Gene list
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Organism: Dictyostelium discoideum AX4, AX4
Number of genes found: 13258
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium discoideum AX4, AX4 | ||||||||
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Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
29C | DDB_G0291255 | similar to DDB_G0278725 contains a predicted signal peptide | DDB0232433 | CDS | 29253 | 555 | - | 0.356757 |
2C | DDB_G0280847 | cyclic AMP-regulated gene underexpressed in gskA-null strain | DDB0232430 | CDS | 3820212 | 297 | - | 0.430976 |
3B-1 | DDB_G0272795 | expressed in prespore cells there is a second copy of this gene | DDB0232429 | CDS | 2321351 | 660 | - | 0.345455 |
3B-2 | DDB_G0274045 | expressed in prespore cells there is a second copy of this gene | DDB0232429 | CDS | 3709694 | 660 | + | 0.345455 |
4cl1 | DDB_G0284831 | catalyzes the reaction ATP 4-coumarate CoA AMP diphosphate 4-coumaroyl-CoA | DDB0232431 | CDS | 2416042 | 1656 | - | 0.316425 |
4cl2 | DDB_G0284745 | catalyzes the reaction ATP 4-coumarate CoA AMP diphosphate 4-coumaroyl-CoA | DDB0232431 | CDS | 2413291 | 1656 | - | 0.31401 |
4cl3 | DDB_G0284743 | catalyzes the reaction ATP 4-coumarate CoA AMP diphosphate 4-coumaroyl-CoA | DDB0232431 | CDS | 2409764 | 1656 | - | 0.307971 |
5NT | DDB_G0287199 | catalyzes the reaction a 5'-ribonucleotide Hsub2subO a ribonucleoside phosphate enriched in prestalk cells | DDB0232431 | CDS | 5397049 | 1737 | - | 0.255037 |
7E | DDB_G0275437 | DDB0232429 | CDS | 5545999 | 294 | + | 0.380952 | |
ChLim | DDB_G0267490 | contains a N-terminal Calponin Homology (CH) domain 3 LIM domains and 4 LIM-related domains (LRDs) | DDB0232428 | CDS | 212712 | 2061 | - | 0.311499 |
D2 | DDB_G0283085 | DDB0232431 | CDS | 276713 | 1608 | + | 0.324627 | |
D7 | DDB_G0284613 | DDB0232431 | CDS | 2275277 | 2553 | - | 0.307873 | |
DB10 | DDB_G0274127 | DDB0232429 | CDS | 3999704 | 1683 | + | 0.272133 | |
DD3-3 | DDB_G0283095 | similar to tunicate proteins involved in O-glycosylation as identified by mRNA differential display | DDB0232431 | CDS | 210212 | 1851 | - | 0.399244 |
DD7-1 | DDB_G0270214 | similar to discoidin I involved in O-glycosylation as identified by mRNA differential display almost identical to its upstream gene | DDB0232428 | CDS | 4418564 | 789 | - | 0.326996 |
DD8-14 | DDB_G0289467 | DDB0232432 | CDS | 2821081 | 1992 | - | 0.317269 | |
DDB_G0267178_RTE | DDB_G0267178 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 1890 | 1398 | + | 0.395565 |
DDB_G0267180_RTE | DDB_G0267180 | ORF1 protein of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 3848 | 1008 | + | 0.365079 |
DDB_G0267182_RTE | DDB_G0267182 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 5505 | 2265 | + | 0.39426 |
DDB_G0267184_RTE | DDB_G0267184 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 8308 | 1215 | - | 0.415638 |
DDB_G0267186_RTE | DDB_G0267186 | ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 9635 | 255 | - | 0.360784 |
DDB_G0267188_RTE | DDB_G0267188 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 10033 | 1971 | + | 0.392187 |
DDB_G0267190_TE | DDB_G0267190 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 12436 | 609 | - | 0.252874 |
DDB_G0267194 | DDB_G0267194 | DDB0232428 | CDS | 17379 | 270 | + | 0.422222 | |
DDB_G0267196 | DDB_G0267196 | DDB0232428 | CDS | 17928 | 372 | + | 0.438172 | |
DDB_G0267198 | DDB_G0267198 | DDB0232428 | CDS | 18497 | 198 | + | 0.439394 | |
DDB_G0267202_TE | DDB_G0267202 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-B refer to AF298202 for full-length consensus element | DDB0232428 | CDS | 20869 | 381 | + | 0.2021 |
DDB_G0267204_ps | DDB_G0267204 | putative pseudogene similar to a family of genes including | DDB0232428 | CDS | 21490 | 408 | + | 0.323529 |
DDB_G0267206_RTE | DDB_G0267206 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 23929 | 2025 | + | 0.391111 |
DDB_G0267208_RTE | DDB_G0267208 | ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 28333 | 588 | + | 0.370748 |
DDB_G0267210_RTE | DDB_G0267210 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 29137 | 2907 | + | 0.396285 |
DDB_G0267212_RTE | DDB_G0267212 | Fused fragments of the DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232432 | CDS | 4280779 | 2064 | + | 0.212209 |
DDB_G0267216 | DDB_G0267216 | DDB0232428 | CDS | 36170 | 498 | - | 0.267068 | |
DDB_G0267218 | DDB_G0267218 | DDB0232428 | CDS | 36858 | 207 | - | 0.256039 | |
DDB_G0267220 | DDB_G0267220 | DDB0232428 | CDS | 37303 | 231 | - | 0.21645 | |
DDB_G0267222 | DDB_G0267222 | DDB0232428 | CDS | 38063 | 480 | - | 0.31875 | |
DDB_G0267224 | DDB_G0267224 | DDB0232428 | CDS | 38714 | 297 | - | 0.360269 | |
DDB_G0267226 | DDB_G0267226 | DDB0232428 | CDS | 39234 | 261 | - | 0.40613 | |
DDB_G0267228_TE | DDB_G0267228 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-B refer to AF298202 for full-length consensus element | DDB0232428 | CDS | 39890 | 2160 | + | 0.215741 |
DDB_G0267230 | DDB_G0267230 | DDB0232428 | CDS | 42193 | 771 | + | 0.341115 | |
DDB_G0267236_RTE | DDB_G0267236 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 46105 | 2265 | - | 0.394702 |
DDB_G0267238_RTE | DDB_G0267238 | ORF1 protein of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 49019 | 1008 | - | 0.367063 |
DDB_G0267240_RTE | DDB_G0267240 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 52425 | 2457 | - | 0.396825 |
DDB_G0267242_RTE | DDB_G0267242 | ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 55333 | 845 | - | 0.377515 |
DDB_G0267244_RTE | DDB_G0267244 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 57242 | 2172 | - | 0.39733 |
DDB_G0267246_RTE | DDB_G0267246 | ORF1 protein of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 60063 | 1008 | - | 0.371032 |
DDB_G0267248_RTE | DDB_G0267248 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 61559 | 663 | - | 0.377074 |
DDB_G0267250_TE | DDB_G0267250 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-B refer to AF298202 for full-length consensus element | DDB0232428 | CDS | 63591 | 2451 | + | 0.221542 |
DDB_G0267252 | DDB_G0267252 | DDB0232428 | CDS | 66189 | 771 | + | 0.341115 | |
DDB_G0267254_ps | DDB_G0267254 | DDB0232428 | CDS | 68992 | 2154 | + | 0.226555 | |
DDB_G0267258_RTE | DDB_G0267258 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 74542 | 2265 | - | 0.392053 |
DDB_G0267260_RTE | DDB_G0267260 | ORF1 protein of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 77456 | 1008 | - | 0.368056 |
DDB_G0267262_RTE | DDB_G0267262 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 79066 | 708 | - | 0.392655 |
DDB_G0267264_RTE | DDB_G0267264 | ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 56374 | 438 | - | 0.363014 |
DDB_G0267270_RTE | DDB_G0267270 | small ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 88569 | 276 | - | 0.355072 |
DDB_G0267272_RTE | DDB_G0267272 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 89316 | 831 | + | 0.373045 |
DDB_G0267274_TE | DDB_G0267274 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 90719 | 1212 | + | 0.224422 |
DDB_G0267278_TE | DDB_G0267278 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 94094 | 543 | - | 0.230203 |
DDB_G0267280_TE | DDB_G0267280 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 94704 | 1284 | - | 0.234424 |
DDB_G0267282_RTE | DDB_G0267282 | ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 97144 | 852 | - | 0.372066 |
DDB_G0267286 | DDB_G0267286 | DDB0232428 | CDS | 100754 | 273 | - | 0.428571 | |
DDB_G0267292_RTE | DDB_G0267292 | ORF1 protein of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 104223 | 1008 | + | 0.373016 |
DDB_G0267294_RTE | DDB_G0267294 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 105880 | 2265 | + | 0.393377 |
DDB_G0267296_RTE | DDB_G0267296 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 108593 | 537 | - | 0.370577 |
DDB_G0267298_TE | DDB_G0267298 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 109429 | 417 | - | 0.232614 |
DDB_G0267300_RTE | DDB_G0267300 | ORF1ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 110783 | 2022 | + | 0.395648 |
DDB_G0267302_TE | DDB_G0267302 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 113142 | 183 | - | 0.289617 |
DDB_G0267304_RTE | DDB_G0267304 | ORF3 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 114394 | 2502 | + | 0.392486 |
DDB_G0267306_RTE | DDB_G0267306 | long terminal repeat retrotransposon Skipper GAG-PRO-POL refer to GenBank AF049230 for full length consensus element | DDB0232428 | CDS | 117148 | 3462 | - | 0.317735 |
DDB_G0267308_RTE | DDB_G0267308 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232428 | CDS | 121433 | 411 | - | 0.40146 |
DDB_G0267310_RTE | DDB_G0267310 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232428 | CDS | 121880 | 519 | - | 0.377649 |
DDB_G0267314_RTE | DDB_G0267314 | fused fragments of the DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 123714 | 951 | - | 0.38591 |
DDB_G0267322_RTE | DDB_G0267322 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 127571 | 516 | - | 0.389535 |
DDB_G0267324_RTE | DDB_G0267324 | ORF1 protein of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 128570 | 1008 | + | 0.371032 |
DDB_G0267326_RTE | DDB_G0267326 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 129934 | 2457 | + | 0.400488 |
DDB_G0267328_RTE | DDB_G0267328 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 132940 | 1719 | - | 0.397324 |
DDB_G0267330_RTE | DDB_G0267330 | ORF1 protein of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 135308 | 1005 | - | 0.369154 |
DDB_G0267332 | DDB_G0267332 | DDB0232428 | CDS | 137038 | 531 | - | 0.438795 | |
DDB_G0267334_RTE | DDB_G0267334 | ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 139298 | 468 | + | 0.354701 |
DDB_G0267336_TE | DDB_G0267336 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-B refer to AF298202 for full-length consensus element | DDB0232428 | CDS | 142027 | 789 | - | 0.311787 |
DDB_G0267338_RTE | DDB_G0267338 | ORF3 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 138334 | 486 | - | 0.374486 |
DDB_G0267342_RTE | DDB_G0267342 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 145444 | 2778 | + | 0.397768 |
DDB_G0267344 | DDB_G0267344 | DDB0232428 | CDS | 149314 | 1011 | + | 0.440158 | |
DDB_G0267346 | DDB_G0267346 | DDB0232428 | CDS | 151286 | 621 | + | 0.436393 | |
DDB_G0267348_TE | DDB_G0267348 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 153529 | 606 | - | 0.234323 |
DDB_G0267350_TE | DDB_G0267350 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 154265 | 546 | - | 0.203297 |
DDB_G0267352_TE | DDB_G0267352 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 158583 | 2442 | + | 0.223178 |
DDB_G0267354_TE | DDB_G0267354 | ORF2 (contains 2 introns) encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 161143 | 663 | + | 0.295626 |
DDB_G0267356_RTE | DDB_G0267356 | long terminal repeat retrotransposon Skipper GAG-PRO-POL refer to GenBank AF049230 for full length consensus element | DDB0232428 | CDS | 162941 | 3969 | - | 0.323507 |
DDB_G0267358_RTE | DDB_G0267358 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232428 | CDS | 167225 | 1149 | - | 0.389034 |
DDB_G0267362_RTE | DDB_G0267362 | long terminal repeat retrotransposon Skipper GAG-PRO-POL refer to GenBank AF049230 for full length consensus element | DDB0232428 | CDS | 169365 | 4008 | - | 0.320858 |
DDB_G0267364_RTE | DDB_G0267364 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232428 | CDS | 173832 | 441 | - | 0.396825 |
DDB_G0267366_RTE | DDB_G0267366 | long terminal repeat retrotransposon Skipper GAG-PRO-POL refer to GenBank AF049230 for full length consensus element | DDB0232428 | CDS | 186996 | 3276 | - | 0.336081 |
DDB_G0267370_TE | DDB_G0267370 | ORF2 (contains 2 introns) encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 191815 | 573 | - | 0.315881 |
DDB_G0267372_RTE | DDB_G0267372 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 193516 | 644 | + | 0.281056 |
DDB_G0267434 | DDB_G0267434 | DDB0232428 | CDS | 1260113 | 2460 | + | 0.116667 | |
DDB_G0267448 | DDB_G0267448 | DDB0232428 | CDS | 481685 | 1146 | - | 0.286213 | |
DDB_G0267458 | DDB_G0267458 | DDB0232428 | CDS | 201217 | 2037 | + | 0.340697 | |
DDB_G0267482 | DDB_G0267482 | DDB0232428 | CDS | 206837 | 240 | + | 0.2875 | |
DDB_G0267486 | DDB_G0267486 | DDB0232428 | CDS | 208945 | 480 | - | 0.26875 | |
DDB_G0267488 | DDB_G0267488 | DDB0232428 | CDS | 210356 | 2040 | + | 0.269118 | |
DDB_G0267492 | DDB_G0267492 | putative metalloprotease of the peptidase M41 family which belong to a larger family of zinc metalloproteases includes the cell division protein FtsH | DDB0232428 | CDS | 215251 | 2163 | - | 0.314378 |
DDB_G0267494 | DDB_G0267494 | DDB0232428 | CDS | 217763 | 603 | + | 0.228856 | |
DDB_G0267496 | DDB_G0267496 | DDB0232428 | CDS | 218913 | 6837 | + | 0.320608 | |
DDB_G0267500 | DDB_G0267500 | DDB0232428 | CDS | 227165 | 1059 | - | 0.334278 | |
DDB_G0267502 | DDB_G0267502 | DDB0232428 | CDS | 236992 | 1419 | - | 0.306554 | |
DDB_G0267504 | DDB_G0267504 | DDB0232428 | CDS | 245416 | 1467 | - | 0.327198 | |
DDB_G0267508 | DDB_G0267508 | DDB0232428 | CDS | 254497 | 294 | - | 0.357143 | |
DDB_G0267510 | DDB_G0267510 | similar to coiled-coil domain containing protein 43 (CCDC43) contains two predicted coiled-coil domains | DDB0232428 | CDS | 256535 | 669 | - | 0.234679 |
DDB_G0267512 | DDB_G0267512 | DDB0232428 | CDS | 257711 | 1011 | - | 0.338279 | |
DDB_G0267514 | DDB_G0267514 | DDB0232428 | CDS | 259066 | 2751 | - | 0.28426 | |
DDB_G0267522 | DDB_G0267522 | DDB0232428 | CDS | 269690 | 2082 | - | 0.231508 | |
DDB_G0267526 | DDB_G0267526 | DDB0232428 | CDS | 272779 | 981 | + | 0.282365 | |
DDB_G0267528 | DDB_G0267528 | DDB0232428 | CDS | 274124 | 1038 | - | 0.350674 | |
DDB_G0267530 | DDB_G0267530 | DDB0232428 | CDS | 276695 | 633 | + | 0.375987 | |
DDB_G0267532 | DDB_G0267532 | DDB0232428 | CDS | 283495 | 2658 | + | 0.256584 | |
DDB_G0267534 | DDB_G0267534 | DDB0232428 | CDS | 288484 | 819 | - | 0.297924 | |
DDB_G0267538 | DDB_G0267538 | DDB0232428 | CDS | 291771 | 1824 | + | 0.313596 | |
DDB_G0267542 | DDB_G0267542 | DDB0232428 | CDS | 303809 | 228 | + | 0.201754 | |
DDB_G0267546 | DDB_G0267546 | DDB0232428 | CDS | 311255 | 1014 | + | 0.301775 | |
DDB_G0267550 | DDB_G0267550 | DDB0232428 | CDS | 323194 | 1404 | + | 0.230057 | |
DDB_G0267552 | DDB_G0267552 | DDB0232428 | CDS | 324845 | 300 | - | 0.36 | |
DDB_G0267554 | DDB_G0267554 | DDB0232428 | CDS | 325873 | 966 | + | 0.233954 | |
DDB_G0267556 | DDB_G0267556 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232428 | CDS | 327145 | 3480 | - | 0.281034 |
DDB_G0267562 | DDB_G0267562 | DDB0232428 | CDS | 339546 | 1674 | + | 0.263441 | |
DDB_G0267564 | DDB_G0267564 | similar to D. purpureum protein contains a predicted signal anchor sequence | DDB0232428 | CDS | 341837 | 1563 | + | 0.274472 |
DDB_G0267566 | DDB_G0267566 | putative protein serinethreonine kinase contains an ankyrin repeat domain similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232428 | CDS | 343868 | 2535 | - | 0.244181 |
DDB_G0267570 | DDB_G0267570 | DDB0232428 | CDS | 358932 | 1785 | - | 0.301961 | |
DDB_G0267572 | DDB_G0267572 | DDB0232428 | CDS | 361555 | 1290 | - | 0.249612 | |
DDB_G0267574 | DDB_G0267574 | DDB0232428 | CDS | 365942 | 678 | + | 0.294985 | |
DDB_G0267576 | DDB_G0267576 | DDB0232428 | CDS | 366936 | 447 | + | 0.201342 | |
DDB_G0267578 | DDB_G0267578 | DDB0232428 | CDS | 368155 | 591 | + | 0.252115 | |
DDB_G0267580 | DDB_G0267580 | DDB0232428 | CDS | 369407 | 600 | + | 0.24 | |
DDB_G0267582 | DDB_G0267582 | DDB0232428 | CDS | 371018 | 1479 | + | 0.313049 | |
DDB_G0267586 | DDB_G0267586 | DDB0232428 | CDS | 375348 | 1389 | + | 0.267099 | |
DDB_G0267590 | DDB_G0267590 | DDB0232428 | CDS | 381029 | 1386 | - | 0.3557 | |
DDB_G0267592 | DDB_G0267592 | DDB0232428 | CDS | 383616 | 1596 | + | 0.309524 | |
DDB_G0267596 | DDB_G0267596 | DDB0232428 | CDS | 390446 | 5139 | - | 0.246546 | |
DDB_G0267598 | DDB_G0267598 | DDB0232428 | CDS | 395715 | 1224 | - | 0.254085 | |
DDB_G0267600 | DDB_G0267600 | similar to HIBCH might have 3-hydroxyisobutyryl-Coenzyme A hydrolase activity | DDB0232428 | CDS | 398417 | 1020 | - | 0.233333 |
DDB_G0267602 | DDB_G0267602 | DDB0232428 | CDS | 400350 | 5424 | - | 0.261799 | |
DDB_G0267608 | DDB_G0267608 | DDB0232428 | CDS | 409670 | 672 | - | 0.251488 | |
DDB_G0267610 | DDB_G0267610 | there is a paralog of this gene | DDB0232428 | CDS | 411512 | 924 | - | 0.24026 |
DDB_G0267612 | DDB_G0267612 | DDB0232428 | CDS | 413651 | 630 | + | 0.28254 | |
DDB_G0267614 | DDB_G0267614 | DDB0232428 | CDS | 420108 | 1080 | - | 0.262037 | |
DDB_G0267616 | DDB_G0267616 | DDB0232428 | CDS | 427853 | 2247 | + | 0.303961 | |
DDB_G0267618_ps | DDB_G0267618 | putative pseudogene fragment similar to D. discoideum gene | DDB0232428 | CDS | 433828 | 1326 | + | 0.19457 |
DDB_G0267620 | DDB_G0267620 | DDB0232428 | CDS | 436026 | 1329 | - | 0.273138 | |
DDB_G0267624 | DDB_G0267624 | DDB0232428 | CDS | 439137 | 1515 | + | 0.307591 | |
DDB_G0267632 | DDB_G0267632 | DDB0232428 | CDS | 445092 | 1230 | - | 0.202439 | |
DDB_G0267634 | DDB_G0267634 | DDB0232428 | CDS | 448892 | 2901 | + | 0.110307 | |
DDB_G0267638 | DDB_G0267638 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232428 | CDS | 464992 | 9210 | + | 0.282953 |
DDB_G0267642 | DDB_G0267642 | DDB0232428 | CDS | 484012 | 1419 | + | 0.200846 | |
DDB_G0267644 | DDB_G0267644 | DDB0232428 | CDS | 488923 | 1092 | - | 0.252747 | |
DDB_G0267648 | DDB_G0267648 | DDB0232428 | CDS | 491895 | 2772 | + | 0.234848 | |
DDB_G0267658 | DDB_G0267658 | DDB0232428 | CDS | 523164 | 3042 | + | 0.214661 | |
DDB_G0267660 | DDB_G0267660 | DDB0232428 | CDS | 526607 | 1011 | - | 0.167161 | |
DDB_G0267662 | DDB_G0267662 | DDB0232428 | CDS | 527773 | 1005 | + | 0.232836 | |
DDB_G0267670 | DDB_G0267670 | DDB0232428 | CDS | 537622 | 738 | - | 0.268293 | |
DDB_G0267672 | DDB_G0267672 | DDB0232428 | CDS | 539176 | 2058 | + | 0.212828 | |
DDB_G0267676 | DDB_G0267676 | DDB0232428 | CDS | 548246 | 1986 | - | 0.205942 | |
DDB_G0267680 | DDB_G0267680 | DDB0232428 | CDS | 557566 | 480 | + | 0.28125 | |
DDB_G0267684 | DDB_G0267684 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D | DDB0232428 | CDS | 561516 | 2295 | + | 0.266667 |
DDB_G0267686 | DDB_G0267686 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats contains an RGS (Regulator of G protein Signaling) domain | DDB0232428 | CDS | 564277 | 6693 | - | 0.276109 |
DDB_G0267692 | DDB_G0267692 | DDB0232428 | CDS | 600250 | 3549 | + | 0.272189 | |
DDB_G0267694 | DDB_G0267694 | DDB0232428 | CDS | 611485 | 1704 | - | 0.198357 | |
DDB_G0267696 | DDB_G0267696 | DDB0232428 | CDS | 622339 | 471 | - | 0.199575 | |
DDB_G0267698 | DDB_G0267698 | DDB0232428 | CDS | 623530 | 372 | - | 0.284946 | |
DDB_G0267700 | DDB_G0267700 | DDB0232428 | CDS | 624602 | 1083 | - | 0.174515 | |
DDB_G0267702 | DDB_G0267702 | DDB0232428 | CDS | 625985 | 846 | - | 0.193853 | |
DDB_G0267706 | DDB_G0267706 | DDB0232428 | CDS | 670002 | 756 | + | 0.232804 | |
DDB_G0267710 | DDB_G0267710 | DDB0232428 | CDS | 673242 | 1656 | + | 0.332126 | |
DDB_G0267712 | DDB_G0267712 | DDB0232428 | CDS | 675419 | 438 | + | 0.33105 | |
DDB_G0267716 | DDB_G0267716 | DDB0232428 | CDS | 678047 | 1530 | - | 0.213725 | |
DDB_G0267718 | DDB_G0267718 | DDB0232428 | CDS | 695658 | 1779 | + | 0.271501 | |
DDB_G0267720 | DDB_G0267720 | DDB0232428 | CDS | 698211 | 1053 | + | 0.298196 | |
DDB_G0267722 | DDB_G0267722 | DDB0232428 | CDS | 699431 | 690 | - | 0.276812 | |
DDB_G0267724 | DDB_G0267724 | DDB0232428 | CDS | 700627 | 2730 | + | 0.182784 | |
DDB_G0267732 | DDB_G0267732 | DDB0232428 | CDS | 723287 | 6147 | - | 0.252969 | |
DDB_G0267734 | DDB_G0267734 | contains a SAM (and some other nucleotide) binding motif similar to bacterial and eukaryotic methyltransferases | DDB0232428 | CDS | 730241 | 873 | + | 0.358534 |
DDB_G0267736_RTE | DDB_G0267736 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232428 | CDS | 734616 | 684 | - | 0.375731 |
DDB_G0267740 | DDB_G0267740 | DDB0232428 | CDS | 746953 | 2616 | - | 0.177752 | |
DDB_G0267742 | DDB_G0267742 | similar to the Dictyostelium hydrolase Apeh the conserved acylamino-acid-releasing enzyme | DDB0232428 | CDS | 764516 | 2334 | + | 0.215081 |
DDB_G0267744 | DDB_G0267744 | DDB0232428 | CDS | 767152 | 1290 | - | 0.24031 | |
DDB_G0267746 | DDB_G0267746 | DDB0232428 | CDS | 774330 | 1608 | + | 0.265547 | |
DDB_G0267750 | DDB_G0267750 | DDB0232428 | CDS | 780178 | 2937 | + | 0.208716 | |
DDB_G0267752 | DDB_G0267752 | DDB0232428 | CDS | 783552 | 2325 | + | 0.231828 | |
DDB_G0267754 | DDB_G0267754 | DDB0232428 | CDS | 786322 | 1389 | - | 0.24982 | |
DDB_G0267756 | DDB_G0267756 | DDB0232428 | CDS | 788307 | 546 | - | 0.254579 | |
DDB_G0267758 | DDB_G0267758 | DDB0232428 | CDS | 789209 | 2637 | - | 0.252939 | |
DDB_G0267762 | DDB_G0267762 | DDB0232428 | CDS | 795721 | 1635 | - | 0.200612 | |
DDB_G0267764 | DDB_G0267764 | DDB0232428 | CDS | 799346 | 1227 | - | 0.220864 | |
DDB_G0267768 | DDB_G0267768 | widely conserved protein very similar to M. musculus Myg1 (melanocyte proliferating gene 1) | DDB0232428 | CDS | 809267 | 990 | + | 0.282828 |
DDB_G0267770 | DDB_G0267770 | DDB0232428 | CDS | 820114 | 1593 | + | 0.214689 | |
DDB_G0267772 | DDB_G0267772 | DDB0232428 | CDS | 824718 | 237 | + | 0.198312 | |
DDB_G0267776 | DDB_G0267776 | DDB0232428 | CDS | 827764 | 4281 | - | 0.328662 | |
DDB_G0267778_RTE | DDB_G0267778 | DDB0232428 | CDS | 835920 | 873 | + | 0.295533 | |
DDB_G0267780_RTE | DDB_G0267780 | DDB0232428 | CDS | 836942 | 3294 | + | 0.334244 | |
DDB_G0267784 | DDB_G0267784 | DDB0232428 | CDS | 849532 | 1764 | - | 0.234127 | |
DDB_G0267786 | DDB_G0267786 | weakly similar to niban protein a marker for renal carcinogenesisbr bCommunity annotation:b DDB_G0267786 appears to be cell-cycle regulated expressed in late G2 at the same time when virtually all S-phase and M-phase specific genes are active (see graph on wiki page). The gene is slightly overexpressed in the rblA disruptant (15-fold) but appears primarily regulated by at present unknown Rb-independent mechanisms. No ortholog of DDB_G0267786 is recognizable in yeast. Harry MacWilliams August 2010br | DDB0232428 | CDS | 852021 | 1587 | - | 0.332073 |
DDB_G0267788 | DDB_G0267788 | DDB0232428 | CDS | 854978 | 840 | - | 0.277381 | |
DDB_G0267790 | DDB_G0267790 | DDB0232428 | CDS | 857737 | 363 | + | 0.272727 | |
DDB_G0267792 | DDB_G0267792 | DDB0232428 | CDS | 858290 | 1380 | - | 0.221014 | |
DDB_G0267794 | DDB_G0267794 | DDB0232428 | CDS | 860671 | 1923 | - | 0.314613 | |
DDB_G0267796 | DDB_G0267796 | conserved protein similar to yeast CWC22 an essential putative spliceosomal component | DDB0232428 | CDS | 863148 | 2778 | + | 0.321814 |
DDB_G0267798 | DDB_G0267798 | DDB0232428 | CDS | 877260 | 3168 | + | 0.216225 | |
DDB_G0267800 | DDB_G0267800 | DDB0232428 | CDS | 889672 | 1866 | + | 0.245981 | |
DDB_G0267802 | DDB_G0267802 | DDB0232428 | CDS | 897809 | 156 | - | 0.275641 | |
DDB_G0267804 | DDB_G0267804 | DDB0232428 | CDS | 899153 | 2970 | + | 0.259933 | |
DDB_G0267808 | DDB_G0267808 | DDB0232428 | CDS | 903471 | 1998 | + | 0.269269 | |
DDB_G0267810 | DDB_G0267810 | DDB0232428 | CDS | 905813 | 2313 | - | 0.236922 | |
DDB_G0267812 | DDB_G0267812 | DDB0232428 | CDS | 909280 | 810 | + | 0.18642 | |
DDB_G0267814 | DDB_G0267814 | DDB0232428 | CDS | 910680 | 1605 | + | 0.274766 | |
DDB_G0267816 | DDB_G0267816 | DDB0232428 | CDS | 913536 | 1077 | + | 0.208914 | |
DDB_G0267818 | DDB_G0267818 | DDB0232428 | CDS | 914771 | 3783 | - | 0.244251 | |
DDB_G0267820 | DDB_G0267820 | DDB0232428 | CDS | 919584 | 1098 | - | 0.224954 | |
DDB_G0267822 | DDB_G0267822 | DDB0232428 | CDS | 920878 | 1098 | + | 0.284153 | |
DDB_G0267824 | DDB_G0267824 | DDB0232428 | CDS | 922136 | 1509 | - | 0.266402 | |
DDB_G0267826 | DDB_G0267826 | DDB0232428 | CDS | 924216 | 1572 | - | 0.211196 | |
DDB_G0267828 | DDB_G0267828 | DDB0232428 | CDS | 926752 | 2484 | + | 0.271739 | |
DDB_G0267832 | DDB_G0267832 | DDB0232428 | CDS | 932664 | 1998 | - | 0.211211 | |
DDB_G0267834 | DDB_G0267834 | DDB0232428 | CDS | 939089 | 1353 | + | 0.266075 | |
DDB_G0267836 | DDB_G0267836 | DDB0232428 | CDS | 940974 | 1695 | + | 0.234218 | |
DDB_G0267838 | DDB_G0267838 | DDB0232428 | CDS | 949001 | 645 | + | 0.251163 | |
DDB_G0267840 | DDB_G0267840 | DDB0232428 | CDS | 954390 | 4299 | + | 0.229588 | |
DDB_G0267842 | DDB_G0267842 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232428 | CDS | 959377 | 921 | + | 0.327904 |
DDB_G0267848 | DDB_G0267848 | DDB0232428 | CDS | 964384 | 999 | + | 0.301301 | |
DDB_G0267850 | DDB_G0267850 | DDB0232428 | CDS | 965758 | 1857 | + | 0.310716 | |
DDB_G0267852 | DDB_G0267852 | the Maf protein is a putative inhibitor of septum formation found in eukaryotes bacteria and archaea | DDB0232428 | CDS | 968117 | 651 | - | 0.262673 |
DDB_G0267856 | DDB_G0267856 | DDB0232428 | CDS | 974099 | 2493 | + | 0.231047 | |
DDB_G0267858 | DDB_G0267858 | DDB0232428 | CDS | 977722 | 2496 | + | 0.227163 | |
DDB_G0267860 | DDB_G0267860 | DDB0232428 | CDS | 983481 | 642 | - | 0.158879 | |
DDB_G0267862 | DDB_G0267862 | DDB0232428 | CDS | 984537 | 870 | + | 0.187356 | |
DDB_G0267864 | DDB_G0267864 | DDB0232428 | CDS | 985707 | 951 | - | 0.179811 | |
DDB_G0267866 | DDB_G0267866 | putative ortholog of H. sapiens POMP similar to S. cerevisiae UMP1 involved in maturation of the 20S proteasome | DDB0232428 | CDS | 991453 | 387 | - | 0.276486 |
DDB_G0267868 | DDB_G0267868 | DDB0232428 | CDS | 992499 | 1971 | - | 0.278031 | |
DDB_G0267872 | DDB_G0267872 | conserved protein containing a Suneukaryotic nucleolar NOL1Nop2p domain | DDB0232428 | CDS | 1012281 | 2043 | - | 0.22467 |
DDB_G0267874 | DDB_G0267874 | DDB0232428 | CDS | 1016994 | 1953 | + | 0.269329 | |
DDB_G0267876 | DDB_G0267876 | similar to D. purpureum protein contains one coiled-coil domain | DDB0232428 | CDS | 1024145 | 558 | - | 0.197133 |
DDB_G0267878 | DDB_G0267878 | DDB0232428 | CDS | 1025189 | 2850 | + | 0.208421 | |
DDB_G0267880 | DDB_G0267880 | similar to bacterial and fungal acetyltransferases member of the GNAT family | DDB0232428 | CDS | 1028328 | 570 | + | 0.233333 |
DDB_G0267882 | DDB_G0267882 | DDB0232428 | CDS | 1029261 | 1614 | - | 0.298637 | |
DDB_G0267886 | DDB_G0267886 | DDB0232428 | CDS | 1036314 | 1692 | - | 0.264184 | |
DDB_G0267888 | DDB_G0267888 | DDB0232428 | CDS | 1038511 | 3495 | - | 0.228612 | |
DDB_G0267890 | DDB_G0267890 | DDB0232428 | CDS | 1042896 | 1242 | - | 0.278583 | |
DDB_G0267892 | DDB_G0267892 | DDB0232428 | CDS | 1045342 | 2577 | - | 0.216531 | |
DDB_G0267894 | DDB_G0267894 | DDB0232428 | CDS | 1051356 | 675 | - | 0.300741 | |
DDB_G0267896 | DDB_G0267896 | DDB0232428 | CDS | 1052627 | 627 | - | 0.272727 | |
DDB_G0267898 | DDB_G0267898 | contains two EGF (epidermal growth factor) repeats expressed in pstAB cells | DDB0232428 | CDS | 1053842 | 1308 | - | 0.287462 |
DDB_G0267902 | DDB_G0267902 | DDB0232428 | CDS | 1071888 | 2535 | + | 0.222091 | |
DDB_G0267904 | DDB_G0267904 | putative ortholog of Xenopus AND-1 (Acidic Nucleoplasmic DNA-binding protein 1) that participates in loading the MCM2-7 helicase complex at the initiation of DNA replication brbr bCommunity annotation:b DDB G0267904 is a wd-repeat protein with moderate similarity to AND-1 also known as CTF4 a wd40 and HMG-box containing protein originally discovered in Xenopus. (see Franke et al AND-1 a natural chimeric DNA-binding protein combines an HMG-box with regulatory WD-repeats.Journal of Cell Science 110 1051-1062) AND-1CTF4 participates in loading the MCM2-7 helicase complex at the initiation of DNA replication (see Zhu et al Genes and Development 21 2288-2299 (2007) also Tanaka et al Genes to Cells 14 807-20 (2009). Recent work suggests that AND-1CTF4 links sister chromatid cohesion with DNA replication(see Tanaka et al Genes to Cells 14 991-1001 (2009).br DDB G0267904 is overexpressed 12-fold [1299 hits to 99 p1e-210] in a Dicty strain lacking the retinoblastoma-like gene rblA. Most genes a | DDB0232428 | CDS | 1077141 | 3267 | - | 0.285277 |
DDB_G0267906 | DDB_G0267906 | related to the Ovarian Tumour (OTU) gene of Drosophila function is unknown but conserved cysteine and histidine and possibly the aspartate residues suggests that those not yet recognized as peptidases could possess cysteine protease activity | DDB0232428 | CDS | 1080926 | 1317 | - | 0.277904 |
DDB_G0267908 | DDB_G0267908 | DDB0232428 | CDS | 1083269 | 300 | + | 0.256667 | |
DDB_G0267910 | DDB_G0267910 | DDB0232428 | CDS | 1106720 | 1614 | - | 0.223048 | |
DDB_G0267914 | DDB_G0267914 | DDB0232428 | CDS | 1112700 | 1554 | - | 0.250322 | |
DDB_G0267918 | DDB_G0267918 | DDB0232428 | CDS | 1118591 | 2514 | + | 0.222355 | |
DDB_G0267920 | DDB_G0267920 | DDB0232428 | CDS | 1121667 | 372 | + | 0.233871 | |
DDB_G0267922_ps | DDB_G0267922 | putative pseudogene fragment similar to gene | DDB0232428 | CDS | 1125084 | 273 | - | 0.223443 |
DDB_G0267924 | DDB_G0267924 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | DDB0232428 | CDS | 1128799 | 3330 | + | 0.331231 |
DDB_G0267930 | DDB_G0267930 | underexpressed in | DDB0232428 | CDS | 1143814 | 252 | + | 0.301587 |
DDB_G0267932 | DDB_G0267932 | DDB0232428 | CDS | 1145056 | 156 | + | 0.237179 | |
DDB_G0267936 | DDB_G0267936 | highly similar to neighboring genes | DDB0232428 | CDS | 1152289 | 246 | + | 0.345528 |
DDB_G0267938 | DDB_G0267938 | DDB0232428 | CDS | 1153178 | 3546 | + | 0.219966 | |
DDB_G0267940 | DDB_G0267940 | DDB0232428 | CDS | 1159902 | 1620 | + | 0.212346 | |
DDB_G0267942 | DDB_G0267942 | DDB0232428 | CDS | 1161933 | 2697 | - | 0.288469 | |
DDB_G0267946 | DDB_G0267946 | DDB0232428 | CDS | 1167122 | 195 | + | 0.384615 | |
DDB_G0267952 | DDB_G0267952 | DDB0232428 | CDS | 1173990 | 831 | - | 0.247894 | |
DDB_G0267954 | DDB_G0267954 | contains a C-terminal Bicoid-interacting 3 domain which occurs in methyltransferases that modify RNA-binding proteins has similarity to mammalian 7SK snRNA methylphosphate capping enzyme | DDB0232428 | CDS | 1175758 | 1302 | + | 0.195853 |
DDB_G0267958 | DDB_G0267958 | DDB0232428 | CDS | 1179370 | 2190 | + | 0.305479 | |
DDB_G0267964 | DDB_G0267964 | DDB0232428 | CDS | 1199077 | 378 | - | 0.238095 | |
DDB_G0267968 | DDB_G0267968 | DDB0232428 | CDS | 1207158 | 1698 | + | 0.207303 | |
DDB_G0267970 | DDB_G0267970 | DDB0232428 | CDS | 1209177 | 162 | - | 0.290123 | |
DDB_G0267974 | DDB_G0267974 | DDB0232428 | CDS | 1214003 | 2865 | - | 0.264223 | |
DDB_G0267984 | DDB_G0267984 | conserved peptidase M20 family zinc metallopeptidases which are glutamate carboxypeptidases contains peptidase dimerization domain | DDB0232428 | CDS | 1236115 | 1560 | - | 0.287179 |
DDB_G0267986 | DDB_G0267986 | DDB0232428 | CDS | 1238363 | 1875 | + | 0.212267 | |
DDB_G0267988 | DDB_G0267988 | DDB0232428 | CDS | 1240356 | 999 | - | 0.2002 | |
DDB_G0267992 | DDB_G0267992 | DDB0232428 | CDS | 1244589 | 789 | - | 0.309252 | |
DDB_G0267994 | DDB_G0267994 | DDB0232428 | CDS | 1246116 | 1227 | - | 0.326813 | |
DDB_G0267996 | DDB_G0267996 | DDB0232428 | CDS | 1248279 | 1230 | + | 0.286992 | |
DDB_G0268002_ps | DDB_G0268002 | putative pseudogene very similar to Dictyostelium PA14 domain-containing proteins | DDB0232428 | CDS | 1279173 | 666 | - | 0.276276 |
DDB_G0268006 | DDB_G0268006 | DDB0232428 | CDS | 1288689 | 435 | - | 0.287356 | |
DDB_G0268008 | DDB_G0268008 | DDB0232428 | CDS | 1290599 | 1296 | - | 0.26929 | |
DDB_G0268010 | DDB_G0268010 | DDB0232428 | CDS | 1301596 | 753 | + | 0.203187 | |
DDB_G0268012 | DDB_G0268012 | DDB0232428 | CDS | 1302705 | 1149 | - | 0.191471 | |
DDB_G0268016 | DDB_G0268016 | DDB0232428 | CDS | 1313476 | 237 | - | 0.236287 | |
DDB_G0268018 | DDB_G0268018 | DDB0232428 | CDS | 1314808 | 1596 | + | 0.280702 | |
DDB_G0268022 | DDB_G0268022 | DDB0232428 | CDS | 1318763 | 522 | - | 0.229885 | |
DDB_G0268026 | DDB_G0268026 | contains 4 putative transmembrane domains similar to D. purpureum protein | DDB0232428 | CDS | 1322688 | 669 | - | 0.303438 |
DDB_G0268028 | DDB_G0268028 | DDB0232428 | CDS | 1325279 | 2322 | - | 0.341085 | |
DDB_G0268030 | DDB_G0268030 | DDB0232428 | CDS | 1334449 | 3666 | - | 0.27114 | |
DDB_G0268034 | DDB_G0268034 | homolog of mammalian Rab GDP dissociation inhibitor alpha forms a soluble complex with Rab proteins thereby preventing exchange of GDP for GTP | DDB0232428 | CDS | 1340557 | 1365 | + | 0.347985 |
DDB_G0268036 | DDB_G0268036 | bifunctional enolase-phosphatase that cleaves the substrates 23-diketo-5-methylthio-1-phosphopentane and 2-hydroxy-3-keto-5-methylthio-1-phosphopentene | DDB0232428 | CDS | 1342458 | 804 | + | 0.288557 |
DDB_G0268040 | DDB_G0268040 | DDB0232428 | CDS | 1345125 | 996 | + | 0.248996 | |
DDB_G0268042 | DDB_G0268042 | DDB0232428 | CDS | 1346481 | 591 | - | 0.34687 | |
DDB_G0268044 | DDB_G0268044 | DDB0232428 | CDS | 1347890 | 3717 | - | 0.308313 | |
DDB_G0268046 | DDB_G0268046 | DDB0232428 | CDS | 1352853 | 138 | + | 0.34058 | |
DDB_G0268048 | DDB_G0268048 | DDB0232428 | CDS | 1353351 | 579 | - | 0.248705 | |
DDB_G0268050 | DDB_G0268050 | DDB0232428 | CDS | 1354807 | 723 | - | 0.215768 | |
DDB_G0268052 | DDB_G0268052 | DDB0232428 | CDS | 1359896 | 3105 | - | 0.298873 | |
DDB_G0268054 | DDB_G0268054 | DDB0232428 | CDS | 1365318 | 360 | - | 0.188889 | |
DDB_G0268060 | DDB_G0268060 | DDB0232428 | CDS | 1380972 | 2445 | - | 0.312883 | |
DDB_G0268062 | DDB_G0268062 | DDB0232428 | CDS | 1391482 | 1761 | + | 0.21749 | |
DDB_G0268064 | DDB_G0268064 | DDB0232428 | CDS | 1393387 | 669 | - | 0.281016 | |
DDB_G0268066 | DDB_G0268066 | DDB0232428 | CDS | 1394864 | 2595 | + | 0.210019 | |
DDB_G0268070 | DDB_G0268070 | DDB0232428 | CDS | 1399546 | 1434 | - | 0.235704 | |
DDB_G0268072 | DDB_G0268072 | DDB0232428 | CDS | 1404967 | 2187 | + | 0.196616 | |
DDB_G0268074 | DDB_G0268074 | DDB0232428 | CDS | 1408319 | 2991 | - | 0.251755 | |
DDB_G0268076 | DDB_G0268076 | DDB0232428 | CDS | 1414125 | 1131 | - | 0.329797 | |
DDB_G0268078 | DDB_G0268078 | DDB0232428 | CDS | 1417972 | 1524 | + | 0.281496 | |
DDB_G0268082 | DDB_G0268082 | DDB0232428 | CDS | 1428341 | 294 | + | 0.289116 | |
DDB_G0268086 | DDB_G0268086 | DDB0232428 | CDS | 1432461 | 186 | + | 0.193548 | |
DDB_G0268090 | DDB_G0268090 | underexpressed in | DDB0232428 | CDS | 1440159 | 783 | - | 0.315453 |
DDB_G0268092 | DDB_G0268092 | similar to human Zinc finger SWIM domain-containing protein 7 a regulator of homologous recombination in eukaryotic cells | DDB0232428 | CDS | 1445229 | 471 | - | 0.254777 |
DDB_G0268094 | DDB_G0268094 | DDB0232428 | CDS | 1446577 | 1149 | + | 0.227154 | |
DDB_G0268096 | DDB_G0268096 | DDB0232428 | CDS | 1448032 | 1554 | - | 0.22973 | |
DDB_G0268102 | DDB_G0268102 | DDB0232428 | CDS | 1455102 | 5586 | + | 0.264232 | |
DDB_G0268106 | DDB_G0268106 | DDB0232428 | CDS | 1463479 | 387 | - | 0.21447 | |
DDB_G0268108 | DDB_G0268108 | DDB0232428 | CDS | 1465335 | 675 | + | 0.285926 | |
DDB_G0268110 | DDB_G0268110 | DDB0232428 | CDS | 1466318 | 1545 | - | 0.241424 | |
DDB_G0268112 | DDB_G0268112 | DDB0232428 | CDS | 1468365 | 600 | + | 0.216667 | |
DDB_G0268114 | DDB_G0268114 | DDB0232428 | CDS | 1473867 | 417 | + | 0.294964 | |
DDB_G0268116 | DDB_G0268116 | similarity to Xenopus F8A1 protein human Factor VIII intron 22 protein | DDB0232428 | CDS | 1479679 | 1113 | - | 0.238095 |
DDB_G0268118 | DDB_G0268118 | DDB0232428 | CDS | 1481369 | 2298 | + | 0.302437 | |
DDB_G0268120_ps | DDB_G0268120 | putative pseudogene similar to | DDB0232428 | CDS | 1483803 | 273 | - | 0.300366 |
DDB_G0268122 | DDB_G0268122 | DDB0232428 | CDS | 1487041 | 501 | - | 0.295409 | |
DDB_G0268124_ps | DDB_G0268124 | putative pseudogene similar to | DDB0232428 | CDS | 1488450 | 708 | - | 0.30791 |
DDB_G0268126 | DDB_G0268126 | ortholog of human HPS4 mutations in human HPS4 have been linked to Hermansky-Pudlak syndrome 4 | DDB0232428 | CDS | 1489512 | 1653 | - | 0.249244 |
DDB_G0268128_RTE | DDB_G0268128 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1507711 | 192 | - | 0.302083 |
DDB_G0268130 | DDB_G0268130 | DDB0232428 | CDS | 1512409 | 1626 | + | 0.302583 | |
DDB_G0268132 | DDB_G0268132 | contains a SET domain involved in histone methylation an AWS (Associated With SET) domain and a post-SET zinc-binding domain | DDB0232428 | CDS | 1516724 | 2697 | + | 0.269559 |
DDB_G0268134 | DDB_G0268134 | DDB0232428 | CDS | 1521691 | 4614 | + | 0.317512 | |
DDB_G0268136 | DDB_G0268136 | DDB0232428 | CDS | 1527025 | 972 | + | 0.270576 | |
DDB_G0268138 | DDB_G0268138 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232428 | CDS | 1528262 | 609 | + | 0.302135 |
DDB_G0268140 | DDB_G0268140 | DDB0232428 | CDS | 1529143 | 2328 | - | 0.294244 | |
DDB_G0268142 | DDB_G0268142 | DDB0232428 | CDS | 1532259 | 1047 | + | 0.254059 | |
DDB_G0268146 | DDB_G0268146 | DDB0232428 | CDS | 1536630 | 1053 | + | 0.249763 | |
DDB_G0268148 | DDB_G0268148 | DDB0232428 | CDS | 1538303 | 1038 | + | 0.264933 | |
DDB_G0268150_ps | DDB_G0268150 | putative pseudogene fragment similar to a small family of Dictyostelium genes including the upstream | DDB0232428 | CDS | 1539632 | 357 | + | 0.246499 |
DDB_G0268152 | DDB_G0268152 | DDB0232428 | CDS | 1542257 | 2463 | - | 0.191636 | |
DDB_G0268154 | DDB_G0268154 | DDB0232428 | CDS | 1545975 | 657 | + | 0.298326 | |
DDB_G0268156 | DDB_G0268156 | DDB0232428 | CDS | 1548695 | 1461 | - | 0.216975 | |
DDB_G0268158 | DDB_G0268158 | DDB0232428 | CDS | 1574564 | 2067 | + | 0.257378 | |
DDB_G0268162 | DDB_G0268162 | DDB0232428 | CDS | 1580521 | 1431 | + | 0.253669 | |
DDB_G0268164 | DDB_G0268164 | DDB0232428 | CDS | 1584255 | 1989 | + | 0.257919 | |
DDB_G0268166 | DDB_G0268166 | similar to uncharacterized bacterial and eukaryotic proteins of the cupin_5 family also predicted to have an RmlC-like jelly roll fold | DDB0232428 | CDS | 1590745 | 540 | + | 0.261111 |
DDB_G0268170 | DDB_G0268170 | DDB0232428 | CDS | 1593660 | 273 | - | 0.322344 | |
DDB_G0268172 | DDB_G0268172 | highly similar to neighboring genes | DDB0232428 | CDS | 1596761 | 264 | - | 0.348485 |
DDB_G0268174 | DDB_G0268174 | highly similar to neighboring genes | DDB0232428 | CDS | 1597570 | 264 | - | 0.344697 |
DDB_G0268176 | DDB_G0268176 | DDB0232428 | CDS | 1600589 | 1434 | - | 0.253138 | |
DDB_G0268180 | DDB_G0268180 | DDB0232428 | CDS | 1615735 | 1902 | - | 0.270242 | |
DDB_G0268182 | DDB_G0268182 | DDB0232428 | CDS | 1618791 | 369 | + | 0.279133 | |
DDB_G0268184 | DDB_G0268184 | DDB0232428 | CDS | 1619582 | 1536 | - | 0.221354 | |
DDB_G0268186 | DDB_G0268186 | DDB0232428 | CDS | 1622398 | 4515 | - | 0.242968 | |
DDB_G0268188 | DDB_G0268188 | DDB0232428 | CDS | 1633311 | 3144 | + | 0.185115 | |
DDB_G0268192 | DDB_G0268192 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232428 | CDS | 1640028 | 465 | - | 0.275269 |
DDB_G0268194 | DDB_G0268194 | catalyzes the reaction Hsub2subO dCTP - NH3 dUTP in de novo biosynthesis of pyrimidine deoxyribonucleotides | DDB0232428 | CDS | 1641107 | 768 | - | 0.311198 |
DDB_G0268196 | DDB_G0268196 | DDB0232428 | CDS | 1642718 | 2325 | + | 0.294624 | |
DDB_G0268200 | DDB_G0268200 | DDB0232428 | CDS | 1653352 | 414 | - | 0.21256 | |
DDB_G0268202 | DDB_G0268202 | DDB0232428 | CDS | 1682484 | 576 | - | 0.234375 | |
DDB_G0268206 | DDB_G0268206 | DDB0232428 | CDS | 1686758 | 894 | + | 0.284116 | |
DDB_G0268208 | DDB_G0268208 | DDB0232428 | CDS | 1693320 | 633 | + | 0.273302 | |
DDB_G0268210 | DDB_G0268210 | DDB0232428 | CDS | 1694068 | 774 | - | 0.29199 | |
DDB_G0268212 | DDB_G0268212 | contains an N-terminal DEADDEAH box helicase a central helicase associated domain (HA2) and a C-terminal domain of unknown function DUF1605 common to DEAD box helicases | DDB0232428 | CDS | 1695570 | 1368 | - | 0.234649 |
DDB_G0268218 | DDB_G0268218 | DDB0232428 | CDS | 1708888 | 2547 | + | 0.217903 | |
DDB_G0268220 | DDB_G0268220 | similar to Ixodes scapularis U2 small nuclear ribonucleoprotein A human c10orf11 has 3 leucine-rich repeats which are involved in protein-protein interactions | DDB0232428 | CDS | 1712183 | 669 | + | 0.252616 |
DDB_G0268222 | DDB_G0268222 | belongs to the metallophosphoesterase superfamily similar to human PAPL (Ironzinc purple acid phosphatase-like protein) contains a predicted signal peptide | DDB0232428 | CDS | 1715767 | 1479 | - | 0.323191 |
DDB_G0268224 | DDB_G0268224 | DDB0232428 | CDS | 1719500 | 1710 | - | 0.276023 | |
DDB_G0268226 | DDB_G0268226 | DDB0232428 | CDS | 1721883 | 189 | - | 0.333333 | |
DDB_G0268228 | DDB_G0268228 | DDB0232428 | CDS | 1723392 | 2421 | - | 0.263527 | |
DDB_G0268230 | DDB_G0268230 | DDB0232428 | CDS | 1727069 | 1764 | + | 0.265306 | |
DDB_G0268232 | DDB_G0268232 | shares a short region of similarity with mammalian Nedd4 binding protein 2BCL-3 binding protein | DDB0232428 | CDS | 1728957 | 3078 | - | 0.269656 |
DDB_G0268234 | DDB_G0268234 | DDB0232428 | CDS | 1732577 | 840 | - | 0.214286 | |
DDB_G0268236 | DDB_G0268236 | DDB0232428 | CDS | 1733949 | 1590 | - | 0.367296 | |
DDB_G0268240 | DDB_G0268240 | DDB0232428 | CDS | 1754914 | 324 | - | 0.237654 | |
DDB_G0268244 | DDB_G0268244 | DDB0232428 | CDS | 1761068 | 2418 | + | 0.283706 | |
DDB_G0268246 | DDB_G0268246 | DDB0232428 | CDS | 1764265 | 2478 | + | 0.166263 | |
DDB_G0268248 | DDB_G0268248 | DDB0232428 | CDS | 1766831 | 1188 | - | 0.255892 | |
DDB_G0268250 | DDB_G0268250 | DDB0232428 | CDS | 1768454 | 1173 | - | 0.27792 | |
DDB_G0268252 | DDB_G0268252 | DDB0232428 | CDS | 1771285 | 966 | - | 0.266046 | |
DDB_G0268254_ps | DDB_G0268254 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 1784155 | 1176 | - | 0.218537 |
DDB_G0268260 | DDB_G0268260 | DDB0232428 | CDS | 198724 | 1176 | - | 0.238095 | |
DDB_G0268264 | DDB_G0268264 | DDB0232428 | CDS | 231364 | 555 | - | 0.463063 | |
DDB_G0268266 | DDB_G0268266 | DDB0232428 | CDS | 233800 | 2070 | + | 0.257005 | |
DDB_G0268268 | DDB_G0268268 | DDB0232428 | CDS | 251537 | 1338 | - | 0.251868 | |
DDB_G0268270 | DDB_G0268270 | DDB0232428 | CDS | 279600 | 2025 | - | 0.304198 | |
DDB_G0268274 | DDB_G0268274 | DDB0232428 | CDS | 320689 | 276 | + | 0.333333 | |
DDB_G0268278 | DDB_G0268278 | DDB0232428 | CDS | 322112 | 606 | + | 0.267327 | |
DDB_G0268280 | DDB_G0268280 | DDB0232428 | CDS | 331477 | 4182 | + | 0.188187 | |
DDB_G0268286 | DDB_G0268286 | DDB0232428 | CDS | 363410 | 1059 | + | 0.29084 | |
DDB_G0268288 | DDB_G0268288 | DDB0232428 | CDS | 386296 | 3792 | - | 0.238397 | |
DDB_G0268290 | DDB_G0268290 | DDB0232428 | CDS | 397569 | 186 | - | 0.204301 | |
DDB_G0268292 | DDB_G0268292 | DDB0232428 | CDS | 416596 | 1104 | - | 0.168478 | |
DDB_G0268294_ps | DDB_G0268294 | putative pseudogene fragment nearly identical to | DDB0232428 | CDS | 426116 | 687 | - | 0.283843 |
DDB_G0268298 | DDB_G0268298 | DDB0232428 | CDS | 447485 | 396 | - | 0.239899 | |
DDB_G0268300 | DDB_G0268300 | DDB0232428 | CDS | 475634 | 192 | + | 0.197917 | |
DDB_G0268310 | DDB_G0268310 | DDB0232428 | CDS | 577816 | 423 | + | 0.20331 | |
DDB_G0268312 | DDB_G0268312 | DDB0232428 | CDS | 580421 | 189 | - | 0.301587 | |
DDB_G0268314 | DDB_G0268314 | DDB0232428 | CDS | 604725 | 3615 | + | 0.254772 | |
DDB_G0268316 | DDB_G0268316 | DDB0232428 | CDS | 613392 | 3681 | - | 0.234719 | |
DDB_G0268318 | DDB_G0268318 | DDB0232428 | CDS | 627395 | 825 | + | 0.242424 | |
DDB_G0268320 | DDB_G0268320 | similar to S. cerevisiae BUD7 (bud site selection protein 7) which is required for the export of specialised cargo from the Golgi. belongs to the CHAPS (Chs5p-Arf1p-binding proteins) family | DDB0232428 | CDS | 637945 | 2712 | - | 0.29646 |
DDB_G0268322 | DDB_G0268322 | DDB0232428 | CDS | 659396 | 1008 | - | 0.340278 | |
DDB_G0268324 | DDB_G0268324 | DDB0232428 | CDS | 679845 | 909 | - | 0.176018 | |
DDB_G0268326 | DDB_G0268326 | DDB0232428 | CDS | 682072 | 882 | - | 0.150794 | |
DDB_G0268328 | DDB_G0268328 | DDB0232428 | CDS | 683499 | 11340 | - | 0.245679 | |
DDB_G0268334 | DDB_G0268334 | DDB0232428 | CDS | 714031 | 2337 | - | 0.273427 | |
DDB_G0268336 | DDB_G0268336 | DDB0232428 | CDS | 731136 | 792 | - | 0.268939 | |
DDB_G0268338 | DDB_G0268338 | DDB0232428 | CDS | 733269 | 714 | + | 0.163866 | |
DDB_G0268340_RTE | DDB_G0268340 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232428 | CDS | 743291 | 3099 | + | 0.349145 |
DDB_G0268342_ps | DDB_G0268342 | putative pseudogene similar to Dictyostelium genes | DDB0232428 | CDS | 778920 | 876 | + | 0.192922 |
DDB_G0268344 | DDB_G0268344 | DDB0232428 | CDS | 798097 | 909 | + | 0.286029 | |
DDB_G0268346 | DDB_G0268346 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232428 | CDS | 866636 | 1269 | + | 0.266351 |
DDB_G0268348 | DDB_G0268348 | DDB0232428 | CDS | 868196 | 4149 | + | 0.185346 | |
DDB_G0268350 | DDB_G0268350 | DDB0232428 | CDS | 881664 | 3027 | + | 0.218698 | |
DDB_G0268352 | DDB_G0268352 | conserved in Dictyostelium contains an immunoglobulin like fold domain contains a predicted signal sequence and C-terminal transmembrane domain | DDB0232428 | CDS | 885149 | 3354 | + | 0.250447 |
DDB_G0268358 | DDB_G0268358 | ortholog of the human SDCCAG10 (Serologically Defined Colon Cancer Antigen 10) PPIase is an enzyme that accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232428 | CDS | 936052 | 1482 | + | 0.262483 |
DDB_G0268360 | DDB_G0268360 | DDB0232428 | CDS | 948334 | 279 | - | 0.354839 | |
DDB_G0268362 | DDB_G0268362 | DDB0232428 | CDS | 980835 | 2316 | + | 0.200777 | |
DDB_G0268364 | DDB_G0268364 | DDB0232428 | CDS | 986994 | 2139 | + | 0.287518 | |
DDB_G0268366 | DDB_G0268366 | DDB0232428 | CDS | 989851 | 1059 | + | 0.25118 | |
DDB_G0268370 | DDB_G0268370 | DDB0232428 | CDS | 1000903 | 141 | - | 0.269504 | |
DDB_G0268376 | DDB_G0268376 | DDB0232428 | CDS | 1015824 | 651 | + | 0.218126 | |
DDB_G0268382 | DDB_G0268382 | DDB0232428 | CDS | 1076498 | 393 | + | 0.279898 | |
DDB_G0268384 | DDB_G0268384 | DDB0232428 | CDS | 1085918 | 2886 | + | 0.30492 | |
DDB_G0268386 | DDB_G0268386 | similar to D. purpureum protein contains one SET domain and one tetratricopeptide repeat (TPR) region | DDB0232428 | CDS | 1104198 | 2031 | - | 0.232398 |
DDB_G0268388_ps | DDB_G0268388 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 1108930 | 1476 | - | 0.243902 |
DDB_G0268390_ps | DDB_G0268390 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 1110833 | 1305 | - | 0.230651 |
DDB_G0268394 | DDB_G0268394 | DDB0232428 | CDS | 1135912 | 3339 | + | 0.259958 | |
DDB_G0268398 | DDB_G0268398 | highly similar to neighboring genes | DDB0232428 | CDS | 1150368 | 246 | - | 0.345528 |
DDB_G0268400 | DDB_G0268400 | highly similar to neighboring genes | DDB0232428 | CDS | 1151178 | 243 | - | 0.349794 |
DDB_G0268404 | DDB_G0268404 | DDB0232428 | CDS | 1184694 | 2535 | + | 0.24931 | |
DDB_G0268406 | DDB_G0268406 | DDB0232428 | CDS | 1206080 | 408 | - | 0.188725 | |
DDB_G0268408_ps | DDB_G0268408 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 1212494 | 831 | + | 0.238267 |
DDB_G0268412 | DDB_G0268412 | DDB0232428 | CDS | 1253447 | 3051 | + | 0.265487 | |
DDB_G0268420 | DDB_G0268420 | DDB0232428 | CDS | 1295307 | 3267 | - | 0.233548 | |
DDB_G0268422 | DDB_G0268422 | DDB0232428 | CDS | 1339034 | 681 | + | 0.221733 | |
DDB_G0268424 | DDB_G0268424 | DDB0232428 | CDS | 1368763 | 1752 | - | 0.255708 | |
DDB_G0268428 | DDB_G0268428 | DDB0232428 | CDS | 1402456 | 2091 | + | 0.151602 | |
DDB_G0268430 | DDB_G0268430 | DDB0232428 | CDS | 1423638 | 2802 | + | 0.246253 | |
DDB_G0268432 | DDB_G0268432 | DDB0232428 | CDS | 1475254 | 2895 | - | 0.161313 | |
DDB_G0268434 | DDB_G0268434 | DDB0232428 | CDS | 1485131 | 729 | - | 0.288066 | |
DDB_G0268438 | DDB_G0268438 | DDB0232428 | CDS | 1491471 | 327 | + | 0.238532 | |
DDB_G0268440_RTE | DDB_G0268440 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1506583 | 642 | - | 0.266355 |
DDB_G0268442 | DDB_G0268442 | DDB0232428 | CDS | 1509432 | 867 | + | 0.324106 | |
DDB_G0268444 | DDB_G0268444 | DDB0232428 | CDS | 1514264 | 1509 | - | 0.220013 | |
DDB_G0268450 | DDB_G0268450 | DDB0232428 | CDS | 1586565 | 1779 | + | 0.19674 | |
DDB_G0268452 | DDB_G0268452 | DDB0232428 | CDS | 1588545 | 813 | - | 0.258303 | |
DDB_G0268454 | DDB_G0268454 | weakly similar to hssA2C7E family genes expression positively regulated by STATa | DDB0232428 | CDS | 1594682 | 246 | - | 0.260163 |
DDB_G0268456 | DDB_G0268456 | highly similar to neighboring genes | DDB0232428 | CDS | 1595915 | 267 | - | 0.340824 |
DDB_G0268458 | DDB_G0268458 | highly similar to neighboring genes | DDB0232428 | CDS | 1598476 | 267 | - | 0.348315 |
DDB_G0268462 | DDB_G0268462 | DDB0232428 | CDS | 1630091 | 1890 | + | 0.292064 | |
DDB_G0268464_RTE | DDB_G0268464 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1691546 | 978 | + | 0.297546 |
DDB_G0268466 | DDB_G0268466 | DDB0232428 | CDS | 1756054 | 171 | - | 0.22807 | |
DDB_G0268470_RTE | DDB_G0268470 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 1791230 | 1128 | - | 0.312057 |
DDB_G0268474_RTE | DDB_G0268474 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 194176 | 675 | + | 0.336296 |
DDB_G0268476_TE | DDB_G0268476 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 195959 | 1026 | - | 0.19883 |
DDB_G0268478 | DDB_G0268478 | DDB0232428 | CDS | 255654 | 402 | + | 0.288557 | |
DDB_G0268482_ps | DDB_G0268482 | putative pseudogene similar to | DDB0232428 | CDS | 318212 | 1179 | + | 0.217981 |
DDB_G0268484_ps | DDB_G0268484 | putative pseudogene fragment similar to | DDB0232428 | CDS | 430688 | 741 | - | 0.330634 |
DDB_G0268486_ps | DDB_G0268486 | putative pseudogene contains protein kinase domain | DDB0232428 | CDS | 498516 | 2820 | - | 0.22305 |
DDB_G0268492 | DDB_G0268492 | DDB0232428 | CDS | 520101 | 2007 | - | 0.247135 | |
DDB_G0268494 | DDB_G0268494 | DDB0232428 | CDS | 542006 | 2259 | + | 0.177512 | |
DDB_G0268496 | DDB_G0268496 | DDB0232428 | CDS | 554652 | 1434 | - | 0.357043 | |
DDB_G0268498 | DDB_G0268498 | DDB0232428 | CDS | 573341 | 2457 | - | 0.334961 | |
DDB_G0268500 | DDB_G0268500 | DDB0232428 | CDS | 590684 | 4485 | - | 0.21204 | |
DDB_G0268502 | DDB_G0268502 | DDB0232428 | CDS | 595744 | 2622 | - | 0.239893 | |
DDB_G0268504 | DDB_G0268504 | contains two putative coiled-coil domains conserved in Dictyostelium and Polysphondylium | DDB0232428 | CDS | 642853 | 15879 | + | 0.239688 |
DDB_G0268506 | DDB_G0268506 | DDB0232428 | CDS | 663020 | 3363 | - | 0.237288 | |
DDB_G0268508_RTE | DDB_G0268508 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 735632 | 4704 | + | 0.31335 |
DDB_G0268510_RTE | DDB_G0268510 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232428 | CDS | 741690 | 1077 | + | 0.416899 |
DDB_G0268518 | DDB_G0268518 | DDB0232428 | CDS | 810583 | 792 | - | 0.272727 | |
DDB_G0268520 | DDB_G0268520 | DDB0232428 | CDS | 811678 | 3921 | - | 0.217547 | |
DDB_G0268524_RTE | DDB_G0268524 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 842918 | 4824 | + | 0.311774 |
DDB_G0268526 | DDB_G0268526 | DDB0232428 | CDS | 874156 | 2277 | + | 0.237593 | |
DDB_G0268528_RTE | DDB_G0268528 | DDB0232428 | CDS | 945806 | 1386 | + | 0.353535 | |
DDB_G0268534 | DDB_G0268534 | DDB0232428 | CDS | 1014659 | 558 | - | 0.286738 | |
DDB_G0268536 | DDB_G0268536 | DDB0232428 | CDS | 1020423 | 2031 | + | 0.248646 | |
DDB_G0268542 | DDB_G0268542 | DDB0232428 | CDS | 1091218 | 216 | + | 0.375 | |
DDB_G0268546 | DDB_G0268546 | DDB0232428 | CDS | 1095713 | 1098 | - | 0.256831 | |
DDB_G0268550 | DDB_G0268550 | kinase domain similar to those of mitogen-activated protein kinases similar to the STE20 family | DDB0232428 | CDS | 1145507 | 1611 | - | 0.189323 |
DDB_G0268552 | DDB_G0268552 | DDB0232428 | CDS | 1182084 | 1557 | + | 0.252408 | |
DDB_G0268554 | DDB_G0268554 | DDB0232428 | CDS | 1209766 | 1863 | + | 0.229737 | |
DDB_G0268558 | DDB_G0268558 | DDB0232428 | CDS | 1292814 | 1380 | + | 0.237681 | |
DDB_G0268560 | DDB_G0268560 | the SWIM domain is found in variety of prokaryotic and eukaryotic proteins it is predicted to have DNA-binding and protein-protein interaction functions in different contexts also contains a P-loop motif and region of tetrapeptide XPTX repeats similar to D. purpureum protein | DDB0232428 | CDS | 1355835 | 3465 | - | 0.232612 |
DDB_G0268564 | DDB_G0268564 | DDB0232428 | CDS | 1377494 | 759 | + | 0.279315 | |
DDB_G0268566 | DDB_G0268566 | DDB0232428 | CDS | 1378934 | 1701 | + | 0.188713 | |
DDB_G0268568_ps | DDB_G0268568 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 1387513 | 216 | + | 0.282407 |
DDB_G0268570 | DDB_G0268570 | DDB0232428 | CDS | 1492031 | 1911 | + | 0.205128 | |
DDB_G0268572 | DDB_G0268572 | DDB0232428 | CDS | 1551637 | 3324 | + | 0.217208 | |
DDB_G0268576 | DDB_G0268576 | DDB0232428 | CDS | 1558253 | 3210 | + | 0.214642 | |
DDB_G0268580_RTE | DDB_G0268580 | DDB0232428 | CDS | 1611083 | 3294 | - | 0.33303 | |
DDB_G0268582_RTE | DDB_G0268582 | DDB0232428 | CDS | 1614526 | 873 | - | 0.297824 | |
DDB_G0268584 | DDB_G0268584 | DDB0232428 | CDS | 1649497 | 1623 | + | 0.260012 | |
DDB_G0268586 | DDB_G0268586 | DDB0232428 | CDS | 1666540 | 1164 | - | 0.262028 | |
DDB_G0268588 | DDB_G0268588 | DDB0232428 | CDS | 1668764 | 2973 | - | 0.223343 | |
DDB_G0268590 | DDB_G0268590 | DDB0232428 | CDS | 1672557 | 1755 | - | 0.291738 | |
DDB_G0268594 | DDB_G0268594 | DDB0232428 | CDS | 1680932 | 1458 | + | 0.20096 | |
DDB_G0268596_RTE | DDB_G0268596 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1688502 | 699 | + | 0.347639 |
DDB_G0268598_RTE | DDB_G0268598 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1690396 | 402 | + | 0.370647 |
DDB_G0268602 | DDB_G0268602 | DDB0232428 | CDS | 1713715 | 285 | + | 0.270175 | |
DDB_G0268604 | DDB_G0268604 | DDB0232428 | CDS | 1746832 | 192 | + | 0.166667 | |
DDB_G0268606_RTE | DDB_G0268606 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 1773769 | 675 | - | 0.334815 |
DDB_G0268608_RTE | DDB_G0268608 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1775368 | 4983 | + | 0.319888 |
DDB_G0268610_RTE | DDB_G0268610 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1782218 | 1497 | + | 0.318637 |
DDB_G0268612_ps | DDB_G0268612 | putative pseudogene similar to a small family of genes including | DDB0232428 | CDS | 1787018 | 1110 | - | 0.276577 |
DDB_G0268624 | DDB_G0268624 | DDB0232428 | CDS | 2362108 | 1017 | + | 0.241888 | |
DDB_G0268626 | DDB_G0268626 | Dictyostelium family protein | DDB0232428 | CDS | 2357127 | 4320 | + | 0.245139 |
DDB_G0268640 | DDB_G0268640 | serine-rich protein very similar to rtoA contains a putative signal sequence | DDB0232428 | CDS | 1799319 | 2355 | + | 0.380892 |
DDB_G0268642 | DDB_G0268642 | related to the GCN2 family of protein kinases which phosphorylate the alpha subunit of eIF2 unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232428 | CDS | 1801909 | 3237 | - | 0.255792 |
DDB_G0268644 | DDB_G0268644 | DDB0232428 | CDS | 1807927 | 663 | + | 0.321267 | |
DDB_G0268646 | DDB_G0268646 | DDB0232428 | CDS | 1826960 | 318 | - | 0.355346 | |
DDB_G0268650 | DDB_G0268650 | DDB0232428 | CDS | 1841483 | 2802 | + | 0.315132 | |
DDB_G0268656 | DDB_G0268656 | highly similar to human ULK (Unc51-like kinase) does not contain the full consensus sequence required for kinase function | DDB0232428 | CDS | 1863917 | 954 | - | 0.220126 |
DDB_G0268660 | DDB_G0268660 | highly similar to neighboring gene | DDB0232428 | CDS | 1873355 | 6945 | - | 0.257307 |
DDB_G0268662 | DDB_G0268662 | highly similar to neighboring gene | DDB0232428 | CDS | 1881042 | 7572 | - | 0.267697 |
DDB_G0268666 | DDB_G0268666 | DDB0232428 | CDS | 1890850 | 402 | - | 0.276119 | |
DDB_G0268670 | DDB_G0268670 | DDB0232428 | CDS | 1893644 | 165 | - | 0.224242 | |
DDB_G0268672 | DDB_G0268672 | DDB0232428 | CDS | 1895260 | 174 | + | 0.264368 | |
DDB_G0268674 | DDB_G0268674 | DDB0232428 | CDS | 1896312 | 165 | - | 0.224242 | |
DDB_G0268676 | DDB_G0268676 | DDB0232428 | CDS | 1897615 | 177 | + | 0.259887 | |
DDB_G0268678 | DDB_G0268678 | component of the multisubunit transcription elongation factor NELF human TH1 interacts with A-Raf | DDB0232428 | CDS | 1901921 | 1983 | + | 0.271306 |
DDB_G0268680 | DDB_G0268680 | DDB0232428 | CDS | 1904782 | 2043 | + | 0.303475 | |
DDB_G0268684 | DDB_G0268684 | DDB0232428 | CDS | 1916625 | 2490 | + | 0.243373 | |
DDB_G0268686 | DDB_G0268686 | contains one C2 domain one MHD1 (Munc13-homology) domain and one MHD2 domain | DDB0232428 | CDS | 1919974 | 4245 | + | 0.244759 |
DDB_G0268688 | DDB_G0268688 | DDB0232428 | CDS | 1924769 | 180 | - | 0.288889 | |
DDB_G0268690 | DDB_G0268690 | DDB0232428 | CDS | 1926730 | 180 | - | 0.272222 | |
DDB_G0268692 | DDB_G0268692 | DDB0232428 | CDS | 1928290 | 978 | + | 0.148262 | |
DDB_G0268694 | DDB_G0268694 | DDB0232428 | CDS | 1929940 | 1086 | + | 0.163904 | |
DDB_G0268696 | DDB_G0268696 | DDB0232428 | CDS | 1935672 | 1632 | + | 0.289216 | |
DDB_G0268698 | DDB_G0268698 | DDB0232428 | CDS | 1938533 | 1926 | - | 0.267394 | |
DDB_G0268704 | DDB_G0268704 | DDB0232428 | CDS | 1943354 | 996 | - | 0.2751 | |
DDB_G0268708 | DDB_G0268708 | DDB0232428 | CDS | 1963368 | 1590 | + | 0.254088 | |
DDB_G0268710 | DDB_G0268710 | DDB0232428 | CDS | 1966394 | 3432 | + | 0.251457 | |
DDB_G0268712 | DDB_G0268712 | DDB0232428 | CDS | 1979347 | 678 | + | 0.212389 | |
DDB_G0268724_RTE | DDB_G0268724 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1999319 | 663 | + | 0.307692 |
DDB_G0268726_ps | DDB_G0268726 | putative pseudogene similar to | DDB0232428 | CDS | 2004451 | 204 | - | 0.343137 |
DDB_G0268730_ps | DDB_G0268730 | putative pseudogene small fragment similar to D. discoideum genes | DDB0232428 | CDS | 2006217 | 180 | - | 0.355556 |
DDB_G0268732 | DDB_G0268732 | DDB0232428 | CDS | 2008794 | 255 | + | 0.356863 | |
DDB_G0268734 | DDB_G0268734 | DDB0232428 | CDS | 2009231 | 459 | - | 0.333333 | |
DDB_G0268738 | DDB_G0268738 | DDB0232428 | CDS | 2019408 | 198 | + | 0.323232 | |
DDB_G0268742 | DDB_G0268742 | DDB0232428 | CDS | 2030028 | 1182 | - | 0.212352 | |
DDB_G0268746 | DDB_G0268746 | contains a UBX domain found in ubiquitin-regulatory proteins | DDB0232428 | CDS | 2032965 | 1230 | - | 0.262602 |
DDB_G0268748 | DDB_G0268748 | DDB0232428 | CDS | 2035070 | 1311 | - | 0.212815 | |
DDB_G0268750 | DDB_G0268750 | DDB0232428 | CDS | 2039946 | 180 | + | 0.233333 | |
DDB_G0268752 | DDB_G0268752 | DDB0232428 | CDS | 2040402 | 180 | - | 0.177778 | |
DDB_G0268754 | DDB_G0268754 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232428 | CDS | 2044869 | 1968 | + | 0.303862 |
DDB_G0268756 | DDB_G0268756 | DDB0232428 | CDS | 2048275 | 372 | + | 0.268817 | |
DDB_G0268762 | DDB_G0268762 | DDB0232428 | CDS | 2055281 | 846 | - | 0.286052 | |
DDB_G0268764 | DDB_G0268764 | DDB0232428 | CDS | 2056699 | 5253 | + | 0.262707 | |
DDB_G0268772 | DDB_G0268772 | DDB0232428 | CDS | 2068280 | 348 | - | 0.310345 | |
DDB_G0268774 | DDB_G0268774 | DDB0232428 | CDS | 2073845 | 1026 | - | 0.192982 | |
DDB_G0268780_ps | DDB_G0268780 | putative pseudogene similar to a large D. discoideum gene family including | DDB0232428 | CDS | 2087968 | 441 | + | 0.213152 |
DDB_G0268782 | DDB_G0268782 | DDB0232428 | CDS | 2097735 | 1278 | + | 0.216745 | |
DDB_G0268784 | DDB_G0268784 | DDB0232428 | CDS | 2104624 | 1815 | - | 0.271625 | |
DDB_G0268786 | DDB_G0268786 | DDB0232428 | CDS | 2108112 | 1965 | - | 0.243766 | |
DDB_G0268788 | DDB_G0268788 | DDB0232428 | CDS | 2116939 | 1317 | + | 0.211845 | |
DDB_G0268790 | DDB_G0268790 | belongs to the synaptotagmin family contains a predicted signal sequence and a transmembrane domain | DDB0232428 | CDS | 2118381 | 561 | - | 0.338681 |
DDB_G0268796 | DDB_G0268796 | DDB0232428 | CDS | 2124707 | 693 | - | 0.249639 | |
DDB_G0268798 | DDB_G0268798 | DDB0232428 | CDS | 2125974 | 1140 | + | 0.205263 | |
DDB_G0268800 | DDB_G0268800 | DDB0232428 | CDS | 2127909 | 903 | + | 0.180509 | |
DDB_G0268806_ps | DDB_G0268806 | putative pseudogene highly similar especially a short 5' stretch and a longer 3' stretch to | DDB0232428 | CDS | 2140091 | 324 | + | 0.290123 |
DDB_G0268808 | DDB_G0268808 | DDB0232428 | CDS | 2141889 | 2874 | - | 0.214683 | |
DDB_G0268810 | DDB_G0268810 | ortholog of bacterial Mgsup2sup transporter mgtA contains eight transmembrane domains | DDB0232428 | CDS | 2146485 | 2865 | + | 0.339965 |
DDB_G0268812 | DDB_G0268812 | DDB0232428 | CDS | 2154156 | 1230 | - | 0.180488 | |
DDB_G0268814 | DDB_G0268814 | DDB0232428 | CDS | 2157480 | 2880 | + | 0.220833 | |
DDB_G0268816 | DDB_G0268816 | DDB0232428 | CDS | 2160760 | 1107 | - | 0.277326 | |
DDB_G0268818 | DDB_G0268818 | DDB0232428 | CDS | 2167055 | 1341 | + | 0.247576 | |
DDB_G0268820 | DDB_G0268820 | DDB0232428 | CDS | 2174037 | 1590 | + | 0.224528 | |
DDB_G0268822 | DDB_G0268822 | DDB0232428 | CDS | 2179084 | 3099 | + | 0.27041 | |
DDB_G0268824 | DDB_G0268824 | DDB0232428 | CDS | 2182743 | 1299 | - | 0.254811 | |
DDB_G0268826 | DDB_G0268826 | DDB0232428 | CDS | 2184410 | 3060 | - | 0.203595 | |
DDB_G0268828 | DDB_G0268828 | contains a predicted signal peptide highly similar to neighboring genes | DDB0232428 | CDS | 2191612 | 459 | - | 0.318083 |
DDB_G0268830 | DDB_G0268830 | DDB0232428 | CDS | 2194306 | 231 | + | 0.285714 | |
DDB_G0268832 | DDB_G0268832 | DDB0232428 | CDS | 2194685 | 453 | - | 0.282561 | |
DDB_G0268834 | DDB_G0268834 | DDB0232428 | CDS | 2196631 | 147 | + | 0.408163 | |
DDB_G0268836 | DDB_G0268836 | DDB0232428 | CDS | 2197263 | 339 | - | 0.294985 | |
DDB_G0268838 | DDB_G0268838 | DDB0232428 | CDS | 2198420 | 468 | + | 0.25 | |
DDB_G0268842 | DDB_G0268842 | DDB0232428 | CDS | 2218538 | 306 | + | 0.232026 | |
DDB_G0268844 | DDB_G0268844 | DDB0232428 | CDS | 2221088 | 1746 | + | 0.264032 | |
DDB_G0268846 | DDB_G0268846 | DDB0232428 | CDS | 2223009 | 1746 | + | 0.260596 | |
DDB_G0268848 | DDB_G0268848 | similar though smaller than H. sapiens SACS a very large protein. The SACS defect causes autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) a neurodegenerative disease D. discoideum contains three nearly identical genes located next to each other contains two putative ATP binding domains. | DDB0232428 | CDS | 2225484 | 7983 | + | 0.262057 |
DDB_G0268850 | DDB_G0268850 | similar though smaller than H. sapiens SACS a very large protein. The SACS defect causes autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) a neurodegenerative disease D. discoideum contains three nearly identical genes located next to each other contains two putative ATP binding domains. | DDB0232428 | CDS | 2235139 | 7986 | + | 0.262334 |
DDB_G0268852 | DDB_G0268852 | similar though smaller than H. sapiens SACS a very large protein. The SACS defect causes autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) a neurodegenerative disease D. discoideum contains three nearly identical genes located next to each other contains two putative ATP binding domains. | DDB0232428 | CDS | 2244141 | 8022 | + | 0.260284 |
DDB_G0268856 | DDB_G0268856 | DDB0232428 | CDS | 2261646 | 1941 | + | 0.267388 | |
DDB_G0268858 | DDB_G0268858 | DDB0232428 | CDS | 2264502 | 588 | - | 0.282313 | |
DDB_G0268862 | DDB_G0268862 | DDB0232428 | CDS | 2271073 | 1869 | - | 0.304441 | |
DDB_G0268864 | DDB_G0268864 | DDB0232428 | CDS | 2276260 | 1110 | - | 0.290991 | |
DDB_G0268866 | DDB_G0268866 | DDB0232428 | CDS | 2278922 | 2493 | + | 0.184517 | |
DDB_G0268870 | DDB_G0268870 | DDB0232428 | CDS | 2286518 | 744 | + | 0.330645 | |
DDB_G0268872 | DDB_G0268872 | similar to members of the ubiquitin specific peptidase (USP) family including USP44 and USP3 | DDB0232428 | CDS | 2287976 | 6378 | + | 0.298056 |
DDB_G0268874 | DDB_G0268874 | DDB0232428 | CDS | 2296806 | 810 | + | 0.258025 | |
DDB_G0268876 | DDB_G0268876 | member of the TKL (tyrosine kinase-like) group of protein kinases contains filamin repeat similar to ABP120 | DDB0232428 | CDS | 2297918 | 4158 | - | 0.279702 |
DDB_G0268878 | DDB_G0268878 | DDB0232428 | CDS | 2304383 | 1101 | + | 0.283379 | |
DDB_G0268882 | DDB_G0268882 | DDB0232428 | CDS | 2308576 | 402 | - | 0.21393 | |
DDB_G0268884 | DDB_G0268884 | ortholog of E. coli OsmC a stress-inducible protein there is another member of this family in Dictyostelium | DDB0232428 | CDS | 2309454 | 471 | + | 0.314225 |
DDB_G0268892 | DDB_G0268892 | DDB0232428 | CDS | 2336357 | 606 | + | 0.353135 | |
DDB_G0268894 | DDB_G0268894 | DDB0232428 | CDS | 2339948 | 192 | - | 0.307292 | |
DDB_G0268896 | DDB_G0268896 | DDB0232428 | CDS | 2340589 | 228 | - | 0.381579 | |
DDB_G0268900 | DDB_G0268900 | DDB0232428 | CDS | 2344800 | 642 | - | 0.193146 | |
DDB_G0268902 | DDB_G0268902 | DDB0232428 | CDS | 2346148 | 1926 | + | 0.20405 | |
DDB_G0268904 | DDB_G0268904 | DDB0232428 | CDS | 2353413 | 2364 | + | 0.191624 | |
DDB_G0268906 | DDB_G0268906 | DDB0232428 | CDS | 2356141 | 363 | + | 0.231405 | |
DDB_G0268914 | DDB_G0268914 | DDB0232428 | CDS | 2371552 | 13623 | - | 0.261396 | |
DDB_G0268916 | DDB_G0268916 | DDB0232428 | CDS | 2389897 | 297 | + | 0.262626 | |
DDB_G0268918 | DDB_G0268918 | DDB0232428 | CDS | 1795565 | 2667 | - | 0.170229 | |
DDB_G0268922 | DDB_G0268922 | DDB0232428 | CDS | 1846133 | 3798 | - | 0.269879 | |
DDB_G0268924 | DDB_G0268924 | DDB0232428 | CDS | 1866297 | 5295 | - | 0.259679 | |
DDB_G0268926_ps | DDB_G0268926 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232428 | CDS | 1872318 | 456 | - | 0.27193 |
DDB_G0268928 | DDB_G0268928 | DDB0232428 | CDS | 1909652 | 1656 | + | 0.298913 | |
DDB_G0268930_ps | DDB_G0268930 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 1911597 | 2964 | - | 0.204116 |
DDB_G0268932 | DDB_G0268932 | DDB0232428 | CDS | 1915657 | 675 | + | 0.21037 | |
DDB_G0268934 | DDB_G0268934 | belongs to a family of short proteins that includes proteins from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | DDB0232428 | CDS | 1937906 | 399 | + | 0.233083 |
DDB_G0268942_RTE | DDB_G0268942 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1970717 | 1209 | + | 0.337469 |
DDB_G0268944_RTE | DDB_G0268944 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1972671 | 3078 | + | 0.304094 |
DDB_G0268946 | DDB_G0268946 | DDB0232428 | CDS | 1980426 | 1944 | + | 0.237654 | |
DDB_G0268948 | DDB_G0268948 | contains a SAM (and some other nucleotide) binding motif similar to bacterial and eukaryotic methyltransferases | DDB0232428 | CDS | 1982796 | 792 | - | 0.291667 |
DDB_G0268958_TE | DDB_G0268958 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232428 | CDS | 2011975 | 2418 | - | 0.29239 |
DDB_G0268960 | DDB_G0268960 | DDB0232428 | CDS | 2015222 | 225 | + | 0.32 | |
DDB_G0268962 | DDB_G0268962 | DDB0232428 | CDS | 2017135 | 450 | - | 0.308889 | |
DDB_G0268968 | DDB_G0268968 | DDB0232428 | CDS | 2047241 | 333 | + | 0.387387 | |
DDB_G0268970 | DDB_G0268970 | homolog of A. thaliana CPI1 (cycloeucalenol cycloisomerase) contains 6 putative transmembrane domains converts pentacyclic cyclopropyl sterols to tetracyclic sterols | DDB0232428 | CDS | 2050767 | 849 | + | 0.320377 |
DDB_G0268974 | DDB_G0268974 | DDB0232428 | CDS | 2052354 | 369 | - | 0.211382 | |
DDB_G0268978_RTE | DDB_G0268978 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 2063551 | 642 | - | 0.277259 |
DDB_G0268980_ps | DDB_G0268980 | putative pseudogene fragment very similar to parts of DDB_G0268948 a putative SAM dependent methyltransferase | DDB0232428 | CDS | 2065538 | 243 | - | 0.288066 |
DDB_G0268982 | DDB_G0268982 | DDB0232428 | CDS | 2066042 | 1338 | - | 0.198804 | |
DDB_G0268984 | DDB_G0268984 | DDB0232428 | CDS | 2069168 | 579 | + | 0.385147 | |
DDB_G0268986_RTE | DDB_G0268986 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 2071718 | 1545 | - | 0.298382 |
DDB_G0268988 | DDB_G0268988 | contains two RNA recognition motif domains (RRMs) conserved in all Dictyostelids | DDB0232428 | CDS | 2077109 | 1146 | - | 0.291449 |
DDB_G0268990 | DDB_G0268990 | DDB0232428 | CDS | 2079025 | 1308 | + | 0.249235 | |
DDB_G0268996 | DDB_G0268996 | DDB0232428 | CDS | 2099731 | 1836 | - | 0.271786 | |
DDB_G0269000 | DDB_G0269000 | DDB0232428 | CDS | 2111460 | 1104 | - | 0.286232 | |
DDB_G0269004 | DDB_G0269004 | DDB0232428 | CDS | 2150422 | 3135 | + | 0.232855 | |
DDB_G0269006 | DDB_G0269006 | DDB0232428 | CDS | 2170094 | 2745 | - | 0.298361 | |
DDB_G0269008 | DDB_G0269008 | contains a predicted signal peptide highly similar to neighboring genes | DDB0232428 | CDS | 2190252 | 444 | - | 0.310811 |
DDB_G0269010 | DDB_G0269010 | DDB0232428 | CDS | 2195578 | 516 | + | 0.333333 | |
DDB_G0269012 | DDB_G0269012 | DDB0232428 | CDS | 2196293 | 270 | + | 0.340741 | |
DDB_G0269014 | DDB_G0269014 | contains a predicted signal sequence and one putative transmembrane domain similar to D. purpureum protein | DDB0232428 | CDS | 2204411 | 8541 | - | 0.273036 |
DDB_G0269018 | DDB_G0269018 | DDB0232428 | CDS | 2258756 | 1953 | + | 0.273938 | |
DDB_G0269020 | DDB_G0269020 | DDB0232428 | CDS | 2274361 | 1482 | - | 0.188934 | |
DDB_G0269022 | DDB_G0269022 | DDB0232428 | CDS | 2295154 | 1041 | + | 0.273775 | |
DDB_G0269028 | DDB_G0269028 | DDB0232428 | CDS | 2367538 | 159 | - | 0.264151 | |
DDB_G0269030_RTE | DDB_G0269030 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 2369649 | 273 | - | 0.29304 |
DDB_G0269032 | DDB_G0269032 | contains two coiled-coil domains central region predicted to have structural similarity to the beta-sandwich domain of the Sec2324 superfamily | DDB0232428 | CDS | 2385345 | 3426 | - | 0.234384 |
DDB_G0269036_RTE | DDB_G0269036 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1793029 | 2345 | + | 0.302345 |
DDB_G0269040 | DDB_G0269040 | DDB0232428 | CDS | 1817324 | 5493 | + | 0.305662 | |
DDB_G0269042_ps | DDB_G0269042 | putative pseudogene similar to a family of FNIP repeat-containing proteins including | DDB0232428 | CDS | 1824333 | 1755 | - | 0.219373 |
DDB_G0269044 | DDB_G0269044 | DDB0232428 | CDS | 1851313 | 1230 | - | 0.284553 | |
DDB_G0269046 | DDB_G0269046 | catalyzes the reaction NADPH NAD NADP NADH | DDB0232428 | CDS | 1853006 | 3492 | - | 0.337343 |
DDB_G0269048 | DDB_G0269048 | DDB0232428 | CDS | 1858322 | 2007 | - | 0.350772 | |
DDB_G0269050 | DDB_G0269050 | DDB0232428 | CDS | 1861999 | 969 | + | 0.303406 | |
DDB_G0269052 | DDB_G0269052 | DDB0232428 | CDS | 1898794 | 1815 | - | 0.230854 | |
DDB_G0269056_RTE | DDB_G0269056 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 1950932 | 3144 | - | 0.338104 |
DDB_G0269058_RTE | DDB_G0269058 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 1954366 | 1335 | - | 0.310861 |
DDB_G0269060 | DDB_G0269060 | DDB0232428 | CDS | 1958550 | 1767 | + | 0.238257 | |
DDB_G0269062 | DDB_G0269062 | DDB0232428 | CDS | 1988769 | 1536 | - | 0.246745 | |
DDB_G0269064_RTE | DDB_G0269064 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 1997520 | 480 | + | 0.352083 |
DDB_G0269066 | DDB_G0269066 | DDB0232428 | CDS | 2003674 | 480 | + | 0.310417 | |
DDB_G0269068 | DDB_G0269068 | DDB0232428 | CDS | 2007191 | 1041 | + | 0.389049 | |
DDB_G0269070 | DDB_G0269070 | conserved hypothetical Dictyostelium proteinidentical to | DDB0232428 | CDS | 2016593 | 141 | + | 0.489362 |
DDB_G0269072 | DDB_G0269072 | DDB0232428 | CDS | 2017892 | 483 | + | 0.277433 | |
DDB_G0269074 | DDB_G0269074 | DDB0232428 | CDS | 2018396 | 336 | + | 0.294643 | |
DDB_G0269076_RTE | DDB_G0269076 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2022160 | 1131 | - | 0.316534 |
DDB_G0269078 | DDB_G0269078 | DDB0232428 | CDS | 2023544 | 909 | - | 0.30473 | |
DDB_G0269080 | DDB_G0269080 | DDB0232428 | CDS | 2069754 | 579 | + | 0.355786 | |
DDB_G0269082 | DDB_G0269082 | similar to D. purpureum protein there is a similar second gene | DDB0232428 | CDS | 2086586 | 570 | - | 0.233333 |
DDB_G0269084 | DDB_G0269084 | DDB0232428 | CDS | 2091187 | 1896 | + | 0.18038 | |
DDB_G0269086 | DDB_G0269086 | contains an N-terminal alphabeta hydrolase fold-1 which is also similar to bacterial lysophospholipases | DDB0232428 | CDS | 2113025 | 2814 | - | 0.38344 |
DDB_G0269088 | DDB_G0269088 | DDB0232428 | CDS | 2134088 | 501 | - | 0.319361 | |
DDB_G0269090 | DDB_G0269090 | DDB0232428 | CDS | 2162449 | 2190 | - | 0.163014 | |
DDB_G0269092 | DDB_G0269092 | contains a predicted signal peptide highly similar to neighboring genes | DDB0232428 | CDS | 2192652 | 450 | - | 0.306667 |
DDB_G0269094_RTE | DDB_G0269094 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2390879 | 1335 | + | 0.307865 |
DDB_G0269096 | DDB_G0269096 | DDB0232428 | CDS | 2393899 | 858 | - | 0.29021 | |
DDB_G0269126 | DDB_G0269126 | contains a signal peptide small gene family in D. discoideum D. purpureum has a single gene REMI mutant arrests at the finger stage (see | DDB0232428 | CDS | 2922116 | 3066 | - | 0.312133 |
DDB_G0269128 | DDB_G0269128 | contains two transmembrane domains REMI mutant forms aberrant fruiting bodies see | DDB0232428 | CDS | 3055800 | 1635 | - | 0.193884 |
DDB_G0269162 | DDB_G0269162 | DDB0232428 | CDS | 4629764 | 2397 | - | 0.275761 | |
DDB_G0269220 | DDB_G0269220 | subunit VIb of cytochrome c oxidase the terminal member of the mitochondrial inner membrane electron transport chain | DDB0232428 | CDS | 3734477 | 324 | + | 0.225309 |
DDB_G0269228 | DDB_G0269228 | DDB0232428 | CDS | 3259661 | 1725 | + | 0.235362 | |
DDB_G0269232 | DDB_G0269232 | conserved in D. purpureum and P. pallidum REMI mutant arrests at the finger stage (see | DDB0232428 | CDS | 2906854 | 1644 | + | 0.252433 |
DDB_G0269256 | DDB_G0269256 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | DDB0232428 | CDS | 2408349 | 465 | + | 0.27957 |
DDB_G0269258_RTE | DDB_G0269258 | DDB0232428 | CDS | 2410260 | 588 | - | 0.365646 | |
DDB_G0269260 | DDB_G0269260 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232428 | CDS | 2415581 | 465 | + | 0.273118 |
DDB_G0269264_RTE | DDB_G0269264 | DDB0232428 | CDS | 2419170 | 816 | - | 0.373774 | |
DDB_G0269266_RTE | DDB_G0269266 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232428 | CDS | 2420227 | 3300 | - | 0.317273 |
DDB_G0269268_RTE | DDB_G0269268 | partial ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232428 | CDS | 2423664 | 546 | - | 0.260073 |
DDB_G0269270 | DDB_G0269270 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | DDB0232428 | CDS | 2428475 | 465 | - | 0.27957 |
DDB_G0269272 | DDB_G0269272 | DDB0232428 | CDS | 2434615 | 3645 | + | 0.257064 | |
DDB_G0269276 | DDB_G0269276 | DDB0232428 | CDS | 2442246 | 264 | + | 0.32197 | |
DDB_G0269278 | DDB_G0269278 | DDB0232428 | CDS | 2442606 | 1323 | - | 0.197279 | |
DDB_G0269280 | DDB_G0269280 | DDB0232428 | CDS | 2444312 | 960 | - | 0.3 | |
DDB_G0269282 | DDB_G0269282 | DDB0232428 | CDS | 2445906 | 975 | - | 0.324103 | |
DDB_G0269284 | DDB_G0269284 | DDB0232428 | CDS | 2449936 | 1533 | - | 0.297456 | |
DDB_G0269286 | DDB_G0269286 | DDB0232428 | CDS | 2451692 | 3708 | - | 0.242988 | |
DDB_G0269288 | DDB_G0269288 | DDB0232428 | CDS | 2456628 | 11052 | - | 0.278502 | |
DDB_G0269294 | DDB_G0269294 | DDB0232428 | CDS | 2471481 | 2553 | - | 0.224442 | |
DDB_G0269296 | DDB_G0269296 | DDB0232428 | CDS | 2474747 | 1155 | + | 0.25368 | |
DDB_G0269300 | DDB_G0269300 | has similarity to human CD2BP2 a CD2 antigen cytoplasmic tail-binding protein and yeast LIN1 a non-essential component of the U5 snRNP | DDB0232428 | CDS | 2481510 | 1272 | + | 0.220126 |
DDB_G0269302 | DDB_G0269302 | DDB0232428 | CDS | 2482897 | 867 | - | 0.222607 | |
DDB_G0269304 | DDB_G0269304 | similar to S. cerevisiae SHQ1 which is required for box HACA small nucleolar ribonucleoprotein particle biogenesis contains one CS domain | DDB0232428 | CDS | 2484101 | 1752 | + | 0.232877 |
DDB_G0269308_ps | DDB_G0269308 | DDB0232428 | CDS | 2491060 | 2118 | + | 0.282814 | |
DDB_G0269312 | DDB_G0269312 | ortholog of S. cerevisiae ESF1 a nucleolar protein involved in pre-rRNA processing | DDB0232428 | CDS | 2497222 | 2511 | - | 0.282358 |
DDB_G0269318 | DDB_G0269318 | DDB0232428 | CDS | 2540112 | 435 | - | 0.149425 | |
DDB_G0269320_ps | DDB_G0269320 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 2541259 | 465 | - | 0.15914 |
DDB_G0269322 | DDB_G0269322 | DDB0232428 | CDS | 2542013 | 864 | - | 0.284722 | |
DDB_G0269328 | DDB_G0269328 | DDB0232428 | CDS | 2548313 | 3423 | + | 0.194566 | |
DDB_G0269330 | DDB_G0269330 | DDB0232428 | CDS | 2552986 | 876 | + | 0.211187 | |
DDB_G0269332 | DDB_G0269332 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232428 | CDS | 2554441 | 1845 | + | 0.280217 |
DDB_G0269334 | DDB_G0269334 | DDB0232428 | CDS | 2556676 | 960 | - | 0.396875 | |
DDB_G0269336 | DDB_G0269336 | DDB0232428 | CDS | 2560862 | 252 | + | 0.253968 | |
DDB_G0269340 | DDB_G0269340 | DDB0232428 | CDS | 2565964 | 834 | + | 0.29976 | |
DDB_G0269342 | DDB_G0269342 | DDB0232428 | CDS | 2567416 | 279 | + | 0.250896 | |
DDB_G0269344 | DDB_G0269344 | DDB0232428 | CDS | 2568156 | 1203 | - | 0.307564 | |
DDB_G0269346 | DDB_G0269346 | DDB0232428 | CDS | 2569786 | 828 | + | 0.149758 | |
DDB_G0269348 | DDB_G0269348 | DDB0232428 | CDS | 2570683 | 1911 | - | 0.244898 | |
DDB_G0269350 | DDB_G0269350 | DDB0232428 | CDS | 2573853 | 2109 | - | 0.245614 | |
DDB_G0269354 | DDB_G0269354 | conserved hypothetical Dictyostelium protein contains one EGF-like type 3 domain | DDB0232428 | CDS | 2578522 | 2928 | + | 0.265369 |
DDB_G0269356 | DDB_G0269356 | DDB0232428 | CDS | 2583576 | 819 | + | 0.246642 | |
DDB_G0269358 | DDB_G0269358 | DDB0232428 | CDS | 2584566 | 969 | - | 0.281734 | |
DDB_G0269360 | DDB_G0269360 | DDB0232428 | CDS | 2585971 | 2013 | - | 0.222057 | |
DDB_G0269368 | DDB_G0269368 | similar to human SYS1 which is involved in protein trafficking contains 4 putative transmembrane domains | DDB0232428 | CDS | 2629488 | 699 | + | 0.281831 |
DDB_G0269370 | DDB_G0269370 | very similar to the human 25 kDa cleavage and polyadenylation specificity factor component of the cleavage factor Im (CFIm) complex that plays a key role in pre-mRNA 3' processing | DDB0232428 | CDS | 2630812 | 603 | + | 0.288557 |
DDB_G0269372 | DDB_G0269372 | DDB0232428 | CDS | 2632261 | 483 | + | 0.331263 | |
DDB_G0269374 | DDB_G0269374 | DDB0232428 | CDS | 2633520 | 2331 | - | 0.221793 | |
DDB_G0269376 | DDB_G0269376 | DDB0232428 | CDS | 2642577 | 852 | - | 0.269953 | |
DDB_G0269380 | DDB_G0269380 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | DDB0232428 | CDS | 2645714 | 3942 | - | 0.348554 |
DDB_G0269384 | DDB_G0269384 | DDB0232428 | CDS | 2655370 | 1932 | + | 0.210145 | |
DDB_G0269390 | DDB_G0269390 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232428 | CDS | 2681142 | 246 | - | 0.264228 |
DDB_G0269392 | DDB_G0269392 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232428 | CDS | 2689530 | 429 | - | 0.275058 |
DDB_G0269398 | DDB_G0269398 | DDB0232428 | CDS | 2708681 | 768 | - | 0.248698 | |
DDB_G0269400 | DDB_G0269400 | DDB0232428 | CDS | 2710210 | 690 | + | 0.271014 | |
DDB_G0269402 | DDB_G0269402 | the SWIM domain is found in variety of prokaryotic and eukaryotic proteins it is predicted to have DNA-binding and protein-protein interaction functions in different contexts | DDB0232428 | CDS | 2711495 | 1527 | - | 0.195809 |
DDB_G0269404 | DDB_G0269404 | similar to human DUSP19 predicted to have dual specificity toward SerThr and Tyr-containing proteins | DDB0232428 | CDS | 2713558 | 639 | - | 0.309859 |
DDB_G0269408 | DDB_G0269408 | DDB0232428 | CDS | 2716911 | 177 | - | 0.372881 | |
DDB_G0269410 | DDB_G0269410 | catalyzes the reaction L-proline NAD(P)supsup 1-pyrroline-5-carboxylate NAD(P)H Hsupsup | DDB0232428 | CDS | 2719928 | 900 | + | 0.353333 |
DDB_G0269418 | DDB_G0269418 | similar to E. coli OsmC a stress-inducible protein and down-regulated by hyperosmotic shock there is another member of this gene family in Dictyostelium | DDB0232428 | CDS | 2728317 | 489 | - | 0.280164 |
DDB_G0269420 | DDB_G0269420 | DDB0232428 | CDS | 2730080 | 306 | + | 0.369281 | |
DDB_G0269422 | DDB_G0269422 | DDB0232428 | CDS | 2730908 | 465 | - | 0.253763 | |
DDB_G0269426 | DDB_G0269426 | DDB0232428 | CDS | 2738058 | 2202 | + | 0.315622 | |
DDB_G0269428 | DDB_G0269428 | DDB0232428 | CDS | 2743300 | 1038 | + | 0.235067 | |
DDB_G0269430 | DDB_G0269430 | Sel1-like repeats are tetratricopeptide repeat sequences originally identified in a C. elegans receptor molecule which is a key negative regulator of the Notch pathway Dictyostelium like mammals has two sel1-like proteins which are located next to each other | DDB0232428 | CDS | 2753471 | 2895 | + | 0.308463 |
DDB_G0269432 | DDB_G0269432 | Sel1-like repeats are tetratricopeptide repeat sequences originally identified in a C. elegans receptor molecule which is a key negative regulator of the Notch pathway Dictyostelium like mammals has two sel1-like proteins which are located next to each other | DDB0232428 | CDS | 2756997 | 3183 | + | 0.270814 |
DDB_G0269434 | DDB_G0269434 | DDB0232428 | CDS | 2760643 | 354 | - | 0.220339 | |
DDB_G0269436 | DDB_G0269436 | conserved Dictyostelium protein contains a putative signal sequence | DDB0232428 | CDS | 2762300 | 537 | + | 0.335196 |
DDB_G0269440 | DDB_G0269440 | DDB0232428 | CDS | 2782084 | 2166 | - | 0.244229 | |
DDB_G0269442 | DDB_G0269442 | DDB0232428 | CDS | 2784673 | 2772 | - | 0.240981 | |
DDB_G0269446 | DDB_G0269446 | DDB0232428 | CDS | 2789495 | 1077 | - | 0.221913 | |
DDB_G0269448 | DDB_G0269448 | DDB0232428 | CDS | 2791078 | 3879 | - | 0.267079 | |
DDB_G0269450 | DDB_G0269450 | DDB0232428 | CDS | 2798117 | 621 | - | 0.233494 | |
DDB_G0269452 | DDB_G0269452 | DDB0232428 | CDS | 2799520 | 2991 | - | 0.248412 | |
DDB_G0269456 | DDB_G0269456 | DDB0232428 | CDS | 2810443 | 213 | + | 0.225352 | |
DDB_G0269460 | DDB_G0269460 | DDB0232428 | CDS | 2818161 | 6666 | - | 0.271377 | |
DDB_G0269462 | DDB_G0269462 | large protein containing two ubiquitin domains has no ortholog in other organisms | DDB0232428 | CDS | 2825931 | 7014 | + | 0.286142 |
DDB_G0269464 | DDB_G0269464 | DDB0232428 | CDS | 2833557 | 228 | - | 0.298246 | |
DDB_G0269466 | DDB_G0269466 | DDB0232428 | CDS | 2834458 | 1005 | + | 0.267662 | |
DDB_G0269468 | DDB_G0269468 | DDB0232428 | CDS | 2836013 | 579 | + | 0.17962 | |
DDB_G0269478 | DDB_G0269478 | DDB0232428 | CDS | 2845861 | 195 | - | 0.235897 | |
DDB_G0269480_ps | DDB_G0269480 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 2851126 | 321 | + | 0.317757 |
DDB_G0269482 | DDB_G0269482 | conserved hypothetical Dictyostelium protein contains a weak von Willebrand factor type A domain | DDB0232428 | CDS | 2852550 | 2211 | + | 0.287653 |
DDB_G0269484 | DDB_G0269484 | DDB0232428 | CDS | 2859071 | 861 | + | 0.250871 | |
DDB_G0269486 | DDB_G0269486 | DDB0232428 | CDS | 2860257 | 3207 | + | 0.258497 | |
DDB_G0269488 | DDB_G0269488 | DDB0232428 | CDS | 2863702 | 387 | - | 0.273902 | |
DDB_G0269492_ps | DDB_G0269492 | putative pseudogene fragment similar to D. discoideum gene | DDB0232428 | CDS | 2869010 | 375 | - | 0.168 |
DDB_G0269494 | DDB_G0269494 | DDB0232428 | CDS | 2875151 | 1821 | - | 0.163646 | |
DDB_G0269498 | DDB_G0269498 | DDB0232428 | CDS | 2883107 | 1053 | - | 0.212726 | |
DDB_G0269500 | DDB_G0269500 | similar to D. purpureum protein contains 5 predicted transmembrane domains | DDB0232428 | CDS | 2887577 | 747 | + | 0.278447 |
DDB_G0269504 | DDB_G0269504 | conserved in Dictyostelids predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) there are two highly similar genes | DDB0232428 | CDS | 2898939 | 714 | - | 0.271709 |
DDB_G0269506 | DDB_G0269506 | conserved in Dictyostelids predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) there are two highly similar genes | DDB0232428 | CDS | 2900455 | 714 | - | 0.278711 |
DDB_G0269508 | DDB_G0269508 | conserved in Dictyostelids predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) there are two highly similar genes | DDB0232428 | CDS | 2902023 | 714 | - | 0.273109 |
DDB_G0269512 | DDB_G0269512 | DDB0232428 | CDS | 2908706 | 228 | - | 0.285088 | |
DDB_G0269514 | DDB_G0269514 | DDB0232428 | CDS | 2909436 | 1113 | - | 0.221024 | |
DDB_G0269516 | DDB_G0269516 | DDB0232428 | CDS | 2912518 | 126 | - | 0.373016 | |
DDB_G0269522 | DDB_G0269522 | DDB0232428 | CDS | 2944304 | 867 | - | 0.286044 | |
DDB_G0269530 | DDB_G0269530 | conserved in Dictyostelium predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) | DDB0232428 | CDS | 2954280 | 714 | + | 0.285714 |
DDB_G0269532 | DDB_G0269532 | DDB0232428 | CDS | 2955284 | 441 | + | 0.315193 | |
DDB_G0269534 | DDB_G0269534 | DDB0232428 | CDS | 2956743 | 711 | + | 0.277075 | |
DDB_G0269536 | DDB_G0269536 | DDB0232428 | CDS | 2958224 | 714 | + | 0.27591 | |
DDB_G0269538 | DDB_G0269538 | DDB0232428 | CDS | 2959764 | 711 | + | 0.277075 | |
DDB_G0269540 | DDB_G0269540 | DDB0232428 | CDS | 2961358 | 714 | + | 0.278711 | |
DDB_G0269542_RTE | DDB_G0269542 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232428 | CDS | 2962520 | 1314 | - | 0.310502 |
DDB_G0269546 | DDB_G0269546 | DDB0232428 | CDS | 2969017 | 4641 | + | 0.290239 | |
DDB_G0269556 | DDB_G0269556 | DDB0232428 | CDS | 2989310 | 702 | + | 0.279202 | |
DDB_G0269560 | DDB_G0269560 | DDB0232428 | CDS | 2996712 | 1728 | - | 0.219329 | |
DDB_G0269562 | DDB_G0269562 | DDB0232428 | CDS | 2998816 | 393 | + | 0.267176 | |
DDB_G0269564 | DDB_G0269564 | DDB0232428 | CDS | 3013601 | 702 | - | 0.290598 | |
DDB_G0269566 | DDB_G0269566 | DDB0232428 | CDS | 3015026 | 462 | - | 0.24026 | |
DDB_G0269572 | DDB_G0269572 | DDB0232428 | CDS | 3034894 | 4539 | - | 0.280238 | |
DDB_G0269576 | DDB_G0269576 | DDB0232428 | CDS | 3049822 | 1572 | + | 0.283715 | |
DDB_G0269578 | DDB_G0269578 | DDB0232428 | CDS | 3051829 | 663 | - | 0.223228 | |
DDB_G0269580 | DDB_G0269580 | DDB0232428 | CDS | 3064049 | 1314 | + | 0.268645 | |
DDB_G0269582 | DDB_G0269582 | DDB0232428 | CDS | 3066210 | 2895 | + | 0.194473 | |
DDB_G0269584 | DDB_G0269584 | DDB0232428 | CDS | 3072947 | 1410 | + | 0.285106 | |
DDB_G0269586 | DDB_G0269586 | DDB0232428 | CDS | 3074692 | 414 | - | 0.202899 | |
DDB_G0269588 | DDB_G0269588 | DDB0232428 | CDS | 3077286 | 1185 | - | 0.335865 | |
DDB_G0269590 | DDB_G0269590 | DDB0232428 | CDS | 3078895 | 4161 | - | 0.280221 | |
DDB_G0269592 | DDB_G0269592 | DDB0232428 | CDS | 3083994 | 1326 | - | 0.257164 | |
DDB_G0269594 | DDB_G0269594 | DDB0232428 | CDS | 3087129 | 2715 | + | 0.335175 | |
DDB_G0269596 | DDB_G0269596 | DDB0232428 | CDS | 3090844 | 993 | + | 0.205438 | |
DDB_G0269598 | DDB_G0269598 | DDB0232428 | CDS | 3092703 | 873 | + | 0.178694 | |
DDB_G0269600 | DDB_G0269600 | DDB0232428 | CDS | 3096976 | 1113 | - | 0.303684 | |
DDB_G0269604_ps | DDB_G0269604 | putative pseudogene fragment similar to neighboring | DDB0232428 | CDS | 3115235 | 276 | + | 0.202899 |
DDB_G0269606 | DDB_G0269606 | DDB0232428 | CDS | 3116884 | 2175 | + | 0.21977 | |
DDB_G0269608 | DDB_G0269608 | DDB0232428 | CDS | 3131550 | 2520 | + | 0.281746 | |
DDB_G0269614 | DDB_G0269614 | DDB0232428 | CDS | 3146250 | 1311 | + | 0.357742 | |
DDB_G0269618 | DDB_G0269618 | DDB0232428 | CDS | 3150646 | 1194 | + | 0.331658 | |
DDB_G0269620 | DDB_G0269620 | DDB0232428 | CDS | 3159757 | 1164 | - | 0.180412 | |
DDB_G0269622 | DDB_G0269622 | DDB0232428 | CDS | 3162116 | 912 | - | 0.23136 | |
DDB_G0269628 | DDB_G0269628 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232428 | CDS | 3183487 | 2214 | - | 0.303975 |
DDB_G0269634 | DDB_G0269634 | DDB0232428 | CDS | 3201588 | 432 | + | 0.25463 | |
DDB_G0269636 | DDB_G0269636 | DDB0232428 | CDS | 3202239 | 1215 | - | 0.268313 | |
DDB_G0269640 | DDB_G0269640 | DDB0232428 | CDS | 3205382 | 495 | - | 0.258586 | |
DDB_G0269644 | DDB_G0269644 | DDB0232428 | CDS | 3214845 | 1650 | + | 0.258182 | |
DDB_G0269646 | DDB_G0269646 | DDB0232428 | CDS | 3217078 | 684 | - | 0.236842 | |
DDB_G0269648 | DDB_G0269648 | DDB0232428 | CDS | 3218681 | 417 | + | 0.285372 | |
DDB_G0269650 | DDB_G0269650 | DDB0232428 | CDS | 3230494 | 144 | - | 0.263889 | |
DDB_G0269652 | DDB_G0269652 | DDB0232428 | CDS | 3231014 | 360 | - | 0.3 | |
DDB_G0269654_ps | DDB_G0269654 | putative pseudogene similar to D. discoideum gene | DDB0232428 | CDS | 3233164 | 2109 | + | 0.180654 |
DDB_G0269656 | DDB_G0269656 | DDB0232428 | CDS | 3235920 | 1851 | + | 0.209616 | |
DDB_G0269658 | DDB_G0269658 | DDB0232428 | CDS | 3247871 | 813 | + | 0.268143 | |
DDB_G0269662_RTE | DDB_G0269662 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232428 | CDS | 3257172 | 495 | + | 0.371717 |
DDB_G0269664 | DDB_G0269664 | DDB0232428 | CDS | 3265296 | 813 | + | 0.313653 | |
DDB_G0269666 | DDB_G0269666 | DDB0232428 | CDS | 3273351 | 390 | - | 0.205128 | |
DDB_G0269668 | DDB_G0269668 | DDB0232428 | CDS | 3278152 | 414 | - | 0.294686 | |
DDB_G0269670 | DDB_G0269670 | contains one C2 domain which is thought to be involved in calcium-dependent phospholipid binding also contains one WW domain which is involved in protein binding | DDB0232428 | CDS | 3279591 | 1707 | - | 0.3058 |
DDB_G0269672 | DDB_G0269672 | DDB0232428 | CDS | 3282508 | 216 | + | 0.310185 | |
DDB_G0269674 | DDB_G0269674 | DDB0232428 | CDS | 3283385 | 222 | + | 0.315315 | |
DDB_G0269676 | DDB_G0269676 | DDB0232428 | CDS | 3289699 | 1557 | - | 0.219011 | |
DDB_G0269680 | DDB_G0269680 | DDB0232428 | CDS | 3305788 | 2778 | - | 0.219582 | |
DDB_G0269684 | DDB_G0269684 | shares a short region of similarity with cell division cycle associated 3 (CDCA3TOME-1) in particular the presence of two DPRSPST(xxx)RTP repeats characterized in Xenopus as a F-box-like protein required for entry into mitosis and that participates in the E3 ligase complexes that mediate the ubiquitination and degradation of WEE1 kinase at G2M phase brbr bCommunity annotation:b DDB_G0269684 is weakly similar to tome-1 (Trigger of Mitotic Entry) also known as cdcA3 a gene first characterized in the mouse which is also found throughout the metazoans budding yeast also contains a related gene a target | DDB0232428 | CDS | 3317582 | 1563 | - | 0.256558 |
DDB_G0269686 | DDB_G0269686 | DDB0232428 | CDS | 3319946 | 2688 | - | 0.289062 | |
DDB_G0269692 | DDB_G0269692 | DDB0232428 | CDS | 3337065 | 1863 | + | 0.215781 | |
DDB_G0269698 | DDB_G0269698 | DDB0232428 | CDS | 3350709 | 735 | - | 0.235374 | |
DDB_G0269700 | DDB_G0269700 | DDB0232428 | CDS | 3352107 | 2622 | + | 0.249809 | |
DDB_G0269702 | DDB_G0269702 | expressed in pstAB cells and in pstA cells pstO cells upper and lower cups and stalk during culmination | DDB0232428 | CDS | 3365719 | 252 | - | 0.400794 |
DDB_G0269704 | DDB_G0269704 | DDB0232428 | CDS | 3367372 | 1272 | - | 0.264151 | |
DDB_G0269706 | DDB_G0269706 | DDB0232428 | CDS | 3373104 | 1692 | + | 0.229314 | |
DDB_G0269708 | DDB_G0269708 | contains an actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domain near its N-terminus and a C-terminal SH3 (src Homology-3) domain predicted to have an N-terminal signal peptide | DDB0232428 | CDS | 3379646 | 918 | + | 0.459695 |
DDB_G0269710 | DDB_G0269710 | DDB0232428 | CDS | 3383680 | 4329 | - | 0.275583 | |
DDB_G0269716 | DDB_G0269716 | DDB0232428 | CDS | 3397004 | 1047 | - | 0.324737 | |
DDB_G0269718 | DDB_G0269718 | DDB0232428 | CDS | 3402124 | 3972 | - | 0.276435 | |
DDB_G0269722 | DDB_G0269722 | belongs to the methyltransferase superfamily ortholog of human WBSCR22 an uncharacterized methyltransferase associated with Williams-Beuren syndrome | DDB0232428 | CDS | 3414230 | 864 | + | 0.340278 |
DDB_G0269724 | DDB_G0269724 | DDB0232428 | CDS | 3424394 | 1065 | + | 0.296714 | |
DDB_G0269730 | DDB_G0269730 | DDB0232428 | CDS | 3429232 | 543 | - | 0.348066 | |
DDB_G0269732 | DDB_G0269732 | DDB0232428 | CDS | 3443410 | 2439 | + | 0.357524 | |
DDB_G0269734 | DDB_G0269734 | DDB0232428 | CDS | 3450462 | 642 | + | 0.221184 | |
DDB_G0269736 | DDB_G0269736 | DDB0232428 | CDS | 3451792 | 2052 | - | 0.207602 | |
DDB_G0269740 | DDB_G0269740 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D | DDB0232428 | CDS | 3463314 | 2268 | + | 0.299824 |
DDB_G0269744 | DDB_G0269744 | DDB0232428 | CDS | 3468500 | 1380 | - | 0.280435 | |
DDB_G0269748 | DDB_G0269748 | DDB0232428 | CDS | 3473013 | 1458 | - | 0.265432 | |
DDB_G0269750 | DDB_G0269750 | DDB0232428 | CDS | 3480476 | 693 | + | 0.343434 | |
DDB_G0269752_ps | DDB_G0269752 | putative pseudogene similar to parts of | DDB0232428 | CDS | 3482394 | 972 | - | 0.283951 |
DDB_G0269754 | DDB_G0269754 | DDB0232428 | CDS | 3484288 | 1062 | + | 0.211864 | |
DDB_G0269756 | DDB_G0269756 | DDB0232428 | CDS | 3489330 | 1788 | - | 0.317673 | |
DDB_G0269758 | DDB_G0269758 | DDB0232428 | CDS | 3496969 | 3297 | + | 0.196239 | |
DDB_G0269760 | DDB_G0269760 | one of many putative Dictyostelium potassium channels contains 3 pentapeptide repeats | DDB0232428 | CDS | 3510769 | 1068 | + | 0.297753 |
DDB_G0269762 | DDB_G0269762 | DDB0232428 | CDS | 3512075 | 2475 | - | 0.314747 | |
DDB_G0269766 | DDB_G0269766 | similar to UPF0451 family proteins contains 3 predicted transmembrane domains there is an almost identical gene | DDB0232428 | CDS | 3517400 | 363 | - | 0.30854 |
DDB_G0269774 | DDB_G0269774 | DDB0232428 | CDS | 3527142 | 795 | + | 0.188679 | |
DDB_G0269776 | DDB_G0269776 | DDB0232428 | CDS | 3528359 | 1158 | - | 0.262522 | |
DDB_G0269778 | DDB_G0269778 | DDB0232428 | CDS | 3547267 | 1083 | + | 0.290859 | |
DDB_G0269780 | DDB_G0269780 | DDB0232428 | CDS | 3549387 | 3099 | + | 0.238464 | |
DDB_G0269782 | DDB_G0269782 | DDB0232428 | CDS | 3553343 | 840 | - | 0.263095 | |
DDB_G0269784 | DDB_G0269784 | DDB0232428 | CDS | 3555282 | 606 | + | 0.283828 | |
DDB_G0269788 | DDB_G0269788 | catalyzes the first of three steps required to remove two C-4 methyl groups from an intermediate in ergosterol biosynthesis almost identical to the neighboring gene | DDB0232428 | CDS | 3558146 | 813 | + | 0.312423 |
DDB_G0269794 | DDB_G0269794 | DDB0232428 | CDS | 3580948 | 768 | + | 0.221354 | |
DDB_G0269796_ps | DDB_G0269796 | putative pseudogene highly similar to | DDB0232428 | CDS | 3588898 | 3621 | + | 0.307374 |
DDB_G0269800 | DDB_G0269800 | putative ortholog of the conserved chromatin assembly factor 1 (CAF1) subunit Bbr bNote:b Do not confuse this gene with | DDB0232428 | CDS | 3628624 | 2115 | - | 0.274704 |
DDB_G0269802 | DDB_G0269802 | DDB0232428 | CDS | 3631591 | 1854 | + | 0.245415 | |
DDB_G0269804 | DDB_G0269804 | DDB0232428 | CDS | 3637012 | 450 | + | 0.308889 | |
DDB_G0269806 | DDB_G0269806 | DDB0232428 | CDS | 3645779 | 279 | - | 0.27957 | |
DDB_G0269808 | DDB_G0269808 | DDB0232428 | CDS | 3646239 | 465 | - | 0.255914 | |
DDB_G0269812 | DDB_G0269812 | DDB0232428 | CDS | 3658614 | 651 | - | 0.253456 | |
DDB_G0269816 | DDB_G0269816 | ortholog of the mammalian kin17 protein a zinc finger nuclear protein | DDB0232428 | CDS | 3664995 | 1338 | + | 0.245142 |
DDB_G0269818 | DDB_G0269818 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232428 | CDS | 3667020 | 276 | - | 0.369565 |
DDB_G0269820 | DDB_G0269820 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232428 | CDS | 3669036 | 276 | + | 0.358696 |
DDB_G0269824 | DDB_G0269824 | DDB0232428 | CDS | 3671523 | 1341 | + | 0.217002 | |
DDB_G0269826 | DDB_G0269826 | DDB0232428 | CDS | 3675572 | 3645 | - | 0.201097 | |
DDB_G0269828 | DDB_G0269828 | putative ortholog of SSSCA1 (Sjogrens syndrome scleroderma autoantigen 1) that might play a role in mitosis | DDB0232428 | CDS | 3682321 | 1257 | + | 0.270485 |
DDB_G0269830 | DDB_G0269830 | DDB0232428 | CDS | 3683818 | 1491 | - | 0.239437 | |
DDB_G0269832 | DDB_G0269832 | DDB0232428 | CDS | 3685708 | 822 | + | 0.274939 | |
DDB_G0269834 | DDB_G0269834 | DDB0232428 | CDS | 3686674 | 1212 | - | 0.306931 | |
DDB_G0269836 | DDB_G0269836 | DDB0232428 | CDS | 3688411 | 786 | - | 0.229008 | |
DDB_G0269838 | DDB_G0269838 | DDB0232428 | CDS | 3690037 | 603 | + | 0.232172 | |
DDB_G0269840 | DDB_G0269840 | contains one putative transmembrane domain similar to D. purpureum protein | DDB0232428 | CDS | 3697371 | 1650 | - | 0.246667 |
DDB_G0269842 | DDB_G0269842 | contains two C2H2-type zinc finger domains contains one coiled-coil domain | DDB0232428 | CDS | 3701971 | 4785 | - | 0.266458 |
DDB_G0269844 | DDB_G0269844 | DDB0232428 | CDS | 3709558 | 126 | - | 0.293651 | |
DDB_G0269846 | DDB_G0269846 | DDB0232428 | CDS | 3710387 | 360 | - | 0.280556 | |
DDB_G0269850 | DDB_G0269850 | contains a signal peptide and a single predicted transmembrane domain at the C-terminus small gene family in D. discoideum D. purpureum has a single gene | DDB0232428 | CDS | 3719484 | 3081 | + | 0.313859 |
DDB_G0269858 | DDB_G0269858 | DDB0232428 | CDS | 3745025 | 1683 | - | 0.193108 | |
DDB_G0269860 | DDB_G0269860 | similar to importin-7 and importin-8 from numerous eukaryotes involved in nuclear protein import | DDB0232428 | CDS | 3747132 | 3198 | + | 0.288618 |
DDB_G0269864 | DDB_G0269864 | DDB0232428 | CDS | 3763159 | 1569 | - | 0.289356 | |
DDB_G0269866 | DDB_G0269866 | DDB0232428 | CDS | 3767514 | 294 | + | 0.244898 | |
DDB_G0269870 | DDB_G0269870 | DDB0232428 | CDS | 3768283 | 477 | + | 0.249476 | |
DDB_G0269874 | DDB_G0269874 | DDB0232428 | CDS | 3773813 | 1095 | + | 0.317808 | |
DDB_G0269880 | DDB_G0269880 | conserved protein may catalyze reversible transfer reactions of coenzyme A groups from CoA-thioesters to free acids | DDB0232428 | CDS | 3785577 | 1416 | + | 0.249294 |
DDB_G0269882 | DDB_G0269882 | similar to bacterial outer membrane lipoprotein Blc lipocalins are involved in the binding and transport of small molecules such as lipids steroid hormones bilins and retinoids | DDB0232428 | CDS | 3787682 | 549 | + | 0.28051 |
DDB_G0269884 | DDB_G0269884 | DDB0232428 | CDS | 3797962 | 2532 | + | 0.232622 | |
DDB_G0269886 | DDB_G0269886 | DDB0232428 | CDS | 3801076 | 1044 | + | 0.264368 | |
DDB_G0269888 | DDB_G0269888 | DDB0232428 | CDS | 3802780 | 810 | + | 0.188889 | |
DDB_G0269890 | DDB_G0269890 | ortholog of human APOA1BP S. pombe mug182 | DDB0232428 | CDS | 3803772 | 708 | + | 0.265537 |
DDB_G0269892 | DDB_G0269892 | DDB0232428 | CDS | 3806514 | 1458 | + | 0.357339 | |
DDB_G0269898 | DDB_G0269898 | DDB0232428 | CDS | 3820454 | 2829 | + | 0.298339 | |
DDB_G0269904 | DDB_G0269904 | DDB0232428 | CDS | 3827661 | 177 | - | 0.305085 | |
DDB_G0269908 | DDB_G0269908 | ortholog of human FA2H S. cerevisiae SCS7 contains a cytochrome b5 heme-binding domain and 4 predicted transmembrane domains | DDB0232428 | CDS | 3831693 | 1122 | - | 0.272727 |
DDB_G0269910 | DDB_G0269910 | DDB0232428 | CDS | 3847028 | 1107 | + | 0.385727 | |
DDB_G0269920 | DDB_G0269920 | DDB0232428 | CDS | 3868370 | 2583 | + | 0.218351 | |
DDB_G0269926 | DDB_G0269926 | DDB0232428 | CDS | 3880004 | 2175 | - | 0.306207 | |
DDB_G0269928 | DDB_G0269928 | contains a predicted signal peptide similar to D. purpureum protein | DDB0232428 | CDS | 3884502 | 714 | - | 0.327731 |
DDB_G0269930 | DDB_G0269930 | DDB0232428 | CDS | 3886301 | 297 | + | 0.245791 | |
DDB_G0269934 | DDB_G0269934 | DDB0232428 | CDS | 3897216 | 6135 | + | 0.351263 | |
DDB_G0269936 | DDB_G0269936 | DDB0232428 | CDS | 3903678 | 1053 | + | 0.235518 | |
DDB_G0269942 | DDB_G0269942 | belongs to the synaptobrevin family ortholog of human SEC22B contains a longin domain and a v-snare coiled-coil domain contains 1 predicted transmembrane domain | DDB0232428 | CDS | 3911017 | 645 | + | 0.24031 |
DDB_G0269944 | DDB_G0269944 | DDB0232428 | CDS | 3913001 | 909 | + | 0.20242 | |
DDB_G0269946 | DDB_G0269946 | DDB0232428 | CDS | 3915625 | 267 | - | 0.262172 | |
DDB_G0269952 | DDB_G0269952 | DDB0232428 | CDS | 3922020 | 795 | - | 0.208805 | |
DDB_G0269954 | DDB_G0269954 | DDB0232428 | CDS | 3923641 | 2385 | + | 0.305241 | |
DDB_G0269956_RTE | DDB_G0269956 | DDB0232428 | CDS | 3927053 | 888 | - | 0.370495 | |
DDB_G0269958 | DDB_G0269958 | DDB0232428 | CDS | 3929456 | 366 | - | 0.325137 | |
DDB_G0269960 | DDB_G0269960 | DDB0232428 | CDS | 3932800 | 558 | + | 0.200717 | |
DDB_G0269962 | DDB_G0269962 | DDB0232428 | CDS | 3933879 | 2367 | - | 0.244613 | |
DDB_G0269964 | DDB_G0269964 | DDB0232428 | CDS | 3938864 | 1998 | + | 0.285285 | |
DDB_G0269968 | DDB_G0269968 | similar to human ARMC1 contains an ARM repeat ARM-repeat proteins are involved in various processes including intracellular signalling and cytoskeletal regulation | DDB0232428 | CDS | 3945381 | 900 | - | 0.313333 |
DDB_G0269970 | DDB_G0269970 | DDB0232428 | CDS | 3946896 | 774 | - | 0.22739 | |
DDB_G0269974 | DDB_G0269974 | DDB0232428 | CDS | 3955288 | 1062 | + | 0.200565 | |
DDB_G0269976 | DDB_G0269976 | DDB0232428 | CDS | 3956916 | 2103 | + | 0.285782 | |
DDB_G0269978 | DDB_G0269978 | DDB0232428 | CDS | 3960032 | 1521 | + | 0.266272 | |
DDB_G0269982 | DDB_G0269982 | similar to human TBC1D22B S. pombe gyp1 | DDB0232428 | CDS | 3972852 | 1635 | - | 0.292966 |
DDB_G0269984 | DDB_G0269984 | DDB0232428 | CDS | 3976381 | 390 | - | 0.192308 | |
DDB_G0269986 | DDB_G0269986 | DDB0232428 | CDS | 3977474 | 2391 | + | 0.24634 | |
DDB_G0269988 | DDB_G0269988 | DDB0232428 | CDS | 3985001 | 420 | + | 0.280952 | |
DDB_G0269992 | DDB_G0269992 | DDB0232428 | CDS | 3988412 | 651 | + | 0.322581 | |
DDB_G0269994 | DDB_G0269994 | DDB0232428 | CDS | 3990838 | 1008 | + | 0.282738 | |
DDB_G0269998 | DDB_G0269998 | DDB0232428 | CDS | 3995432 | 3243 | + | 0.211224 | |
DDB_G0270000 | DDB_G0270000 | DDB0232428 | CDS | 3999184 | 1275 | + | 0.21098 | |
DDB_G0270002 | DDB_G0270002 | DDB0232428 | CDS | 4001179 | 1284 | + | 0.19704 | |
DDB_G0270004 | DDB_G0270004 | DDB0232428 | CDS | 4011450 | 444 | - | 0.286036 | |
DDB_G0270008 | DDB_G0270008 | DDB0232428 | CDS | 4022273 | 378 | + | 0.396825 | |
DDB_G0270010 | DDB_G0270010 | DDB0232428 | CDS | 4023401 | 210 | + | 0.285714 | |
DDB_G0270012 | DDB_G0270012 | DDB0232428 | CDS | 4024276 | 315 | + | 0.425397 | |
DDB_G0270014 | DDB_G0270014 | DDB0232428 | CDS | 4026325 | 621 | + | 0.326892 | |
DDB_G0270016 | DDB_G0270016 | DDB0232428 | CDS | 4029381 | 909 | - | 0.225523 | |
DDB_G0270018 | DDB_G0270018 | DDB0232428 | CDS | 4030543 | 942 | - | 0.291932 | |
DDB_G0270022 | DDB_G0270022 | DDB0232428 | CDS | 4041315 | 1335 | + | 0.266667 | |
DDB_G0270026 | DDB_G0270026 | DDB0232428 | CDS | 4051948 | 798 | + | 0.285714 | |
DDB_G0270028 | DDB_G0270028 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232428 | CDS | 4053112 | 1488 | + | 0.350806 |
DDB_G0270030 | DDB_G0270030 | DDB0232428 | CDS | 4058777 | 1068 | + | 0.272472 | |
DDB_G0270032 | DDB_G0270032 | DDB0232428 | CDS | 4060239 | 1074 | + | 0.258845 | |
DDB_G0270034 | DDB_G0270034 | DDB0232428 | CDS | 4066936 | 768 | + | 0.283854 | |
DDB_G0270038 | DDB_G0270038 | DDB0232428 | CDS | 4074913 | 492 | - | 0.278455 | |
DDB_G0270040 | DDB_G0270040 | DDB0232428 | CDS | 4075572 | 3240 | - | 0.228395 | |
DDB_G0270044 | DDB_G0270044 | DDB0232428 | CDS | 4092193 | 1254 | - | 0.259968 | |
DDB_G0270046 | DDB_G0270046 | DDB0232428 | CDS | 4094301 | 1806 | + | 0.281838 | |
DDB_G0270048 | DDB_G0270048 | DDB0232428 | CDS | 4103221 | 1566 | + | 0.233078 | |
DDB_G0270050 | DDB_G0270050 | DDB0232428 | CDS | 4105655 | 663 | + | 0.309201 | |
DDB_G0270052 | DDB_G0270052 | DDB0232428 | CDS | 4106977 | 4128 | - | 0.204457 | |
DDB_G0270054 | DDB_G0270054 | DDB0232428 | CDS | 4111305 | 390 | + | 0.287179 | |
DDB_G0270056 | DDB_G0270056 | DDB0232428 | CDS | 4130694 | 4299 | - | 0.25378 | |
DDB_G0270058 | DDB_G0270058 | DDB0232428 | CDS | 4143232 | 3414 | + | 0.306385 | |
DDB_G0270060 | DDB_G0270060 | highly similar to | DDB0232428 | CDS | 4148273 | 3414 | + | 0.306093 |
DDB_G0270062 | DDB_G0270062 | DDB0232428 | CDS | 4152838 | 4488 | + | 0.227718 | |
DDB_G0270064_RTE | DDB_G0270064 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 4159771 | 855 | + | 0.291228 |
DDB_G0270066 | DDB_G0270066 | DDB0232428 | CDS | 4165016 | 5736 | - | 0.284693 | |
DDB_G0270068 | DDB_G0270068 | DDB0232428 | CDS | 4175523 | 3891 | + | 0.271139 | |
DDB_G0270070 | DDB_G0270070 | DDB0232428 | CDS | 4180324 | 1284 | + | 0.342679 | |
DDB_G0270072 | DDB_G0270072 | contains two coiled-coil domains brbr bCommunity annotation:b There is a chance that DDB_G0270072 codes for an SMC protein. The blast homology to Ciona XCAP-E is weak but when the predicted XCAP-E protein is compared with DDB_G0270072 by Blast2Sequences multiple regions of homology are found and the overall E-value is 0001. The strongest homology is in the N-terminus where SMC proteins are generally strongly conserved. SMC proteins contain two prominent coiled-coil domains (separated by a hinge region) according to the Dictybase curators these regions are present in DDB_G0270072. SMC proteins are involved in sister chromosome cohesion and mitotic chromosome condensation. Most genes with functions in cell cycle progression are overexpressed in a strain lacking the Dicty Rb ortholog rblA. The Dicty SMC genes are highly overexpressed in this strain(10-15-fold) DDB_G0270072 is overexpressed 23-fold (p4e-28) a really exceptional value. Harry MacWilliams May 2010br | DDB0232428 | CDS | 4182087 | 1815 | - | 0.239118 |
DDB_G0270074 | DDB_G0270074 | belongs to the glycoside hydrolase 5 (cellulase) family 5 contains a predicted signal sequence | DDB0232428 | CDS | 4187072 | 1530 | - | 0.309804 |
DDB_G0270076 | DDB_G0270076 | DDB0232428 | CDS | 4189203 | 714 | - | 0.278711 | |
DDB_G0270078 | DDB_G0270078 | DDB0232428 | CDS | 4191196 | 714 | - | 0.281513 | |
DDB_G0270080 | DDB_G0270080 | DDB0232428 | CDS | 4192479 | 345 | - | 0.281159 | |
DDB_G0270084_ps | DDB_G0270084 | putative pseudogene similar to Dictyostelium genes | DDB0232428 | CDS | 4193386 | 363 | + | 0.214876 |
DDB_G0270086 | DDB_G0270086 | similar to bacterial outer membrane lipoprotein Blc lipocalins are involved in the binding and transport of small molecules such as lipids steroid hormones bilins and retinoids | DDB0232428 | CDS | 4194168 | 540 | - | 0.287037 |
DDB_G0270088 | DDB_G0270088 | DDB0232428 | CDS | 4195432 | 1680 | - | 0.325 | |
DDB_G0270090 | DDB_G0270090 | DDB0232428 | CDS | 4198052 | 774 | + | 0.22093 | |
DDB_G0270092 | DDB_G0270092 | DDB0232428 | CDS | 4199147 | 771 | + | 0.223087 | |
DDB_G0270094_ps | DDB_G0270094 | putative pseudogene highly similar to | DDB0232428 | CDS | 4203953 | 675 | + | 0.275556 |
DDB_G0270096 | DDB_G0270096 | DDB0232428 | CDS | 4205387 | 2373 | - | 0.292035 | |
DDB_G0270100 | DDB_G0270100 | DDB0232428 | CDS | 4212241 | 1827 | + | 0.238643 | |
DDB_G0270104 | DDB_G0270104 | similar to plant and fungi NADH dehydrogenases such as S. cerevisiae NDE1 and NDE2 the external mitochondrial NADH dehydrogenases that catalyze the oxidation of cytosolic NADH | DDB0232428 | CDS | 4225842 | 1356 | - | 0.297935 |
DDB_G0270106 | DDB_G0270106 | DDB0232428 | CDS | 4238878 | 2925 | - | 0.321026 | |
DDB_G0270108_ps | DDB_G0270108 | putative pseudogene almost identical to parts of the putative NADH dehydrogenase | DDB0232428 | CDS | 4243063 | 390 | + | 0.317949 |
DDB_G0270112 | DDB_G0270112 | DDB0232428 | CDS | 4251451 | 1611 | - | 0.258845 | |
DDB_G0270114 | DDB_G0270114 | DDB0232428 | CDS | 4260144 | 1101 | - | 0.220708 | |
DDB_G0270116 | DDB_G0270116 | DDB0232428 | CDS | 4262007 | 951 | + | 0.256572 | |
DDB_G0270118 | DDB_G0270118 | contains a PPI_Ypi1 domain which is predicted to be involved in protein phosphatase regulation | DDB0232428 | CDS | 4271883 | 393 | - | 0.328244 |
DDB_G0270128 | DDB_G0270128 | DDB0232428 | CDS | 4289930 | 2667 | + | 0.243345 | |
DDB_G0270130 | DDB_G0270130 | DDB0232428 | CDS | 4293863 | 1767 | + | 0.285229 | |
DDB_G0270132 | DDB_G0270132 | DDB0232428 | CDS | 4296112 | 462 | + | 0.316017 | |
DDB_G0270134 | DDB_G0270134 | DDB0232428 | CDS | 4297045 | 459 | + | 0.309368 | |
DDB_G0270136 | DDB_G0270136 | DDB0232428 | CDS | 4297732 | 366 | - | 0.237705 | |
DDB_G0270144_ps | DDB_G0270144 | putative pseudogene similar to D. discoideum genes | DDB0232428 | CDS | 4302709 | 408 | + | 0.291667 |
DDB_G0270146 | DDB_G0270146 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis | DDB0232428 | CDS | 4304005 | 1908 | - | 0.287212 |
DDB_G0270154 | DDB_G0270154 | DDB0232428 | CDS | 4327219 | 1125 | + | 0.266667 | |
DDB_G0270156 | DDB_G0270156 | DDB0232428 | CDS | 4329080 | 2703 | - | 0.27488 | |
DDB_G0270158 | DDB_G0270158 | DDB0232428 | CDS | 4337917 | 588 | + | 0.238095 | |
DDB_G0270160 | DDB_G0270160 | DDB0232428 | CDS | 4339530 | 645 | + | 0.355039 | |
DDB_G0270164 | DDB_G0270164 | DDB0232428 | CDS | 4350714 | 273 | + | 0.358974 | |
DDB_G0270166 | DDB_G0270166 | DDB0232428 | CDS | 4352624 | 255 | + | 0.368627 | |
DDB_G0270168 | DDB_G0270168 | DDB0232428 | CDS | 4358663 | 684 | + | 0.27193 | |
DDB_G0270170 | DDB_G0270170 | atypical protein kinase GTE group weakly simlar to A. thaliana bromodomain-containing protein (GenBank NP_201138) | DDB0232428 | CDS | 4360881 | 4737 | + | 0.299979 |
DDB_G0270172 | DDB_G0270172 | DDB0232428 | CDS | 4366498 | 552 | - | 0.226449 | |
DDB_G0270176 | DDB_G0270176 | the amino terminus contains leucine-rich repeats and the carboxyl terminus a protein phosphatase 2C domain a serinethreonine specific protein phosphatase with broad substrate specificity and dependent on divalent cations (mainly manganese and magnesium) for its activity | DDB0232428 | CDS | 4369737 | 4080 | + | 0.239216 |
DDB_G0270180 | DDB_G0270180 | DDB0232428 | CDS | 4377432 | 357 | + | 0.263305 | |
DDB_G0270182 | DDB_G0270182 | DDB0232428 | CDS | 4377987 | 1089 | - | 0.258035 | |
DDB_G0270186 | DDB_G0270186 | putative copper transporter contains 3 predicted transmembrane domains | DDB0232428 | CDS | 4381272 | 471 | + | 0.212314 |
DDB_G0270190 | DDB_G0270190 | similar to bacterial endo-14-beta-glucanase expressed in pstAO cells | DDB0232428 | CDS | 4384621 | 1719 | - | 0.294939 |
DDB_G0270192 | DDB_G0270192 | conserved from bacteria to plants to alveolata contains 10 predicted transmembrane domains | DDB0232428 | CDS | 4389263 | 1284 | + | 0.246885 |
DDB_G0270194 | DDB_G0270194 | DDB0232428 | CDS | 4391158 | 471 | + | 0.261146 | |
DDB_G0270196 | DDB_G0270196 | DDB0232428 | CDS | 4393614 | 1125 | + | 0.264 | |
DDB_G0270200 | DDB_G0270200 | DDB0232428 | CDS | 4397167 | 2088 | - | 0.246169 | |
DDB_G0270202 | DDB_G0270202 | DDB0232428 | CDS | 4400104 | 714 | + | 0.298319 | |
DDB_G0270206 | DDB_G0270206 | DDB0232428 | CDS | 4404424 | 3465 | + | 0.223954 | |
DDB_G0270208 | DDB_G0270208 | DDB0232428 | CDS | 4413499 | 1068 | - | 0.176966 | |
DDB_G0270212 | DDB_G0270212 | similar to discoidin I almost identical to its downstream gene DD7-1 | DDB0232428 | CDS | 4416314 | 789 | - | 0.326996 |
DDB_G0270216 | DDB_G0270216 | DDB0232428 | CDS | 4420069 | 3033 | - | 0.132212 | |
DDB_G0270220 | DDB_G0270220 | DDB0232428 | CDS | 4432689 | 2520 | + | 0.314683 | |
DDB_G0270222 | DDB_G0270222 | DDB0232428 | CDS | 4435722 | 468 | - | 0.217949 | |
DDB_G0270224 | DDB_G0270224 | DDB0232428 | CDS | 4437084 | 3615 | + | 0.15823 | |
DDB_G0270226 | DDB_G0270226 | DDB0232428 | CDS | 4441377 | 183 | + | 0.26776 | |
DDB_G0270232 | DDB_G0270232 | DDB0232428 | CDS | 4457457 | 2307 | + | 0.219766 | |
DDB_G0270234 | DDB_G0270234 | DDB0232428 | CDS | 4466006 | 159 | - | 0.345912 | |
DDB_G0270236 | DDB_G0270236 | DDB0232428 | CDS | 4474318 | 192 | + | 0.234375 | |
DDB_G0270238 | DDB_G0270238 | DDB0232428 | CDS | 4474835 | 4002 | - | 0.290605 | |
DDB_G0270240 | DDB_G0270240 | DDB0232428 | CDS | 4481557 | 246 | + | 0.337398 | |
DDB_G0270242 | DDB_G0270242 | DDB0232428 | CDS | 4484790 | 759 | - | 0.227931 | |
DDB_G0270244 | DDB_G0270244 | DDB0232428 | CDS | 4485669 | 840 | + | 0.192857 | |
DDB_G0270246 | DDB_G0270246 | DDB0232428 | CDS | 4514326 | 1725 | - | 0.225507 | |
DDB_G0270250 | DDB_G0270250 | DDB0232428 | CDS | 4517624 | 1257 | + | 0.222753 | |
DDB_G0270252 | DDB_G0270252 | DDB0232428 | CDS | 4519307 | 2043 | - | 0.256975 | |
DDB_G0270254 | DDB_G0270254 | DDB0232428 | CDS | 4521755 | 351 | + | 0.222222 | |
DDB_G0270256 | DDB_G0270256 | DDB0232428 | CDS | 4522306 | 405 | - | 0.279012 | |
DDB_G0270258 | DDB_G0270258 | DDB0232428 | CDS | 4523481 | 1158 | - | 0.196028 | |
DDB_G0270262 | DDB_G0270262 | DDB0232428 | CDS | 4528758 | 627 | + | 0.23764 | |
DDB_G0270266 | DDB_G0270266 | DDB0232428 | CDS | 4534905 | 2661 | - | 0.195039 | |
DDB_G0270268 | DDB_G0270268 | DDB0232428 | CDS | 4540670 | 1617 | + | 0.222016 | |
DDB_G0270274_RTE | DDB_G0270274 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 4551821 | 288 | + | 0.340278 |
DDB_G0270276 | DDB_G0270276 | DDB0232428 | CDS | 4552978 | 381 | - | 0.288714 | |
DDB_G0270278 | DDB_G0270278 | DDB0232428 | CDS | 4558267 | 3390 | + | 0.259587 | |
DDB_G0270280 | DDB_G0270280 | DDB0232428 | CDS | 4567595 | 219 | + | 0.383562 | |
DDB_G0270282 | DDB_G0270282 | DDB0232428 | CDS | 4576953 | 1326 | - | 0.242081 | |
DDB_G0270284 | DDB_G0270284 | contains an N-terminal DOMON domain as it occurs in dopamine beta-monooxygenases the Dictyostelium protein is followed by a cytochrome b561 domain which contains 5 putative transmembrane regions in addition the protein contains a putative signal peptide | DDB0232428 | CDS | 4579488 | 1173 | + | 0.277067 |
DDB_G0270286 | DDB_G0270286 | DDB0232428 | CDS | 4590927 | 1938 | + | 0.20227 | |
DDB_G0270288 | DDB_G0270288 | DDB0232428 | CDS | 4593105 | 417 | - | 0.292566 | |
DDB_G0270290 | DDB_G0270290 | DDB0232428 | CDS | 4594432 | 417 | - | 0.29976 | |
DDB_G0270292 | DDB_G0270292 | DDB0232428 | CDS | 4595762 | 375 | - | 0.309333 | |
DDB_G0270294 | DDB_G0270294 | DDB0232428 | CDS | 4597029 | 417 | - | 0.297362 | |
DDB_G0270300 | DDB_G0270300 | DDB0232428 | CDS | 4604758 | 801 | - | 0.227216 | |
DDB_G0270302 | DDB_G0270302 | DDB0232428 | CDS | 4605944 | 657 | - | 0.251142 | |
DDB_G0270304 | DDB_G0270304 | DDB0232428 | CDS | 4607306 | 630 | - | 0.284127 | |
DDB_G0270306 | DDB_G0270306 | DDB0232428 | CDS | 4610085 | 1449 | + | 0.277433 | |
DDB_G0270308 | DDB_G0270308 | DDB0232428 | CDS | 4611669 | 1710 | - | 0.19883 | |
DDB_G0270310 | DDB_G0270310 | DDB0232428 | CDS | 4614754 | 993 | + | 0.270896 | |
DDB_G0270312 | DDB_G0270312 | members of this family are membrane proteins involved in long chain fatty acid elongation systems that produce 26-carbon precursors for ceramide and sphingolipid synthesis contains 7 putative transmembrane domains | DDB0232428 | CDS | 4616748 | 792 | + | 0.255051 |
DDB_G0270318 | DDB_G0270318 | DDB0232428 | CDS | 4638217 | 1041 | + | 0.292988 | |
DDB_G0270322 | DDB_G0270322 | DDB0232428 | CDS | 4641717 | 2163 | + | 0.266297 | |
DDB_G0270324 | DDB_G0270324 | similar to N-myc downstream regulated gene 1 (NDRG1) defects in NDRG1 are the cause of Charcot-Marie-Tooth disease type 4D (CMT4D) also known as hereditary motor and sensory neuropathy Lom type (HMSNL) | DDB0232428 | CDS | 4644690 | 981 | + | 0.275229 |
DDB_G0270326 | DDB_G0270326 | DDB0232428 | CDS | 4649483 | 3231 | + | 0.205509 | |
DDB_G0270328 | DDB_G0270328 | contains 7 Dictyostelium (slime mold) repeats nearly identical to | DDB0232428 | CDS | 4652829 | 1113 | - | 0.324349 |
DDB_G0270330 | DDB_G0270330 | nearly identical to | DDB0232428 | CDS | 4654733 | 1548 | + | 0.288114 |
DDB_G0270342 | DDB_G0270342 | DDB0232428 | CDS | 4671955 | 1695 | - | 0.323304 | |
DDB_G0270344 | DDB_G0270344 | DDB0232428 | CDS | 4674130 | 4644 | - | 0.225668 | |
DDB_G0270348 | DDB_G0270348 | DDB0232428 | CDS | 4683008 | 408 | - | 0.306373 | |
DDB_G0270350_ps | DDB_G0270350 | putative pseudogene similar to D. discoideum gene | DDB0232428 | CDS | 4690187 | 834 | + | 0.311751 |
DDB_G0270352 | DDB_G0270352 | DDB0232428 | CDS | 4693514 | 1887 | + | 0.323264 | |
DDB_G0270358 | DDB_G0270358 | ortholog of mammalian ubxn7 (UBX domain-containing protein 7) contains a UBX domain found in ubiquitin-regulatory proteins | DDB0232428 | CDS | 4701032 | 1512 | + | 0.29828 |
DDB_G0270364 | DDB_G0270364 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon but a shorter second exon | DDB0232428 | CDS | 4714774 | 192 | + | 0.322917 |
DDB_G0270366 | DDB_G0270366 | nearly identical to | DDB0232428 | CDS | 4718091 | 1548 | - | 0.291344 |
DDB_G0270368 | DDB_G0270368 | contains 7 Dictyostelium (slime mold) repeats nearly identical to | DDB0232428 | CDS | 4720670 | 1113 | + | 0.325247 |
DDB_G0270372_ps | DDB_G0270372 | putative pseudogene fragment similar to | DDB0232428 | CDS | 4721881 | 804 | - | 0.218905 |
DDB_G0270374_ps | DDB_G0270374 | putative pseudogene similar to a family of small D. discoideum genes including | DDB0232428 | CDS | 4724596 | 129 | + | 0.426357 |
DDB_G0270376 | DDB_G0270376 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232428 | CDS | 4726483 | 252 | + | 0.349206 |
DDB_G0270378 | DDB_G0270378 | similar to human TTC39C matches PFAM outer membrane protein IML2 mitochondrialtetratricopeptide repeat protein 39 | DDB0232428 | CDS | 4727960 | 1596 | + | 0.311404 |
DDB_G0270382 | DDB_G0270382 | DDB0232428 | CDS | 4732515 | 975 | + | 0.321026 | |
DDB_G0270386 | DDB_G0270386 | DDB0232428 | CDS | 4735593 | 1719 | + | 0.267016 | |
DDB_G0270388 | DDB_G0270388 | DDB0232428 | CDS | 4737656 | 2901 | - | 0.386763 | |
DDB_G0270390 | DDB_G0270390 | DDB0232428 | CDS | 4742507 | 2241 | + | 0.264614 | |
DDB_G0270394 | DDB_G0270394 | DDB0232428 | CDS | 4751920 | 327 | - | 0.256881 | |
DDB_G0270400 | DDB_G0270400 | DDB0232428 | CDS | 4773468 | 1629 | - | 0.263966 | |
DDB_G0270402 | DDB_G0270402 | contains a putative Like-Sm (Lsm) domain possible homolog of LSM12 | DDB0232428 | CDS | 4784022 | 657 | + | 0.286149 |
DDB_G0270408 | DDB_G0270408 | DDB0232428 | CDS | 4810031 | 1209 | + | 0.27378 | |
DDB_G0270410 | DDB_G0270410 | DDB0232428 | CDS | 4811940 | 6315 | - | 0.304513 | |
DDB_G0270412 | DDB_G0270412 | DDB0232428 | CDS | 4819722 | 1983 | + | 0.2824 | |
DDB_G0270416 | DDB_G0270416 | DDB0232428 | CDS | 4823455 | 2646 | + | 0.228647 | |
DDB_G0270420 | DDB_G0270420 | DDB0232428 | CDS | 4840357 | 966 | - | 0.308489 | |
DDB_G0270426 | DDB_G0270426 | DDB0232428 | CDS | 4851386 | 459 | + | 0.267974 | |
DDB_G0270428 | DDB_G0270428 | DDB0232428 | CDS | 4852185 | 690 | - | 0.227536 | |
DDB_G0270432 | DDB_G0270432 | DDB0232428 | CDS | 4857327 | 2865 | - | 0.253403 | |
DDB_G0270436 | DDB_G0270436 | DDB0232428 | CDS | 4873137 | 1566 | - | 0.297573 | |
DDB_G0270438 | DDB_G0270438 | DDB0232428 | CDS | 4881217 | 345 | + | 0.301449 | |
DDB_G0270440 | DDB_G0270440 | DDB0232428 | CDS | 4882133 | 519 | + | 0.235067 | |
DDB_G0270444 | DDB_G0270444 | kinase domain similar to mitogen-activated protein kinases does not contain the consensus sequences required for kinase function N-terminus contains WD40 repeats | DDB0232428 | CDS | 4890352 | 4083 | + | 0.281411 |
DDB_G0270446 | DDB_G0270446 | DDB0232428 | CDS | 4899926 | 2979 | - | 0.249413 | |
DDB_G0270448 | DDB_G0270448 | DDB0232428 | CDS | 4903242 | 1347 | + | 0.203415 | |
DDB_G0270450 | DDB_G0270450 | RRM domain similar to that of splicing factor RBM17 (RNA binding motif 17) a splice factor | DDB0232428 | CDS | 4904923 | 1119 | - | 0.258266 |
DDB_G0270452 | DDB_G0270452 | DDB0232428 | CDS | 4906213 | 2493 | + | 0.215804 | |
DDB_G0270454 | DDB_G0270454 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232428 | CDS | 4909508 | 456 | + | 0.247807 |
DDB_G0270456_TE | DDB_G0270456 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232428 | CDS | 4916220 | 231 | - | 0.277056 |
DDB_G0270458_RTE | DDB_G0270458 | DDB0232428 | CDS | 2404459 | 2517 | + | 0.340882 | |
DDB_G0270460_RTE | DDB_G0270460 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 2411033 | 642 | - | 0.277259 |
DDB_G0270462_RTE | DDB_G0270462 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2425241 | 531 | - | 0.310734 |
DDB_G0270464_RTE | DDB_G0270464 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2425838 | 1620 | + | 0.350617 |
DDB_G0270466 | DDB_G0270466 | DDB0232428 | CDS | 2429715 | 1395 | - | 0.200717 | |
DDB_G0270468 | DDB_G0270468 | DDB0232428 | CDS | 2447181 | 1197 | - | 0.201337 | |
DDB_G0270470 | DDB_G0270470 | DDB0232428 | CDS | 2488609 | 1251 | - | 0.257394 | |
DDB_G0270472 | DDB_G0270472 | DDB0232428 | CDS | 2493841 | 2754 | - | 0.232752 | |
DDB_G0270474 | DDB_G0270474 | DDB0232428 | CDS | 2500071 | 420 | - | 0.264286 | |
DDB_G0270476_ps | DDB_G0270476 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 2504768 | 1161 | - | 0.258398 |
DDB_G0270478_ps | DDB_G0270478 | putative pseudogene IPTTIG family protein | DDB0232428 | CDS | 2519831 | 2409 | - | 0.287256 |
DDB_G0270480 | DDB_G0270480 | DDB0232428 | CDS | 2529046 | 9588 | + | 0.290572 | |
DDB_G0270488 | DDB_G0270488 | DDB0232428 | CDS | 2594752 | 10563 | + | 0.348859 | |
DDB_G0270490 | DDB_G0270490 | DDB0232428 | CDS | 2607006 | 495 | + | 0.266667 | |
DDB_G0270492 | DDB_G0270492 | DDB0232428 | CDS | 2607973 | 1026 | + | 0.233918 | |
DDB_G0270494 | DDB_G0270494 | DDB0232428 | CDS | 2611408 | 750 | - | 0.217333 | |
DDB_G0270496 | DDB_G0270496 | putative ortholog of H. sapiens AATF apoptosis-antagonizing transcription factorbrbr bCommunity annotation:b DDB_G0270496 shows extensive similarities with the | DDB0232428 | CDS | 2636802 | 1572 | + | 0.262087 |
DDB_G0270502_RTE | DDB_G0270502 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2685505 | 597 | - | 0.335008 |
DDB_G0270504_RTE | DDB_G0270504 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2686145 | 690 | - | 0.284058 |
DDB_G0270506 | DDB_G0270506 | DDB0232428 | CDS | 2687898 | 1239 | - | 0.243745 | |
DDB_G0270508 | DDB_G0270508 | DDB0232428 | CDS | 2717192 | 225 | - | 0.262222 | |
DDB_G0270512_ps | DDB_G0270512 | putative pseudogene similar to D. discoideum genes | DDB0232428 | CDS | 2731859 | 675 | + | 0.256296 |
DDB_G0270514_ps | DDB_G0270514 | putative pseudogene similar to gene | DDB0232428 | CDS | 2741124 | 894 | + | 0.228188 |
DDB_G0270518 | DDB_G0270518 | conserved Dictyostelium protein contains a putative signal sequence | DDB0232428 | CDS | 2764361 | 537 | + | 0.337058 |
DDB_G0270520 | DDB_G0270520 | DDB0232428 | CDS | 2765942 | 1281 | + | 0.193599 | |
DDB_G0270522 | DDB_G0270522 | DDB0232428 | CDS | 2769350 | 1407 | - | 0.253731 | |
DDB_G0270524 | DDB_G0270524 | DDB0232428 | CDS | 2771493 | 1416 | - | 0.217514 | |
DDB_G0270530 | DDB_G0270530 | DDB0232428 | CDS | 2809230 | 630 | - | 0.239683 | |
DDB_G0270532 | DDB_G0270532 | DDB0232428 | CDS | 2814532 | 1458 | - | 0.269547 | |
DDB_G0270536_RTE | DDB_G0270536 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2855765 | 1335 | + | 0.304869 |
DDB_G0270538 | DDB_G0270538 | DDB0232428 | CDS | 2869907 | 2244 | - | 0.220143 | |
DDB_G0270540 | DDB_G0270540 | DDB0232428 | CDS | 2873819 | 1041 | + | 0.260327 | |
DDB_G0270552 | DDB_G0270552 | contains one C2H2-type zinc finger motif and 2 ankyrin repeats contains 2 predicted coiled-coil domains | DDB0232428 | CDS | 2951187 | 2364 | + | 0.301184 |
DDB_G0270554 | DDB_G0270554 | DDB0232428 | CDS | 2988150 | 687 | + | 0.250364 | |
DDB_G0270558 | DDB_G0270558 | DDB0232428 | CDS | 3016390 | 1113 | + | 0.222821 | |
DDB_G0270564 | DDB_G0270564 | DDB0232428 | CDS | 3054343 | 1383 | + | 0.227766 | |
DDB_G0270566 | DDB_G0270566 | DDB0232428 | CDS | 3070710 | 1551 | + | 0.300451 | |
DDB_G0270568 | DDB_G0270568 | very similar to D. purpureum protein | DDB0232428 | CDS | 3075849 | 1260 | + | 0.244444 |
DDB_G0270570 | DDB_G0270570 | DDB0232428 | CDS | 3093873 | 555 | + | 0.207207 | |
DDB_G0270574 | DDB_G0270574 | DDB0232428 | CDS | 3112632 | 2085 | + | 0.191847 | |
DDB_G0270578 | DDB_G0270578 | DDB0232428 | CDS | 3141822 | 2277 | - | 0.26043 | |
DDB_G0270580 | DDB_G0270580 | DDB0232428 | CDS | 3152348 | 930 | + | 0.211828 | |
DDB_G0270582 | DDB_G0270582 | peptidase M20 family zinc metallopeptidases which are glutamate carboxypeptidases contains peptidase dimerization domain | DDB0232428 | CDS | 3155421 | 1458 | + | 0.285322 |
DDB_G0270584 | DDB_G0270584 | DDB0232428 | CDS | 3164918 | 834 | - | 0.23741 | |
DDB_G0270586 | DDB_G0270586 | DDB0232428 | CDS | 3181593 | 1464 | + | 0.249317 | |
DDB_G0270588 | DDB_G0270588 | DDB0232428 | CDS | 3189061 | 345 | + | 0.202899 | |
DDB_G0270590 | DDB_G0270590 | DDB0232428 | CDS | 3209615 | 2034 | + | 0.301377 | |
DDB_G0270592 | DDB_G0270592 | DDB0232428 | CDS | 3212380 | 303 | + | 0.264026 | |
DDB_G0270594 | DDB_G0270594 | DDB0232428 | CDS | 3247124 | 207 | - | 0.246377 | |
DDB_G0270596 | DDB_G0270596 | DDB0232428 | CDS | 3250824 | 1929 | - | 0.202696 | |
DDB_G0270598 | DDB_G0270598 | DDB0232428 | CDS | 3253076 | 1353 | - | 0.208426 | |
DDB_G0270600 | DDB_G0270600 | DDB0232428 | CDS | 3270165 | 984 | - | 0.257114 | |
DDB_G0270604 | DDB_G0270604 | conserved D. discoideum protein | DDB0232428 | CDS | 3272420 | 252 | - | 0.373016 |
DDB_G0270606 | DDB_G0270606 | DDB0232428 | CDS | 3287288 | 2334 | + | 0.268209 | |
DDB_G0270610 | DDB_G0270610 | DDB0232428 | CDS | 3299624 | 354 | - | 0.228814 | |
DDB_G0270614 | DDB_G0270614 | DDB0232428 | CDS | 3326879 | 615 | - | 0.239024 | |
DDB_G0270618 | DDB_G0270618 | DDB0232428 | CDS | 3364045 | 1233 | + | 0.281427 | |
DDB_G0270620 | DDB_G0270620 | DDB0232428 | CDS | 3369226 | 138 | + | 0.144928 | |
DDB_G0270622 | DDB_G0270622 | DDB0232428 | CDS | 3391069 | 255 | + | 0.298039 | |
DDB_G0270624 | DDB_G0270624 | DDB0232428 | CDS | 3394961 | 339 | - | 0.19469 | |
DDB_G0270628 | DDB_G0270628 | DDB0232428 | CDS | 3456576 | 3741 | + | 0.179364 | |
DDB_G0270630 | DDB_G0270630 | DDB0232428 | CDS | 3470541 | 684 | + | 0.200292 | |
DDB_G0270632 | DDB_G0270632 | DDB0232428 | CDS | 3492337 | 2388 | - | 0.202261 | |
DDB_G0270634 | DDB_G0270634 | similar to TNRC4 (TriNucleotide Repeat Containing 4 protein) and Bruno-like proteins contains 3 RRM domains | DDB0232428 | CDS | 3530459 | 1107 | + | 0.317073 |
DDB_G0270636 | DDB_G0270636 | contains two predicted transmembrane domains one at amino terminus and one at carboxyl terminus | DDB0232428 | CDS | 3534092 | 3099 | + | 0.327525 |
DDB_G0270638_RTE | DDB_G0270638 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232428 | CDS | 3577989 | 1290 | - | 0.303101 |
DDB_G0270640 | DDB_G0270640 | matches PFAM HMM for SPB_interacting (spindle pole body) protein similar to D.purpureum protein | DDB0232428 | CDS | 3581899 | 2670 | - | 0.317603 |
DDB_G0270642 | DDB_G0270642 | DDB0232428 | CDS | 3586235 | 2349 | - | 0.286079 | |
DDB_G0270644 | DDB_G0270644 | DDB0232428 | CDS | 3610258 | 2373 | - | 0.278129 | |
DDB_G0270646 | DDB_G0270646 | DDB0232428 | CDS | 3633884 | 2028 | + | 0.228304 | |
DDB_G0270648_RTE | DDB_G0270648 | DDB0232428 | CDS | 3639054 | 1149 | - | 0.357702 | |
DDB_G0270650_RTE | DDB_G0270650 | DDB0232428 | CDS | 3640332 | 1029 | - | 0.321672 | |
DDB_G0270652 | DDB_G0270652 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232428 | CDS | 3647265 | 1122 | + | 0.266488 |
DDB_G0270654 | DDB_G0270654 | DDB0232428 | CDS | 3660860 | 468 | + | 0.25641 | |
DDB_G0270656_ps | DDB_G0270656 | putative pseudogene hssA2C7E family gene | DDB0232428 | CDS | 3667800 | 288 | - | 0.298611 |
DDB_G0270660 | DDB_G0270660 | DDB0232428 | CDS | 3695166 | 369 | - | 0.322493 | |
DDB_G0270662 | DDB_G0270662 | DDB0232428 | CDS | 3696190 | 294 | - | 0.292517 | |
DDB_G0270664 | DDB_G0270664 | DDB0232428 | CDS | 3699523 | 2160 | + | 0.206019 | |
DDB_G0270686 | DDB_G0270686 | DDB0232428 | CDS | 3829651 | 903 | - | 0.336656 | |
DDB_G0270690 | DDB_G0270690 | DDB0232428 | CDS | 3883017 | 432 | - | 0.261574 | |
DDB_G0270692 | DDB_G0270692 | contains 6 ankyrin repeats contains one VPS9 (vacuolar sorting protein 9) domain similar to D. purpureum protein | DDB0232428 | CDS | 3887599 | 3024 | - | 0.276786 |
DDB_G0270694 | DDB_G0270694 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains one predicted transmembrane domain | DDB0232428 | CDS | 3908437 | 1125 | - | 0.310222 |
DDB_G0270700 | DDB_G0270700 | contains a predicted signal sequence and a putative C-terminal transmembrane domain contains 7 calcium-binding EGF domains | DDB0232428 | CDS | 4002803 | 2445 | + | 0.274438 |
DDB_G0270704_ps | DDB_G0270704 | putative pseudogene similar to Dictyostelium genes | DDB0232428 | CDS | 4034417 | 3270 | + | 0.242202 |
DDB_G0270706_ps | DDB_G0270706 | putative pseudogene fragment similar to D. discoideum genes | DDB0232428 | CDS | 4039201 | 1308 | - | 0.278287 |
DDB_G0270708 | DDB_G0270708 | DDB0232428 | CDS | 4062615 | 3231 | - | 0.260291 | |
DDB_G0270710 | DDB_G0270710 | DDB0232428 | CDS | 4079745 | 612 | - | 0.24183 | |
DDB_G0270714_ps | DDB_G0270714 | putative pseudogene similar to a family of genes including | DDB0232428 | CDS | 4096586 | 621 | + | 0.31562 |
DDB_G0270718 | DDB_G0270718 | DDB0232428 | CDS | 4098007 | 4173 | + | 0.260724 | |
DDB_G0270720 | DDB_G0270720 | DDB0232428 | CDS | 4125800 | 1560 | + | 0.239744 | |
DDB_G0270722 | DDB_G0270722 | DDB0232428 | CDS | 4127506 | 2271 | - | 0.235139 | |
DDB_G0270724_ps | DDB_G0270724 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232428 | CDS | 4171732 | 654 | - | 0.301223 |
DDB_G0270728_ps | DDB_G0270728 | putative pseudogene similar to D. discoideum gene | DDB0232428 | CDS | 4234614 | 411 | - | 0.243309 |
DDB_G0270732 | DDB_G0270732 | DDB0232428 | CDS | 4247306 | 1911 | + | 0.121402 | |
DDB_G0270734 | DDB_G0270734 | DDB0232428 | CDS | 4274869 | 1728 | - | 0.23206 | |
DDB_G0270738 | DDB_G0270738 | DDB0232428 | CDS | 4307771 | 729 | - | 0.264746 | |
DDB_G0270740 | DDB_G0270740 | DDB0232428 | CDS | 4310650 | 279 | + | 0.218638 | |
DDB_G0270742 | DDB_G0270742 | protein with large regions of low complexity conserved in Dictyostelids though the low complexity regions diverge | DDB0232428 | CDS | 4313687 | 1194 | - | 0.291457 |
DDB_G0270744 | DDB_G0270744 | DDB0232428 | CDS | 4332329 | 2580 | - | 0.282558 | |
DDB_G0270746 | DDB_G0270746 | putative ortholog of H. sapiens transducin beta-like 2 (TBL2) deleted in patients with Williams-Beuren syndrome (WBS) | DDB0232428 | CDS | 4336075 | 1377 | - | 0.257807 |
DDB_G0270750 | DDB_G0270750 | contains six kelch repeats which are known to be involved in various biological processes | DDB0232428 | CDS | 4356679 | 1458 | + | 0.341564 |
DDB_G0270752 | DDB_G0270752 | DDB0232428 | CDS | 4392160 | 555 | + | 0.317117 | |
DDB_G0270758 | DDB_G0270758 | DDB0232428 | CDS | 4456371 | 588 | + | 0.236395 | |
DDB_G0270760 | DDB_G0270760 | DDB0232428 | CDS | 4460065 | 2946 | - | 0.307196 | |
DDB_G0270766 | DDB_G0270766 | DDB0232428 | CDS | 4499254 | 2994 | + | 0.257515 | |
DDB_G0270768 | DDB_G0270768 | DDB0232428 | CDS | 4534439 | 171 | + | 0.239766 | |
DDB_G0270770_RTE | DDB_G0270770 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232428 | CDS | 4549776 | 1800 | - | 0.348889 |
DDB_G0270772 | DDB_G0270772 | DDB0232428 | CDS | 4556824 | 462 | - | 0.201299 | |
DDB_G0270774 | DDB_G0270774 | DDB0232428 | CDS | 4621793 | 5223 | - | 0.285085 | |
DDB_G0270776 | DDB_G0270776 | conserved eukaryotic protein of unknown function ortholog of human SPATA20 (spermatogenesis associated 20) | DDB0232428 | CDS | 4646538 | 2475 | + | 0.273939 |
DDB_G0270778 | DDB_G0270778 | DDB0232428 | CDS | 4659316 | 1254 | - | 0.295853 | |
DDB_G0270786 | DDB_G0270786 | DDB0232428 | CDS | 4686330 | 1848 | - | 0.284091 | |
DDB_G0270788 | DDB_G0270788 | conserved Dictyostelium protein similar to bacterial proteins contains a predicted signal peptide | DDB0232428 | CDS | 4691410 | 402 | - | 0.323383 |
DDB_G0270790_RTE | DDB_G0270790 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232428 | CDS | 4703859 | 1128 | - | 0.344858 |
DDB_G0270792_RTE | DDB_G0270792 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232428 | CDS | 4705053 | 1986 | - | 0.357503 |
DDB_G0270794 | DDB_G0270794 | DDB0232428 | CDS | 4715122 | 348 | - | 0.336207 | |
DDB_G0270798 | DDB_G0270798 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232428 | CDS | 4725378 | 243 | + | 0.341564 |
DDB_G0270800 | DDB_G0270800 | DDB0232428 | CDS | 4734866 | 186 | + | 0.317204 | |
DDB_G0270802 | DDB_G0270802 | DDB0232428 | CDS | 4745422 | 3126 | + | 0.222009 | |
DDB_G0270810 | DDB_G0270810 | DDB0232428 | CDS | 4837019 | 2358 | - | 0.186175 | |
DDB_G0270812 | DDB_G0270812 | DDB0232428 | CDS | 4839738 | 132 | - | 0.234848 | |
DDB_G0270816 | DDB_G0270816 | DDB0232428 | CDS | 4879000 | 1341 | - | 0.295302 | |
DDB_G0270820_TE | DDB_G0270820 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 4912005 | 909 | + | 0.20462 |
DDB_G0270822_TE | DDB_G0270822 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232428 | CDS | 4913554 | 765 | + | 0.247059 |
DDB_G0270824_TE | DDB_G0270824 | fusion of the DNA transposon Tdd-4 (downstream of exon 2) and and thugS an AT-rich low copy repetitive element (exon 1) | DDB0232428 | CDS | 4916854 | 2310 | - | 0.312121 |
DDB_G0270828 | DDB_G0270828 | DDB0232428 | CDS | 3009708 | 2880 | - | 0.241319 | |
DDB_G0270840_RTE | DDB_G0270840 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2402920 | 503 | - | 0.312127 |
DDB_G0270842_RTE | DDB_G0270842 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2501983 | 1335 | - | 0.307865 |
DDB_G0270848_ps | DDB_G0270848 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 2517195 | 1545 | - | 0.284142 |
DDB_G0270850 | DDB_G0270850 | DDB0232428 | CDS | 2525862 | 2397 | - | 0.279516 | |
DDB_G0270852_RTE | DDB_G0270852 | DDB0232428 | CDS | 2559165 | 978 | + | 0.335378 | |
DDB_G0270856 | DDB_G0270856 | DDB0232428 | CDS | 2591243 | 2496 | + | 0.271635 | |
DDB_G0270858 | DDB_G0270858 | DDB0232428 | CDS | 2676041 | 1521 | + | 0.239974 | |
DDB_G0270860_RTE | DDB_G0270860 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2691885 | 3144 | - | 0.338422 |
DDB_G0270862_RTE | DDB_G0270862 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2695319 | 1335 | - | 0.310861 |
DDB_G0270864 | DDB_G0270864 | DDB0232428 | CDS | 2744495 | 2892 | - | 0.357538 | |
DDB_G0270868 | DDB_G0270868 | DDB0232428 | CDS | 2774064 | 2634 | - | 0.214882 | |
DDB_G0270872_ps | DDB_G0270872 | putative pseudogene similar to the conserved hypothetical Dictyostelium protein that contains a weak von Willebrand factor type A domain | DDB0232428 | CDS | 2850392 | 339 | + | 0.292035 |
DDB_G0270878 | DDB_G0270878 | DDB0232428 | CDS | 2931465 | 987 | - | 0.256332 | |
DDB_G0270886_RTE | DDB_G0270886 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232428 | CDS | 2963981 | 1992 | - | 0.318273 |
DDB_G0270888_RTE | DDB_G0270888 | partial ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232428 | CDS | 2966061 | 711 | - | 0.274262 |
DDB_G0270890 | DDB_G0270890 | DDB0232428 | CDS | 3096057 | 726 | + | 0.207989 | |
DDB_G0270892 | DDB_G0270892 | DDB0232428 | CDS | 3109107 | 768 | + | 0.223958 | |
DDB_G0270896_RTE | DDB_G0270896 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 3221057 | 675 | - | 0.336296 |
DDB_G0270898 | DDB_G0270898 | DDB0232428 | CDS | 3223232 | 2232 | - | 0.25 | |
DDB_G0270902 | DDB_G0270902 | DDB0232428 | CDS | 3239824 | 3621 | + | 0.257387 | |
DDB_G0270910 | DDB_G0270910 | DDB0232428 | CDS | 3293315 | 2934 | + | 0.293115 | |
DDB_G0270912 | DDB_G0270912 | DDB0232428 | CDS | 3297321 | 207 | - | 0.251208 | |
DDB_G0270914 | DDB_G0270914 | DDB0232428 | CDS | 3328824 | 993 | + | 0.387714 | |
DDB_G0270916 | DDB_G0270916 | DDB0232428 | CDS | 3330425 | 774 | + | 0.232558 | |
DDB_G0270918 | DDB_G0270918 | DDB0232428 | CDS | 3332298 | 4029 | + | 0.269794 | |
DDB_G0270920 | DDB_G0270920 | DDB0232428 | CDS | 3375140 | 3339 | - | 0.262953 | |
DDB_G0270922 | DDB_G0270922 | DDB0232428 | CDS | 3381332 | 327 | + | 0.318043 | |
DDB_G0270924 | DDB_G0270924 | DDB0232428 | CDS | 3383025 | 285 | + | 0.242105 | |
DDB_G0270926 | DDB_G0270926 | DDB0232428 | CDS | 3393751 | 993 | + | 0.225579 | |
DDB_G0270932 | DDB_G0270932 | DDB0232428 | CDS | 3418520 | 3039 | + | 0.29253 | |
DDB_G0270934 | DDB_G0270934 | DDB0232428 | CDS | 3485944 | 864 | - | 0.315972 | |
DDB_G0270936 | DDB_G0270936 | DDB0232428 | CDS | 3488110 | 663 | - | 0.288084 | |
DDB_G0270938_ps | DDB_G0270938 | putative pseudogene similar to D. discoideum gene | DDB0232428 | CDS | 3495532 | 285 | + | 0.319298 |
DDB_G0270940 | DDB_G0270940 | DDB0232428 | CDS | 3508370 | 987 | - | 0.219858 | |
DDB_G0270942 | DDB_G0270942 | similar to UPF0451 family proteins contains 3 predicted transmembrane domains there is an almost identical gene | DDB0232428 | CDS | 3518935 | 363 | - | 0.316804 |
DDB_G0270946 | DDB_G0270946 | catalyzes the first of three steps required to remove two C-4 methyl groups from an intermediate in ergosterol biosynthesis almost identical to the neighboring gene | DDB0232428 | CDS | 3559643 | 804 | + | 0.291045 |
DDB_G0270950_RTE | DDB_G0270950 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232428 | CDS | 3567457 | 3435 | - | 0.346143 |
DDB_G0270952_RTE | DDB_G0270952 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232428 | CDS | 3572251 | 1149 | + | 0.389034 |
DDB_G0270954_RTE | DDB_G0270954 | long terminal repeat retrotransposon Skipper GAG-PRO-POL refer to GenBank AF049230 for full length consensus element | DDB0232428 | CDS | 3573682 | 3969 | + | 0.322499 |
DDB_G0270958 | DDB_G0270958 | DDB0232428 | CDS | 3595722 | 2415 | - | 0.274534 | |
DDB_G0270962 | DDB_G0270962 | DDB0232428 | CDS | 3599415 | 9597 | + | 0.291654 | |
DDB_G0270964_ps | DDB_G0270964 | putative pseudogene highly similar to | DDB0232428 | CDS | 3616147 | 11259 | + | 0.27276 |
DDB_G0270966 | DDB_G0270966 | DDB0232428 | CDS | 3627252 | 1116 | + | 0.272401 | |
DDB_G0270968_RTE | DDB_G0270968 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232428 | CDS | 3642654 | 1077 | - | 0.415042 |
DDB_G0270970 | DDB_G0270970 | DDB0232428 | CDS | 3644457 | 849 | - | 0.275618 | |
DDB_G0270972 | DDB_G0270972 | DDB0232428 | CDS | 3691172 | 900 | - | 0.332222 | |
DDB_G0270974 | DDB_G0270974 | DDB0232428 | CDS | 3694605 | 375 | - | 0.277333 | |
DDB_G0270976_ps | DDB_G0270976 | putative pseudogene fragment similar to laminin-type EGF-like domain-containing proteins such as | DDB0232428 | CDS | 3754803 | 339 | - | 0.297935 |
DDB_G0270978 | DDB_G0270978 | conserved protein of unknown function contains a putative signal peptide followed by a transmembrane domain | DDB0232428 | CDS | 3757657 | 171 | - | 0.321637 |
DDB_G0270980 | DDB_G0270980 | DDB0232428 | CDS | 3766207 | 591 | + | 0.269036 | |
DDB_G0270982 | DDB_G0270982 | DDB0232428 | CDS | 3771006 | 213 | + | 0.276995 | |
DDB_G0270990 | DDB_G0270990 | very similar to acyl-coenzyme A oxidases but lacks the full domain | DDB0232428 | CDS | 3834760 | 2079 | + | 0.341029 |
DDB_G0270996 | DDB_G0270996 | DDB0232428 | CDS | 3845549 | 1008 | + | 0.264881 | |
DDB_G0270998_ps | DDB_G0270998 | putative pseudogene fragment similar to the large family of EGF domain-containing proteins including | DDB0232428 | CDS | 3865926 | 801 | - | 0.259675 |
DDB_G0271002 | DDB_G0271002 | DDB0232428 | CDS | 3981529 | 2004 | - | 0.273453 | |
DDB_G0271006_RTE | DDB_G0271006 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 4005997 | 2934 | - | 0.301977 |
DDB_G0271008_ps | DDB_G0271008 | putative pseudogene similar to a D. discoideum gene family including the just upstream | DDB0232428 | CDS | 4013407 | 447 | - | 0.275168 |
DDB_G0271010 | DDB_G0271010 | DDB0232428 | CDS | 4014521 | 441 | + | 0.249433 | |
DDB_G0271014 | DDB_G0271014 | DDB0232428 | CDS | 4089972 | 1944 | + | 0.328704 | |
DDB_G0271016 | DDB_G0271016 | DDB0232428 | CDS | 4112718 | 4830 | - | 0.210352 | |
DDB_G0271018_RTE | DDB_G0271018 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 4119220 | 3144 | - | 0.338422 |
DDB_G0271020_RTE | DDB_G0271020 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 4122654 | 1335 | - | 0.306367 |
DDB_G0271024 | DDB_G0271024 | DDB0232428 | CDS | 4138891 | 2931 | + | 0.297168 | |
DDB_G0271026_RTE | DDB_G0271026 | DDB0232428 | CDS | 4157920 | 849 | - | 0.378092 | |
DDB_G0271028_RTE | DDB_G0271028 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 4160763 | 375 | + | 0.376 |
DDB_G0271030_ps | DDB_G0271030 | putative pseudogene fragment highly similar to | DDB0232428 | CDS | 4200105 | 885 | - | 0.267797 |
DDB_G0271032 | DDB_G0271032 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232428 | CDS | 4228148 | 4116 | - | 0.262391 |
DDB_G0271034 | DDB_G0271034 | DDB0232428 | CDS | 4256212 | 3264 | + | 0.257659 | |
DDB_G0271038 | DDB_G0271038 | DDB0232428 | CDS | 4263564 | 195 | + | 0.282051 | |
DDB_G0271042 | DDB_G0271042 | DDB0232428 | CDS | 4340831 | 3000 | + | 0.301 | |
DDB_G0271044 | DDB_G0271044 | contains Sec23Sec24 zinc finger trunk and helical domains yeast Sec23Sec24 is a component of COPII (coat protein complex II) involved in ER to Golgi transport | DDB0232428 | CDS | 4346844 | 2391 | - | 0.26056 |
DDB_G0271046_ps | DDB_G0271046 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 4444375 | 240 | + | 0.3875 |
DDB_G0271054 | DDB_G0271054 | contains one SMADFHA domain contains one coiled-coil domain | DDB0232428 | CDS | 4565256 | 1737 | - | 0.235463 |
DDB_G0271056 | DDB_G0271056 | DDB0232428 | CDS | 4568604 | 2142 | + | 0.197012 | |
DDB_G0271060 | DDB_G0271060 | DDB0232428 | CDS | 4581402 | 2073 | + | 0.207911 | |
DDB_G0271062 | DDB_G0271062 | conserved hypothetical Dictyostelium protein containing two FNIP repeats | DDB0232428 | CDS | 4587614 | 2703 | + | 0.224565 |
DDB_G0271066 | DDB_G0271066 | ortholog of human ELOVL4 members of this family are membrane proteins involved in long chain fatty acid elongation systems that produce 26-carbon precursors for ceramide and sphingolipid synthesis contains 6 putative transmembrane domains | DDB0232428 | CDS | 4618383 | 810 | - | 0.250617 |
DDB_G0271070 | DDB_G0271070 | DDB0232428 | CDS | 4634981 | 261 | + | 0.210728 | |
DDB_G0271074 | DDB_G0271074 | conserved Dictyostelium protein similar to bacterial proteins contains a predicted signal peptide | DDB0232428 | CDS | 4657372 | 402 | + | 0.320896 |
DDB_G0271076_RTE | DDB_G0271076 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232428 | CDS | 4707908 | 732 | - | 0.401639 |
DDB_G0271080 | DDB_G0271080 | DDB0232428 | CDS | 4771263 | 234 | - | 0.24359 | |
DDB_G0271084 | DDB_G0271084 | DDB0232428 | CDS | 4795072 | 495 | + | 0.240404 | |
DDB_G0271086 | DDB_G0271086 | DDB0232428 | CDS | 4808484 | 933 | + | 0.30761 | |
DDB_G0271098 | DDB_G0271098 | DDB0232429 | CDS | 49746 | 558 | - | 0.258065 | |
DDB_G0271100 | DDB_G0271100 | DDB0232429 | CDS | 47597 | 1581 | - | 0.248577 | |
DDB_G0271102 | DDB_G0271102 | DDB0232429 | CDS | 44348 | 192 | - | 0.0729167 | |
DDB_G0271104 | DDB_G0271104 | DDB0232429 | CDS | 39516 | 951 | + | 0.232387 | |
DDB_G0271108 | DDB_G0271108 | DDB0232429 | CDS | 28810 | 978 | + | 0.260736 | |
DDB_G0271110 | DDB_G0271110 | small Dictyostelium protein family absent from other organisms | DDB0232429 | CDS | 19444 | 240 | + | 0.3125 |
DDB_G0271112 | DDB_G0271112 | DDB0232429 | CDS | 16144 | 1920 | + | 0.252083 | |
DDB_G0271114 | DDB_G0271114 | DDB0232429 | CDS | 13927 | 1494 | + | 0.204819 | |
DDB_G0271118_ps | DDB_G0271118 | putative pseudogene bromodomain protein | DDB0232429 | CDS | 25027 | 831 | + | 0.274368 |
DDB_G0271120 | DDB_G0271120 | very similar to the mammalian glucosidase II subunit beta also known as protein kinase C substrate 80K-H which catalyzes the sequential removal of two alpha-13-linked glucose residues in the second step of N-linked oligosaccharide processing also similar to yeast GTB1 defects in human PRKCSH are a cause of polycystic liver disease (PCLD) | DDB0232429 | CDS | 30690 | 1575 | - | 0.265397 |
DDB_G0271124 | DDB_G0271124 | DDB0232429 | CDS | 37151 | 1950 | + | 0.225128 | |
DDB_G0271128_ps | DDB_G0271128 | putative pseudogene SAP DNA-binding domain protein | DDB0232429 | CDS | 43353 | 444 | - | 0.155405 |
DDB_G0271130 | DDB_G0271130 | DDB0232429 | CDS | 45087 | 1902 | + | 0.223449 | |
DDB_G0271132 | DDB_G0271132 | DDB0232429 | CDS | 51145 | 2556 | + | 0.160407 | |
DDB_G0271150 | DDB_G0271150 | DDB0232429 | CDS | 376705 | 489 | - | 0.263804 | |
DDB_G0271152 | DDB_G0271152 | DDB0232429 | CDS | 375288 | 498 | - | 0.253012 | |
DDB_G0271154_TE | DDB_G0271154 | DDB0232429 | CDS | 373067 | 426 | - | 0.328638 | |
DDB_G0271156_ps | DDB_G0271156 | putative pseudogene fragment similar to gene | DDB0232429 | CDS | 370188 | 1119 | + | 0.226095 |
DDB_G0271158_ps | DDB_G0271158 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 365065 | 1104 | + | 0.222826 |
DDB_G0271160 | DDB_G0271160 | DDB0232429 | CDS | 361149 | 1302 | - | 0.316436 | |
DDB_G0271162 | DDB_G0271162 | DDB0232429 | CDS | 356657 | 291 | - | 0.340206 | |
DDB_G0271164_ps | DDB_G0271164 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 355407 | 867 | + | 0.215686 |
DDB_G0271166 | DDB_G0271166 | DDB0232429 | CDS | 351938 | 2679 | + | 0.226577 | |
DDB_G0271168_ps | DDB_G0271168 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 350196 | 309 | + | 0.213592 |
DDB_G0271172_TE | DDB_G0271172 | DDB0232429 | CDS | 349161 | 537 | + | 0.32216 | |
DDB_G0271176_ps | DDB_G0271176 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 343079 | 1323 | + | 0.234316 |
DDB_G0271178 | DDB_G0271178 | DDB0232429 | CDS | 341330 | 321 | - | 0.311526 | |
DDB_G0271180_ps | DDB_G0271180 | putative pseudogene similar to a large family of D. discoideum proteins including | DDB0232429 | CDS | 338345 | 417 | + | 0.206235 |
DDB_G0271184_ps | DDB_G0271184 | DDB0232429 | CDS | 336811 | 837 | - | 0.333333 | |
DDB_G0271186_ps | DDB_G0271186 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 333149 | 372 | + | 0.120968 |
DDB_G0271188 | DDB_G0271188 | DDB0232429 | CDS | 328676 | 1197 | - | 0.238095 | |
DDB_G0271190_ps | DDB_G0271190 | DDB0232429 | CDS | 326565 | 1461 | + | 0.203285 | |
DDB_G0271192 | DDB_G0271192 | DDB0232429 | CDS | 319239 | 138 | - | 0.471014 | |
DDB_G0271194_TE | DDB_G0271194 | DDB0232429 | CDS | 306767 | 438 | - | 0.3379 | |
DDB_G0271196 | DDB_G0271196 | DDB0232429 | CDS | 306087 | 321 | + | 0.299065 | |
DDB_G0271198 | DDB_G0271198 | DDB0232429 | CDS | 303072 | 138 | + | 0.311594 | |
DDB_G0271202 | DDB_G0271202 | DDB0232429 | CDS | 297663 | 1854 | + | 0.181769 | |
DDB_G0271204_ps | DDB_G0271204 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 293096 | 540 | - | 0.333333 |
DDB_G0271210 | DDB_G0271210 | DDB0232429 | CDS | 290849 | 120 | - | 0.333333 | |
DDB_G0271212 | DDB_G0271212 | DDB0232429 | CDS | 290676 | 120 | - | 0.3 | |
DDB_G0271214 | DDB_G0271214 | DDB0232429 | CDS | 288473 | 1980 | + | 0.194949 | |
DDB_G0271216 | DDB_G0271216 | DDB0232429 | CDS | 285190 | 1923 | + | 0.182007 | |
DDB_G0271218 | DDB_G0271218 | DDB0232429 | CDS | 275867 | 3081 | + | 0.21876 | |
DDB_G0271220 | DDB_G0271220 | DDB0232429 | CDS | 274412 | 363 | + | 0.258953 | |
DDB_G0271226_ps | DDB_G0271226 | putative pseudogene similar to a larger gene family including | DDB0232429 | CDS | 262858 | 135 | + | 0.237037 |
DDB_G0271228 | DDB_G0271228 | DDB0232429 | CDS | 258017 | 1899 | + | 0.1901 | |
DDB_G0271232_ps | DDB_G0271232 | putative pseudogene similar to the putative extracellular matrix protein DDB_G0271722 and other family members | DDB0232429 | CDS | 256636 | 843 | + | 0.33452 |
DDB_G0271236_ps | DDB_G0271236 | putative pseudogene member of a Dictyostelium-specific gene family | DDB0232429 | CDS | 248591 | 3612 | + | 0.26938 |
DDB_G0271238 | DDB_G0271238 | DDB0232429 | CDS | 244515 | 3582 | + | 0.266052 | |
DDB_G0271242 | DDB_G0271242 | DDB0232429 | CDS | 232357 | 1512 | - | 0.292989 | |
DDB_G0271244 | DDB_G0271244 | DDB0232429 | CDS | 230689 | 1635 | + | 0.21896 | |
DDB_G0271248 | DDB_G0271248 | DDB0232429 | CDS | 226562 | 1248 | + | 0.293269 | |
DDB_G0271250 | DDB_G0271250 | DDB0232429 | CDS | 214985 | 1278 | + | 0.234742 | |
DDB_G0271252 | DDB_G0271252 | DDB0232429 | CDS | 213313 | 270 | + | 0.2 | |
DDB_G0271254 | DDB_G0271254 | DDB0232429 | CDS | 210375 | 837 | + | 0.307049 | |
DDB_G0271256_ps | DDB_G0271256 | putative pseudogene similar to a large gene family including | DDB0232429 | CDS | 205101 | 273 | - | 0.197802 |
DDB_G0271260 | DDB_G0271260 | DDB0232429 | CDS | 192510 | 210 | - | 0.290476 | |
DDB_G0271266 | DDB_G0271266 | DDB0232429 | CDS | 182683 | 210 | - | 0.233333 | |
DDB_G0271268 | DDB_G0271268 | DDB0232429 | CDS | 181275 | 561 | + | 0.276292 | |
DDB_G0271270 | DDB_G0271270 | DDB0232429 | CDS | 179519 | 1080 | - | 0.287963 | |
DDB_G0271272 | DDB_G0271272 | DDB0232429 | CDS | 174413 | 4386 | - | 0.262426 | |
DDB_G0271274 | DDB_G0271274 | DDB0232429 | CDS | 171780 | 588 | - | 0.282313 | |
DDB_G0271276_ps | DDB_G0271276 | putative pseudogene highly similar to | DDB0232429 | CDS | 165859 | 1008 | - | 0.327381 |
DDB_G0271280 | DDB_G0271280 | DDB0232429 | CDS | 162882 | 1842 | + | 0.27633 | |
DDB_G0271288 | DDB_G0271288 | ortholog of the putative tumor suppressor candidate 4 protein (TUSC4) the nitrogen permease regulator 2 (NPR2) family of regulators are involved in post-translational control of nitrogen permease | DDB0232429 | CDS | 154060 | 1179 | + | 0.276506 |
DDB_G0271290 | DDB_G0271290 | DDB0232429 | CDS | 149480 | 891 | - | 0.320988 | |
DDB_G0271292 | DDB_G0271292 | DDB0232429 | CDS | 145979 | 774 | - | 0.25323 | |
DDB_G0271294 | DDB_G0271294 | DDB0232429 | CDS | 143922 | 486 | - | 0.26749 | |
DDB_G0271296 | DDB_G0271296 | DDB0232429 | CDS | 141746 | 1875 | + | 0.2304 | |
DDB_G0271300 | DDB_G0271300 | DDB0232429 | CDS | 139580 | 441 | + | 0.22449 | |
DDB_G0271302 | DDB_G0271302 | DDB0232429 | CDS | 136477 | 2448 | - | 0.200572 | |
DDB_G0271304 | DDB_G0271304 | DDB0232429 | CDS | 132172 | 921 | + | 0.239957 | |
DDB_G0271308 | DDB_G0271308 | DDB0232429 | CDS | 127309 | 2238 | + | 0.256479 | |
DDB_G0271316 | DDB_G0271316 | DDB0232429 | CDS | 120793 | 657 | - | 0.231355 | |
DDB_G0271318 | DDB_G0271318 | DDB0232429 | CDS | 113549 | 168 | - | 0.22619 | |
DDB_G0271320 | DDB_G0271320 | DDB0232429 | CDS | 107780 | 321 | + | 0.29595 | |
DDB_G0271322_ps | DDB_G0271322 | putative pseudogene fragment similar to | DDB0232429 | CDS | 106314 | 495 | - | 0.19596 |
DDB_G0271324 | DDB_G0271324 | DDB0232429 | CDS | 104273 | 816 | - | 0.295343 | |
DDB_G0271326 | DDB_G0271326 | DDB0232429 | CDS | 102030 | 321 | + | 0.299065 | |
DDB_G0271328_ps | DDB_G0271328 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 100329 | 699 | - | 0.228898 |
DDB_G0271330 | DDB_G0271330 | DDB0232429 | CDS | 97475 | 1857 | - | 0.210016 | |
DDB_G0271332 | DDB_G0271332 | DDB0232429 | CDS | 93170 | 633 | + | 0.203791 | |
DDB_G0271334 | DDB_G0271334 | contains a dilute domain found at the carboxyl terminus of non-muscle myosin V | DDB0232429 | CDS | 87969 | 4518 | + | 0.279991 |
DDB_G0271336 | DDB_G0271336 | DDB0232429 | CDS | 84159 | 552 | + | 0.306159 | |
DDB_G0271340 | DDB_G0271340 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub expressed in pstAB cells and in upper cup during culmination | DDB0232429 | CDS | 76522 | 1926 | + | 0.28297 |
DDB_G0271348 | DDB_G0271348 | DDB0232429 | CDS | 62552 | 3114 | + | 0.221901 | |
DDB_G0271350 | DDB_G0271350 | DDB0232429 | CDS | 54276 | 828 | - | 0.242754 | |
DDB_G0271352_TE | DDB_G0271352 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232429 | CDS | 312077 | 231 | - | 0.277056 |
DDB_G0271354 | DDB_G0271354 | DDB0232429 | CDS | 56277 | 765 | + | 0.266667 | |
DDB_G0271356 | DDB_G0271356 | contains 3 zinc-binding LIM domains LIM domains are found in proteins with differing functions including gene expression and cytoskeleton organisation and development | DDB0232429 | CDS | 72258 | 561 | + | 0.301248 |
DDB_G0271358 | DDB_G0271358 | DDB0232429 | CDS | 79477 | 633 | + | 0.271722 | |
DDB_G0271360 | DDB_G0271360 | DDB0232429 | CDS | 85049 | 1698 | - | 0.196702 | |
DDB_G0271362 | DDB_G0271362 | DDB0232429 | CDS | 94411 | 1851 | - | 0.202053 | |
DDB_G0271364_ps | DDB_G0271364 | putative pseudogene fragment similar to | DDB0232429 | CDS | 105543 | 570 | + | 0.249123 |
DDB_G0271366 | DDB_G0271366 | DDB0232429 | CDS | 111179 | 531 | - | 0.316384 | |
DDB_G0271368 | DDB_G0271368 | DDB0232429 | CDS | 111944 | 918 | - | 0.319172 | |
DDB_G0271370 | DDB_G0271370 | DDB0232429 | CDS | 115000 | 933 | + | 0.222937 | |
DDB_G0271372 | DDB_G0271372 | similar to human TIF1a atypical protein kinase RING and B-box zinc finger containing protein kelch repeat-containing protein | DDB0232429 | CDS | 117705 | 3000 | + | 0.271 |
DDB_G0271374 | DDB_G0271374 | DDB0232429 | CDS | 135005 | 1245 | + | 0.31004 | |
DDB_G0271376 | DDB_G0271376 | DDB0232429 | CDS | 144988 | 762 | + | 0.295276 | |
DDB_G0271378 | DDB_G0271378 | DDB0232429 | CDS | 147174 | 1689 | - | 0.201895 | |
DDB_G0271380_ps | DDB_G0271380 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 159603 | 618 | + | 0.268608 |
DDB_G0271384 | DDB_G0271384 | DDB0232429 | CDS | 168234 | 3123 | + | 0.23375 | |
DDB_G0271386 | DDB_G0271386 | DDB0232429 | CDS | 190327 | 1725 | + | 0.173913 | |
DDB_G0271390_ps | DDB_G0271390 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 203789 | 792 | - | 0.166667 |
DDB_G0271392_ps | DDB_G0271392 | putative pseudogene similar to a D. discoideum gene family including | DDB0232429 | CDS | 207386 | 1743 | - | 0.199082 |
DDB_G0271394 | DDB_G0271394 | DDB0232429 | CDS | 211402 | 411 | - | 0.23601 | |
DDB_G0271396 | DDB_G0271396 | similar to human EXOSC6 and S. pombe mtr3 which are components of the exosome a 3'-5' exoribonuclease complex involved in RNA processing | DDB0232429 | CDS | 213822 | 654 | + | 0.318043 |
DDB_G0271402 | DDB_G0271402 | DDB0232429 | CDS | 241165 | 2298 | + | 0.309835 | |
DDB_G0271404 | DDB_G0271404 | DDB0232429 | CDS | 260280 | 2082 | + | 0.212296 | |
DDB_G0271406 | DDB_G0271406 | DDB0232429 | CDS | 279448 | 1989 | + | 0.183007 | |
DDB_G0271408 | DDB_G0271408 | DDB0232429 | CDS | 282899 | 1929 | + | 0.190254 | |
DDB_G0271410_ps | DDB_G0271410 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 287435 | 378 | - | 0.325397 |
DDB_G0271412 | DDB_G0271412 | DDB0232429 | CDS | 294765 | 1854 | + | 0.178533 | |
DDB_G0271414 | DDB_G0271414 | DDB0232429 | CDS | 303584 | 957 | - | 0.213166 | |
DDB_G0271418 | DDB_G0271418 | DDB0232429 | CDS | 309490 | 1983 | + | 0.196167 | |
DDB_G0271422_TE | DDB_G0271422 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232429 | CDS | 314547 | 663 | - | 0.340875 |
DDB_G0271424_ps | DDB_G0271424 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 317314 | 1719 | + | 0.182083 |
DDB_G0271426_ps | DDB_G0271426 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 319621 | 327 | + | 0.299694 |
DDB_G0271428_ps | DDB_G0271428 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 321627 | 921 | - | 0.262758 |
DDB_G0271430 | DDB_G0271430 | DDB0232429 | CDS | 323360 | 2097 | + | 0.188364 | |
DDB_G0271434 | DDB_G0271434 | DDB0232429 | CDS | 334485 | 1911 | + | 0.190999 | |
DDB_G0271438 | DDB_G0271438 | DDB0232429 | CDS | 358067 | 2832 | + | 0.226342 | |
DDB_G0271440_TE | DDB_G0271440 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232429 | CDS | 366668 | 2316 | - | 0.311313 |
DDB_G0271444_ps | DDB_G0271444 | DDB0232429 | CDS | 371956 | 330 | - | 0.181818 | |
DDB_G0271446_ps | DDB_G0271446 | putative pseudogene fragment similar to a large family of genes including | DDB0232429 | CDS | 374110 | 219 | - | 0.246575 |
DDB_G0271448_RTE | DDB_G0271448 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 377800 | 642 | - | 0.271028 |
DDB_G0271450_RTE | DDB_G0271450 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 378769 | 537 | - | 0.294227 |
DDB_G0271452_RTE | DDB_G0271452 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 382297 | 2052 | - | 0.352827 |
DDB_G0271454_RTE | DDB_G0271454 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 384873 | 951 | - | 0.425867 |
DDB_G0271456_RTE | DDB_G0271456 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232429 | CDS | 386778 | 1929 | - | 0.268533 |
DDB_G0271458 | DDB_G0271458 | DDB0232429 | CDS | 389413 | 3036 | + | 0.210804 | |
DDB_G0271460 | DDB_G0271460 | DDB0232429 | CDS | 393193 | 3162 | + | 0.203669 | |
DDB_G0271462 | DDB_G0271462 | DDB0232429 | CDS | 396914 | 3054 | + | 0.20465 | |
DDB_G0271466_ps | DDB_G0271466 | putative pseudogene similar to a D. discoideum gene family including | DDB0232429 | CDS | 401358 | 714 | + | 0.197479 |
DDB_G0271468 | DDB_G0271468 | DDB0232429 | CDS | 403904 | 2733 | + | 0.197951 | |
DDB_G0271470 | DDB_G0271470 | DDB0232429 | CDS | 406925 | 528 | - | 0.284091 | |
DDB_G0271472 | DDB_G0271472 | DDB0232429 | CDS | 408255 | 1950 | + | 0.264103 | |
DDB_G0271474_ps | DDB_G0271474 | putative pseudogene fragment of D. discoideum gene | DDB0232429 | CDS | 411947 | 309 | + | 0.297735 |
DDB_G0271476 | DDB_G0271476 | DDB0232429 | CDS | 413395 | 1893 | + | 0.268885 | |
DDB_G0271478 | DDB_G0271478 | DDB0232429 | CDS | 415978 | 1950 | - | 0.175385 | |
DDB_G0271480 | DDB_G0271480 | DDB0232429 | CDS | 418580 | 3648 | + | 0.261787 | |
DDB_G0271482 | DDB_G0271482 | DDB0232429 | CDS | 422622 | 3963 | + | 0.206662 | |
DDB_G0271484 | DDB_G0271484 | DDB0232429 | CDS | 427690 | 1485 | + | 0.256566 | |
DDB_G0271486 | DDB_G0271486 | DDB0232429 | CDS | 430036 | 318 | + | 0.418239 | |
DDB_G0271508_ps | DDB_G0271508 | putative pseudogene similar to | DDB0232429 | CDS | 459066 | 1125 | - | 0.194667 |
DDB_G0271510 | DDB_G0271510 | DDB0232429 | CDS | 464711 | 2229 | - | 0.290265 | |
DDB_G0271516 | DDB_G0271516 | DDB0232429 | CDS | 494360 | 1101 | - | 0.255223 | |
DDB_G0271526 | DDB_G0271526 | DDB0232429 | CDS | 517604 | 519 | - | 0.223507 | |
DDB_G0271528 | DDB_G0271528 | DDB0232429 | CDS | 527305 | 390 | + | 0.289744 | |
DDB_G0271532 | DDB_G0271532 | there is an identical copy of this gene on chromosome 5 | DDB0232429 | CDS | 550427 | 1755 | - | 0.317949 |
DDB_G0271534 | DDB_G0271534 | DDB0232429 | CDS | 553300 | 564 | + | 0.262411 | |
DDB_G0271538 | DDB_G0271538 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family expressed in pstO cells | DDB0232429 | CDS | 568653 | 1584 | - | 0.285985 |
DDB_G0271542_ps | DDB_G0271542 | putative pseudogene similar to family of D. discoideum genes including | DDB0232429 | CDS | 590623 | 2034 | - | 0.224189 |
DDB_G0271546 | DDB_G0271546 | DDB0232429 | CDS | 620269 | 1137 | - | 0.248901 | |
DDB_G0271548 | DDB_G0271548 | DDB0232429 | CDS | 632125 | 942 | + | 0.250531 | |
DDB_G0271550 | DDB_G0271550 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | DDB0232429 | CDS | 634463 | 1179 | + | 0.267176 |
DDB_G0271552 | DDB_G0271552 | DDB0232429 | CDS | 637163 | 2286 | + | 0.332021 | |
DDB_G0271554 | DDB_G0271554 | DDB0232429 | CDS | 639768 | 183 | - | 0.180328 | |
DDB_G0271558 | DDB_G0271558 | DDB0232429 | CDS | 654748 | 333 | + | 0.312312 | |
DDB_G0271560 | DDB_G0271560 | DDB0232429 | CDS | 665896 | 192 | - | 0.203125 | |
DDB_G0271568_RTE | DDB_G0271568 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 529289 | 1041 | - | 0.278578 |
DDB_G0271570 | DDB_G0271570 | DDB0232429 | CDS | 577332 | 1038 | - | 0.197495 | |
DDB_G0271574 | DDB_G0271574 | DDB0232429 | CDS | 616734 | 783 | - | 0.162197 | |
DDB_G0271576_RTE | DDB_G0271576 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 618122 | 1398 | + | 0.288984 |
DDB_G0271578 | DDB_G0271578 | DDB0232429 | CDS | 640693 | 186 | - | 0.193548 | |
DDB_G0271588 | DDB_G0271588 | DDB0232429 | CDS | 666617 | 186 | - | 0.241935 | |
DDB_G0271592 | DDB_G0271592 | DDB0232429 | CDS | 697134 | 1485 | - | 0.245791 | |
DDB_G0271594_ps | DDB_G0271594 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 445806 | 2496 | - | 0.192308 |
DDB_G0271596 | DDB_G0271596 | DDB0232429 | CDS | 448767 | 2550 | - | 0.195686 | |
DDB_G0271602 | DDB_G0271602 | DDB0232429 | CDS | 461460 | 2169 | - | 0.201014 | |
DDB_G0271606 | DDB_G0271606 | DDB0232429 | CDS | 474534 | 3639 | - | 0.290464 | |
DDB_G0271610 | DDB_G0271610 | DDB0232429 | CDS | 488534 | 5082 | - | 0.266824 | |
DDB_G0271622_ps | DDB_G0271622 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232429 | CDS | 539055 | 1320 | + | 0.256061 |
DDB_G0271624 | DDB_G0271624 | DDB0232429 | CDS | 557800 | 3234 | - | 0.246444 | |
DDB_G0271634 | DDB_G0271634 | DDB0232429 | CDS | 583523 | 2991 | + | 0.245069 | |
DDB_G0271636 | DDB_G0271636 | DDB0232429 | CDS | 587121 | 3075 | + | 0.244228 | |
DDB_G0271638 | DDB_G0271638 | DDB0232429 | CDS | 593663 | 3201 | + | 0.249297 | |
DDB_G0271640 | DDB_G0271640 | DDB0232429 | CDS | 597228 | 1944 | - | 0.221708 | |
DDB_G0271656 | DDB_G0271656 | highly similar to | DDB0232429 | CDS | 665072 | 201 | - | 0.263682 |
DDB_G0271658 | DDB_G0271658 | DDB0232429 | CDS | 667530 | 186 | - | 0.252688 | |
DDB_G0271664 | DDB_G0271664 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | DDB0232429 | CDS | 442827 | 2772 | + | 0.297258 |
DDB_G0271672 | DDB_G0271672 | member of the ZIP (Zrt- and Irt-like Protein) family capable of transporting zinc and other metal ions contains 6 transmembrane domains | DDB0232429 | CDS | 818432 | 1170 | + | 0.357265 |
DDB_G0271674_ps | DDB_G0271674 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 814850 | 570 | + | 0.254386 |
DDB_G0271676 | DDB_G0271676 | DDB0232429 | CDS | 812738 | 1602 | + | 0.327091 | |
DDB_G0271680 | DDB_G0271680 | DDB0232429 | CDS | 796698 | 1008 | + | 0.324405 | |
DDB_G0271682 | DDB_G0271682 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats contains two kinase domains one of which is predicted to be inactive | DDB0232429 | CDS | 792553 | 3075 | + | 0.247154 |
DDB_G0271690 | DDB_G0271690 | DDB0232429 | CDS | 763571 | 2349 | + | 0.286505 | |
DDB_G0271694 | DDB_G0271694 | DDB0232429 | CDS | 750344 | 2142 | - | 0.355742 | |
DDB_G0271698 | DDB_G0271698 | DDB0232429 | CDS | 736637 | 1137 | + | 0.226913 | |
DDB_G0271700 | DDB_G0271700 | contains a thioredoxin domain which functions as a general disulfide isomerase enriched in gametes | DDB0232429 | CDS | 730777 | 900 | - | 0.26 |
DDB_G0271702 | DDB_G0271702 | DDB0232429 | CDS | 725506 | 702 | - | 0.294872 | |
DDB_G0271704 | DDB_G0271704 | DDB0232429 | CDS | 724441 | 396 | - | 0.363636 | |
DDB_G0271710_ps | DDB_G0271710 | DDB0232429 | CDS | 834356 | 330 | - | 0.290909 | |
DDB_G0271712 | DDB_G0271712 | highly similar to other Dictyostelium small proteins antibodies against this protein inhibits aggregation | DDB0232429 | CDS | 835390 | 270 | + | 0.366667 |
DDB_G0271714 | DDB_G0271714 | developmental expression pattern altered in GBF null cells highly similar to other Dictyostelium small proteins | DDB0232429 | CDS | 836349 | 267 | - | 0.363296 |
DDB_G0271716 | DDB_G0271716 | highly similar to other Dictyostelium small proteins antibodies against this protein inhibits aggregation | DDB0232429 | CDS | 841529 | 270 | - | 0.355556 |
DDB_G0271718 | DDB_G0271718 | highly similar to other Dictyostelium small proteins antibodies against this protein inhibits aggregation | DDB0232429 | CDS | 842563 | 270 | + | 0.355556 |
DDB_G0271720 | DDB_G0271720 | almost identical to | DDB0232429 | CDS | 843067 | 1029 | - | 0.290573 |
DDB_G0271722 | DDB_G0271722 | similar to extracellular matrix protein contains a putative signal peptide | DDB0232429 | CDS | 844656 | 1044 | + | 0.361111 |
DDB_G0271724 | DDB_G0271724 | DDB0232429 | CDS | 857132 | 876 | + | 0.26484 | |
DDB_G0271726 | DDB_G0271726 | DDB0232429 | CDS | 858649 | 516 | + | 0.333333 | |
DDB_G0271728 | DDB_G0271728 | DDB0232429 | CDS | 866554 | 408 | - | 0.269608 | |
DDB_G0271730 | DDB_G0271730 | DDB0232429 | CDS | 868232 | 3978 | + | 0.311714 | |
DDB_G0271732 | DDB_G0271732 | highly similar to mammalian DNA-binding protein SMUBP-2 (IGHMBP2) involved in muscular atrophy and other diseases putative ortholog of S. cerevisiae HCS1 a DNA helicase associated with alpha DNA polymerase | DDB0232429 | CDS | 872358 | 3075 | - | 0.267967 |
DDB_G0271740 | DDB_G0271740 | DDB0232429 | CDS | 897538 | 1008 | + | 0.329365 | |
DDB_G0271742 | DDB_G0271742 | DDB0232429 | CDS | 910931 | 651 | - | 0.322581 | |
DDB_G0271748_ps | DDB_G0271748 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 711253 | 876 | + | 0.261416 |
DDB_G0271752 | DDB_G0271752 | DDB0232429 | CDS | 734961 | 1218 | + | 0.328407 | |
DDB_G0271754 | DDB_G0271754 | contains one PHD-type zinc finger domain contains one SPRY domain weak similarity to human ASH2L (Set1Ash2 histone methyltransferase complex subunit ASH2) | DDB0232429 | CDS | 743389 | 3066 | - | 0.29028 |
DDB_G0271756 | DDB_G0271756 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232429 | CDS | 749196 | 213 | - | 0.267606 |
DDB_G0271762_ps | DDB_G0271762 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 849998 | 123 | + | 0.268293 |
DDB_G0271764 | DDB_G0271764 | DDB0232429 | CDS | 851193 | 1521 | + | 0.2643 | |
DDB_G0271770 | DDB_G0271770 | this gene is very similar to four almost identical genes on C4 ( | DDB0232429 | CDS | 877919 | 180 | - | 0.372222 |
DDB_G0271780 | DDB_G0271780 | DDB0232429 | CDS | 899784 | 1026 | + | 0.312865 | |
DDB_G0271784 | DDB_G0271784 | DDB0232429 | CDS | 706981 | 1764 | + | 0.248299 | |
DDB_G0271786 | DDB_G0271786 | DDB0232429 | CDS | 712435 | 3492 | - | 0.201031 | |
DDB_G0271796 | DDB_G0271796 | DDB0232429 | CDS | 753355 | 951 | + | 0.233438 | |
DDB_G0271798 | DDB_G0271798 | DDB0232429 | CDS | 755175 | 2511 | + | 0.240143 | |
DDB_G0271800 | DDB_G0271800 | DDB0232429 | CDS | 770369 | 207 | + | 0.217391 | |
DDB_G0271802 | DDB_G0271802 | DDB0232429 | CDS | 783832 | 954 | + | 0.267296 | |
DDB_G0271804 | DDB_G0271804 | DDB0232429 | CDS | 785458 | 279 | + | 0.243728 | |
DDB_G0271808 | DDB_G0271808 | DDB0232429 | CDS | 798398 | 3990 | + | 0.261654 | |
DDB_G0271810 | DDB_G0271810 | DDB0232429 | CDS | 803219 | 180 | - | 0.211111 | |
DDB_G0271812 | DDB_G0271812 | similar to H. sapiens formin-binding protein 1 (FNBP1) involved in regulation of the actin cytoskeleton during endocytosis chromosomal aberrations involving FNBP1 are also found in acute leukemias | DDB0232429 | CDS | 805322 | 1497 | - | 0.350033 |
DDB_G0271814 | DDB_G0271814 | DDB0232429 | CDS | 815855 | 732 | - | 0.254098 | |
DDB_G0271816 | DDB_G0271816 | DDB0232429 | CDS | 825354 | 3726 | + | 0.318304 | |
DDB_G0271818 | DDB_G0271818 | DDB0232429 | CDS | 837375 | 267 | + | 0.363296 | |
DDB_G0271820 | DDB_G0271820 | almost identical to | DDB0232429 | CDS | 837872 | 1035 | - | 0.284058 |
DDB_G0271822 | DDB_G0271822 | highly similar to other Dictyostelium small proteins antibodies against this protein inhibits aggregation | DDB0232429 | CDS | 839761 | 267 | - | 0.363296 |
DDB_G0271824 | DDB_G0271824 | highly similar to other Dictyostelium small proteins antibodies against this protein inhibits aggregation | DDB0232429 | CDS | 840762 | 270 | + | 0.355556 |
DDB_G0271826_ps | DDB_G0271826 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 845885 | 3651 | + | 0.209532 |
DDB_G0271828 | DDB_G0271828 | DDB0232429 | CDS | 853054 | 2562 | - | 0.271663 | |
DDB_G0271830 | DDB_G0271830 | DDB0232429 | CDS | 876349 | 1065 | + | 0.196244 | |
DDB_G0271832 | DDB_G0271832 | DDB0232429 | CDS | 887242 | 2319 | - | 0.236309 | |
DDB_G0271834 | DDB_G0271834 | DDB0232429 | CDS | 901139 | 2445 | - | 0.256442 | |
DDB_G0271836 | DDB_G0271836 | DDB0232429 | CDS | 904078 | 615 | - | 0.297561 | |
DDB_G0271838 | DDB_G0271838 | DDB0232429 | CDS | 905039 | 3885 | - | 0.215187 | |
DDB_G0271840 | DDB_G0271840 | DDB0232429 | CDS | 909593 | 447 | - | 0.275168 | |
DDB_G0271844 | DDB_G0271844 | DDB0232429 | CDS | 914753 | 4812 | - | 0.257273 | |
DDB_G0271850 | DDB_G0271850 | DDB0232429 | CDS | 957017 | 2202 | + | 0.268847 | |
DDB_G0271854 | DDB_G0271854 | DDB0232429 | CDS | 969621 | 849 | + | 0.269729 | |
DDB_G0271860 | DDB_G0271860 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232429 | CDS | 939689 | 1683 | + | 0.263815 |
DDB_G0271866 | DDB_G0271866 | belongs to the crotonase superfamily similar to fungal and bacterial proteins of the enoyl-CoA hydratasesomerase family predicted to be mitochondrial | DDB0232429 | CDS | 980879 | 900 | + | 0.292222 |
DDB_G0271872 | DDB_G0271872 | DDB0232429 | CDS | 926405 | 438 | - | 0.239726 | |
DDB_G0271876 | DDB_G0271876 | DDB0232429 | CDS | 967334 | 1500 | - | 0.241333 | |
DDB_G0271878 | DDB_G0271878 | DDB0232429 | CDS | 925396 | 438 | - | 0.239726 | |
DDB_G0271880 | DDB_G0271880 | similar to the uncharacterized H. sapiens C16orf70 | DDB0232429 | CDS | 930648 | 1560 | + | 0.228846 |
DDB_G0271884 | DDB_G0271884 | conserved putative quinone oxidoreductase belongs to the broader superfamily of zinc-dependent alcohol dehydrogenases | DDB0232429 | CDS | 973836 | 996 | - | 0.358434 |
DDB_G0271886 | DDB_G0271886 | DDB0232429 | CDS | 981925 | 3123 | - | 0.327249 | |
DDB_G0271888 | DDB_G0271888 | DDB0232429 | CDS | 1032903 | 225 | + | 0.28 | |
DDB_G0271890 | DDB_G0271890 | DDB0232429 | CDS | 1033465 | 1137 | - | 0.297274 | |
DDB_G0271892 | DDB_G0271892 | similar to bacterial glutathione S-transferase catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 1035063 | 684 | - | 0.302632 |
DDB_G0271894 | DDB_G0271894 | DDB0232429 | CDS | 1037222 | 2067 | + | 0.355104 | |
DDB_G0271896 | DDB_G0271896 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232429 | CDS | 1041429 | 264 | - | 0.30303 |
DDB_G0271898 | DDB_G0271898 | DDB0232429 | CDS | 1042985 | 549 | - | 0.196721 | |
DDB_G0271900 | DDB_G0271900 | DDB0232429 | CDS | 1044061 | 3354 | - | 0.271318 | |
DDB_G0271904 | DDB_G0271904 | catalyzes the reaction GTP oxaloacetate GDP phosphoenolpyruvate COsub2sub in gluconeogenesis and the TCA cycle | DDB0232429 | CDS | 1058890 | 1962 | - | 0.349134 |
DDB_G0271910 | DDB_G0271910 | ortholog of human MCTS1 which is an anti-oncogene that may play a role in cell cycle regulation contains a PUA domain which is predicted to bind RNA | DDB0232429 | CDS | 1018193 | 549 | + | 0.26776 |
DDB_G0271912 | DDB_G0271912 | DDB0232429 | CDS | 1004091 | 1608 | + | 0.251244 | |
DDB_G0271914 | DDB_G0271914 | DDB0232429 | CDS | 1000440 | 675 | - | 0.358519 | |
DDB_G0271918 | DDB_G0271918 | DDB0232429 | CDS | 1028566 | 195 | + | 0.169231 | |
DDB_G0271920 | DDB_G0271920 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232429 | CDS | 1028961 | 213 | - | 0.28169 |
DDB_G0271926 | DDB_G0271926 | DDB0232429 | CDS | 1066723 | 3009 | + | 0.170156 | |
DDB_G0271928 | DDB_G0271928 | DDB0232429 | CDS | 1052190 | 4305 | + | 0.253194 | |
DDB_G0271930 | DDB_G0271930 | DDB0232429 | CDS | 1027709 | 192 | - | 0.265625 | |
DDB_G0271934 | DDB_G0271934 | weakly similar to hssA2C7E family protein N terminal exon is 10 nt rather than 13 as the other genes of that family | DDB0232429 | CDS | 1039722 | 231 | - | 0.316017 |
DDB_G0271936 | DDB_G0271936 | DDB0232429 | CDS | 1030563 | 1254 | + | 0.274322 | |
DDB_G0271938 | DDB_G0271938 | putative pseudogene similar to a large gene family encoding FNIP repeat-containing proteins including | DDB0232429 | CDS | 1025973 | 1305 | - | 0.172414 |
DDB_G0271944 | DDB_G0271944 | DDB0232429 | CDS | 1016342 | 1518 | - | 0.249671 | |
DDB_G0271946 | DDB_G0271946 | DDB0232429 | CDS | 1009716 | 4098 | + | 0.300878 | |
DDB_G0271948 | DDB_G0271948 | DDB0232429 | CDS | 1006829 | 2154 | + | 0.221913 | |
DDB_G0271950 | DDB_G0271950 | DDB0232429 | CDS | 1002205 | 1344 | - | 0.235119 | |
DDB_G0271952_RTE | DDB_G0271952 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 996675 | 1335 | + | 0.305618 |
DDB_G0271954_RTE | DDB_G0271954 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 994788 | 1209 | - | 0.333333 |
DDB_G0271956 | DDB_G0271956 | member of the TRIAD family which contain an IBR Zn finger (C6HC domain) flanked by two RING fingers | DDB0232429 | CDS | 1020910 | 2628 | - | 0.230213 |
DDB_G0271958 | DDB_G0271958 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 1074422 | 717 | - | 0.1841 |
DDB_G0271962 | DDB_G0271962 | DDB0232429 | CDS | 1080455 | 1401 | - | 0.271235 | |
DDB_G0271964_ps | DDB_G0271964 | putative pseudogene poly(ADP-ribose) polymerase family protein | DDB0232429 | CDS | 1084003 | 303 | + | 0.273927 |
DDB_G0271966 | DDB_G0271966 | DDB0232429 | CDS | 1085006 | 423 | + | 0.274232 | |
DDB_G0271968 | DDB_G0271968 | similar to human LMAN1 (lectin mannose-binding protein 1) belongs to the legume-like lectin family contains 1 predicted transmembrane domain similar to D. purpureum protein | DDB0232429 | CDS | 1086145 | 1710 | + | 0.281287 |
DDB_G0271970 | DDB_G0271970 | DDB0232429 | CDS | 1088983 | 1707 | + | 0.341535 | |
DDB_G0271972 | DDB_G0271972 | DDB0232429 | CDS | 1092100 | 219 | + | 0.351598 | |
DDB_G0271982 | DDB_G0271982 | DDB0232429 | CDS | 1103704 | 1890 | - | 0.284127 | |
DDB_G0271986 | DDB_G0271986 | DDB0232429 | CDS | 1118852 | 531 | + | 0.229755 | |
DDB_G0271988 | DDB_G0271988 | contains 7 putative transmembrane domains similar to D. purpureum protein | DDB0232429 | CDS | 1144876 | 1476 | + | 0.285908 |
DDB_G0271990 | DDB_G0271990 | DDB0232429 | CDS | 1143353 | 840 | + | 0.271429 | |
DDB_G0271992 | DDB_G0271992 | DDB0232429 | CDS | 1142461 | 426 | + | 0.347418 | |
DDB_G0271994 | DDB_G0271994 | bCommunity annotation: bThis protein may be a highly diverged monomeric a target | DDB0232429 | CDS | 1129144 | 1515 | - | 0.240924 |
DDB_G0271996 | DDB_G0271996 | contains four FNIP repeats similar to cmbB cigB and other conserved hypothetical Dictyostelium proteins | DDB0232429 | CDS | 1132270 | 2814 | - | 0.290334 |
DDB_G0272000 | DDB_G0272000 | DDB0232429 | CDS | 1137998 | 2859 | - | 0.243442 | |
DDB_G0272006 | DDB_G0272006 | similar to H. sapiens Down syndrome critical region protein 5 the Dictyostelium protein is much longer (602 amino acids compared to 134 amino acids for the human gene) has two predicted transmembrane domains | DDB0232429 | CDS | 1167768 | 1809 | - | 0.294085 |
DDB_G0272012 | DDB_G0272012 | members of this family are membrane proteins involved in long chain fatty acid elongation systems that produce 26-carbon precursors for ceramide and sphingolipid synthesis contains 7 putative transmembrane domains | DDB0232429 | CDS | 1170947 | 891 | + | 0.264871 |
DDB_G0272014 | DDB_G0272014 | belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family similar to human AADAT (kynureninealpha-aminoadipate aminotransferase) and S. cerevisiae ARO8 (aromatic amino acid aminotransferase) | DDB0232429 | CDS | 1172213 | 1446 | - | 0.278008 |
DDB_G0272016 | DDB_G0272016 | the DCUN1 domain is found in the eukaryotic 'defective in cullin neddylation' (DCN) protein family | DDB0232429 | CDS | 1175168 | 738 | + | 0.314363 |
DDB_G0272020 | DDB_G0272020 | contains an N-terminal F-box domain a central SH2 domain and C-terminal ankyrin repeats | DDB0232429 | CDS | 1179282 | 2412 | + | 0.246269 |
DDB_G0272024 | DDB_G0272024 | DDB0232429 | CDS | 1183612 | 1530 | - | 0.209804 | |
DDB_G0272026 | DDB_G0272026 | DDB0232429 | CDS | 1185842 | 327 | - | 0.391437 | |
DDB_G0272028 | DDB_G0272028 | DDB0232429 | CDS | 1186737 | 1827 | - | 0.310892 | |
DDB_G0272030 | DDB_G0272030 | DDB0232429 | CDS | 1189650 | 678 | - | 0.361357 | |
DDB_G0272034 | DDB_G0272034 | DDB0232429 | CDS | 1075826 | 1914 | - | 0.211599 | |
DDB_G0272040 | DDB_G0272040 | DDB0232429 | CDS | 1123795 | 309 | - | 0.333333 | |
DDB_G0272042 | DDB_G0272042 | DDB0232429 | CDS | 1162280 | 1167 | - | 0.302485 | |
DDB_G0272048 | DDB_G0272048 | DDB0232429 | CDS | 1193466 | 1176 | - | 0.271259 | |
DDB_G0272050_ps | DDB_G0272050 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 1194853 | 243 | - | 0.26749 |
DDB_G0272052 | DDB_G0272052 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D | DDB0232429 | CDS | 1070817 | 2211 | + | 0.284034 |
DDB_G0272054 | DDB_G0272054 | DDB0232429 | CDS | 1100914 | 1236 | - | 0.306634 | |
DDB_G0272056 | DDB_G0272056 | putative ortholog of H. sapiens CNOT3 and S. cerevisiae NOT3 component of the CCR4-NOT transcription complex | DDB0232429 | CDS | 1115108 | 2601 | + | 0.329489 |
DDB_G0272058 | DDB_G0272058 | similar to other Dictyostelium genes although shorter at the carboxyl terminus | DDB0232429 | CDS | 1124620 | 2652 | - | 0.18175 |
DDB_G0272060 | DDB_G0272060 | DDB0232429 | CDS | 1146550 | 1536 | - | 0.169922 | |
DDB_G0272062 | DDB_G0272062 | DDB0232429 | CDS | 1148337 | 441 | - | 0.285714 | |
DDB_G0272064 | DDB_G0272064 | DDB0232429 | CDS | 1150556 | 8169 | + | 0.281307 | |
DDB_G0272066 | DDB_G0272066 | DDB0232429 | CDS | 1159049 | 1851 | - | 0.251756 | |
DDB_G0272068_ps | DDB_G0272068 | putative pseudogene fragment of D. discoideum genes | DDB0232429 | CDS | 1199474 | 168 | - | 0.27381 |
DDB_G0272070 | DDB_G0272070 | DDB0232429 | CDS | 1201188 | 2145 | - | 0.250816 | |
DDB_G0272072 | DDB_G0272072 | DDB0232429 | CDS | 1214216 | 1203 | - | 0.27182 | |
DDB_G0272074 | DDB_G0272074 | DDB0232429 | CDS | 1216065 | 576 | + | 0.289931 | |
DDB_G0272082 | DDB_G0272082 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232429 | CDS | 1245702 | 5517 | + | 0.237992 |
DDB_G0272086_ps | DDB_G0272086 | putative pseudogene fragment similar to | DDB0232429 | CDS | 1196033 | 120 | + | 0.325 |
DDB_G0272088_ps | DDB_G0272088 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 1200085 | 300 | + | 0.266667 |
DDB_G0272090 | DDB_G0272090 | contains 5 putative transmembrane domains similar to D. purpureum protein | DDB0232429 | CDS | 1216702 | 2343 | - | 0.28041 |
DDB_G0272092 | DDB_G0272092 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family contains a C2 domain (Ca2-dependent membrane-targeting module) an ankyrin repeat region and a SAM (Sterile alpha motif) domain | DDB0232429 | CDS | 1251605 | 2961 | - | 0.296184 |
DDB_G0272094 | DDB_G0272094 | conserved Dictyostelium protein similar to bacterial proteins contains a predicted signal peptide | DDB0232429 | CDS | 1197926 | 417 | - | 0.302158 |
DDB_G0272096 | DDB_G0272096 | DDB0232429 | CDS | 1203890 | 4941 | + | 0.243473 | |
DDB_G0272098 | DDB_G0272098 | DDB0232429 | CDS | 1209397 | 3255 | - | 0.252535 | |
DDB_G0272100 | DDB_G0272100 | DDB0232429 | CDS | 1227402 | 5673 | + | 0.241671 | |
DDB_G0272102 | DDB_G0272102 | DDB0232429 | CDS | 1233762 | 4959 | + | 0.20125 | |
DDB_G0272108 | DDB_G0272108 | shares a short region of similarity with the splicing regulator TIA-1 REMI mutant forms aberrant fruiting bodies see | DDB0232429 | CDS | 1281320 | 1410 | - | 0.274468 |
DDB_G0272122 | DDB_G0272122 | DDB0232429 | CDS | 1381315 | 6063 | - | 0.242289 | |
DDB_G0272126 | DDB_G0272126 | DDB0232429 | CDS | 1376138 | 219 | + | 0.178082 | |
DDB_G0272128 | DDB_G0272128 | belongs to the short chain dehydrogenasesreductases family ortholog of human HSD17B10 which is involved in mitochondrial tRNA maturation and by interacting with intracellular amyloid-beta may contribute to the neuronal dysfunction associated with Alzheimer disease | DDB0232429 | CDS | 1375029 | 795 | + | 0.328302 |
DDB_G0272130 | DDB_G0272130 | DDB0232429 | CDS | 1366581 | 618 | + | 0.260518 | |
DDB_G0272134 | DDB_G0272134 | DDB0232429 | CDS | 1489722 | 2271 | - | 0.217525 | |
DDB_G0272140 | DDB_G0272140 | DDB0232429 | CDS | 1481911 | 369 | - | 0.308943 | |
DDB_G0272142 | DDB_G0272142 | contains one RF-1 domain similar to human ICT1 (immature colon carcinoma transcript 1 protein) | DDB0232429 | CDS | 1480927 | 648 | + | 0.239198 |
DDB_G0272144 | DDB_G0272144 | DDB0232429 | CDS | 1477294 | 2205 | + | 0.248526 | |
DDB_G0272146 | DDB_G0272146 | DDB0232429 | CDS | 1475387 | 816 | - | 0.3125 | |
DDB_G0272148 | DDB_G0272148 | DDB0232429 | CDS | 1472039 | 2706 | - | 0.216925 | |
DDB_G0272152 | DDB_G0272152 | DDB0232429 | CDS | 1595785 | 408 | + | 0.254902 | |
DDB_G0272154 | DDB_G0272154 | DDB0232429 | CDS | 1594214 | 906 | - | 0.378587 | |
DDB_G0272156 | DDB_G0272156 | DDB0232429 | CDS | 1588042 | 1623 | - | 0.187924 | |
DDB_G0272160 | DDB_G0272160 | DDB0232429 | CDS | 1582590 | 711 | - | 0.357243 | |
DDB_G0272162 | DDB_G0272162 | DDB0232429 | CDS | 1555450 | 1977 | - | 0.222559 | |
DDB_G0272164 | DDB_G0272164 | DDB0232429 | CDS | 1554645 | 453 | + | 0.309051 | |
DDB_G0272174 | DDB_G0272174 | DDB0232429 | CDS | 1524938 | 1845 | - | 0.228726 | |
DDB_G0272176 | DDB_G0272176 | conserved eukaryotic protein ortholog of S. cerevisiae LAS1 an essential nuclear protein possibly involved in bud formation and morphogenesis | DDB0232429 | CDS | 1520760 | 1845 | + | 0.233604 |
DDB_G0272178 | DDB_G0272178 | DDB0232429 | CDS | 1520067 | 420 | - | 0.22619 | |
DDB_G0272180 | DDB_G0272180 | DDB0232429 | CDS | 1518514 | 1008 | + | 0.240079 | |
DDB_G0272182 | DDB_G0272182 | catalyzes the reaction L-arginine Hsub2subO L-citrulline NHsub3sub N-terminal half highly similar to bacterial argnine deiminase an amidinotransferase | DDB0232429 | CDS | 1515537 | 2409 | + | 0.33956 |
DDB_G0272184 | DDB_G0272184 | very conserved protein among bacteria and fungi zinc-binding ADH's are dimeric or tetrameric enzymes that bind two atoms of zinc per subunit | DDB0232429 | CDS | 1513508 | 966 | - | 0.385093 |
DDB_G0272186 | DDB_G0272186 | DDB0232429 | CDS | 1509530 | 3153 | - | 0.292103 | |
DDB_G0272188 | DDB_G0272188 | DDB0232429 | CDS | 1507098 | 246 | + | 0.247967 | |
DDB_G0272192 | DDB_G0272192 | DDB0232429 | CDS | 1412468 | 1497 | + | 0.329993 | |
DDB_G0272194 | DDB_G0272194 | DDB0232429 | CDS | 1431432 | 882 | + | 0.239229 | |
DDB_G0272196 | DDB_G0272196 | contains one VWFA domain and one copine domain copines are phospholipid-binding proteins | DDB0232429 | CDS | 1467056 | 855 | - | 0.336842 |
DDB_G0272198 | DDB_G0272198 | DDB0232429 | CDS | 1615667 | 606 | - | 0.287129 | |
DDB_G0272200 | DDB_G0272200 | DDB0232429 | CDS | 1626168 | 2634 | + | 0.312073 | |
DDB_G0272202 | DDB_G0272202 | DDB0232429 | CDS | 1651021 | 1617 | + | 0.310451 | |
DDB_G0272204 | DDB_G0272204 | DDB0232429 | CDS | 1653467 | 585 | + | 0.147009 | |
DDB_G0272206 | DDB_G0272206 | DDB0232429 | CDS | 1658418 | 5340 | + | 0.265169 | |
DDB_G0272212 | DDB_G0272212 | DDB0232429 | CDS | 1673975 | 2508 | - | 0.289075 | |
DDB_G0272214 | DDB_G0272214 | DDB0232429 | CDS | 1678306 | 1845 | + | 0.241734 | |
DDB_G0272218 | DDB_G0272218 | DDB0232429 | CDS | 1690375 | 1809 | + | 0.290216 | |
DDB_G0272220 | DDB_G0272220 | DDB0232429 | CDS | 1693684 | 2616 | + | 0.270642 | |
DDB_G0272224 | DDB_G0272224 | phosphorylates NAD to NADP | DDB0232429 | CDS | 1711679 | 1389 | + | 0.258459 |
DDB_G0272226 | DDB_G0272226 | DDB0232429 | CDS | 1713237 | 1656 | - | 0.263889 | |
DDB_G0272228 | DDB_G0272228 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232429 | CDS | 1715738 | 264 | + | 0.371212 |
DDB_G0272230 | DDB_G0272230 | DDB0232429 | CDS | 1716242 | 675 | - | 0.245926 | |
DDB_G0272232 | DDB_G0272232 | DDB0232429 | CDS | 1717674 | 339 | - | 0.292035 | |
DDB_G0272238 | DDB_G0272238 | DDB0232429 | CDS | 1724431 | 210 | + | 0.27619 | |
DDB_G0272252 | DDB_G0272252 | DDB0232429 | CDS | 1388787 | 495 | + | 0.246465 | |
DDB_G0272254 | DDB_G0272254 | member of the TKL (tyrosine kinase-like) group contains a galactose oxidase central domain and three Kelch motifs | DDB0232429 | CDS | 1396081 | 3996 | - | 0.264765 |
DDB_G0272262 | DDB_G0272262 | DDB0232429 | CDS | 1429556 | 780 | + | 0.179487 | |
DDB_G0272264 | DDB_G0272264 | contains two coiled-coil domains predicted to have structural similarity to the beta-sandwich domain of the Sec2324 superfamily | DDB0232429 | CDS | 1442939 | 2895 | + | 0.230052 |
DDB_G0272268_RTE | DDB_G0272268 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 1460129 | 642 | - | 0.272586 |
DDB_G0272270_RTE | DDB_G0272270 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 1461355 | 276 | - | 0.297101 |
DDB_G0272272 | DDB_G0272272 | DDB0232429 | CDS | 1470684 | 1215 | + | 0.201646 | |
DDB_G0272278_ps | DDB_G0272278 | putative pseudogene similar to a Dictyostelium family of genes including | DDB0232429 | CDS | 1558001 | 1041 | - | 0.239193 |
DDB_G0272280 | DDB_G0272280 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232429 | CDS | 1570828 | 546 | + | 0.287546 |
DDB_G0272282 | DDB_G0272282 | member of the AGC kinase group similar to kinase domains of NDR (nuclear Dbf2-related) and MAST (microtubule-associated serinethreonine kinase) | DDB0232429 | CDS | 1572926 | 6309 | + | 0.272468 |
DDB_G0272288 | DDB_G0272288 | DDB0232429 | CDS | 1605368 | 1047 | - | 0.333333 | |
DDB_G0272290_RTE | DDB_G0272290 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 1612117 | 3180 | + | 0.349686 |
DDB_G0272292_TE | DDB_G0272292 | DDB0232429 | CDS | 1631049 | 594 | + | 0.240741 | |
DDB_G0272294 | DDB_G0272294 | DDB0232429 | CDS | 1633573 | 2949 | + | 0.287894 | |
DDB_G0272298 | DDB_G0272298 | DDB0232429 | CDS | 1664020 | 918 | - | 0.310458 | |
DDB_G0272302 | DDB_G0272302 | DDB0232429 | CDS | 1692695 | 246 | - | 0.260163 | |
DDB_G0272310_ps | DDB_G0272310 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 1259741 | 2574 | - | 0.238539 |
DDB_G0272314 | DDB_G0272314 | DDB0232429 | CDS | 1264510 | 5073 | - | 0.241672 | |
DDB_G0272316 | DDB_G0272316 | highly similar to | DDB0232429 | CDS | 1270771 | 192 | + | 0.260417 |
DDB_G0272318 | DDB_G0272318 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) | DDB0232429 | CDS | 1278811 | 1551 | + | 0.350097 |
DDB_G0272322 | DDB_G0272322 | DDB0232429 | CDS | 1285359 | 963 | - | 0.318795 | |
DDB_G0272328 | DDB_G0272328 | DDB0232429 | CDS | 1298775 | 747 | + | 0.290495 | |
DDB_G0272330_ps | DDB_G0272330 | putative pseudogene similar to EGF repeat-containing proteins such as | DDB0232429 | CDS | 1300433 | 1370 | + | 0.269343 |
DDB_G0272334_ps | DDB_G0272334 | putative pseudogene similar to EGF repeat-containing proteins such as | DDB0232429 | CDS | 1305873 | 3441 | + | 0.282476 |
DDB_G0272336_ps | DDB_G0272336 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 1311861 | 3312 | + | 0.281401 |
DDB_G0272338 | DDB_G0272338 | DDB0232429 | CDS | 1326566 | 5052 | - | 0.223674 | |
DDB_G0272340 | DDB_G0272340 | DDB0232429 | CDS | 1331957 | 1350 | - | 0.264444 | |
DDB_G0272342 | DDB_G0272342 | DDB0232429 | CDS | 1338747 | 1281 | + | 0.330211 | |
DDB_G0272348 | DDB_G0272348 | DDB0232429 | CDS | 1358012 | 1788 | - | 0.250559 | |
DDB_G0272356 | DDB_G0272356 | DDB0232429 | CDS | 1290469 | 1914 | - | 0.372518 | |
DDB_G0272358 | DDB_G0272358 | DDB0232429 | CDS | 1293361 | 753 | + | 0.243028 | |
DDB_G0272364 | DDB_G0272364 | contains a predicted signal sequence and a putative C-terminal transmembrane domain contains 2 EGF-like domains | DDB0232429 | CDS | 1317794 | 3891 | + | 0.28219 |
DDB_G0272366 | DDB_G0272366 | contains EGF-like domain and an immunoglobulin E-set domain contains a predicted signal peptide and a putative C-terminal transmembrane domain | DDB0232429 | CDS | 1322780 | 3390 | + | 0.275221 |
DDB_G0272370 | DDB_G0272370 | DDB0232429 | CDS | 1361017 | 3543 | + | 0.18967 | |
DDB_G0272376 | DDB_G0272376 | DDB0232429 | CDS | 1389998 | 816 | + | 0.269608 | |
DDB_G0272378 | DDB_G0272378 | DDB0232429 | CDS | 1392021 | 2682 | + | 0.219985 | |
DDB_G0272380 | DDB_G0272380 | DDB0232429 | CDS | 1395088 | 702 | + | 0.27208 | |
DDB_G0272382 | DDB_G0272382 | DDB0232429 | CDS | 1401273 | 2337 | - | 0.279418 | |
DDB_G0272384 | DDB_G0272384 | E.coli ATP-dependent DNA helicase RecQ is involved in genome maintenance similar to Bloom syndrome protein defects in BLM cause genetic instability including a high level of sister chromatid exchanges associated with a greatly increased predisposition to a wide range of cancers | DDB0232429 | CDS | 1405577 | 2922 | + | 0.255305 |
DDB_G0272386 | DDB_G0272386 | DDB0232429 | CDS | 1415836 | 1344 | + | 0.296875 | |
DDB_G0272388 | DDB_G0272388 | DDB0232429 | CDS | 1417426 | 2022 | - | 0.250247 | |
DDB_G0272396 | DDB_G0272396 | DDB0232429 | CDS | 1435063 | 1188 | - | 0.305556 | |
DDB_G0272398 | DDB_G0272398 | DDB0232429 | CDS | 1448193 | 306 | + | 0.316993 | |
DDB_G0272400_RTE | DDB_G0272400 | partial and rearranged ORF1and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 1461647 | 2400 | - | 0.326667 |
DDB_G0272402 | DDB_G0272402 | DDB0232429 | CDS | 1469033 | 876 | + | 0.157534 | |
DDB_G0272404 | DDB_G0272404 | DDB0232429 | CDS | 1479556 | 816 | - | 0.245098 | |
DDB_G0272406 | DDB_G0272406 | DDB0232429 | CDS | 1486400 | 3066 | + | 0.304305 | |
DDB_G0272408_RTE | DDB_G0272408 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 1493180 | 684 | + | 0.336257 |
DDB_G0272410_ps | DDB_G0272410 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232429 | CDS | 1495444 | 3876 | + | 0.237358 |
DDB_G0272416 | DDB_G0272416 | DDB0232429 | CDS | 1500467 | 2574 | - | 0.272727 | |
DDB_G0272418 | DDB_G0272418 | DDB0232429 | CDS | 1503629 | 399 | - | 0.285714 | |
DDB_G0272420 | DDB_G0272420 | DDB0232429 | CDS | 1507846 | 1083 | - | 0.301016 | |
DDB_G0272424 | DDB_G0272424 | similar to bacterial MarR family protein a transcriptional regulator | DDB0232429 | CDS | 1533902 | 459 | + | 0.250545 |
DDB_G0272432 | DDB_G0272432 | DDB0232429 | CDS | 1560308 | 1434 | - | 0.243375 | |
DDB_G0272434 | DDB_G0272434 | DDB0232429 | CDS | 1564450 | 4044 | - | 0.32542 | |
DDB_G0272436 | DDB_G0272436 | DDB0232429 | CDS | 1579848 | 729 | - | 0.397805 | |
DDB_G0272438 | DDB_G0272438 | DDB0232429 | CDS | 1590421 | 3639 | + | 0.205826 | |
DDB_G0272440 | DDB_G0272440 | very similar to the H. sapiens tumor protein p53-inducible protein 3 (TP53I3) belongs to the broader superfamily of zinc-dependent alcohol dehydrogenases | DDB0232429 | CDS | 1596579 | 1008 | - | 0.340278 |
DDB_G0272442 | DDB_G0272442 | DDB0232429 | CDS | 1598330 | 705 | - | 0.307801 | |
DDB_G0272448_RTE | DDB_G0272448 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 1610513 | 1080 | + | 0.414815 |
DDB_G0272450 | DDB_G0272450 | DDB0232429 | CDS | 1616616 | 4677 | - | 0.286081 | |
DDB_G0272454 | DDB_G0272454 | DDB0232429 | CDS | 1636769 | 1788 | - | 0.241051 | |
DDB_G0272456 | DDB_G0272456 | DDB0232429 | CDS | 1639732 | 4566 | + | 0.250548 | |
DDB_G0272458 | DDB_G0272458 | DDB0232429 | CDS | 1656497 | 750 | - | 0.225333 | |
DDB_G0272460 | DDB_G0272460 | DDB0232429 | CDS | 1680676 | 1644 | + | 0.297445 | |
DDB_G0272464 | DDB_G0272464 | DDB0232429 | CDS | 1705340 | 396 | + | 0.224747 | |
DDB_G0272466 | DDB_G0272466 | DDB0232429 | CDS | 1706359 | 867 | - | 0.304498 | |
DDB_G0272468 | DDB_G0272468 | DDB0232429 | CDS | 1707789 | 2247 | - | 0.272363 | |
DDB_G0272470 | DDB_G0272470 | DDB0232429 | CDS | 1732877 | 3009 | + | 0.258225 | |
DDB_G0272472 | DDB_G0272472 | DDB0232429 | CDS | 1736613 | 4527 | + | 0.299978 | |
DDB_G0272474 | DDB_G0272474 | DDB0232429 | CDS | 1745284 | 1644 | + | 0.216545 | |
DDB_G0272476 | DDB_G0272476 | DDB0232429 | CDS | 1747963 | 375 | - | 0.290667 | |
DDB_G0272480 | DDB_G0272480 | DDB0232429 | CDS | 1751987 | 3990 | - | 0.254637 | |
DDB_G0272482 | DDB_G0272482 | DDB0232429 | CDS | 1756945 | 1917 | + | 0.209703 | |
DDB_G0272484 | DDB_G0272484 | contains the metal-dependent phosphohydrolase HD region similar to the H. sapiens SAM domain and HD domain-containing protein 1 (SAMHD1) but lacking the N-terminal SAM domain | DDB0232429 | CDS | 1760557 | 1545 | - | 0.297735 |
DDB_G0272490_ps | DDB_G0272490 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 1783111 | 1821 | + | 0.217463 |
DDB_G0272492 | DDB_G0272492 | DDB0232429 | CDS | 1771698 | 4221 | + | 0.270315 | |
DDB_G0272494 | DDB_G0272494 | DDB0232429 | CDS | 1799833 | 1110 | + | 0.400901 | |
DDB_G0272496 | DDB_G0272496 | DDB0232429 | CDS | 1802094 | 1374 | + | 0.199418 | |
DDB_G0272500 | DDB_G0272500 | DDB0232429 | CDS | 1806966 | 1239 | - | 0.290557 | |
DDB_G0272502 | DDB_G0272502 | DDB0232429 | CDS | 1817675 | 3381 | + | 0.300799 | |
DDB_G0272504 | DDB_G0272504 | DDB0232429 | CDS | 1821204 | 669 | - | 0.279522 | |
DDB_G0272506 | DDB_G0272506 | DDB0232429 | CDS | 1822376 | 213 | + | 0.309859 | |
DDB_G0272508 | DDB_G0272508 | DDB0232429 | CDS | 1841723 | 315 | + | 0.307937 | |
DDB_G0272510 | DDB_G0272510 | belongs to a gene family conserved in amoeba contains a putative metal-binding domain | DDB0232429 | CDS | 1844774 | 1050 | + | 0.274286 |
DDB_G0272512 | DDB_G0272512 | weakly similar to mammalian tenascin expressed in pstAO cells | DDB0232429 | CDS | 1848141 | 927 | - | 0.255663 |
DDB_G0272514 | DDB_G0272514 | DDB0232429 | CDS | 1849663 | 162 | - | 0.320988 | |
DDB_G0272516 | DDB_G0272516 | DDB0232429 | CDS | 1766680 | 1398 | + | 0.263949 | |
DDB_G0272518 | DDB_G0272518 | DDB0232429 | CDS | 1770352 | 246 | - | 0.243902 | |
DDB_G0272528 | DDB_G0272528 | DDB0232429 | CDS | 1815902 | 708 | + | 0.185028 | |
DDB_G0272530 | DDB_G0272530 | DDB0232429 | CDS | 1826463 | 906 | + | 0.321192 | |
DDB_G0272532 | DDB_G0272532 | DDB0232429 | CDS | 1827873 | 4482 | + | 0.283579 | |
DDB_G0272534 | DDB_G0272534 | DDB0232429 | CDS | 1768175 | 1959 | + | 0.308321 | |
DDB_G0272536_ps | DDB_G0272536 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 1777162 | 1245 | - | 0.195181 |
DDB_G0272538 | DDB_G0272538 | DDB0232429 | CDS | 1778862 | 1761 | - | 0.187394 | |
DDB_G0272540 | DDB_G0272540 | DDB0232429 | CDS | 1786441 | 1812 | + | 0.211921 | |
DDB_G0272544 | DDB_G0272544 | similar to folate and thymidine transporters contains 11 transmembrane domains | DDB0232429 | CDS | 1796154 | 1701 | - | 0.219283 |
DDB_G0272546 | DDB_G0272546 | DDB0232429 | CDS | 1814324 | 843 | + | 0.28707 | |
DDB_G0272548_RTE | DDB_G0272548 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 1823720 | 855 | - | 0.34269 |
DDB_G0272550 | DDB_G0272550 | belongs to the POT (proton-dependent oligopeptide transport) family contains 12 putative transmembrane domains | DDB0232429 | CDS | 1832689 | 1749 | - | 0.302459 |
DDB_G0272554_RTE | DDB_G0272554 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232429 | CDS | 1837120 | 2265 | + | 0.393377 |
DDB_G0272558 | DDB_G0272558 | DDB0232429 | CDS | 1851656 | 3241 | + | 0.294971 | |
DDB_G0272570 | DDB_G0272570 | there is a second copy of this gene | DDB0232429 | CDS | 2456931 | 687 | - | 0.251819 |
DDB_G0272572 | DDB_G0272572 | there is a second copy of this gene | DDB0232429 | CDS | 2458351 | 585 | - | 0.273504 |
DDB_G0272576 | DDB_G0272576 | there is a second copy of this gene | DDB0232429 | CDS | 2466189 | 543 | - | 0.276243 |
DDB_G0272580 | DDB_G0272580 | similar to human RWDD1 S. cerevisiae GIR2 S. cerevisiae GIR2 binds to and regulates the expression of GTP-binding protein DRG2 there is a second copy of this gene | DDB0232429 | CDS | 2380443 | 696 | + | 0.303161 |
DDB_G0272586 | DDB_G0272586 | expressed in prespore cells there is a second copy of this gene | DDB0232429 | CDS | 2390435 | 855 | + | 0.298246 |
DDB_G0272592 | DDB_G0272592 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 2400265 | 4188 | + | 0.255492 |
DDB_G0272594_ps | DDB_G0272594 | putative pseudogene very similar to the putative importin subunit alpha C gene | DDB0232429 | CDS | 2405347 | 747 | - | 0.293173 |
DDB_G0272596 | DDB_G0272596 | there is a second copy of this gene | DDB0232429 | CDS | 2419091 | 303 | - | 0.287129 |
DDB_G0272598_ps | DDB_G0272598 | putative pseudogene similar to to a large family of EGF like domain-containing proteins there is a second copy of this pseudogene | DDB0232429 | CDS | 2425859 | 681 | - | 0.26138 |
DDB_G0272600 | DDB_G0272600 | ortholog of human HPS5 mutations in human HPS5 have been linked to Hermansky-Pudlak syndrome 5 contains a putative RING Zn finger there is a second copy of this gene | DDB0232429 | CDS | 2437736 | 4611 | - | 0.284971 |
DDB_G0272602 | DDB_G0272602 | there is a second copy of this gene | DDB0232429 | CDS | 2447280 | 1569 | + | 0.260038 |
DDB_G0272606 | DDB_G0272606 | there is a second copy of this gene | DDB0232429 | CDS | 2334392 | 858 | + | 0.305361 |
DDB_G0272610 | DDB_G0272610 | weakly similar to glycoproteins GP138A-D and gp130 there is a second copy of this gene | DDB0232429 | CDS | 2342908 | 2046 | - | 0.251222 |
DDB_G0272612 | DDB_G0272612 | there is a second copy of this gene | DDB0232429 | CDS | 2350685 | 1638 | + | 0.333333 |
DDB_G0272614 | DDB_G0272614 | similar to the THAP domain in the mammalian THAP domain-containing protein 4 underexpressed in | DDB0232429 | CDS | 2352791 | 480 | - | 0.302083 |
DDB_G0272620 | DDB_G0272620 | similar to human HSBP1 HSBP1 is a negative regulator of the heat shock response there is a second copy of this gene | DDB0232429 | CDS | 2363352 | 309 | + | 0.28479 |
DDB_G0272622 | DDB_G0272622 | there is a second copy of this gene | DDB0232429 | CDS | 2367362 | 1614 | - | 0.226766 |
DDB_G0272626 | DDB_G0272626 | DDB0232429 | CDS | 2272326 | 1278 | - | 0.187011 | |
DDB_G0272628 | DDB_G0272628 | underexpressed in | DDB0232429 | CDS | 2278778 | 1023 | - | 0.333333 |
DDB_G0272630 | DDB_G0272630 | there is a second copy of this gene | DDB0232429 | CDS | 2280592 | 621 | - | 0.241546 |
DDB_G0272632 | DDB_G0272632 | catalyzes the reaction RX glutathione HX R-S-glutathione there is a second copy of this gene | DDB0232429 | CDS | 2282062 | 597 | + | 0.309883 |
DDB_G0272636 | DDB_G0272636 | there is a second copy of this gene | DDB0232429 | CDS | 2295735 | 1221 | + | 0.284193 |
DDB_G0272638 | DDB_G0272638 | PIP5K catalyze the formation of phosphoinositol-45-bisphosphate via the phosphorylation of phosphatidylinositol-4-phosphate a precursor in the phosphinositide signaling pathway there is a second copy of this gene | DDB0232429 | CDS | 2297189 | 3240 | - | 0.264506 |
DDB_G0272640 | DDB_G0272640 | there is a second copy of this gene | DDB0232429 | CDS | 2304323 | 828 | - | 0.214976 |
DDB_G0272642 | DDB_G0272642 | there is a second copy of this gene | DDB0232429 | CDS | 2307287 | 1563 | + | 0.198337 |
DDB_G0272644 | DDB_G0272644 | contains 3 FNIP repeats there is a second copy of this gene | DDB0232429 | CDS | 2309231 | 1473 | + | 0.205024 |
DDB_G0272648 | DDB_G0272648 | there is a second copy of this gene | DDB0232429 | CDS | 2312521 | 672 | + | 0.181548 |
DDB_G0272650 | DDB_G0272650 | there is a second copy of this gene | DDB0232429 | CDS | 2313660 | 396 | - | 0.333333 |
DDB_G0272654 | DDB_G0272654 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232429 | CDS | 2255996 | 267 | - | 0.348315 |
DDB_G0272656 | DDB_G0272656 | DDB0232429 | CDS | 2258985 | 270 | + | 0.355556 | |
DDB_G0272658 | DDB_G0272658 | expressed at post-aggregation stage regulated by the MADS-box transcription factor SrfA during development | DDB0232429 | CDS | 2259874 | 270 | - | 0.344444 |
DDB_G0272662 | DDB_G0272662 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232429 | CDS | 2246849 | 492 | + | 0.296748 |
DDB_G0272664 | DDB_G0272664 | DDB0232429 | CDS | 2249594 | 393 | + | 0.302799 | |
DDB_G0272666 | DDB_G0272666 | DDB0232429 | CDS | 1858373 | 3930 | + | 0.265903 | |
DDB_G0272670 | DDB_G0272670 | DDB0232429 | CDS | 1945680 | 903 | + | 0.174972 | |
DDB_G0272672 | DDB_G0272672 | DDB0232429 | CDS | 2048228 | 366 | + | 0.355191 | |
DDB_G0272674 | DDB_G0272674 | DDB0232429 | CDS | 2041459 | 5730 | + | 0.2363 | |
DDB_G0272678 | DDB_G0272678 | DDB0232429 | CDS | 2007612 | 2211 | + | 0.291723 | |
DDB_G0272680 | DDB_G0272680 | protein phosphatase 2C is a serinethreonine specific protein phosphatase with broad substrate specificity and dependent on divalent cations (mainly manganese and magnesium) for its activity | DDB0232429 | CDS | 2003225 | 3447 | + | 0.286916 |
DDB_G0272682 | DDB_G0272682 | partial similarity to cry34 the Bacillus thuringiensis proteinaceous crystal and insecticidal toxin formed during sporulation contains an endonucleaseexonucleasephosphatase domain which is found in proteins such as magnesium dependent endonucleases and phosphatases involved in intracellular signalling | DDB0232429 | CDS | 1987848 | 3324 | + | 0.274368 |
DDB_G0272686 | DDB_G0272686 | DDB0232429 | CDS | 1983840 | 1368 | + | 0.25731 | |
DDB_G0272688 | DDB_G0272688 | DDB0232429 | CDS | 1980098 | 900 | - | 0.31 | |
DDB_G0272690 | DDB_G0272690 | DDB0232429 | CDS | 1968947 | 2271 | + | 0.265962 | |
DDB_G0272692 | DDB_G0272692 | DDB0232429 | CDS | 1960823 | 1209 | + | 0.17866 | |
DDB_G0272696 | DDB_G0272696 | DDB0232429 | CDS | 1925752 | 13482 | + | 0.282228 | |
DDB_G0272698_ps | DDB_G0272698 | putative pseudogene small fragment of D. discoideum gene | DDB0232429 | CDS | 1925070 | 174 | + | 0.264368 |
DDB_G0272700 | DDB_G0272700 | DDB0232429 | CDS | 1921731 | 621 | - | 0.330113 | |
DDB_G0272702 | DDB_G0272702 | DDB0232429 | CDS | 1919477 | 231 | - | 0.294372 | |
DDB_G0272706 | DDB_G0272706 | DDB0232429 | CDS | 1911544 | 1089 | - | 0.273646 | |
DDB_G0272708 | DDB_G0272708 | belongs to the methyltransferase superfamily AML1 family similar to human N6AMT2 S. cerevisiae AML1 | DDB0232429 | CDS | 1910511 | 636 | + | 0.235849 |
DDB_G0272714 | DDB_G0272714 | DDB0232429 | CDS | 1901589 | 1077 | + | 0.26091 | |
DDB_G0272716 | DDB_G0272716 | DDB0232429 | CDS | 1899910 | 1056 | - | 0.261364 | |
DDB_G0272718 | DDB_G0272718 | highly similar to | DDB0232429 | CDS | 1887722 | 270 | - | 0.448148 |
DDB_G0272720 | DDB_G0272720 | highly similar to | DDB0232429 | CDS | 1886873 | 255 | - | 0.462745 |
DDB_G0272722_ps | DDB_G0272722 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 1885747 | 318 | - | 0.248428 |
DDB_G0272724 | DDB_G0272724 | DDB0232429 | CDS | 1875234 | 315 | - | 0.498413 | |
DDB_G0272726 | DDB_G0272726 | DDB0232429 | CDS | 1873658 | 1134 | + | 0.271605 | |
DDB_G0272728 | DDB_G0272728 | DDB0232429 | CDS | 2214393 | 1218 | - | 0.142036 | |
DDB_G0272734 | DDB_G0272734 | DDB0232429 | CDS | 2221948 | 492 | + | 0.300813 | |
DDB_G0272740 | DDB_G0272740 | bCommunity annotation:b DDB_G0272740 is similar to histone2a-related transcription factors of the Hap5CBFNF-Y family which bind to the subsequence CCAAT and is threefold upregulated (p3E-7) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (Doquang et al in preparation). Most genes associated with S-phase or mitosis are upregulated in this strain. This is is consistent with the idea that factors of the the Hap5CBFNF-Y factors are involved in cell cycle progression in Dictyostelium as they are in animal cells. Harry MacWilliams September 2009br Closer examination of the blast results suggests that this gene does NOT code for an NF-Y subunit. Real orthologs to DDB_G0272740 do seem to occur in some fungi for instance Aspergillis and Ajellomyces although there are none in budding yeast. Insects also have a protein that is much more closely related to DDB_G0272740 than it is to nfyC it is called chrac-16 and is a component of the chromatin accessibility complex | DDB0232429 | CDS | 2228582 | 477 | + | 0.283019 |
DDB_G0272742 | DDB_G0272742 | DDB0232429 | CDS | 2229610 | 1038 | + | 0.267823 | |
DDB_G0272744 | DDB_G0272744 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232429 | CDS | 2238625 | 276 | + | 0.355072 |
DDB_G0272746 | DDB_G0272746 | DDB0232429 | CDS | 2239128 | 1140 | - | 0.220175 | |
DDB_G0272748 | DDB_G0272748 | DDB0232429 | CDS | 2092080 | 1956 | + | 0.21319 | |
DDB_G0272750_ps | DDB_G0272750 | putative pseudogene fragment similar to a D. discoideum patatin gene family including | DDB0232429 | CDS | 2096672 | 630 | + | 0.261905 |
DDB_G0272752 | DDB_G0272752 | contains a C2 calciumlipid-binding region (CaLB) | DDB0232429 | CDS | 2097426 | 537 | - | 0.324022 |
DDB_G0272762 | DDB_G0272762 | DDB0232429 | CDS | 2117004 | 390 | - | 0.189744 | |
DDB_G0272765 | DDB_G0272765 | DDB0232429 | CDS | 2137821 | 5130 | + | 0.301559 | |
DDB_G0272767 | DDB_G0272767 | DDB0232429 | CDS | 2144128 | 720 | - | 0.269444 | |
DDB_G0272769 | DDB_G0272769 | DDB0232429 | CDS | 2145765 | 2337 | + | 0.291827 | |
DDB_G0272773 | DDB_G0272773 | contains a predicted signal peptide there are two similar genes in D. discoideum | DDB0232429 | CDS | 2159393 | 618 | + | 0.257282 |
DDB_G0272777 | DDB_G0272777 | member of the same super family as valosin-containing protein (VCP) and CDC48brbr bCommunity annotation:b DDB G0272777 appears to be the Dicty-specific AAA-ATPase related cdc48 (cdcD) in Dicty and other organisms. When | DDB0232429 | CDS | 2164739 | 2217 | + | 0.249436 |
DDB_G0272785 | DDB_G0272785 | similar to human AOAH (acyloxyacyl hydrolase) removes the secondary (acyloxyacyl-linked) fatty acyl chains from the lipid A region of bacterial lipopolysaccharides contains a predicted signal peptide contains 1 saposin B-type domain | DDB0232429 | CDS | 2173913 | 1695 | - | 0.320944 |
DDB_G0272793 | DDB_G0272793 | there is a second copy of this gene | DDB0232429 | CDS | 2276143 | 552 | + | 0.280797 |
DDB_G0272797 | DDB_G0272797 | similar to cyclin dependent protein kinases there is a second copy of this gene | DDB0232429 | CDS | 2368968 | 2043 | - | 0.313754 |
DDB_G0272801 | DDB_G0272801 | there is a second copy of this gene | DDB0232429 | CDS | 2392581 | 2172 | - | 0.234807 |
DDB_G0272803 | DDB_G0272803 | there is a second copy of this gene | DDB0232429 | CDS | 2408163 | 231 | + | 0.311688 |
DDB_G0272805 | DDB_G0272805 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 2408810 | 4137 | + | 0.259367 |
DDB_G0272807 | DDB_G0272807 | there is a second copy of this gene | DDB0232429 | CDS | 2443179 | 2913 | + | 0.274288 |
DDB_G0272809 | DDB_G0272809 | DDB0232429 | CDS | 2251460 | 1947 | + | 0.24602 | |
DDB_G0272821 | DDB_G0272821 | DDB0232429 | CDS | 1962368 | 582 | + | 0.16323 | |
DDB_G0272823 | DDB_G0272823 | DDB0232429 | CDS | 2015699 | 2100 | - | 0.242381 | |
DDB_G0272829 | DDB_G0272829 | DDB0232429 | CDS | 2085728 | 1593 | - | 0.227872 | |
DDB_G0272839 | DDB_G0272839 | has a short region of similarity to aprataxin a Hint related protein that is mutated in individuals with ataxia with oculomotor apraxia | DDB0232429 | CDS | 2148504 | 1173 | + | 0.224211 |
DDB_G0272841 | DDB_G0272841 | belongs to the metallophosphoesterase superfamily similar to A. thaliana PAP6 (purple acid phosphatase) contains a predicted signal peptide and putative C-terminal transmembrane domain | DDB0232429 | CDS | 2241089 | 1755 | + | 0.334473 |
DDB_G0272843 | DDB_G0272843 | DDB0232429 | CDS | 2231078 | 1716 | + | 0.170746 | |
DDB_G0272845 | DDB_G0272845 | DDB0232429 | CDS | 2190439 | 2439 | + | 0.263223 | |
DDB_G0272849 | DDB_G0272849 | contains two putative EGF repeats an N-terminal signal sequence and a C-terminal transmembrane domain thus this seems to be an extracellular protein that is anchored in the membrane | DDB0232429 | CDS | 2179680 | 3414 | - | 0.268893 |
DDB_G0272851_ps | DDB_G0272851 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232429 | CDS | 2167082 | 1815 | - | 0.276584 |
DDB_G0272853 | DDB_G0272853 | DDB0232429 | CDS | 2114192 | 411 | - | 0.182482 | |
DDB_G0272855 | DDB_G0272855 | DDB0232429 | CDS | 2098484 | 480 | - | 0.270833 | |
DDB_G0272863 | DDB_G0272863 | DDB0232429 | CDS | 2069719 | 1362 | + | 0.263583 | |
DDB_G0272865 | DDB_G0272865 | DDB0232429 | CDS | 2067475 | 1932 | - | 0.219462 | |
DDB_G0272873 | DDB_G0272873 | there is a second copy of this gene | DDB0232429 | CDS | 2277326 | 1356 | + | 0.20059 |
DDB_G0272877 | DDB_G0272877 | contains 4 coiled-coil domains there is a second copy of this gene | DDB0232429 | CDS | 2317791 | 1677 | + | 0.305903 |
DDB_G0272879 | DDB_G0272879 | there is a second copy of this gene | DDB0232429 | CDS | 2319732 | 240 | - | 0.2125 |
DDB_G0272881 | DDB_G0272881 | highly similar to | DDB0232429 | CDS | 2332988 | 756 | - | 0.215608 |
DDB_G0272891_ps | DDB_G0272891 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 2391829 | 636 | + | 0.212264 |
DDB_G0272897 | DDB_G0272897 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 2414215 | 4143 | + | 0.260681 |
DDB_G0272901 | DDB_G0272901 | conserved Dictyostelium protein contains a weak putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 2429907 | 4227 | - | 0.255974 |
DDB_G0272903 | DDB_G0272903 | hypothetical protein there is a second copy of this gene | DDB0232429 | CDS | 2435526 | 2028 | + | 0.204142 |
DDB_G0272907_ps | DDB_G0272907 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 2463205 | 564 | - | 0.237589 |
DDB_G0272909 | DDB_G0272909 | DDB0232429 | CDS | 1856367 | 1080 | + | 0.165741 | |
DDB_G0272911 | DDB_G0272911 | DDB0232429 | CDS | 1864276 | 519 | + | 0.248555 | |
DDB_G0272913 | DDB_G0272913 | DDB0232429 | CDS | 1908716 | 762 | + | 0.26378 | |
DDB_G0272917 | DDB_G0272917 | DDB0232429 | CDS | 1919957 | 1464 | - | 0.314891 | |
DDB_G0272919 | DDB_G0272919 | DDB0232429 | CDS | 1923213 | 1275 | + | 0.258039 | |
DDB_G0272921 | DDB_G0272921 | DDB0232429 | CDS | 1942697 | 1554 | + | 0.181467 | |
DDB_G0272923 | DDB_G0272923 | DDB0232429 | CDS | 1992058 | 1089 | + | 0.215794 | |
DDB_G0272927 | DDB_G0272927 | conserved hypothetical Dictyostelium prestalk protein possible coiled-coil protein | DDB0232429 | CDS | 2260937 | 270 | + | 0.351852 |
DDB_G0272933 | DDB_G0272933 | DDB0232429 | CDS | 1863483 | 474 | + | 0.236287 | |
DDB_G0272937 | DDB_G0272937 | DDB0232429 | CDS | 1869111 | 4140 | + | 0.161594 | |
DDB_G0272939 | DDB_G0272939 | highly similar to | DDB0232429 | CDS | 1876171 | 732 | - | 0.233607 |
DDB_G0272947 | DDB_G0272947 | overexpressed in aspidocytes highly similar to | DDB0232429 | CDS | 1888648 | 282 | - | 0.386525 |
DDB_G0272949 | DDB_G0272949 | DDB0232429 | CDS | 1889671 | 3630 | - | 0.298623 | |
DDB_G0272951 | DDB_G0272951 | DDB0232429 | CDS | 1894598 | 1680 | - | 0.260119 | |
DDB_G0272953 | DDB_G0272953 | DDB0232429 | CDS | 1904183 | 1545 | + | 0.212945 | |
DDB_G0272955 | DDB_G0272955 | DDB0232429 | CDS | 1906038 | 1284 | - | 0.264798 | |
DDB_G0272957 | DDB_G0272957 | DDB0232429 | CDS | 1907750 | 741 | - | 0.221323 | |
DDB_G0272961 | DDB_G0272961 | DDB0232429 | CDS | 1939687 | 2643 | + | 0.180098 | |
DDB_G0272963 | DDB_G0272963 | DDB0232429 | CDS | 1944524 | 831 | + | 0.160048 | |
DDB_G0272965 | DDB_G0272965 | DDB0232429 | CDS | 1946792 | 1767 | - | 0.300509 | |
DDB_G0272971 | DDB_G0272971 | DDB0232429 | CDS | 1954958 | 795 | + | 0.262893 | |
DDB_G0272973 | DDB_G0272973 | DDB0232429 | CDS | 1963629 | 4542 | + | 0.192206 | |
DDB_G0272975 | DDB_G0272975 | DDB0232429 | CDS | 1974054 | 2079 | + | 0.275132 | |
DDB_G0272977 | DDB_G0272977 | DDB0232429 | CDS | 1976953 | 3054 | + | 0.173543 | |
DDB_G0272979 | DDB_G0272979 | DDB0232429 | CDS | 1981430 | 1416 | - | 0.288842 | |
DDB_G0272983 | DDB_G0272983 | contains one DnaJ N-terminal domain and one MYND-type zinc finger domain contains 8 putative transmembrane domains | DDB0232429 | CDS | 2010405 | 1719 | - | 0.268179 |
DDB_G0272993 | DDB_G0272993 | DDB0232429 | CDS | 2051969 | 2973 | - | 0.216953 | |
DDB_G0272995 | DDB_G0272995 | DDB0232429 | CDS | 2061113 | 3639 | + | 0.263809 | |
DDB_G0272997 | DDB_G0272997 | DDB0232429 | CDS | 2081848 | 3345 | - | 0.23707 | |
DDB_G0273005 | DDB_G0273005 | DDB0232429 | CDS | 2121552 | 1974 | + | 0.240628 | |
DDB_G0273009 | DDB_G0273009 | DDB0232429 | CDS | 2150157 | 1701 | - | 0.190476 | |
DDB_G0273011_ps | DDB_G0273011 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 2152302 | 1494 | - | 0.208835 |
DDB_G0273017 | DDB_G0273017 | catalyzes the reaction isocitrate glyoxylate succinate | DDB0232429 | CDS | 2236569 | 1407 | + | 0.369581 |
DDB_G0273019_ps | DDB_G0273019 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 2245384 | 195 | - | 0.317949 |
DDB_G0273021 | DDB_G0273021 | DDB0232429 | CDS | 2257063 | 264 | + | 0.348485 | |
DDB_G0273023 | DDB_G0273023 | DDB0232429 | CDS | 2257906 | 267 | - | 0.35206 | |
DDB_G0273025 | DDB_G0273025 | there is a second copy of this gene | DDB0232429 | CDS | 2262117 | 228 | + | 0.337719 |
DDB_G0273027 | DDB_G0273027 | there is a second copy of this gene | DDB0232429 | CDS | 2293392 | 1137 | - | 0.287599 |
DDB_G0273029 | DDB_G0273029 | there is a second copy of this gene | DDB0232429 | CDS | 2294733 | 342 | - | 0.225146 |
DDB_G0273031 | DDB_G0273031 | there is a second copy of this gene | DDB0232429 | CDS | 2322900 | 657 | + | 0.255708 |
DDB_G0273033 | DDB_G0273033 | there is a second copy of this gene | DDB0232429 | CDS | 2328058 | 4698 | + | 0.254364 |
DDB_G0273041 | DDB_G0273041 | there is a second copy of this gene | DDB0232429 | CDS | 2381533 | 1344 | - | 0.299851 |
DDB_G0273043 | DDB_G0273043 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 2420797 | 4176 | + | 0.257423 |
DDB_G0273049 | DDB_G0273049 | there is a second copy of this gene | DDB0232429 | CDS | 2461135 | 939 | - | 0.234292 |
DDB_G0273053 | DDB_G0273053 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog there is a second copy of this gene | DDB0232429 | CDS | 2288541 | 4557 | - | 0.250384 |
DDB_G0273075 | DDB_G0273075 | there is a second copy of this gene | DDB0232429 | CDS | 2647848 | 4143 | - | 0.177649 |
DDB_G0273077 | DDB_G0273077 | there is a second copy of this gene | DDB0232429 | CDS | 2646033 | 1632 | + | 0.259804 |
DDB_G0273079 | DDB_G0273079 | there is a second copy of this gene | DDB0232429 | CDS | 2641934 | 375 | + | 0.354667 |
DDB_G0273081 | DDB_G0273081 | similar to histidine ammonia-lyase which catalyzes the reaction L-histidine urocanate NHsub3sub there is a second copy of this gene | DDB0232429 | CDS | 2625067 | 1590 | + | 0.264151 |
DDB_G0273083 | DDB_G0273083 | member of the Dyp-type peroxidase family lacking a typical heme-binding region does not appear to be present in higher organisms there is a second copy of this gene | DDB0232429 | CDS | 2623576 | 921 | - | 0.334419 |
DDB_G0273085 | DDB_G0273085 | contains a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 2621919 | 1332 | + | 0.292042 |
DDB_G0273087_ps | DDB_G0273087 | putative pseudogene similar to Dictyostelium genes | DDB0232429 | CDS | 2605221 | 4356 | - | 0.288567 |
DDB_G0273091 | DDB_G0273091 | member of the ZIP (Zrt- and Irt-like Protein) family capable of transporting zinc and other metal ions contains 6 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 2599717 | 1128 | + | 0.337766 |
DDB_G0273093 | DDB_G0273093 | similar to the mammalian Hypoxia up-regulated protein 1 (HYOU1) a protein that plays a role in cytoprotective cellular mechanisms triggered by oxygen deprivation there is a second copy of this gene | DDB0232429 | CDS | 2591482 | 2781 | - | 0.280834 |
DDB_G0273095 | DDB_G0273095 | similar to human PDAP1 (PDGFA-associated protein 1) there is a second copy of this gene | DDB0232429 | CDS | 2590732 | 627 | + | 0.338118 |
DDB_G0273101 | DDB_G0273101 | there is a second copy of this gene | DDB0232429 | CDS | 2569065 | 6147 | + | 0.284041 |
DDB_G0273103 | DDB_G0273103 | there is a second copy of this gene | DDB0232429 | CDS | 2565766 | 717 | + | 0.319386 |
DDB_G0273105 | DDB_G0273105 | introduces a double bond at the delta position of fatty acids during the biosynthesis of monounsaturated fatty acids there is a second copy of this gene | DDB0232429 | CDS | 2562086 | 2361 | + | 0.309615 |
DDB_G0273109 | DDB_G0273109 | there is a second copy of this gene | DDB0232429 | CDS | 2552049 | 963 | - | 0.263759 |
DDB_G0273111 | DDB_G0273111 | there is a second copy of this gene | DDB0232429 | CDS | 2548178 | 210 | - | 0.219048 |
DDB_G0273113 | DDB_G0273113 | there is a second copy of this gene | DDB0232429 | CDS | 2546637 | 753 | - | 0.285525 |
DDB_G0273115 | DDB_G0273115 | there is a second copy of this gene | DDB0232429 | CDS | 2545999 | 531 | + | 0.308851 |
DDB_G0273119 | DDB_G0273119 | there is a second copy of this gene | DDB0232429 | CDS | 2535890 | 177 | - | 0.310734 |
DDB_G0273123 | DDB_G0273123 | there is a second copy of this gene | DDB0232429 | CDS | 2531335 | 1083 | + | 0.317636 |
DDB_G0273125 | DDB_G0273125 | there is a second copy of this gene | DDB0232429 | CDS | 2528420 | 2205 | - | 0.221769 |
DDB_G0273133 | DDB_G0273133 | there is a second copy of this gene | DDB0232429 | CDS | 2836914 | 2166 | + | 0.201754 |
DDB_G0273135 | DDB_G0273135 | there is a second copy of this gene | DDB0232429 | CDS | 2846671 | 1029 | + | 0.221574 |
DDB_G0273137 | DDB_G0273137 | there is a second copy of this gene | DDB0232429 | CDS | 2854787 | 1818 | + | 0.262376 |
DDB_G0273143 | DDB_G0273143 | there is a second copy of this gene | DDB0232429 | CDS | 2866004 | 321 | - | 0.267913 |
DDB_G0273145 | DDB_G0273145 | there is a second copy of this gene | DDB0232429 | CDS | 2872889 | 1065 | - | 0.252582 |
DDB_G0273147 | DDB_G0273147 | has similarity to the S. cerevisisae ATP10 a mitochondrial inner membrane protein required for assembly of the mitochondrial F1F0 ATP synthase there is a second copy of this gene | DDB0232429 | CDS | 2874426 | 783 | - | 0.240102 |
DDB_G0273149 | DDB_G0273149 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) there is a second copy of this gene | DDB0232429 | CDS | 2875789 | 1653 | - | 0.333333 |
DDB_G0273151 | DDB_G0273151 | there is a second copy of this gene | DDB0232429 | CDS | 2523859 | 2118 | - | 0.219075 |
DDB_G0273153 | DDB_G0273153 | weakly similar to glutathione S-transferases there is a second copy of this gene | DDB0232429 | CDS | 2469557 | 603 | + | 0.223881 |
DDB_G0273155 | DDB_G0273155 | there is a second copy of this gene | DDB0232429 | CDS | 2472439 | 1011 | - | 0.346192 |
DDB_G0273159 | DDB_G0273159 | there is a second copy of this gene | DDB0232429 | CDS | 2480367 | 216 | + | 0.25463 |
DDB_G0273161 | DDB_G0273161 | there is a second copy of this gene | DDB0232429 | CDS | 2481710 | 300 | + | 0.256667 |
DDB_G0273165 | DDB_G0273165 | catalyses the endonucleolytic cleavage of apurinic or apyrimidinic sites to generate products with a 5'-phosphate there is a second copy of this gene | DDB0232429 | CDS | 2484199 | 969 | - | 0.252838 |
DDB_G0273167 | DDB_G0273167 | there is a second copy of this gene | DDB0232429 | CDS | 2485605 | 444 | - | 0.236486 |
DDB_G0273169 | DDB_G0273169 | there is a second copy of this gene | DDB0232429 | CDS | 2498827 | 1740 | + | 0.18908 |
DDB_G0273173 | DDB_G0273173 | there is a second copy of this gene | DDB0232429 | CDS | 2502953 | 2301 | + | 0.156454 |
DDB_G0273177 | DDB_G0273177 | there is a second copy of this gene | DDB0232429 | CDS | 2526700 | 378 | - | 0.261905 |
DDB_G0273179 | DDB_G0273179 | there is a second copy of this gene | DDB0232429 | CDS | 2584694 | 1506 | - | 0.189907 |
DDB_G0273181 | DDB_G0273181 | contains no functional domains and is not similar to any other protein there is a second copy of this gene | DDB0232429 | CDS | 2602576 | 192 | + | 0.213542 |
DDB_G0273183 | DDB_G0273183 | there is a second copy of this gene | DDB0232429 | CDS | 2612260 | 225 | + | 0.306667 |
DDB_G0273185 | DDB_G0273185 | there is a second copy of this gene | DDB0232429 | CDS | 2673521 | 3651 | + | 0.212271 |
DDB_G0273187 | DDB_G0273187 | there is a second copy of this gene | DDB0232429 | CDS | 2677894 | 192 | + | 0.234375 |
DDB_G0273189 | DDB_G0273189 | there is a second copy of this gene | DDB0232429 | CDS | 2679135 | 2427 | + | 0.264524 |
DDB_G0273193 | DDB_G0273193 | shares a short region of similarity with the human gene TEX2 (expressed in testis) there is a second copy of this gene | DDB0232429 | CDS | 2684717 | 1728 | - | 0.282407 |
DDB_G0273195 | DDB_G0273195 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 2690707 | 1764 | - | 0.294218 |
DDB_G0273201 | DDB_G0273201 | similar to MAD2 and REV7 there is a second copy of this gene | DDB0232429 | CDS | 2699843 | 612 | + | 0.27451 |
DDB_G0273205 | DDB_G0273205 | contains an EF hand but shows little similarity to other proteins there is a second copy of this gene | DDB0232429 | CDS | 2704086 | 3033 | + | 0.279261 |
DDB_G0273217 | DDB_G0273217 | there is a second copy of this gene | DDB0232429 | CDS | 2728893 | 594 | - | 0.272727 |
DDB_G0273219 | DDB_G0273219 | there is a second copy of this gene | DDB0232429 | CDS | 2729906 | 1449 | - | 0.189786 |
DDB_G0273221 | DDB_G0273221 | conserved protein of unknown function contains a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 2732471 | 678 | + | 0.348083 |
DDB_G0273231 | DDB_G0273231 | there is a second copy of this gene | DDB0232429 | CDS | 2760431 | 2484 | - | 0.23913 |
DDB_G0273233 | DDB_G0273233 | there is a second copy of this gene | DDB0232429 | CDS | 2763989 | 1119 | - | 0.217158 |
DDB_G0273235 | DDB_G0273235 | contains 8 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 2765356 | 3843 | - | 0.284934 |
DDB_G0273237 | DDB_G0273237 | there is a second copy of this gene | DDB0232429 | CDS | 2770909 | 1158 | + | 0.277202 |
DDB_G0273241 | DDB_G0273241 | there is a second copy of this gene | DDB0232429 | CDS | 2784903 | 195 | + | 0.266667 |
DDB_G0273243 | DDB_G0273243 | there is a second copy of this gene | DDB0232429 | CDS | 2785722 | 171 | + | 0.251462 |
DDB_G0273245 | DDB_G0273245 | there is a second copy of this gene | DDB0232429 | CDS | 2791662 | 2778 | + | 0.172426 |
DDB_G0273247 | DDB_G0273247 | there is a second copy of this gene | DDB0232429 | CDS | 2794534 | 4683 | - | 0.325432 |
DDB_G0273253 | DDB_G0273253 | there is a second copy of this gene | DDB0232429 | CDS | 2884698 | 1161 | + | 0.221361 |
DDB_G0273255 | DDB_G0273255 | there is a second copy of this gene | DDB0232429 | CDS | 2887233 | 192 | - | 0.255208 |
DDB_G0273263_RTE | DDB_G0273263 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element there is a second copy of this gene | DDB0232429 | CDS | 2492298 | 2373 | - | 0.2933 |
DDB_G0273265 | DDB_G0273265 | there is a second copy of this gene | DDB0232429 | CDS | 2495550 | 333 | - | 0.339339 |
DDB_G0273269_ps | DDB_G0273269 | putative pseudogene fragment similar to UNC93-like protein MFSD11 family members | DDB0232429 | CDS | 2508437 | 147 | - | 0.346939 |
DDB_G0273271_RTE | DDB_G0273271 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element there is a second copy of this gene | DDB0232429 | CDS | 2514908 | 378 | + | 0.314815 |
DDB_G0273273 | DDB_G0273273 | there is a second copy of this gene | DDB0232429 | CDS | 2550408 | 579 | - | 0.300518 |
DDB_G0273275 | DDB_G0273275 | there is a second copy of this gene | DDB0232429 | CDS | 2566700 | 1476 | - | 0.22561 |
DDB_G0273277 | DDB_G0273277 | there is a second copy of this gene | DDB0232429 | CDS | 2575884 | 1374 | - | 0.3377 |
DDB_G0273279 | DDB_G0273279 | there is a second copy of this gene | DDB0232429 | CDS | 2578304 | 1110 | + | 0.193694 |
DDB_G0273281 | DDB_G0273281 | there is a second copy of this gene | DDB0232429 | CDS | 2581380 | 1434 | - | 0.232915 |
DDB_G0273283 | DDB_G0273283 | there is a second copy of this gene | DDB0232429 | CDS | 2583982 | 408 | + | 0.215686 |
DDB_G0273285 | DDB_G0273285 | there is a second copy of this gene | DDB0232429 | CDS | 2613529 | 6951 | - | 0.243274 |
DDB_G0273289 | DDB_G0273289 | no homologs in other organisms there is a second copy of this gene | DDB0232429 | CDS | 2626943 | 777 | - | 0.293436 |
DDB_G0273293 | DDB_G0273293 | DDB0232429 | CDS | 2636071 | 1413 | - | 0.265393 | |
DDB_G0273295 | DDB_G0273295 | there is a second copy of this gene | DDB0232429 | CDS | 2642763 | 369 | - | 0.273713 |
DDB_G0273297 | DDB_G0273297 | there is a second copy of this gene | DDB0232429 | CDS | 2643893 | 507 | + | 0.224852 |
DDB_G0273299 | DDB_G0273299 | there is a second copy of this gene | DDB0232429 | CDS | 2652628 | 1017 | + | 0.222222 |
DDB_G0273301 | DDB_G0273301 | there is a second copy of this gene | DDB0232429 | CDS | 2668726 | 1926 | - | 0.323988 |
DDB_G0273307_ps | DDB_G0273307 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 2772386 | 1074 | - | 0.214153 |
DDB_G0273311 | DDB_G0273311 | contains no functional domains there is a second copy of this gene | DDB0232429 | CDS | 2829694 | 645 | + | 0.252713 |
DDB_G0273313 | DDB_G0273313 | there is a second copy of this gene | DDB0232429 | CDS | 2845293 | 672 | - | 0.168155 |
DDB_G0273315 | DDB_G0273315 | there is a second copy of this gene | DDB0232429 | CDS | 2851916 | 1365 | + | 0.214652 |
DDB_G0273319 | DDB_G0273319 | DDB0232429 | CDS | 2870213 | 273 | - | 0.274725 | |
DDB_G0273321 | DDB_G0273321 | there is a second copy of this gene | DDB0232429 | CDS | 2476242 | 1605 | - | 0.261682 |
DDB_G0273323_RTE | DDB_G0273323 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE there is a second copy of this gene | DDB0232429 | CDS | 2497136 | 537 | - | 0.307263 |
DDB_G0273325_RTE | DDB_G0273325 | partial ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-C there is a second copy of this gene | DDB0232429 | CDS | 2517024 | 882 | + | 0.298186 |
DDB_G0273327_RTE | DDB_G0273327 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-C there is a second copy of this gene | DDB0232429 | CDS | 2518055 | 2586 | + | 0.324439 |
DDB_G0273329_RTE | DDB_G0273329 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-C there is a second copy of this gene | DDB0232429 | CDS | 2520747 | 540 | + | 0.375926 |
DDB_G0273331 | DDB_G0273331 | there is a second copy of this gene | DDB0232429 | CDS | 2538856 | 657 | + | 0.242009 |
DDB_G0273337_ps | DDB_G0273337 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 2549398 | 222 | - | 0.252252 |
DDB_G0273339 | DDB_G0273339 | there is a second copy of this gene | DDB0232429 | CDS | 2595096 | 3468 | - | 0.21684 |
DDB_G0273341 | DDB_G0273341 | there is a second copy of this gene | DDB0232429 | CDS | 2612891 | 159 | + | 0.289308 |
DDB_G0273343 | DDB_G0273343 | there is a second copy of this gene | DDB0232429 | CDS | 2638627 | 1158 | - | 0.212435 |
DDB_G0273345_RTE | DDB_G0273345 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE there is a second copy of this gene | DDB0232429 | CDS | 2655025 | 3144 | - | 0.338422 |
DDB_G0273347_RTE | DDB_G0273347 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE there is a second copy of this gene | DDB0232429 | CDS | 2658459 | 1335 | - | 0.31161 |
DDB_G0273351 | DDB_G0273351 | there is a second copy of this gene | DDB0232429 | CDS | 2663113 | 5058 | - | 0.169237 |
DDB_G0273357 | DDB_G0273357 | there is a second copy of this gene | DDB0232429 | CDS | 2693104 | 1980 | - | 0.377273 |
DDB_G0273361 | DDB_G0273361 | contains 5 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 2727455 | 936 | - | 0.244658 |
DDB_G0273367 | DDB_G0273367 | there is a second copy of this gene | DDB0232429 | CDS | 2754939 | 366 | + | 0.363388 |
DDB_G0273371 | DDB_G0273371 | there is a second copy of this gene | DDB0232429 | CDS | 2756320 | 3834 | + | 0.199009 |
DDB_G0273373 | DDB_G0273373 | there is a second copy of this gene | DDB0232429 | CDS | 2781320 | 189 | + | 0.306878 |
DDB_G0273375_TE | DDB_G0273375 | AT-rich low copy repetitive element which is thought to have no protein-coding capacity there is a second copy of this gene | DDB0232429 | CDS | 2783058 | 381 | + | 0.32021 |
DDB_G0273377 | DDB_G0273377 | there is a second copy of this gene | DDB0232429 | CDS | 2789660 | 1170 | - | 0.240171 |
DDB_G0273379 | DDB_G0273379 | there is a second copy of this gene | DDB0232429 | CDS | 2802060 | 3363 | + | 0.249182 |
DDB_G0273381 | DDB_G0273381 | there is a second copy of this gene | DDB0232429 | CDS | 2813973 | 4095 | + | 0.263736 |
DDB_G0273385 | DDB_G0273385 | there is a second copy of this gene | DDB0232429 | CDS | 2840909 | 3459 | - | 0.194276 |
DDB_G0273387 | DDB_G0273387 | expressed in pstAO cells and in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 2859896 | 663 | + | 0.279035 |
DDB_G0273391 | DDB_G0273391 | there is a second copy of this gene | DDB0232429 | CDS | 2879174 | 2340 | - | 0.20812 |
DDB_G0273393 | DDB_G0273393 | there is a second copy of this gene | DDB0232429 | CDS | 2883211 | 1242 | + | 0.217391 |
DDB_G0273395 | DDB_G0273395 | there is a second copy of this gene | DDB0232429 | CDS | 2886386 | 147 | - | 0.265306 |
DDB_G0273403 | DDB_G0273403 | there is a second copy of this gene | DDB0232429 | CDS | 2893976 | 156 | + | 0.25641 |
DDB_G0273405_ps | DDB_G0273405 | putative pseudogene similar to coactosin contains an ADF (actin depolymerisation factorcofilin-like) domain there is a second copy of this gene | DDB0232429 | CDS | 2913032 | 819 | + | 0.316239 |
DDB_G0273411 | DDB_G0273411 | there is a second copy of this gene | DDB0232429 | CDS | 2935949 | 669 | + | 0.282511 |
DDB_G0273413 | DDB_G0273413 | there is a second copy of this gene | DDB0232429 | CDS | 2940321 | 1371 | + | 0.243618 |
DDB_G0273415 | DDB_G0273415 | there is a second copy of this gene | DDB0232429 | CDS | 2941844 | 996 | - | 0.26506 |
DDB_G0273417 | DDB_G0273417 | similar to bacterial S-adenosyl-L-methionine (SAM) methyltransferases similar to D. purpureum protein there is a second copy of this gene | DDB0232429 | CDS | 2943449 | 1407 | + | 0.25231 |
DDB_G0273419 | DDB_G0273419 | there is a second copy of this gene | DDB0232429 | CDS | 2955221 | 3024 | + | 0.308201 |
DDB_G0273421 | DDB_G0273421 | there is a second copy of this gene | DDB0232429 | CDS | 2972872 | 2238 | + | 0.319482 |
DDB_G0273423 | DDB_G0273423 | there is a second copy of this gene | DDB0232429 | CDS | 2975860 | 1233 | - | 0.300081 |
DDB_G0273427 | DDB_G0273427 | there is a second copy of this gene | DDB0232429 | CDS | 2982372 | 375 | - | 0.218667 |
DDB_G0273431 | DDB_G0273431 | there is a second copy of this gene | DDB0232429 | CDS | 2990349 | 870 | + | 0.213793 |
DDB_G0273433 | DDB_G0273433 | there is a second copy of this gene | DDB0232429 | CDS | 2992272 | 1353 | + | 0.269771 |
DDB_G0273435 | DDB_G0273435 | there is a second copy of this gene | DDB0232429 | CDS | 2997078 | 1230 | - | 0.252846 |
DDB_G0273437 | DDB_G0273437 | there is a second copy of this gene | DDB0232429 | CDS | 2999157 | 1140 | - | 0.276316 |
DDB_G0273441 | DDB_G0273441 | there is a second copy of this gene | DDB0232429 | CDS | 3008502 | 2310 | + | 0.257143 |
DDB_G0273449 | DDB_G0273449 | part of a small Dictyostelium protein family enriched in gametes contains a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 2891795 | 999 | - | 0.311311 |
DDB_G0273451 | DDB_G0273451 | there is a second copy of this gene | DDB0232429 | CDS | 2894718 | 16893 | - | 0.258273 |
DDB_G0273453 | DDB_G0273453 | there is a second copy of this gene | DDB0232429 | CDS | 2914216 | 2520 | - | 0.265476 |
DDB_G0273459 | DDB_G0273459 | there is a second copy of this gene | DDB0232429 | CDS | 2986448 | 822 | + | 0.238443 |
DDB_G0273463 | DDB_G0273463 | there is a second copy of this gene | DDB0232429 | CDS | 3006071 | 1065 | - | 0.224413 |
DDB_G0273465 | DDB_G0273465 | there is a second copy of this gene | DDB0232429 | CDS | 3011236 | 813 | - | 0.307503 |
DDB_G0273467 | DDB_G0273467 | there is a second copy of this gene | DDB0232429 | CDS | 2890795 | 429 | + | 0.2331 |
DDB_G0273473 | DDB_G0273473 | conserved hypothetical protein similar to esophageal cancer associated protein there is a second copy of this gene | DDB0232429 | CDS | 2922562 | 2964 | - | 0.283063 |
DDB_G0273477 | DDB_G0273477 | there is a second copy of this gene | DDB0232429 | CDS | 2933551 | 1509 | - | 0.204109 |
DDB_G0273481 | DDB_G0273481 | there is a second copy of this gene | DDB0232429 | CDS | 2951458 | 2025 | + | 0.196543 |
DDB_G0273483 | DDB_G0273483 | there is a second copy of this gene | DDB0232429 | CDS | 2959446 | 888 | - | 0.313063 |
DDB_G0273485 | DDB_G0273485 | there is a second copy of this gene | DDB0232429 | CDS | 3012756 | 912 | + | 0.317982 |
DDB_G0273487 | DDB_G0273487 | there is a second copy of this gene | DDB0232429 | CDS | 3014131 | 708 | - | 0.271186 |
DDB_G0273491 | DDB_G0273491 | there is a second copy of this gene | DDB0232429 | CDS | 3016853 | 708 | + | 0.271186 |
DDB_G0273493 | DDB_G0273493 | there is a second copy of this gene | DDB0232429 | CDS | 3018032 | 912 | - | 0.317982 |
DDB_G0273495 | DDB_G0273495 | there is a second copy of this gene | DDB0232429 | CDS | 3019580 | 813 | + | 0.307503 |
DDB_G0273497 | DDB_G0273497 | there is a second copy of this gene | DDB0232429 | CDS | 3020778 | 2310 | - | 0.257143 |
DDB_G0273499 | DDB_G0273499 | there is a second copy of this gene | DDB0232429 | CDS | 3024348 | 1065 | + | 0.224413 |
DDB_G0273503 | DDB_G0273503 | there is a second copy of this gene | DDB0232429 | CDS | 3031281 | 1140 | + | 0.276316 |
DDB_G0273505 | DDB_G0273505 | there is a second copy of this gene | DDB0232429 | CDS | 3033401 | 1230 | + | 0.252846 |
DDB_G0273509 | DDB_G0273509 | there is a second copy of this gene | DDB0232429 | CDS | 3038057 | 1353 | - | 0.269771 |
DDB_G0273511 | DDB_G0273511 | there is a second copy of this gene | DDB0232429 | CDS | 3040382 | 870 | - | 0.213793 |
DDB_G0273515 | DDB_G0273515 | there is a second copy of this gene | DDB0232429 | CDS | 3044517 | 822 | - | 0.238443 |
DDB_G0273521 | DDB_G0273521 | there is a second copy of this gene | DDB0232429 | CDS | 3048967 | 375 | + | 0.218667 |
DDB_G0273527 | DDB_G0273527 | there is a second copy of this gene | DDB0232429 | CDS | 3054694 | 1233 | + | 0.300081 |
DDB_G0273529 | DDB_G0273529 | there is a second copy of this gene | DDB0232429 | CDS | 3056199 | 2238 | - | 0.319482 |
DDB_G0273537 | DDB_G0273537 | there is a second copy of this gene | DDB0232429 | CDS | 3070673 | 888 | + | 0.313063 |
DDB_G0273539 | DDB_G0273539 | there is a second copy of this gene | DDB0232429 | CDS | 3072578 | 3024 | - | 0.308201 |
DDB_G0273543 | DDB_G0273543 | there is a second copy of this gene | DDB0232429 | CDS | 3078093 | 2025 | - | 0.196543 |
DDB_G0273547 | DDB_G0273547 | similar to bacterial S-adenosyl-L-methionine (SAM) methyltransferases similar to D. purpureum protein there is a second copy of this gene | DDB0232429 | CDS | 3086765 | 1407 | - | 0.25231 |
DDB_G0273549 | DDB_G0273549 | there is a second copy of this gene | DDB0232429 | CDS | 3088869 | 996 | + | 0.26506 |
DDB_G0273551 | DDB_G0273551 | there is a second copy of this gene | DDB0232429 | CDS | 3090095 | 1371 | - | 0.243618 |
DDB_G0273555 | DDB_G0273555 | there is a second copy of this gene | DDB0232429 | CDS | 3095016 | 669 | - | 0.282511 |
DDB_G0273557 | DDB_G0273557 | there is a second copy of this gene | DDB0232429 | CDS | 3096406 | 1509 | + | 0.204109 |
DDB_G0273559 | DDB_G0273559 | conserved hypothetical protein similar to esophageal cancer associated protein there is a second copy of this gene | DDB0232429 | CDS | 3105660 | 2964 | + | 0.283063 |
DDB_G0273565 | DDB_G0273565 | there is a second copy of this gene | DDB0232429 | CDS | 3114676 | 2520 | + | 0.265476 |
DDB_G0273569_ps | DDB_G0273569 | putative pseudogene similar to coactosin contains an ADF (actin depolymerisation factorcofilin-like) domain there is a second copy of this gene | DDB0232429 | CDS | 3117781 | 819 | - | 0.316239 |
DDB_G0273573 | DDB_G0273573 | there is a second copy of this gene | DDB0232429 | CDS | 3119869 | 16893 | + | 0.258213 |
DDB_G0273575 | DDB_G0273575 | there is a second copy of this gene | DDB0232429 | CDS | 3137655 | 156 | - | 0.25641 |
DDB_G0273577 | DDB_G0273577 | part of a small Dictyostelium protein family enriched in gametes contains a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 3138626 | 999 | + | 0.311311 |
DDB_G0273579 | DDB_G0273579 | there is a second copy of this gene | DDB0232429 | CDS | 3140434 | 429 | - | 0.2331 |
DDB_G0273585 | DDB_G0273585 | there is a second copy of this gene | DDB0232429 | CDS | 3144362 | 192 | + | 0.255208 |
DDB_G0273587 | DDB_G0273587 | there is a second copy of this gene | DDB0232429 | CDS | 3145254 | 147 | + | 0.265306 |
DDB_G0273589 | DDB_G0273589 | there is a second copy of this gene | DDB0232429 | CDS | 3145928 | 1161 | - | 0.221361 |
DDB_G0273591 | DDB_G0273591 | there is a second copy of this gene | DDB0232429 | CDS | 3147334 | 1242 | - | 0.217391 |
DDB_G0273593 | DDB_G0273593 | there is a second copy of this gene | DDB0232429 | CDS | 3150139 | 2340 | + | 0.20812 |
DDB_G0273595 | DDB_G0273595 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) there is a second copy of this gene | DDB0232429 | CDS | 3154181 | 1653 | + | 0.333333 |
DDB_G0273597 | DDB_G0273597 | has similarity to the S. cerevisisae ATP10 a mitochondrial inner membrane protein required for assembly of the mitochondrial F1F0 ATP synthase there is a second copy of this gene | DDB0232429 | CDS | 3156381 | 783 | + | 0.240102 |
DDB_G0273599 | DDB_G0273599 | there is a second copy of this gene | DDB0232429 | CDS | 3157833 | 1065 | + | 0.252582 |
DDB_G0273603 | DDB_G0273603 | there is a second copy of this gene | DDB0232429 | CDS | 3161301 | 273 | + | 0.274725 |
DDB_G0273607 | DDB_G0273607 | there is a second copy of this gene | DDB0232429 | CDS | 3165261 | 321 | + | 0.267913 |
DDB_G0273613 | DDB_G0273613 | expressed in pstAO cells and in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 3171066 | 663 | - | 0.279035 |
DDB_G0273617 | DDB_G0273617 | there is a second copy of this gene | DDB0232429 | CDS | 3174939 | 1818 | - | 0.262376 |
DDB_G0273621 | DDB_G0273621 | there is a second copy of this gene | DDB0232429 | CDS | 3178423 | 1365 | - | 0.214652 |
DDB_G0273625 | DDB_G0273625 | there is a second copy of this gene | DDB0232429 | CDS | 3184086 | 1029 | - | 0.221574 |
DDB_G0273627 | DDB_G0273627 | there is a second copy of this gene | DDB0232429 | CDS | 3185739 | 672 | + | 0.168155 |
DDB_G0273629 | DDB_G0273629 | there is a second copy of this gene | DDB0232429 | CDS | 3187419 | 3459 | + | 0.194565 |
DDB_G0273633 | DDB_G0273633 | there is a second copy of this gene | DDB0232429 | CDS | 3192182 | 2166 | - | 0.202216 |
DDB_G0273637 | DDB_G0273637 | contains no functional domains there is a second copy of this gene | DDB0232429 | CDS | 3201360 | 645 | - | 0.252713 |
DDB_G0273643 | DDB_G0273643 | there is a second copy of this gene | DDB0232429 | CDS | 3213141 | 4095 | - | 0.263736 |
DDB_G0273647 | DDB_G0273647 | there is a second copy of this gene | DDB0232429 | CDS | 3226059 | 3363 | - | 0.249182 |
DDB_G0273651 | DDB_G0273651 | there is a second copy of this gene | DDB0232429 | CDS | 3232367 | 4683 | + | 0.325432 |
DDB_G0273653 | DDB_G0273653 | there is a second copy of this gene | DDB0232429 | CDS | 3237347 | 2778 | - | 0.172426 |
DDB_G0273655 | DDB_G0273655 | there is a second copy of this gene | DDB0232429 | CDS | 3240778 | 1170 | + | 0.240171 |
DDB_G0273659 | DDB_G0273659 | there is a second copy of this gene | DDB0232429 | CDS | 3245894 | 171 | - | 0.251462 |
DDB_G0273661 | DDB_G0273661 | there is a second copy of this gene | DDB0232429 | CDS | 3246689 | 195 | - | 0.266667 |
DDB_G0273663_TE | DDB_G0273663 | AT-rich low copy repetitive element which is thought to have no protein-coding capacity there is a second copy of this gene | DDB0232429 | CDS | 3247453 | 381 | - | 0.32021 |
DDB_G0273667 | DDB_G0273667 | there is a second copy of this gene | DDB0232429 | CDS | 3250010 | 189 | - | 0.306878 |
DDB_G0273671_ps | DDB_G0273671 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 3258387 | 1074 | + | 0.214153 |
DDB_G0273673 | DDB_G0273673 | there is a second copy of this gene | DDB0232429 | CDS | 3259720 | 1158 | - | 0.277202 |
DDB_G0273675 | DDB_G0273675 | contains eight transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 3262518 | 3843 | + | 0.284934 |
DDB_G0273677 | DDB_G0273677 | there is a second copy of this gene | DDB0232429 | CDS | 3266679 | 1119 | + | 0.217158 |
DDB_G0273679 | DDB_G0273679 | there is a second copy of this gene | DDB0232429 | CDS | 3268768 | 2484 | + | 0.23913 |
DDB_G0273681 | DDB_G0273681 | there is a second copy of this gene | DDB0232429 | CDS | 3271631 | 3834 | - | 0.199009 |
DDB_G0273685 | DDB_G0273685 | there is a second copy of this gene | DDB0232429 | CDS | 3276482 | 366 | - | 0.363388 |
DDB_G0273701 | DDB_G0273701 | conserved protein of unknown function contains a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 3298556 | 678 | - | 0.348083 |
DDB_G0273703 | DDB_G0273703 | there is a second copy of this gene | DDB0232429 | CDS | 3300432 | 1449 | + | 0.189786 |
DDB_G0273705 | DDB_G0273705 | there is a second copy of this gene | DDB0232429 | CDS | 3302300 | 594 | + | 0.272727 |
DDB_G0273707 | DDB_G0273707 | contains 5 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 3303396 | 936 | + | 0.244658 |
DDB_G0273723 | DDB_G0273723 | contains an EF hand but shows little similarity to other proteins there is a second copy of this gene | DDB0232429 | CDS | 3324668 | 3033 | - | 0.279261 |
DDB_G0273727 | DDB_G0273727 | similar to MAD2 and REV7 there is a second copy of this gene | DDB0232429 | CDS | 3331134 | 612 | - | 0.27451 |
DDB_G0273733 | DDB_G0273733 | there is a second copy of this gene | DDB0232429 | CDS | 3336611 | 1980 | + | 0.377273 |
DDB_G0273735 | DDB_G0273735 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 3339316 | 1764 | + | 0.294218 |
DDB_G0273739 | DDB_G0273739 | shares a short region of similarity with the human gene TEX2 (expressed in testis) there is a second copy of this gene | DDB0232429 | CDS | 3345112 | 1728 | + | 0.282407 |
DDB_G0273745 | DDB_G0273745 | there is a second copy of this gene | DDB0232429 | CDS | 3350147 | 2427 | - | 0.264524 |
DDB_G0273747 | DDB_G0273747 | there is a second copy of this gene | DDB0232429 | CDS | 3353701 | 192 | - | 0.234375 |
DDB_G0273749 | DDB_G0273749 | there is a second copy of this gene | DDB0232429 | CDS | 3354615 | 3651 | - | 0.212545 |
DDB_G0273753 | DDB_G0273753 | there is a second copy of this gene | DDB0232429 | CDS | 3360515 | 1926 | + | 0.323988 |
DDB_G0273755 | DDB_G0273755 | there is a second copy of this gene | DDB0232429 | CDS | 3363343 | 5058 | + | 0.169237 |
DDB_G0273759_RTE | DDB_G0273759 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE there is a second copy of this gene | DDB0232429 | CDS | 3371993 | 1335 | + | 0.31161 |
DDB_G0273761_RTE | DDB_G0273761 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE there is a second copy of this gene | DDB0232429 | CDS | 3373618 | 3144 | + | 0.338422 |
DDB_G0273763 | DDB_G0273763 | there is a second copy of this gene | DDB0232429 | CDS | 3377741 | 1017 | - | 0.222222 |
DDB_G0273765 | DDB_G0273765 | there is a second copy of this gene | DDB0232429 | CDS | 3379796 | 4143 | + | 0.177649 |
DDB_G0273767 | DDB_G0273767 | there is a second copy of this gene | DDB0232429 | CDS | 3384122 | 1632 | - | 0.259804 |
DDB_G0273769 | DDB_G0273769 | there is a second copy of this gene | DDB0232429 | CDS | 3387269 | 507 | - | 0.224852 |
DDB_G0273771 | DDB_G0273771 | there is a second copy of this gene | DDB0232429 | CDS | 3388529 | 369 | + | 0.273713 |
DDB_G0273773 | DDB_G0273773 | there is a second copy of this gene | DDB0232429 | CDS | 3389376 | 375 | - | 0.354667 |
DDB_G0273777 | DDB_G0273777 | there is a second copy of this gene | DDB0232429 | CDS | 3392002 | 1158 | + | 0.212435 |
DDB_G0273779 | DDB_G0273779 | there is a second copy of this gene | DDB0232429 | CDS | 3394303 | 1413 | + | 0.265393 |
DDB_G0273785 | DDB_G0273785 | no homologs in other organisms there is a second copy of this gene | DDB0232429 | CDS | 3404067 | 777 | + | 0.293436 |
DDB_G0273787 | DDB_G0273787 | similar to histidine ammonia-lyase which catalyzes the reaction L-histidine urocanate NHsub3sub there is a second copy of this gene | DDB0232429 | CDS | 3405130 | 1590 | - | 0.264151 |
DDB_G0273789 | DDB_G0273789 | member of the Dyp-type peroxidase family lacking a typical heme-binding region does not appear to be present in higher organisms there is a second copy of this gene | DDB0232429 | CDS | 3407290 | 921 | + | 0.334419 |
DDB_G0273791 | DDB_G0273791 | contains a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 3408281 | 1332 | - | 0.292042 |
DDB_G0273795 | DDB_G0273795 | there is a second copy of this gene | DDB0232429 | CDS | 3410837 | 6951 | + | 0.243274 |
DDB_G0273797 | DDB_G0273797 | there is a second copy of this gene | DDB0232429 | CDS | 3418714 | 159 | - | 0.289308 |
DDB_G0273799 | DDB_G0273799 | there is a second copy of this gene | DDB0232429 | CDS | 3419302 | 225 | - | 0.306667 |
DDB_G0273801_ps | DDB_G0273801 | putative pseudogene similar to Dictyostelium genes | DDB0232429 | CDS | 3420827 | 4356 | + | 0.288567 |
DDB_G0273807 | DDB_G0273807 | contains no functional domains and is not similar to any other protein there is a second copy of this gene | DDB0232429 | CDS | 3428943 | 192 | - | 0.213542 |
DDB_G0273809 | DDB_G0273809 | member of the ZIP (Zrt- and Irt-like Protein) family capable of transporting zinc and other metal ions contains 6 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 3430856 | 1128 | - | 0.337766 |
DDB_G0273811 | DDB_G0273811 | there is a second copy of this gene | DDB0232429 | CDS | 3433152 | 3468 | + | 0.21684 |
DDB_G0273813 | DDB_G0273813 | similar to the mammalian Hypoxia up-regulated protein 1 (HYOU1) a protein that plays a role in cytoprotective cellular mechanisms triggered by oxygen deprivation there is a second copy of this gene | DDB0232429 | CDS | 3437085 | 2781 | + | 0.280834 |
DDB_G0273815 | DDB_G0273815 | similar to human PDAP1 (PDGFA-associated protein 1) there is a second copy of this gene | DDB0232429 | CDS | 3440428 | 627 | - | 0.338118 |
DDB_G0273819 | DDB_G0273819 | there is a second copy of this gene | DDB0232429 | CDS | 3445587 | 1506 | + | 0.189907 |
DDB_G0273821 | DDB_G0273821 | there is a second copy of this gene | DDB0232429 | CDS | 3447237 | 408 | - | 0.215686 |
DDB_G0273823 | DDB_G0273823 | there is a second copy of this gene | DDB0232429 | CDS | 3448973 | 1434 | + | 0.232915 |
DDB_G0273827 | DDB_G0273827 | there is a second copy of this gene | DDB0232429 | CDS | 3452373 | 1110 | - | 0.193694 |
DDB_G0273829 | DDB_G0273829 | there is a second copy of this gene | DDB0232429 | CDS | 3454255 | 1374 | + | 0.3377 |
DDB_G0273831 | DDB_G0273831 | there is a second copy of this gene | DDB0232429 | CDS | 3456169 | 6147 | - | 0.284041 |
DDB_G0273833 | DDB_G0273833 | there is a second copy of this gene | DDB0232429 | CDS | 3463611 | 1476 | + | 0.22561 |
DDB_G0273835 | DDB_G0273835 | there is a second copy of this gene | DDB0232429 | CDS | 3465226 | 717 | - | 0.319386 |
DDB_G0273837 | DDB_G0273837 | introduces a double bond at the delta position of fatty acids during the biosynthesis of monounsaturated fatty acids there is a second copy of this gene | DDB0232429 | CDS | 3466919 | 2361 | - | 0.309615 |
DDB_G0273841 | DDB_G0273841 | there is a second copy of this gene | DDB0232429 | CDS | 3478561 | 963 | + | 0.263759 |
DDB_G0273843 | DDB_G0273843 | there is a second copy of this gene | DDB0232429 | CDS | 3480800 | 579 | + | 0.300518 |
DDB_G0273845_ps | DDB_G0273845 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 3482185 | 222 | + | 0.252252 |
DDB_G0273849 | DDB_G0273849 | there is a second copy of this gene | DDB0232429 | CDS | 3483399 | 210 | + | 0.219048 |
DDB_G0273851 | DDB_G0273851 | there is a second copy of this gene | DDB0232429 | CDS | 3484397 | 753 | + | 0.285525 |
DDB_G0273853 | DDB_G0273853 | there is a second copy of this gene | DDB0232429 | CDS | 3485257 | 531 | - | 0.308851 |
DDB_G0273855 | DDB_G0273855 | there is a second copy of this gene | DDB0232429 | CDS | 3486160 | 915 | + | 0.243716 |
DDB_G0273859 | DDB_G0273859 | there is a second copy of this gene | DDB0232429 | CDS | 3492274 | 657 | - | 0.242009 |
DDB_G0273863 | DDB_G0273863 | there is a second copy of this gene | DDB0232429 | CDS | 3495454 | 177 | + | 0.310734 |
DDB_G0273867 | DDB_G0273867 | there is a second copy of this gene | DDB0232429 | CDS | 3499369 | 1083 | - | 0.317636 |
DDB_G0273869 | DDB_G0273869 | there is a second copy of this gene | DDB0232429 | CDS | 3501162 | 2205 | + | 0.221769 |
DDB_G0273871 | DDB_G0273871 | there is a second copy of this gene | DDB0232429 | CDS | 3504469 | 378 | + | 0.261905 |
DDB_G0273873 | DDB_G0273873 | there is a second copy of this gene | DDB0232429 | CDS | 3505655 | 2118 | + | 0.219075 |
DDB_G0273877_RTE | DDB_G0273877 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-C there is a second copy of this gene | DDB0232429 | CDS | 3510436 | 540 | - | 0.375926 |
DDB_G0273879_RTE | DDB_G0273879 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-C there is a second copy of this gene | DDB0232429 | CDS | 3511146 | 2586 | - | 0.324439 |
DDB_G0273881_RTE | DDB_G0273881 | partial ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-C there is a second copy of this gene | DDB0232429 | CDS | 3513881 | 882 | - | 0.298186 |
DDB_G0273883_RTE | DDB_G0273883 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element there is a second copy of this gene | DDB0232429 | CDS | 3515045 | 378 | - | 0.314815 |
DDB_G0273889_ps | DDB_G0273889 | putative pseudogene fragment similar to UNC93-like protein MFSD11 family members | DDB0232429 | CDS | 3522887 | 147 | + | 0.346939 |
DDB_G0273893 | DDB_G0273893 | there is a second copy of this gene | DDB0232429 | CDS | 3526533 | 2301 | - | 0.156454 |
DDB_G0273895 | DDB_G0273895 | there is a second copy of this gene | DDB0232429 | CDS | 3531220 | 1740 | - | 0.18908 |
DDB_G0273897_RTE | DDB_G0273897 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE there is a second copy of this gene | DDB0232429 | CDS | 3533786 | 537 | + | 0.307263 |
DDB_G0273899 | DDB_G0273899 | there is a second copy of this gene | DDB0232429 | CDS | 3535904 | 333 | + | 0.339339 |
DDB_G0273901_RTE | DDB_G0273901 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element there is a second copy of this gene | DDB0232429 | CDS | 3536552 | 2373 | + | 0.2933 |
DDB_G0273905 | DDB_G0273905 | there is a second copy of this gene | DDB0232429 | CDS | 3545738 | 444 | + | 0.236486 |
DDB_G0273907 | DDB_G0273907 | catalyses the endonucleolytic cleavage of apurinic or apyrimidinic sites to generate products with a 5'-phosphate there is a second copy of this gene | DDB0232429 | CDS | 3546510 | 969 | + | 0.252838 |
DDB_G0273911 | DDB_G0273911 | there is a second copy of this gene | DDB0232429 | CDS | 3549347 | 300 | - | 0.253333 |
DDB_G0273913 | DDB_G0273913 | there is a second copy of this gene | DDB0232429 | CDS | 3551204 | 216 | - | 0.25463 |
DDB_G0273917 | DDB_G0273917 | there is a second copy of this gene | DDB0232429 | CDS | 3553792 | 1605 | + | 0.261682 |
DDB_G0273921 | DDB_G0273921 | there is a second copy of this gene | DDB0232429 | CDS | 3558114 | 1011 | + | 0.346192 |
DDB_G0273923 | DDB_G0273923 | weakly similar to glutathione S-transferases there is a second copy of this gene | DDB0232429 | CDS | 3561472 | 603 | - | 0.223881 |
DDB_G0273925_ps | DDB_G0273925 | putative pseudogene hssAB family gene | DDB0232429 | CDS | 3766470 | 168 | - | 0.410714 |
DDB_G0273927 | DDB_G0273927 | there is a second copy of this gene | DDB0232429 | CDS | 3564872 | 543 | + | 0.276243 |
DDB_G0273929_ps | DDB_G0273929 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 3567518 | 564 | + | 0.237589 |
DDB_G0273933 | DDB_G0273933 | there is a second copy of this gene | DDB0232429 | CDS | 3569600 | 939 | + | 0.234292 |
DDB_G0273937 | DDB_G0273937 | there is a second copy of this gene | DDB0232429 | CDS | 3572851 | 585 | + | 0.273504 |
DDB_G0273939 | DDB_G0273939 | there is a second copy of this gene | DDB0232429 | CDS | 3574169 | 687 | + | 0.251819 |
DDB_G0273947 | DDB_G0273947 | there is a second copy of this gene | DDB0232429 | CDS | 3582853 | 1569 | - | 0.260038 |
DDB_G0273949 | DDB_G0273949 | there is a second copy of this gene | DDB0232429 | CDS | 3584650 | 2913 | - | 0.274288 |
DDB_G0273951 | DDB_G0273951 | ortholog of human HPS5 mutations in human HPS5 have been linked to Hermansky-Pudlak syndrome 5 contains a putative RING Zn finger there is a second copy of this gene | DDB0232429 | CDS | 3589328 | 4611 | + | 0.284971 |
DDB_G0273953 | DDB_G0273953 | hypothetical protein there is a second copy of this gene | DDB0232429 | CDS | 3594233 | 2028 | - | 0.204142 |
DDB_G0273955 | DDB_G0273955 | conserved Dictyostelium protein contains a weak putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 3597027 | 4227 | + | 0.255974 |
DDB_G0273959_ps | DDB_G0273959 | putative pseudogene similar to to a large family of EGF like domain-containing proteins there is a second copy of this pseudogene | DDB0232429 | CDS | 3604314 | 681 | + | 0.26138 |
DDB_G0273961 | DDB_G0273961 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 3606161 | 4176 | - | 0.257663 |
DDB_G0273963 | DDB_G0273963 | there is a second copy of this gene | DDB0232429 | CDS | 3612304 | 303 | + | 0.287129 |
DDB_G0273965 | DDB_G0273965 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 3613046 | 4143 | - | 0.260681 |
DDB_G0273967 | DDB_G0273967 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 3618473 | 4137 | - | 0.259367 |
DDB_G0273969 | DDB_G0273969 | there is a second copy of this gene | DDB0232429 | CDS | 3623393 | 231 | - | 0.311688 |
DDB_G0273973_ps | DDB_G0273973 | putative pseudogene very similar to the putative importin subunit alpha C gene | DDB0232429 | CDS | 3624846 | 747 | + | 0.293173 |
DDB_G0273975 | DDB_G0273975 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain there is a second copy of this gene | DDB0232429 | CDS | 3626926 | 4188 | - | 0.255492 |
DDB_G0273985 | DDB_G0273985 | there is a second copy of this gene | DDB0232429 | CDS | 3636917 | 2172 | + | 0.234807 |
DDB_G0273987_ps | DDB_G0273987 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 3639322 | 636 | - | 0.212264 |
DDB_G0273989 | DDB_G0273989 | expressed in prespore cells there is a second copy of this gene | DDB0232429 | CDS | 3640497 | 855 | - | 0.298246 |
DDB_G0273997 | DDB_G0273997 | there is a second copy of this gene | DDB0232429 | CDS | 3648910 | 1344 | + | 0.299851 |
DDB_G0273999 | DDB_G0273999 | similar to human RWDD1 S. cerevisiae GIR2 S. cerevisiae GIR2 binds to and regulates the expression of GTP-binding protein DRG2 there is a second copy of this gene | DDB0232429 | CDS | 3650442 | 696 | - | 0.303161 |
DDB_G0274007 | DDB_G0274007 | similar to cyclin dependent protein kinases there is a second copy of this gene | DDB0232429 | CDS | 3660427 | 2043 | + | 0.313754 |
DDB_G0274009 | DDB_G0274009 | there is a second copy of this gene | DDB0232429 | CDS | 3662811 | 1614 | + | 0.226766 |
DDB_G0274013 | DDB_G0274013 | similar to human HSBP1 HSBP1 is a negative regulator of the heat shock response there is a second copy of this gene | DDB0232429 | CDS | 3667910 | 309 | - | 0.28479 |
DDB_G0274025 | DDB_G0274025 | similar to the THAP domain in the mammalian THAP domain-containing protein 4 underexpressed in | DDB0232429 | CDS | 3678442 | 480 | + | 0.302083 |
DDB_G0274027 | DDB_G0274027 | there is a second copy of this gene | DDB0232429 | CDS | 3679259 | 1638 | - | 0.333333 |
DDB_G0274031 | DDB_G0274031 | weakly similar to glycoproteins GP138A-D and gp130 there is a second copy of this gene | DDB0232429 | CDS | 3686525 | 2046 | + | 0.251222 |
DDB_G0274037 | DDB_G0274037 | there is a second copy of this gene | DDB0232429 | CDS | 3696537 | 858 | - | 0.305361 |
DDB_G0274039 | DDB_G0274039 | highly similar to | DDB0232429 | CDS | 3697844 | 756 | + | 0.215608 |
DDB_G0274041 | DDB_G0274041 | there is a second copy of this gene | DDB0232429 | CDS | 3698912 | 4698 | - | 0.254364 |
DDB_G0274043 | DDB_G0274043 | there is a second copy of this gene | DDB0232429 | CDS | 3708092 | 657 | - | 0.255708 |
DDB_G0274047 | DDB_G0274047 | there is a second copy of this gene | DDB0232429 | CDS | 3711697 | 240 | + | 0.2125 |
DDB_G0274049 | DDB_G0274049 | contains 4 coiled-coil domains there is a second copy of this gene | DDB0232429 | CDS | 3712319 | 1677 | - | 0.305903 |
DDB_G0274053 | DDB_G0274053 | there is a second copy of this gene | DDB0232429 | CDS | 3717731 | 396 | + | 0.333333 |
DDB_G0274055 | DDB_G0274055 | there is a second copy of this gene | DDB0232429 | CDS | 3718398 | 672 | - | 0.181548 |
DDB_G0274061 | DDB_G0274061 | contains 3 FNIP repeats there is a second copy of this gene | DDB0232429 | CDS | 3721083 | 1473 | - | 0.205024 |
DDB_G0274063 | DDB_G0274063 | there is a second copy of this gene | DDB0232429 | CDS | 3722937 | 1563 | - | 0.198337 |
DDB_G0274065 | DDB_G0274065 | there is a second copy of this gene | DDB0232429 | CDS | 3726636 | 828 | + | 0.214976 |
DDB_G0274067 | DDB_G0274067 | PIP5K catalyze the formation of phosphoinositol-45-bisphosphate via the phosphorylation of phosphatidylinositol-4-phosphate a precursor in the phosphinositide signaling pathway there is a second copy of this gene | DDB0232429 | CDS | 3730947 | 3240 | + | 0.264506 |
DDB_G0274069 | DDB_G0274069 | there is a second copy of this gene | DDB0232429 | CDS | 3734831 | 1221 | - | 0.284193 |
DDB_G0274071 | DDB_G0274071 | there is a second copy of this gene | DDB0232429 | CDS | 3736604 | 342 | + | 0.225146 |
DDB_G0274073 | DDB_G0274073 | there is a second copy of this gene | DDB0232429 | CDS | 3737258 | 1137 | + | 0.287599 |
DDB_G0274075 | DDB_G0274075 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog there is a second copy of this gene | DDB0232429 | CDS | 3738689 | 4557 | + | 0.250384 |
DDB_G0274081 | DDB_G0274081 | catalyzes the reaction RX glutathione HX R-S-glutathione there is a second copy of this gene | DDB0232429 | CDS | 3748941 | 597 | - | 0.309883 |
DDB_G0274083 | DDB_G0274083 | there is a second copy of this gene | DDB0232429 | CDS | 3750393 | 621 | + | 0.241546 |
DDB_G0274085 | DDB_G0274085 | underexpressed in | DDB0232429 | CDS | 3751889 | 1023 | + | 0.333333 |
DDB_G0274087 | DDB_G0274087 | there is a second copy of this gene | DDB0232429 | CDS | 3753105 | 1356 | - | 0.20059 |
DDB_G0274089 | DDB_G0274089 | there is a second copy of this gene | DDB0232429 | CDS | 3755009 | 552 | - | 0.280797 |
DDB_G0274091 | DDB_G0274091 | DDB0232429 | CDS | 3758069 | 1278 | + | 0.187011 | |
DDB_G0274097 | DDB_G0274097 | there is a second copy of this gene | DDB0232429 | CDS | 3765352 | 228 | - | 0.337719 |
DDB_G0274141 | DDB_G0274141 | DDB0232429 | CDS | 4917455 | 576 | - | 0.366319 | |
DDB_G0274143 | DDB_G0274143 | DDB0232429 | CDS | 4916421 | 711 | + | 0.261603 | |
DDB_G0274145 | DDB_G0274145 | DDB0232429 | CDS | 4882054 | 999 | - | 0.139139 | |
DDB_G0274147_ps | DDB_G0274147 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 4883520 | 318 | - | 0.248428 |
DDB_G0274149 | DDB_G0274149 | DDB0232429 | CDS | 4884886 | 3678 | + | 0.281675 | |
DDB_G0274151_ps | DDB_G0274151 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 4889468 | 468 | + | 0.32906 |
DDB_G0274153 | DDB_G0274153 | protein phosphatase 2C is a serinethreonine specific protein phosphatase with broad substrate specificity and dependent on divalent cations (mainly manganese and magnesium) for its activity | DDB0232429 | CDS | 4909656 | 1932 | + | 0.315217 |
DDB_G0274155 | DDB_G0274155 | DDB0232429 | CDS | 4912583 | 2304 | + | 0.231337 | |
DDB_G0274157 | DDB_G0274157 | DDB0232429 | CDS | 4881571 | 387 | + | 0.235142 | |
DDB_G0274161 | DDB_G0274161 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repressionbrbr bCommunity annotation:b DDB_G0274161 is similar to nmr1 originally identified as a Neurospora gene which binds to the transcription factor nit2 and prevents its binding to and activating genes required for nitrogen utilization. The human ortholog is | DDB0232429 | CDS | 4878022 | 927 | + | 0.311758 |
DDB_G0274163 | DDB_G0274163 | DDB0232429 | CDS | 4874703 | 132 | - | 0.257576 | |
DDB_G0274165 | DDB_G0274165 | DDB0232429 | CDS | 4870104 | 2484 | - | 0.242754 | |
DDB_G0274169 | DDB_G0274169 | DDB0232429 | CDS | 4865070 | 345 | + | 0.228986 | |
DDB_G0274171 | DDB_G0274171 | similar to Fraser syndrome protein von Willebrand factor and kielin expressed in pstAO cells and in upper cup during culmination | DDB0232429 | CDS | 4853650 | 1356 | - | 0.375369 |
DDB_G0274173 | DDB_G0274173 | DDB0232429 | CDS | 4852122 | 405 | - | 0.266667 | |
DDB_G0274175 | DDB_G0274175 | DDB0232429 | CDS | 4841279 | 996 | - | 0.208835 | |
DDB_G0274177 | DDB_G0274177 | DDB0232429 | CDS | 4833721 | 5757 | + | 0.295814 | |
DDB_G0274179_ps | DDB_G0274179 | putative pseudogene similar to it's neighboring gene ( | DDB0232429 | CDS | 4832304 | 150 | + | 0.36 |
DDB_G0274181 | DDB_G0274181 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide | DDB0232429 | CDS | 4831162 | 639 | + | 0.375587 |
DDB_G0274183 | DDB_G0274183 | DDB0232429 | CDS | 4819660 | 2643 | - | 0.287552 | |
DDB_G0274185 | DDB_G0274185 | contains an N-terminal oxidoreductase domain and a partial C-terminal oxidoreductase domain the GfoIdhMocA family proteins utilize NADP or NAD | DDB0232429 | CDS | 4815159 | 1293 | - | 0.336427 |
DDB_G0274187 | DDB_G0274187 | DDB0232429 | CDS | 4810741 | 1713 | - | 0.242849 | |
DDB_G0274195 | DDB_G0274195 | DDB0232429 | CDS | 4790573 | 2184 | - | 0.308608 | |
DDB_G0274199 | DDB_G0274199 | DDB0232429 | CDS | 4796097 | 1281 | + | 0.291179 | |
DDB_G0274201 | DDB_G0274201 | DDB0232429 | CDS | 4797968 | 951 | + | 0.268139 | |
DDB_G0274203 | DDB_G0274203 | DDB0232429 | CDS | 4799224 | 735 | - | 0.414966 | |
DDB_G0274205 | DDB_G0274205 | DDB0232429 | CDS | 4800486 | 741 | - | 0.280702 | |
DDB_G0274207 | DDB_G0274207 | DDB0232429 | CDS | 4778748 | 3777 | - | 0.243315 | |
DDB_G0274209 | DDB_G0274209 | DDB0232429 | CDS | 4783187 | 1236 | - | 0.271845 | |
DDB_G0274211 | DDB_G0274211 | DDB0232429 | CDS | 4768104 | 5187 | - | 0.277232 | |
DDB_G0274215 | DDB_G0274215 | DDB0232429 | CDS | 4763951 | 1842 | + | 0.279045 | |
DDB_G0274219 | DDB_G0274219 | DDB0232429 | CDS | 4749133 | 3540 | + | 0.216102 | |
DDB_G0274223 | DDB_G0274223 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 4720551 | 783 | + | 0.273308 |
DDB_G0274227 | DDB_G0274227 | DDB0232429 | CDS | 4710807 | 459 | - | 0.224401 | |
DDB_G0274231 | DDB_G0274231 | DDB0232429 | CDS | 4700982 | 1656 | - | 0.236715 | |
DDB_G0274235 | DDB_G0274235 | DDB0232429 | CDS | 4698594 | 225 | + | 0.266667 | |
DDB_G0274237 | DDB_G0274237 | DDB0232429 | CDS | 4696078 | 330 | + | 0.381818 | |
DDB_G0274245 | DDB_G0274245 | DDB0232429 | CDS | 4218420 | 663 | + | 0.307692 | |
DDB_G0274249 | DDB_G0274249 | DDB0232429 | CDS | 4154286 | 417 | - | 0.256595 | |
DDB_G0274251 | DDB_G0274251 | DDB0232429 | CDS | 4152834 | 1077 | + | 0.226555 | |
DDB_G0274253 | DDB_G0274253 | DDB0232429 | CDS | 4109588 | 579 | + | 0.260794 | |
DDB_G0274255 | DDB_G0274255 | DDB0232429 | CDS | 4120597 | 3327 | + | 0.242861 | |
DDB_G0274259 | DDB_G0274259 | DDB0232429 | CDS | 4126091 | 3507 | + | 0.260907 | |
DDB_G0274261 | DDB_G0274261 | DDB0232429 | CDS | 4129800 | 1104 | - | 0.237319 | |
DDB_G0274263 | DDB_G0274263 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 4131815 | 678 | + | 0.328909 |
DDB_G0274265 | DDB_G0274265 | DDB0232429 | CDS | 4139227 | 1803 | - | 0.291736 | |
DDB_G0274267 | DDB_G0274267 | contains a galactose oxidasekelch beta-propeller domain galactose oxidase catalyzes the oxidation of the C6 hydroxyl group in D-galactose kelch may have a cytoskeletal function similar to D. purpureum gene | DDB0232429 | CDS | 4004221 | 2004 | - | 0.252994 |
DDB_G0274269 | DDB_G0274269 | highly similar to H. sapiens and S. cerevisiae HAT1 a subunit of the HAT1HAT2 histone acetyltransferase complex | DDB0232429 | CDS | 4007291 | 1461 | - | 0.234086 |
DDB_G0274271 | DDB_G0274271 | DDB0232429 | CDS | 4009424 | 348 | - | 0.267241 | |
DDB_G0274273 | DDB_G0274273 | DDB0232429 | CDS | 4010059 | 963 | - | 0.36864 | |
DDB_G0274275 | DDB_G0274275 | DDB0232429 | CDS | 4012481 | 10254 | - | 0.277453 | |
DDB_G0274277 | DDB_G0274277 | DDB0232429 | CDS | 4031010 | 3357 | + | 0.181412 | |
DDB_G0274283 | DDB_G0274283 | DDB0232429 | CDS | 4044553 | 1179 | - | 0.310433 | |
DDB_G0274289 | DDB_G0274289 | DDB0232429 | CDS | 4059892 | 1572 | + | 0.199109 | |
DDB_G0274291 | DDB_G0274291 | DDB0232429 | CDS | 4062693 | 513 | - | 0.276803 | |
DDB_G0274293 | DDB_G0274293 | DDB0232429 | CDS | 4065363 | 1497 | + | 0.281229 | |
DDB_G0274295 | DDB_G0274295 | The RWP-RK domain is named after a conserved motif at its C-terminus found in Chlamydomonas plant proteins involved in nitrogen-controlled development and in Dictyostelium | DDB0232429 | CDS | 4068268 | 1647 | - | 0.292046 |
DDB_G0274299 | DDB_G0274299 | DDB0232429 | CDS | 4085599 | 252 | + | 0.412698 | |
DDB_G0274301 | DDB_G0274301 | DDB0232429 | CDS | 4097612 | 2697 | + | 0.239155 | |
DDB_G0274303 | DDB_G0274303 | DDB0232429 | CDS | 3981595 | 507 | - | 0.299803 | |
DDB_G0274305 | DDB_G0274305 | DDB0232429 | CDS | 3982536 | 1701 | - | 0.289242 | |
DDB_G0274307 | DDB_G0274307 | DDB0232429 | CDS | 3987188 | 1473 | - | 0.276307 | |
DDB_G0274309 | DDB_G0274309 | DDB0232429 | CDS | 3996443 | 858 | - | 0.298368 | |
DDB_G0274311 | DDB_G0274311 | similar to the mammalian NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13 (NDUFA13) contains one predicted transmembrane domain | DDB0232429 | CDS | 3938972 | 342 | - | 0.362573 |
DDB_G0274317 | DDB_G0274317 | DDB0232429 | CDS | 3944535 | 1242 | - | 0.301932 | |
DDB_G0274319 | DDB_G0274319 | DDB0232429 | CDS | 3952988 | 939 | + | 0.198083 | |
DDB_G0274323 | DDB_G0274323 | DDB0232429 | CDS | 3956333 | 840 | - | 0.242857 | |
DDB_G0274327 | DDB_G0274327 | ortholog of S. cerevisiae SPN1 (ISW1) a probable transcriptional elongation factor | DDB0232429 | CDS | 3920096 | 1947 | + | 0.325629 |
DDB_G0274329 | DDB_G0274329 | DDB0232429 | CDS | 3880324 | 609 | - | 0.269294 | |
DDB_G0274331 | DDB_G0274331 | DDB0232429 | CDS | 3887023 | 774 | + | 0.329457 | |
DDB_G0274333 | DDB_G0274333 | DDB0232429 | CDS | 3888367 | 327 | - | 0.278287 | |
DDB_G0274335 | DDB_G0274335 | DDB0232429 | CDS | 3889250 | 894 | - | 0.324385 | |
DDB_G0274337 | DDB_G0274337 | DDB0232429 | CDS | 3891057 | 1530 | + | 0.339869 | |
DDB_G0274339 | DDB_G0274339 | belongs to the thiolase family similar to human ACAA1 | DDB0232429 | CDS | 3898333 | 1251 | + | 0.409273 |
DDB_G0274341 | DDB_G0274341 | DDB0232429 | CDS | 3900148 | 2577 | - | 0.298021 | |
DDB_G0274343 | DDB_G0274343 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232429 | CDS | 3907672 | 207 | + | 0.294686 |
DDB_G0274345 | DDB_G0274345 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains an N-terminal transmembrane domain that might be a signal sequence | DDB0232429 | CDS | 3908527 | 1005 | + | 0.271642 |
DDB_G0274347 | DDB_G0274347 | DDB0232429 | CDS | 3836054 | 2115 | - | 0.292671 | |
DDB_G0274349 | DDB_G0274349 | DDB0232429 | CDS | 3833248 | 1989 | - | 0.28356 | |
DDB_G0274351 | DDB_G0274351 | DDB0232429 | CDS | 3830152 | 1569 | - | 0.236456 | |
DDB_G0274353 | DDB_G0274353 | DDB0232429 | CDS | 3820360 | 1182 | - | 0.29357 | |
DDB_G0274355 | DDB_G0274355 | DDB0232429 | CDS | 3817435 | 498 | - | 0.329317 | |
DDB_G0274357 | DDB_G0274357 | contains two EF hands very similar to Dictyostelium cbpK and cbpJ belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232429 | CDS | 3816301 | 558 | - | 0.304659 |
DDB_G0274363 | DDB_G0274363 | DDB0232429 | CDS | 3796506 | 1536 | - | 0.212891 | |
DDB_G0274365 | DDB_G0274365 | DDB0232429 | CDS | 3794897 | 906 | + | 0.261589 | |
DDB_G0274367 | DDB_G0274367 | DDB0232429 | CDS | 3791790 | 2688 | - | 0.30878 | |
DDB_G0274369 | DDB_G0274369 | DDB0232429 | CDS | 3790253 | 1059 | + | 0.227573 | |
DDB_G0274377 | DDB_G0274377 | DDB0232429 | CDS | 3773769 | 375 | - | 0.434667 | |
DDB_G0274379 | DDB_G0274379 | DDB0232429 | CDS | 4375605 | 261 | + | 0.233716 | |
DDB_G0274385 | DDB_G0274385 | DDB0232429 | CDS | 4876346 | 1077 | + | 0.311978 | |
DDB_G0274393 | DDB_G0274393 | DDB0232429 | CDS | 4776106 | 1167 | - | 0.265638 | |
DDB_G0274397 | DDB_G0274397 | DDB0232429 | CDS | 4686286 | 1305 | - | 0.31341 | |
DDB_G0274399 | DDB_G0274399 | similar to ATP-dependent RNA helicase M NAM7and to putative helicases involved in RNA maturation SEN1 human senataxin imlicated in ataxia-ocular apraxia 2 (AOA2) and amyotrophic lateral sclerosis 4 (ALS4) also belongs to this family | DDB0232429 | CDS | 4681340 | 2904 | + | 0.333333 |
DDB_G0274401 | DDB_G0274401 | DDB0232429 | CDS | 4667606 | 1593 | - | 0.209667 | |
DDB_G0274405 | DDB_G0274405 | DDB0232429 | CDS | 4663584 | 1134 | - | 0.22134 | |
DDB_G0274407 | DDB_G0274407 | DDB0232429 | CDS | 4661589 | 549 | - | 0.360656 | |
DDB_G0274411_ps | DDB_G0274411 | DDB0232429 | CDS | 4640782 | 1221 | - | 0.271089 | |
DDB_G0274413_ps | DDB_G0274413 | DDB0232429 | CDS | 4636251 | 507 | - | 0.167653 | |
DDB_G0274415 | DDB_G0274415 | DDB0232429 | CDS | 4635738 | 186 | + | 0.301075 | |
DDB_G0274417 | DDB_G0274417 | DDB0232429 | CDS | 4635539 | 138 | + | 0.304348 | |
DDB_G0274419 | DDB_G0274419 | bCommunity annotation:b DDB_G0274419 appears to encode a DNA polymerase with closest affinities to pol I of bacteria (the Kornberg polymerase). This is a low-processivity polymerase thought to function in DNA repair. DDB_G0274419 is only marginally (2x)overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (Doquang et al in preparation). DNA polymerases associated with replication show overexpression factors of 5- to 14-fold in this strain as as do several genes associated with replication-coupled repair while most genes associated with replication-independent repair pathways show overexpression factors of 2 or less. This suggests that DDB_G0274419 acts in replication-uncoupled DNA repair. Harry MacWilliams September 2009 | DDB0232429 | CDS | 4627713 | 3354 | - | 0.230471 |
DDB_G0274423 | DDB_G0274423 | DDB0232429 | CDS | 4625298 | 2091 | + | 0.31803 | |
DDB_G0274425 | DDB_G0274425 | the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232429 | CDS | 4618827 | 4197 | - | 0.286633 |
DDB_G0274427 | DDB_G0274427 | DDB0232429 | CDS | 4613288 | 4245 | - | 0.288104 | |
DDB_G0274429 | DDB_G0274429 | DDB0232429 | CDS | 4607655 | 4332 | - | 0.289935 | |
DDB_G0274433 | DDB_G0274433 | bCommunity annotation:b DDB G0274433 is weakly similar to SDS23 and SDS24 of budding yeast which are themselves homologues of sds23 from fission yeast. The fission yeast gene interacts with the anaphase promoting complex in a manner which is not understood molecularly. The APC must be dephosphoryated by PPI for normal mitosis and sds23 overexpressers bypass the requirement for PPI (Ishii et al EMBO Journal 15 6629-6640 (1996). Deletion of sds23 gives very slowly growing cells with multiple nuclei and extremely prolonged anaphase. In budding yeast however the double deletion is viable with changes mainly in the size of the vacuole. In Dicty a role of DDB_G0274433 in cell cycle control is suggested by the gene's fivefold overexpression in a Dicty strain deficient in the Dictyostelium | DDB0232429 | CDS | 4606302 | 1062 | + | 0.29661 |
DDB_G0274435 | DDB_G0274435 | DDB0232429 | CDS | 4603856 | 1524 | + | 0.253281 | |
DDB_G0274439 | DDB_G0274439 | in E. coli bolA plays a role in general stress response and affects cellular morphogenesis this protein is about 50 amino acids shorter on the amino terminus compared to homologs | DDB0232429 | CDS | 4596108 | 159 | + | 0.27673 |
DDB_G0274451 | DDB_G0274451 | DDB0232429 | CDS | 4573546 | 1191 | + | 0.269521 | |
DDB_G0274453_ps | DDB_G0274453 | putative pseudogene fragment similar to D. discoideum genes | DDB0232429 | CDS | 4547444 | 576 | - | 0.291667 |
DDB_G0274459 | DDB_G0274459 | conserved hypothetical Dictyostelium protein identical to | DDB0232429 | CDS | 4523083 | 141 | + | 0.489362 |
DDB_G0274461 | DDB_G0274461 | DDB0232429 | CDS | 4508759 | 1194 | + | 0.312395 | |
DDB_G0274465 | DDB_G0274465 | conserved hypothetical protein contains an N-terminal hydrophobic region | DDB0232429 | CDS | 4494014 | 483 | - | 0.242236 |
DDB_G0274467 | DDB_G0274467 | DDB0232429 | CDS | 4490494 | 846 | + | 0.22695 | |
DDB_G0274469 | DDB_G0274469 | DDB0232429 | CDS | 4482749 | 315 | - | 0.352381 | |
DDB_G0274473 | DDB_G0274473 | DDB0232429 | CDS | 4476400 | 2367 | + | 0.260245 | |
DDB_G0274475 | DDB_G0274475 | DDB0232429 | CDS | 4451947 | 1098 | - | 0.265938 | |
DDB_G0274477 | DDB_G0274477 | DDB0232429 | CDS | 4450801 | 336 | - | 0.241071 | |
DDB_G0274479 | DDB_G0274479 | DDB0232429 | CDS | 4449564 | 639 | - | 0.289515 | |
DDB_G0274481 | DDB_G0274481 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | DDB0232429 | CDS | 4437706 | 3162 | - | 0.28463 |
DDB_G0274483 | DDB_G0274483 | DDB0232429 | CDS | 4423293 | 4917 | - | 0.273744 | |
DDB_G0274485 | DDB_G0274485 | DDB0232429 | CDS | 4416444 | 558 | - | 0.385305 | |
DDB_G0274487 | DDB_G0274487 | DDB0232429 | CDS | 4406975 | 1668 | + | 0.339928 | |
DDB_G0274489 | DDB_G0274489 | DDB0232429 | CDS | 4405595 | 603 | - | 0.26534 | |
DDB_G0274491 | DDB_G0274491 | similar to human L antigen family member 3 (LAGE3)brbr bCommunity annotation:b DDB G0274491 codes for a small protein with significant similarities to | DDB0232429 | CDS | 4404875 | 345 | - | 0.228986 |
DDB_G0274495 | DDB_G0274495 | contains one HTTM (horizontally transferred transmembrane) domain contains 5 transmembrane domains | DDB0232429 | CDS | 4387839 | 2442 | - | 0.279279 |
DDB_G0274499 | DDB_G0274499 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity contains a predicted signal peptide | DDB0232429 | CDS | 4386087 | 942 | + | 0.316348 |
DDB_G0274505 | DDB_G0274505 | DDB0232429 | CDS | 4376727 | 1509 | - | 0.297548 | |
DDB_G0274507 | DDB_G0274507 | DDB0232429 | CDS | 4347895 | 225 | + | 0.342222 | |
DDB_G0274509 | DDB_G0274509 | DDB0232429 | CDS | 4332352 | 1497 | - | 0.225785 | |
DDB_G0274511 | DDB_G0274511 | ortholog of vitellogenic carboxypeptidase a conserved serine carboxypeptidase expressed in mosquito ovaries contains a predicted signal peptide | DDB0232429 | CDS | 4330307 | 1503 | + | 0.296075 |
DDB_G0274513 | DDB_G0274513 | DDB0232429 | CDS | 4309796 | 1671 | - | 0.183124 | |
DDB_G0274515 | DDB_G0274515 | DDB0232429 | CDS | 4306433 | 1443 | + | 0.227997 | |
DDB_G0274523 | DDB_G0274523 | DDB0232429 | CDS | 4286028 | 2715 | - | 0.239779 | |
DDB_G0274527 | DDB_G0274527 | DDB0232429 | CDS | 4275808 | 1428 | - | 0.298319 | |
DDB_G0274533 | DDB_G0274533 | DDB0232429 | CDS | 4264802 | 1668 | - | 0.233813 | |
DDB_G0274535 | DDB_G0274535 | DDB0232429 | CDS | 4263139 | 1368 | + | 0.256579 | |
DDB_G0274537 | DDB_G0274537 | contains a sac phosphatase domain similar to D. discoideum sac1 similar to D. purpureum protein | DDB0232429 | CDS | 4257363 | 4317 | - | 0.281214 |
DDB_G0274539 | DDB_G0274539 | similar to D. purpureum protein there is a similar second gene | DDB0232429 | CDS | 4254270 | 561 | + | 0.272727 |
DDB_G0274541 | DDB_G0274541 | DDB0232429 | CDS | 4235469 | 2382 | - | 0.215365 | |
DDB_G0274543 | DDB_G0274543 | DDB0232429 | CDS | 4215708 | 705 | - | 0.197163 | |
DDB_G0274547 | DDB_G0274547 | DDB0232429 | CDS | 4197500 | 1554 | + | 0.279923 | |
DDB_G0274549 | DDB_G0274549 | contains a central single transmembrane domain | DDB0232429 | CDS | 4195122 | 231 | - | 0.34632 |
DDB_G0274557 | DDB_G0274557 | DDB0232429 | CDS | 4163363 | 702 | - | 0.346154 | |
DDB_G0274573 | DDB_G0274573 | DDB0232429 | CDS | 3963501 | 1263 | + | 0.216152 | |
DDB_G0274581 | DDB_G0274581 | DDB0232429 | CDS | 3871056 | 1716 | + | 0.27972 | |
DDB_G0274583 | DDB_G0274583 | DDB0232429 | CDS | 3870555 | 276 | - | 0.23913 | |
DDB_G0274585 | DDB_G0274585 | similar to A. thaliana short chain specific acyl-Coa oxidase ACX4 which catalyzes the first step of peroxisomal fatty acid beta-oxidation | DDB0232429 | CDS | 3869123 | 1293 | + | 0.314772 |
DDB_G0274609 | DDB_G0274609 | DDB0232429 | CDS | 4922788 | 1068 | - | 0.283708 | |
DDB_G0274611_ps | DDB_G0274611 | putative pseudogene fragment similar to | DDB0232429 | CDS | 4896937 | 279 | + | 0.268817 |
DDB_G0274613 | DDB_G0274613 | kinase domain similar to mitogen-activated protein kinases does not contain the consensus sequences known to be required for kinase function contains a RING zinc finger domain | DDB0232429 | CDS | 4893134 | 2496 | - | 0.260417 |
DDB_G0274615 | DDB_G0274615 | DDB0232429 | CDS | 4881010 | 168 | - | 0.255952 | |
DDB_G0274617 | DDB_G0274617 | DDB0232429 | CDS | 4859710 | 1578 | + | 0.260456 | |
DDB_G0274629 | DDB_G0274629 | DDB0232429 | CDS | 4658071 | 210 | + | 0.261905 | |
DDB_G0274631 | DDB_G0274631 | DDB0232429 | CDS | 4645992 | 1968 | - | 0.21748 | |
DDB_G0274635_ps | DDB_G0274635 | putative pseudogene similar to a small family of genes including the neighboring | DDB0232429 | CDS | 4643728 | 1611 | - | 0.240223 |
DDB_G0274637 | DDB_G0274637 | DDB0232429 | CDS | 4637236 | 1980 | - | 0.244949 | |
DDB_G0274641 | DDB_G0274641 | DDB0232429 | CDS | 4569510 | 1203 | + | 0.241895 | |
DDB_G0274643 | DDB_G0274643 | DDB0232429 | CDS | 4531583 | 855 | + | 0.352047 | |
DDB_G0274645_TE | DDB_G0274645 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232429 | CDS | 4517216 | 1167 | - | 0.300771 |
DDB_G0274647_TE | DDB_G0274647 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232429 | CDS | 4516555 | 228 | - | 0.276316 |
DDB_G0274649 | DDB_G0274649 | DDB0232429 | CDS | 4499141 | 4935 | + | 0.240324 | |
DDB_G0274653 | DDB_G0274653 | DDB0232429 | CDS | 4491792 | 2178 | + | 0.200184 | |
DDB_G0274655 | DDB_G0274655 | DDB0232429 | CDS | 4479756 | 765 | + | 0.366013 | |
DDB_G0274657 | DDB_G0274657 | related to glutaredoxin which functions as an electron carrier in the glutathione-dependent synthesis of deoxyribonucleotides | DDB0232429 | CDS | 4453801 | 432 | + | 0.305556 |
DDB_G0274659 | DDB_G0274659 | DDB0232429 | CDS | 4429085 | 1407 | - | 0.283582 | |
DDB_G0274661 | DDB_G0274661 | DDB0232429 | CDS | 4411951 | 576 | + | 0.366319 | |
DDB_G0274663 | DDB_G0274663 | similar to human PRSS16 (thymus-specific serine protease) contains a putative signal peptide | DDB0232429 | CDS | 4408799 | 1464 | - | 0.347678 |
DDB_G0274665_ps | DDB_G0274665 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 4398044 | 1050 | - | 0.244762 |
DDB_G0274669 | DDB_G0274669 | DDB0232429 | CDS | 4395991 | 879 | - | 0.25711 | |
DDB_G0274671_RTE | DDB_G0274671 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 4355252 | 765 | + | 0.32549 |
DDB_G0274673_RTE | DDB_G0274673 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 4353208 | 1506 | - | 0.295485 |
DDB_G0274675 | DDB_G0274675 | DDB0232429 | CDS | 4339292 | 1539 | - | 0.283951 | |
DDB_G0274677 | DDB_G0274677 | conserved in Dictyostelium weak similarity to putative cell number regulator contains a predicted signal anchor sequence | DDB0232429 | CDS | 4304114 | 1770 | + | 0.248023 |
DDB_G0274679 | DDB_G0274679 | DDB0232429 | CDS | 4301386 | 2025 | + | 0.219753 | |
DDB_G0274681 | DDB_G0274681 | DDB0232429 | CDS | 4298827 | 1677 | + | 0.206321 | |
DDB_G0274685 | DDB_G0274685 | DDB0232429 | CDS | 4249771 | 1485 | - | 0.177778 | |
DDB_G0274687 | DDB_G0274687 | DDB0232429 | CDS | 4246508 | 3015 | + | 0.276949 | |
DDB_G0274689 | DDB_G0274689 | DDB0232429 | CDS | 4245076 | 1119 | - | 0.228776 | |
DDB_G0274691 | DDB_G0274691 | DDB0232429 | CDS | 4238537 | 2325 | - | 0.289032 | |
DDB_G0274693 | DDB_G0274693 | contains a BRCT domain (C-terminal domain of a breast cancer susceptibility protein) which is often found in proteins involved in cell cycle checkpoint | DDB0232429 | CDS | 4233488 | 1365 | - | 0.301832 |
DDB_G0274695 | DDB_G0274695 | ortholog of human CD2 binding proteinproline-serine-threonine phosphatase-interacting protein 1 | DDB0232429 | CDS | 4207853 | 1170 | + | 0.289744 |
DDB_G0274701 | DDB_G0274701 | DDB0232429 | CDS | 4200277 | 825 | + | 0.232727 | |
DDB_G0274703 | DDB_G0274703 | DDB0232429 | CDS | 4184904 | 2808 | + | 0.275997 | |
DDB_G0274705 | DDB_G0274705 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 4155932 | 780 | + | 0.261538 |
DDB_G0274709 | DDB_G0274709 | DDB0232429 | CDS | 4143013 | 282 | - | 0.223404 | |
DDB_G0274711 | DDB_G0274711 | DDB0232429 | CDS | 4141983 | 303 | - | 0.207921 | |
DDB_G0274713 | DDB_G0274713 | catalyzes the reaction S-adenosyl-L-methionine 1-aminocyclopropane-1-carboxylate methylthioadenosine | DDB0232429 | CDS | 4137196 | 1449 | + | 0.285024 |
DDB_G0274715 | DDB_G0274715 | DDB0232429 | CDS | 4110567 | 1332 | - | 0.231982 | |
DDB_G0274717_RTE | DDB_G0274717 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 4108767 | 276 | - | 0.32971 |
DDB_G0274719_RTE | DDB_G0274719 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 4108028 | 642 | - | 0.274143 |
DDB_G0274721_RTE | DDB_G0274721 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 4101568 | 1335 | - | 0.307865 |
DDB_G0274723 | DDB_G0274723 | DDB0232429 | CDS | 4086866 | 804 | - | 0.235075 | |
DDB_G0274725 | DDB_G0274725 | DDB0232429 | CDS | 4063639 | 708 | - | 0.240113 | |
DDB_G0274731 | DDB_G0274731 | conserved in Dictyostelium contains 7 FNIP repeat regions | DDB0232429 | CDS | 4029040 | 1698 | + | 0.207303 |
DDB_G0274735 | DDB_G0274735 | bears no significant similarity with any other protein other than containing several evenly spaced cysteine residues | DDB0232429 | CDS | 3985805 | 1014 | + | 0.270217 |
DDB_G0274739 | DDB_G0274739 | DDB0232429 | CDS | 3941346 | 1341 | + | 0.226696 | |
DDB_G0274745 | DDB_G0274745 | DDB0232429 | CDS | 3918064 | 1068 | - | 0.281835 | |
DDB_G0274747 | DDB_G0274747 | DDB0232429 | CDS | 3917072 | 528 | - | 0.225379 | |
DDB_G0274751 | DDB_G0274751 | DDB0232429 | CDS | 3914880 | 1179 | - | 0.27905 | |
DDB_G0274753_RTE | DDB_G0274753 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 3848103 | 4653 | - | 0.309908 |
DDB_G0274757 | DDB_G0274757 | DDB0232429 | CDS | 3781238 | 573 | - | 0.319372 | |
DDB_G0274759_ps | DDB_G0274759 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 3780331 | 204 | - | 0.245098 |
DDB_G0274763_RTE | DDB_G0274763 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232429 | CDS | 3772081 | 297 | - | 0.393939 |
DDB_G0274765 | DDB_G0274765 | DDB0232429 | CDS | 3770260 | 771 | + | 0.342412 | |
DDB_G0274769_ps | DDB_G0274769 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 3775956 | 279 | + | 0.272401 |
DDB_G0274771 | DDB_G0274771 | DDB0232429 | CDS | 3788355 | 627 | + | 0.279107 | |
DDB_G0274777 | DDB_G0274777 | similar to Dna2 a DNA replication factor required for Okazaki fragment processing and involved in DNA repair pathways | DDB0232429 | CDS | 3809416 | 5517 | + | 0.240348 |
DDB_G0274779 | DDB_G0274779 | contains a predicted signal peptide similar to D. purpureum protein | DDB0232429 | CDS | 3818302 | 543 | + | 0.320442 |
DDB_G0274781 | DDB_G0274781 | contains three EF hands similar to mammalian neuron specific calcium-binding protein hippocalcin belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232429 | CDS | 3825256 | 678 | + | 0.29646 |
DDB_G0274785 | DDB_G0274785 | similar to the H. sapiens TATA element modulatory factor (TMF1) which binds the HIV-1 TATA element and inhibits transcriptional activation by the TATA-binding protein TBP | DDB0232429 | CDS | 3826769 | 3255 | + | 0.2553 |
DDB_G0274787 | DDB_G0274787 | DDB0232429 | CDS | 3832237 | 597 | - | 0.261307 | |
DDB_G0274789 | DDB_G0274789 | DDB0232429 | CDS | 3841237 | 6309 | + | 0.277223 | |
DDB_G0274793 | DDB_G0274793 | DDB0232429 | CDS | 3855208 | 1710 | - | 0.183626 | |
DDB_G0274795 | DDB_G0274795 | very similar to mammalian USP48 ubiquitin-specific protease catalyzes the hydrolysis of various forms of polymeric ubiquitin sequences and removes ubiquitin from larger groups | DDB0232429 | CDS | 3857138 | 4074 | - | 0.241041 |
DDB_G0274801 | DDB_G0274801 | DDB0232429 | CDS | 3911402 | 2562 | - | 0.369243 | |
DDB_G0274803 | DDB_G0274803 | DDB0232429 | CDS | 3928531 | 4395 | - | 0.268487 | |
DDB_G0274807 | DDB_G0274807 | DDB0232429 | CDS | 3946871 | 1851 | - | 0.222582 | |
DDB_G0274813 | DDB_G0274813 | conserved protein mainly among fungi and plants | DDB0232429 | CDS | 3971713 | 2817 | + | 0.302449 |
DDB_G0274819 | DDB_G0274819 | DDB0232429 | CDS | 3989396 | 3009 | - | 0.199402 | |
DDB_G0274821 | DDB_G0274821 | DDB0232429 | CDS | 3992986 | 2565 | - | 0.181287 | |
DDB_G0274823 | DDB_G0274823 | DDB0232429 | CDS | 4001854 | 1782 | - | 0.182379 | |
DDB_G0274825 | DDB_G0274825 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D | DDB0232429 | CDS | 4034427 | 2505 | - | 0.263872 |
DDB_G0274827 | DDB_G0274827 | DDB0232429 | CDS | 4039593 | 2760 | - | 0.267391 | |
DDB_G0274831 | DDB_G0274831 | DDB0232429 | CDS | 4061568 | 513 | - | 0.270955 | |
DDB_G0274835 | DDB_G0274835 | DDB0232429 | CDS | 4088247 | 369 | + | 0.238482 | |
DDB_G0274837_RTE | DDB_G0274837 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 4103316 | 1968 | + | 0.348577 |
DDB_G0274839_RTE | DDB_G0274839 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 4106680 | 600 | - | 0.298333 |
DDB_G0274845 | DDB_G0274845 | DDB0232429 | CDS | 4169606 | 3612 | - | 0.212071 | |
DDB_G0274847 | DDB_G0274847 | DDB0232429 | CDS | 4177568 | 5643 | + | 0.270069 | |
DDB_G0274849 | DDB_G0274849 | DDB0232429 | CDS | 4189206 | 189 | + | 0.227513 | |
DDB_G0274851 | DDB_G0274851 | DDB0232429 | CDS | 4190323 | 2307 | + | 0.186389 | |
DDB_G0274853 | DDB_G0274853 | DDB0232429 | CDS | 4210021 | 1602 | + | 0.154806 | |
DDB_G0274861 | DDB_G0274861 | DDB0232429 | CDS | 4216447 | 1293 | - | 0.217324 | |
DDB_G0274863 | DDB_G0274863 | DDB0232429 | CDS | 4225429 | 1281 | + | 0.192818 | |
DDB_G0274865 | DDB_G0274865 | DDB0232429 | CDS | 4252777 | 690 | + | 0.23913 | |
DDB_G0274867 | DDB_G0274867 | DDB0232429 | CDS | 4256257 | 693 | + | 0.20202 | |
DDB_G0274877 | DDB_G0274877 | DDB0232429 | CDS | 4317924 | 2226 | - | 0.261905 | |
DDB_G0274879 | DDB_G0274879 | DDB0232429 | CDS | 4324545 | 5304 | + | 0.326735 | |
DDB_G0274881 | DDB_G0274881 | DDB0232429 | CDS | 4334242 | 1353 | - | 0.233555 | |
DDB_G0274883 | DDB_G0274883 | DDB0232429 | CDS | 4336031 | 1536 | - | 0.231771 | |
DDB_G0274887 | DDB_G0274887 | DDB0232429 | CDS | 4345083 | 1044 | + | 0.251916 | |
DDB_G0274891 | DDB_G0274891 | DDB0232429 | CDS | 4356640 | 1701 | - | 0.219283 | |
DDB_G0274893 | DDB_G0274893 | DDB0232429 | CDS | 4359088 | 2748 | - | 0.270742 | |
DDB_G0274895 | DDB_G0274895 | DDB0232429 | CDS | 4363008 | 957 | - | 0.31348 | |
DDB_G0274897 | DDB_G0274897 | DDB0232429 | CDS | 4364366 | 2733 | - | 0.312477 | |
DDB_G0274899 | DDB_G0274899 | DDB0232429 | CDS | 4368652 | 3927 | - | 0.269926 | |
DDB_G0274901 | DDB_G0274901 | DDB0232429 | CDS | 4391451 | 1377 | - | 0.17284 | |
DDB_G0274903 | DDB_G0274903 | DDB0232429 | CDS | 4393027 | 663 | - | 0.184012 | |
DDB_G0274905 | DDB_G0274905 | DDB0232429 | CDS | 4394654 | 870 | - | 0.156322 | |
DDB_G0274907 | DDB_G0274907 | DDB0232429 | CDS | 4412777 | 3315 | + | 0.198492 | |
DDB_G0274909 | DDB_G0274909 | DDB0232429 | CDS | 4419877 | 822 | - | 0.268856 | |
DDB_G0274911_ps | DDB_G0274911 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 4421760 | 1470 | - | 0.182993 |
DDB_G0274915 | DDB_G0274915 | DDB0232429 | CDS | 4442899 | 5520 | - | 0.352717 | |
DDB_G0274919 | DDB_G0274919 | DDB0232429 | CDS | 4484019 | 3450 | - | 0.186667 | |
DDB_G0274921 | DDB_G0274921 | DDB0232429 | CDS | 4488656 | 1065 | - | 0.210329 | |
DDB_G0274923 | DDB_G0274923 | DDB0232429 | CDS | 4513889 | 1872 | + | 0.254274 | |
DDB_G0274925_ps | DDB_G0274925 | putative pseudogene fragment similar to the genes | DDB0232429 | CDS | 4518975 | 2247 | + | 0.258122 |
DDB_G0274927 | DDB_G0274927 | DDB0232429 | CDS | 4526720 | 1818 | - | 0.231023 | |
DDB_G0274931 | DDB_G0274931 | DDB0232429 | CDS | 4542146 | 4182 | + | 0.277857 | |
DDB_G0274933 | DDB_G0274933 | DDB0232429 | CDS | 4548951 | 579 | + | 0.260794 | |
DDB_G0274935 | DDB_G0274935 | DDB0232429 | CDS | 4555761 | 1482 | + | 0.269231 | |
DDB_G0274945_ps | DDB_G0274945 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232429 | CDS | 4591973 | 786 | + | 0.260814 |
DDB_G0274947 | DDB_G0274947 | DDB0232429 | CDS | 4598646 | 4401 | - | 0.234719 | |
DDB_G0274949 | DDB_G0274949 | DDB0232429 | CDS | 4631680 | 1977 | - | 0.242792 | |
DDB_G0274951 | DDB_G0274951 | DDB0232429 | CDS | 4634989 | 423 | - | 0.295508 | |
DDB_G0274953 | DDB_G0274953 | DDB0232429 | CDS | 4652461 | 1893 | - | 0.228737 | |
DDB_G0274957_ps | DDB_G0274957 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 4659350 | 789 | + | 0.257288 |
DDB_G0274961 | DDB_G0274961 | DDB0232429 | CDS | 4670597 | 1215 | - | 0.235391 | |
DDB_G0274963 | DDB_G0274963 | DDB0232429 | CDS | 4672730 | 3711 | + | 0.181622 | |
DDB_G0274965 | DDB_G0274965 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232429 | CDS | 4676573 | 4203 | - | 0.281704 |
DDB_G0274969 | DDB_G0274969 | similar to mammalian lysophosphatidic acid acyltransferase zeta (1-acylglycerol-3-phosphate O-acyltransferase 6) contains 3 putative transmembrane domains | DDB0232429 | CDS | 4689182 | 1467 | + | 0.276074 |
DDB_G0274971 | DDB_G0274971 | DDB0232429 | CDS | 4712814 | 873 | + | 0.341352 | |
DDB_G0274973 | DDB_G0274973 | DDB0232429 | CDS | 4725095 | 2148 | + | 0.180168 | |
DDB_G0274975 | DDB_G0274975 | DDB0232429 | CDS | 4730779 | 4398 | - | 0.31105 | |
DDB_G0274977 | DDB_G0274977 | DDB0232429 | CDS | 4753411 | 201 | - | 0.338308 | |
DDB_G0274979 | DDB_G0274979 | DDB0232429 | CDS | 4754213 | 2421 | + | 0.220983 | |
DDB_G0274981 | DDB_G0274981 | DDB0232429 | CDS | 4760642 | 2514 | - | 0.265314 | |
DDB_G0274985_ps | DDB_G0274985 | putative pseudogene conserved hypothetical Dictyostelium protein | DDB0232429 | CDS | 4814216 | 222 | - | 0.301802 |
DDB_G0274987 | DDB_G0274987 | DDB0232429 | CDS | 4816957 | 660 | - | 0.306061 | |
DDB_G0274991 | DDB_G0274991 | DDB0232429 | CDS | 4818450 | 873 | + | 0.229095 | |
DDB_G0274995 | DDB_G0274995 | DDB0232429 | CDS | 4844842 | 3315 | + | 0.246154 | |
DDB_G0274997 | DDB_G0274997 | DDB0232429 | CDS | 4848528 | 2832 | - | 0.227048 | |
DDB_G0275001 | DDB_G0275001 | DDB0232429 | CDS | 4873769 | 564 | + | 0.351064 | |
DDB_G0275003 | DDB_G0275003 | DDB0232429 | CDS | 4890449 | 1881 | - | 0.23126 | |
DDB_G0275005 | DDB_G0275005 | putative ortholog of H. sapiens CNOT4 and S. cerevisiae MOT2 component of the CCR4-NOT transcription complex | DDB0232429 | CDS | 4898014 | 4461 | + | 0.30195 |
DDB_G0275015 | DDB_G0275015 | DDB0232429 | CDS | 5186347 | 2631 | + | 0.240593 | |
DDB_G0275017 | DDB_G0275017 | contains a MOZSAS-like domain (Monocytic leukemia Zinc fingerSomething About Silencing) predicted to have histone acetyltransferase activity | DDB0232429 | CDS | 5183368 | 1920 | - | 0.336979 |
DDB_G0275019 | DDB_G0275019 | DDB0232429 | CDS | 5181844 | 924 | + | 0.281385 | |
DDB_G0275025 | DDB_G0275025 | contains one thioredoxin domain similar to human PDIA6 (protein disulfide isomerase A6) | DDB0232429 | CDS | 5326205 | 1230 | + | 0.264228 |
DDB_G0275027 | DDB_G0275027 | DDB0232429 | CDS | 5323069 | 276 | - | 0.297101 | |
DDB_G0275031 | DDB_G0275031 | DDB0232429 | CDS | 5315972 | 213 | + | 0.333333 | |
DDB_G0275033 | DDB_G0275033 | conserved hypothetical Dictyostelium protein | DDB0232429 | CDS | 5311440 | 2073 | - | 0.235408 |
DDB_G0275039 | DDB_G0275039 | conserved hypothetical protein contains 13 predicted transmembrane domains and a partial endonucleaseexonucleasephosphatase domain | DDB0232429 | CDS | 5278271 | 2145 | - | 0.332401 |
DDB_G0275041 | DDB_G0275041 | DDB0232429 | CDS | 5273798 | 1026 | + | 0.220273 | |
DDB_G0275043 | DDB_G0275043 | DDB0232429 | CDS | 5268701 | 186 | + | 0.263441 | |
DDB_G0275047 | DDB_G0275047 | DDB0232429 | CDS | 5250735 | 705 | - | 0.195745 | |
DDB_G0275049 | DDB_G0275049 | DDB0232429 | CDS | 5249449 | 924 | + | 0.313853 | |
DDB_G0275051_ps | DDB_G0275051 | putative pseudogene hssA2C7E family protein | DDB0232429 | CDS | 5240500 | 192 | - | 0.40625 |
DDB_G0275053 | DDB_G0275053 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232429 | CDS | 5239346 | 918 | + | 0.33878 |
DDB_G0275057 | DDB_G0275057 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | DDB0232429 | CDS | 5089988 | 1050 | + | 0.33619 |
DDB_G0275059 | DDB_G0275059 | DDB0232429 | CDS | 5091816 | 816 | - | 0.294118 | |
DDB_G0275063 | DDB_G0275063 | DDB0232429 | CDS | 5094579 | 762 | - | 0.307087 | |
DDB_G0275067 | DDB_G0275067 | DDB0232429 | CDS | 5107775 | 1161 | + | 0.283376 | |
DDB_G0275075 | DDB_G0275075 | ortholog of mammalian NARG1 and yeast NAT1 part of a complex that displays alpha (N-terminal) acetyltransferase activity | DDB0232429 | CDS | 5130987 | 2445 | + | 0.285072 |
DDB_G0275081 | DDB_G0275081 | similar to bacterial proteins of the YjgF superfamily homolog of Psedomonas sp. amnD (2-aminomuconate deaminase) also matches PFAM HMM for endoribonuclease L-PSP | DDB0232429 | CDS | 5148814 | 426 | + | 0.316901 |
DDB_G0275083 | DDB_G0275083 | DDB0232429 | CDS | 5153248 | 471 | - | 0.29087 | |
DDB_G0275087 | DDB_G0275087 | DDB0232429 | CDS | 5163252 | 1440 | + | 0.20625 | |
DDB_G0275089 | DDB_G0275089 | DDB0232429 | CDS | 5165037 | 1680 | - | 0.225595 | |
DDB_G0275091 | DDB_G0275091 | contains one predicted coiled-coil domain similar to D. purpureum protein | DDB0232429 | CDS | 5172500 | 1950 | + | 0.262051 |
DDB_G0275093 | DDB_G0275093 | similar to ubiquitin in the N-terminal region contains one von Willebrand factor (vWF) type A domain | DDB0232429 | CDS | 5056195 | 2055 | - | 0.30219 |
DDB_G0275097 | DDB_G0275097 | DDB0232429 | CDS | 5060014 | 2256 | + | 0.321809 | |
DDB_G0275099 | DDB_G0275099 | DDB0232429 | CDS | 5062455 | 1356 | - | 0.291298 | |
DDB_G0275103 | DDB_G0275103 | contains an N-terminal B-box zinc finger domain and 4 FNIP repeats contains a predicted coiled-coil domain | DDB0232429 | CDS | 5065612 | 1785 | + | 0.235854 |
DDB_G0275105_ps | DDB_G0275105 | putative pseudogene fragment similar to D. discoideum genes | DDB0232429 | CDS | 5067904 | 222 | + | 0.256757 |
DDB_G0275107 | DDB_G0275107 | DDB0232429 | CDS | 5025157 | 1356 | - | 0.308997 | |
DDB_G0275109 | DDB_G0275109 | DDB0232429 | CDS | 5033896 | 1845 | - | 0.197832 | |
DDB_G0275111 | DDB_G0275111 | contains a predicted signal peptide conserved in Dictyostelium and Polysphondylium | DDB0232429 | CDS | 5037232 | 864 | + | 0.306713 |
DDB_G0275113 | DDB_G0275113 | DDB0232429 | CDS | 5041441 | 1638 | - | 0.247863 | |
DDB_G0275117 | DDB_G0275117 | DDB0232429 | CDS | 5047947 | 1917 | - | 0.248826 | |
DDB_G0275127 | DDB_G0275127 | DDB0232429 | CDS | 4987975 | 1008 | - | 0.251984 | |
DDB_G0275131 | DDB_G0275131 | DDB0232429 | CDS | 4929416 | 171 | - | 0.216374 | |
DDB_G0275133 | DDB_G0275133 | DDB0232429 | CDS | 4930622 | 696 | - | 0.248563 | |
DDB_G0275135 | DDB_G0275135 | DDB0232429 | CDS | 4932274 | 186 | - | 0.22043 | |
DDB_G0275137 | DDB_G0275137 | DDB0232429 | CDS | 4934269 | 180 | - | 0.205556 | |
DDB_G0275139 | DDB_G0275139 | DDB0232429 | CDS | 4953641 | 1788 | + | 0.199664 | |
DDB_G0275143 | DDB_G0275143 | DDB0232429 | CDS | 4958210 | 1971 | - | 0.217149 | |
DDB_G0275145 | DDB_G0275145 | contains one RING-type zinc finger and one IBR (In Between Ring fingers) domain similar to S. cerevisiae RING finger protein YKR017C | DDB0232429 | CDS | 4960811 | 1746 | - | 0.310424 |
DDB_G0275147 | DDB_G0275147 | DDB0232429 | CDS | 4963654 | 657 | - | 0.210046 | |
DDB_G0275149 | DDB_G0275149 | similar to S. cerevisiae AKR1 (palmitoyltransferase AKR1) contains 5 ankyrin repeats and 1 zinc finger DHHC domain contains 6 putative transmembrane domains | DDB0232429 | CDS | 4965140 | 2097 | + | 0.299475 |
DDB_G0275151 | DDB_G0275151 | DDB0232429 | CDS | 5180306 | 315 | - | 0.32381 | |
DDB_G0275155 | DDB_G0275155 | DDB0232429 | CDS | 5260668 | 1425 | + | 0.397895 | |
DDB_G0275159 | DDB_G0275159 | probable ortholog of H. sapiens and S. cerevisiae HAT1 a subunit of the HAT1HAT2 histone acetyltransferase complex | DDB0232429 | CDS | 5204831 | 1401 | + | 0.254818 |
DDB_G0275161 | DDB_G0275161 | DDB0232429 | CDS | 5203376 | 564 | - | 0.292553 | |
DDB_G0275163 | DDB_G0275163 | DDB0232429 | CDS | 5152512 | 324 | - | 0.299383 | |
DDB_G0275165 | DDB_G0275165 | DDB0232429 | CDS | 5143836 | 2766 | - | 0.298988 | |
DDB_G0275169 | DDB_G0275169 | DDB0232429 | CDS | 5084018 | 3873 | + | 0.268009 | |
DDB_G0275171 | DDB_G0275171 | DDB0232429 | CDS | 5072046 | 1449 | - | 0.224293 | |
DDB_G0275175 | DDB_G0275175 | DDB0232429 | CDS | 4926006 | 165 | - | 0.242424 | |
DDB_G0275179 | DDB_G0275179 | similar to H. sapiens CECR1 protein (Swiss Prot Q9NZK5) | DDB0232429 | CDS | 5345936 | 1632 | + | 0.273284 |
DDB_G0275189 | DDB_G0275189 | DDB0232429 | CDS | 5256632 | 876 | + | 0.27968 | |
DDB_G0275195 | DDB_G0275195 | DDB0232429 | CDS | 5206472 | 3642 | - | 0.31933 | |
DDB_G0275201 | DDB_G0275201 | DDB0232429 | CDS | 5147013 | 171 | + | 0.169591 | |
DDB_G0275203 | DDB_G0275203 | DDB0232429 | CDS | 5105558 | 1707 | + | 0.176333 | |
DDB_G0275205 | DDB_G0275205 | DDB0232429 | CDS | 5081463 | 1533 | - | 0.270711 | |
DDB_G0275213 | DDB_G0275213 | DDB0232429 | CDS | 5010279 | 705 | + | 0.217021 | |
DDB_G0275215 | DDB_G0275215 | DDB0232429 | CDS | 5007231 | 2076 | - | 0.244701 | |
DDB_G0275217_RTE | DDB_G0275217 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 4983192 | 174 | - | 0.327586 |
DDB_G0275219_RTE | DDB_G0275219 | partial ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232429 | CDS | 4982711 | 153 | - | 0.339869 |
DDB_G0275221_RTE | DDB_G0275221 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 4967851 | 3627 | - | 0.311828 |
DDB_G0275223 | DDB_G0275223 | DDB0232429 | CDS | 4937448 | 309 | - | 0.262136 | |
DDB_G0275225 | DDB_G0275225 | DDB0232429 | CDS | 4936614 | 480 | - | 0.2875 | |
DDB_G0275227 | DDB_G0275227 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | DDB0232429 | CDS | 4935740 | 324 | - | 0.361111 |
DDB_G0275229_ps | DDB_G0275229 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 4924842 | 168 | - | 0.202381 |
DDB_G0275231 | DDB_G0275231 | DDB0232429 | CDS | 4927229 | 195 | - | 0.25641 | |
DDB_G0275233 | DDB_G0275233 | DDB0232429 | CDS | 4928353 | 177 | - | 0.259887 | |
DDB_G0275237 | DDB_G0275237 | DDB0232429 | CDS | 4941790 | 1815 | - | 0.17135 | |
DDB_G0275243 | DDB_G0275243 | belongs to the PLAC8 family (placenta-specific gene 8 protein) a family of cysteine-rich proteins with highly divergent low complexity amino terminal regions | DDB0232429 | CDS | 4990595 | 330 | + | 0.375758 |
DDB_G0275245 | DDB_G0275245 | DDB0232429 | CDS | 4995682 | 4254 | + | 0.242595 | |
DDB_G0275247 | DDB_G0275247 | DDB0232429 | CDS | 5000529 | 1911 | - | 0.178441 | |
DDB_G0275251 | DDB_G0275251 | DDB0232429 | CDS | 5029263 | 924 | + | 0.205628 | |
DDB_G0275253 | DDB_G0275253 | DDB0232429 | CDS | 5031311 | 861 | + | 0.321719 | |
DDB_G0275255 | DDB_G0275255 | DDB0232429 | CDS | 5032870 | 870 | + | 0.277011 | |
DDB_G0275259 | DDB_G0275259 | similar to a D. purpureum protein contains a predicted signal peptide | DDB0232429 | CDS | 5053540 | 144 | + | 0.284722 |
DDB_G0275269 | DDB_G0275269 | DDB0232429 | CDS | 5126494 | 1626 | + | 0.288438 | |
DDB_G0275271 | DDB_G0275271 | DDB0232429 | CDS | 5150001 | 633 | + | 0.208531 | |
DDB_G0275273 | DDB_G0275273 | DDB0232429 | CDS | 5150712 | 1236 | - | 0.197411 | |
DDB_G0275275 | DDB_G0275275 | DDB0232429 | CDS | 5161132 | 1629 | + | 0.275015 | |
DDB_G0275277 | DDB_G0275277 | DDB0232429 | CDS | 5167778 | 1980 | + | 0.288384 | |
DDB_G0275279 | DDB_G0275279 | member of a gene family comprising | DDB0232429 | CDS | 5170228 | 969 | - | 0.236326 |
DDB_G0275283 | DDB_G0275283 | DDB0232429 | CDS | 5192598 | 3009 | - | 0.251911 | |
DDB_G0275285 | DDB_G0275285 | DDB0232429 | CDS | 5198095 | 2283 | + | 0.233027 | |
DDB_G0275287 | DDB_G0275287 | DDB0232429 | CDS | 5218487 | 6324 | - | 0.246521 | |
DDB_G0275289 | DDB_G0275289 | DDB0232429 | CDS | 5225979 | 2826 | - | 0.209837 | |
DDB_G0275291 | DDB_G0275291 | DDB0232429 | CDS | 5242381 | 144 | + | 0.326389 | |
DDB_G0275297 | DDB_G0275297 | DDB0232429 | CDS | 5270344 | 1098 | + | 0.26776 | |
DDB_G0275301 | DDB_G0275301 | DDB0232429 | CDS | 5275007 | 1035 | - | 0.311111 | |
DDB_G0275303 | DDB_G0275303 | DDB0232429 | CDS | 5281471 | 5265 | - | 0.252422 | |
DDB_G0275305 | DDB_G0275305 | DDB0232429 | CDS | 5302345 | 8607 | + | 0.297084 | |
DDB_G0275307 | DDB_G0275307 | DDB0232429 | CDS | 5319128 | 810 | - | 0.22716 | |
DDB_G0275309 | DDB_G0275309 | DDB0232429 | CDS | 5320535 | 1851 | - | 0.147488 | |
DDB_G0275311 | DDB_G0275311 | DDB0232429 | CDS | 5329126 | 1383 | + | 0.366594 | |
DDB_G0275315 | DDB_G0275315 | DDB0232429 | CDS | 5337299 | 759 | - | 0.258235 | |
DDB_G0275317 | DDB_G0275317 | DDB0232429 | CDS | 5339600 | 1110 | + | 0.24955 | |
DDB_G0275319 | DDB_G0275319 | DDB0232429 | CDS | 5341225 | 1692 | - | 0.190898 | |
DDB_G0275321 | DDB_G0275321 | DDB0232429 | CDS | 5348199 | 1914 | + | 0.133751 | |
DDB_G0275325 | DDB_G0275325 | DDB0232429 | CDS | 5350193 | 171 | - | 0.192982 | |
DDB_G0275329 | DDB_G0275329 | similar to | DDB0232429 | CDS | 5357606 | 558 | + | 0.249104 |
DDB_G0275331 | DDB_G0275331 | DDB0232429 | CDS | 5365929 | 3147 | + | 0.280902 | |
DDB_G0275333 | DDB_G0275333 | DDB0232429 | CDS | 5369983 | 1437 | - | 0.263048 | |
DDB_G0275335 | DDB_G0275335 | DDB0232429 | CDS | 5382119 | 426 | + | 0.307512 | |
DDB_G0275337 | DDB_G0275337 | DDB0232429 | CDS | 5383223 | 1041 | + | 0.309318 | |
DDB_G0275339 | DDB_G0275339 | DDB0232429 | CDS | 5391099 | 1308 | + | 0.239297 | |
DDB_G0275341 | DDB_G0275341 | DDB0232429 | CDS | 5392651 | 1071 | + | 0.300654 | |
DDB_G0275343 | DDB_G0275343 | DDB0232429 | CDS | 5393905 | 1638 | - | 0.234432 | |
DDB_G0275345 | DDB_G0275345 | DDB0232429 | CDS | 5397156 | 2109 | + | 0.266477 | |
DDB_G0275347 | DDB_G0275347 | DDB0232429 | CDS | 5399825 | 276 | - | 0.286232 | |
DDB_G0275349 | DDB_G0275349 | DDB0232429 | CDS | 5401406 | 318 | + | 0.320755 | |
DDB_G0275351 | DDB_G0275351 | contains 1 C2H2-type zinc finger homolog of human ZNF593 and S. cerevisiae BUD20 (bud site selection protein 20) | DDB0232429 | CDS | 5402357 | 426 | + | 0.293427 |
DDB_G0275353 | DDB_G0275353 | DDB0232429 | CDS | 5409975 | 1443 | + | 0.27027 | |
DDB_G0275357 | DDB_G0275357 | DDB0232429 | CDS | 5417695 | 276 | - | 0.326087 | |
DDB_G0275359 | DDB_G0275359 | DDB0232429 | CDS | 5424566 | 1389 | - | 0.397408 | |
DDB_G0275363_ps | DDB_G0275363 | putative pseudogene fragment similar to gene | DDB0232429 | CDS | 5426347 | 459 | - | 0.189542 |
DDB_G0275365 | DDB_G0275365 | DDB0232429 | CDS | 5428576 | 2088 | + | 0.346264 | |
DDB_G0275367 | DDB_G0275367 | similar to uncharacterized eukaryotic proteins of the DUF1909 (4F5) family | DDB0232429 | CDS | 5434710 | 243 | - | 0.374486 |
DDB_G0275369 | DDB_G0275369 | DDB0232429 | CDS | 5451865 | 141 | - | 0.276596 | |
DDB_G0275371 | DDB_G0275371 | similar to the esterase encoded by | DDB0232429 | CDS | 5452633 | 1095 | + | 0.277626 |
DDB_G0275373 | DDB_G0275373 | DDB0232429 | CDS | 5467402 | 1362 | - | 0.169604 | |
DDB_G0275375 | DDB_G0275375 | DDB0232429 | CDS | 5469261 | 5103 | - | 0.22477 | |
DDB_G0275377 | DDB_G0275377 | DDB0232429 | CDS | 5475784 | 939 | + | 0.251331 | |
DDB_G0275379 | DDB_G0275379 | DDB0232429 | CDS | 5477021 | 282 | - | 0.276596 | |
DDB_G0275381 | DDB_G0275381 | belongs to the RAMP4 (ribosome-associated membrane protein) family homolog of human SERP1 (stress-associated endoplasmic reticulum protein) contains one predicted transmembrane domain | DDB0232429 | CDS | 5477733 | 180 | - | 0.327778 |
DDB_G0275383 | DDB_G0275383 | similar to small genes conserved in plants contains one central transmembrane domain | DDB0232429 | CDS | 5480068 | 207 | - | 0.400966 |
DDB_G0275385 | DDB_G0275385 | DDB0232429 | CDS | 5482191 | 666 | + | 0.28979 | |
DDB_G0275389 | DDB_G0275389 | DDB0232429 | CDS | 5493095 | 1608 | + | 0.298507 | |
DDB_G0275393 | DDB_G0275393 | DDB0232429 | CDS | 5354537 | 2616 | - | 0.195719 | |
DDB_G0275399 | DDB_G0275399 | DDB0232429 | CDS | 5375069 | 6531 | + | 0.239473 | |
DDB_G0275401 | DDB_G0275401 | DDB0232429 | CDS | 5385395 | 5256 | + | 0.272831 | |
DDB_G0275403 | DDB_G0275403 | similar to human NOC4L belongs to the CBFMAK21 family contains a CCAAT-binding_factor domain | DDB0232429 | CDS | 5403180 | 2139 | - | 0.249182 |
DDB_G0275409 | DDB_G0275409 | DDB0232429 | CDS | 5421845 | 2214 | + | 0.247967 | |
DDB_G0275411 | DDB_G0275411 | DDB0232429 | CDS | 5431261 | 1035 | - | 0.279227 | |
DDB_G0275413 | DDB_G0275413 | DDB0232429 | CDS | 5435452 | 3807 | - | 0.24166 | |
DDB_G0275415 | DDB_G0275415 | DDB0232429 | CDS | 5440439 | 8976 | + | 0.29434 | |
DDB_G0275417 | DDB_G0275417 | DDB0232429 | CDS | 5450465 | 1092 | + | 0.192308 | |
DDB_G0275419 | DDB_G0275419 | contains a predicted signal peptide similarity to bacterial NUDIX hydrolases and dipeptidyl-peptidases | DDB0232429 | CDS | 5454847 | 1623 | - | 0.234134 |
DDB_G0275421 | DDB_G0275421 | contains 2 GRAM domains one RabGAPTBC domain and one EF hand domain | DDB0232429 | CDS | 5459788 | 3672 | + | 0.232026 |
DDB_G0275423 | DDB_G0275423 | DDB0232429 | CDS | 5465798 | 1296 | + | 0.243056 | |
DDB_G0275431 | DDB_G0275431 | DDB0232429 | CDS | 5483235 | 4791 | - | 0.262784 | |
DDB_G0275433 | DDB_G0275433 | DDB0232429 | CDS | 5488651 | 381 | + | 0.217848 | |
DDB_G0275435 | DDB_G0275435 | DDB0232429 | CDS | 5500328 | 269 | - | 0.178439 | |
DDB_G0275457 | DDB_G0275457 | DDB0232429 | CDS | 6112474 | 780 | + | 0.284615 | |
DDB_G0275459 | DDB_G0275459 | DDB0232429 | CDS | 6113524 | 900 | + | 0.428889 | |
DDB_G0275461_ps | DDB_G0275461 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 6115320 | 336 | - | 0.267857 |
DDB_G0275463 | DDB_G0275463 | DDB0232429 | CDS | 6116744 | 249 | + | 0.317269 | |
DDB_G0275465_ps | DDB_G0275465 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 6117739 | 1308 | - | 0.237768 |
DDB_G0275467 | DDB_G0275467 | catalyzes the reaction a 5'-ribonucleotide Hsub2subO a ribonucleoside phosphate | DDB0232429 | CDS | 6119794 | 1776 | - | 0.273649 |
DDB_G0275469 | DDB_G0275469 | similar to endonuclease V which catalyses the endonucleolytic cleavage of apurinic or apyrimidinic sites to generate products with a 5'-phosphate | DDB0232429 | CDS | 6096697 | 1617 | - | 0.29128 |
DDB_G0275475 | DDB_G0275475 | DDB0232429 | CDS | 6086909 | 1041 | + | 0.292988 | |
DDB_G0275477 | DDB_G0275477 | DDB0232429 | CDS | 6081078 | 162 | + | 0.209877 | |
DDB_G0275479 | DDB_G0275479 | DDB0232429 | CDS | 5986809 | 381 | - | 0.301837 | |
DDB_G0275481 | DDB_G0275481 | DDB0232429 | CDS | 5988394 | 1077 | + | 0.393686 | |
DDB_G0275483 | DDB_G0275483 | DDB0232429 | CDS | 5990519 | 255 | + | 0.352941 | |
DDB_G0275485 | DDB_G0275485 | DDB0232429 | CDS | 5991516 | 129 | + | 0.24031 | |
DDB_G0275487 | DDB_G0275487 | DDB0232429 | CDS | 5992334 | 957 | + | 0.272727 | |
DDB_G0275489 | DDB_G0275489 | DDB0232429 | CDS | 5994199 | 246 | - | 0.349593 | |
DDB_G0275491 | DDB_G0275491 | DDB0232429 | CDS | 5997672 | 249 | - | 0.317269 | |
DDB_G0275497 | DDB_G0275497 | DDB0232429 | CDS | 6007182 | 1974 | + | 0.324721 | |
DDB_G0275503 | DDB_G0275503 | DDB0232429 | CDS | 6017175 | 834 | + | 0.260192 | |
DDB_G0275505 | DDB_G0275505 | DDB0232429 | CDS | 6018482 | 3393 | + | 0.325965 | |
DDB_G0275507 | DDB_G0275507 | similar to bacterial acetyltransferases homolog of E. coli maa (maltose O-acetyltransferase) | DDB0232429 | CDS | 6022499 | 591 | - | 0.314721 |
DDB_G0275509 | DDB_G0275509 | DDB0232429 | CDS | 6023716 | 2607 | + | 0.197929 | |
DDB_G0275511 | DDB_G0275511 | DDB0232429 | CDS | 6026463 | 402 | - | 0.164179 | |
DDB_G0275513 | DDB_G0275513 | conserved in bacteria plants and protozoans contains two transmembrane domains | DDB0232429 | CDS | 6033383 | 315 | - | 0.28254 |
DDB_G0275519 | DDB_G0275519 | DDB0232429 | CDS | 6062122 | 921 | + | 0.330076 | |
DDB_G0275521 | DDB_G0275521 | DDB0232429 | CDS | 6066450 | 1434 | + | 0.26848 | |
DDB_G0275523 | DDB_G0275523 | DDB0232429 | CDS | 6068094 | 2556 | - | 0.294601 | |
DDB_G0275527 | DDB_G0275527 | DDB0232429 | CDS | 5891053 | 438 | + | 0.308219 | |
DDB_G0275529 | DDB_G0275529 | DDB0232429 | CDS | 5892491 | 4269 | - | 0.223003 | |
DDB_G0275531 | DDB_G0275531 | DDB0232429 | CDS | 5908177 | 207 | - | 0.2657 | |
DDB_G0275533 | DDB_G0275533 | DDB0232429 | CDS | 5909271 | 5910 | - | 0.311168 | |
DDB_G0275535 | DDB_G0275535 | DDB0232429 | CDS | 5868742 | 3477 | + | 0.300546 | |
DDB_G0275539 | DDB_G0275539 | DDB0232429 | CDS | 5727073 | 3975 | - | 0.272453 | |
DDB_G0275541 | DDB_G0275541 | DDB0232429 | CDS | 5731969 | 1182 | + | 0.28088 | |
DDB_G0275543 | DDB_G0275543 | DDB0232429 | CDS | 5736589 | 1005 | + | 0.21791 | |
DDB_G0275545 | DDB_G0275545 | DDB0232429 | CDS | 5754202 | 294 | + | 0.302721 | |
DDB_G0275547 | DDB_G0275547 | DDB0232429 | CDS | 5770895 | 1008 | + | 0.274802 | |
DDB_G0275549 | DDB_G0275549 | DDB0232429 | CDS | 5648871 | 945 | + | 0.219048 | |
DDB_G0275551 | DDB_G0275551 | DDB0232429 | CDS | 5655917 | 333 | - | 0.267267 | |
DDB_G0275553 | DDB_G0275553 | DDB0232429 | CDS | 5674643 | 1011 | - | 0.252226 | |
DDB_G0275555 | DDB_G0275555 | DDB0232429 | CDS | 5684935 | 723 | + | 0.271093 | |
DDB_G0275557 | DDB_G0275557 | DDB0232429 | CDS | 5616992 | 555 | - | 0.223423 | |
DDB_G0275559 | DDB_G0275559 | underexpressed in | DDB0232429 | CDS | 5618738 | 873 | + | 0.316151 |
DDB_G0275563 | DDB_G0275563 | DDB0232429 | CDS | 5506678 | 4404 | + | 0.221844 | |
DDB_G0275565 | DDB_G0275565 | DDB0232429 | CDS | 5516663 | 198 | - | 0.0656566 | |
DDB_G0275569 | DDB_G0275569 | DDB0232429 | CDS | 5519854 | 1053 | - | 0.220323 | |
DDB_G0275571 | DDB_G0275571 | DDB0232429 | CDS | 5522231 | 2793 | + | 0.3029 | |
DDB_G0275575 | DDB_G0275575 | DDB0232429 | CDS | 5530051 | 984 | + | 0.166667 | |
DDB_G0275577 | DDB_G0275577 | DDB0232429 | CDS | 5533870 | 1953 | - | 0.275474 | |
DDB_G0275579 | DDB_G0275579 | DDB0232429 | CDS | 5538592 | 282 | - | 0.37234 | |
DDB_G0275581 | DDB_G0275581 | DDB0232429 | CDS | 5550573 | 2736 | - | 0.299708 | |
DDB_G0275583 | DDB_G0275583 | DDB0232429 | CDS | 5553795 | 612 | - | 0.222222 | |
DDB_G0275585 | DDB_G0275585 | DDB0232429 | CDS | 5554964 | 1422 | + | 0.227848 | |
DDB_G0275587 | DDB_G0275587 | DDB0232429 | CDS | 5556745 | 162 | - | 0.191358 | |
DDB_G0275591 | DDB_G0275591 | DDB0232429 | CDS | 5562777 | 2082 | + | 0.304995 | |
DDB_G0275593 | DDB_G0275593 | DDB0232429 | CDS | 5568361 | 1221 | - | 0.232596 | |
DDB_G0275595 | DDB_G0275595 | DDB0232429 | CDS | 5571932 | 2052 | - | 0.220273 | |
DDB_G0275597 | DDB_G0275597 | DDB0232429 | CDS | 5577263 | 318 | + | 0.198113 | |
DDB_G0275599 | DDB_G0275599 | DDB0232429 | CDS | 5578557 | 768 | - | 0.251302 | |
DDB_G0275603 | DDB_G0275603 | DDB0232429 | CDS | 5583526 | 1782 | + | 0.319865 | |
DDB_G0275605_ps | DDB_G0275605 | putative pseudogene similar to gene | DDB0232429 | CDS | 5585797 | 1407 | - | 0.329069 |
DDB_G0275609 | DDB_G0275609 | DDB0232429 | CDS | 5594155 | 345 | - | 0.205797 | |
DDB_G0275613 | DDB_G0275613 | DDB0232429 | CDS | 5606831 | 1314 | + | 0.289954 | |
DDB_G0275615_ps | DDB_G0275615 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 5609342 | 2181 | - | 0.215956 |
DDB_G0275621 | DDB_G0275621 | DDB0232429 | CDS | 5934525 | 1581 | + | 0.250474 | |
DDB_G0275625 | DDB_G0275625 | DDB0232429 | CDS | 5947660 | 876 | + | 0.276256 | |
DDB_G0275629 | DDB_G0275629 | DDB0232429 | CDS | 5954835 | 171 | + | 0.280702 | |
DDB_G0275631 | DDB_G0275631 | the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232429 | CDS | 5956945 | 2307 | + | 0.332466 |
DDB_G0275633 | DDB_G0275633 | ortholog of human SKIV2L2 (SuperKIller Viralicitic 2L2) protein and yeast MTR4 a helicase required for mRNA export from the nucleus | DDB0232429 | CDS | 5972320 | 3387 | + | 0.346324 |
DDB_G0275639 | DDB_G0275639 | DDB0232429 | CDS | 6080040 | 177 | + | 0.180791 | |
DDB_G0275641 | DDB_G0275641 | DDB0232429 | CDS | 6082396 | 159 | + | 0.188679 | |
DDB_G0275643 | DDB_G0275643 | DDB0232429 | CDS | 5864931 | 1275 | + | 0.219608 | |
DDB_G0275647 | DDB_G0275647 | DDB0232429 | CDS | 5858199 | 477 | - | 0.283019 | |
DDB_G0275649 | DDB_G0275649 | DDB0232429 | CDS | 5854199 | 2076 | + | 0.251927 | |
DDB_G0275659 | DDB_G0275659 | DDB0232429 | CDS | 5815544 | 2997 | + | 0.303971 | |
DDB_G0275661 | DDB_G0275661 | DDB0232429 | CDS | 5806627 | 1389 | + | 0.180706 | |
DDB_G0275665 | DDB_G0275665 | DDB0232429 | CDS | 5789524 | 912 | - | 0.308114 | |
DDB_G0275667 | DDB_G0275667 | homolog of human and S. cerevisiae KTI12 (killer toxin insensitivity protein 12) S. cerevisiae KTI12 interacts with the Elongator complex a component of the elongating form of RNA polymerase II | DDB0232429 | CDS | 5787522 | 822 | - | 0.283455 |
DDB_G0275669 | DDB_G0275669 | involved in proline metabolism catalyzes the reaction L-proline acceptor (S)-1-pyrroline-5-carboxylate reduced acceptor | DDB0232429 | CDS | 5784538 | 1719 | - | 0.2484 |
DDB_G0275671 | DDB_G0275671 | putative serine esterase similar to hypothetical proteins in plants and yeast | DDB0232429 | CDS | 5687040 | 1239 | + | 0.268765 |
DDB_G0275673 | DDB_G0275673 | DDB0232429 | CDS | 5694864 | 363 | + | 0.250689 | |
DDB_G0275677 | DDB_G0275677 | DDB0232429 | CDS | 5700254 | 1389 | - | 0.154068 | |
DDB_G0275681 | DDB_G0275681 | DDB0232429 | CDS | 5715872 | 198 | + | 0.222222 | |
DDB_G0275683 | DDB_G0275683 | DDB0232429 | CDS | 5719223 | 1110 | + | 0.209009 | |
DDB_G0275685 | DDB_G0275685 | DDB0232429 | CDS | 5720646 | 150 | - | 0.266667 | |
DDB_G0275691 | DDB_G0275691 | DDB0232429 | CDS | 5504962 | 798 | - | 0.166667 | |
DDB_G0275693 | DDB_G0275693 | DDB0232429 | CDS | 5531426 | 2103 | + | 0.300048 | |
DDB_G0275705 | DDB_G0275705 | DDB0232429 | CDS | 6126263 | 168 | + | 0.22619 | |
DDB_G0275707 | DDB_G0275707 | weakly similar to ints10 component of a multiprotein mediator of small nuclear RNA processing | DDB0232429 | CDS | 6082948 | 2976 | + | 0.209005 |
DDB_G0275709_ps | DDB_G0275709 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 6053556 | 819 | - | 0.21978 |
DDB_G0275713 | DDB_G0275713 | conserved hypothetical protein contains a putative N-terminal signal sequence | DDB0232429 | CDS | 6040578 | 936 | - | 0.24359 |
DDB_G0275715 | DDB_G0275715 | DDB0232429 | CDS | 6031763 | 423 | - | 0.193853 | |
DDB_G0275721 | DDB_G0275721 | DDB0232429 | CDS | 5987883 | 348 | - | 0.298851 | |
DDB_G0275723 | DDB_G0275723 | DDB0232429 | CDS | 5987198 | 327 | - | 0.302752 | |
DDB_G0275725 | DDB_G0275725 | DDB0232429 | CDS | 5985888 | 585 | + | 0.295727 | |
DDB_G0275735 | DDB_G0275735 | DDB0232429 | CDS | 5905995 | 894 | + | 0.233781 | |
DDB_G0275737 | DDB_G0275737 | DDB0232429 | CDS | 5899852 | 2004 | + | 0.322854 | |
DDB_G0275739 | DDB_G0275739 | contains one HEAT repeat region similar to D. purpureum protein | DDB0232429 | CDS | 5887655 | 1647 | + | 0.246509 |
DDB_G0275743 | DDB_G0275743 | DDB0232429 | CDS | 5881476 | 1173 | - | 0.208866 | |
DDB_G0275747 | DDB_G0275747 | DDB0232429 | CDS | 5872794 | 2400 | - | 0.268333 | |
DDB_G0275749 | DDB_G0275749 | DDB0232429 | CDS | 5863253 | 543 | - | 0.296501 | |
DDB_G0275751 | DDB_G0275751 | belongs to the IF-2 family an essential component for the initiation of protein synthesis | DDB0232429 | CDS | 5859705 | 2979 | - | 0.335347 |
DDB_G0275755 | DDB_G0275755 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232429 | CDS | 5846616 | 597 | - | 0.274707 |
DDB_G0275757_ps | DDB_G0275757 | putative pseudogene fragment similar to D. discoideum genes | DDB0232429 | CDS | 5819427 | 213 | + | 0.206573 |
DDB_G0275761 | DDB_G0275761 | DDB0232429 | CDS | 5788919 | 219 | + | 0.269406 | |
DDB_G0275763 | DDB_G0275763 | DDB0232429 | CDS | 5779278 | 237 | + | 0.219409 | |
DDB_G0275765 | DDB_G0275765 | DDB0232429 | CDS | 5735439 | 555 | - | 0.2 | |
DDB_G0275767 | DDB_G0275767 | DDB0232429 | CDS | 5733694 | 732 | + | 0.285519 | |
DDB_G0275773 | DDB_G0275773 | DDB0232429 | CDS | 5716350 | 1488 | - | 0.261425 | |
DDB_G0275777 | DDB_G0275777 | DDB0232429 | CDS | 5681724 | 2499 | + | 0.270508 | |
DDB_G0275783 | DDB_G0275783 | contains a predicted signal anchor contains 3 coiled coil domains | DDB0232429 | CDS | 5653320 | 1734 | + | 0.252018 |
DDB_G0275785 | DDB_G0275785 | DDB0232429 | CDS | 5650203 | 2535 | - | 0.231953 | |
DDB_G0275789 | DDB_G0275789 | DDB0232429 | CDS | 5620256 | 3561 | + | 0.278012 | |
DDB_G0275791 | DDB_G0275791 | DDB0232429 | CDS | 5615906 | 603 | + | 0.230514 | |
DDB_G0275793 | DDB_G0275793 | DDB0232429 | CDS | 5611769 | 1593 | - | 0.2285 | |
DDB_G0275795 | DDB_G0275795 | DDB0232429 | CDS | 5596338 | 2427 | - | 0.301607 | |
DDB_G0275797 | DDB_G0275797 | DDB0232429 | CDS | 5595268 | 849 | + | 0.111896 | |
DDB_G0275799 | DDB_G0275799 | DDB0232429 | CDS | 5576194 | 579 | - | 0.255613 | |
DDB_G0275801 | DDB_G0275801 | contains two putative WWE domains which are predicted to mediate protein-protein interactions in ubiquitin and ADP ribose conjugation systems | DDB0232429 | CDS | 5574827 | 1152 | + | 0.263021 |
DDB_G0275803_ps | DDB_G0275803 | putative pseudogene fragment similar to D. discoideum genes | DDB0232429 | CDS | 5570659 | 1188 | + | 0.209596 |
DDB_G0275805 | DDB_G0275805 | DDB0232429 | CDS | 5565701 | 2154 | + | 0.285051 | |
DDB_G0275807 | DDB_G0275807 | DDB0232429 | CDS | 5544915 | 282 | + | 0.35461 | |
DDB_G0275813 | DDB_G0275813 | DDB0232429 | CDS | 5526799 | 2244 | - | 0.250891 | |
DDB_G0275817 | DDB_G0275817 | weakly similar to hssA2C7E family genes | DDB0232429 | CDS | 5539448 | 276 | - | 0.289855 |
DDB_G0275819 | DDB_G0275819 | weakly similar to hssA2C7E family genes | DDB0232429 | CDS | 5541223 | 291 | - | 0.381443 |
DDB_G0275821 | DDB_G0275821 | DDB0232429 | CDS | 5541988 | 2382 | - | 0.210327 | |
DDB_G0275825 | DDB_G0275825 | conserved hypothetical Dictyostelium protein contains no functional protein domains | DDB0232429 | CDS | 5559641 | 198 | + | 0.207071 |
DDB_G0275827 | DDB_G0275827 | DDB0232429 | CDS | 5560910 | 183 | + | 0.240437 | |
DDB_G0275829 | DDB_G0275829 | DDB0232429 | CDS | 5561391 | 492 | - | 0.278455 | |
DDB_G0275831 | DDB_G0275831 | DDB0232429 | CDS | 5578081 | 216 | + | 0.337963 | |
DDB_G0275835 | DDB_G0275835 | DDB0232429 | CDS | 5581974 | 819 | - | 0.29304 | |
DDB_G0275843 | DDB_G0275843 | DDB0232429 | CDS | 5657920 | 2226 | - | 0.310422 | |
DDB_G0275847 | DDB_G0275847 | belongs to the UPF0568 family homolog of human C14orf166 | DDB0232429 | CDS | 5673341 | 816 | - | 0.224265 |
DDB_G0275849 | DDB_G0275849 | conserved small protein of unknown function contains two predicted transmembrane domains | DDB0232429 | CDS | 5676909 | 297 | - | 0.289562 |
DDB_G0275851 | DDB_G0275851 | has similarity to human OS-9 a protein that might play a role in the ER-associated degradation of misfolded glycoproteins | DDB0232429 | CDS | 5678003 | 957 | + | 0.247649 |
DDB_G0275853 | DDB_G0275853 | conserved protein contains 11 putative transmembrane domains | DDB0232429 | CDS | 5691217 | 2460 | - | 0.254065 |
DDB_G0275855 | DDB_G0275855 | DDB0232429 | CDS | 5697759 | 2007 | - | 0.19432 | |
DDB_G0275859 | DDB_G0275859 | DDB0232429 | CDS | 5722920 | 873 | - | 0.243986 | |
DDB_G0275861 | DDB_G0275861 | DDB0232429 | CDS | 5745037 | 7551 | - | 0.243809 | |
DDB_G0275865 | DDB_G0275865 | DDB0232429 | CDS | 5772751 | 1584 | - | 0.351641 | |
DDB_G0275867 | DDB_G0275867 | DDB0232429 | CDS | 5776448 | 2658 | + | 0.269752 | |
DDB_G0275869 | DDB_G0275869 | DDB0232429 | CDS | 5793308 | 2625 | + | 0.211048 | |
DDB_G0275871 | DDB_G0275871 | DDB0232429 | CDS | 5796327 | 3492 | - | 0.286655 | |
DDB_G0275873 | DDB_G0275873 | DDB0232429 | CDS | 5800903 | 3873 | - | 0.288407 | |
DDB_G0275875 | DDB_G0275875 | DDB0232429 | CDS | 5828810 | 5808 | + | 0.2698 | |
DDB_G0275885 | DDB_G0275885 | DDB0232429 | CDS | 5885784 | 786 | - | 0.26972 | |
DDB_G0275889 | DDB_G0275889 | ortholog of human HPS3 mutations in human HPS3 have been linked to Hermansky-Pudlak syndrome 3 | DDB0232429 | CDS | 5924463 | 4410 | + | 0.265079 |
DDB_G0275891_ps | DDB_G0275891 | putative pseudogene member of a gene family comprising | DDB0232429 | CDS | 5929362 | 775 | + | 0.249032 |
DDB_G0275893 | DDB_G0275893 | DDB0232429 | CDS | 5930653 | 3165 | - | 0.153554 | |
DDB_G0275897 | DDB_G0275897 | putative pseudogene similar to a large gene family encoding FNIP repeat-containing proteins including | DDB0232429 | CDS | 5960620 | 2550 | + | 0.218431 |
DDB_G0275899 | DDB_G0275899 | contains 12 putative transmembrane domains similar to D. purpureum protein | DDB0232429 | CDS | 5966546 | 3738 | - | 0.277956 |
DDB_G0275901 | DDB_G0275901 | DDB0232429 | CDS | 5976071 | 207 | - | 0.280193 | |
DDB_G0275903 | DDB_G0275903 | DDB0232429 | CDS | 5981905 | 231 | - | 0.337662 | |
DDB_G0275905 | DDB_G0275905 | DDB0232429 | CDS | 5982746 | 642 | + | 0.339564 | |
DDB_G0275907_ps | DDB_G0275907 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 5996541 | 309 | + | 0.249191 |
DDB_G0275909 | DDB_G0275909 | DDB0232429 | CDS | 6013021 | 393 | - | 0.351145 | |
DDB_G0275911 | DDB_G0275911 | DDB0232429 | CDS | 6027807 | 1158 | - | 0.33247 | |
DDB_G0275913 | DDB_G0275913 | similar to bacterial acetyltransferases homolog of E. coli maa (maltose O-acetyltransferase) similar to D. purpureum protein | DDB0232429 | CDS | 6029488 | 573 | - | 0.340314 |
DDB_G0275915 | DDB_G0275915 | DDB0232429 | CDS | 6030307 | 249 | - | 0.361446 | |
DDB_G0275917 | DDB_G0275917 | DDB0232429 | CDS | 6034546 | 3069 | + | 0.289019 | |
DDB_G0275919 | DDB_G0275919 | DDB0232429 | CDS | 6037798 | 2409 | - | 0.249481 | |
DDB_G0275921 | DDB_G0275921 | DDB0232429 | CDS | 6054662 | 912 | - | 0.274123 | |
DDB_G0275923 | DDB_G0275923 | DDB0232429 | CDS | 6059162 | 501 | - | 0.219561 | |
DDB_G0275927 | DDB_G0275927 | DDB0232429 | CDS | 6071471 | 2289 | - | 0.238532 | |
DDB_G0275933 | DDB_G0275933 | homolog of S. cerevisiae CMC1 (COX assembly mitochondrial protein) which is a copper-binding protein required for mitochondrial cytochrome c oxidase assembly | DDB0232429 | CDS | 6090814 | 366 | + | 0.289617 |
DDB_G0275935 | DDB_G0275935 | DDB0232429 | CDS | 6095467 | 807 | - | 0.2057 | |
DDB_G0275937 | DDB_G0275937 | DDB0232429 | CDS | 6099175 | 3813 | + | 0.199056 | |
DDB_G0275941_RTE | DDB_G0275941 | DDB0232429 | CDS | 6128275 | 435 | + | 0.317241 | |
DDB_G0275943_RTE | DDB_G0275943 | DDB0232429 | CDS | 6128899 | 2625 | + | 0.322286 | |
DDB_G0275945_RTE | DDB_G0275945 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 6133220 | 642 | + | 0.277259 |
DDB_G0275947_RTE | DDB_G0275947 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 6134212 | 2175 | + | 0.324138 |
DDB_G0275949 | DDB_G0275949 | DDB0232429 | CDS | 5502985 | 459 | - | 0.305011 | |
DDB_G0275951 | DDB_G0275951 | DDB0232429 | CDS | 5814130 | 711 | + | 0.341772 | |
DDB_G0275953 | DDB_G0275953 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232429 | CDS | 6210610 | 1044 | - | 0.272031 |
DDB_G0275959 | DDB_G0275959 | DDB0232429 | CDS | 6214903 | 744 | + | 0.293011 | |
DDB_G0275961 | DDB_G0275961 | DDB0232429 | CDS | 6217776 | 1287 | - | 0.190365 | |
DDB_G0275963 | DDB_G0275963 | DDB0232429 | CDS | 6216012 | 1407 | - | 0.170576 | |
DDB_G0275965 | DDB_G0275965 | DDB0232429 | CDS | 6213523 | 198 | + | 0.222222 | |
DDB_G0275967 | DDB_G0275967 | DDB0232429 | CDS | 6187951 | 1914 | - | 0.283699 | |
DDB_G0275971 | DDB_G0275971 | DDB0232429 | CDS | 6175233 | 2100 | + | 0.335714 | |
DDB_G0275973 | DDB_G0275973 | DDB0232429 | CDS | 6173352 | 666 | + | 0.27027 | |
DDB_G0275975 | DDB_G0275975 | DDB0232429 | CDS | 6165066 | 231 | - | 0.367965 | |
DDB_G0275981 | DDB_G0275981 | DDB0232429 | CDS | 6148751 | 1635 | + | 0.301529 | |
DDB_G0275987 | DDB_G0275987 | DDB0232429 | CDS | 6143298 | 1053 | + | 0.235518 | |
DDB_G0275989 | DDB_G0275989 | DDB0232429 | CDS | 6141360 | 1203 | + | 0.212801 | |
DDB_G0275991 | DDB_G0275991 | DDB0232429 | CDS | 6139718 | 1047 | - | 0.230181 | |
DDB_G0275993 | DDB_G0275993 | DDB0232429 | CDS | 6150629 | 687 | - | 0.227074 | |
DDB_G0275995_ps | DDB_G0275995 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 6156043 | 645 | - | 0.207752 |
DDB_G0275997 | DDB_G0275997 | DDB0232429 | CDS | 6157246 | 948 | - | 0.200422 | |
DDB_G0276001 | DDB_G0276001 | DDB0232429 | CDS | 6162439 | 168 | - | 0.208333 | |
DDB_G0276005 | DDB_G0276005 | DDB0232429 | CDS | 6165936 | 5955 | - | 0.213602 | |
DDB_G0276007 | DDB_G0276007 | DDB0232429 | CDS | 6178436 | 639 | + | 0.27543 | |
DDB_G0276009_RTE | DDB_G0276009 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232429 | CDS | 6182669 | 1770 | + | 0.269492 |
DDB_G0276011_RTE | DDB_G0276011 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 6185531 | 1335 | - | 0.305618 |
DDB_G0276013 | DDB_G0276013 | DDB0232429 | CDS | 6191275 | 2247 | - | 0.304406 | |
DDB_G0276015 | DDB_G0276015 | DDB0232429 | CDS | 6195575 | 1545 | - | 0.264725 | |
DDB_G0276017 | DDB_G0276017 | DDB0232429 | CDS | 6201276 | 1317 | + | 0.23918 | |
DDB_G0276021 | DDB_G0276021 | DDB0232429 | CDS | 6219625 | 314 | - | 0.171975 | |
DDB_G0276029 | DDB_G0276029 | putative ortholog of H. sapiens CNOT1 and S. cerevisiae CDC39 REMI mutant forms aberrant fruiting bodies (see | DDB0232429 | CDS | 6435703 | 7581 | - | 0.303654 |
DDB_G0276031 | DDB_G0276031 | similar human THO complex subunit 3 (THOC3) although D. discoideum seems to be lacking THOC4 and THOC5 | DDB0232429 | CDS | 6461770 | 1437 | + | 0.302714 |
DDB_G0276035 | DDB_G0276035 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232429 | CDS | 6541243 | 4131 | - | 0.255628 |
DDB_G0276037 | DDB_G0276037 | DDB0232429 | CDS | 6539160 | 1020 | + | 0.269608 | |
DDB_G0276039 | DDB_G0276039 | DDB0232429 | CDS | 6521223 | 906 | - | 0.282561 | |
DDB_G0276045 | DDB_G0276045 | DDB0232429 | CDS | 6496624 | 900 | + | 0.3 | |
DDB_G0276047 | DDB_G0276047 | DDB0232429 | CDS | 6489001 | 6693 | - | 0.262812 | |
DDB_G0276049 | DDB_G0276049 | weakly similar to NLPP60 domain-containing proteins bacterial cell wall-associated hydrolases | DDB0232429 | CDS | 6486635 | 789 | - | 0.434727 |
DDB_G0276051 | DDB_G0276051 | DDB0232429 | CDS | 6484404 | 1062 | + | 0.231638 | |
DDB_G0276057 | DDB_G0276057 | DDB0232429 | CDS | 6469384 | 1623 | - | 0.32902 | |
DDB_G0276059 | DDB_G0276059 | DDB0232429 | CDS | 6468555 | 675 | + | 0.183704 | |
DDB_G0276061 | DDB_G0276061 | DDB0232429 | CDS | 6465016 | 411 | - | 0.250608 | |
DDB_G0276063 | DDB_G0276063 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232429 | CDS | 6452850 | 243 | - | 0.300412 |
DDB_G0276065 | DDB_G0276065 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub | DDB0232429 | CDS | 6450283 | 1887 | - | 0.327504 |
DDB_G0276075 | DDB_G0276075 | DDB0232429 | CDS | 6429266 | 1113 | + | 0.297394 | |
DDB_G0276081 | DDB_G0276081 | DDB0232429 | CDS | 6421444 | 771 | - | 0.207523 | |
DDB_G0276085 | DDB_G0276085 | DDB0232429 | CDS | 6360342 | 2439 | + | 0.242722 | |
DDB_G0276087 | DDB_G0276087 | DDB0232429 | CDS | 6358797 | 1230 | + | 0.279675 | |
DDB_G0276089 | DDB_G0276089 | DDB0232429 | CDS | 6350255 | 4890 | - | 0.274847 | |
DDB_G0276093 | DDB_G0276093 | DDB0232429 | CDS | 6339087 | 2487 | + | 0.198633 | |
DDB_G0276095 | DDB_G0276095 | DDB0232429 | CDS | 6333535 | 1317 | + | 0.312073 | |
DDB_G0276097 | DDB_G0276097 | DDB0232429 | CDS | 6328288 | 1701 | + | 0.284539 | |
DDB_G0276099 | DDB_G0276099 | DDB0232429 | CDS | 6326680 | 1020 | + | 0.32549 | |
DDB_G0276107 | DDB_G0276107 | DDB0232429 | CDS | 6288449 | 2145 | - | 0.257809 | |
DDB_G0276109 | DDB_G0276109 | contains one MPPN (mitotic phosphoprotein N' end) domain | DDB0232429 | CDS | 6272283 | 1569 | - | 0.268961 |
DDB_G0276111 | DDB_G0276111 | DDB0232429 | CDS | 6270826 | 1248 | + | 0.308494 | |
DDB_G0276113 | DDB_G0276113 | DDB0232429 | CDS | 6269416 | 717 | - | 0.260809 | |
DDB_G0276117 | DDB_G0276117 | DDB0232429 | CDS | 6262508 | 615 | - | 0.21626 | |
DDB_G0276121 | DDB_G0276121 | DDB0232429 | CDS | 6256669 | 2142 | + | 0.339869 | |
DDB_G0276123 | DDB_G0276123 | DDB0232429 | CDS | 6255698 | 267 | + | 0.131086 | |
DDB_G0276125 | DDB_G0276125 | DDB0232429 | CDS | 6248649 | 4017 | - | 0.301718 | |
DDB_G0276127 | DDB_G0276127 | DDB0232429 | CDS | 6247229 | 513 | + | 0.183236 | |
DDB_G0276131 | DDB_G0276131 | DDB0232429 | CDS | 6243302 | 1089 | + | 0.274564 | |
DDB_G0276133 | DDB_G0276133 | DDB0232429 | CDS | 6240850 | 1905 | + | 0.212073 | |
DDB_G0276135 | DDB_G0276135 | DDB0232429 | CDS | 6238985 | 918 | + | 0.237473 | |
DDB_G0276139 | DDB_G0276139 | DDB0232429 | CDS | 6226640 | 396 | - | 0.335859 | |
DDB_G0276145 | DDB_G0276145 | DDB0232429 | CDS | 6522877 | 678 | + | 0.29056 | |
DDB_G0276147 | DDB_G0276147 | DDB0232429 | CDS | 6401716 | 2943 | - | 0.251104 | |
DDB_G0276151 | DDB_G0276151 | belongs to the crotonase superfamily conserved in bacteria contains a predicted peroxisomal targeting signal | DDB0232429 | CDS | 6392232 | 816 | - | 0.270833 |
DDB_G0276161 | DDB_G0276161 | DDB0232429 | CDS | 6225937 | 156 | - | 0.230769 | |
DDB_G0276165 | DDB_G0276165 | DDB0232429 | CDS | 6540411 | 183 | - | 0.306011 | |
DDB_G0276167 | DDB_G0276167 | DDB0232429 | CDS | 6516957 | 1107 | - | 0.252033 | |
DDB_G0276169 | DDB_G0276169 | similar to S. cerevisiae MSP1 a mitochondrial protein involved in sorting of proteins in the mitochondria | DDB0232429 | CDS | 6497773 | 993 | + | 0.286002 |
DDB_G0276171_RTE | DDB_G0276171 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6476907 | 3180 | - | 0.350629 |
DDB_G0276173 | DDB_G0276173 | DDB0232429 | CDS | 6466369 | 390 | + | 0.25641 | |
DDB_G0276179 | DDB_G0276179 | contains a predicted signal peptide weakly similar to DDB_G0272504 | DDB0232429 | CDS | 6427907 | 684 | + | 0.248538 |
DDB_G0276181 | DDB_G0276181 | member of the TKL (tyrosine kinase-like) group of protein kinases contains a PH (pleckstrin homology) domain | DDB0232429 | CDS | 6410071 | 4668 | - | 0.262853 |
DDB_G0276183 | DDB_G0276183 | DDB0232429 | CDS | 6408604 | 687 | - | 0.227074 | |
DDB_G0276189 | DDB_G0276189 | DDB0232429 | CDS | 6390838 | 966 | + | 0.246377 | |
DDB_G0276193 | DDB_G0276193 | contains repeats found in several Chlamydia polymorphic membrane proteins has a signal peptide and a carboxy-terminus transmembrane domain | DDB0232429 | CDS | 6387804 | 1563 | - | 0.307102 |
DDB_G0276195_RTE | DDB_G0276195 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 6384158 | 1365 | - | 0.310623 |
DDB_G0276197_RTE | DDB_G0276197 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 6380617 | 3435 | - | 0.346143 |
DDB_G0276201_RTE | DDB_G0276201 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 6378549 | 450 | - | 0.386667 |
DDB_G0276203 | DDB_G0276203 | DDB0232429 | CDS | 6376612 | 1212 | - | 0.271452 | |
DDB_G0276205 | DDB_G0276205 | DDB0232429 | CDS | 6371487 | 1500 | - | 0.299333 | |
DDB_G0276209_RTE | DDB_G0276209 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 6365054 | 1335 | + | 0.307865 |
DDB_G0276211_RTE | DDB_G0276211 | DDB0232429 | CDS | 6363456 | 912 | - | 0.367325 | |
DDB_G0276213 | DDB_G0276213 | DDB0232429 | CDS | 6356046 | 1407 | + | 0.187633 | |
DDB_G0276215 | DDB_G0276215 | DDB0232429 | CDS | 6342811 | 1947 | + | 0.313303 | |
DDB_G0276217 | DDB_G0276217 | DDB0232429 | CDS | 6335483 | 171 | - | 0.222222 | |
DDB_G0276219 | DDB_G0276219 | DDB0232429 | CDS | 6331145 | 1635 | + | 0.310092 | |
DDB_G0276223 | DDB_G0276223 | DDB0232429 | CDS | 6263547 | 2046 | + | 0.319159 | |
DDB_G0276225 | DDB_G0276225 | similar to yeast ERG28 an endoplasmic reticulum protein involved in ergosterol biosynthesis contains 4 putative transmembrane domains | DDB0232429 | CDS | 6247906 | 372 | - | 0.255376 |
DDB_G0276227 | DDB_G0276227 | DDB0232429 | CDS | 6222654 | 2514 | + | 0.239061 | |
DDB_G0276231 | DDB_G0276231 | DDB0232429 | CDS | 6232165 | 156 | + | 0.294872 | |
DDB_G0276235 | DDB_G0276235 | DDB0232429 | CDS | 6281262 | 669 | - | 0.209268 | |
DDB_G0276237 | DDB_G0276237 | DDB0232429 | CDS | 6306373 | 1077 | + | 0.275766 | |
DDB_G0276239 | DDB_G0276239 | involved in vesicle-mediated transport similar to VPS33 | DDB0232429 | CDS | 6373737 | 2577 | - | 0.217307 |
DDB_G0276243 | DDB_G0276243 | contains one DUF1620 domain homolog of human KIAA0090 (uncharacterized protein KIAA0090) contains 2 putative transmembrane domains | DDB0232429 | CDS | 6418177 | 2973 | + | 0.263707 |
DDB_G0276245 | DDB_G0276245 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub | DDB0232429 | CDS | 6454072 | 1890 | - | 0.32381 |
DDB_G0276247 | DDB_G0276247 | DDB0232429 | CDS | 6464158 | 246 | - | 0.296748 | |
DDB_G0276249_RTE | DDB_G0276249 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6480611 | 1080 | - | 0.415741 |
DDB_G0276251 | DDB_G0276251 | similar to H. sapiens GP17 involved in modification of glycosylphosphatidylinositol contains 16 transmembrane domains | DDB0232429 | CDS | 6500338 | 4329 | + | 0.260799 |
DDB_G0276253 | DDB_G0276253 | a bifunctional enzyme that catalyses both the synthesis and the degradation of fructose-2 6-bisphosphate | DDB0232429 | CDS | 6504888 | 1527 | - | 0.301899 |
DDB_G0276255 | DDB_G0276255 | DDB0232429 | CDS | 6507776 | 2526 | - | 0.291766 | |
DDB_G0276257 | DDB_G0276257 | DDB0232429 | CDS | 6527471 | 1245 | - | 0.203213 | |
DDB_G0276259 | DDB_G0276259 | contains 5 predicted transmembrane domains and an additional putative signal sequence similar to D. purpureum protein | DDB0232429 | CDS | 6529676 | 1119 | - | 0.280608 |
DDB_G0276263 | DDB_G0276263 | DDB0232429 | CDS | 6536235 | 2286 | + | 0.209099 | |
DDB_G0276265 | DDB_G0276265 | DDB0232429 | CDS | 6220039 | 1884 | - | 0.165605 | |
DDB_G0276271 | DDB_G0276271 | DDB0232429 | CDS | 6637140 | 1641 | - | 0.203534 | |
DDB_G0276275 | DDB_G0276275 | DDB0232429 | CDS | 6628998 | 735 | + | 0.27619 | |
DDB_G0276277 | DDB_G0276277 | DDB0232429 | CDS | 6627741 | 690 | + | 0.32029 | |
DDB_G0276279 | DDB_G0276279 | DDB0232429 | CDS | 6610188 | 1089 | + | 0.331497 | |
DDB_G0276281 | DDB_G0276281 | DDB0232429 | CDS | 6608304 | 1032 | - | 0.223837 | |
DDB_G0276285 | DDB_G0276285 | DDB0232429 | CDS | 6594215 | 1878 | + | 0.367945 | |
DDB_G0276289 | DDB_G0276289 | DDB0232429 | CDS | 6570030 | 492 | - | 0.193089 | |
DDB_G0276291 | DDB_G0276291 | DDB0232429 | CDS | 6564892 | 399 | + | 0.290727 | |
DDB_G0276293 | DDB_G0276293 | DDB0232429 | CDS | 6559102 | 1473 | - | 0.304141 | |
DDB_G0276297 | DDB_G0276297 | DDB0232429 | CDS | 6556293 | 1056 | + | 0.294508 | |
DDB_G0276303 | DDB_G0276303 | contains weak similarity to EGF-like domain contains both a predicted N-terminal signal sequence and C-terminal transmembrane domain | DDB0232429 | CDS | 6614400 | 4248 | - | 0.274011 |
DDB_G0276305 | DDB_G0276305 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232429 | CDS | 6612090 | 1878 | + | 0.356762 |
DDB_G0276307 | DDB_G0276307 | DDB0232429 | CDS | 6603655 | 4431 | - | 0.183029 | |
DDB_G0276309 | DDB_G0276309 | DDB0232429 | CDS | 6597404 | 2169 | + | 0.320424 | |
DDB_G0276313_RTE | DDB_G0276313 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6573478 | 3180 | + | 0.349686 |
DDB_G0276315 | DDB_G0276315 | DDB0232429 | CDS | 6552432 | 276 | - | 0.300725 | |
DDB_G0276317 | DDB_G0276317 | DDB0232429 | CDS | 6561863 | 1794 | + | 0.27146 | |
DDB_G0276321 | DDB_G0276321 | similar to mammalian SA hypertension-associated homolog and to acetoacetyl-CoA synthetases which catalyze the first step of the mevalonate pathway of isoprenoid biosynthesis via isopentenyl diphosphate | DDB0232429 | CDS | 6567409 | 1914 | - | 0.263323 |
DDB_G0276323_RTE | DDB_G0276323 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6571874 | 1080 | + | 0.417593 |
DDB_G0276325 | DDB_G0276325 | DDB0232429 | CDS | 6633638 | 3012 | + | 0.255312 | |
DDB_G0276327 | DDB_G0276327 | DDB0232429 | CDS | 6639378 | 378 | - | 0.396825 | |
DDB_G0276329_RTE | DDB_G0276329 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6641376 | 248 | + | 0.415323 |
DDB_G0276337 | DDB_G0276337 | DDB0232429 | CDS | 6659047 | 1791 | + | 0.269123 | |
DDB_G0276339_ps | DDB_G0276339 | putative pseudogene similar to | DDB0232429 | CDS | 6661296 | 507 | - | 0.353057 |
DDB_G0276347 | DDB_G0276347 | DDB0232429 | CDS | 6697417 | 1071 | + | 0.288515 | |
DDB_G0276351 | DDB_G0276351 | similar to bacterial glutathione S-transferase catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 6703448 | 693 | + | 0.292929 |
DDB_G0276361 | DDB_G0276361 | DDB0232429 | CDS | 6745195 | 2370 | + | 0.332489 | |
DDB_G0276365 | DDB_G0276365 | has similarity to H. sapiens di-N-acetylchitobiase (CBTS) a hydrolase involved in the degradation of asparagine-linked glycoproteins contains a putative N-terminal signal sequence | DDB0232429 | CDS | 6760197 | 1110 | + | 0.236937 |
DDB_G0276367 | DDB_G0276367 | DDB0232429 | CDS | 6761550 | 1095 | + | 0.260274 | |
DDB_G0276375 | DDB_G0276375 | DDB0232429 | CDS | 6671139 | 3804 | - | 0.226078 | |
DDB_G0276379 | DDB_G0276379 | DDB0232429 | CDS | 6705904 | 168 | - | 0.196429 | |
DDB_G0276381 | DDB_G0276381 | DDB0232429 | CDS | 6722202 | 651 | + | 0.274962 | |
DDB_G0276383 | DDB_G0276383 | DDB0232429 | CDS | 6735925 | 6081 | + | 0.258017 | |
DDB_G0276387_RTE | DDB_G0276387 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6642428 | 3066 | + | 0.351598 |
DDB_G0276389 | DDB_G0276389 | DDB0232429 | CDS | 6651958 | 3864 | + | 0.219203 | |
DDB_G0276391_ps | DDB_G0276391 | putative pseudogene EGF family protein | DDB0232429 | CDS | 6666022 | 1131 | + | 0.274978 |
DDB_G0276393 | DDB_G0276393 | DDB0232429 | CDS | 6724904 | 867 | + | 0.362168 | |
DDB_G0276397_RTE | DDB_G0276397 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6767487 | 1012 | + | 0.413043 |
DDB_G0276401 | DDB_G0276401 | DDB0232429 | CDS | 6789174 | 3075 | + | 0.225691 | |
DDB_G0276403 | DDB_G0276403 | DDB0232429 | CDS | 6815001 | 3129 | + | 0.240652 | |
DDB_G0276407 | DDB_G0276407 | DDB0232429 | CDS | 6832640 | 1236 | + | 0.279935 | |
DDB_G0276409_ps | DDB_G0276409 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 6834384 | 3207 | - | 0.228874 |
DDB_G0276413 | DDB_G0276413 | conserved protein ortholog or HEATR3 (HEAT repeat containing 3) | DDB0232429 | CDS | 6843825 | 2151 | + | 0.234775 |
DDB_G0276419 | DDB_G0276419 | DDB0232429 | CDS | 6871013 | 495 | - | 0.264646 | |
DDB_G0276421 | DDB_G0276421 | DDB0232429 | CDS | 6881042 | 138 | + | 0.318841 | |
DDB_G0276429 | DDB_G0276429 | DDB0232429 | CDS | 6932540 | 1422 | - | 0.270042 | |
DDB_G0276431 | DDB_G0276431 | DDB0232429 | CDS | 6930950 | 1182 | + | 0.318951 | |
DDB_G0276433 | DDB_G0276433 | DDB0232429 | CDS | 6921413 | 147 | + | 0.380952 | |
DDB_G0276435 | DDB_G0276435 | DDB0232429 | CDS | 6919395 | 1287 | - | 0.20979 | |
DDB_G0276437 | DDB_G0276437 | DDB0232429 | CDS | 6910190 | 1881 | - | 0.267943 | |
DDB_G0276439 | DDB_G0276439 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide has similarity to D. discoideum counting factor components cf50 and cf45-1. | DDB0232429 | CDS | 6954075 | 1443 | + | 0.383229 |
DDB_G0276445 | DDB_G0276445 | highly similar to human HSPA5 (78 kDa glucose-regulated protein precursor GRP78) contains a predicted endoplasmic reticulum targeting sequence | DDB0232429 | CDS | 6984336 | 1977 | - | 0.373293 |
DDB_G0276447 | DDB_G0276447 | has a BAR domain at the N terminus and a DNAJ heat shock N-terminal domain at the carboxyl domain shares a short region of similarity with plant auxilin-like protein a heat shock protein binding | DDB0232429 | CDS | 6979797 | 2193 | + | 0.302782 |
DDB_G0276449 | DDB_G0276449 | DDB0232429 | CDS | 6977542 | 1206 | - | 0.254561 | |
DDB_G0276451 | DDB_G0276451 | bCommunity annotation:b DDB_G0276451 has only one recognizable blast hit outside the Amebozoans this is to the proapoptotic protein SIVA. The homology is weak but when vertebrate SIVA is blasted back to Dicty DDB_G0276451 is the only hit. SIVA is a suspected transcriptional target of E2F1 [Fortin et al Journal of Biological Chemistry 279 28706-28714 (2004)]. E2F1 is well known to be bound and inactivated by the retinoblastoma protein. Interestingly DDB_G0276451 is tenfold overexpressed in a Dicty strain lacking the Dicty retinoblastoma homologue (p4e-15). This suggests that DDB_G0276451 is also a direct or indirect E2F target in Dicty. The promoter contains the 8-mer CCCGCCAA which is roughly 20-fold enriched in the promoters of rblA-repressed genes (p2e-13). In Dicty multicellular development DDB_G0276451 shows an expression trajectory (see DictyExpress) which is highly typical of rblA-repressed putative cell-cycle regulated genes. Harry MacWilliams May 2010br | DDB0232429 | CDS | 6974621 | 537 | - | 0.242086 |
DDB_G0276461 | DDB_G0276461 | putative protein serinethreonine kinase similar to the kinase domains of AAK1 (AP2 associated kinase) and BMP-inducible protein kinase (BIKe) | DDB0232429 | CDS | 6904331 | 2397 | - | 0.267418 |
DDB_G0276467 | DDB_G0276467 | DDB0232429 | CDS | 6988198 | 168 | + | 0.142857 | |
DDB_G0276471 | DDB_G0276471 | DDB0232429 | CDS | 7014397 | 315 | + | 0.273016 | |
DDB_G0276473 | DDB_G0276473 | DDB0232429 | CDS | 7015380 | 1092 | - | 0.340659 | |
DDB_G0276477 | DDB_G0276477 | DDB0232429 | CDS | 7025054 | 246 | - | 0.48374 | |
DDB_G0276483 | DDB_G0276483 | DDB0232429 | CDS | 6787819 | 789 | - | 0.217997 | |
DDB_G0276485 | DDB_G0276485 | DDB0232429 | CDS | 6809778 | 1221 | - | 0.2457 | |
DDB_G0276489 | DDB_G0276489 | contains 1 RING-type zinc finger contains one putative transmembrane domain similar to human ZFPL1 (zinc finger protein-like 1) | DDB0232429 | CDS | 6853485 | 1065 | - | 0.25446 |
DDB_G0276495_RTE | DDB_G0276495 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 6863657 | 561 | + | 0.351159 |
DDB_G0276497 | DDB_G0276497 | DDB0232429 | CDS | 6865567 | 387 | - | 0.242894 | |
DDB_G0276499 | DDB_G0276499 | DDB0232429 | CDS | 6893167 | 177 | + | 0.214689 | |
DDB_G0276501_ps | DDB_G0276501 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 6893904 | 219 | + | 0.242009 |
DDB_G0276503 | DDB_G0276503 | very similar to the H. sapiens PISD a mitochondrial proenzyme that is cleaved into a phosphatidylserine decarboxylase alpha and beta chain contains one putative transmembrane domain | DDB0232429 | CDS | 6908594 | 1200 | + | 0.291667 |
DDB_G0276505 | DDB_G0276505 | DDB0232429 | CDS | 6923091 | 159 | + | 0.358491 | |
DDB_G0276507 | DDB_G0276507 | DDB0232429 | CDS | 6925108 | 138 | + | 0.355072 | |
DDB_G0276509 | DDB_G0276509 | DDB0232429 | CDS | 6935162 | 1101 | + | 0.173479 | |
DDB_G0276511 | DDB_G0276511 | DDB0232429 | CDS | 6982368 | 492 | - | 0.050813 | |
DDB_G0276513 | DDB_G0276513 | DDB0232429 | CDS | 6983477 | 363 | - | 0.391185 | |
DDB_G0276515 | DDB_G0276515 | DDB0232429 | CDS | 6990870 | 1176 | + | 0.221088 | |
DDB_G0276517_ps | DDB_G0276517 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 7006417 | 504 | - | 0.230159 |
DDB_G0276521 | DDB_G0276521 | DDB0232429 | CDS | 7012325 | 300 | - | 0.3 | |
DDB_G0276523 | DDB_G0276523 | MBOAT family protein membrane proteins that contains a variety of acyltransferase enzymes contains 8 predicted transmembrane domains | DDB0232429 | CDS | 7020725 | 1557 | - | 0.242775 |
DDB_G0276525_RTE | DDB_G0276525 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6769215 | 756 | - | 0.407407 |
DDB_G0276527 | DDB_G0276527 | contains 3 major domains: one RCC1 domain one protein kinase domain and one HECT domain N-terminal region beongs to the SerThr protein kinase family C-terminal region belongs to the CAMK SerThr protein kinase family. | DDB0232429 | CDS | 6772155 | 5664 | - | 0.240643 |
DDB_G0276529 | DDB_G0276529 | DDB0232429 | CDS | 6780883 | 6480 | + | 0.268519 | |
DDB_G0276531 | DDB_G0276531 | similar to elaC and TRZ a zinc phosphodiesterase with tRNA 3'-processing endonuclease activity and probably involved in tRNA maturation by removing a 3'-trailer from precursor tRNAbrbr bCommunity annotation:b similar to elaC an endoribonuclease conserved from bacteria to humans sequence variants of which are associated with aggressive prostate cancer. Nothing seems to be known about the connection between elaC and cell proliferation. The possible involvement of the Dicty gene in cell cycle control is suggested by its 34-fold overexpression in a Dicty strain lacking the retinoblastoma like gene | DDB0232429 | CDS | 6795915 | 2871 | - | 0.27621 |
DDB_G0276533 | DDB_G0276533 | DDB0232429 | CDS | 6804850 | 624 | - | 0.205128 | |
DDB_G0276535 | DDB_G0276535 | DDB0232429 | CDS | 6806163 | 1224 | - | 0.172386 | |
DDB_G0276537 | DDB_G0276537 | DDB0232429 | CDS | 6807798 | 348 | + | 0.232759 | |
DDB_G0276539_ps | DDB_G0276539 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 6811793 | 2388 | + | 0.236181 |
DDB_G0276541 | DDB_G0276541 | DDB0232429 | CDS | 6819663 | 5490 | - | 0.298725 | |
DDB_G0276543 | DDB_G0276543 | DDB0232429 | CDS | 6826555 | 2451 | + | 0.286822 | |
DDB_G0276545 | DDB_G0276545 | DDB0232429 | CDS | 6829983 | 1032 | - | 0.293605 | |
DDB_G0276547_ps | DDB_G0276547 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 6839123 | 3543 | - | 0.223539 |
DDB_G0276549 | DDB_G0276549 | DDB0232429 | CDS | 6867377 | 2568 | + | 0.253505 | |
DDB_G0276551 | DDB_G0276551 | protein family conserved in protozoans fungi and invertebrate animals | DDB0232429 | CDS | 6872132 | 2250 | + | 0.230667 |
DDB_G0276553 | DDB_G0276553 | DDB0232429 | CDS | 6875533 | 2703 | + | 0.260451 | |
DDB_G0276555 | DDB_G0276555 | DDB0232429 | CDS | 6885788 | 2436 | + | 0.204844 | |
DDB_G0276557 | DDB_G0276557 | DDB0232429 | CDS | 6896381 | 705 | + | 0.300709 | |
DDB_G0276559 | DDB_G0276559 | DDB0232429 | CDS | 6897934 | 4848 | + | 0.229992 | |
DDB_G0276563 | DDB_G0276563 | DDB0232429 | CDS | 6929458 | 600 | - | 0.25 | |
DDB_G0276565_RTE | DDB_G0276565 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 6947282 | 684 | - | 0.334795 |
DDB_G0276567 | DDB_G0276567 | homolog of S. cerevisiae CDC50 (cell division control protein 50) which is required for polarized cell growth contains two putative transmembrane domains | DDB0232429 | CDS | 6951075 | 939 | - | 0.292865 |
DDB_G0276569 | DDB_G0276569 | DDB0232429 | CDS | 6958359 | 1176 | + | 0.234694 | |
DDB_G0276573 | DDB_G0276573 | DDB0232429 | CDS | 6975985 | 1146 | + | 0.271379 | |
DDB_G0276581 | DDB_G0276581 | DDB0232429 | CDS | 7007643 | 1668 | + | 0.220624 | |
DDB_G0276583 | DDB_G0276583 | DDB0232429 | CDS | 7017424 | 2673 | - | 0.171343 | |
DDB_G0276585 | DDB_G0276585 | DDB0232429 | CDS | 7027413 | 162 | - | 0.197531 | |
DDB_G0276589 | DDB_G0276589 | DDB0232429 | CDS | 7029406 | 174 | - | 0.212644 | |
DDB_G0276591 | DDB_G0276591 | DDB0232429 | CDS | 7030998 | 162 | - | 0.203704 | |
DDB_G0276593 | DDB_G0276593 | DDB0232429 | CDS | 7042853 | 741 | - | 0.287449 | |
DDB_G0276595 | DDB_G0276595 | DDB0232429 | CDS | 7041687 | 171 | - | 0.210526 | |
DDB_G0276597 | DDB_G0276597 | DDB0232429 | CDS | 7040401 | 741 | - | 0.294197 | |
DDB_G0276599 | DDB_G0276599 | DDB0232429 | CDS | 7039288 | 171 | - | 0.192982 | |
DDB_G0276601 | DDB_G0276601 | DDB0232429 | CDS | 7037927 | 741 | - | 0.2861 | |
DDB_G0276603 | DDB_G0276603 | DDB0232429 | CDS | 7035596 | 741 | - | 0.292848 | |
DDB_G0276605 | DDB_G0276605 | DDB0232429 | CDS | 7032998 | 171 | - | 0.204678 | |
DDB_G0276609 | DDB_G0276609 | DDB0232429 | CDS | 7034410 | 171 | - | 0.210526 | |
DDB_G0276611 | DDB_G0276611 | DDB0232429 | CDS | 7044161 | 124 | - | 0.225806 | |
DDB_G0276613 | DDB_G0276613 | identical to | DDB0232429 | CDS | 7074258 | 162 | + | 0.209877 |
DDB_G0276619 | DDB_G0276619 | DDB0232429 | CDS | 7045093 | 165 | - | 0.193939 | |
DDB_G0276621 | DDB_G0276621 | DDB0232429 | CDS | 7046443 | 168 | + | 0.160714 | |
DDB_G0276623 | DDB_G0276623 | DDB0232429 | CDS | 7051390 | 537 | - | 0.320298 | |
DDB_G0276625 | DDB_G0276625 | belongs to the drugmetabolite transporter superfamily similar to human SLC35D1 (UDP-glucuronic acidUDP-N-acetylgalactosamine transporter) and S. cerevisiae VRG4 (GDP-mannose transporter 1) contains 8 putative transmembrane domains | DDB0232429 | CDS | 7055459 | 945 | - | 0.271958 |
DDB_G0276627 | DDB_G0276627 | DDB0232429 | CDS | 7057900 | 1218 | + | 0.267652 | |
DDB_G0276629 | DDB_G0276629 | DDB0232429 | CDS | 7059622 | 129 | - | 0.20155 | |
DDB_G0276631 | DDB_G0276631 | DDB0232429 | CDS | 7060113 | 948 | + | 0.227848 | |
DDB_G0276633 | DDB_G0276633 | DDB0232429 | CDS | 7061709 | 2496 | + | 0.262019 | |
DDB_G0276635 | DDB_G0276635 | DDB0232429 | CDS | 7072784 | 162 | - | 0.209877 | |
DDB_G0276637 | DDB_G0276637 | DDB0232429 | CDS | 7072164 | 174 | + | 0.281609 | |
DDB_G0276639 | DDB_G0276639 | DDB0232429 | CDS | 7070220 | 162 | - | 0.185185 | |
DDB_G0276641 | DDB_G0276641 | DDB0232429 | CDS | 7069335 | 165 | - | 0.230303 | |
DDB_G0276643 | DDB_G0276643 | DDB0232429 | CDS | 7068237 | 165 | + | 0.266667 | |
DDB_G0276645_TE | DDB_G0276645 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232429 | CDS | 7066186 | 1719 | - | 0.315881 |
DDB_G0276647_TE | DDB_G0276647 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232429 | CDS | 7065552 | 231 | - | 0.277056 |
DDB_G0276649 | DDB_G0276649 | DDB0232429 | CDS | 7044385 | 162 | + | 0.228395 | |
DDB_G0276651 | DDB_G0276651 | DDB0232429 | CDS | 7078494 | 162 | - | 0.222222 | |
DDB_G0276653 | DDB_G0276653 | DDB0232429 | CDS | 7079602 | 180 | + | 0.166667 | |
DDB_G0276655 | DDB_G0276655 | DDB0232429 | CDS | 7080607 | 159 | + | 0.207547 | |
DDB_G0276659_ps | DDB_G0276659 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 7086569 | 1761 | + | 0.232822 |
DDB_G0276661 | DDB_G0276661 | DDB0232429 | CDS | 7093016 | 1377 | + | 0.312273 | |
DDB_G0276663 | DDB_G0276663 | DDB0232429 | CDS | 7094813 | 2835 | - | 0.292064 | |
DDB_G0276665_ps | DDB_G0276665 | putative pseudogene fragment similar to | DDB0232429 | CDS | 7099421 | 345 | + | 0.336232 |
DDB_G0276671 | DDB_G0276671 | DDB0232429 | CDS | 7101219 | 996 | + | 0.216867 | |
DDB_G0276673 | DDB_G0276673 | DDB0232429 | CDS | 7102352 | 3360 | - | 0.269345 | |
DDB_G0276675 | DDB_G0276675 | DDB0232429 | CDS | 7106291 | 906 | + | 0.246137 | |
DDB_G0276677 | DDB_G0276677 | DDB0232429 | CDS | 7107804 | 3117 | + | 0.278473 | |
DDB_G0276679 | DDB_G0276679 | DDB0232429 | CDS | 7116545 | 354 | - | 0.299435 | |
DDB_G0276681 | DDB_G0276681 | DDB0232429 | CDS | 7117771 | 2307 | + | 0.29042 | |
DDB_G0276683 | DDB_G0276683 | DDB0232429 | CDS | 7120524 | 708 | + | 0.299435 | |
DDB_G0276685 | DDB_G0276685 | DDB0232429 | CDS | 7126405 | 219 | + | 0.406393 | |
DDB_G0276687 | DDB_G0276687 | DDB0232429 | CDS | 7127174 | 222 | - | 0.400901 | |
DDB_G0276689 | DDB_G0276689 | DDB0232429 | CDS | 7128289 | 8319 | - | 0.221661 | |
DDB_G0276693 | DDB_G0276693 | DDB0232429 | CDS | 7140104 | 1005 | + | 0.2 | |
DDB_G0276695 | DDB_G0276695 | DDB0232429 | CDS | 7141543 | 1941 | + | 0.301391 | |
DDB_G0276697 | DDB_G0276697 | DDB0232429 | CDS | 7143862 | 672 | + | 0.27381 | |
DDB_G0276699 | DDB_G0276699 | DDB0232429 | CDS | 7145278 | 162 | - | 0.228395 | |
DDB_G0276701 | DDB_G0276701 | DDB0232429 | CDS | 7147104 | 171 | + | 0.216374 | |
DDB_G0276703 | DDB_G0276703 | DDB0232429 | CDS | 7148982 | 171 | + | 0.222222 | |
DDB_G0276705 | DDB_G0276705 | DDB0232429 | CDS | 7149874 | 672 | + | 0.278274 | |
DDB_G0276707 | DDB_G0276707 | identical to | DDB0232429 | CDS | 7077584 | 162 | + | 0.209877 |
DDB_G0276709 | DDB_G0276709 | DDB0232429 | CDS | 7088764 | 2055 | - | 0.230657 | |
DDB_G0276713 | DDB_G0276713 | DDB0232429 | CDS | 7112533 | 3534 | + | 0.29966 | |
DDB_G0276717_RTE | DDB_G0276717 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 7121701 | 684 | - | 0.372807 |
DDB_G0276719 | DDB_G0276719 | DDB0232429 | CDS | 7123870 | 2268 | + | 0.22619 | |
DDB_G0276723 | DDB_G0276723 | DDB0232429 | CDS | 7150803 | 162 | - | 0.222222 | |
DDB_G0276725 | DDB_G0276725 | DDB0232429 | CDS | 7175956 | 237 | + | 0.265823 | |
DDB_G0276727 | DDB_G0276727 | DDB0232429 | CDS | 7175547 | 132 | + | 0.174242 | |
DDB_G0276729 | DDB_G0276729 | DDB0232429 | CDS | 7173981 | 591 | + | 0.265651 | |
DDB_G0276731 | DDB_G0276731 | DDB0232429 | CDS | 7172694 | 558 | + | 0.267025 | |
DDB_G0276733 | DDB_G0276733 | DDB0232429 | CDS | 7166909 | 4410 | + | 0.280045 | |
DDB_G0276735 | DDB_G0276735 | DDB0232429 | CDS | 7162758 | 792 | + | 0.27904 | |
DDB_G0276737 | DDB_G0276737 | DDB0232429 | CDS | 7160082 | 162 | - | 0.209877 | |
DDB_G0276739 | DDB_G0276739 | DDB0232429 | CDS | 7159124 | 639 | + | 0.280125 | |
DDB_G0276741 | DDB_G0276741 | DDB0232429 | CDS | 7158214 | 165 | + | 0.236364 | |
DDB_G0276743 | DDB_G0276743 | DDB0232429 | CDS | 7156375 | 162 | - | 0.222222 | |
DDB_G0276745 | DDB_G0276745 | DDB0232429 | CDS | 7155346 | 672 | + | 0.275298 | |
DDB_G0276747 | DDB_G0276747 | DDB0232429 | CDS | 7151707 | 672 | + | 0.285714 | |
DDB_G0276749 | DDB_G0276749 | DDB0232429 | CDS | 7152617 | 162 | - | 0.203704 | |
DDB_G0276751 | DDB_G0276751 | DDB0232429 | CDS | 7154411 | 171 | + | 0.216374 | |
DDB_G0276755 | DDB_G0276755 | DDB0232429 | CDS | 7163692 | 1377 | - | 0.248366 | |
DDB_G0276769 | DDB_G0276769 | DDB0232429 | CDS | 7284177 | 660 | - | 0.307576 | |
DDB_G0276773_ps | DDB_G0276773 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 7277816 | 2337 | + | 0.212238 |
DDB_G0276775_ps | DDB_G0276775 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 7274148 | 2667 | + | 0.214098 |
DDB_G0276777 | DDB_G0276777 | DDB0232429 | CDS | 7287390 | 249 | + | 0.297189 | |
DDB_G0276779 | DDB_G0276779 | similar to AAAS also known as achalasia adrenocortical insufficiency alacrimia (Allgrove triple-A) | DDB0232429 | CDS | 7288118 | 1416 | - | 0.275424 |
DDB_G0276781 | DDB_G0276781 | DDB0232429 | CDS | 7290266 | 798 | - | 0.303258 | |
DDB_G0276783 | DDB_G0276783 | homolog of human EXOSC3 (exosome component 3) and S. cerevisiae RRP40 (Ribosomal RNA-processing protein 40) S. cerevisiae RRP40 is a component of the exosome 3'-5' exoribonuclease complex but lacks exonuclease activity | DDB0232429 | CDS | 7291532 | 714 | - | 0.278711 |
DDB_G0276785 | DDB_G0276785 | DDB0232429 | CDS | 7306921 | 1224 | - | 0.216503 | |
DDB_G0276787 | DDB_G0276787 | DDB0232429 | CDS | 7311292 | 1887 | + | 0.208267 | |
DDB_G0276789 | DDB_G0276789 | DDB0232429 | CDS | 7329318 | 402 | - | 0.236318 | |
DDB_G0276791 | DDB_G0276791 | DDB0232429 | CDS | 7326201 | 2649 | + | 0.328048 | |
DDB_G0276793 | DDB_G0276793 | DDB0232429 | CDS | 7318662 | 1314 | + | 0.281583 | |
DDB_G0276801 | DDB_G0276801 | DDB0232429 | CDS | 7352564 | 2265 | - | 0.277263 | |
DDB_G0276805 | DDB_G0276805 | DDB0232429 | CDS | 7366504 | 3126 | + | 0.238644 | |
DDB_G0276807 | DDB_G0276807 | DDB0232429 | CDS | 7375327 | 1200 | + | 0.260833 | |
DDB_G0276809 | DDB_G0276809 | DDB0232429 | CDS | 7385987 | 519 | + | 0.248555 | |
DDB_G0276811 | DDB_G0276811 | DDB0232429 | CDS | 7386858 | 2736 | + | 0.26462 | |
DDB_G0276813 | DDB_G0276813 | weak similarity to NAP family proteins which are involved in nucleosome assembly the SWIM domain is found in variety of prokaryotic and eukaryotic proteins it is predicted to have DNA-binding and protein-protein interaction functions in different contexts | DDB0232429 | CDS | 7389875 | 585 | - | 0.294017 |
DDB_G0276815 | DDB_G0276815 | contains 7 WD repeats belongs to the WD repeat WDSOF1 family homolog of human WDSOF1 S. cerevisiae SOF1 S. cerevisiae SOF1 is required for ribosomal RNA processing | DDB0232429 | CDS | 7390722 | 1338 | - | 0.309417 |
DDB_G0276817 | DDB_G0276817 | DDB0232429 | CDS | 7392401 | 744 | - | 0.270161 | |
DDB_G0276819 | DDB_G0276819 | DDB0232429 | CDS | 7395512 | 411 | - | 0.29927 | |
DDB_G0276821 | DDB_G0276821 | similar to antiquitin aldehyde dehydrogenase family 7 catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232429 | CDS | 7397249 | 1530 | - | 0.391503 |
DDB_G0276823 | DDB_G0276823 | DDB0232429 | CDS | 7402781 | 633 | + | 0.236967 | |
DDB_G0276825 | DDB_G0276825 | DDB0232429 | CDS | 7408795 | 207 | + | 0.294686 | |
DDB_G0276827 | DDB_G0276827 | DDB0232429 | CDS | 7411298 | 1245 | - | 0.240161 | |
DDB_G0276831 | DDB_G0276831 | DDB0232429 | CDS | 7417052 | 678 | - | 0.165192 | |
DDB_G0276837 | DDB_G0276837 | DDB0232429 | CDS | 7454063 | 219 | + | 0.347032 | |
DDB_G0276839 | DDB_G0276839 | DDB0232429 | CDS | 7462954 | 1164 | + | 0.250859 | |
DDB_G0276841 | DDB_G0276841 | DDB0232429 | CDS | 7464543 | 996 | + | 0.266064 | |
DDB_G0276843 | DDB_G0276843 | DDB0232429 | CDS | 7468613 | 1254 | - | 0.238437 | |
DDB_G0276845 | DDB_G0276845 | DDB0232429 | CDS | 7470616 | 636 | + | 0.352201 | |
DDB_G0276847 | DDB_G0276847 | DDB0232429 | CDS | 7479610 | 1905 | - | 0.264042 | |
DDB_G0276853 | DDB_G0276853 | DDB0232429 | CDS | 7488908 | 783 | + | 0.232439 | |
DDB_G0276855 | DDB_G0276855 | DDB0232429 | CDS | 7489987 | 2193 | + | 0.300958 | |
DDB_G0276857 | DDB_G0276857 | DDB0232429 | CDS | 7492421 | 1203 | - | 0.260183 | |
DDB_G0276859 | DDB_G0276859 | DDB0232429 | CDS | 7500743 | 1296 | - | 0.203704 | |
DDB_G0276861 | DDB_G0276861 | conserved protein of unknown function localizes to adherens junctions in zebrafish | DDB0232429 | CDS | 7503468 | 1068 | - | 0.258427 |
DDB_G0276867 | DDB_G0276867 | weakly similar to PCNA contains one putative transmembrane domain at the C terminus | DDB0232429 | CDS | 7532126 | 495 | + | 0.187879 |
DDB_G0276873 | DDB_G0276873 | DDB0232429 | CDS | 7544433 | 2388 | - | 0.34129 | |
DDB_G0276879 | DDB_G0276879 | DDB0232429 | CDS | 7566354 | 885 | + | 0.242938 | |
DDB_G0276881 | DDB_G0276881 | contains one AN1-type zinc finger and one A20-type zinc finger similar to A. thaliana SAP7 (stress-associated protein) | DDB0232429 | CDS | 7569897 | 522 | - | 0.331418 |
DDB_G0276895 | DDB_G0276895 | DDB0232429 | CDS | 7315144 | 708 | - | 0.200565 | |
DDB_G0276897 | DDB_G0276897 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232429 | CDS | 7267534 | 1494 | + | 0.299197 |
DDB_G0276899 | DDB_G0276899 | conserved hypothetical protein similar to failed axon connections family proteins | DDB0232429 | CDS | 7264174 | 882 | - | 0.278912 |
DDB_G0276901 | DDB_G0276901 | DDB0232429 | CDS | 7263655 | 264 | - | 0.19697 | |
DDB_G0276905 | DDB_G0276905 | DDB0232429 | CDS | 7256369 | 1062 | - | 0.243879 | |
DDB_G0276907 | DDB_G0276907 | DDB0232429 | CDS | 7254558 | 1137 | - | 0.258575 | |
DDB_G0276911 | DDB_G0276911 | DDB0232429 | CDS | 7251359 | 933 | - | 0.23687 | |
DDB_G0276913 | DDB_G0276913 | DDB0232429 | CDS | 7248197 | 1176 | - | 0.191327 | |
DDB_G0276915 | DDB_G0276915 | DDB0232429 | CDS | 7236466 | 150 | + | 0.3 | |
DDB_G0276921 | DDB_G0276921 | member of a Dictyostelium-specific gene family contains a signal peptide | DDB0232429 | CDS | 7182465 | 771 | - | 0.277562 |
DDB_G0276923_ps | DDB_G0276923 | putative pseudogene highly similar to | DDB0232429 | CDS | 7183824 | 798 | - | 0.283208 |
DDB_G0276925 | DDB_G0276925 | member of a Dictyostelium-specific gene family contains a signal peptide | DDB0232429 | CDS | 7185219 | 768 | - | 0.282552 |
DDB_G0276927 | DDB_G0276927 | DDB0232429 | CDS | 7191923 | 438 | - | 0.299087 | |
DDB_G0276929 | DDB_G0276929 | DDB0232429 | CDS | 7196605 | 1815 | - | 0.236915 | |
DDB_G0276931 | DDB_G0276931 | DDB0232429 | CDS | 7206700 | 1809 | - | 0.281371 | |
DDB_G0276935 | DDB_G0276935 | DDB0232429 | CDS | 7220481 | 2037 | - | 0.238586 | |
DDB_G0276955 | DDB_G0276955 | DDB0232429 | CDS | 7582702 | 1053 | - | 0.177588 | |
DDB_G0276957 | DDB_G0276957 | DDB0232429 | CDS | 7586125 | 1020 | - | 0.196078 | |
DDB_G0276959 | DDB_G0276959 | DDB0232429 | CDS | 7589219 | 3459 | - | 0.270598 | |
DDB_G0276961 | DDB_G0276961 | C-terminus similar to Arabidopsis thaliana plant adhesion molecule 1 Drosophila melanogaster extracellular matrix adhesion protein Pollux and human rab6 GTPase activating protein GAPCENA | DDB0232429 | CDS | 7212385 | 1536 | - | 0.266927 |
DDB_G0276969 | DDB_G0276969 | highly similar to | DDB0232429 | CDS | 7477013 | 1608 | - | 0.31903 |
DDB_G0276975_RTE | DDB_G0276975 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 7521491 | 1335 | - | 0.310112 |
DDB_G0276979_RTE | DDB_G0276979 | DDB0232429 | CDS | 7437663 | 600 | + | 0.37 | |
DDB_G0276981_RTE | DDB_G0276981 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232429 | CDS | 7435825 | 1638 | + | 0.312576 |
DDB_G0276983_RTE | DDB_G0276983 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 7431540 | 1953 | + | 0.34767 |
DDB_G0276987 | DDB_G0276987 | DDB0232429 | CDS | 7382245 | 189 | + | 0.100529 | |
DDB_G0276989 | DDB_G0276989 | DDB0232429 | CDS | 7379194 | 2832 | - | 0.277542 | |
DDB_G0276991 | DDB_G0276991 | DDB0232429 | CDS | 7376660 | 1860 | - | 0.192473 | |
DDB_G0276997 | DDB_G0276997 | DDB0232429 | CDS | 7293362 | 1305 | + | 0.276628 | |
DDB_G0276999 | DDB_G0276999 | contains four transmembrane domains no homolog sequences in other organisms | DDB0232429 | CDS | 7269337 | 777 | - | 0.178893 |
DDB_G0277003 | DDB_G0277003 | DDB0232429 | CDS | 7259970 | 1080 | + | 0.224074 | |
DDB_G0277005_ps | DDB_G0277005 | putative pseudogene similar to a larger gene family including | DDB0232429 | CDS | 7253376 | 849 | + | 0.243816 |
DDB_G0277007 | DDB_G0277007 | homolog of human SLC35C1 (GDP-fucose transporter 1) defects in human SLC35C1 are the cause of leukocyte adhesion deficiency type II contains 10 putative transmembrane domains | DDB0232429 | CDS | 7200459 | 1107 | + | 0.272809 |
DDB_G0277009 | DDB_G0277009 | DDB0232429 | CDS | 7202546 | 840 | + | 0.257143 | |
DDB_G0277011 | DDB_G0277011 | bCommunity annotation:b DDB_G0277011 is highly similar in an N-terminal domain to the bShakerb voltage-gated potassium channel of vertebrates and is the best hit in the Dicty genome when searched with the sequence of this channel. The channel is strongly expressed in several classes of neurons in adult animals and appears to regulate neuronal excitability. The channel is also expressed during embryonic development where it shows a correlation with proliferation [see Hallows and Tempel Journal of Neuroscience 15 5682-5691 (1998)]. Older work shows clear correlation between expression and proliferation in cultured Schwann cells and blockade of potassium conduction inhibits proliferation (reviewed in Hallows and Tempel).br DDB_GO277011 is fourfold overexpressed (p3E-70)in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (Doquang et al in preparation). Most genes whose products have roles in S-phase or mitosis are overexpressed in this strain and most of the ove | DDB0232429 | CDS | 7203757 | 1104 | - | 0.296196 |
DDB_G0277021_ps | DDB_G0277021 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 7249627 | 966 | - | 0.242236 |
DDB_G0277023 | DDB_G0277023 | DDB0232429 | CDS | 7258388 | 1026 | - | 0.205653 | |
DDB_G0277025 | DDB_G0277025 | DDB0232429 | CDS | 7262534 | 714 | + | 0.257703 | |
DDB_G0277031 | DDB_G0277031 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232429 | CDS | 7281651 | 1533 | - | 0.297456 |
DDB_G0277035 | DDB_G0277035 | DDB0232429 | CDS | 7300081 | 573 | - | 0.289703 | |
DDB_G0277039 | DDB_G0277039 | DDB0232429 | CDS | 7313618 | 1260 | + | 0.246825 | |
DDB_G0277043 | DDB_G0277043 | structural similarity to Zn-dependent peptidases contains a a predicted signal anchor sequence and 4 putative transmembrane domains | DDB0232429 | CDS | 7322606 | 2187 | - | 0.288523 |
DDB_G0277045 | DDB_G0277045 | DDB0232429 | CDS | 7343113 | 1902 | - | 0.370137 | |
DDB_G0277047 | DDB_G0277047 | DDB0232429 | CDS | 7348550 | 3483 | + | 0.250072 | |
DDB_G0277049 | DDB_G0277049 | ortholog of S. cerevisiae TAM41 a mitochondrial protein involved in protein import into the mitochondrial matrix | DDB0232429 | CDS | 7355862 | 1284 | + | 0.237539 |
DDB_G0277051 | DDB_G0277051 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232429 | CDS | 7358123 | 1899 | + | 0.278568 |
DDB_G0277053 | DDB_G0277053 | DDB0232429 | CDS | 7363809 | 2250 | + | 0.230222 | |
DDB_G0277055 | DDB_G0277055 | DDB0232429 | CDS | 7373453 | 1119 | + | 0.264522 | |
DDB_G0277057 | DDB_G0277057 | DDB0232429 | CDS | 7382833 | 240 | + | 0.1 | |
DDB_G0277059 | DDB_G0277059 | DDB0232429 | CDS | 7400698 | 1182 | - | 0.274958 | |
DDB_G0277063 | DDB_G0277063 | DDB0232429 | CDS | 7409167 | 939 | + | 0.251331 | |
DDB_G0277065 | DDB_G0277065 | DDB0232429 | CDS | 7427326 | 2346 | + | 0.285592 | |
DDB_G0277067_RTE | DDB_G0277067 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 7430633 | 525 | + | 0.346667 |
DDB_G0277073_ps | DDB_G0277073 | putative pseudogene similar to D. discoideum genes | DDB0232429 | CDS | 7454940 | 624 | + | 0.245192 |
DDB_G0277077 | DDB_G0277077 | contains a UvrBUvrC domain however does not share similarity with UvrB or UvrC | DDB0232429 | CDS | 7466122 | 2190 | + | 0.252968 |
DDB_G0277081 | DDB_G0277081 | DDB0232429 | CDS | 7472098 | 1179 | - | 0.262935 | |
DDB_G0277091 | DDB_G0277091 | DDB0232429 | CDS | 7494067 | 564 | + | 0.320922 | |
DDB_G0277093 | DDB_G0277093 | DDB0232429 | CDS | 7495473 | 855 | + | 0.231579 | |
DDB_G0277095 | DDB_G0277095 | DDB0232429 | CDS | 7496528 | 1029 | - | 0.202138 | |
DDB_G0277103 | DDB_G0277103 | DDB0232429 | CDS | 7511199 | 3357 | + | 0.243074 | |
DDB_G0277105 | DDB_G0277105 | DDB0232429 | CDS | 7528689 | 2595 | + | 0.180347 | |
DDB_G0277109 | DDB_G0277109 | DDB0232429 | CDS | 7547283 | 4191 | - | 0.241708 | |
DDB_G0277111 | DDB_G0277111 | DDB0232429 | CDS | 7555133 | 2061 | + | 0.235808 | |
DDB_G0277117 | DDB_G0277117 | DDB0232429 | CDS | 7576790 | 1002 | - | 0.193613 | |
DDB_G0277121_ps | DDB_G0277121 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 7579760 | 675 | - | 0.18963 |
DDB_G0277127_ps | DDB_G0277127 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 7593644 | 4164 | - | 0.303074 |
DDB_G0277129 | DDB_G0277129 | DDB0232429 | CDS | 7609682 | 513 | - | 0.28655 | |
DDB_G0277133 | DDB_G0277133 | DDB0232429 | CDS | 7601973 | 1434 | - | 0.237796 | |
DDB_G0277137 | DDB_G0277137 | conserved protein ortholog of mouse adult male hypothalamus cDNA clone:A230106L22 | DDB0232429 | CDS | 7600198 | 1464 | + | 0.261612 |
DDB_G0277149 | DDB_G0277149 | contains 3 TPR domains homolog of human TTC35 (tetratricopeptide repeat protein 35) | DDB0232429 | CDS | 7777377 | 969 | + | 0.26935 |
DDB_G0277151 | DDB_G0277151 | DDB0232429 | CDS | 7889956 | 1455 | - | 0.22543 | |
DDB_G0277153 | DDB_G0277153 | DDB0232429 | CDS | 7923209 | 963 | - | 0.316719 | |
DDB_G0277159 | DDB_G0277159 | DDB0232429 | CDS | 7913689 | 1017 | - | 0.228122 | |
DDB_G0277161 | DDB_G0277161 | DDB0232429 | CDS | 7912606 | 882 | + | 0.241497 | |
DDB_G0277163 | DDB_G0277163 | DDB0232429 | CDS | 7909800 | 1314 | + | 0.256469 | |
DDB_G0277165 | DDB_G0277165 | CAMKL family protein kinase the protein kinase domain is similar to those of the CAMKLBRSK subfamily which are named based on brain-specific expression in human and neuronal expression in worm | DDB0232429 | CDS | 7893420 | 2502 | - | 0.271783 |
DDB_G0277167 | DDB_G0277167 | DDB0232429 | CDS | 7668593 | 1392 | + | 0.257902 | |
DDB_G0277169 | DDB_G0277169 | DDB0232429 | CDS | 7670938 | 3633 | - | 0.293146 | |
DDB_G0277171 | DDB_G0277171 | DDB0232429 | CDS | 7678365 | 1272 | - | 0.233491 | |
DDB_G0277177 | DDB_G0277177 | DDB0232429 | CDS | 7686538 | 1599 | - | 0.218887 | |
DDB_G0277179 | DDB_G0277179 | DDB0232429 | CDS | 7688578 | 1584 | + | 0.270833 | |
DDB_G0277181 | DDB_G0277181 | DDB0232429 | CDS | 7692473 | 969 | - | 0.26419 | |
DDB_G0277185 | DDB_G0277185 | DDB0232429 | CDS | 7699060 | 6855 | + | 0.307513 | |
DDB_G0277187 | DDB_G0277187 | DDB0232429 | CDS | 7707361 | 1119 | + | 0.268097 | |
DDB_G0277189 | DDB_G0277189 | DDB0232429 | CDS | 7715722 | 369 | + | 0.252033 | |
DDB_G0277191 | DDB_G0277191 | DDB0232429 | CDS | 7723058 | 483 | + | 0.310559 | |
DDB_G0277193_ps | DDB_G0277193 | putative pseudogene similar to many other hypothetical Dictyostelium proteins | DDB0232429 | CDS | 7730515 | 324 | - | 0.20679 |
DDB_G0277197 | DDB_G0277197 | DDB0232429 | CDS | 7732529 | 678 | + | 0.205015 | |
DDB_G0277201 | DDB_G0277201 | DDB0232429 | CDS | 7738970 | 717 | - | 0.377964 | |
DDB_G0277203 | DDB_G0277203 | members of the NAD-dependent epimerasedehydratase family use nucleotide-sugar substrates for a variety of chemical reactions | DDB0232429 | CDS | 7744744 | 1008 | + | 0.293651 |
DDB_G0277205 | DDB_G0277205 | DDB0232429 | CDS | 7746561 | 567 | + | 0.340388 | |
DDB_G0277207 | DDB_G0277207 | DDB0232429 | CDS | 7618079 | 432 | - | 0.222222 | |
DDB_G0277209 | DDB_G0277209 | DDB0232429 | CDS | 7627453 | 375 | + | 0.189333 | |
DDB_G0277211 | DDB_G0277211 | ortholog of human SKIV2L (SuperKIller Viralicitic 2L) protein and yeast SKI2 a helicase required for repressing propagation of dsRNA viruses | DDB0232429 | CDS | 7627913 | 4137 | - | 0.292966 |
DDB_G0277213 | DDB_G0277213 | DDB0232429 | CDS | 7638955 | 705 | + | 0.370213 | |
DDB_G0277217 | DDB_G0277217 | DDB0232429 | CDS | 7655048 | 3492 | - | 0.278351 | |
DDB_G0277225 | DDB_G0277225 | DDB0232429 | CDS | 7748048 | 2004 | + | 0.15519 | |
DDB_G0277227 | DDB_G0277227 | DDB0232429 | CDS | 7750722 | 603 | + | 0.270315 | |
DDB_G0277229 | DDB_G0277229 | DDB0232429 | CDS | 7752528 | 2145 | + | 0.20979 | |
DDB_G0277233 | DDB_G0277233 | expressed in pstO cells highly similar to | DDB0232429 | CDS | 7758796 | 264 | + | 0.363636 |
DDB_G0277235 | DDB_G0277235 | DDB0232429 | CDS | 7759588 | 1500 | - | 0.22 | |
DDB_G0277239 | DDB_G0277239 | DDB0232429 | CDS | 7764969 | 5868 | - | 0.223926 | |
DDB_G0277243 | DDB_G0277243 | similar to mammalian TNF receptor-associated factors 5 and 6 (TRAF5 TRAF6) | DDB0232429 | CDS | 7783025 | 1272 | + | 0.283019 |
DDB_G0277245 | DDB_G0277245 | catalyzes the reaction L-threonine 2-oxobutanoate NHsub3sub | DDB0232429 | CDS | 7799232 | 3522 | + | 0.315446 |
DDB_G0277249 | DDB_G0277249 | DDB0232429 | CDS | 7817927 | 849 | - | 0.34629 | |
DDB_G0277251 | DDB_G0277251 | DDB0232429 | CDS | 7821349 | 1674 | - | 0.250896 | |
DDB_G0277255 | DDB_G0277255 | DDB0232429 | CDS | 7827595 | 3372 | - | 0.253559 | |
DDB_G0277257 | DDB_G0277257 | DDB0232429 | CDS | 7833225 | 1404 | - | 0.340456 | |
DDB_G0277259 | DDB_G0277259 | DDB0232429 | CDS | 7835294 | 411 | + | 0.194647 | |
DDB_G0277261 | DDB_G0277261 | DDB0232429 | CDS | 7836022 | 411 | - | 0.240876 | |
DDB_G0277263 | DDB_G0277263 | DDB0232429 | CDS | 7842734 | 1068 | + | 0.279963 | |
DDB_G0277265 | DDB_G0277265 | DDB0232429 | CDS | 7848602 | 1389 | + | 0.25414 | |
DDB_G0277271 | DDB_G0277271 | DDB0232429 | CDS | 7915485 | 1053 | - | 0.252612 | |
DDB_G0277279 | DDB_G0277279 | DDB0232429 | CDS | 7911260 | 588 | - | 0.238095 | |
DDB_G0277281_RTE | DDB_G0277281 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 7879581 | 1335 | + | 0.306367 |
DDB_G0277283_RTE | DDB_G0277283 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232429 | CDS | 7874573 | 1899 | - | 0.266983 |
DDB_G0277285_RTE | DDB_G0277285 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 7872301 | 1335 | + | 0.307116 |
DDB_G0277287 | DDB_G0277287 | DDB0232429 | CDS | 7868434 | 2502 | - | 0.155076 | |
DDB_G0277291 | DDB_G0277291 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232429 | CDS | 7790152 | 4197 | + | 0.264475 |
DDB_G0277297_RTE | DDB_G0277297 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 7677105 | 501 | + | 0.343313 |
DDB_G0277299_RTE | DDB_G0277299 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 7676172 | 684 | + | 0.375731 |
DDB_G0277301 | DDB_G0277301 | DDB0232429 | CDS | 7618748 | 4389 | - | 0.256095 | |
DDB_G0277305 | DDB_G0277305 | DDB0232429 | CDS | 7632373 | 723 | - | 0.239281 | |
DDB_G0277307 | DDB_G0277307 | highly similar to H. sapiens LONP1 and S. cerevisiae PIM1 Lon protease family members are often located in the mitochondria there is a second Lon protease in Dictyostelium | DDB0232429 | CDS | 7634314 | 2511 | - | 0.322979 |
DDB_G0277311 | DDB_G0277311 | DDB0232429 | CDS | 7649277 | 2049 | + | 0.235237 | |
DDB_G0277313 | DDB_G0277313 | similar to TAPT1 (Transmembrane Anterior Posterior Transformation) a conserved eukaryotic gene when mutated in mouse causes skeletal homeotic transformations | DDB0232429 | CDS | 7659066 | 2487 | - | 0.26538 |
DDB_G0277315 | DDB_G0277315 | DDB0232429 | CDS | 7664995 | 849 | + | 0.256773 | |
DDB_G0277317 | DDB_G0277317 | DDB0232429 | CDS | 7667169 | 708 | + | 0.252825 | |
DDB_G0277323 | DDB_G0277323 | contains four FNIP repeats similar to CigB and other conserved hypothetical Dictyostelium proteins | DDB0232429 | CDS | 7696333 | 1095 | - | 0.198174 |
DDB_G0277325 | DDB_G0277325 | DDB0232429 | CDS | 7711176 | 3048 | + | 0.260827 | |
DDB_G0277327 | DDB_G0277327 | DDB0232429 | CDS | 7723793 | 3354 | - | 0.304114 | |
DDB_G0277329 | DDB_G0277329 | N-terminal region similar to ubiquitin central region contains one von Willebrand factor (vWF) type A domain C-terminal region similar to P-loop containing nucleoside triphosphate hydrolases | DDB0232429 | CDS | 7727570 | 2397 | - | 0.272841 |
DDB_G0277331 | DDB_G0277331 | bCommunity annotation:b DDB_GO277331 is similar (blasts both ways) to a widely conserved histone lysine methyl transferease called ASHR1 in plants but known as the Set and MYnd Domain-containing protein SMYD3 in metazoans. In humans SMYD3 is upregulated in the majority of colorectal and hepatic cancers it is thought to participate in transactivating genes involved in cell cycle regulation [see Hamamoto et al Nature Cell Biology 6 731-740 (2004)]. The protein binds to the motif bCCCTCCb which is found in the promoters of many such genes in humans.br DDB_G0277331 is fivefold overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (Doquang et al. in preparation). The SMYD3 target bCCCTCCb is rare in Dictyostelium promoters but highly enriched in the promoters of genes which the rblA disruptant overexpresses. Most of these genes have functions in cell cycle progression they include three kifs two DNA polymerases two centrosomal proteins and cdk1. It th | DDB0232429 | CDS | 7763036 | 1650 | + | 0.211515 |
DDB_G0277333 | DDB_G0277333 | DDB0232429 | CDS | 7771869 | 792 | + | 0.299242 | |
DDB_G0277335 | DDB_G0277335 | DDB0232429 | CDS | 7773309 | 609 | + | 0.261084 | |
DDB_G0277337 | DDB_G0277337 | DDB0232429 | CDS | 7774136 | 2658 | - | 0.307374 | |
DDB_G0277341 | DDB_G0277341 | contains a plant homeodomain (PHD) finger a C4HC3 zinc-finger-like motif found in nuclear proteins thought to be involved in chromatin-mediated transcriptional regulation | DDB0232429 | CDS | 7779263 | 2745 | + | 0.261202 |
DDB_G0277347 | DDB_G0277347 | DDB0232429 | CDS | 7797355 | 1278 | - | 0.2723 | |
DDB_G0277349 | DDB_G0277349 | DDB0232429 | CDS | 7803232 | 759 | - | 0.310935 | |
DDB_G0277353 | DDB_G0277353 | DDB0232429 | CDS | 7808700 | 1902 | - | 0.325973 | |
DDB_G0277355 | DDB_G0277355 | DDB0232429 | CDS | 7838828 | 969 | - | 0.415893 | |
DDB_G0277357 | DDB_G0277357 | contains a putative cupin RmlC-type domain found in RmlC a dTDP-sugar isomerase | DDB0232429 | CDS | 7850366 | 3147 | - | 0.261837 |
DDB_G0277359 | DDB_G0277359 | DDB0232429 | CDS | 7855699 | 1161 | + | 0.209302 | |
DDB_G0277361 | DDB_G0277361 | DDB0232429 | CDS | 7860770 | 1014 | + | 0.216963 | |
DDB_G0277363_RTE | DDB_G0277363 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 7882048 | 1335 | + | 0.31161 |
DDB_G0277365_RTE | DDB_G0277365 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232429 | CDS | 7883673 | 3144 | + | 0.337786 |
DDB_G0277367 | DDB_G0277367 | DDB0232429 | CDS | 7889390 | 486 | + | 0.255144 | |
DDB_G0277369 | DDB_G0277369 | similar to SETPhosphatase 2A inhibitor and other NAP domain-containing proteins | DDB0232429 | CDS | 7892019 | 714 | - | 0.253501 |
DDB_G0277373 | DDB_G0277373 | DDB0232429 | CDS | 7901323 | 1035 | + | 0.239614 | |
DDB_G0277375 | DDB_G0277375 | DDB0232429 | CDS | 7905630 | 3207 | - | 0.309947 | |
DDB_G0277383 | DDB_G0277383 | DDB0232429 | CDS | 7941454 | 1491 | - | 0.316566 | |
DDB_G0277385 | DDB_G0277385 | DDB0232429 | CDS | 7940048 | 1008 | + | 0.190476 | |
DDB_G0277387 | DDB_G0277387 | DDB0232429 | CDS | 7936707 | 2286 | - | 0.244532 | |
DDB_G0277389 | DDB_G0277389 | DDB0232429 | CDS | 7930691 | 1575 | - | 0.273016 | |
DDB_G0277391 | DDB_G0277391 | DDB0232429 | CDS | 7927670 | 2397 | + | 0.299124 | |
DDB_G0277395 | DDB_G0277395 | DDB0232429 | CDS | 7945233 | 1086 | + | 0.212707 | |
DDB_G0277405 | DDB_G0277405 | DDB0232429 | CDS | 7966950 | 1101 | - | 0.354223 | |
DDB_G0277407 | DDB_G0277407 | DDB0232429 | CDS | 7966182 | 378 | + | 0.206349 | |
DDB_G0277409 | DDB_G0277409 | DDB0232429 | CDS | 7964365 | 675 | - | 0.334815 | |
DDB_G0277411 | DDB_G0277411 | DDB0232429 | CDS | 7962538 | 681 | - | 0.330396 | |
DDB_G0277415 | DDB_G0277415 | DDB0232429 | CDS | 8036179 | 837 | - | 0.301075 | |
DDB_G0277417 | DDB_G0277417 | DDB0232429 | CDS | 8034298 | 837 | - | 0.299881 | |
DDB_G0277419 | DDB_G0277419 | DDB0232429 | CDS | 8052660 | 7878 | - | 0.248159 | |
DDB_G0277421 | DDB_G0277421 | DDB0232429 | CDS | 8051193 | 837 | + | 0.30227 | |
DDB_G0277423 | DDB_G0277423 | DDB0232429 | CDS | 8049469 | 837 | + | 0.298686 | |
DDB_G0277425 | DDB_G0277425 | DDB0232429 | CDS | 8047664 | 837 | + | 0.297491 | |
DDB_G0277427 | DDB_G0277427 | DDB0232429 | CDS | 8043662 | 1911 | + | 0.299843 | |
DDB_G0277429 | DDB_G0277429 | DDB0232429 | CDS | 8039644 | 2550 | - | 0.296863 | |
DDB_G0277431 | DDB_G0277431 | DDB0232429 | CDS | 8079828 | 3294 | - | 0.265938 | |
DDB_G0277443 | DDB_G0277443 | DDB0232429 | CDS | 8114815 | 1992 | + | 0.212349 | |
DDB_G0277445 | DDB_G0277445 | DDB0232429 | CDS | 8116895 | 207 | - | 0.10628 | |
DDB_G0277447 | DDB_G0277447 | DDB0232429 | CDS | 8117419 | 1914 | + | 0.204807 | |
DDB_G0277449 | DDB_G0277449 | member of the AGC kinase group similar to kinase domains of SGK (serum and glucocorticoid responsive kinase) AktPKB and RSK (ribosomal S6 kinase) family members | DDB0232429 | CDS | 8121319 | 1371 | + | 0.300511 |
DDB_G0277453 | DDB_G0277453 | DDB0232429 | CDS | 8131041 | 246 | + | 0.365854 | |
DDB_G0277457 | DDB_G0277457 | DDB0232429 | CDS | 8136499 | 459 | + | 0.331155 | |
DDB_G0277459 | DDB_G0277459 | DDB0232429 | CDS | 8137150 | 216 | - | 0.337963 | |
DDB_G0277461 | DDB_G0277461 | DDB0232429 | CDS | 8138236 | 186 | - | 0.327957 | |
DDB_G0277463 | DDB_G0277463 | DDB0232429 | CDS | 8138567 | 210 | + | 0.290476 | |
DDB_G0277465 | DDB_G0277465 | DDB0232429 | CDS | 8139057 | 555 | + | 0.340541 | |
DDB_G0277467 | DDB_G0277467 | DDB0232429 | CDS | 8139803 | 945 | + | 0.315344 | |
DDB_G0277469 | DDB_G0277469 | DDB0232429 | CDS | 8142776 | 573 | + | 0.22164 | |
DDB_G0277471 | DDB_G0277471 | homolog of human PAAF1 (proteasomal ATPase-associated factor 1) which inhibits proteasome 26S assembly and activity contains 3 WD repeats | DDB0232429 | CDS | 8143567 | 1278 | - | 0.305164 |
DDB_G0277473 | DDB_G0277473 | DDB0232429 | CDS | 8145872 | 864 | + | 0.291667 | |
DDB_G0277475 | DDB_G0277475 | DDB0232429 | CDS | 8147736 | 1395 | + | 0.317563 | |
DDB_G0277477 | DDB_G0277477 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub | DDB0232429 | CDS | 8149300 | 1917 | - | 0.303078 |
DDB_G0277479 | DDB_G0277479 | DDB0232429 | CDS | 8152464 | 1596 | + | 0.244987 | |
DDB_G0277481 | DDB_G0277481 | DDB0232429 | CDS | 7953876 | 1176 | + | 0.244048 | |
DDB_G0277483 | DDB_G0277483 | DDB0232429 | CDS | 7973999 | 2199 | + | 0.246021 | |
DDB_G0277487 | DDB_G0277487 | DDB0232429 | CDS | 7985968 | 558 | + | 0.229391 | |
DDB_G0277489 | DDB_G0277489 | DDB0232429 | CDS | 7988276 | 399 | + | 0.345865 | |
DDB_G0277495 | DDB_G0277495 | DDB0232429 | CDS | 8005050 | 1980 | + | 0.221212 | |
DDB_G0277499 | DDB_G0277499 | DDB0232429 | CDS | 8026900 | 156 | - | 0.275641 | |
DDB_G0277507 | DDB_G0277507 | DDB0232429 | CDS | 7970770 | 1125 | - | 0.275556 | |
DDB_G0277513_ps | DDB_G0277513 | putative pseudogene similar to parts of gene | DDB0232429 | CDS | 8071368 | 1407 | - | 0.248045 |
DDB_G0277515 | DDB_G0277515 | DDB0232429 | CDS | 8077667 | 1542 | - | 0.323606 | |
DDB_G0277519_RTE | DDB_G0277519 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 8084696 | 1365 | + | 0.308425 |
DDB_G0277521_RTE | DDB_G0277521 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 8086854 | 2949 | + | 0.344184 |
DDB_G0277523_RTE | DDB_G0277523 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 8089978 | 309 | + | 0.355987 |
DDB_G0277525 | DDB_G0277525 | DDB0232429 | CDS | 8090925 | 3399 | - | 0.259782 | |
DDB_G0277531 | DDB_G0277531 | conserved hypothetical Dictyostelium protein contains one EGF-like type 3 domain | DDB0232429 | CDS | 7955427 | 2856 | - | 0.240896 |
DDB_G0277533 | DDB_G0277533 | similar to human WDR48 a WD repeat endosomal protein | DDB0232429 | CDS | 7976869 | 3519 | - | 0.24524 |
DDB_G0277537 | DDB_G0277537 | subunit of PI4K responsible for the phosphorylation of phosphatidylinositol (PI) to PI4P (ATP 1-phosphatidyl-1D-myo-inositol ADP 1-phosphatidyl-1D-myo-inositol 4-phosphate) the first committed step in the generation of phosphatidylinositol 45-bisphosphate (PIP2) a precursor of the second messenger inositol 145-trisphosphate (InsP3) | DDB0232429 | CDS | 7989159 | 7383 | + | 0.301233 |
DDB_G0277539 | DDB_G0277539 | putative protein tyrosine kinase similar to human wee1 inhibitor of mitosis through phosphorylation of cdc2 | DDB0232429 | CDS | 8010617 | 2997 | - | 0.248248 |
DDB_G0277541 | DDB_G0277541 | DDB0232429 | CDS | 8015733 | 2283 | - | 0.240911 | |
DDB_G0277543 | DDB_G0277543 | DDB0232429 | CDS | 8021040 | 4974 | - | 0.283273 | |
DDB_G0277547 | DDB_G0277547 | DDB0232429 | CDS | 8045819 | 1404 | - | 0.180199 | |
DDB_G0277555 | DDB_G0277555 | DDB0232429 | CDS | 8102198 | 3342 | + | 0.247157 | |
DDB_G0277557 | DDB_G0277557 | DDB0232429 | CDS | 8106401 | 3327 | + | 0.243463 | |
DDB_G0277559 | DDB_G0277559 | contains a predicted signal peptide and a putative C-terminal transmembrane domain similar to D. purpureum protein | DDB0232429 | CDS | 8125465 | 1938 | - | 0.209494 |
DDB_G0277563 | DDB_G0277563 | DDB0232429 | CDS | 8135123 | 543 | - | 0.307551 | |
DDB_G0277567 | DDB_G0277567 | DDB0232429 | CDS | 8163219 | 1761 | - | 0.321408 | |
DDB_G0277569 | DDB_G0277569 | members of this family are membrane proteins involved in long chain fatty acid elongation systems that produce 26-carbon precursors for ceramide and sphingolipid synthesis contains 7 putative transmembrane domains | DDB0232429 | CDS | 8161171 | 939 | + | 0.263046 |
DDB_G0277571 | DDB_G0277571 | DDB0232429 | CDS | 8158069 | 2259 | + | 0.266932 | |
DDB_G0277573 | DDB_G0277573 | DDB0232429 | CDS | 8170344 | 1017 | + | 0.277286 | |
DDB_G0277575 | DDB_G0277575 | DDB0232429 | CDS | 8169746 | 387 | - | 0.271318 | |
DDB_G0277577 | DDB_G0277577 | DDB0232429 | CDS | 8171700 | 864 | + | 0.201389 | |
DDB_G0277581 | DDB_G0277581 | DDB0232429 | CDS | 8272981 | 1479 | - | 0.292765 | |
DDB_G0277583 | DDB_G0277583 | DDB0232429 | CDS | 8264672 | 690 | - | 0.176812 | |
DDB_G0277585 | DDB_G0277585 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8228651 | 3873 | + | 0.221275 |
DDB_G0277593 | DDB_G0277593 | DDB0232429 | CDS | 8183598 | 177 | + | 0.20904 | |
DDB_G0277595 | DDB_G0277595 | conserved hypothetical Dictyostelium protein identical to | DDB0232429 | CDS | 8209423 | 141 | - | 0.496454 |
DDB_G0277599 | DDB_G0277599 | DDB0232429 | CDS | 8263837 | 561 | - | 0.26025 | |
DDB_G0277601 | DDB_G0277601 | DDB0232429 | CDS | 8291535 | 1383 | + | 0.205351 | |
DDB_G0277603 | DDB_G0277603 | DDB0232429 | CDS | 8295204 | 2730 | + | 0.271062 | |
DDB_G0277605 | DDB_G0277605 | DDB0232429 | CDS | 8298219 | 465 | - | 0.154839 | |
DDB_G0277607 | DDB_G0277607 | DDB0232429 | CDS | 8299059 | 792 | - | 0.300505 | |
DDB_G0277613 | DDB_G0277613 | DDB0232429 | CDS | 8310859 | 468 | + | 0.215812 | |
DDB_G0277615 | DDB_G0277615 | proteins containing the actin depolymerisation factor (ADF)cofilin-like domain sever actin filaments and bind to actin monomers | DDB0232429 | CDS | 8184492 | 1569 | - | 0.339069 |
DDB_G0277617_ps | DDB_G0277617 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 8203285 | 456 | - | 0.210526 |
DDB_G0277619 | DDB_G0277619 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8219196 | 4158 | + | 0.224146 |
DDB_G0277621_ps | DDB_G0277621 | putative pseudogene fragment similar to D. discoideum genes | DDB0232429 | CDS | 8227373 | 270 | - | 0.307407 |
DDB_G0277623_ps | DDB_G0277623 | putative pseudogene small fragment very similar to neighboring genes that belong to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8234081 | 366 | + | 0.180328 |
DDB_G0277625 | DDB_G0277625 | DDB0232429 | CDS | 8269607 | 1263 | - | 0.278702 | |
DDB_G0277631 | DDB_G0277631 | DDB0232429 | CDS | 8282560 | 633 | - | 0.281201 | |
DDB_G0277633_ps | DDB_G0277633 | putative pseudogene small fragment similar to prespore specific (psp) - and spore coat (cot) protein encoding genes | DDB0232429 | CDS | 8289542 | 189 | - | 0.301587 |
DDB_G0277637 | DDB_G0277637 | DDB0232429 | CDS | 8186997 | 3753 | - | 0.221956 | |
DDB_G0277639 | DDB_G0277639 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8191422 | 3984 | + | 0.223143 |
DDB_G0277641_ps | DDB_G0277641 | putative pseudogene very similar to neighboring genes that belong to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8196187 | 1797 | + | 0.224263 |
DDB_G0277643 | DDB_G0277643 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8198851 | 3900 | + | 0.215641 |
DDB_G0277645 | DDB_G0277645 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8204055 | 4062 | + | 0.222797 |
DDB_G0277647_ps | DDB_G0277647 | putative pseudogene very similar to neighboring genes that belong to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8210587 | 3300 | + | 0.225758 |
DDB_G0277651_ps | DDB_G0277651 | putative pseudogene very similar to neighboring genes that belong to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8224157 | 1863 | + | 0.21256 |
DDB_G0277653 | DDB_G0277653 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8235037 | 3729 | + | 0.22982 |
DDB_G0277655_ps | DDB_G0277655 | putative pseudogene very similar to neighboring genes that belong to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8243854 | 3055 | + | 0.235025 |
DDB_G0277657 | DDB_G0277657 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8247429 | 4188 | + | 0.223734 |
DDB_G0277659 | DDB_G0277659 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8252136 | 4164 | + | 0.222382 |
DDB_G0277661 | DDB_G0277661 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8257035 | 4245 | + | 0.21437 |
DDB_G0277663 | DDB_G0277663 | DDB0232429 | CDS | 8265860 | 3207 | - | 0.278765 | |
DDB_G0277665 | DDB_G0277665 | DDB0232429 | CDS | 8271819 | 453 | + | 0.286976 | |
DDB_G0277667 | DDB_G0277667 | DDB0232429 | CDS | 8286817 | 1392 | + | 0.283764 | |
DDB_G0277669 | DDB_G0277669 | similar to aldose 1-epimerase (mutarotase) the enzyme responsible for the anomeric interconversion of D-glucose and other aldoses between their alpha- and beta-form | DDB0232429 | CDS | 8293206 | 987 | - | 0.261398 |
DDB_G0277673 | DDB_G0277673 | DDB0232429 | CDS | 8312031 | 290 | + | 0.165517 | |
DDB_G0277675 | DDB_G0277675 | DDB0232429 | CDS | 8331577 | 2112 | - | 0.288826 | |
DDB_G0277679 | DDB_G0277679 | DDB0232429 | CDS | 8347286 | 1101 | + | 0.257039 | |
DDB_G0277685 | DDB_G0277685 | DDB0232429 | CDS | 8335817 | 6561 | + | 0.299192 | |
DDB_G0277687 | DDB_G0277687 | DDB0232429 | CDS | 8316109 | 5757 | + | 0.258121 | |
DDB_G0277689 | DDB_G0277689 | DDB0232429 | CDS | 8322084 | 1308 | + | 0.232416 | |
DDB_G0277693 | DDB_G0277693 | DDB0232429 | CDS | 8329000 | 2025 | + | 0.290864 | |
DDB_G0277695 | DDB_G0277695 | DDB0232429 | CDS | 8344683 | 1074 | + | 0.297952 | |
DDB_G0277697 | DDB_G0277697 | conserved protein similar to DDB_G0278913 | DDB0232429 | CDS | 8312721 | 1146 | + | 0.28185 |
DDB_G0277699 | DDB_G0277699 | DDB0232429 | CDS | 8366249 | 681 | - | 0.234949 | |
DDB_G0277705 | DDB_G0277705 | DDB0232429 | CDS | 8352571 | 1524 | - | 0.229659 | |
DDB_G0277707 | DDB_G0277707 | DDB0232429 | CDS | 8354614 | 2046 | - | 0.221408 | |
DDB_G0277709 | DDB_G0277709 | DDB0232429 | CDS | 8357628 | 306 | + | 0.261438 | |
DDB_G0277711_RTE | DDB_G0277711 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 8359557 | 3435 | - | 0.346725 |
DDB_G0277713_RTE | DDB_G0277713 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232429 | CDS | 8363091 | 1356 | - | 0.311947 |
DDB_G0277715_RTE | DDB_G0277715 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232429 | CDS | 8365162 | 684 | + | 0.339181 |
DDB_G0277717 | DDB_G0277717 | DDB0232429 | CDS | 8370232 | 422 | - | 0.151659 | |
DDB_G0277719 | DDB_G0277719 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain REMI mutant form aberrant fruiting bodies (see | DDB0232429 | CDS | 8390719 | 4050 | + | 0.241481 |
DDB_G0277729 | DDB_G0277729 | DDB0232429 | CDS | 8389301 | 819 | + | 0.352869 | |
DDB_G0277731 | DDB_G0277731 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232429 | CDS | 8396089 | 4131 | + | 0.254176 |
DDB_G0277735 | DDB_G0277735 | DDB0232429 | CDS | 8406382 | 816 | + | 0.20098 | |
DDB_G0277737 | DDB_G0277737 | DDB0232429 | CDS | 8407484 | 2742 | + | 0.310722 | |
DDB_G0277739 | DDB_G0277739 | highly similar to neighboring gene | DDB0232429 | CDS | 8410519 | 237 | - | 0.388186 |
DDB_G0277741 | DDB_G0277741 | contains a predicted coiled-coil region found in a group of Dictyostelium proteins known to be regulated by cAMP highly similar to neighboring gene | DDB0232429 | CDS | 8411530 | 237 | + | 0.388186 |
DDB_G0277745 | DDB_G0277745 | DDB0232429 | CDS | 8419128 | 882 | - | 0.290249 | |
DDB_G0277747 | DDB_G0277747 | DDB0232429 | CDS | 8420426 | 939 | - | 0.255591 | |
DDB_G0277749 | DDB_G0277749 | DDB0232429 | CDS | 8434187 | 5040 | + | 0.242262 | |
DDB_G0277753 | DDB_G0277753 | DDB0232429 | CDS | 8444919 | 690 | + | 0.282609 | |
DDB_G0277757 | DDB_G0277757 | DDB0232429 | CDS | 8456100 | 1128 | + | 0.301418 | |
DDB_G0277761 | DDB_G0277761 | similar to bacterial endoribonucleases similar to human HRSP12 (ribonuclease UK114) an endoribonuclease which cleaves mRNA and inhibits protein synthesis | DDB0232429 | CDS | 8470556 | 390 | + | 0.346154 |
DDB_G0277763 | DDB_G0277763 | DDB0232429 | CDS | 8471398 | 1350 | - | 0.292593 | |
DDB_G0277765_RTE | DDB_G0277765 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232429 | CDS | 8476009 | 159 | + | 0.45283 |
DDB_G0277767 | DDB_G0277767 | DDB0232429 | CDS | 8373298 | 2406 | - | 0.216958 | |
DDB_G0277769 | DDB_G0277769 | putative secreted protein contains a signal sequence | DDB0232429 | CDS | 8413951 | 597 | + | 0.266332 |
DDB_G0277771 | DDB_G0277771 | DDB0232429 | CDS | 8416365 | 561 | + | 0.269162 | |
DDB_G0277773 | DDB_G0277773 | DDB0232429 | CDS | 8461506 | 1395 | - | 0.286022 | |
DDB_G0277775 | DDB_G0277775 | DDB0232429 | CDS | 8465643 | 375 | - | 0.333333 | |
DDB_G0277777 | DDB_G0277777 | DDB0232429 | CDS | 8467444 | 2598 | + | 0.270593 | |
DDB_G0277779_RTE | DDB_G0277779 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232429 | CDS | 8476605 | 477 | + | 0.352201 |
DDB_G0277781_RTE | DDB_G0277781 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232429 | CDS | 8478382 | 882 | + | 0.396825 |
DDB_G0277783_TE | DDB_G0277783 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232429 | CDS | 8480176 | 672 | + | 0.230655 |
DDB_G0277785_TE | DDB_G0277785 | ORF2 (contains 2 introns) encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232429 | CDS | 8480964 | 390 | + | 0.328205 |
DDB_G0277787 | DDB_G0277787 | DDB0232429 | CDS | 8370803 | 1806 | + | 0.313953 | |
DDB_G0277789 | DDB_G0277789 | similar to a conserved eukaryotic protein contains two transmembrane domains | DDB0232429 | CDS | 8381890 | 3408 | + | 0.265845 |
DDB_G0277793 | DDB_G0277793 | conserved hypothetical protein contains a putative signal peptide | DDB0232429 | CDS | 8412296 | 1014 | + | 0.233728 |
DDB_G0277795 | DDB_G0277795 | DDB0232429 | CDS | 8415694 | 246 | + | 0.341463 | |
DDB_G0277799 | DDB_G0277799 | DDB0232429 | CDS | 8427032 | 2307 | + | 0.255743 | |
DDB_G0277805 | DDB_G0277805 | DDB0232429 | CDS | 8433000 | 903 | + | 0.139535 | |
DDB_G0277807 | DDB_G0277807 | DDB0232429 | CDS | 8439922 | 1833 | + | 0.19749 | |
DDB_G0277813 | DDB_G0277813 | DDB0232429 | CDS | 8445920 | 2325 | + | 0.237849 | |
DDB_G0277819 | DDB_G0277819 | DDB0232429 | CDS | 8481872 | 771 | - | 0.341115 | |
DDB_G0277821_TE | DDB_G0277821 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-B refer to AF298202 for full-length consensus element | DDB0232429 | CDS | 8483067 | 504 | - | 0.214286 |
DDB_G0277895 | DDB_G0277895 | DDB0232430 | CDS | 94751 | 462 | + | 0.409091 | |
DDB_G0277899 | DDB_G0277899 | DDB0232430 | CDS | 439645 | 864 | + | 0.22338 | |
DDB_G0277931 | DDB_G0277931 | DDB0232430 | CDS | 29762 | 768 | - | 0.276042 | |
DDB_G0277933_ps | DDB_G0277933 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 30749 | 396 | + | 0.292929 |
DDB_G0277937 | DDB_G0277937 | DDB0232430 | CDS | 32996 | 2691 | + | 0.212932 | |
DDB_G0277939 | DDB_G0277939 | DDB0232430 | CDS | 37703 | 1476 | - | 0.156504 | |
DDB_G0277941 | DDB_G0277941 | similar to HIRA histone cell cycle regulation defective homolog A | DDB0232430 | CDS | 39336 | 1431 | + | 0.288609 |
DDB_G0277951 | DDB_G0277951 | DDB0232430 | CDS | 55112 | 609 | - | 0.27422 | |
DDB_G0277957 | DDB_G0277957 | putative ras GTPase-activating protein-binding protein similar to H. sapiens ras GTPase-activating protein-binding protein 1 (G3BP1) | DDB0232430 | CDS | 62453 | 1551 | + | 0.32882 |
DDB_G0277961 | DDB_G0277961 | DDB0232430 | CDS | 66831 | 1452 | - | 0.199725 | |
DDB_G0277963 | DDB_G0277963 | DDB0232430 | CDS | 68797 | 1236 | - | 0.291262 | |
DDB_G0277965 | DDB_G0277965 | DDB0232430 | CDS | 70947 | 390 | - | 0.269231 | |
DDB_G0277967 | DDB_G0277967 | DDB0232430 | CDS | 72018 | 3144 | + | 0.26145 | |
DDB_G0277969 | DDB_G0277969 | DDB0232430 | CDS | 78242 | 1230 | + | 0.298374 | |
DDB_G0277973 | DDB_G0277973 | DDB0232430 | CDS | 83008 | 915 | + | 0.183607 | |
DDB_G0277981_ps | DDB_G0277981 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 92490 | 177 | - | 0.344633 |
DDB_G0277985 | DDB_G0277985 | DDB0232430 | CDS | 99770 | 447 | - | 0.214765 | |
DDB_G0277989 | DDB_G0277989 | DDB0232430 | CDS | 119614 | 4302 | + | 0.225477 | |
DDB_G0277993 | DDB_G0277993 | importins function in nuclear protein import however this protein does not contain the N-terminal importin beta binding domain (IBB domain) | DDB0232430 | CDS | 126886 | 1575 | + | 0.31873 |
DDB_G0277997 | DDB_G0277997 | DDB0232430 | CDS | 130346 | 9849 | + | 0.222155 | |
DDB_G0277999 | DDB_G0277999 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232430 | CDS | 144948 | 1182 | - | 0.265651 |
DDB_G0278001 | DDB_G0278001 | DDB0232430 | CDS | 146554 | 393 | - | 0.221374 | |
DDB_G0278003 | DDB_G0278003 | DDB0232430 | CDS | 147404 | 1074 | - | 0.238361 | |
DDB_G0278005 | DDB_G0278005 | DDB0232430 | CDS | 151993 | 999 | - | 0.173173 | |
DDB_G0278007 | DDB_G0278007 | DDB0232430 | CDS | 153604 | 207 | - | 0.207729 | |
DDB_G0278013 | DDB_G0278013 | DDB0232430 | CDS | 162120 | 258 | - | 0.329457 | |
DDB_G0278015 | DDB_G0278015 | DDB0232430 | CDS | 164355 | 2322 | - | 0.273471 | |
DDB_G0278017 | DDB_G0278017 | DDB0232430 | CDS | 167304 | 561 | - | 0.233512 | |
DDB_G0278021 | DDB_G0278021 | DDB0232430 | CDS | 170689 | 1371 | + | 0.28884 | |
DDB_G0278025 | DDB_G0278025 | DDB0232430 | CDS | 174453 | 675 | + | 0.368889 | |
DDB_G0278029 | DDB_G0278029 | DDB0232430 | CDS | 176737 | 1446 | - | 0.2213 | |
DDB_G0278031 | DDB_G0278031 | DDB0232430 | CDS | 178451 | 771 | - | 0.217899 | |
DDB_G0278045 | DDB_G0278045 | DDB0232430 | CDS | 190215 | 1014 | + | 0.228797 | |
DDB_G0278047 | DDB_G0278047 | DDB0232430 | CDS | 191972 | 1164 | - | 0.285223 | |
DDB_G0278049 | DDB_G0278049 | DDB0232430 | CDS | 193898 | 222 | + | 0.243243 | |
DDB_G0278059 | DDB_G0278059 | similar to the human acetyl-coenzyme A transporter 1 contains 10 putative transmembrane domains | DDB0232430 | CDS | 207407 | 1857 | - | 0.234787 |
DDB_G0278063 | DDB_G0278063 | highly similar to H. sapiens LONP1 and S. cerevisiae PIM1 Lon protease family members are often located in the mitochondria there is a second Lon protease in Dictyostelium | DDB0232430 | CDS | 211823 | 2871 | + | 0.290143 |
DDB_G0278065 | DDB_G0278065 | contains no functional domains weakly similar to Candida glabrata XP_449244 | DDB0232430 | CDS | 214953 | 246 | - | 0.227642 |
DDB_G0278067 | DDB_G0278067 | DDB0232430 | CDS | 216614 | 570 | + | 0.177193 | |
DDB_G0278071 | DDB_G0278071 | DDB0232430 | CDS | 227597 | 960 | - | 0.239583 | |
DDB_G0278073 | DDB_G0278073 | DDB0232430 | CDS | 229027 | 3633 | - | 0.24305 | |
DDB_G0278075 | DDB_G0278075 | DDB0232430 | CDS | 233703 | 699 | + | 0.271817 | |
DDB_G0278081_ps | DDB_G0278081 | putative pseudogene acetyl-CoA synthetase fragment | DDB0232430 | CDS | 248036 | 786 | - | 0.212468 |
DDB_G0278083 | DDB_G0278083 | highly similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA | DDB0232430 | CDS | 249687 | 2160 | - | 0.224537 |
DDB_G0278087_ps | DDB_G0278087 | putative pseudogene containing a partial protein kinase domain and a partial ankyrin repeat | DDB0232430 | CDS | 256195 | 1557 | - | 0.285806 |
DDB_G0278091 | DDB_G0278091 | DDB0232430 | CDS | 258121 | 924 | - | 0.313853 | |
DDB_G0278093 | DDB_G0278093 | DDB0232430 | CDS | 259686 | 2454 | - | 0.187857 | |
DDB_G0278097 | DDB_G0278097 | DDB0232430 | CDS | 264255 | 6198 | + | 0.261052 | |
DDB_G0278099_ps | DDB_G0278099 | putative pseudogene kinase motif-containing (KMC) | DDB0232430 | CDS | 270787 | 678 | - | 0.222714 |
DDB_G0278103 | DDB_G0278103 | DDB0232430 | CDS | 278742 | 1155 | + | 0.29697 | |
DDB_G0278105 | DDB_G0278105 | highly similar to HNRNPL a heterogeneous ribonucleoprotein that plays a role in pre-mRNA splicing | DDB0232430 | CDS | 280166 | 1593 | - | 0.314501 |
DDB_G0278107 | DDB_G0278107 | catalyzes the reaction pyridoxamine 5'-phosphate Hsub2subO Osub2sub pyridoxal 5'-phosphate NHsub3sub Hsub2subOsub2sub | DDB0232430 | CDS | 283161 | 684 | + | 0.30117 |
DDB_G0278111 | DDB_G0278111 | DDB0232430 | CDS | 294308 | 354 | - | 0.327684 | |
DDB_G0278113 | DDB_G0278113 | similar to protein-tyrosine phosphatases but probably not catalytically active due to lack of conservation of active site residues similar to human PTPLA (protein-tyrosine phosphatase-like member A) contains 4 putative transmembrane domains | DDB0232430 | CDS | 295249 | 678 | - | 0.297935 |
DDB_G0278119 | DDB_G0278119 | DDB0232430 | CDS | 307681 | 1284 | - | 0.284268 | |
DDB_G0278121 | DDB_G0278121 | DDB0232430 | CDS | 321235 | 4422 | - | 0.205337 | |
DDB_G0278123 | DDB_G0278123 | DDB0232430 | CDS | 326427 | 222 | - | 0.405405 | |
DDB_G0278125 | DDB_G0278125 | DDB0232430 | CDS | 327348 | 2496 | - | 0.333333 | |
DDB_G0278127 | DDB_G0278127 | DDB0232430 | CDS | 335063 | 168 | - | 0.327381 | |
DDB_G0278131_ps | DDB_G0278131 | putative pseudogene similar to | DDB0232430 | CDS | 335988 | 789 | - | 0.250951 |
DDB_G0278133 | DDB_G0278133 | DDB0232430 | CDS | 338266 | 1413 | - | 0.261146 | |
DDB_G0278137_ps | DDB_G0278137 | putative pseudogene similar to | DDB0232430 | CDS | 340292 | 564 | - | 0.248227 |
DDB_G0278139_ps | DDB_G0278139 | putative pseudogene fragment similar to | DDB0232430 | CDS | 342260 | 411 | - | 0.26764 |
DDB_G0278143 | DDB_G0278143 | DDB0232430 | CDS | 347205 | 6408 | + | 0.302903 | |
DDB_G0278151 | DDB_G0278151 | DDB0232430 | CDS | 372488 | 1455 | - | 0.294845 | |
DDB_G0278161 | DDB_G0278161 | members of the multi antimicrobial extrusion (MATE) family function as drugsodium antiporters and are found in bacteria archaea and eukaryotes these proteins are predicted to have 12 alpha-helical transmembrane regions | DDB0232430 | CDS | 385354 | 1869 | + | 0.318352 |
DDB_G0278163 | DDB_G0278163 | contains a conserved TM2 domain a pair of transmembrane alpha helices connected by a short linker | DDB0232430 | CDS | 387740 | 486 | - | 0.37037 |
DDB_G0278167 | DDB_G0278167 | highly similar to a part of DDB_G0291514 an immunoglobulin E-set domain-containing protein however much shorter (other members of the family are between 850 and 100 amino acids in length) | DDB0232430 | CDS | 391115 | 153 | + | 0.294118 |
DDB_G0278169 | DDB_G0278169 | DDB0232430 | CDS | 391453 | 825 | - | 0.209697 | |
DDB_G0278171 | DDB_G0278171 | DDB0232430 | CDS | 393144 | 2748 | + | 0.319869 | |
DDB_G0278173 | DDB_G0278173 | DDB0232430 | CDS | 395988 | 1659 | - | 0.209162 | |
DDB_G0278177 | DDB_G0278177 | DDB0232430 | CDS | 398692 | 1506 | + | 0.312085 | |
DDB_G0278179 | DDB_G0278179 | contains two myb domains similar to Arabidopsis thaliana DNAJ heat shock N-terminal domain-containing protein (NP_187752.1) and Mus musculus zuotin related factor 2 (NP_033610.1) | DDB0232430 | CDS | 400484 | 1905 | - | 0.371129 |
DDB_G0278181 | DDB_G0278181 | DDB0232430 | CDS | 405756 | 2802 | + | 0.283726 | |
DDB_G0278183 | DDB_G0278183 | DDB0232430 | CDS | 408831 | 1806 | - | 0.235327 | |
DDB_G0278193 | DDB_G0278193 | ortholog of the asparagine synthetase domain containing protein 1 conserved from yeast to human | DDB0232430 | CDS | 444626 | 2229 | + | 0.277703 |
DDB_G0278195 | DDB_G0278195 | DDB0232430 | CDS | 447655 | 363 | + | 0.269972 | |
DDB_G0278197 | DDB_G0278197 | DDB0232430 | CDS | 448708 | 5442 | - | 0.281882 | |
DDB_G0278199 | DDB_G0278199 | DDB0232430 | CDS | 464388 | 2019 | + | 0.158494 | |
DDB_G0278201 | DDB_G0278201 | DDB0232430 | CDS | 470480 | 348 | - | 0.206897 | |
DDB_G0278209 | DDB_G0278209 | DDB0232430 | CDS | 475574 | 2109 | + | 0.253675 | |
DDB_G0278211 | DDB_G0278211 | DDB0232430 | CDS | 477809 | 2040 | - | 0.218627 | |
DDB_G0278213 | DDB_G0278213 | DDB0232430 | CDS | 481110 | 1320 | + | 0.245455 | |
DDB_G0278215 | DDB_G0278215 | contains a predicted signal sequence and 7 putative transmembrane domains conserved in Dictyostelium and Polysphondylium | DDB0232430 | CDS | 484147 | 5700 | + | 0.295965 |
DDB_G0278219 | DDB_G0278219 | DDB0232430 | CDS | 492709 | 1404 | - | 0.194444 | |
DDB_G0278221_RTE | DDB_G0278221 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232430 | CDS | 495104 | 504 | + | 0.367063 |
DDB_G0278227 | DDB_G0278227 | DDB0232430 | CDS | 509789 | 1620 | - | 0.247531 | |
DDB_G0278229 | DDB_G0278229 | DDB0232430 | CDS | 512537 | 2673 | - | 0.263749 | |
DDB_G0278231 | DDB_G0278231 | DDB0232430 | CDS | 515488 | 408 | - | 0.254902 | |
DDB_G0278233 | DDB_G0278233 | DDB0232430 | CDS | 516517 | 915 | + | 0.269945 | |
DDB_G0278235 | DDB_G0278235 | DDB0232430 | CDS | 523540 | 1314 | - | 0.215373 | |
DDB_G0278239 | DDB_G0278239 | DDB0232430 | CDS | 533251 | 1263 | - | 0.231987 | |
DDB_G0278247 | DDB_G0278247 | DDB0232430 | CDS | 552139 | 2667 | + | 0.175853 | |
DDB_G0278249 | DDB_G0278249 | DDB0232430 | CDS | 554945 | 750 | + | 0.225333 | |
DDB_G0278251_ps | DDB_G0278251 | putative pseudogene fragment similar to gene | DDB0232430 | CDS | 565585 | 396 | - | 0.320707 |
DDB_G0278253 | DDB_G0278253 | DDB0232430 | CDS | 566464 | 1710 | - | 0.27076 | |
DDB_G0278255 | DDB_G0278255 | DDB0232430 | CDS | 568794 | 1545 | - | 0.260841 | |
DDB_G0278257 | DDB_G0278257 | similar to human BROX contains one BRO1 domain | DDB0232430 | CDS | 571285 | 1551 | - | 0.296583 |
DDB_G0278261 | DDB_G0278261 | similar to the H. sapiens proton myo-inositol cotransporter SLC2A13 contains 10 putative transmembrane domains | DDB0232430 | CDS | 577308 | 1893 | + | 0.270998 |
DDB_G0278265 | DDB_G0278265 | DDB0232430 | CDS | 581627 | 1983 | + | 0.252647 | |
DDB_G0278267 | DDB_G0278267 | DDB0232430 | CDS | 586381 | 2631 | + | 0.259597 | |
DDB_G0278269 | DDB_G0278269 | DDB0232430 | CDS | 593095 | 861 | + | 0.275261 | |
DDB_G0278271 | DDB_G0278271 | DDB0232430 | CDS | 599596 | 987 | + | 0.276596 | |
DDB_G0278279 | DDB_G0278279 | DDB0232430 | CDS | 610480 | 1020 | - | 0.230392 | |
DDB_G0278281 | DDB_G0278281 | DDB0232430 | CDS | 614554 | 1194 | - | 0.247069 | |
DDB_G0278291 | DDB_G0278291 | DDB0232430 | CDS | 628601 | 4230 | + | 0.212057 | |
DDB_G0278295 | DDB_G0278295 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232430 | CDS | 638585 | 426 | + | 0.377934 |
DDB_G0278297 | DDB_G0278297 | DDB0232430 | CDS | 639451 | 1203 | - | 0.270989 | |
DDB_G0278299 | DDB_G0278299 | DDB0232430 | CDS | 644203 | 1908 | + | 0.298218 | |
DDB_G0278301 | DDB_G0278301 | DDB0232430 | CDS | 647938 | 3447 | + | 0.262547 | |
DDB_G0278303_ps | DDB_G0278303 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232430 | CDS | 652045 | 2175 | - | 0.243678 |
DDB_G0278311 | DDB_G0278311 | similar to myotubularin a dual-specific lipid phosphatase that dephosphorylates phosphatidylinositol 3-phosphate and phosphatidylinositol (35)-bi-phosphate | DDB0232430 | CDS | 668576 | 3009 | - | 0.312396 |
DDB_G0278313 | DDB_G0278313 | underexpressed in | DDB0232430 | CDS | 673736 | 1752 | + | 0.298516 |
DDB_G0278315 | DDB_G0278315 | DDB0232430 | CDS | 683079 | 1704 | + | 0.230047 | |
DDB_G0278323 | DDB_G0278323 | DDB0232430 | CDS | 704452 | 141 | + | 0.312057 | |
DDB_G0278325 | DDB_G0278325 | DDB0232430 | CDS | 705714 | 1854 | + | 0.187702 | |
DDB_G0278327 | DDB_G0278327 | DDB0232430 | CDS | 707798 | 1677 | + | 0.268933 | |
DDB_G0278329 | DDB_G0278329 | DDB0232430 | CDS | 709648 | 906 | - | 0.260486 | |
DDB_G0278331 | DDB_G0278331 | DDB0232430 | CDS | 711190 | 2481 | + | 0.294236 | |
DDB_G0278333 | DDB_G0278333 | DDB0232430 | CDS | 713907 | 1950 | - | 0.315385 | |
DDB_G0278337 | DDB_G0278337 | DDB0232430 | CDS | 717847 | 417 | - | 0.275779 | |
DDB_G0278339 | DDB_G0278339 | DDB0232430 | CDS | 719660 | 2148 | + | 0.317039 | |
DDB_G0278341 | DDB_G0278341 | highly similar to ACLY which catalyzes the reaction ADP phosphate acetyl-CoA oxaloacetate ATP citrate CoA | DDB0232430 | CDS | 722601 | 1353 | - | 0.308943 |
DDB_G0278347 | DDB_G0278347 | DDB0232430 | CDS | 729623 | 345 | + | 0.301449 | |
DDB_G0278351 | DDB_G0278351 | DDB0232430 | CDS | 734436 | 2991 | + | 0.265129 | |
DDB_G0278355 | DDB_G0278355 | DDB0232430 | CDS | 739670 | 2070 | + | 0.282126 | |
DDB_G0278357 | DDB_G0278357 | DDB0232430 | CDS | 742074 | 201 | - | 0.318408 | |
DDB_G0278359 | DDB_G0278359 | DDB0232430 | CDS | 749797 | 2580 | - | 0.213178 | |
DDB_G0278361_ps | DDB_G0278361 | putative pseudogene very similar to DDB_G0278909 an ARMK family protein | DDB0232430 | CDS | 759575 | 252 | + | 0.313492 |
DDB_G0278363 | DDB_G0278363 | DDB0232430 | CDS | 761869 | 702 | + | 0.32906 | |
DDB_G0278365 | DDB_G0278365 | DDB0232430 | CDS | 762818 | 144 | + | 0.319444 | |
DDB_G0278367 | DDB_G0278367 | similar to DNA polymerase epsilon subunit B in yeast and vertebrates thought to be involved in DNA replication DNA repair and cell-cycle checkpoint control in eukaryotes | DDB0232430 | CDS | 766301 | 2031 | - | 0.255047 |
DDB_G0278369 | DDB_G0278369 | DDB0232430 | CDS | 768975 | 1170 | + | 0.22735 | |
DDB_G0278373 | DDB_G0278373 | at the N-terminus very similar to human ATPBD4 (ATP binding domain 4) also similar to plant and fungal endoribonuclease L-PSP family proteins | DDB0232430 | CDS | 771365 | 2259 | - | 0.232846 |
DDB_G0278375 | DDB_G0278375 | DDB0232430 | CDS | 779475 | 942 | + | 0.309979 | |
DDB_G0278377 | DDB_G0278377 | DDB0232430 | CDS | 782698 | 1932 | - | 0.169772 | |
DDB_G0278383 | DDB_G0278383 | DDB0232430 | CDS | 803175 | 351 | + | 0.31339 | |
DDB_G0278385 | DDB_G0278385 | DDB0232430 | CDS | 810765 | 237 | + | 0.21097 | |
DDB_G0278391 | DDB_G0278391 | DDB0232430 | CDS | 815812 | 627 | + | 0.259968 | |
DDB_G0278393 | DDB_G0278393 | DDB0232430 | CDS | 817359 | 1494 | + | 0.250335 | |
DDB_G0278395 | DDB_G0278395 | DDB0232430 | CDS | 819227 | 1767 | - | 0.262592 | |
DDB_G0278399 | DDB_G0278399 | DDB0232430 | CDS | 821871 | 453 | + | 0.322296 | |
DDB_G0278405 | DDB_G0278405 | DDB0232430 | CDS | 830272 | 1794 | + | 0.244147 | |
DDB_G0278407 | DDB_G0278407 | DDB0232430 | CDS | 833181 | 2685 | + | 0.239106 | |
DDB_G0278411 | DDB_G0278411 | DDB0232430 | CDS | 849816 | 1005 | + | 0.250746 | |
DDB_G0278415 | DDB_G0278415 | DDB0232430 | CDS | 857716 | 945 | + | 0.295238 | |
DDB_G0278421 | DDB_G0278421 | DDB0232430 | CDS | 865177 | 435 | + | 0.282759 | |
DDB_G0278423 | DDB_G0278423 | DDB0232430 | CDS | 866013 | 441 | + | 0.331066 | |
DDB_G0278425 | DDB_G0278425 | DDB0232430 | CDS | 866714 | 3273 | - | 0.276199 | |
DDB_G0278427 | DDB_G0278427 | DDB0232430 | CDS | 870597 | 666 | + | 0.268769 | |
DDB_G0278431 | DDB_G0278431 | DDB0232430 | CDS | 872674 | 1440 | - | 0.30625 | |
DDB_G0278433 | DDB_G0278433 | DDB0232430 | CDS | 875590 | 1518 | + | 0.353096 | |
DDB_G0278435 | DDB_G0278435 | DDB0232430 | CDS | 877848 | 2661 | - | 0.269823 | |
DDB_G0278437 | DDB_G0278437 | DDB0232430 | CDS | 880882 | 441 | - | 0.321995 | |
DDB_G0278439 | DDB_G0278439 | DDB0232430 | CDS | 881959 | 441 | - | 0.312925 | |
DDB_G0278441 | DDB_G0278441 | DDB0232430 | CDS | 883102 | 1062 | - | 0.277778 | |
DDB_G0278443 | DDB_G0278443 | DDB0232430 | CDS | 885094 | 1626 | + | 0.250308 | |
DDB_G0278451 | DDB_G0278451 | DDB0232430 | CDS | 898275 | 1797 | + | 0.189761 | |
DDB_G0278453 | DDB_G0278453 | contains 5 coiled-coil domains highly repetitive glutamine and glutamic acid-rich protein | DDB0232430 | CDS | 901380 | 2472 | + | 0.330097 |
DDB_G0278455 | DDB_G0278455 | DDB0232430 | CDS | 904324 | 1101 | - | 0.229791 | |
DDB_G0278459 | DDB_G0278459 | DDB0232430 | CDS | 909148 | 327 | - | 0.24159 | |
DDB_G0278461 | DDB_G0278461 | DDB0232430 | CDS | 910604 | 2847 | + | 0.270109 | |
DDB_G0278463 | DDB_G0278463 | DDB0232430 | CDS | 913723 | 2034 | + | 0.247296 | |
DDB_G0278465 | DDB_G0278465 | DDB0232430 | CDS | 916080 | 177 | - | 0.242938 | |
DDB_G0278467 | DDB_G0278467 | DDB0232430 | CDS | 918286 | 180 | - | 0.222222 | |
DDB_G0278469 | DDB_G0278469 | DDB0232430 | CDS | 924371 | 2148 | + | 0.282123 | |
DDB_G0278471 | DDB_G0278471 | DDB0232430 | CDS | 926878 | 1584 | - | 0.304293 | |
DDB_G0278473 | DDB_G0278473 | DDB0232430 | CDS | 929409 | 1995 | - | 0.277694 | |
DDB_G0278475 | DDB_G0278475 | DDB0232430 | CDS | 932374 | 1806 | + | 0.253599 | |
DDB_G0278479 | DDB_G0278479 | DDB0232430 | CDS | 936199 | 1434 | + | 0.239191 | |
DDB_G0278487 | DDB_G0278487 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases belongs to the CMGC group of protein kinases | DDB0232430 | CDS | 959760 | 1911 | + | 0.288854 |
DDB_G0278489 | DDB_G0278489 | DDB0232430 | CDS | 962952 | 1350 | - | 0.214815 | |
DDB_G0278491 | DDB_G0278491 | DDB0232430 | CDS | 965453 | 1356 | - | 0.231563 | |
DDB_G0278493 | DDB_G0278493 | DDB0232430 | CDS | 967226 | 528 | + | 0.263258 | |
DDB_G0278499 | DDB_G0278499 | protein phosphatase 2C is a serinethreonine specific protein phosphatase with broad substrate specificity and dependent on divalent cations (mainly manganese and magnesium) for its activity similar to P. pallidum protein | DDB0232430 | CDS | 971318 | 2076 | + | 0.322254 |
DDB_G0278501 | DDB_G0278501 | weakly similar to yeast transmembrane ubiquitin ligase E3 (TUL1) protein involved in ubiquitinating and sorting certain membrane proteins contains 6 predicted transmembrane domains and one additional signal sequence | DDB0232430 | CDS | 976180 | 2001 | + | 0.246877 |
DDB_G0278503 | DDB_G0278503 | DDB0232430 | CDS | 979308 | 666 | + | 0.273273 | |
DDB_G0278505 | DDB_G0278505 | conserved in bacteria similar to human HEMK1 (hemK methyltransferase family member 1) and S. cerevisiae MTQ1 (mitochondrial N(5)-glutamine methyltransferase MTQ1) | DDB0232430 | CDS | 980321 | 1032 | + | 0.194767 |
DDB_G0278507 | DDB_G0278507 | DDB0232430 | CDS | 981524 | 1908 | - | 0.277254 | |
DDB_G0278509 | DDB_G0278509 | DDB0232430 | CDS | 984753 | 3747 | + | 0.238858 | |
DDB_G0278511_ps | DDB_G0278511 | putative pseudogene fragment highly similar to neighboring | DDB0232430 | CDS | 988851 | 303 | - | 0.257426 |
DDB_G0278513 | DDB_G0278513 | DDB0232430 | CDS | 990043 | 2226 | - | 0.284367 | |
DDB_G0278515_ps | DDB_G0278515 | putative pseudogene highly similar to neighboring | DDB0232430 | CDS | 993620 | 321 | - | 0.261682 |
DDB_G0278517 | DDB_G0278517 | DDB0232430 | CDS | 995255 | 810 | + | 0.234568 | |
DDB_G0278519 | DDB_G0278519 | DDB0232430 | CDS | 997978 | 606 | + | 0.292079 | |
DDB_G0278521 | DDB_G0278521 | member of the TKL (tyrosine kinase-like) group the MLK (mixed lineage kinase) family and the HH498 subfamily contains an ankyrin repeat | DDB0232430 | CDS | 1000912 | 2727 | - | 0.226989 |
DDB_G0278523 | DDB_G0278523 | DDB0232430 | CDS | 1018779 | 459 | - | 0.357298 | |
DDB_G0278527 | DDB_G0278527 | DDB0232430 | CDS | 1022106 | 2826 | + | 0.274947 | |
DDB_G0278529 | DDB_G0278529 | DDB0232430 | CDS | 1025609 | 582 | - | 0.266323 | |
DDB_G0278531 | DDB_G0278531 | DDB0232430 | CDS | 1028305 | 4107 | - | 0.244704 | |
DDB_G0278535 | DDB_G0278535 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family contains an ankyrin repeat region and a SAM (Sterile alpha motif) domain | DDB0232430 | CDS | 1034770 | 2547 | + | 0.329407 |
DDB_G0278537 | DDB_G0278537 | DDB0232430 | CDS | 1038088 | 543 | - | 0.300184 | |
DDB_G0278541 | DDB_G0278541 | MBOAT family protein membrane proteins that contains a variety of acyltransferase enzymes most similar to S. cerevisiae ALE1 and mammalian MBOAT2 contains 9 predicted transmembrane domains | DDB0232430 | CDS | 1041012 | 1410 | - | 0.334752 |
DDB_G0278547 | DDB_G0278547 | DDB0232430 | CDS | 1050062 | 2214 | - | 0.268744 | |
DDB_G0278551 | DDB_G0278551 | DDB0232430 | CDS | 1060290 | 2220 | - | 0.345495 | |
DDB_G0278553 | DDB_G0278553 | small amoebozoan gene family absent in other organisms | DDB0232430 | CDS | 1066866 | 447 | - | 0.35123 |
DDB_G0278557 | DDB_G0278557 | small amoebozoan gene family absent in other organisms | DDB0232430 | CDS | 1071153 | 462 | - | 0.311688 |
DDB_G0278559 | DDB_G0278559 | small amoebozoan gene family absent in other organisms | DDB0232430 | CDS | 1073057 | 435 | - | 0.312644 |
DDB_G0278561 | DDB_G0278561 | small amoebozoan gene family absent in other organisms | DDB0232430 | CDS | 1075082 | 417 | - | 0.314149 |
DDB_G0278563 | DDB_G0278563 | DDB0232430 | CDS | 1076940 | 600 | - | 0.395 | |
DDB_G0278565 | DDB_G0278565 | small amoebozoan gene family absent in other organisms | DDB0232430 | CDS | 1078278 | 462 | - | 0.311688 |
DDB_G0278567 | DDB_G0278567 | catalyzes the reaction NADH 2 ferricytochrome b5 NAD() H() 2 ferrocytochrome involved in desaturation and elongation of fatty acids cholesterol biosynthesis and drug metabolism | DDB0232430 | CDS | 1089249 | 1386 | + | 0.227273 |
DDB_G0278569 | DDB_G0278569 | DDB0232430 | CDS | 1091191 | 642 | + | 0.275701 | |
DDB_G0278571 | DDB_G0278571 | conserved protein contains two transmembrane domains | DDB0232430 | CDS | 1092876 | 351 | - | 0.373219 |
DDB_G0278573 | DDB_G0278573 | DDB0232430 | CDS | 1094317 | 810 | + | 0.245679 | |
DDB_G0278575 | DDB_G0278575 | DDB0232430 | CDS | 1095238 | 1539 | - | 0.323587 | |
DDB_G0278577 | DDB_G0278577 | contains one putative transmembrane domain contains a predicted signal sequence similar to D. purpureum protein | DDB0232430 | CDS | 1097386 | 456 | + | 0.274123 |
DDB_G0278585 | DDB_G0278585 | DDB0232430 | CDS | 26113 | 2664 | + | 0.202327 | |
DDB_G0278587 | DDB_G0278587 | DDB0232430 | CDS | 36191 | 948 | + | 0.385021 | |
DDB_G0278591 | DDB_G0278591 | DDB0232430 | CDS | 225002 | 2094 | + | 0.281757 | |
DDB_G0278597 | DDB_G0278597 | DDB0232430 | CDS | 287423 | 831 | - | 0.305656 | |
DDB_G0278601 | DDB_G0278601 | DDB0232430 | CDS | 297893 | 3909 | + | 0.240727 | |
DDB_G0278603 | DDB_G0278603 | DDB0232430 | CDS | 311161 | 441 | + | 0.23356 | |
DDB_G0278609 | DDB_G0278609 | DDB0232430 | CDS | 316046 | 1725 | + | 0.291014 | |
DDB_G0278611 | DDB_G0278611 | DDB0232430 | CDS | 318473 | 2640 | + | 0.182197 | |
DDB_G0278613 | DDB_G0278613 | N-terminus similar to matrilin a vertebrate extracellular matrix protein expressed in cartilage C-terminus similar to other Dictyostelium EGF repeat-containing proteins contains 11 EGF (epidermal growth factor) repeats | DDB0232430 | CDS | 358498 | 2898 | - | 0.3147 |
DDB_G0278617 | DDB_G0278617 | DDB0232430 | CDS | 369004 | 2964 | + | 0.247638 | |
DDB_G0278621 | DDB_G0278621 | DDB0232430 | CDS | 427974 | 2571 | + | 0.266044 | |
DDB_G0278623 | DDB_G0278623 | DDB0232430 | CDS | 430729 | 1005 | - | 0.331343 | |
DDB_G0278625 | DDB_G0278625 | DDB0232430 | CDS | 432237 | 2862 | + | 0.206848 | |
DDB_G0278627 | DDB_G0278627 | contains 2 coiled-coil domains similar to D. purpureum protein | DDB0232430 | CDS | 435839 | 2634 | - | 0.243356 |
DDB_G0278629 | DDB_G0278629 | DDB0232430 | CDS | 459553 | 2115 | + | 0.299291 | |
DDB_G0278631 | DDB_G0278631 | putative ortholog of H. sapiens SLC35D2 UDP-N-acetylglucosamineUDP-glucoseGDP-mannose transporter contains 10 putative transmembrane domains | DDB0232430 | CDS | 462648 | 1149 | + | 0.222802 |
DDB_G0278633_RTE | DDB_G0278633 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232430 | CDS | 506205 | 1497 | + | 0.301269 |
DDB_G0278635 | DDB_G0278635 | similar to mammalian ribonucleaseangiogenesis inhibitor proteins | DDB0232430 | CDS | 519532 | 1875 | - | 0.256533 |
DDB_G0278641_RTE | DDB_G0278641 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 546702 | 1335 | - | 0.307116 |
DDB_G0278645 | DDB_G0278645 | DDB0232430 | CDS | 594341 | 2070 | - | 0.282609 | |
DDB_G0278647 | DDB_G0278647 | DDB0232430 | CDS | 612467 | 1020 | - | 0.226471 | |
DDB_G0278655 | DDB_G0278655 | DDB0232430 | CDS | 672611 | 867 | + | 0.302191 | |
DDB_G0278657_ps | DDB_G0278657 | putative pseudogene similar to DDB_G0293286 and DDB_G0293288 | DDB0232430 | CDS | 676729 | 4128 | + | 0.336725 |
DDB_G0278659 | DDB_G0278659 | DDB0232430 | CDS | 692443 | 2559 | - | 0.205549 | |
DDB_G0278661 | DDB_G0278661 | DDB0232430 | CDS | 695788 | 4023 | - | 0.316182 | |
DDB_G0278663 | DDB_G0278663 | DDB0232430 | CDS | 701606 | 1908 | - | 0.249476 | |
DDB_G0278665 | DDB_G0278665 | DDB0232430 | CDS | 753135 | 3273 | - | 0.31103 | |
DDB_G0278667 | DDB_G0278667 | DDB0232430 | CDS | 758682 | 543 | + | 0.327808 | |
DDB_G0278669 | DDB_G0278669 | DDB0232430 | CDS | 781169 | 1230 | - | 0.225203 | |
DDB_G0278671 | DDB_G0278671 | DDB0232430 | CDS | 784969 | 1656 | - | 0.240338 | |
DDB_G0278675 | DDB_G0278675 | DDB0232430 | CDS | 789665 | 1752 | - | 0.261986 | |
DDB_G0278677 | DDB_G0278677 | DDB0232430 | CDS | 803909 | 894 | - | 0.227069 | |
DDB_G0278681 | DDB_G0278681 | DDB0232430 | CDS | 827063 | 1935 | + | 0.239276 | |
DDB_G0278683 | DDB_G0278683 | DDB0232430 | CDS | 839543 | 570 | + | 0.280702 | |
DDB_G0278689 | DDB_G0278689 | DDB0232430 | CDS | 923436 | 219 | - | 0.251142 | |
DDB_G0278691 | DDB_G0278691 | DDB0232430 | CDS | 937883 | 1395 | - | 0.268817 | |
DDB_G0278693 | DDB_G0278693 | DDB0232430 | CDS | 939361 | 1926 | - | 0.20405 | |
DDB_G0278695 | DDB_G0278695 | putative secreted protein contains a predicted signal sequence | DDB0232430 | CDS | 999218 | 198 | + | 0.272727 |
DDB_G0278697 | DDB_G0278697 | DDB0232430 | CDS | 1000143 | 615 | + | 0.380488 | |
DDB_G0278699 | DDB_G0278699 | contains a weak tweety (tty) domain which is of unknown function | DDB0232430 | CDS | 1004448 | 1674 | + | 0.310633 |
DDB_G0278705 | DDB_G0278705 | DDB0232430 | CDS | 1058155 | 1428 | - | 0.282913 | |
DDB_G0278707 | DDB_G0278707 | small amoebozoan gene family absent in other organisms | DDB0232430 | CDS | 1079955 | 462 | - | 0.307359 |
DDB_G0278709 | DDB_G0278709 | DDB0232430 | CDS | 1084792 | 1122 | + | 0.292335 | |
DDB_G0278719 | DDB_G0278719 | DDB0232430 | CDS | 499808 | 1605 | - | 0.174455 | |
DDB_G0278743 | DDB_G0278743 | DDB0232430 | CDS | 1109794 | 753 | + | 0.240372 | |
DDB_G0278745 | DDB_G0278745 | DDB0232430 | CDS | 1111389 | 756 | + | 0.277778 | |
DDB_G0278747 | DDB_G0278747 | DDB0232430 | CDS | 1113093 | 1689 | + | 0.255773 | |
DDB_G0278749 | DDB_G0278749 | DDB0232430 | CDS | 1114992 | 1833 | - | 0.310966 | |
DDB_G0278751 | DDB_G0278751 | similar to S. cerevisiae UPF0399 protein YOR287C which may be involved in rRNA-processing and ribosome biosynthesis contains two putative coiled-coil domains | DDB0232430 | CDS | 1117749 | 897 | + | 0.274247 |
DDB_G0278757 | DDB_G0278757 | DDB0232430 | CDS | 1123519 | 4032 | - | 0.308532 | |
DDB_G0278759 | DDB_G0278759 | DDB0232430 | CDS | 1128110 | 2484 | + | 0.231079 | |
DDB_G0278761 | DDB_G0278761 | DDB0232430 | CDS | 1131314 | 5382 | + | 0.281865 | |
DDB_G0278763 | DDB_G0278763 | DDB0232430 | CDS | 1137106 | 699 | - | 0.216023 | |
DDB_G0278765 | DDB_G0278765 | DDB0232430 | CDS | 1138348 | 648 | - | 0.285494 | |
DDB_G0278767 | DDB_G0278767 | DDB0232430 | CDS | 1139276 | 1911 | + | 0.200942 | |
DDB_G0278771 | DDB_G0278771 | DDB0232430 | CDS | 1143468 | 4053 | - | 0.278806 | |
DDB_G0278773 | DDB_G0278773 | similar to human VAPA and VAPB defects in VAPB cause amyotrophic lateral sclerosis 8 (ALS8) | DDB0232430 | CDS | 1149897 | 933 | - | 0.276527 |
DDB_G0278777_ps | DDB_G0278777 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 1160699 | 687 | + | 0.22853 |
DDB_G0278785 | DDB_G0278785 | DDB0232430 | CDS | 1176379 | 891 | + | 0.332211 | |
DDB_G0278787 | DDB_G0278787 | DDB0232430 | CDS | 1177436 | 804 | - | 0.220149 | |
DDB_G0278789 | DDB_G0278789 | similar to DNAJA3 DnaJ homolog subfamily A member 3 | DDB0232430 | CDS | 1182227 | 1383 | + | 0.336226 |
DDB_G0278791 | DDB_G0278791 | DDB0232430 | CDS | 1184009 | 1185 | - | 0.228692 | |
DDB_G0278793 | DDB_G0278793 | DDB0232430 | CDS | 1186077 | 690 | + | 0.350725 | |
DDB_G0278797 | DDB_G0278797 | DDB0232430 | CDS | 1192386 | 1233 | - | 0.316302 | |
DDB_G0278801 | DDB_G0278801 | DDB0232430 | CDS | 1206396 | 1491 | - | 0.221999 | |
DDB_G0278805 | DDB_G0278805 | DDB0232430 | CDS | 1209711 | 972 | + | 0.282922 | |
DDB_G0278807 | DDB_G0278807 | DDB0232430 | CDS | 1213734 | 288 | + | 0.326389 | |
DDB_G0278811 | DDB_G0278811 | DDB0232430 | CDS | 1230143 | 297 | + | 0.215488 | |
DDB_G0278813 | DDB_G0278813 | DDB0232430 | CDS | 1230925 | 336 | + | 0.309524 | |
DDB_G0278817 | DDB_G0278817 | DDB0232430 | CDS | 1235984 | 1818 | + | 0.205721 | |
DDB_G0278819 | DDB_G0278819 | ortholog of human CRNKL1 (crooked neck-like) involved in pre-mRNA splicing contains 11 HAT (Half A TPR) repeats | DDB0232430 | CDS | 1238183 | 2118 | + | 0.283758 |
DDB_G0278823 | DDB_G0278823 | similar to human FDPS (farnesyl pyrophosphate synthetase) which is a key enzyme in isoprenoid biosynthesis may have both dimethylallyltranstransferase and geranyltranstransferase activities | DDB0232430 | CDS | 1243679 | 1071 | - | 0.267974 |
DDB_G0278825 | DDB_G0278825 | DDB0232430 | CDS | 1248051 | 2718 | + | 0.316409 | |
DDB_G0278827 | DDB_G0278827 | DDB0232430 | CDS | 1252983 | 5451 | - | 0.259035 | |
DDB_G0278829 | DDB_G0278829 | DDB0232430 | CDS | 1258942 | 1692 | - | 0.232861 | |
DDB_G0278831 | DDB_G0278831 | DDB0232430 | CDS | 1261226 | 531 | + | 0.346516 | |
DDB_G0278833 | DDB_G0278833 | DDB0232430 | CDS | 1262058 | 129 | - | 0.410853 | |
DDB_G0278835 | DDB_G0278835 | DDB0232430 | CDS | 1262788 | 108 | - | 0.277778 | |
DDB_G0278837 | DDB_G0278837 | DDB0232430 | CDS | 1263275 | 132 | - | 0.401515 | |
DDB_G0278839 | DDB_G0278839 | DDB0232430 | CDS | 1264354 | 822 | + | 0.243309 | |
DDB_G0278841 | DDB_G0278841 | DDB0232430 | CDS | 1265394 | 1560 | - | 0.253846 | |
DDB_G0278845 | DDB_G0278845 | member of the AGC kinase group similar to kinase domains of NDR (nuclear Dbf2-related) family members | DDB0232430 | CDS | 1269374 | 4053 | - | 0.265976 |
DDB_G0278851 | DDB_G0278851 | bCommunity annotation:b DDB G0278851 is similar to the rik1-associated factor raf1 of S. pombe. Raf1 (as well as rik1) participates in the Clr4 methyltransferase complex (see Horn et al Genes and Development 19 1705-1714) which methylates H3K9 important in silencing centromeric and telomeric repeats. It has recently been shown that these repeats are transcribed for a limited period during S-phase (Chen et al Nature 451 734-737 (2008) that this transcription is essential for RNA-interference mediated heterochromatin assembly and that the repeats are transcriptionally repressed outside of S-phase.br DDB_G0278851 and a second member of the Clr4 complex the methyl transferase clr4suvA are both overexpressed about threefold (p2e-63) in a Dicty strain in which the retinoblastoma-like protein rblA has been disrupted. Most genes associated with S-phase or mitosis are overexpressed in this strain. The activity of the clr4 complex is thus likely to be S-phase associated. All these observations a | DDB0232430 | CDS | 1278474 | 2757 | - | 0.318099 |
DDB_G0278853 | DDB_G0278853 | DDB0232430 | CDS | 1282301 | 390 | + | 0.120513 | |
DDB_G0278857 | DDB_G0278857 | DDB0232430 | CDS | 1289087 | 618 | + | 0.224919 | |
DDB_G0278859 | DDB_G0278859 | DDB0232430 | CDS | 1292767 | 2718 | - | 0.18028 | |
DDB_G0278861 | DDB_G0278861 | DDB0232430 | CDS | 1295784 | 1449 | - | 0.235335 | |
DDB_G0278865 | DDB_G0278865 | DDB0232430 | CDS | 1303121 | 591 | + | 0.336717 | |
DDB_G0278869 | DDB_G0278869 | DDB0232430 | CDS | 1313132 | 3126 | + | 0.242802 | |
DDB_G0278871 | DDB_G0278871 | DDB0232430 | CDS | 1320697 | 549 | + | 0.216758 | |
DDB_G0278881 | DDB_G0278881 | weakly similar to mannose-6-phosphatensulin-like growth factor 2 receptor | DDB0232430 | CDS | 1333528 | 1119 | + | 0.223414 |
DDB_G0278883 | DDB_G0278883 | DDB0232430 | CDS | 1337376 | 675 | + | 0.265185 | |
DDB_G0278891 | DDB_G0278891 | DDB0232430 | CDS | 1344963 | 1065 | + | 0.258216 | |
DDB_G0278897 | DDB_G0278897 | DDB0232430 | CDS | 1358187 | 654 | + | 0.295107 | |
DDB_G0278899 | DDB_G0278899 | DDB0232430 | CDS | 1359880 | 1206 | + | 0.157546 | |
DDB_G0278901 | DDB_G0278901 | DDB0232430 | CDS | 1361340 | 4488 | - | 0.282308 | |
DDB_G0278903 | DDB_G0278903 | DDB0232430 | CDS | 1368428 | 1413 | + | 0.206653 | |
DDB_G0278905 | DDB_G0278905 | DDB0232430 | CDS | 1370259 | 2667 | + | 0.194601 | |
DDB_G0278909 | DDB_G0278909 | member of the TKL (tyrosine kinase-like) group and the ARMK (armadillo repeat-containing kinase) family contains an N-terminal LRR and a C-terminal armadillobeta-catenin repeat unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232430 | CDS | 1376167 | 5811 | + | 0.293581 |
DDB_G0278911 | DDB_G0278911 | DDB0232430 | CDS | 1382986 | 804 | + | 0.226368 | |
DDB_G0278913 | DDB_G0278913 | DDB0232430 | CDS | 1384248 | 1251 | + | 0.221423 | |
DDB_G0278915 | DDB_G0278915 | DDB0232430 | CDS | 1392137 | 1965 | + | 0.231043 | |
DDB_G0278917 | DDB_G0278917 | DDB0232430 | CDS | 1397821 | 498 | - | 0.206827 | |
DDB_G0278919 | DDB_G0278919 | DDB0232430 | CDS | 1399877 | 4239 | + | 0.241802 | |
DDB_G0278921 | DDB_G0278921 | DDB0232430 | CDS | 1404420 | 2766 | - | 0.236081 | |
DDB_G0278923 | DDB_G0278923 | DDB0232430 | CDS | 1407772 | 2379 | + | 0.265658 | |
DDB_G0278925 | DDB_G0278925 | DDB0232430 | CDS | 1410371 | 1818 | + | 0.257426 | |
DDB_G0278927 | DDB_G0278927 | DDB0232430 | CDS | 1414868 | 1488 | + | 0.202957 | |
DDB_G0278933 | DDB_G0278933 | DDB0232430 | CDS | 1421183 | 468 | + | 0.309829 | |
DDB_G0278937 | DDB_G0278937 | DDB0232430 | CDS | 1214678 | 2715 | + | 0.271455 | |
DDB_G0278939 | DDB_G0278939 | DDB0232430 | CDS | 1222621 | 1530 | - | 0.20719 | |
DDB_G0278941 | DDB_G0278941 | DDB0232430 | CDS | 1224203 | 585 | - | 0.276923 | |
DDB_G0278943 | DDB_G0278943 | tRNA-specific adenosine deaminase deaminates adenosine-37 to inosine in tRNA-Ala ortholog of S. cerevisiae TAD1 and H. sapiens adat1 | DDB0232430 | CDS | 1240717 | 1638 | + | 0.21917 |
DDB_G0278945 | DDB_G0278945 | DDB0232430 | CDS | 1251221 | 960 | + | 0.292708 | |
DDB_G0278951 | DDB_G0278951 | DDB0232430 | CDS | 1318190 | 264 | - | 0.359848 | |
DDB_G0278953 | DDB_G0278953 | contains four CBS domains similar to protein kinase 5'AMP activated gamma subunit expressed in prespore cells | DDB0232430 | CDS | 1335145 | 1080 | - | 0.312963 |
DDB_G0278955 | DDB_G0278955 | DDB0232430 | CDS | 1366879 | 1212 | + | 0.263201 | |
DDB_G0278957 | DDB_G0278957 | DDB0232430 | CDS | 1385676 | 858 | - | 0.251748 | |
DDB_G0278961 | DDB_G0278961 | belongs to the PhyH family homolog of human PHYHD1 | DDB0232430 | CDS | 1412506 | 849 | - | 0.286219 |
DDB_G0278973 | DDB_G0278973 | DDB0232430 | CDS | 1448552 | 1845 | - | 0.197832 | |
DDB_G0278975 | DDB_G0278975 | DDB0232430 | CDS | 1450854 | 4248 | - | 0.29096 | |
DDB_G0278977 | DDB_G0278977 | DDB0232430 | CDS | 1457351 | 2250 | + | 0.188889 | |
DDB_G0278979 | DDB_G0278979 | DDB0232430 | CDS | 1466872 | 1068 | - | 0.264045 | |
DDB_G0278981 | DDB_G0278981 | ortholog of the E3 ubiquitin-protein ligase TRIAD1 (Two RING fingers And Double RING finger Linked) which is involved in the proteasomal degradation pathway contains a ubiqutin associalte (UBA) domain and 2 RING-type zinc fingers sourrounding a cysteine-rich domain (C6HC) | DDB0232430 | CDS | 1470681 | 1692 | - | 0.303782 |
DDB_G0278985 | DDB_G0278985 | DDB0232430 | CDS | 1475884 | 699 | - | 0.288984 | |
DDB_G0278987 | DDB_G0278987 | DDB0232430 | CDS | 1477419 | 987 | - | 0.29078 | |
DDB_G0278989 | DDB_G0278989 | DDB0232430 | CDS | 1479334 | 465 | + | 0.331183 | |
DDB_G0278993 | DDB_G0278993 | DDB0232430 | CDS | 1489337 | 573 | + | 0.239092 | |
DDB_G0278995 | DDB_G0278995 | DDB0232430 | CDS | 1494607 | 3168 | + | 0.223169 | |
DDB_G0278997 | DDB_G0278997 | conserved in bacteria and plants there is an almost identical gene | DDB0232430 | CDS | 1499624 | 876 | + | 0.270548 |
DDB_G0278999 | DDB_G0278999 | conserved in bacteria and plants there is an almost identical gene | DDB0232430 | CDS | 1501033 | 876 | + | 0.270548 |
DDB_G0279003 | DDB_G0279003 | DDB0232430 | CDS | 1503809 | 2328 | + | 0.334192 | |
DDB_G0279005 | DDB_G0279005 | DDB0232430 | CDS | 1507522 | 1929 | + | 0.270607 | |
DDB_G0279011 | DDB_G0279011 | DDB0232430 | CDS | 1513004 | 270 | - | 0.296296 | |
DDB_G0279015 | DDB_G0279015 | DDB0232430 | CDS | 1515905 | 1188 | + | 0.286195 | |
DDB_G0279017 | DDB_G0279017 | DDB0232430 | CDS | 1517215 | 915 | - | 0.197814 | |
DDB_G0279019 | DDB_G0279019 | DDB0232430 | CDS | 1519155 | 885 | + | 0.250847 | |
DDB_G0279021 | DDB_G0279021 | DDB0232430 | CDS | 1522629 | 2997 | + | 0.243911 | |
DDB_G0279023 | DDB_G0279023 | contains a predicted signal peptide and a putative transmembrane domain contains a serine-rich region similar to bacterial SASA repeat | DDB0232430 | CDS | 1526543 | 1215 | + | 0.331687 |
DDB_G0279033 | DDB_G0279033 | DDB0232430 | CDS | 1534984 | 1890 | - | 0.24709 | |
DDB_G0279035 | DDB_G0279035 | DDB0232430 | CDS | 1538571 | 1029 | + | 0.283771 | |
DDB_G0279039 | DDB_G0279039 | DDB0232430 | CDS | 1541078 | 2886 | + | 0.21483 | |
DDB_G0279041 | DDB_G0279041 | DDB0232430 | CDS | 1545614 | 1914 | + | 0.242947 | |
DDB_G0279043 | DDB_G0279043 | DDB0232430 | CDS | 1548959 | 603 | + | 0.310116 | |
DDB_G0279045 | DDB_G0279045 | DDB0232430 | CDS | 1551325 | 1746 | + | 0.321306 | |
DDB_G0279047 | DDB_G0279047 | conserved protein contains a signal peptide | DDB0232430 | CDS | 1553555 | 453 | - | 0.238411 |
DDB_G0279049 | DDB_G0279049 | conserved in dictyostelids contains a predicted peroxisomal targeting signal | DDB0232430 | CDS | 1554715 | 2550 | + | 0.236863 |
DDB_G0279051 | DDB_G0279051 | DDB0232430 | CDS | 1559805 | 3537 | + | 0.197908 | |
DDB_G0279053 | DDB_G0279053 | catalyzes the reaction a 5'-ribonucleotide Hsub2subO a ribonucleoside phosphate | DDB0232430 | CDS | 1563766 | 1779 | + | 0.296796 |
DDB_G0279055_RTE | DDB_G0279055 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 1568998 | 3180 | - | 0.349686 |
DDB_G0279057 | DDB_G0279057 | DDB0232430 | CDS | 1574903 | 174 | - | 0.241379 | |
DDB_G0279059 | DDB_G0279059 | DDB0232430 | CDS | 1576793 | 759 | + | 0.320158 | |
DDB_G0279065 | DDB_G0279065 | DDB0232430 | CDS | 1468580 | 1710 | + | 0.191813 | |
DDB_G0279067 | DDB_G0279067 | DDB0232430 | CDS | 1520762 | 1434 | + | 0.266388 | |
DDB_G0279069 | DDB_G0279069 | DDB0232430 | CDS | 1528089 | 693 | - | 0.266955 | |
DDB_G0279073 | DDB_G0279073 | DDB0232430 | CDS | 1550621 | 258 | + | 0.224806 | |
DDB_G0279077_RTE | DDB_G0279077 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 1572702 | 1080 | - | 0.415741 |
DDB_G0279089 | DDB_G0279089 | DDB0232430 | CDS | 1601965 | 4191 | - | 0.272727 | |
DDB_G0279091 | DDB_G0279091 | DDB0232430 | CDS | 1608785 | 4002 | - | 0.305847 | |
DDB_G0279093 | DDB_G0279093 | similar to kelch proteins that contain the BTBPOZ domain and are actin binding proteins such as mayven and actinfilin the BTBPOZ domain contains the K channel tertramerization domain | DDB0232430 | CDS | 1618503 | 2349 | + | 0.257982 |
DDB_G0279097_ps | DDB_G0279097 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232430 | CDS | 1625351 | 195 | + | 0.282051 |
DDB_G0279099 | DDB_G0279099 | ortholog of DEPDC5 a conserved eukaryotic protein that may be involved in intracellular signaling | DDB0232430 | CDS | 1626037 | 6729 | - | 0.281171 |
DDB_G0279101 | DDB_G0279101 | DDB0232430 | CDS | 1633445 | 324 | - | 0.243827 | |
DDB_G0279103 | DDB_G0279103 | DDB0232430 | CDS | 1634323 | 300 | - | 0.24 | |
DDB_G0279105 | DDB_G0279105 | DDB0232430 | CDS | 1635440 | 3261 | + | 0.274149 | |
DDB_G0279107 | DDB_G0279107 | DDB0232430 | CDS | 1638888 | 3717 | - | 0.283562 | |
DDB_G0279111 | DDB_G0279111 | DDB0232430 | CDS | 1646736 | 1122 | + | 0.251337 | |
DDB_G0279115 | DDB_G0279115 | DDB0232430 | CDS | 1651481 | 3138 | + | 0.288719 | |
DDB_G0279117 | DDB_G0279117 | DDB0232430 | CDS | 1657313 | 171 | + | 0.222222 | |
DDB_G0279119 | DDB_G0279119 | DDB0232430 | CDS | 1658914 | 639 | - | 0.305164 | |
DDB_G0279121 | DDB_G0279121 | DDB0232430 | CDS | 1660011 | 459 | + | 0.326797 | |
DDB_G0279125 | DDB_G0279125 | DDB0232430 | CDS | 1658002 | 171 | - | 0.321637 | |
DDB_G0279127_RTE | DDB_G0279127 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232430 | CDS | 1660925 | 2858 | - | 0.29846 |
DDB_G0279131 | DDB_G0279131 | GFA enzymes catalyze the condensation of formaldehyde and glutathione to S-hydroxymethylglutathione all known members of this family contain 5 strongly conserved cysteine residues | DDB0232430 | CDS | 1671588 | 465 | - | 0.292473 |
DDB_G0279135 | DDB_G0279135 | DDB0232430 | CDS | 1673721 | 813 | - | 0.204182 | |
DDB_G0279137 | DDB_G0279137 | catalyzes the reaction 5-methyltetrahydrofolate NADPsupsup 510-methylenetetrahydrofolate NADPH Hsupsup in various biosynthetic pathways | DDB0232430 | CDS | 1675769 | 1884 | - | 0.379512 |
DDB_G0279139 | DDB_G0279139 | homolog of human ANKRD29 contains 8 ankyrin repeats | DDB0232430 | CDS | 1678974 | 1143 | + | 0.297463 |
DDB_G0279143 | DDB_G0279143 | DDB0232430 | CDS | 1684165 | 2127 | + | 0.238834 | |
DDB_G0279145 | DDB_G0279145 | DDB0232430 | CDS | 1686583 | 1587 | - | 0.31758 | |
DDB_G0279153_RTE | DDB_G0279153 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 1669827 | 1077 | - | 0.414113 |
DDB_G0279155 | DDB_G0279155 | DDB0232430 | CDS | 1698727 | 1356 | + | 0.247788 | |
DDB_G0279161 | DDB_G0279161 | DDB0232430 | CDS | 1711904 | 537 | + | 0.13594 | |
DDB_G0279163 | DDB_G0279163 | similar to hypothetical Dictyostelium proteins enriched in gametes | DDB0232430 | CDS | 1712573 | 867 | - | 0.327566 |
DDB_G0279165 | DDB_G0279165 | DDB0232430 | CDS | 1706026 | 2016 | + | 0.378472 | |
DDB_G0279177 | DDB_G0279177 | DDB0232430 | CDS | 1734898 | 1281 | + | 0.234973 | |
DDB_G0279179 | DDB_G0279179 | DDB0232430 | CDS | 1715076 | 2779 | + | 0.348687 | |
DDB_G0279181 | DDB_G0279181 | DDB0232430 | CDS | 1728295 | 1836 | + | 0.254902 | |
DDB_G0279197 | DDB_G0279197 | DDB0232430 | CDS | 1738130 | 186 | + | 0.247312 | |
DDB_G0279203 | DDB_G0279203 | DDB0232430 | CDS | 1741814 | 1218 | - | 0.212644 | |
DDB_G0279205 | DDB_G0279205 | similar to the conserved CAATT binding factor which is essential for growth and necessary for 60S ribosomal subunit biogenesis | DDB0232430 | CDS | 1747299 | 3162 | - | 0.280519 |
DDB_G0279209 | DDB_G0279209 | DDB0232430 | CDS | 1761272 | 399 | - | 0.265664 | |
DDB_G0279211 | DDB_G0279211 | catalyzes the reaction homocysteine 5-methyltetrahydropteroyltri-L-glutamate L-methionine tetrahydropteroyltri-L-glutamate | DDB0232430 | CDS | 1762684 | 2478 | - | 0.311945 |
DDB_G0279213 | DDB_G0279213 | DDB0232430 | CDS | 1768231 | 1911 | + | 0.263213 | |
DDB_G0279215 | DDB_G0279215 | DDB0232430 | CDS | 1771918 | 756 | - | 0.285714 | |
DDB_G0279217_RTE | DDB_G0279217 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232430 | CDS | 1773941 | 1932 | - | 0.26501 |
DDB_G0279219 | DDB_G0279219 | similar to D. purpureum protein contains a cysteine-rich repeat motif found in Dictyostelium proteins (PF00526) | DDB0232430 | CDS | 1779089 | 1794 | + | 0.345596 |
DDB_G0279221 | DDB_G0279221 | DDB0232430 | CDS | 1781444 | 264 | + | 0.268939 | |
DDB_G0279223 | DDB_G0279223 | contains a nucleic acid binding domain the oligonucleotideoligosaccharide binding motif (OB fold) | DDB0232430 | CDS | 1790126 | 552 | + | 0.309783 |
DDB_G0279225 | DDB_G0279225 | DDB0232430 | CDS | 1791010 | 2166 | - | 0.240997 | |
DDB_G0279227 | DDB_G0279227 | DDB0232430 | CDS | 1794406 | 735 | + | 0.289796 | |
DDB_G0279229 | DDB_G0279229 | DDB0232430 | CDS | 1796021 | 753 | - | 0.284197 | |
DDB_G0279231 | DDB_G0279231 | DDB0232430 | CDS | 1797887 | 804 | + | 0.272388 | |
DDB_G0279233_RTE | DDB_G0279233 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 1806047 | 1335 | - | 0.306367 |
DDB_G0279237 | DDB_G0279237 | DDB0232430 | CDS | 1809065 | 2931 | + | 0.235756 | |
DDB_G0279241 | DDB_G0279241 | DDB0232430 | CDS | 1814829 | 2760 | - | 0.236594 | |
DDB_G0279243 | DDB_G0279243 | DDB0232430 | CDS | 1820687 | 1545 | - | 0.191586 | |
DDB_G0279247 | DDB_G0279247 | DDB0232430 | CDS | 1830468 | 729 | + | 0.259259 | |
DDB_G0279249 | DDB_G0279249 | DDB0232430 | CDS | 1832140 | 963 | + | 0.15161 | |
DDB_G0279251 | DDB_G0279251 | weakly similar to ints5 component of a multiprotein mediator of small nuclear RNA processing | DDB0232430 | CDS | 1833200 | 4692 | - | 0.213342 |
DDB_G0279253 | DDB_G0279253 | DDB0232430 | CDS | 1838283 | 1539 | - | 0.238467 | |
DDB_G0279255 | DDB_G0279255 | DDB0232430 | CDS | 1840170 | 5097 | - | 0.249755 | |
DDB_G0279259 | DDB_G0279259 | DDB0232430 | CDS | 1848643 | 2526 | + | 0.266825 | |
DDB_G0279261 | DDB_G0279261 | DDB0232430 | CDS | 1855053 | 1911 | + | 0.22449 | |
DDB_G0279263 | DDB_G0279263 | DDB0232430 | CDS | 1857138 | 2229 | - | 0.261104 | |
DDB_G0279265 | DDB_G0279265 | DDB0232430 | CDS | 1859879 | 687 | - | 0.28821 | |
DDB_G0279271 | DDB_G0279271 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains an N-terminal transmembrane domain that might be a signal sequence | DDB0232430 | CDS | 1870767 | 1029 | + | 0.276968 |
DDB_G0279273 | DDB_G0279273 | DDB0232430 | CDS | 1872529 | 243 | - | 0.246914 | |
DDB_G0279275 | DDB_G0279275 | DDB0232430 | CDS | 1874332 | 1704 | + | 0.286385 | |
DDB_G0279277 | DDB_G0279277 | DDB0232430 | CDS | 1876664 | 1086 | + | 0.257827 | |
DDB_G0279279 | DDB_G0279279 | DDB0232430 | CDS | 1878087 | 1164 | + | 0.255155 | |
DDB_G0279285 | DDB_G0279285 | DDB0232430 | CDS | 1882454 | 1722 | + | 0.277003 | |
DDB_G0279287 | DDB_G0279287 | catalyzes the reaction L-cysteine [enzyme]-cysteine L-alanine [enzyme]-S-sulfanylcysteine | DDB0232430 | CDS | 1892317 | 1353 | + | 0.345898 |
DDB_G0279291 | DDB_G0279291 | DDB0232430 | CDS | 1895354 | 1422 | + | 0.348101 | |
DDB_G0279293 | DDB_G0279293 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232430 | CDS | 1897152 | 249 | - | 0.325301 |
DDB_G0279295 | DDB_G0279295 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232430 | CDS | 1898671 | 243 | - | 0.341564 |
DDB_G0279297 | DDB_G0279297 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232430 | CDS | 1899385 | 258 | + | 0.352713 |
DDB_G0279299 | DDB_G0279299 | DDB0232430 | CDS | 1899915 | 411 | + | 0.277372 | |
DDB_G0279309 | DDB_G0279309 | DDB0232430 | CDS | 1913378 | 3627 | - | 0.359802 | |
DDB_G0279317 | DDB_G0279317 | conserved protein similar to the human C19orf29 a putative splice factor identified in the spliceosome C complex | DDB0232430 | CDS | 1928580 | 2184 | - | 0.300824 |
DDB_G0279319 | DDB_G0279319 | DDB0232430 | CDS | 1931110 | 1062 | + | 0.1629 | |
DDB_G0279321 | DDB_G0279321 | DDB0232430 | CDS | 1932547 | 1488 | + | 0.298387 | |
DDB_G0279323 | DDB_G0279323 | has similarity to H. sapiens Selenocysteine insertion sequence-binding protein 2 (SECISBP2) that binds to the 3'-UTR of some mRNAs encoding selenoproteins | DDB0232430 | CDS | 1934535 | 1740 | + | 0.245402 |
DDB_G0279325 | DDB_G0279325 | DDB0232430 | CDS | 1936679 | 4311 | + | 0.271399 | |
DDB_G0279329 | DDB_G0279329 | DDB0232430 | CDS | 1945987 | 3912 | + | 0.213701 | |
DDB_G0279335 | DDB_G0279335 | DDB0232430 | CDS | 1951807 | 2097 | + | 0.259895 | |
DDB_G0279337 | DDB_G0279337 | DDB0232430 | CDS | 1954714 | 1125 | + | 0.401778 | |
DDB_G0279339 | DDB_G0279339 | DDB0232430 | CDS | 1955944 | 1032 | - | 0.282946 | |
DDB_G0279341 | DDB_G0279341 | DDB0232430 | CDS | 1957657 | 1275 | + | 0.200784 | |
DDB_G0279347 | DDB_G0279347 | DDB0232430 | CDS | 1965450 | 4410 | + | 0.229705 | |
DDB_G0279351 | DDB_G0279351 | DDB0232430 | CDS | 1974768 | 474 | - | 0.303797 | |
DDB_G0279353 | DDB_G0279353 | DDB0232430 | CDS | 1978760 | 2337 | + | 0.284553 | |
DDB_G0279355 | DDB_G0279355 | DDB0232430 | CDS | 1981638 | 1146 | + | 0.283595 | |
DDB_G0279357 | DDB_G0279357 | very similar to E.coli ybiK a putative L-asparaginase of the asparagine 2 family with the likely catalytic activity L-asparagine Hsub2subO L-aspartate NHsub3sub contains InterPro 'Peptidase T2 asparaginase 2' domain which includes L-asparaginases and glycosylasparaginases | DDB0232430 | CDS | 1983573 | 1041 | - | 0.307397 |
DDB_G0279361 | DDB_G0279361 | DDB0232430 | CDS | 1986517 | 825 | + | 0.338182 | |
DDB_G0279363 | DDB_G0279363 | DDB0232430 | CDS | 1987447 | 516 | - | 0.244186 | |
DDB_G0279365 | DDB_G0279365 | DDB0232430 | CDS | 1988545 | 3495 | - | 0.246638 | |
DDB_G0279367 | DDB_G0279367 | DDB0232430 | CDS | 1993529 | 1500 | - | 0.273333 | |
DDB_G0279369 | DDB_G0279369 | DDB0232430 | CDS | 1995959 | 2190 | - | 0.232877 | |
DDB_G0279375 | DDB_G0279375 | related to the Ovarian Tumour (OTU) gene of Drosophila function is unknown but conserved cysteine and histidine and possibly the aspartate residues suggests that those not yet recognized as peptidases could possess cysteine protease activity | DDB0232430 | CDS | 2006606 | 1023 | - | 0.250244 |
DDB_G0279381 | DDB_G0279381 | DDB0232430 | CDS | 2014573 | 1758 | + | 0.212742 | |
DDB_G0279383 | DDB_G0279383 | DDB0232430 | CDS | 2017692 | 1011 | + | 0.23541 | |
DDB_G0279385 | DDB_G0279385 | DDB0232430 | CDS | 1736871 | 939 | + | 0.253461 | |
DDB_G0279389_RTE | DDB_G0279389 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 1799975 | 2943 | - | 0.33809 |
DDB_G0279391_RTE | DDB_G0279391 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 1803409 | 1335 | - | 0.31161 |
DDB_G0279393 | DDB_G0279393 | DDB0232430 | CDS | 1851382 | 1239 | - | 0.17272 | |
DDB_G0279395 | DDB_G0279395 | DDB0232430 | CDS | 1853231 | 1341 | - | 0.247576 | |
DDB_G0279397 | DDB_G0279397 | DDB0232430 | CDS | 1884785 | 6180 | - | 0.256311 | |
DDB_G0279399_ps | DDB_G0279399 | putative pseudogene hssA2C7E family gene | DDB0232430 | CDS | 1897976 | 294 | - | 0.282313 |
DDB_G0279405 | DDB_G0279405 | CAMKL family protein kinase the protein kinase domain has similarity to those of calciumcalmodulin-dependent protein kinase kinases (CAMKK) that belong to a proposed calcium-triggered signaling cascade involved in a number of cellular processes | DDB0232430 | CDS | 1975813 | 2088 | + | 0.290709 |
DDB_G0279421 | DDB_G0279421 | DDB0232430 | CDS | 2022765 | 816 | - | 0.261029 | |
DDB_G0279425 | DDB_G0279425 | DDB0232430 | CDS | 2025317 | 3717 | + | 0.267689 | |
DDB_G0279427 | DDB_G0279427 | highly similar to sestrin1 p53-regulated protein PA26 in human a potential regulator of cellular growth | DDB0232430 | CDS | 2032053 | 1806 | - | 0.324474 |
DDB_G0279429 | DDB_G0279429 | DDB0232430 | CDS | 2037686 | 2064 | - | 0.315407 | |
DDB_G0279431 | DDB_G0279431 | DDB0232430 | CDS | 2040372 | 1581 | - | 0.251107 | |
DDB_G0279435 | DDB_G0279435 | DDB0232430 | CDS | 2045716 | 1461 | - | 0.299795 | |
DDB_G0279437 | DDB_G0279437 | contains an N-terminal DOMON domain as it occurs in dopamine beta-monooxygenases the Dictyostelium protein is followed by a cytochrome b561 domain which contains 5 putative transmembrane regions in addition the protein contains a putative signal peptide | DDB0232430 | CDS | 2047840 | 1122 | - | 0.339572 |
DDB_G0279449 | DDB_G0279449 | DDB0232430 | CDS | 2062975 | 3303 | + | 0.350288 | |
DDB_G0279453 | DDB_G0279453 | DDB0232430 | CDS | 2068536 | 2595 | - | 0.234297 | |
DDB_G0279455 | DDB_G0279455 | DDB0232430 | CDS | 2074339 | 840 | + | 0.239286 | |
DDB_G0279457_ps | DDB_G0279457 | putative pseudogene small fragment similar to gene | DDB0232430 | CDS | 2076549 | 225 | + | 0.346667 |
DDB_G0279459 | DDB_G0279459 | bCommunity Annotationb DDB G0279459 contains a forkhead-associated domain which is similar to the corresponding domain in the KI-67 antigen a very widely used clinical proliferation marker and is the only hit when the KI-67 sequence is blasted against Dicty proteins. Direct comparison of the Dd sequence with KI-67 by Blast2Sequences identifies two regions of homology and gives an expected value of 4e-08 suggesting that the similarity may be real. The KI-67 antigen in humans is nuclear and present throughout the cell cycle in proliferating cells but undetectable in cells in G0. Recent work suggests that the protein is involved in ribosomal RNA synthesis ((Bullwinkel et al J Cell Physiology 206 624-635 (2005) Rahmanzadeh et al Cell and Molecular Biology 40 422-430 (2007). A role in chromatin compaction has also been ascribed to KI-67 (Kametaka et al Genes Cells 7 1231-42 (2002) but this appears to involve the C-terminus. The Dicty protein is significantly shorter than the human protein a | DDB0232430 | CDS | 2077799 | 3099 | - | 0.310745 |
DDB_G0279461 | DDB_G0279461 | protein phosphatase 2C is a serinethreonine specific protein phosphatase with broad substrate specificity and dependent on divalent cations (mainly manganese and magnesium) for its activity | DDB0232430 | CDS | 2082919 | 3021 | + | 0.28335 |
DDB_G0279463 | DDB_G0279463 | DDB0232430 | CDS | 2087531 | 1623 | + | 0.260628 | |
DDB_G0279467 | DDB_G0279467 | DDB0232430 | CDS | 2101459 | 126 | - | 0.34127 | |
DDB_G0279469_RTE | DDB_G0279469 | ORF2 protein short fragment of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 2102943 | 123 | - | 0.243902 |
DDB_G0279471 | DDB_G0279471 | DDB0232430 | CDS | 2106661 | 339 | + | 0.268437 | |
DDB_G0279473 | DDB_G0279473 | DDB0232430 | CDS | 2107184 | 1230 | - | 0.297561 | |
DDB_G0279477 | DDB_G0279477 | DDB0232430 | CDS | 2114897 | 4263 | + | 0.24091 | |
DDB_G0279479 | DDB_G0279479 | DDB0232430 | CDS | 2120059 | 201 | + | 0.223881 | |
DDB_G0279485 | DDB_G0279485 | DDB0232430 | CDS | 2127093 | 4137 | - | 0.246072 | |
DDB_G0279487 | DDB_G0279487 | DDB0232430 | CDS | 2132450 | 8004 | - | 0.305597 | |
DDB_G0279489 | DDB_G0279489 | DDB0232430 | CDS | 2144687 | 2541 | - | 0.23416 | |
DDB_G0279491 | DDB_G0279491 | DDB0232430 | CDS | 2147617 | 1725 | - | 0.277681 | |
DDB_G0279493 | DDB_G0279493 | DDB0232430 | CDS | 2150258 | 2019 | + | 0.34522 | |
DDB_G0279495 | DDB_G0279495 | DDB0232430 | CDS | 2153440 | 375 | + | 0.328 | |
DDB_G0279497 | DDB_G0279497 | DDB0232430 | CDS | 2157078 | 1668 | - | 0.27518 | |
DDB_G0279499 | DDB_G0279499 | DDB0232430 | CDS | 2159836 | 588 | - | 0.294218 | |
DDB_G0279501 | DDB_G0279501 | DDB0232430 | CDS | 2160865 | 4881 | + | 0.238681 | |
DDB_G0279503 | DDB_G0279503 | DDB0232430 | CDS | 2170637 | 657 | + | 0.3379 | |
DDB_G0279505 | DDB_G0279505 | DDB0232430 | CDS | 2172140 | 447 | - | 0.223714 | |
DDB_G0279509 | DDB_G0279509 | DDB0232430 | CDS | 2176877 | 3597 | + | 0.227134 | |
DDB_G0279511 | DDB_G0279511 | DDB0232430 | CDS | 2181977 | 3690 | + | 0.263957 | |
DDB_G0279513 | DDB_G0279513 | DDB0232430 | CDS | 2186381 | 1854 | + | 0.28425 | |
DDB_G0279517 | DDB_G0279517 | DDB0232430 | CDS | 2192375 | 1653 | + | 0.155475 | |
DDB_G0279521 | DDB_G0279521 | DDB0232430 | CDS | 2196884 | 636 | - | 0.194969 | |
DDB_G0279523 | DDB_G0279523 | DDB0232430 | CDS | 2198274 | 1944 | - | 0.3107 | |
DDB_G0279525 | DDB_G0279525 | DDB0232430 | CDS | 2201116 | 513 | + | 0.323587 | |
DDB_G0279527 | DDB_G0279527 | DDB0232430 | CDS | 2202606 | 3702 | + | 0.323609 | |
DDB_G0279531 | DDB_G0279531 | DDB0232430 | CDS | 2217133 | 699 | - | 0.226037 | |
DDB_G0279533 | DDB_G0279533 | DDB0232430 | CDS | 2218849 | 1686 | - | 0.201068 | |
DDB_G0279535 | DDB_G0279535 | putative ortholog to H. sapiens U4U6.U5 tri-snRNP-associated protein 3 also known as nucleic acid-binding protein RY-1 | DDB0232430 | CDS | 2220986 | 891 | + | 0.337823 |
DDB_G0279539 | DDB_G0279539 | DDB0232430 | CDS | 2228944 | 1122 | + | 0.344029 | |
DDB_G0279541 | DDB_G0279541 | DDB0232430 | CDS | 2235559 | 657 | + | 0.357686 | |
DDB_G0279543 | DDB_G0279543 | DDB0232430 | CDS | 2236357 | 249 | - | 0.333333 | |
DDB_G0279545 | DDB_G0279545 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232430 | CDS | 2237325 | 879 | - | 0.290102 |
DDB_G0279547 | DDB_G0279547 | DDB0232430 | CDS | 2239673 | 1023 | + | 0.208211 | |
DDB_G0279551 | DDB_G0279551 | DDB0232430 | CDS | 2242950 | 714 | - | 0.280112 | |
DDB_G0279557 | DDB_G0279557 | contains 8 PUF domains D. melanogaster pumilio binds through a PUF domain to the 3' UTR of target mRNAs | DDB0232430 | CDS | 2250584 | 4488 | - | 0.343806 |
DDB_G0279561 | DDB_G0279561 | protein that contains a conserved domain shared by acyl-CoA synthetases long chain fatty acid Co-A ligase and various other closely-related synthetases | DDB0232430 | CDS | 2261454 | 1629 | - | 0.354819 |
DDB_G0279563 | DDB_G0279563 | DDB0232430 | CDS | 2264498 | 864 | + | 0.274306 | |
DDB_G0279565 | DDB_G0279565 | DDB0232430 | CDS | 2265879 | 3285 | - | 0.269406 | |
DDB_G0279567 | DDB_G0279567 | DDB0232430 | CDS | 2271017 | 831 | + | 0.184116 | |
DDB_G0279571 | DDB_G0279571 | DDB0232430 | CDS | 2278573 | 1614 | - | 0.293061 | |
DDB_G0279573 | DDB_G0279573 | DDB0232430 | CDS | 2280534 | 5220 | - | 0.30364 | |
DDB_G0279575 | DDB_G0279575 | DDB0232430 | CDS | 2286922 | 5328 | - | 0.303303 | |
DDB_G0279577 | DDB_G0279577 | DDB0232430 | CDS | 2293478 | 5223 | - | 0.300785 | |
DDB_G0279581 | DDB_G0279581 | DDB0232430 | CDS | 2301120 | 294 | - | 0.309524 | |
DDB_G0279583 | DDB_G0279583 | DDB0232430 | CDS | 2302296 | 2766 | + | 0.230296 | |
DDB_G0279585 | DDB_G0279585 | DDB0232430 | CDS | 2305662 | 1185 | + | 0.266667 | |
DDB_G0279587 | DDB_G0279587 | DDB0232430 | CDS | 2307458 | 852 | + | 0.245305 | |
DDB_G0279589 | DDB_G0279589 | DDB0232430 | CDS | 2089639 | 453 | + | 0.280353 | |
DDB_G0279593 | DDB_G0279593 | putative ortholog of human KIAA0082 RrmJ (FtsJ) is a well conserved heat shock protein in prokaryotes responsible for methylating the 23 S rRNA at position U2552 in the aminoacyl (A)1-site of the ribosome | DDB0232430 | CDS | 2141942 | 2274 | + | 0.262093 |
DDB_G0279595_RTE | DDB_G0279595 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 2155142 | 1077 | - | 0.419684 |
DDB_G0279597 | DDB_G0279597 | DDB0232430 | CDS | 2166622 | 3627 | + | 0.216984 | |
DDB_G0279609 | DDB_G0279609 | similar to Physarum polycephalum actin-fragmin kinase enriched in gametes | DDB0232430 | CDS | 2313265 | 1260 | - | 0.215873 |
DDB_G0279611 | DDB_G0279611 | DDB0232430 | CDS | 2316340 | 846 | - | 0.286052 | |
DDB_G0279613 | DDB_G0279613 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232430 | CDS | 2317988 | 1770 | + | 0.334463 |
DDB_G0279615 | DDB_G0279615 | DDB0232430 | CDS | 2320738 | 333 | + | 0.267267 | |
DDB_G0279617 | DDB_G0279617 | DDB0232430 | CDS | 2321489 | 633 | - | 0.21169 | |
DDB_G0279619 | DDB_G0279619 | DDB0232430 | CDS | 2325510 | 528 | - | 0.195076 | |
DDB_G0279621 | DDB_G0279621 | DDB0232430 | CDS | 2327562 | 516 | - | 0.186047 | |
DDB_G0279623 | DDB_G0279623 | DDB0232430 | CDS | 2329430 | 489 | - | 0.206544 | |
DDB_G0279625 | DDB_G0279625 | DDB0232430 | CDS | 2333074 | 147 | - | 0.272109 | |
DDB_G0279627 | DDB_G0279627 | DDB0232430 | CDS | 2333694 | 405 | - | 0.254321 | |
DDB_G0279635 | DDB_G0279635 | DDB0232430 | CDS | 2345293 | 1200 | + | 0.269167 | |
DDB_G0279637 | DDB_G0279637 | DDB0232430 | CDS | 2347354 | 903 | + | 0.286822 | |
DDB_G0279639 | DDB_G0279639 | DDB0232430 | CDS | 2350407 | 3030 | - | 0.356766 | |
DDB_G0279643 | DDB_G0279643 | DDB0232430 | CDS | 2356584 | 2340 | + | 0.308974 | |
DDB_G0279645 | DDB_G0279645 | DDB0232430 | CDS | 2359062 | 1161 | - | 0.197244 | |
DDB_G0279647 | DDB_G0279647 | DDB0232430 | CDS | 2361407 | 1137 | + | 0.294635 | |
DDB_G0279651 | DDB_G0279651 | DDB0232430 | CDS | 2369571 | 255 | - | 0.388235 | |
DDB_G0279653 | DDB_G0279653 | DDB0232430 | CDS | 2372697 | 2280 | - | 0.271053 | |
DDB_G0279655 | DDB_G0279655 | similar to Dictyostelium and H. sapiens ppp2r4 (PTPA) the phosphatase 2A regulatory subunit B' | DDB0232430 | CDS | 2376263 | 1407 | - | 0.257996 |
DDB_G0279661 | DDB_G0279661 | shares a short region of similarity with the SOX transcription factors contains a single HMG12 box | DDB0232430 | CDS | 2401539 | 537 | + | 0.258845 |
DDB_G0279663 | DDB_G0279663 | DDB0232430 | CDS | 2402323 | 777 | - | 0.324324 | |
DDB_G0279665 | DDB_G0279665 | DDB0232430 | CDS | 2405211 | 4134 | + | 0.293904 | |
DDB_G0279671 | DDB_G0279671 | DDB0232430 | CDS | 2414162 | 1605 | - | 0.202492 | |
DDB_G0279673 | DDB_G0279673 | DDB0232430 | CDS | 2416668 | 1941 | - | 0.263782 | |
DDB_G0279675 | DDB_G0279675 | belongs to the carbon-nitrogen hydrolase family similar to human VNN1 (pantetheine hydrolase) contains a predicted signal anchor sequence | DDB0232430 | CDS | 2426331 | 1623 | - | 0.262477 |
DDB_G0279679 | DDB_G0279679 | DDB0232430 | CDS | 2429651 | 855 | - | 0.226901 | |
DDB_G0279681 | DDB_G0279681 | DDB0232430 | CDS | 2440539 | 474 | + | 0.2827 | |
DDB_G0279683 | DDB_G0279683 | DDB0232430 | CDS | 2441695 | 819 | + | 0.252747 | |
DDB_G0279685 | DDB_G0279685 | DDB0232430 | CDS | 2442573 | 1044 | - | 0.185824 | |
DDB_G0279687 | DDB_G0279687 | DDB0232430 | CDS | 2445627 | 270 | + | 0.318519 | |
DDB_G0279691_RTE | DDB_G0279691 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 2450743 | 1953 | + | 0.347158 |
DDB_G0279693 | DDB_G0279693 | contains 1 importin N-terminal domain homolog of human IPO11 (importin-11) and S. cerevisiae KAP120 (importin beta-like protein) both of which function in nuclear protein import as a nuclear transport receptor | DDB0232430 | CDS | 2453262 | 3078 | - | 0.294997 |
DDB_G0279695 | DDB_G0279695 | similar D. melanogaster ORF CG8021 and the RRM domain is similar to that of human RBM3 | DDB0232430 | CDS | 2457402 | 255 | + | 0.298039 |
DDB_G0279697 | DDB_G0279697 | DDB0232430 | CDS | 2458047 | 294 | - | 0.306122 | |
DDB_G0279699 | DDB_G0279699 | contains a MOZSAS-like domain (Monocytic leukemia Zinc finger and Something About Silencing) predicted to have histone acetyltransferase activity | DDB0232430 | CDS | 2459375 | 1974 | + | 0.31155 |
DDB_G0279701 | DDB_G0279701 | DDB0232430 | CDS | 2464297 | 1125 | - | 0.273778 | |
DDB_G0279709 | DDB_G0279709 | member of a Dictyostelium protein family that includes | DDB0232430 | CDS | 2471727 | 756 | - | 0.304233 |
DDB_G0279717 | DDB_G0279717 | DDB0232430 | CDS | 2477453 | 1602 | - | 0.378901 | |
DDB_G0279719 | DDB_G0279719 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232430 | CDS | 2480611 | 2829 | - | 0.265111 |
DDB_G0279727 | DDB_G0279727 | DDB0232430 | CDS | 2394194 | 2142 | - | 0.315126 | |
DDB_G0279731 | DDB_G0279731 | DDB0232430 | CDS | 2431375 | 798 | + | 0.256892 | |
DDB_G0279741 | DDB_G0279741 | DDB0232430 | CDS | 2491660 | 3255 | + | 0.284485 | |
DDB_G0279743 | DDB_G0279743 | DDB0232430 | CDS | 2495088 | 1248 | - | 0.260417 | |
DDB_G0279745 | DDB_G0279745 | DDB0232430 | CDS | 2496825 | 1233 | - | 0.25223 | |
DDB_G0279747 | DDB_G0279747 | DDB0232430 | CDS | 2498789 | 870 | + | 0.316092 | |
DDB_G0279749 | DDB_G0279749 | DDB0232430 | CDS | 2499904 | 324 | - | 0.262346 | |
DDB_G0279751 | DDB_G0279751 | DDB0232430 | CDS | 2501638 | 2568 | + | 0.285436 | |
DDB_G0279753 | DDB_G0279753 | DDB0232430 | CDS | 2506085 | 3855 | + | 0.239948 | |
DDB_G0279755 | DDB_G0279755 | contains a nucleic acid binding domain the oligonucleotideoligosaccharide binding motif (OB fold) similar to conserved hypothetical fungal proteins | DDB0232430 | CDS | 2510417 | 1650 | + | 0.279394 |
DDB_G0279757 | DDB_G0279757 | DDB0232430 | CDS | 2520955 | 978 | + | 0.231084 | |
DDB_G0279759 | DDB_G0279759 | DDB0232430 | CDS | 2522049 | 1950 | - | 0.302051 | |
DDB_G0279761 | DDB_G0279761 | atypical protein kinase similar to human G11 serine threonine protein kinase (STK19 part of the major histocompatibility complex) | DDB0232430 | CDS | 2526528 | 1176 | - | 0.221939 |
DDB_G0279765 | DDB_G0279765 | DDB0232430 | CDS | 2530587 | 2448 | - | 0.252042 | |
DDB_G0279767 | DDB_G0279767 | DDB0232430 | CDS | 2533940 | 1557 | + | 0.189467 | |
DDB_G0279771_RTE | DDB_G0279771 | DDB0232430 | CDS | 2537528 | 816 | - | 0.372549 | |
DDB_G0279773_RTE | DDB_G0279773 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232430 | CDS | 2538990 | 645 | - | 0.294574 |
DDB_G0279775 | DDB_G0279775 | DDB0232430 | CDS | 2540030 | 3384 | - | 0.242317 | |
DDB_G0279781_ps | DDB_G0279781 | putative pseudogene fragment similar to D. discoideum gene | DDB0232430 | CDS | 2544557 | 519 | - | 0.244701 |
DDB_G0279783 | DDB_G0279783 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232430 | CDS | 2546062 | 888 | - | 0.240991 |
DDB_G0279787 | DDB_G0279787 | DDB0232430 | CDS | 2516476 | 609 | + | 0.200328 | |
DDB_G0279789 | DDB_G0279789 | DDB0232430 | CDS | 2517567 | 591 | + | 0.245347 | |
DDB_G0279803 | DDB_G0279803 | DDB0232430 | CDS | 2556336 | 1734 | + | 0.21684 | |
DDB_G0279805 | DDB_G0279805 | DDB0232430 | CDS | 2558407 | 1257 | + | 0.216388 | |
DDB_G0279807 | DDB_G0279807 | DDB0232430 | CDS | 2563367 | 1908 | - | 0.321803 | |
DDB_G0279809 | DDB_G0279809 | DDB0232430 | CDS | 2572023 | 2931 | + | 0.253497 | |
DDB_G0279811 | DDB_G0279811 | DDB0232430 | CDS | 2575486 | 312 | - | 0.185897 | |
DDB_G0279813 | DDB_G0279813 | DDB0232430 | CDS | 2578911 | 2346 | + | 0.249361 | |
DDB_G0279815 | DDB_G0279815 | DDB0232430 | CDS | 2582186 | 447 | - | 0.210291 | |
DDB_G0279817 | DDB_G0279817 | DDB0232430 | CDS | 2583923 | 669 | - | 0.294469 | |
DDB_G0279819 | DDB_G0279819 | DDB0232430 | CDS | 2585071 | 1209 | - | 0.163772 | |
DDB_G0279821 | DDB_G0279821 | DDB0232430 | CDS | 2586560 | 1749 | - | 0.263579 | |
DDB_G0279823 | DDB_G0279823 | DDB0232430 | CDS | 2588778 | 2685 | - | 0.299814 | |
DDB_G0279825 | DDB_G0279825 | DDB0232430 | CDS | 2593261 | 3672 | + | 0.227397 | |
DDB_G0279829 | DDB_G0279829 | contains six putative transmembrane domains and is similar to DUF1295 a protein family of unknown function | DDB0232430 | CDS | 2599428 | 804 | - | 0.24005 |
DDB_G0279831 | DDB_G0279831 | putative protein serinethreonine kinase CAMK group the protein kinase domain is similar to those of mammalian CAM kinase I | DDB0232430 | CDS | 2602496 | 2787 | + | 0.267671 |
DDB_G0279835 | DDB_G0279835 | DDB0232430 | CDS | 2606276 | 1644 | + | 0.223236 | |
DDB_G0279843 | DDB_G0279843 | DDB0232430 | CDS | 2627370 | 816 | + | 0.305147 | |
DDB_G0279845 | DDB_G0279845 | DDB0232430 | CDS | 2628470 | 2499 | - | 0.158063 | |
DDB_G0279851 | DDB_G0279851 | putative histone acetyltransferase highly similar to bacterial GCN5-related N-acetyltransferase (GNAT) | DDB0232430 | CDS | 2640159 | 516 | - | 0.284884 |
DDB_G0279859 | DDB_G0279859 | conserved Dictyostelium protein contains 2 EGF-like domains contains both a predicted N-terminal signal sequence and C-terminal transmembrane domain | DDB0232430 | CDS | 2618546 | 3426 | + | 0.27087 |
DDB_G0279861_RTE | DDB_G0279861 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 2633026 | 1080 | + | 0.417593 |
DDB_G0279863 | DDB_G0279863 | DDB0232430 | CDS | 2641846 | 3852 | - | 0.314901 | |
DDB_G0279867_RTE | DDB_G0279867 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 2675830 | 1335 | + | 0.307865 |
DDB_G0279871 | DDB_G0279871 | member of a large D. discoideum gene family that seems to be more diverse and not so expanded in D. purpureum and P. pallidumbr bCommunity annotation:b Significantly down-regulated after infection with Legionella pneumophila and underexpressed in uninfected dupA mutants (Li et al. Cell Host Microbe. 2009 Sep 176(3):253-67). Gareth Bloomfield December 2010br | DDB0232430 | CDS | 2672370 | 1197 | - | 0.238931 |
DDB_G0279873 | DDB_G0279873 | DDB0232430 | CDS | 2670350 | 1197 | - | 0.23726 | |
DDB_G0279877 | DDB_G0279877 | DDB0232430 | CDS | 2664394 | 1218 | - | 0.234811 | |
DDB_G0279879 | DDB_G0279879 | DDB0232430 | CDS | 2661756 | 1185 | - | 0.236287 | |
DDB_G0279881_ps | DDB_G0279881 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232430 | CDS | 2659791 | 357 | - | 0.240896 |
DDB_G0279885_ps | DDB_G0279885 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 2658208 | 480 | - | 0.30625 |
DDB_G0279889_ps | DDB_G0279889 | putative pseudogene similar to a conserved family of zinc finger FNIP domain-containing proteins including | DDB0232430 | CDS | 2653100 | 444 | - | 0.295045 |
DDB_G0279891 | DDB_G0279891 | DDB0232430 | CDS | 2648955 | 1188 | - | 0.238215 | |
DDB_G0279893 | DDB_G0279893 | bCommunity annotation:b This appears to be a gene fragment resulting from degeneration of a member of a large family of uncharacterised Dictyostelium genes which encode proteins containing B-box zinc fingers and FNIP repeats. Although it seems unlikely to encode a functional protein its mRNA as found to be expressed and responsive: it was significantly down-regulated six hours after Legionella pneumophila infection in AX4 cells (Li et al. Cell Host Microbe. 2009 Sep 176(3):253-67). A closely related apparently intact gene DDB_G0279871 is similarly down-regulated suggesting a connection with the response to infection. Gareth Bloomfield December 2010br | DDB0232430 | CDS | 2648228 | 312 | - | 0.317308 |
DDB_G0279895_TE | DDB_G0279895 | DDB0232430 | CDS | 2646397 | 537 | - | 0.325885 | |
DDB_G0279897 | DDB_G0279897 | DDB0232430 | CDS | 2651015 | 1182 | - | 0.230964 | |
DDB_G0279899 | DDB_G0279899 | DDB0232430 | CDS | 2656014 | 1182 | - | 0.243655 | |
DDB_G0279901 | DDB_G0279901 | DDB0232430 | CDS | 2668171 | 1245 | - | 0.215261 | |
DDB_G0279905 | DDB_G0279905 | DDB0232430 | CDS | 2680036 | 876 | + | 0.223744 | |
DDB_G0279907 | DDB_G0279907 | DDB0232430 | CDS | 2681663 | 963 | + | 0.354102 | |
DDB_G0279929_RTE | DDB_G0279929 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 2697801 | 1362 | + | 0.34141 |
DDB_G0279931_RTE | DDB_G0279931 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232430 | CDS | 2701058 | 1911 | + | 0.267399 |
DDB_G0279933 | DDB_G0279933 | DDB0232430 | CDS | 2703861 | 1797 | - | 0.258765 | |
DDB_G0279935 | DDB_G0279935 | contains one C2 domain which is is a Ca2-dependent membrane-targeting module found in many cellular proteins involved in signal transduction or membrane trafficking contains a predicted peroxisomal targeting signal | DDB0232430 | CDS | 2707384 | 513 | + | 0.259259 |
DDB_G0279937 | DDB_G0279937 | DDB0232430 | CDS | 2708291 | 3324 | - | 0.236763 | |
DDB_G0279939 | DDB_G0279939 | conserved in plants and fungi contains one putative transmembrane domain | DDB0232430 | CDS | 2716529 | 165 | - | 0.381818 |
DDB_G0279941 | DDB_G0279941 | DDB0232430 | CDS | 2718242 | 2643 | - | 0.341657 | |
DDB_G0279943 | DDB_G0279943 | belongs to the major facilitator superefamily contains 12 putative transmembrane domains | DDB0232430 | CDS | 2721717 | 1488 | - | 0.309812 |
DDB_G0279945 | DDB_G0279945 | DDB0232430 | CDS | 2737032 | 1926 | - | 0.240395 | |
DDB_G0279949 | DDB_G0279949 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232430 | CDS | 2741741 | 456 | - | 0.307018 |
DDB_G0279951 | DDB_G0279951 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232430 | CDS | 2743413 | 459 | - | 0.276688 |
DDB_G0279953 | DDB_G0279953 | DDB0232430 | CDS | 2745921 | 1404 | - | 0.342593 | |
DDB_G0279955 | DDB_G0279955 | DDB0232430 | CDS | 2748541 | 999 | + | 0.302302 | |
DDB_G0279957 | DDB_G0279957 | DDB0232430 | CDS | 2750436 | 1401 | - | 0.326196 | |
DDB_G0279963 | DDB_G0279963 | DDB0232430 | CDS | 2767341 | 297 | - | 0.316498 | |
DDB_G0279965 | DDB_G0279965 | members of the NAD-dependent epimerasedehydratase family use nucleotide-sugar substrates for a variety of chemical reactions contains a putative signal peptide | DDB0232430 | CDS | 2775437 | 1203 | - | 0.305902 |
DDB_G0279967 | DDB_G0279967 | DDB0232430 | CDS | 2780826 | 828 | + | 0.206522 | |
DDB_G0279969 | DDB_G0279969 | DDB0232430 | CDS | 2781830 | 2280 | - | 0.272807 | |
DDB_G0279971 | DDB_G0279971 | DDB0232430 | CDS | 2799462 | 1194 | - | 0.264657 | |
DDB_G0279973 | DDB_G0279973 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232430 | CDS | 2800822 | 459 | - | 0.296296 |
DDB_G0279975 | DDB_G0279975 | DDB0232430 | CDS | 2802732 | 1815 | - | 0.198347 | |
DDB_G0279979 | DDB_G0279979 | DDB0232430 | CDS | 2806294 | 2172 | - | 0.269337 | |
DDB_G0279981 | DDB_G0279981 | DDB0232430 | CDS | 2809171 | 912 | + | 0.260965 | |
DDB_G0279985 | DDB_G0279985 | conserved hypothetical protein contains a signal peptide and two predicted transmembrane domains | DDB0232430 | CDS | 2817297 | 2901 | + | 0.270252 |
DDB_G0279987 | DDB_G0279987 | DDB0232430 | CDS | 2820923 | 675 | + | 0.216296 | |
DDB_G0279989 | DDB_G0279989 | DDB0232430 | CDS | 2823865 | 465 | + | 0.193548 | |
DDB_G0279993 | DDB_G0279993 | DDB0232430 | CDS | 2832531 | 165 | - | 0.260606 | |
DDB_G0279995 | DDB_G0279995 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232430 | CDS | 2833406 | 2523 | - | 0.309948 |
DDB_G0279999 | DDB_G0279999 | contains 3 EGF-like domains contains a predicted signal peptide and a C-terminal transmembrane domain | DDB0232430 | CDS | 2841134 | 3315 | + | 0.24917 |
DDB_G0280001 | DDB_G0280001 | DDB0232430 | CDS | 2845223 | 3327 | + | 0.250075 | |
DDB_G0280003 | DDB_G0280003 | DDB0232430 | CDS | 2849525 | 3324 | + | 0.252407 | |
DDB_G0280005_ps | DDB_G0280005 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232430 | CDS | 2860281 | 3228 | + | 0.255266 |
DDB_G0280007 | DDB_G0280007 | DDB0232430 | CDS | 2864348 | 3033 | - | 0.246621 | |
DDB_G0280011_TE | DDB_G0280011 | complex cluster of transposon fragments contains TRE3-A ORF2 and an ORF for DDT-A | DDB0232430 | CDS | 2692188 | 1953 | + | 0.328213 |
DDB_G0280015 | DDB_G0280015 | DDB0232430 | CDS | 2764702 | 2226 | + | 0.263702 | |
DDB_G0280017 | DDB_G0280017 | DDB0232430 | CDS | 2788130 | 6774 | + | 0.255536 | |
DDB_G0280019 | DDB_G0280019 | conserved in bacteria and fungi similar to S. cerevisiae HSP31 (heat shock protein 31) a putative protease | DDB0232430 | CDS | 2796272 | 702 | + | 0.339031 |
DDB_G0280023 | DDB_G0280023 | DDB0232430 | CDS | 2810254 | 255 | - | 0.196078 | |
DDB_G0280025 | DDB_G0280025 | DDB0232430 | CDS | 2821744 | 1809 | - | 0.144831 | |
DDB_G0280029_ps | DDB_G0280029 | putative pseudogene similar to a large D. discoideum gene family including | DDB0232430 | CDS | 2854428 | 3099 | + | 0.249113 |
DDB_G0280031_RTE | DDB_G0280031 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 2870918 | 3180 | - | 0.348742 |
DDB_G0280051 | DDB_G0280051 | DDB0232430 | CDS | 3281113 | 960 | - | 0.371875 | |
DDB_G0280063 | DDB_G0280063 | DDB0232430 | CDS | 2879114 | 906 | + | 0.209713 | |
DDB_G0280065 | DDB_G0280065 | DDB0232430 | CDS | 2880772 | 4209 | + | 0.274174 | |
DDB_G0280067 | DDB_G0280067 | similar to T-cell activation protein phosphatase 2C the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232430 | CDS | 2886853 | 1551 | + | 0.295938 |
DDB_G0280069 | DDB_G0280069 | DDB0232430 | CDS | 2889026 | 1032 | - | 0.263566 | |
DDB_G0280071 | DDB_G0280071 | DDB0232430 | CDS | 2891601 | 2457 | + | 0.239316 | |
DDB_G0280073 | DDB_G0280073 | DDB0232430 | CDS | 2894240 | 1194 | - | 0.281407 | |
DDB_G0280075 | DDB_G0280075 | DDB0232430 | CDS | 2895929 | 1587 | - | 0.176434 | |
DDB_G0280085 | DDB_G0280085 | DDB0232430 | CDS | 2908403 | 798 | - | 0.342105 | |
DDB_G0280089 | DDB_G0280089 | DDB0232430 | CDS | 2915769 | 1374 | - | 0.342795 | |
DDB_G0280091 | DDB_G0280091 | homolog of human UBE2H (ubiquitin-conjugating enzyme E2 H) and S. pombe ubc8 catalyzes the covalent attachment of ubiquitin to other proteins | DDB0232430 | CDS | 2919337 | 558 | - | 0.310036 |
DDB_G0280095 | DDB_G0280095 | DDB0232430 | CDS | 2928904 | 258 | - | 0.22093 | |
DDB_G0280097 | DDB_G0280097 | contains a signal peptide a weak PA14 domain and 2 Dictyostelium-specific repeats | DDB0232430 | CDS | 2930052 | 1383 | - | 0.326103 |
DDB_G0280099_ps | DDB_G0280099 | putative pseudogene similar to DDB_G0280097 | DDB0232430 | CDS | 2932544 | 1344 | - | 0.265625 |
DDB_G0280101_ps | DDB_G0280101 | putative pseudogene similar to Dictyostelium PA14 domain-containing proteins | DDB0232430 | CDS | 2934621 | 852 | - | 0.306338 |
DDB_G0280103 | DDB_G0280103 | DDB0232430 | CDS | 2937406 | 399 | + | 0.243108 | |
DDB_G0280105 | DDB_G0280105 | catalyzes the preferential release of a C-terminal arginine or lysine residue expressed in pstAB cells and in upper cup during culmination | DDB0232430 | CDS | 2938222 | 1692 | - | 0.292553 |
DDB_G0280107 | DDB_G0280107 | DDB0232430 | CDS | 2941138 | 369 | - | 0.273713 | |
DDB_G0280111 | DDB_G0280111 | putative protein serinethreonine kinase similar to the kinase domains of AAK1 (AP2 associated kinase) and BMP-inducible protein kinase (BIKe) | DDB0232430 | CDS | 2948944 | 3381 | - | 0.280982 |
DDB_G0280115 | DDB_G0280115 | DDB0232430 | CDS | 2958706 | 1602 | - | 0.209738 | |
DDB_G0280117 | DDB_G0280117 | DDB0232430 | CDS | 2961104 | 3429 | + | 0.273549 | |
DDB_G0280119 | DDB_G0280119 | DDB0232430 | CDS | 2971976 | 3606 | - | 0.235164 | |
DDB_G0280121 | DDB_G0280121 | similar to human ZMAT2 zinc finger matrin type 2 and yeast SNU23 a component of the U4U6.U5 snRNP involved in mRNA splicing | DDB0232430 | CDS | 2976788 | 885 | - | 0.228249 |
DDB_G0280123 | DDB_G0280123 | DDB0232430 | CDS | 2978017 | 708 | + | 0.262712 | |
DDB_G0280125 | DDB_G0280125 | DDB0232430 | CDS | 2979381 | 3804 | + | 0.26551 | |
DDB_G0280129 | DDB_G0280129 | DDB0232430 | CDS | 2984895 | 243 | + | 0.27572 | |
DDB_G0280131 | DDB_G0280131 | member of the TKL (tyrosine kinase-like) group and the ARMK (armadillo repeat-containing kinase) family contains armadillobeta-catenin-like repeats unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232430 | CDS | 2985578 | 3579 | - | 0.308187 |
DDB_G0280133 | DDB_G0280133 | CAMK family protein kinase protein kinase domain similar to those of mammalian SNF1 like kinases | DDB0232430 | CDS | 2991402 | 4518 | + | 0.285967 |
DDB_G0280135 | DDB_G0280135 | DDB0232430 | CDS | 2996500 | 984 | - | 0.292683 | |
DDB_G0280137 | DDB_G0280137 | DDB0232430 | CDS | 2997946 | 975 | - | 0.236923 | |
DDB_G0280139 | DDB_G0280139 | DDB0232430 | CDS | 2999177 | 72 | + | 0.333333 | |
DDB_G0280141 | DDB_G0280141 | DDB0232430 | CDS | 3002773 | 1851 | + | 0.293355 | |
DDB_G0280143 | DDB_G0280143 | DDB0232430 | CDS | 3004846 | 1986 | - | 0.270896 | |
DDB_G0280145 | DDB_G0280145 | DDB0232430 | CDS | 3012864 | 2607 | + | 0.259302 | |
DDB_G0280149 | DDB_G0280149 | DDB0232430 | CDS | 3018896 | 3939 | - | 0.263519 | |
DDB_G0280153 | DDB_G0280153 | DDB0232430 | CDS | 3024229 | 690 | + | 0.157971 | |
DDB_G0280155_ps | DDB_G0280155 | putative pseudogene fragment similar to the neighboring genes | DDB0232430 | CDS | 3025070 | 1233 | - | 0.287105 |
DDB_G0280157 | DDB_G0280157 | DDB0232430 | CDS | 3027046 | 4026 | - | 0.25534 | |
DDB_G0280159 | DDB_G0280159 | one of three paralogs in Dictyostelium (other genes: | DDB0232430 | CDS | 3031994 | 2727 | - | 0.314998 |
DDB_G0280163 | DDB_G0280163 | DDB0232430 | CDS | 3036716 | 1215 | + | 0.266667 | |
DDB_G0280165 | DDB_G0280165 | DDB0232430 | CDS | 3038985 | 2439 | + | 0.271013 | |
DDB_G0280177 | DDB_G0280177 | DDB0232430 | CDS | 3054033 | 3666 | + | 0.346699 | |
DDB_G0280181 | DDB_G0280181 | contains three ankyrin repeats and an RA domain which plays a role in RasGTP activation in mammals and mating in yeast highly similar to | DDB0232430 | CDS | 3067276 | 1002 | - | 0.278443 |
DDB_G0280185 | DDB_G0280185 | conserved hypothetical protein contains a putative signal peptide | DDB0232430 | CDS | 3076448 | 1044 | - | 0.245211 |
DDB_G0280187 | DDB_G0280187 | similar to cathepsin Z a papain cysteine protease family protein | DDB0232430 | CDS | 3078456 | 876 | + | 0.374429 |
DDB_G0280189 | DDB_G0280189 | DDB0232430 | CDS | 3081325 | 1293 | + | 0.276875 | |
DDB_G0280191 | DDB_G0280191 | DDB0232430 | CDS | 3082696 | 1323 | - | 0.230537 | |
DDB_G0280193 | DDB_G0280193 | DDB0232430 | CDS | 3084374 | 2466 | - | 0.227088 | |
DDB_G0280201 | DDB_G0280201 | conserved hypothetical protein contains a putative signal peptide | DDB0232430 | CDS | 3099615 | 753 | - | 0.310757 |
DDB_G0280203_ps | DDB_G0280203 | putative pseudogene similar to pirin family proteins especially to DDB_G0281115 and DDB_G0280725 | DDB0232430 | CDS | 3101331 | 654 | + | 0.314985 |
DDB_G0280205 | DDB_G0280205 | DDB0232430 | CDS | 3106631 | 2508 | - | 0.307815 | |
DDB_G0280209 | DDB_G0280209 | DDB0232430 | CDS | 3109725 | 4770 | - | 0.244654 | |
DDB_G0280211 | DDB_G0280211 | DDB0232430 | CDS | 3115387 | 750 | - | 0.334667 | |
DDB_G0280215 | DDB_G0280215 | DDB0232430 | CDS | 3121269 | 1251 | + | 0.343725 | |
DDB_G0280217 | DDB_G0280217 | DDB0232430 | CDS | 3122881 | 183 | - | 0.245902 | |
DDB_G0280221 | DDB_G0280221 | DDB0232430 | CDS | 3129179 | 6531 | - | 0.27469 | |
DDB_G0280225 | DDB_G0280225 | similar to conserved hypothetical proteins expressed in pstO cells and upper cup during culmination | DDB0232430 | CDS | 3138804 | 240 | + | 0.341667 |
DDB_G0280227 | DDB_G0280227 | DDB0232430 | CDS | 3139657 | 1737 | - | 0.176166 | |
DDB_G0280231_ps | DDB_G0280231 | putative pseudogene fragment similar to gene | DDB0232430 | CDS | 3143880 | 237 | + | 0.227848 |
DDB_G0280233 | DDB_G0280233 | DDB0232430 | CDS | 3144889 | 975 | + | 0.295385 | |
DDB_G0280235 | DDB_G0280235 | DDB0232430 | CDS | 3146638 | 1182 | - | 0.262267 | |
DDB_G0280239 | DDB_G0280239 | has a short region of similarity with CARD4 (caspase recruitment domain family member 4) | DDB0232430 | CDS | 3151038 | 1929 | + | 0.217211 |
DDB_G0280241 | DDB_G0280241 | DDB0232430 | CDS | 3153116 | 633 | - | 0.202212 | |
DDB_G0280243 | DDB_G0280243 | DDB0232430 | CDS | 3154238 | 903 | - | 0.264673 | |
DDB_G0280247 | DDB_G0280247 | DDB0232430 | CDS | 3159963 | 999 | - | 0.268268 | |
DDB_G0280249 | DDB_G0280249 | member of the MAP65ASE1 family of microtubule associated proteins the putative yeast orthologs is an anaphase spindle elongation protein brbr bCommunity annotation:b The provisional identification of this gene as Ase1 is supported by its threefold overexpression in a Dicty strain lacking the Dicty retinoblastoma-like gene rblA (Doquang et al in preparation). Most genes whose products are involved in cell cycle progression are overexpressed in this strain. br Ase1 is a microtubule associated protein resident in the midbody of the mitotic spindle it is phosphorylated by cdk1 during mitotic entry dephosphorylated by the mitotic-exit specific phosphatase cdc14 and degraded by the anaphase promoting complex (see Khmelinskii and Schiebel Cell Cycle 7 283-6 (2008). In budding yeast ase1 is required for spindle elongation and stabilization. br Harry MacWilliams April 2009 | DDB0232430 | CDS | 3162671 | 2316 | - | 0.262522 |
DDB_G0280251 | DDB_G0280251 | similar to human EXOSC7 which is a component of the exosome a 3'-5' exoribonuclease complex involved in RNA processing | DDB0232430 | CDS | 3165971 | 975 | - | 0.285128 |
DDB_G0280253 | DDB_G0280253 | DDB0232430 | CDS | 3167632 | 3522 | + | 0.26519 | |
DDB_G0280257 | DDB_G0280257 | DDB0232430 | CDS | 3173383 | 1245 | + | 0.324498 | |
DDB_G0280259 | DDB_G0280259 | DDB0232430 | CDS | 3176428 | 1530 | - | 0.267974 | |
DDB_G0280261 | DDB_G0280261 | contains one LisH domain and 7 WD40 domains similar to human TBL1X (F-box-likeWD repeat-containing protein) which plays a role in transcription activation mediated by nuclear receptors | DDB0232430 | CDS | 3178567 | 1743 | - | 0.324154 |
DDB_G0280263 | DDB_G0280263 | DDB0232430 | CDS | 3180987 | 825 | - | 0.286061 | |
DDB_G0280265 | DDB_G0280265 | DDB0232430 | CDS | 3182303 | 543 | + | 0.232044 | |
DDB_G0280269 | DDB_G0280269 | DDB0232430 | CDS | 3190136 | 1824 | - | 0.201754 | |
DDB_G0280271 | DDB_G0280271 | conserved in amoeba fungi and alveolates | DDB0232430 | CDS | 3192876 | 546 | + | 0.307692 |
DDB_G0280277 | DDB_G0280277 | DDB0232430 | CDS | 3198023 | 474 | + | 0.301688 | |
DDB_G0280279 | DDB_G0280279 | DDB0232430 | CDS | 3199016 | 165 | + | 0.363636 | |
DDB_G0280281 | DDB_G0280281 | DDB0232430 | CDS | 3200265 | 1836 | + | 0.270697 | |
DDB_G0280283 | DDB_G0280283 | DDB0232430 | CDS | 3203048 | 3168 | + | 0.255051 | |
DDB_G0280285 | DDB_G0280285 | weakly similar to ints8 component of a multiprotein mediator of small nuclear RNA processing | DDB0232430 | CDS | 3206520 | 597 | + | 0.247906 |
DDB_G0280287 | DDB_G0280287 | DDB0232430 | CDS | 3207518 | 600 | - | 0.3 | |
DDB_G0280289 | DDB_G0280289 | DDB0232430 | CDS | 3208817 | 2961 | - | 0.333671 | |
DDB_G0280291 | DDB_G0280291 | bifunctional enzyme that catalyzes the reactions methylene-tetrahydrofolate NADP NADPH methenyl-Hsub4subF and NADPH methenyl-Hsub4subF methylene-tetrahydrofolate NADP | DDB0232430 | CDS | 3212417 | 1323 | + | 0.254724 |
DDB_G0280295_ps | DDB_G0280295 | putative pseudogene fragment similar to D. discoideum gene | DDB0232430 | CDS | 3217053 | 765 | + | 0.34902 |
DDB_G0280299 | DDB_G0280299 | DDB0232430 | CDS | 3219540 | 1389 | + | 0.325414 | |
DDB_G0280303_ps | DDB_G0280303 | putative pseudogene similar to | DDB0232430 | CDS | 3222079 | 876 | - | 0.284247 |
DDB_G0280305 | DDB_G0280305 | DDB0232430 | CDS | 3223200 | 153 | - | 0.248366 | |
DDB_G0280307 | DDB_G0280307 | DDB0232430 | CDS | 3228229 | 1647 | - | 0.297511 | |
DDB_G0280311 | DDB_G0280311 | DDB0232430 | CDS | 3241213 | 3255 | + | 0.256221 | |
DDB_G0280315 | DDB_G0280315 | DDB0232430 | CDS | 3247016 | 975 | - | 0.226667 | |
DDB_G0280317 | DDB_G0280317 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232430 | CDS | 3248423 | 615 | - | 0.284553 |
DDB_G0280323 | DDB_G0280323 | DDB0232430 | CDS | 3260852 | 147 | - | 0.333333 | |
DDB_G0280325 | DDB_G0280325 | DDB0232430 | CDS | 3261453 | 147 | - | 0.346939 | |
DDB_G0280327 | DDB_G0280327 | DDB0232430 | CDS | 3262207 | 129 | - | 0.333333 | |
DDB_G0280329 | DDB_G0280329 | DDB0232430 | CDS | 3262966 | 1128 | + | 0.221631 | |
DDB_G0280331 | DDB_G0280331 | DDB0232430 | CDS | 3265565 | 147 | + | 0.0612245 | |
DDB_G0280333 | DDB_G0280333 | DDB0232430 | CDS | 3275255 | 693 | - | 0.262626 | |
DDB_G0280335 | DDB_G0280335 | DDB0232430 | CDS | 3276492 | 432 | - | 0.243056 | |
DDB_G0280337 | DDB_G0280337 | DDB0232430 | CDS | 3277418 | 378 | - | 0.325397 | |
DDB_G0280339 | DDB_G0280339 | DDB0232430 | CDS | 3278339 | 714 | - | 0.280112 | |
DDB_G0280341 | DDB_G0280341 | DDB0232430 | CDS | 3283772 | 408 | + | 0.267157 | |
DDB_G0280343 | DDB_G0280343 | DDB0232430 | CDS | 3284706 | 966 | + | 0.301242 | |
DDB_G0280347 | DDB_G0280347 | DDB0232430 | CDS | 3287782 | 378 | + | 0.306878 | |
DDB_G0280349 | DDB_G0280349 | DDB0232430 | CDS | 3288732 | 693 | - | 0.282828 | |
DDB_G0280357 | DDB_G0280357 | DDB0232430 | CDS | 3299810 | 912 | + | 0.253289 | |
DDB_G0280365_RTE | DDB_G0280365 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 2877474 | 561 | + | 0.347594 |
DDB_G0280367 | DDB_G0280367 | DDB0232430 | CDS | 2917996 | 909 | + | 0.190319 | |
DDB_G0280369 | DDB_G0280369 | DDB0232430 | CDS | 2942956 | 4443 | - | 0.244655 | |
DDB_G0280371 | DDB_G0280371 | homolog of human GK and S. cerevisiae GUT1 (glycerol utilization) catalyzes the reaction ATP glycerol ADP sn-glycerol 3-phosphate | DDB0232430 | CDS | 3007522 | 1620 | - | 0.327161 |
DDB_G0280373 | DDB_G0280373 | DDB0232430 | CDS | 3009655 | 573 | - | 0.256545 | |
DDB_G0280375 | DDB_G0280375 | DDB0232430 | CDS | 3061638 | 4812 | + | 0.264339 | |
DDB_G0280377 | DDB_G0280377 | DDB0232430 | CDS | 3071897 | 2355 | + | 0.265393 | |
DDB_G0280379 | DDB_G0280379 | DDB0232430 | CDS | 3074704 | 1659 | + | 0.222423 | |
DDB_G0280383 | DDB_G0280383 | DDB0232430 | CDS | 3118643 | 663 | + | 0.286576 | |
DDB_G0280385 | DDB_G0280385 | DDB0232430 | CDS | 3156312 | 1332 | + | 0.294294 | |
DDB_G0280387 | DDB_G0280387 | DDB0232430 | CDS | 3195244 | 90 | + | 0.355556 | |
DDB_G0280389 | DDB_G0280389 | DDB0232430 | CDS | 3197151 | 90 | + | 0.422222 | |
DDB_G0280391 | DDB_G0280391 | DDB0232430 | CDS | 3240109 | 426 | + | 0.206573 | |
DDB_G0280393 | DDB_G0280393 | DDB0232430 | CDS | 3254509 | 1239 | + | 0.338983 | |
DDB_G0280395_ps | DDB_G0280395 | putative pseudogene similar to EGF-like domain-containing protein such as | DDB0232430 | CDS | 3268225 | 1302 | - | 0.240399 |
DDB_G0280397 | DDB_G0280397 | DDB0232430 | CDS | 3271724 | 3123 | + | 0.258085 | |
DDB_G0280405 | DDB_G0280405 | DDB0232430 | CDS | 3310609 | 531 | - | 0.227872 | |
DDB_G0280409 | DDB_G0280409 | DDB0232430 | CDS | 3314622 | 1620 | - | 0.139506 | |
DDB_G0280411 | DDB_G0280411 | belongs to the anaerobic coproporphyrinogen-III oxidase family similar to human RSAD1 | DDB0232430 | CDS | 3317501 | 1341 | + | 0.260254 |
DDB_G0280413 | DDB_G0280413 | DDB0232430 | CDS | 3319399 | 3333 | + | 0.229223 | |
DDB_G0280415 | DDB_G0280415 | weak similarity to profilinallergen HMM similar to D. purpureum protein | DDB0232430 | CDS | 3323965 | 378 | + | 0.246032 |
DDB_G0280417 | DDB_G0280417 | DDB0232430 | CDS | 3324590 | 717 | - | 0.205021 | |
DDB_G0280419 | DDB_G0280419 | DDB0232430 | CDS | 3326559 | 2568 | + | 0.227804 | |
DDB_G0280421 | DDB_G0280421 | DDB0232430 | CDS | 3329289 | 654 | - | 0.253823 | |
DDB_G0280423 | DDB_G0280423 | DDB0232430 | CDS | 3330748 | 1089 | + | 0.28742 | |
DDB_G0280425 | DDB_G0280425 | DDB0232430 | CDS | 3332494 | 1002 | - | 0.260479 | |
DDB_G0280429 | DDB_G0280429 | DDB0232430 | CDS | 3339591 | 3639 | - | 0.271503 | |
DDB_G0280433 | DDB_G0280433 | hypothetical protein similar to the EST-supported | DDB0232430 | CDS | 3347454 | 171 | + | 0.25731 |
DDB_G0280437 | DDB_G0280437 | DDB0232430 | CDS | 3353124 | 897 | - | 0.222965 | |
DDB_G0280441 | DDB_G0280441 | DDB0232430 | CDS | 3356050 | 837 | + | 0.203106 | |
DDB_G0280443 | DDB_G0280443 | contains 4 FNIP repeats conserved in Dictyostelium | DDB0232430 | CDS | 3356914 | 1584 | - | 0.255051 |
DDB_G0280445 | DDB_G0280445 | GFA enzymes catalyze the condensation of formaldehyde and glutathione to S-hydroxymethylglutathione all known members of this family contain 5 strongly conserved cysteine residues | DDB0232430 | CDS | 3367339 | 432 | - | 0.270833 |
DDB_G0280451 | DDB_G0280451 | conserved protein very similar to TR4 orphan receptor associated protein containing a galactose-binding domain-like fold | DDB0232430 | CDS | 3372581 | 444 | + | 0.263514 |
DDB_G0280453 | DDB_G0280453 | conserved in Drosophila predicted to have a structural domain found in several acyl-CoA acyltransferase enzymes | DDB0232430 | CDS | 3373444 | 681 | - | 0.279001 |
DDB_G0280457 | DDB_G0280457 | DDB0232430 | CDS | 3378782 | 1278 | - | 0.29421 | |
DDB_G0280461 | DDB_G0280461 | DDB0232430 | CDS | 3391535 | 1257 | - | 0.24105 | |
DDB_G0280463 | DDB_G0280463 | DDB0232430 | CDS | 3394025 | 2241 | - | 0.262383 | |
DDB_G0280465 | DDB_G0280465 | similar to bacterial 3-hydroxybutyryl-CoA dehydrogenase similar to human HADH (3-hydroxyacyl-CoA dehydrogenase) | DDB0232430 | CDS | 3396577 | 900 | + | 0.3 |
DDB_G0280467 | DDB_G0280467 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232430 | CDS | 3398652 | 255 | - | 0.34902 |
DDB_G0280471 | DDB_G0280471 | DDB0232430 | CDS | 3403854 | 5487 | + | 0.303445 | |
DDB_G0280477 | DDB_G0280477 | DDB0232430 | CDS | 3425404 | 1353 | - | 0.2949 | |
DDB_G0280481 | DDB_G0280481 | DDB0232430 | CDS | 3429343 | 2148 | - | 0.257914 | |
DDB_G0280487 | DDB_G0280487 | DDB0232430 | CDS | 3435776 | 915 | - | 0.265574 | |
DDB_G0280491 | DDB_G0280491 | The RWP-RK domain is named after a conserved motif at its C-terminus found in Chlamydomonas plant proteins involved in nitrogen-controlled development and in Dictyostelium | DDB0232430 | CDS | 3445379 | 2517 | + | 0.304331 |
DDB_G0280493 | DDB_G0280493 | DDB0232430 | CDS | 3448667 | 1803 | + | 0.198003 | |
DDB_G0280497 | DDB_G0280497 | DDB0232430 | CDS | 3452686 | 420 | + | 0.221429 | |
DDB_G0280501 | DDB_G0280501 | DDB0232430 | CDS | 3454488 | 651 | + | 0.198157 | |
DDB_G0280503 | DDB_G0280503 | DDB0232430 | CDS | 3455362 | 1584 | - | 0.237374 | |
DDB_G0280507 | DDB_G0280507 | DDB0232430 | CDS | 3459592 | 1359 | - | 0.260486 | |
DDB_G0280509 | DDB_G0280509 | DDB0232430 | CDS | 3464216 | 2655 | - | 0.179284 | |
DDB_G0280511 | DDB_G0280511 | DDB0232430 | CDS | 3467320 | 3186 | + | 0.251099 | |
DDB_G0280513 | DDB_G0280513 | DDB0232430 | CDS | 3471532 | 2868 | - | 0.322524 | |
DDB_G0280515_ps | DDB_G0280515 | putative pseudogene very similar to | DDB0232430 | CDS | 3477222 | 1368 | - | 0.151316 |
DDB_G0280517 | DDB_G0280517 | DDB0232430 | CDS | 3480039 | 279 | - | 0.168459 | |
DDB_G0280521_RTE | DDB_G0280521 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232430 | CDS | 3359342 | 4269 | + | 0.284844 |
DDB_G0280523_RTE | DDB_G0280523 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 3364554 | 1329 | - | 0.30775 |
DDB_G0280525 | DDB_G0280525 | DDB0232430 | CDS | 3381127 | 4614 | + | 0.252492 | |
DDB_G0280527 | DDB_G0280527 | putative ortholog of TSC2 a GTPase activator involved in tuberous sclerosis belongs to the tuberin family | DDB0232430 | CDS | 3416378 | 8772 | + | 0.256042 |
DDB_G0280549 | DDB_G0280549 | DDB0232430 | CDS | 3481319 | 1116 | + | 0.269713 | |
DDB_G0280551 | DDB_G0280551 | DDB0232430 | CDS | 3483317 | 1038 | + | 0.273603 | |
DDB_G0280555 | DDB_G0280555 | DDB0232430 | CDS | 3490523 | 4410 | + | 0.211791 | |
DDB_G0280557 | DDB_G0280557 | similar to erkA and erkB and other MAP kinases does not contain the consensus sequences required for kinase function | DDB0232430 | CDS | 3496721 | 1383 | + | 0.237889 |
DDB_G0280559 | DDB_G0280559 | similar to many different classes of kinases including several MAPKs unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232430 | CDS | 3499719 | 642 | + | 0.252336 |
DDB_G0280561 | DDB_G0280561 | DDB0232430 | CDS | 3505318 | 300 | - | 0.34 | |
DDB_G0280563 | DDB_G0280563 | DDB0232430 | CDS | 3506050 | 171 | - | 0.192982 | |
DDB_G0280565 | DDB_G0280565 | DDB0232430 | CDS | 3506773 | 2529 | - | 0.324634 | |
DDB_G0280573 | DDB_G0280573 | DDB0232430 | CDS | 3516876 | 765 | + | 0.267974 | |
DDB_G0280575 | DDB_G0280575 | DDB0232430 | CDS | 3519504 | 3060 | + | 0.260784 | |
DDB_G0280577 | DDB_G0280577 | DDB0232430 | CDS | 3522934 | 615 | + | 0.227642 | |
DDB_G0280579 | DDB_G0280579 | DDB0232430 | CDS | 3523763 | 804 | - | 0.263682 | |
DDB_G0280581 | DDB_G0280581 | DDB0232430 | CDS | 3524824 | 2070 | - | 0.20628 | |
DDB_G0280583 | DDB_G0280583 | DDB0232430 | CDS | 3528408 | 2898 | - | 0.256384 | |
DDB_G0280591 | DDB_G0280591 | DDB0232430 | CDS | 3537587 | 1344 | - | 0.241815 | |
DDB_G0280593 | DDB_G0280593 | DDB0232430 | CDS | 3540460 | 2835 | + | 0.258554 | |
DDB_G0280597 | DDB_G0280597 | DDB0232430 | CDS | 3546928 | 183 | - | 0.333333 | |
DDB_G0280601 | DDB_G0280601 | DDB0232430 | CDS | 3558531 | 240 | + | 0.275 | |
DDB_G0280605 | DDB_G0280605 | DDB0232430 | CDS | 3563786 | 399 | + | 0.225564 | |
DDB_G0280613 | DDB_G0280613 | DDB0232430 | CDS | 3568288 | 1380 | - | 0.178986 | |
DDB_G0280615 | DDB_G0280615 | DDB0232430 | CDS | 3570182 | 1878 | + | 0.21033 | |
DDB_G0280619 | DDB_G0280619 | DDB0232430 | CDS | 3575172 | 1791 | + | 0.189838 | |
DDB_G0280629_ps | DDB_G0280629 | DDB0232430 | CDS | 3585207 | 246 | + | 0.223577 | |
DDB_G0280637 | DDB_G0280637 | DDB0232430 | CDS | 3590686 | 945 | + | 0.257143 | |
DDB_G0280641 | DDB_G0280641 | DDB0232430 | CDS | 3597358 | 141 | - | 0.241135 | |
DDB_G0280643 | DDB_G0280643 | similar to many CMGC family members including several MAPKs | DDB0232430 | CDS | 3598294 | 1329 | - | 0.261851 |
DDB_G0280655 | DDB_G0280655 | DDB0232430 | CDS | 3616454 | 189 | + | 0.354497 | |
DDB_G0280659 | DDB_G0280659 | DDB0232430 | CDS | 3616982 | 480 | - | 0.397917 | |
DDB_G0280661 | DDB_G0280661 | DDB0232430 | CDS | 3617623 | 603 | - | 0.343284 | |
DDB_G0280663 | DDB_G0280663 | DDB0232430 | CDS | 3618324 | 417 | + | 0.407674 | |
DDB_G0280665 | DDB_G0280665 | DDB0232430 | CDS | 3618907 | 447 | + | 0.375839 | |
DDB_G0280673 | DDB_G0280673 | DDB0232430 | CDS | 3620960 | 498 | - | 0.351406 | |
DDB_G0280675 | DDB_G0280675 | DDB0232430 | CDS | 3621809 | 438 | - | 0.363014 | |
DDB_G0280677_ps | DDB_G0280677 | putative pseudogene similar to | DDB0232430 | CDS | 3623268 | 579 | + | 0.238342 |
DDB_G0280685_ps | DDB_G0280685 | putative pseudogene very similar to argonaut genes agnA and agnB as well as to portions of midasin (mdn1)br bCommunity annotation:b DDB_G0280685 is twentyfold overexpressed in a Dictyostelium strain in which the retinoblastoma-like protein rblA has been disrupted (Doquang et al in preparation). The promoter region of this gene contains an element (GCGCCAAA) which is highly enriched in rblA-repressed promoters. It appears likely that DDB_G0280685 is a highly mutated and no longer makes a functional protein. The mutations in the coding sequence are also present in Nc4b (G. Bloomfield private communication). Harry MacWilliams February 2010br | DDB0232430 | CDS | 3627702 | 222 | - | 0.301802 |
DDB_G0280691 | DDB_G0280691 | DDB0232430 | CDS | 3638436 | 393 | + | 0.236641 | |
DDB_G0280703 | DDB_G0280703 | DDB0232430 | CDS | 3648372 | 270 | + | 0.314815 | |
DDB_G0280707 | DDB_G0280707 | DDB0232430 | CDS | 3660989 | 420 | - | 0.321429 | |
DDB_G0280709 | DDB_G0280709 | DDB0232430 | CDS | 3662714 | 429 | + | 0.298368 | |
DDB_G0280711_ps | DDB_G0280711 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 3666726 | 2283 | - | 0.246167 |
DDB_G0280717 | DDB_G0280717 | member of the AGC kinase group similar to the kinase domains of PKC (protein kinase C) and MAST (microtubule-associated serinethreonine kinase) | DDB0232430 | CDS | 3670258 | 1236 | - | 0.258091 |
DDB_G0280721 | DDB_G0280721 | DDB0232430 | CDS | 3676594 | 1005 | - | 0.284577 | |
DDB_G0280723_ps | DDB_G0280723 | putative pseudogene fragment similar to D. discoideum gene | DDB0232430 | CDS | 3686392 | 564 | - | 0.333333 |
DDB_G0280725 | DDB_G0280725 | almost identical to | DDB0232430 | CDS | 3688197 | 888 | - | 0.335586 |
DDB_G0280727 | DDB_G0280727 | DDB0232430 | CDS | 3690296 | 753 | + | 0.293493 | |
DDB_G0280729_ps | DDB_G0280729 | putative pseudogene belongs to the pirin family | DDB0232430 | CDS | 3691400 | 840 | - | 0.333333 |
DDB_G0280733 | DDB_G0280733 | DDB0232430 | CDS | 3693324 | 756 | + | 0.292328 | |
DDB_G0280735_ps | DDB_G0280735 | putative pseudogene predicted translation contains the C-terminal domain of pirin a nuclear protein of unknown function | DDB0232430 | CDS | 3696501 | 207 | + | 0.357488 |
DDB_G0280737_ps | DDB_G0280737 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232430 | CDS | 3696977 | 681 | - | 0.292217 |
DDB_G0280741 | DDB_G0280741 | DDB0232430 | CDS | 3591954 | 1086 | - | 0.203499 | |
DDB_G0280747 | DDB_G0280747 | DDB0232430 | CDS | 3657513 | 933 | - | 0.258307 | |
DDB_G0280751 | DDB_G0280751 | DDB0232430 | CDS | 3679412 | 831 | - | 0.148014 | |
DDB_G0280757 | DDB_G0280757 | DDB0232430 | CDS | 3700406 | 2217 | + | 0.129905 | |
DDB_G0280759 | DDB_G0280759 | DDB0232430 | CDS | 3703604 | 1431 | + | 0.275332 | |
DDB_G0280761 | DDB_G0280761 | belongs to the major facilitator superefamily contains 12 putative transmembrane domains | DDB0232430 | CDS | 3705496 | 1608 | - | 0.277985 |
DDB_G0280765 | DDB_G0280765 | DDB0232430 | CDS | 3715566 | 2334 | + | 0.321765 | |
DDB_G0280767 | DDB_G0280767 | DDB0232430 | CDS | 3718300 | 1269 | + | 0.312057 | |
DDB_G0280769 | DDB_G0280769 | DDB0232430 | CDS | 3719733 | 603 | - | 0.242123 | |
DDB_G0280771 | DDB_G0280771 | DDB0232430 | CDS | 3721618 | 294 | - | 0.278912 | |
DDB_G0280773 | DDB_G0280773 | DDB0232430 | CDS | 3724009 | 2985 | + | 0.236181 | |
DDB_G0280777 | DDB_G0280777 | DDB0232430 | CDS | 3729649 | 5472 | + | 0.252193 | |
DDB_G0280779 | DDB_G0280779 | DDB0232430 | CDS | 3735901 | 921 | - | 0.326819 | |
DDB_G0280781 | DDB_G0280781 | DDB0232430 | CDS | 3737208 | 939 | - | 0.225772 | |
DDB_G0280783 | DDB_G0280783 | DDB0232430 | CDS | 3739979 | 375 | + | 0.248 | |
DDB_G0280785 | DDB_G0280785 | DDB0232430 | CDS | 3740763 | 2919 | - | 0.217198 | |
DDB_G0280787 | DDB_G0280787 | DDB0232430 | CDS | 3744078 | 2811 | - | 0.213447 | |
DDB_G0280791_ps | DDB_G0280791 | putative pseudogene similar to the family of SAP DNA-binding domain-containing proteins | DDB0232430 | CDS | 3754836 | 822 | - | 0.223844 |
DDB_G0280793 | DDB_G0280793 | DDB0232430 | CDS | 3756319 | 933 | - | 0.251876 | |
DDB_G0280795 | DDB_G0280795 | DDB0232430 | CDS | 3757477 | 1992 | - | 0.220382 | |
DDB_G0280797 | DDB_G0280797 | similar to S. cerevisiae RRP12 (ribosomal RNA-processing protein 12) contains one NUC173 domain and an armadillo repeat region | DDB0232430 | CDS | 3760317 | 4284 | - | 0.288049 |
DDB_G0280799 | DDB_G0280799 | DDB0232430 | CDS | 3765398 | 126 | - | 0.34127 | |
DDB_G0280801 | DDB_G0280801 | DDB0232430 | CDS | 3766917 | 3807 | + | 0.328343 | |
DDB_G0280803 | DDB_G0280803 | DDB0232430 | CDS | 3777864 | 1221 | + | 0.288288 | |
DDB_G0280805 | DDB_G0280805 | homolog of human and S. cerevisiae KRR1 (KRR-R motif-containing protein) contains one RNA-binding KH domain S. cerevisiae KRR1 is required for 40S ribosome biogenesis | DDB0232430 | CDS | 3779782 | 1125 | - | 0.277333 |
DDB_G0280809 | DDB_G0280809 | DDB0232430 | CDS | 3747630 | 2952 | - | 0.217141 | |
DDB_G0280811 | DDB_G0280811 | DDB0232430 | CDS | 3751748 | 2673 | - | 0.212121 | |
DDB_G0280813 | DDB_G0280813 | DDB0232430 | CDS | 3771010 | 3690 | - | 0.295664 | |
DDB_G0280817 | DDB_G0280817 | DDB0232430 | CDS | 3781925 | 1031 | - | 0.346266 | |
DDB_G0280825 | DDB_G0280825 | similar to bacterial acetyltransferases homolog of E. coli maa (maltose O-acetyltransferase) similar to D. purpureum protein | DDB0232430 | CDS | 1441074 | 576 | + | 0.326389 |
DDB_G0280829 | DDB_G0280829 | DDB0232430 | CDS | 1435464 | 2322 | + | 0.198966 | |
DDB_G0280831 | DDB_G0280831 | DDB0232430 | CDS | 1432985 | 1641 | - | 0.313224 | |
DDB_G0280833_RTE | DDB_G0280833 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 1430947 | 312 | + | 0.208333 |
DDB_G0280835 | DDB_G0280835 | conserved protein in Dictyostelium fungi and bacteria | DDB0232430 | CDS | 1430323 | 579 | - | 0.278066 |
DDB_G0280837 | DDB_G0280837 | DDB0232430 | CDS | 1428903 | 630 | - | 0.215873 | |
DDB_G0280839 | DDB_G0280839 | DDB0232430 | CDS | 1427744 | 603 | - | 0.242123 | |
DDB_G0280841 | DDB_G0280841 | DDB0232430 | CDS | 1425826 | 1560 | - | 0.216026 | |
DDB_G0280845 | DDB_G0280845 | DDB0232430 | CDS | 1421922 | 2185 | + | 0.279634 | |
DDB_G0280851 | DDB_G0280851 | similar to human PIPOX which has both sarcosine oxidase and L-pipecolate oxidase activity | DDB0232430 | CDS | 3787769 | 1323 | - | 0.269841 |
DDB_G0280855 | DDB_G0280855 | similar to erkA and erkB and other MAP kinases unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232430 | CDS | 3794487 | 1179 | + | 0.25106 |
DDB_G0280857 | DDB_G0280857 | DDB0232430 | CDS | 3799596 | 1149 | + | 0.21671 | |
DDB_G0280859 | DDB_G0280859 | DDB0232430 | CDS | 3801882 | 642 | + | 0.23676 | |
DDB_G0280861_ps | DDB_G0280861 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232430 | CDS | 3803076 | 552 | - | 0.240942 |
DDB_G0280863 | DDB_G0280863 | DDB0232430 | CDS | 3805307 | 843 | + | 0.223013 | |
DDB_G0280865 | DDB_G0280865 | DDB0232430 | CDS | 3806833 | 978 | - | 0.242331 | |
DDB_G0280867 | DDB_G0280867 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232430 | CDS | 3809804 | 4176 | + | 0.25455 |
DDB_G0280869 | DDB_G0280869 | DDB0232430 | CDS | 3814959 | 2277 | - | 0.253404 | |
DDB_G0280871 | DDB_G0280871 | DDB0232430 | CDS | 3818142 | 294 | - | 0.418367 | |
DDB_G0280873 | DDB_G0280873 | DDB0232430 | CDS | 3822028 | 297 | - | 0.420875 | |
DDB_G0280875 | DDB_G0280875 | DDB0232430 | CDS | 3824495 | 363 | - | 0.247934 | |
DDB_G0280877 | DDB_G0280877 | DDB0232430 | CDS | 3825256 | 2100 | + | 0.261429 | |
DDB_G0280879 | DDB_G0280879 | DDB0232430 | CDS | 3827972 | 1725 | - | 0.209275 | |
DDB_G0280881 | DDB_G0280881 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232430 | CDS | 3830874 | 783 | - | 0.274585 |
DDB_G0280885 | DDB_G0280885 | DDB0232430 | CDS | 3832886 | 213 | - | 0.361502 | |
DDB_G0280889 | DDB_G0280889 | DDB0232430 | CDS | 3835530 | 897 | - | 0.238573 | |
DDB_G0280895 | DDB_G0280895 | has the same domain composition as fbxA and | DDB0232430 | CDS | 3841507 | 4506 | - | 0.264536 |
DDB_G0280903 | DDB_G0280903 | DDB0232430 | CDS | 3859774 | 810 | + | 0.203704 | |
DDB_G0280905 | DDB_G0280905 | DDB0232430 | CDS | 3861062 | 486 | - | 0.269547 | |
DDB_G0280911 | DDB_G0280911 | DDB0232430 | CDS | 3870282 | 3204 | + | 0.235019 | |
DDB_G0280913 | DDB_G0280913 | DDB0232430 | CDS | 3873660 | 1587 | - | 0.245117 | |
DDB_G0280915 | DDB_G0280915 | DDB0232430 | CDS | 3877405 | 510 | - | 0.215686 | |
DDB_G0280919 | DDB_G0280919 | DDB0232430 | CDS | 3879930 | 234 | - | 0.363248 | |
DDB_G0280921 | DDB_G0280921 | contains a PX (phox) domain which is found in various proteins involved in intracellular signaling | DDB0232430 | CDS | 3881788 | 3150 | + | 0.32381 |
DDB_G0280923 | DDB_G0280923 | DDB0232430 | CDS | 3886092 | 282 | + | 0.326241 | |
DDB_G0280925 | DDB_G0280925 | DDB0232430 | CDS | 3889710 | 294 | - | 0.418367 | |
DDB_G0280927 | DDB_G0280927 | DDB0232430 | CDS | 3890823 | 297 | - | 0.410774 | |
DDB_G0280929 | DDB_G0280929 | DDB0232430 | CDS | 3892080 | 303 | - | 0.39934 | |
DDB_G0280931 | DDB_G0280931 | DDB0232430 | CDS | 3893288 | 294 | - | 0.394558 | |
DDB_G0280933 | DDB_G0280933 | DDB0232430 | CDS | 3894494 | 297 | - | 0.414141 | |
DDB_G0280935 | DDB_G0280935 | DDB0232430 | CDS | 3898059 | 2055 | + | 0.375669 | |
DDB_G0280937_ps | DDB_G0280937 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 3785488 | 1464 | - | 0.245219 |
DDB_G0280939 | DDB_G0280939 | DDB0232430 | CDS | 3797710 | 330 | - | 0.20303 | |
DDB_G0280941 | DDB_G0280941 | DDB0232430 | CDS | 3808603 | 324 | - | 0.200617 | |
DDB_G0280945 | DDB_G0280945 | DDB0232430 | CDS | 3867097 | 1533 | - | 0.217221 | |
DDB_G0280947 | DDB_G0280947 | DDB0232430 | CDS | 3886790 | 2157 | - | 0.269356 | |
DDB_G0280949 | DDB_G0280949 | DDB0232430 | CDS | 3900382 | 306 | - | 0.418301 | |
DDB_G0280951 | DDB_G0280951 | DDB0232430 | CDS | 3901597 | 300 | - | 0.4 | |
DDB_G0280953 | DDB_G0280953 | DDB0232430 | CDS | 3902909 | 300 | - | 0.413333 | |
DDB_G0280955 | DDB_G0280955 | GTPase activator for rab8A involved in the regulation of contractile vacuole function during hypoosmotic stress | DDB0232430 | CDS | 3904017 | 2202 | - | 0.262489 |
DDB_G0280957 | DDB_G0280957 | DDB0232430 | CDS | 3783056 | 449 | - | 0.318486 | |
DDB_G0280987 | DDB_G0280987 | DDB0232430 | CDS | 3916236 | 855 | + | 0.224561 | |
DDB_G0280991 | DDB_G0280991 | DDB0232430 | CDS | 3918547 | 1776 | - | 0.213964 | |
DDB_G0280993 | DDB_G0280993 | similar to serologically defined breast cancer antigen 84 (sdbcag84ERGIC3) putative transmembrane protein that may have a role transport between endoplasmic reticulum and Golgi | DDB0232430 | CDS | 3921693 | 1266 | + | 0.305687 |
DDB_G0280997 | DDB_G0280997 | DDB0232430 | CDS | 3926681 | 1029 | - | 0.295432 | |
DDB_G0280999 | DDB_G0280999 | DDB0232430 | CDS | 3928566 | 252 | + | 0.293651 | |
DDB_G0281001 | DDB_G0281001 | DDB0232430 | CDS | 3929799 | 294 | + | 0.421769 | |
DDB_G0281003 | DDB_G0281003 | underexpressed in gskA-null strain highly similar to other Dictyostelium small coiled-coil proteins | DDB0232430 | CDS | 3930956 | 288 | + | 0.395833 |
DDB_G0281005 | DDB_G0281005 | DDB0232430 | CDS | 3932248 | 279 | + | 0.379928 | |
DDB_G0281007 | DDB_G0281007 | DDB0232430 | CDS | 3933475 | 294 | + | 0.394558 | |
DDB_G0281009_ps | DDB_G0281009 | putative pseudogene hssA2C7E family gene | DDB0232430 | CDS | 3934450 | 150 | + | 0.373333 |
DDB_G0281011 | DDB_G0281011 | DDB0232430 | CDS | 3935487 | 294 | + | 0.391156 | |
DDB_G0281013 | DDB_G0281013 | contains a predicted coiled-coil region found in a group of Dictyostelium proteins known to be regulated by cAMP highly similar to | DDB0232430 | CDS | 3936625 | 285 | + | 0.389474 |
DDB_G0281015 | DDB_G0281015 | DDB0232430 | CDS | 3937648 | 297 | + | 0.400673 | |
DDB_G0281017 | DDB_G0281017 | DDB0232430 | CDS | 3938819 | 285 | + | 0.375439 | |
DDB_G0281019 | DDB_G0281019 | DDB0232430 | CDS | 3939911 | 276 | + | 0.373188 | |
DDB_G0281021 | DDB_G0281021 | similar to yeast ERG28 an endoplasmic reticulum protein involved in ergosterol biosynthesis | DDB0232430 | CDS | 3940485 | 375 | - | 0.232 |
DDB_G0281025 | DDB_G0281025 | DDB0232430 | CDS | 3944292 | 2643 | + | 0.282633 | |
DDB_G0281027 | DDB_G0281027 | DDB0232430 | CDS | 3947337 | 276 | - | 0.351449 | |
DDB_G0281029 | DDB_G0281029 | DDB0232430 | CDS | 3948101 | 2592 | + | 0.180941 | |
DDB_G0281033 | DDB_G0281033 | DDB0232430 | CDS | 3956014 | 171 | - | 0.315789 | |
DDB_G0281035 | DDB_G0281035 | DDB0232430 | CDS | 3957131 | 1032 | + | 0.248062 | |
DDB_G0281037 | DDB_G0281037 | DDB0232430 | CDS | 3958898 | 762 | + | 0.276903 | |
DDB_G0281039 | DDB_G0281039 | DDB0232430 | CDS | 3959819 | 1128 | - | 0.296986 | |
DDB_G0281041 | DDB_G0281041 | DDB0232430 | CDS | 3961441 | 162 | - | 0.179012 | |
DDB_G0281043 | DDB_G0281043 | DDB0232430 | CDS | 3963633 | 1905 | + | 0.271391 | |
DDB_G0281045 | DDB_G0281045 | DDB0232430 | CDS | 3967277 | 5805 | + | 0.316968 | |
DDB_G0281049 | DDB_G0281049 | DDB0232430 | CDS | 3977638 | 762 | + | 0.330709 | |
DDB_G0281053 | DDB_G0281053 | conserved hypothetical Dictyostelium protein similar to bacterial ubiquinonemenaquinone biosynthesis methyltransferase ubiE | DDB0232430 | CDS | 3982008 | 864 | + | 0.278935 |
DDB_G0281055 | DDB_G0281055 | conserved hypothetical Dictyostelium protein similar to bacterial ubiquinonemenaquinone biosynthesis methyltransferase ubiE | DDB0232430 | CDS | 3983103 | 864 | + | 0.260417 |
DDB_G0281057 | DDB_G0281057 | DDB0232430 | CDS | 3984594 | 1518 | + | 0.23913 | |
DDB_G0281059 | DDB_G0281059 | DDB0232430 | CDS | 3994227 | 1068 | + | 0.256554 | |
DDB_G0281065 | DDB_G0281065 | DDB0232430 | CDS | 4001320 | 468 | + | 0.365385 | |
DDB_G0281067 | DDB_G0281067 | DDB0232430 | CDS | 4002363 | 903 | - | 0.34773 | |
DDB_G0281069 | DDB_G0281069 | DDB0232430 | CDS | 4003785 | 1716 | + | 0.300117 | |
DDB_G0281073 | DDB_G0281073 | DDB0232430 | CDS | 4009657 | 2109 | - | 0.218587 | |
DDB_G0281075 | DDB_G0281075 | DDB0232430 | CDS | 4013016 | 1287 | - | 0.34188 | |
DDB_G0281077 | DDB_G0281077 | DDB0232430 | CDS | 4020721 | 1989 | - | 0.296631 | |
DDB_G0281079 | DDB_G0281079 | DDB0232430 | CDS | 4024099 | 1995 | - | 0.300752 | |
DDB_G0281081 | DDB_G0281081 | DDB0232430 | CDS | 4027472 | 1944 | + | 0.288066 | |
DDB_G0281083 | DDB_G0281083 | DDB0232430 | CDS | 4029591 | 1737 | - | 0.312608 | |
DDB_G0281091 | DDB_G0281091 | contains 3 leucine-rich repeat regions similar to D. purpureum protein | DDB0232430 | CDS | 4039994 | 1770 | + | 0.271751 |
DDB_G0281095 | DDB_G0281095 | DDB0232430 | CDS | 4046834 | 3294 | - | 0.221008 | |
DDB_G0281097 | DDB_G0281097 | DDB0232430 | CDS | 4057793 | 1737 | - | 0.274036 | |
DDB_G0281099 | DDB_G0281099 | DDB0232430 | CDS | 4060002 | 1254 | + | 0.315789 | |
DDB_G0281105 | DDB_G0281105 | DDB0232430 | CDS | 4066214 | 603 | + | 0.215589 | |
DDB_G0281107_RTE | DDB_G0281107 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232430 | CDS | 4067396 | 468 | - | 0.365385 |
DDB_G0281111 | DDB_G0281111 | DDB0232430 | CDS | 4071325 | 1971 | - | 0.256722 | |
DDB_G0281113 | DDB_G0281113 | underexpressed in | DDB0232430 | CDS | 4074835 | 2688 | - | 0.15253 |
DDB_G0281115 | DDB_G0281115 | almost identical to | DDB0232430 | CDS | 4078245 | 888 | + | 0.323198 |
DDB_G0281117 | DDB_G0281117 | DDB0232430 | CDS | 4079565 | 750 | - | 0.301333 | |
DDB_G0281119_ps | DDB_G0281119 | putative pseudogene similar to pirin family proteins especially to parts of DDB_G0281115 and DDB_G0280725 | DDB0232430 | CDS | 4081406 | 591 | + | 0.329949 |
DDB_G0281121 | DDB_G0281121 | DDB0232430 | CDS | 4082329 | 750 | - | 0.304 | |
DDB_G0281123_ps | DDB_G0281123 | putative pseudogene similar to Dictyostelium genes | DDB0232430 | CDS | 4083976 | 387 | + | 0.307494 |
DDB_G0281127_ps | DDB_G0281127 | putative pseudogene fragment similar to D. discoideum gene | DDB0232430 | CDS | 4085395 | 639 | + | 0.29421 |
DDB_G0281131 | DDB_G0281131 | DDB0232430 | CDS | 4085896 | 750 | - | 0.298667 | |
DDB_G0281133 | DDB_G0281133 | DDB0232430 | CDS | 4087597 | 372 | + | 0.287634 | |
DDB_G0281135 | DDB_G0281135 | DDB0232430 | CDS | 4088225 | 750 | - | 0.3 | |
DDB_G0281137 | DDB_G0281137 | DDB0232430 | CDS | 4091325 | 1794 | + | 0.240245 | |
DDB_G0281139 | DDB_G0281139 | DDB0232430 | CDS | 4093647 | 960 | - | 0.242708 | |
DDB_G0281141 | DDB_G0281141 | DDB0232430 | CDS | 4094898 | 2949 | - | 0.264836 | |
DDB_G0281143 | DDB_G0281143 | DDB0232430 | CDS | 4098849 | 570 | - | 0.280702 | |
DDB_G0281145 | DDB_G0281145 | DDB0232430 | CDS | 4100184 | 216 | - | 0.189815 | |
DDB_G0281147 | DDB_G0281147 | DDB0232430 | CDS | 4100955 | 360 | - | 0.236111 | |
DDB_G0281149 | DDB_G0281149 | DDB0232430 | CDS | 4101872 | 582 | - | 0.247423 | |
DDB_G0281151 | DDB_G0281151 | DDB0232430 | CDS | 4103245 | 2118 | - | 0.273371 | |
DDB_G0281155 | DDB_G0281155 | putative sugar transporter contains 12 putative transmembrane domains | DDB0232430 | CDS | 4113808 | 1614 | + | 0.29368 |
DDB_G0281157 | DDB_G0281157 | DDB0232430 | CDS | 4116092 | 1218 | + | 0.20197 | |
DDB_G0281159 | DDB_G0281159 | DDB0232430 | CDS | 4117529 | 3249 | + | 0.232687 | |
DDB_G0281161 | DDB_G0281161 | DDB0232430 | CDS | 4123947 | 489 | - | 0.179959 | |
DDB_G0281165 | DDB_G0281165 | DDB0232430 | CDS | 4129870 | 2256 | + | 0.290337 | |
DDB_G0281169 | DDB_G0281169 | DDB0232430 | CDS | 4146807 | 171 | + | 0.380117 | |
DDB_G0281173 | DDB_G0281173 | DDB0232430 | CDS | 4159819 | 240 | + | 0.316667 | |
DDB_G0281181 | DDB_G0281181 | DDB0232430 | CDS | 4171126 | 1131 | - | 0.222812 | |
DDB_G0281183 | DDB_G0281183 | similar to topoisomerase 1-binding RING finger proteins has similarity to the mammalian ubiquitin-protein E3 ligase TOPORS (topoisomerase I-binding arginineserine-rich protein) | DDB0232430 | CDS | 4173081 | 1647 | + | 0.191864 |
DDB_G0281185 | DDB_G0281185 | DDB0232430 | CDS | 4176225 | 1350 | + | 0.303704 | |
DDB_G0281187 | DDB_G0281187 | DDB0232430 | CDS | 4179327 | 837 | - | 0.286738 | |
DDB_G0281189 | DDB_G0281189 | DDB0232430 | CDS | 4180654 | 180 | - | 0.294444 | |
DDB_G0281191 | DDB_G0281191 | DDB0232430 | CDS | 4181682 | 180 | + | 0.288889 | |
DDB_G0281193 | DDB_G0281193 | DDB0232430 | CDS | 4182117 | 837 | - | 0.289128 | |
DDB_G0281195 | DDB_G0281195 | DDB0232430 | CDS | 4183476 | 180 | - | 0.283333 | |
DDB_G0281197 | DDB_G0281197 | DDB0232430 | CDS | 4184500 | 180 | + | 0.288889 | |
DDB_G0281199 | DDB_G0281199 | conserved hypothetical 278 aa Dictyostelium protein centrosomal component | DDB0232430 | CDS | 4184950 | 837 | - | 0.290323 |
DDB_G0281201 | DDB_G0281201 | conserved hypothetical 278 aa Dictyostelium protein centrosomal component | DDB0232430 | CDS | 4186363 | 837 | + | 0.290323 |
DDB_G0281203_ps | DDB_G0281203 | putative pseudogene very similar to the large neighboring gene | DDB0232430 | CDS | 4194901 | 4077 | - | 0.264655 |
DDB_G0281207 | DDB_G0281207 | contains a predicted signal peptide and a C-terminal transmembrane domain conserved in Dictyostelium and Polysphondylium | DDB0232430 | CDS | 4199950 | 4173 | - | 0.253774 |
DDB_G0281209 | DDB_G0281209 | DDB0232430 | CDS | 4207203 | 1566 | + | 0.250319 | |
DDB_G0281217 | DDB_G0281217 | DDB0232430 | CDS | 4231408 | 2025 | + | 0.251852 | |
DDB_G0281219 | DDB_G0281219 | DDB0232430 | CDS | 4234799 | 1131 | - | 0.290893 | |
DDB_G0281223 | DDB_G0281223 | DDB0232430 | CDS | 4239018 | 1296 | + | 0.22608 | |
DDB_G0281225 | DDB_G0281225 | DDB0232430 | CDS | 4242261 | 1464 | - | 0.243169 | |
DDB_G0281227 | DDB_G0281227 | DDB0232430 | CDS | 4244319 | 372 | + | 0.236559 | |
DDB_G0281231 | DDB_G0281231 | DDB0232430 | CDS | 4247788 | 4521 | + | 0.28445 | |
DDB_G0281233 | DDB_G0281233 | DDB0232430 | CDS | 4253054 | 450 | + | 0.317778 | |
DDB_G0281235 | DDB_G0281235 | DDB0232430 | CDS | 4255795 | 990 | - | 0.29798 | |
DDB_G0281237 | DDB_G0281237 | DDB0232430 | CDS | 4257593 | 3117 | + | 0.230029 | |
DDB_G0281243 | DDB_G0281243 | DDB0232430 | CDS | 4265275 | 444 | - | 0.292793 | |
DDB_G0281245_RTE | DDB_G0281245 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232430 | CDS | 4268319 | 681 | + | 0.377386 |
DDB_G0281247_RTE | DDB_G0281247 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232430 | CDS | 4269757 | 180 | - | 0.294444 |
DDB_G0281249 | DDB_G0281249 | DDB0232430 | CDS | 4272791 | 4242 | - | 0.188119 | |
DDB_G0281251 | DDB_G0281251 | DDB0232430 | CDS | 4282030 | 4590 | + | 0.262963 | |
DDB_G0281257 | DDB_G0281257 | DDB0232430 | CDS | 4301960 | 3390 | + | 0.20118 | |
DDB_G0281259 | DDB_G0281259 | similar to the DREV (DORA reverse strand) protein found in other eukaryotes believed to be a methyltransferase but is of unknown function | DDB0232430 | CDS | 4305745 | 1230 | + | 0.243089 |
DDB_G0281261 | DDB_G0281261 | DDB0232430 | CDS | 4307171 | 3342 | - | 0.264213 | |
DDB_G0281263 | DDB_G0281263 | DDB0232430 | CDS | 4310870 | 411 | + | 0.257908 | |
DDB_G0281265 | DDB_G0281265 | DDB0232430 | CDS | 4311777 | 1914 | - | 0.277429 | |
DDB_G0281269 | DDB_G0281269 | DDB0232430 | CDS | 4314924 | 1353 | + | 0.251293 | |
DDB_G0281271 | DDB_G0281271 | DDB0232430 | CDS | 4316503 | 639 | - | 0.190923 | |
DDB_G0281273 | DDB_G0281273 | DDB0232430 | CDS | 4317752 | 234 | - | 0.371795 | |
DDB_G0281275 | DDB_G0281275 | DDB0232430 | CDS | 4322092 | 168 | - | 0.220238 | |
DDB_G0281279 | DDB_G0281279 | DDB0232430 | CDS | 4333375 | 2037 | + | 0.382425 | |
DDB_G0281281 | DDB_G0281281 | DDB0232430 | CDS | 4335971 | 765 | - | 0.347712 | |
DDB_G0281283 | DDB_G0281283 | DDB0232430 | CDS | 4337681 | 660 | + | 0.283333 | |
DDB_G0281285 | DDB_G0281285 | DDB0232430 | CDS | 4338670 | 795 | - | 0.249057 | |
DDB_G0281287 | DDB_G0281287 | DDB0232430 | CDS | 4345792 | 900 | + | 0.29 | |
DDB_G0281289 | DDB_G0281289 | DDB0232430 | CDS | 4358553 | 1347 | + | 0.282108 | |
DDB_G0281291 | DDB_G0281291 | DDB0232430 | CDS | 4360504 | 792 | - | 0.285354 | |
DDB_G0281295 | DDB_G0281295 | DDB0232430 | CDS | 3996913 | 285 | + | 0.414035 | |
DDB_G0281297_RTE | DDB_G0281297 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232430 | CDS | 4014814 | 2745 | + | 0.307468 |
DDB_G0281299_ps | DDB_G0281299 | putative pseudogene similar to the 5' half of a small family of genes including | DDB0232430 | CDS | 4018746 | 1014 | - | 0.280079 |
DDB_G0281301 | DDB_G0281301 | DDB0232430 | CDS | 4051226 | 2862 | - | 0.20021 | |
DDB_G0281303_ps | DDB_G0281303 | putative pseudogene similar to family of SAP DNA-binding domain-containing proteins in D. discoideum | DDB0232430 | CDS | 4054526 | 1458 | - | 0.195473 |
DDB_G0281309 | DDB_G0281309 | DDB0232430 | CDS | 4120970 | 603 | - | 0.296849 | |
DDB_G0281311 | DDB_G0281311 | DDB0232430 | CDS | 4122141 | 510 | - | 0.176471 | |
DDB_G0281313 | DDB_G0281313 | DDB0232430 | CDS | 4150932 | 1614 | + | 0.29368 | |
DDB_G0281317 | DDB_G0281317 | DDB0232430 | CDS | 4155822 | 1620 | + | 0.238272 | |
DDB_G0281319 | DDB_G0281319 | DDB0232430 | CDS | 4160503 | 2124 | - | 0.272128 | |
DDB_G0281321 | DDB_G0281321 | DDB0232430 | CDS | 4178520 | 522 | + | 0.216475 | |
DDB_G0281323 | DDB_G0281323 | DDB0232430 | CDS | 4187406 | 2217 | - | 0.271538 | |
DDB_G0281325 | DDB_G0281325 | similar to prtein in D. purpureum an in the see anemone N. vectensis contains an N-terminal signal sequence and a C-terminal transmembrane domain | DDB0232430 | CDS | 4191095 | 1614 | + | 0.358116 |
DDB_G0281329_ps | DDB_G0281329 | putative pseudogene fragment similar to D. discoideum FNIP repeat-containing proteins including | DDB0232430 | CDS | 4270661 | 1953 | + | 0.219662 |
DDB_G0281331 | DDB_G0281331 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis contains 7 predicted transmembrane domains | DDB0232430 | CDS | 4278355 | 2115 | + | 0.259102 |
DDB_G0281333 | DDB_G0281333 | DDB0232430 | CDS | 4318553 | 2700 | - | 0.266667 | |
DDB_G0281339 | DDB_G0281339 | DDB0232430 | CDS | 4368638 | 675 | + | 0.300741 | |
DDB_G0281341 | DDB_G0281341 | DDB0232430 | CDS | 4370112 | 315 | + | 0.253968 | |
DDB_G0281345 | DDB_G0281345 | DDB0232430 | CDS | 4379229 | 597 | + | 0.269682 | |
DDB_G0281349_ps | DDB_G0281349 | fragment very similar to | DDB0232430 | CDS | 4380507 | 1752 | + | 0.281963 |
DDB_G0281351 | DDB_G0281351 | DDB0232430 | CDS | 4385822 | 1809 | - | 0.263682 | |
DDB_G0281353 | DDB_G0281353 | DDB0232430 | CDS | 4388160 | 6504 | + | 0.281212 | |
DDB_G0281355_RTE | DDB_G0281355 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232430 | CDS | 4395483 | 972 | - | 0.300412 |
DDB_G0281357_RTE | DDB_G0281357 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232430 | CDS | 4397502 | 1512 | - | 0.316799 |
DDB_G0281359 | DDB_G0281359 | DDB0232430 | CDS | 4401226 | 1032 | + | 0.251938 | |
DDB_G0281361 | DDB_G0281361 | DDB0232430 | CDS | 4403294 | 1902 | + | 0.242902 | |
DDB_G0281363 | DDB_G0281363 | putative ortholog of H. sapiens CNOT10 contains several putative TPR repeats | DDB0232430 | CDS | 4410114 | 2805 | + | 0.252406 |
DDB_G0281365 | DDB_G0281365 | DDB0232430 | CDS | 4413139 | 147 | - | 0.204082 | |
DDB_G0281367 | DDB_G0281367 | DDB0232430 | CDS | 4413764 | 504 | - | 0.265873 | |
DDB_G0281369 | DDB_G0281369 | DDB0232430 | CDS | 4370772 | 1206 | - | 0.308458 | |
DDB_G0281371 | DDB_G0281371 | DDB0232430 | CDS | 4372875 | 1302 | - | 0.221966 | |
DDB_G0281377 | DDB_G0281377 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D | DDB0232430 | CDS | 4405679 | 2262 | + | 0.263926 |
DDB_G0281379 | DDB_G0281379 | DDB0232430 | CDS | 4415599 | 1188 | + | 0.236532 | |
DDB_G0281395 | DDB_G0281395 | DDB0232430 | CDS | 4422701 | 414 | - | 0.193237 | |
DDB_G0281399 | DDB_G0281399 | DDB0232430 | CDS | 4424611 | 1515 | - | 0.310891 | |
DDB_G0281401 | DDB_G0281401 | DDB0232430 | CDS | 4429232 | 3771 | + | 0.307611 | |
DDB_G0281413 | DDB_G0281413 | DDB0232430 | CDS | 4442749 | 360 | + | 0.197222 | |
DDB_G0281415 | DDB_G0281415 | DDB0232430 | CDS | 4443494 | 2412 | + | 0.279022 | |
DDB_G0281417 | DDB_G0281417 | unknown protein contains 4 predicted transmembrane domains | DDB0232430 | CDS | 4451020 | 912 | - | 0.299342 |
DDB_G0281421 | DDB_G0281421 | DDB0232430 | CDS | 4458420 | 2949 | + | 0.194303 | |
DDB_G0281423 | DDB_G0281423 | DDB0232430 | CDS | 4461687 | 2979 | + | 0.191339 | |
DDB_G0281425 | DDB_G0281425 | DDB0232430 | CDS | 4468486 | 1356 | - | 0.285398 | |
DDB_G0281427 | DDB_G0281427 | DDB0232430 | CDS | 4470521 | 4176 | - | 0.256944 | |
DDB_G0281429 | DDB_G0281429 | DDB0232430 | CDS | 4475058 | 1161 | + | 0.250646 | |
DDB_G0281431 | DDB_G0281431 | DDB0232430 | CDS | 4477171 | 2763 | + | 0.26131 | |
DDB_G0281433 | DDB_G0281433 | DDB0232430 | CDS | 4495953 | 1044 | + | 0.299808 | |
DDB_G0281439 | DDB_G0281439 | DDB0232430 | CDS | 4501721 | 123 | + | 0.390244 | |
DDB_G0281443 | DDB_G0281443 | belongs to the fatty acid hydroxylase superfamily contains 8 putative transmembrane domains | DDB0232430 | CDS | 4509300 | 2043 | + | 0.198727 |
DDB_G0281447 | DDB_G0281447 | DDB0232430 | CDS | 4516135 | 714 | + | 0.232493 | |
DDB_G0281449_RTE | DDB_G0281449 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232430 | CDS | 4522479 | 288 | - | 0.375 |
DDB_G0281451_RTE | DDB_G0281451 | DDB0232430 | CDS | 4525070 | 333 | + | 0.291291 | |
DDB_G0281453_RTE | DDB_G0281453 | DDB0232430 | CDS | 4525480 | 462 | + | 0.309524 | |
DDB_G0281455_RTE | DDB_G0281455 | DDB0232430 | CDS | 4526091 | 3294 | + | 0.334244 | |
DDB_G0281463 | DDB_G0281463 | DDB0232430 | CDS | 4539251 | 1023 | + | 0.289345 | |
DDB_G0281465 | DDB_G0281465 | DDB0232430 | CDS | 4545446 | 1356 | + | 0.238938 | |
DDB_G0281467 | DDB_G0281467 | DDB0232430 | CDS | 4547456 | 1044 | + | 0.240421 | |
DDB_G0281473 | DDB_G0281473 | DDB0232430 | CDS | 4553203 | 2172 | + | 0.231584 | |
DDB_G0281479_RTE | DDB_G0281479 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232430 | CDS | 4578097 | 639 | + | 0.386541 |
DDB_G0281481 | DDB_G0281481 | DDB0232430 | CDS | 4579212 | 1620 | - | 0.215432 | |
DDB_G0281485 | DDB_G0281485 | DDB0232430 | CDS | 4599041 | 4422 | + | 0.246721 | |
DDB_G0281487 | DDB_G0281487 | ortholog of the human NSDHL protein and the yeast ERG26 protein belongs to the 3beta-HSD family | DDB0232430 | CDS | 4603817 | 1050 | + | 0.31619 |
DDB_G0281489 | DDB_G0281489 | homolog of human TMCO1 (transmembrane and coiled-coil domain-containing protein 1) contains 2 putative transmembrane domains contains a putative coiled-coil region | DDB0232430 | CDS | 4605058 | 561 | - | 0.26738 |
DDB_G0281491_RTE | DDB_G0281491 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 4608468 | 3180 | + | 0.350943 |
DDB_G0281495 | DDB_G0281495 | DDB0232430 | CDS | 4613870 | 1263 | + | 0.270784 | |
DDB_G0281497 | DDB_G0281497 | DDB0232430 | CDS | 4615481 | 1665 | - | 0.267267 | |
DDB_G0281501 | DDB_G0281501 | contains 2 putative transmembrane domains has weak similarity to the N-terminal domain of cytochrome b561 | DDB0232430 | CDS | 4634453 | 2379 | + | 0.254729 |
DDB_G0281503 | DDB_G0281503 | DDB0232430 | CDS | 4637514 | 3360 | + | 0.285417 | |
DDB_G0281505 | DDB_G0281505 | DDB0232430 | CDS | 4641293 | 1014 | - | 0.287968 | |
DDB_G0281509 | DDB_G0281509 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232430 | CDS | 4647716 | 210 | + | 0.185714 |
DDB_G0281513 | DDB_G0281513 | DDB0232430 | CDS | 4652073 | 1449 | - | 0.218772 | |
DDB_G0281515 | DDB_G0281515 | DDB0232430 | CDS | 4654406 | 1569 | - | 0.219885 | |
DDB_G0281521 | DDB_G0281521 | member of the bromo-AAAATPase (BRAT) class of chromatin assembly proteins | DDB0232430 | CDS | 4480305 | 5403 | - | 0.277624 |
DDB_G0281523 | DDB_G0281523 | DDB0232430 | CDS | 4486206 | 1104 | - | 0.294384 | |
DDB_G0281527 | DDB_G0281527 | DDB0232430 | CDS | 4520387 | 1878 | + | 0.205005 | |
DDB_G0281529_TE | DDB_G0281529 | DDB0232430 | CDS | 4529784 | 270 | + | 0.337037 | |
DDB_G0281531_ps | DDB_G0281531 | putative pseudogene similar to EGF domain-containing proteins like | DDB0232430 | CDS | 4532369 | 3399 | + | 0.246543 |
DDB_G0281533_RTE | DDB_G0281533 | ORF1 encoding GAG and protease (PRO) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232430 | CDS | 4571394 | 1149 | + | 0.394256 |
DDB_G0281535_RTE | DDB_G0281535 | long terminal repeat -retrotransposon Skipper GAG-PRO-POL refer to GenBank AF049230 for full length consensus element | DDB0232430 | CDS | 4572825 | 3969 | + | 0.323003 |
DDB_G0281537 | DDB_G0281537 | DDB0232430 | CDS | 4581015 | 1887 | - | 0.229465 | |
DDB_G0281539_RTE | DDB_G0281539 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 4606867 | 1077 | + | 0.410399 |
DDB_G0281541 | DDB_G0281541 | DDB0232430 | CDS | 4627625 | 1572 | - | 0.232824 | |
DDB_G0281543 | DDB_G0281543 | DDB0232430 | CDS | 4629488 | 4020 | - | 0.230846 | |
DDB_G0281559 | DDB_G0281559 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog REMI mutant forms large sori see | DDB0232430 | CDS | 4978870 | 3066 | - | 0.299739 |
DDB_G0281575 | DDB_G0281575 | DDB0232430 | CDS | 4657789 | 681 | + | 0.123348 | |
DDB_G0281577 | DDB_G0281577 | DDB0232430 | CDS | 4658517 | 1170 | + | 0.184615 | |
DDB_G0281579_RTE | DDB_G0281579 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 4660486 | 1119 | + | 0.343164 |
DDB_G0281583 | DDB_G0281583 | DDB0232430 | CDS | 4664590 | 246 | + | 0.211382 | |
DDB_G0281589 | DDB_G0281589 | very similar to mammalian CBWD1 and CBWD2 ubiquitiously expressed COBW domain-containing proteins prokaryotic CobW involved in cobalamin (vitamin B12) biosynthesis | DDB0232430 | CDS | 4676319 | 1191 | - | 0.246012 |
DDB_G0281597 | DDB_G0281597 | DDB0232430 | CDS | 4693112 | 120 | + | 0.3 | |
DDB_G0281601 | DDB_G0281601 | DDB0232430 | CDS | 4697870 | 429 | - | 0.261072 | |
DDB_G0281603 | DDB_G0281603 | DDB0232430 | CDS | 4698687 | 1926 | + | 0.246106 | |
DDB_G0281607 | DDB_G0281607 | DDB0232430 | CDS | 4703616 | 801 | - | 0.277154 | |
DDB_G0281609 | DDB_G0281609 | DDB0232430 | CDS | 4706235 | 933 | + | 0.325831 | |
DDB_G0281611 | DDB_G0281611 | DDB0232430 | CDS | 4707985 | 162 | + | 0.395062 | |
DDB_G0281613 | DDB_G0281613 | conserved hypothetical 278 aa Dictyostelium protein centrosomal component | DDB0232430 | CDS | 4711308 | 837 | - | 0.291517 |
DDB_G0281615 | DDB_G0281615 | DDB0232430 | CDS | 4712751 | 177 | - | 0.237288 | |
DDB_G0281617 | DDB_G0281617 | DDB0232430 | CDS | 4713358 | 837 | - | 0.291517 | |
DDB_G0281619 | DDB_G0281619 | DDB0232430 | CDS | 4714928 | 1515 | + | 0.213861 | |
DDB_G0281621 | DDB_G0281621 | ortholog of the human SART1 identified in the spliceosome C complex also similar to yeast SNU66 which plays a role in mRNA splicing | DDB0232430 | CDS | 4716452 | 2067 | - | 0.253507 |
DDB_G0281625 | DDB_G0281625 | conserved hypothetical protein present in bacteria nematodes plants and fungi | DDB0232430 | CDS | 4723898 | 462 | - | 0.242424 |
DDB_G0281627 | DDB_G0281627 | DDB0232430 | CDS | 4725130 | 1827 | + | 0.305419 | |
DDB_G0281629_ps | DDB_G0281629 | putative pseudogene fragment similar to D. discoideum gene | DDB0232430 | CDS | 4727952 | 831 | + | 0.157641 |
DDB_G0281631_ps | DDB_G0281631 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 4729446 | 2553 | + | 0.167254 |
DDB_G0281633_ps | DDB_G0281633 | putative pseudogene fragment similar to pirin family proteins especially to the C-terminal half of DDB_G0281115 and DDB_G0280725 | DDB0232430 | CDS | 4738827 | 327 | + | 0.299694 |
DDB_G0281635 | DDB_G0281635 | DDB0232430 | CDS | 4739504 | 750 | - | 0.304 | |
DDB_G0281637 | DDB_G0281637 | DDB0232430 | CDS | 4742882 | 2865 | + | 0.195812 | |
DDB_G0281639 | DDB_G0281639 | DDB0232430 | CDS | 4746209 | 2391 | + | 0.240485 | |
DDB_G0281643 | DDB_G0281643 | DDB0232430 | CDS | 4751182 | 2787 | + | 0.22605 | |
DDB_G0281645 | DDB_G0281645 | DDB0232430 | CDS | 4754331 | 1584 | - | 0.279672 | |
DDB_G0281647 | DDB_G0281647 | putative pseudogene fragment similar to the neighboring gene | DDB0232430 | CDS | 4756428 | 327 | - | 0.272171 |
DDB_G0281653 | DDB_G0281653 | DDB0232430 | CDS | 4768142 | 1128 | - | 0.261525 | |
DDB_G0281655 | DDB_G0281655 | DDB0232430 | CDS | 4769979 | 288 | + | 0.21875 | |
DDB_G0281657 | DDB_G0281657 | DDB0232430 | CDS | 4770616 | 2925 | - | 0.27453 | |
DDB_G0281665 | DDB_G0281665 | DDB0232430 | CDS | 4789355 | 1422 | - | 0.190577 | |
DDB_G0281671 | DDB_G0281671 | DDB0232430 | CDS | 4794386 | 4170 | - | 0.243885 | |
DDB_G0281673 | DDB_G0281673 | DDB0232430 | CDS | 4799865 | 822 | + | 0.290754 | |
DDB_G0281675 | DDB_G0281675 | DDB0232430 | CDS | 4800986 | 438 | - | 0.221461 | |
DDB_G0281679 | DDB_G0281679 | DDB0232430 | CDS | 4804047 | 1176 | + | 0.244898 | |
DDB_G0281687 | DDB_G0281687 | DDB0232430 | CDS | 4813506 | 2856 | + | 0.279412 | |
DDB_G0281689 | DDB_G0281689 | similar to | DDB0232430 | CDS | 4816615 | 534 | - | 0.310861 |
DDB_G0281691 | DDB_G0281691 | similar to | DDB0232430 | CDS | 4817955 | 528 | + | 0.299242 |
DDB_G0281693 | DDB_G0281693 | DDB0232430 | CDS | 4833441 | 843 | + | 0.300119 | |
DDB_G0281695 | DDB_G0281695 | DDB0232430 | CDS | 4836494 | 1257 | - | 0.263325 | |
DDB_G0281697 | DDB_G0281697 | DDB0232430 | CDS | 4838618 | 240 | - | 0.258333 | |
DDB_G0281699 | DDB_G0281699 | DDB0232430 | CDS | 4849870 | 1212 | + | 0.292904 | |
DDB_G0281701 | DDB_G0281701 | DDB0232430 | CDS | 4851537 | 243 | - | 0.308642 | |
DDB_G0281705 | DDB_G0281705 | DDB0232430 | CDS | 4853137 | 936 | - | 0.314103 | |
DDB_G0281707 | DDB_G0281707 | DDB0232430 | CDS | 4855046 | 621 | - | 0.297907 | |
DDB_G0281709 | DDB_G0281709 | DDB0232430 | CDS | 4862322 | 3804 | + | 0.259727 | |
DDB_G0281713 | DDB_G0281713 | DDB0232430 | CDS | 4869216 | 255 | - | 0.258824 | |
DDB_G0281719 | DDB_G0281719 | DDB0232430 | CDS | 4874420 | 2943 | - | 0.266735 | |
DDB_G0281723 | DDB_G0281723 | DDB0232430 | CDS | 4880176 | 1380 | - | 0.447826 | |
DDB_G0281727 | DDB_G0281727 | DDB0232430 | CDS | 4885508 | 795 | - | 0.416352 | |
DDB_G0281729 | DDB_G0281729 | DDB0232430 | CDS | 4886865 | 1167 | - | 0.279349 | |
DDB_G0281733 | DDB_G0281733 | DDB0232430 | CDS | 4889095 | 2496 | + | 0.276442 | |
DDB_G0281735 | DDB_G0281735 | contains 9 transmembrane domains as predicted by TMHMM2.0 enriched in gametes | DDB0232430 | CDS | 4892895 | 1728 | - | 0.278935 |
DDB_G0281737 | DDB_G0281737 | DDB0232430 | CDS | 4897459 | 855 | - | 0.273684 | |
DDB_G0281743 | DDB_G0281743 | DDB0232430 | CDS | 4905122 | 3990 | - | 0.246366 | |
DDB_G0281745 | DDB_G0281745 | DDB0232430 | CDS | 4910382 | 1794 | + | 0.337793 | |
DDB_G0281747 | DDB_G0281747 | conserved protein family similar to S. cerevisiae OPI10 (OverProducer of Inositol) possibly involved in phospholipid biosynthesis | DDB0232430 | CDS | 4912687 | 654 | + | 0.237003 |
DDB_G0281749 | DDB_G0281749 | DDB0232430 | CDS | 4915108 | 1026 | + | 0.20078 | |
DDB_G0281751 | DDB_G0281751 | DDB0232430 | CDS | 4916395 | 822 | - | 0.287105 | |
DDB_G0281753 | DDB_G0281753 | DDB0232430 | CDS | 4920824 | 219 | + | 0.251142 | |
DDB_G0281757 | DDB_G0281757 | DDB0232430 | CDS | 4923705 | 204 | + | 0.25 | |
DDB_G0281759 | DDB_G0281759 | DDB0232430 | CDS | 4924793 | 1191 | - | 0.212427 | |
DDB_G0281761 | DDB_G0281761 | DDB0232430 | CDS | 4926150 | 888 | - | 0.211712 | |
DDB_G0281763 | DDB_G0281763 | RNA-binding protein similar to human SSB (Sjoegren Syndrome type B antigen) that plays a role in the transcription of RNA polymerase III and yeast LHP1 protein a molecular chaperone which is required for maturation of tRNA and snRNA precursors | DDB0232430 | CDS | 4927454 | 1065 | - | 0.321127 |
DDB_G0281767 | DDB_G0281767 | DDB0232430 | CDS | 4930354 | 2652 | + | 0.255656 | |
DDB_G0281769 | DDB_G0281769 | DDB0232430 | CDS | 4934294 | 183 | + | 0.295082 | |
DDB_G0281771 | DDB_G0281771 | contains a predicted signal peptide similar to D. purpureum protein | DDB0232430 | CDS | 4943706 | 471 | + | 0.278132 |
DDB_G0281775 | DDB_G0281775 | DDB0232430 | CDS | 4948067 | 1248 | + | 0.306891 | |
DDB_G0281777 | DDB_G0281777 | DDB0232430 | CDS | 4951421 | 1224 | - | 0.31781 | |
DDB_G0281781 | DDB_G0281781 | DDB0232430 | CDS | 4965873 | 1863 | - | 0.285561 | |
DDB_G0281783 | DDB_G0281783 | DDB0232430 | CDS | 4968465 | 2346 | - | 0.322251 | |
DDB_G0281785 | DDB_G0281785 | DDB0232430 | CDS | 4971939 | 2823 | - | 0.253985 | |
DDB_G0281789 | DDB_G0281789 | DDB0232430 | CDS | 4983430 | 1410 | - | 0.367376 | |
DDB_G0281793 | DDB_G0281793 | DDB0232430 | CDS | 4985633 | 570 | + | 0.282456 | |
DDB_G0281805 | DDB_G0281805 | DDB0232430 | CDS | 4737151 | 828 | - | 0.277778 | |
DDB_G0281807_ps | DDB_G0281807 | putative pseudogene fragment similar to pirin family protein | DDB0232430 | CDS | 4741312 | 333 | + | 0.321321 |
DDB_G0281809 | DDB_G0281809 | conserved protein containing a Rapran-GAP (GTPase activating protein) domain | DDB0232430 | CDS | 4840109 | 4860 | - | 0.304733 |
DDB_G0281811 | DDB_G0281811 | DDB0232430 | CDS | 4857991 | 423 | - | 0.451537 | |
DDB_G0281813 | DDB_G0281813 | DDB0232430 | CDS | 4859387 | 2568 | - | 0.241822 | |
DDB_G0281815 | DDB_G0281815 | DDB0232430 | CDS | 4913622 | 930 | - | 0.28172 | |
DDB_G0281817 | DDB_G0281817 | DDB0232430 | CDS | 4963446 | 1626 | - | 0.266913 | |
DDB_G0281819 | DDB_G0281819 | DDB0232430 | CDS | 4975775 | 561 | - | 0.263815 | |
DDB_G0281831 | DDB_G0281831 | conserved in bacteria a member of the NK (nucleosidenucleotide kinase) superfamily also belongs to the zeta toxin family which in bacteria is a component of a postregulational killing system | DDB0232430 | CDS | 4993575 | 507 | - | 0.262327 |
DDB_G0281833 | DDB_G0281833 | DDB0232430 | CDS | 4994441 | 456 | - | 0.313596 | |
DDB_G0281835 | DDB_G0281835 | DDB0232430 | CDS | 4995492 | 1146 | + | 0.19808 | |
DDB_G0281837 | DDB_G0281837 | DDB0232430 | CDS | 4996941 | 528 | - | 0.25 | |
DDB_G0281839 | DDB_G0281839 | DDB0232430 | CDS | 4997894 | 2502 | + | 0.328937 | |
DDB_G0281843 | DDB_G0281843 | similar to D. purpureum protein also contains two EGF repeats | DDB0232430 | CDS | 5003890 | 1236 | - | 0.311489 |
DDB_G0281845 | DDB_G0281845 | DDB0232430 | CDS | 5006578 | 4032 | + | 0.255208 | |
DDB_G0281847 | DDB_G0281847 | DDB0232430 | CDS | 5011508 | 225 | + | 0.244444 | |
DDB_G0281851 | DDB_G0281851 | DDB0232430 | CDS | 5014229 | 2565 | - | 0.183626 | |
DDB_G0281857 | DDB_G0281857 | DDB0232430 | CDS | 5030913 | 4113 | - | 0.181862 | |
DDB_G0281861 | DDB_G0281861 | DDB0232430 | CDS | 5038245 | 1785 | + | 0.345658 | |
DDB_G0281867 | DDB_G0281867 | DDB0232430 | CDS | 5045020 | 141 | - | 0.255319 | |
DDB_G0281869 | DDB_G0281869 | DDB0232430 | CDS | 5050887 | 132 | - | 0.310606 | |
DDB_G0281871 | DDB_G0281871 | DDB0232430 | CDS | 5051942 | 2634 | + | 0.312832 | |
DDB_G0281875 | DDB_G0281875 | DDB0232430 | CDS | 5056031 | 612 | + | 0.320261 | |
DDB_G0281879 | DDB_G0281879 | DDB0232430 | CDS | 5060032 | 177 | - | 0.20339 | |
DDB_G0281883 | DDB_G0281883 | DDB0232430 | CDS | 5062706 | 705 | - | 0.236879 | |
DDB_G0281887 | DDB_G0281887 | DDB0232430 | CDS | 5073921 | 186 | + | 0.236559 | |
DDB_G0281897 | DDB_G0281897 | DDB0232430 | CDS | 5087099 | 606 | + | 0.267327 | |
DDB_G0281903 | DDB_G0281903 | DDB0232430 | CDS | 5094433 | 1218 | + | 0.254516 | |
DDB_G0281905 | DDB_G0281905 | DDB0232430 | CDS | 5096179 | 2739 | + | 0.16831 | |
DDB_G0281907 | DDB_G0281907 | weakly similar to human ATPase family AAA domain-containing protein 5 (ATAD5) that is involved in DNA damage response and to yeast ELG1 (Enhanced Level of Genomic instability) which is required for S phase progression telomere homeostasis and homologous recombination-mediated DNA repairbrbr bCommunity annotation:b DDB_G0281907 is weakly similar to elg1 a protein related to rfc1 which together with rfc2-5 participates in the loading and perhaps unloading of the | DDB0232430 | CDS | 5099224 | 3996 | + | 0.227728 |
DDB_G0281909 | DDB_G0281909 | DDB0232430 | CDS | 5103620 | 1836 | - | 0.289216 | |
DDB_G0281911 | DDB_G0281911 | DDB0232430 | CDS | 5106919 | 1077 | + | 0.276695 | |
DDB_G0281913 | DDB_G0281913 | conserved in plants fungi and bacteria | DDB0232430 | CDS | 5108423 | 1530 | - | 0.375817 |
DDB_G0281915 | DDB_G0281915 | unknown protein contains 4 predicted transmembrane domains | DDB0232430 | CDS | 5110614 | 915 | - | 0.260109 |
DDB_G0281917 | DDB_G0281917 | DDB0232430 | CDS | 5121103 | 954 | + | 0.29979 | |
DDB_G0281919 | DDB_G0281919 | DDB0232430 | CDS | 5122667 | 1398 | + | 0.214592 | |
DDB_G0281921 | DDB_G0281921 | member of the ZIP (Zrt- and Irt-like Protein) family capable of transporting zinc and other metal ions contains 6 transmembrane domains | DDB0232430 | CDS | 5124821 | 1116 | + | 0.280466 |
DDB_G0281925 | DDB_G0281925 | DDB0232430 | CDS | 5132437 | 1761 | - | 0.366269 | |
DDB_G0281927 | DDB_G0281927 | DDB0232430 | CDS | 5152552 | 942 | + | 0.272824 | |
DDB_G0281929 | DDB_G0281929 | DDB0232430 | CDS | 5153973 | 1887 | - | 0.266031 | |
DDB_G0281931 | DDB_G0281931 | DDB0232430 | CDS | 5156500 | 3636 | - | 0.242849 | |
DDB_G0281935 | DDB_G0281935 | DDB0232430 | CDS | 5163572 | 1959 | - | 0.322103 | |
DDB_G0281937 | DDB_G0281937 | DDB0232430 | CDS | 5037215 | 594 | + | 0.304714 | |
DDB_G0281939 | DDB_G0281939 | DDB0232430 | CDS | 5047304 | 3204 | + | 0.252497 | |
DDB_G0281941_RTE | DDB_G0281941 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5065537 | 3144 | - | 0.33874 |
DDB_G0281943_RTE | DDB_G0281943 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5068971 | 1335 | - | 0.310112 |
DDB_G0281945 | DDB_G0281945 | DDB0232430 | CDS | 5071587 | 1125 | + | 0.206222 | |
DDB_G0281953 | DDB_G0281953 | DDB0232430 | CDS | 5193203 | 501 | - | 0.279441 | |
DDB_G0281961 | DDB_G0281961 | DDB0232430 | CDS | 5172400 | 285 | + | 0.284211 | |
DDB_G0281963 | DDB_G0281963 | DDB0232430 | CDS | 5173395 | 1185 | + | 0.296203 | |
DDB_G0281965 | DDB_G0281965 | DDB0232430 | CDS | 5175300 | 453 | + | 0.242826 | |
DDB_G0281967 | DDB_G0281967 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D | DDB0232430 | CDS | 5181089 | 2124 | - | 0.278249 |
DDB_G0281971 | DDB_G0281971 | DDB0232430 | CDS | 5200691 | 717 | + | 0.25523 | |
DDB_G0281973 | DDB_G0281973 | DDB0232430 | CDS | 5202408 | 513 | + | 0.276803 | |
DDB_G0281975 | DDB_G0281975 | DDB0232430 | CDS | 5203577 | 672 | - | 0.306548 | |
DDB_G0281977 | DDB_G0281977 | DDB0232430 | CDS | 5207662 | 171 | - | 0.187135 | |
DDB_G0281979 | DDB_G0281979 | DDB0232430 | CDS | 5208875 | 855 | - | 0.281871 | |
DDB_G0281981 | DDB_G0281981 | DDB0232430 | CDS | 5213481 | 1254 | + | 0.299841 | |
DDB_G0281991 | DDB_G0281991 | DDB0232430 | CDS | 5222837 | 1104 | + | 0.293478 | |
DDB_G0281993 | DDB_G0281993 | DDB0232430 | CDS | 5224852 | 1047 | + | 0.293219 | |
DDB_G0281995 | DDB_G0281995 | DDB0232430 | CDS | 5226169 | 183 | - | 0.234973 | |
DDB_G0281997 | DDB_G0281997 | DDB0232430 | CDS | 5227597 | 204 | - | 0.303922 | |
DDB_G0281999 | DDB_G0281999 | DDB0232430 | CDS | 5230177 | 711 | + | 0.322082 | |
DDB_G0282001 | DDB_G0282001 | DDB0232430 | CDS | 5231139 | 2913 | + | 0.210436 | |
DDB_G0282005 | DDB_G0282005 | DDB0232430 | CDS | 5234911 | 681 | + | 0.30837 | |
DDB_G0282011 | DDB_G0282011 | very similar to the mammalian CDC91L1 and yeast GAB1 (CDC91) a proteinGPI transamidase subunit involved in attachment of glycosylphosphatidylinositol (GPI) anchors to proteins | DDB0232430 | CDS | 5241503 | 1683 | + | 0.259655 |
DDB_G0282013 | DDB_G0282013 | DDB0232430 | CDS | 5243942 | 300 | + | 0.236667 | |
DDB_G0282015 | DDB_G0282015 | DDB0232430 | CDS | 5245292 | 171 | + | 0.28655 | |
DDB_G0282017 | DDB_G0282017 | involved in vesicle-mediated transport similar to VPS33 | DDB0232430 | CDS | 5245886 | 1944 | + | 0.237654 |
DDB_G0282019 | DDB_G0282019 | DDB0232430 | CDS | 5248124 | 1209 | - | 0.169562 | |
DDB_G0282021 | DDB_G0282021 | DDB0232430 | CDS | 5249750 | 636 | - | 0.300314 | |
DDB_G0282025 | DDB_G0282025 | DDB0232430 | CDS | 5253354 | 2052 | - | 0.251462 | |
DDB_G0282033 | DDB_G0282033 | very similar to major vault proteins however much smaller including D. discoideum mvpA and mvpB which are double the length | DDB0232430 | CDS | 5295248 | 1263 | + | 0.327791 |
DDB_G0282037 | DDB_G0282037 | DDB0232430 | CDS | 5318807 | 189 | + | 0.328042 | |
DDB_G0282039 | DDB_G0282039 | DDB0232430 | CDS | 5319634 | 192 | + | 0.3125 | |
DDB_G0282041 | DDB_G0282041 | DDB0232430 | CDS | 5320048 | 945 | - | 0.271958 | |
DDB_G0282051_RTE | DDB_G0282051 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5335654 | 1056 | + | 0.311553 |
DDB_G0282055 | DDB_G0282055 | DDB0232430 | CDS | 5339807 | 1395 | - | 0.232258 | |
DDB_G0282057 | DDB_G0282057 | DDB0232430 | CDS | 5342487 | 5250 | + | 0.225905 | |
DDB_G0282059 | DDB_G0282059 | DDB0232430 | CDS | 5353948 | 3462 | - | 0.219237 | |
DDB_G0282061 | DDB_G0282061 | DDB0232430 | CDS | 5358457 | 906 | - | 0.336645 | |
DDB_G0282063 | DDB_G0282063 | DDB0232430 | CDS | 5360341 | 1386 | - | 0.209235 | |
DDB_G0282065 | DDB_G0282065 | DDB0232430 | CDS | 5362723 | 330 | + | 0.230303 | |
DDB_G0282067 | DDB_G0282067 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232430 | CDS | 5363274 | 1722 | - | 0.349013 |
DDB_G0282071 | DDB_G0282071 | DDB0232430 | CDS | 5185590 | 360 | - | 0.15 | |
DDB_G0282077 | DDB_G0282077 | DDB0232430 | CDS | 5256784 | 570 | + | 0.426316 | |
DDB_G0282083_TE | DDB_G0282083 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232430 | CDS | 5278421 | 1719 | + | 0.315881 |
DDB_G0282085_TE | DDB_G0282085 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232430 | CDS | 5280749 | 231 | + | 0.277056 |
DDB_G0282087 | DDB_G0282087 | DDB0232430 | CDS | 5297220 | 1140 | + | 0.257895 | |
DDB_G0282089_ps | DDB_G0282089 | DDB0232430 | CDS | 5303301 | 4950 | + | 0.256566 | |
DDB_G0282093 | DDB_G0282093 | DDB0232430 | CDS | 5314939 | 2610 | - | 0.191188 | |
DDB_G0282095 | DDB_G0282095 | DDB0232430 | CDS | 5351024 | 2694 | + | 0.291017 | |
DDB_G0282101 | DDB_G0282101 | DDB0232430 | CDS | 5369694 | 3006 | + | 0.276114 | |
DDB_G0282105 | DDB_G0282105 | protein phosphatase 2C is a serinethreonine specific protein phosphatase with broad substrate specificity and dependent on divalent cations (mainly manganese and magnesium) for its activity | DDB0232430 | CDS | 5377643 | 2877 | + | 0.269378 |
DDB_G0282107 | DDB_G0282107 | similar to Aspergillus oryzae phosphatidylglycerolphosphatidylinositol transfer protein expressed in pstO cells during culmination | DDB0232430 | CDS | 5384175 | 444 | - | 0.290541 |
DDB_G0282109 | DDB_G0282109 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232430 | CDS | 5385033 | 429 | - | 0.305361 |
DDB_G0282111 | DDB_G0282111 | DDB0232430 | CDS | 5385904 | 3036 | - | 0.200922 | |
DDB_G0282113 | DDB_G0282113 | DDB0232430 | CDS | 5398887 | 639 | + | 0.255086 | |
DDB_G0282115 | DDB_G0282115 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232430 | CDS | 5399711 | 4923 | - | 0.275848 |
DDB_G0282117 | DDB_G0282117 | DDB0232430 | CDS | 5408423 | 726 | - | 0.316804 | |
DDB_G0282121 | DDB_G0282121 | underexpressed in | DDB0232430 | CDS | 5419274 | 1458 | + | 0.342936 |
DDB_G0282123 | DDB_G0282123 | DDB0232430 | CDS | 5421032 | 1470 | - | 0.255782 | |
DDB_G0282125 | DDB_G0282125 | DDB0232430 | CDS | 5425596 | 2652 | + | 0.27187 | |
DDB_G0282127 | DDB_G0282127 | DDB0232430 | CDS | 5429045 | 1038 | + | 0.220617 | |
DDB_G0282129 | DDB_G0282129 | DDB0232430 | CDS | 5430867 | 2298 | + | 0.232811 | |
DDB_G0282131 | DDB_G0282131 | contains a predicted signal sequence and a putative C-terminal transmembrane domain similar to D. purpureum protein | DDB0232430 | CDS | 5381150 | 2568 | + | 0.253115 |
DDB_G0282133 | DDB_G0282133 | DDB0232430 | CDS | 5389429 | 8610 | - | 0.221022 | |
DDB_G0282135 | DDB_G0282135 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232430 | CDS | 5405787 | 1551 | + | 0.283688 |
DDB_G0282137 | DDB_G0282137 | DDB0232430 | CDS | 5423413 | 1623 | + | 0.273567 | |
DDB_G0282139 | DDB_G0282139 | DDB0232430 | CDS | 5434030 | 1977 | + | 0.232676 | |
DDB_G0282149 | DDB_G0282149 | DDB0232430 | CDS | 5446691 | 6798 | + | 0.246102 | |
DDB_G0282151 | DDB_G0282151 | DDB0232430 | CDS | 5456198 | 2358 | + | 0.296862 | |
DDB_G0282155 | DDB_G0282155 | DDB0232430 | CDS | 5462477 | 1065 | - | 0.201878 | |
DDB_G0282157 | DDB_G0282157 | DDB0232430 | CDS | 5467686 | 1668 | + | 0.209832 | |
DDB_G0282159 | DDB_G0282159 | DDB0232430 | CDS | 5469433 | 1635 | - | 0.327217 | |
DDB_G0282161 | DDB_G0282161 | similar to small ubiquitin-related modifier (SUMO) however the encoded protein is much larger | DDB0232430 | CDS | 5471894 | 1317 | + | 0.261959 |
DDB_G0282165 | DDB_G0282165 | DDB0232430 | CDS | 5477142 | 771 | + | 0.206226 | |
DDB_G0282167 | DDB_G0282167 | DDB0232430 | CDS | 5478048 | 1323 | - | 0.259259 | |
DDB_G0282169 | DDB_G0282169 | DDB0232430 | CDS | 5479724 | 1140 | - | 0.20614 | |
DDB_G0282171 | DDB_G0282171 | DDB0232430 | CDS | 5485189 | 684 | - | 0.387427 | |
DDB_G0282177 | DDB_G0282177 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232430 | CDS | 5490516 | 450 | + | 0.344444 |
DDB_G0282179 | DDB_G0282179 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232430 | CDS | 5491825 | 438 | + | 0.257991 |
DDB_G0282185 | DDB_G0282185 | DDB0232430 | CDS | 5463972 | 2373 | - | 0.269701 | |
DDB_G0282187 | DDB_G0282187 | DDB0232430 | CDS | 5492546 | 2947 | - | 0.304717 | |
DDB_G0282193 | DDB_G0282193 | DDB0232430 | CDS | 5505181 | 435 | + | 0.305747 | |
DDB_G0282197 | DDB_G0282197 | DDB0232430 | CDS | 5507533 | 1443 | + | 0.277893 | |
DDB_G0282201 | DDB_G0282201 | DDB0232430 | CDS | 5515941 | 2025 | - | 0.200494 | |
DDB_G0282207_ps | DDB_G0282207 | putative pseudogene similar to D. discoideum genes | DDB0232430 | CDS | 5520305 | 1137 | - | 0.239226 |
DDB_G0282209 | DDB_G0282209 | weakly related to Sec23Sec24 involved in COPII-coated vesicles intracellular transport | DDB0232430 | CDS | 5522317 | 2097 | - | 0.315689 |
DDB_G0282211 | DDB_G0282211 | DDB0232430 | CDS | 5525043 | 1467 | + | 0.299932 | |
DDB_G0282213 | DDB_G0282213 | DDB0232430 | CDS | 5526720 | 1464 | - | 0.239071 | |
DDB_G0282215 | DDB_G0282215 | DDB0232430 | CDS | 5528630 | 1605 | - | 0.261682 | |
DDB_G0282221 | DDB_G0282221 | DDB0232430 | CDS | 5532383 | 4161 | + | 0.208123 | |
DDB_G0282223 | DDB_G0282223 | DDB0232430 | CDS | 5536930 | 1863 | + | 0.227053 | |
DDB_G0282225 | DDB_G0282225 | DDB0232430 | CDS | 5540643 | 2124 | + | 0.197269 | |
DDB_G0282227 | DDB_G0282227 | DDB0232430 | CDS | 5543803 | 2367 | + | 0.189269 | |
DDB_G0282229 | DDB_G0282229 | DDB0232430 | CDS | 5549011 | 651 | - | 0.298003 | |
DDB_G0282233 | DDB_G0282233 | DDB0232430 | CDS | 5550968 | 1707 | + | 0.322203 | |
DDB_G0282237 | DDB_G0282237 | DDB0232430 | CDS | 5556336 | 2658 | - | 0.284801 | |
DDB_G0282239 | DDB_G0282239 | very similar to the uncharacterized H. sapiens C9orf41 | DDB0232430 | CDS | 5559700 | 1392 | - | 0.236351 |
DDB_G0282241 | DDB_G0282241 | DDB0232430 | CDS | 5561439 | 2478 | + | 0.24778 | |
DDB_G0282251 | DDB_G0282251 | DDB0232430 | CDS | 5576769 | 1464 | - | 0.229508 | |
DDB_G0282253 | DDB_G0282253 | DDB0232430 | CDS | 5579342 | 252 | + | 0.253968 | |
DDB_G0282255 | DDB_G0282255 | DDB0232430 | CDS | 5579876 | 1152 | - | 0.366319 | |
DDB_G0282257 | DDB_G0282257 | DDB0232430 | CDS | 5583350 | 600 | + | 0.22 | |
DDB_G0282259 | DDB_G0282259 | DDB0232430 | CDS | 5584485 | 753 | + | 0.179283 | |
DDB_G0282263 | DDB_G0282263 | DDB0232430 | CDS | 5586895 | 2625 | + | 0.271619 | |
DDB_G0282267 | DDB_G0282267 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | DDB0232430 | CDS | 5592466 | 402 | + | 0.310945 |
DDB_G0282269 | DDB_G0282269 | DDB0232430 | CDS | 5594139 | 810 | + | 0.332099 | |
DDB_G0282275 | DDB_G0282275 | DDB0232430 | CDS | 5598918 | 531 | + | 0.269303 | |
DDB_G0282279 | DDB_G0282279 | DDB0232430 | CDS | 5600791 | 621 | + | 0.178744 | |
DDB_G0282281 | DDB_G0282281 | DDB0232430 | CDS | 5601674 | 486 | - | 0.238683 | |
DDB_G0282285 | DDB_G0282285 | DDB0232430 | CDS | 5511594 | 1578 | - | 0.247148 | |
DDB_G0282287 | DDB_G0282287 | DDB0232430 | CDS | 5546265 | 1794 | - | 0.296544 | |
DDB_G0282299 | DDB_G0282299 | DDB0232430 | CDS | 5607244 | 2508 | - | 0.219298 | |
DDB_G0282301 | DDB_G0282301 | DDB0232430 | CDS | 5610071 | 243 | + | 0.320988 | |
DDB_G0282303 | DDB_G0282303 | DDB0232430 | CDS | 5610805 | 2364 | - | 0.249154 | |
DDB_G0282305 | DDB_G0282305 | DDB0232430 | CDS | 5613858 | 2547 | - | 0.258736 | |
DDB_G0282307 | DDB_G0282307 | DDB0232430 | CDS | 5618181 | 291 | - | 0.388316 | |
DDB_G0282311 | DDB_G0282311 | DDB0232430 | CDS | 5621318 | 1992 | + | 0.314759 | |
DDB_G0282313 | DDB_G0282313 | DDB0232430 | CDS | 5624970 | 1092 | - | 0.320513 | |
DDB_G0282315 | DDB_G0282315 | highly similar to neighboring genes | DDB0232430 | CDS | 5627326 | 264 | + | 0.314394 |
DDB_G0282317 | DDB_G0282317 | underexpressed in gskA-null strain highly similar to neighboring genes | DDB0232430 | CDS | 5628480 | 264 | + | 0.32197 |
DDB_G0282319 | DDB_G0282319 | highly similar to neighboring genes | DDB0232430 | CDS | 5629614 | 264 | + | 0.32197 |
DDB_G0282321 | DDB_G0282321 | highly similar to neighboring genes | DDB0232430 | CDS | 5630697 | 264 | + | 0.310606 |
DDB_G0282323 | DDB_G0282323 | highly similar to neighboring genes | DDB0232430 | CDS | 5631690 | 264 | + | 0.318182 |
DDB_G0282325 | DDB_G0282325 | highly similar to neighboring gene | DDB0232430 | CDS | 5645911 | 186 | + | 0.22043 |
DDB_G0282327 | DDB_G0282327 | highly similar to neighboring gene | DDB0232430 | CDS | 5647342 | 180 | + | 0.227778 |
DDB_G0282329 | DDB_G0282329 | DDB0232430 | CDS | 5648019 | 963 | - | 0.268951 | |
DDB_G0282331 | DDB_G0282331 | DDB0232430 | CDS | 5649510 | 345 | - | 0.228986 | |
DDB_G0282333 | DDB_G0282333 | DDB0232430 | CDS | 5651269 | 672 | - | 0.239583 | |
DDB_G0282335_RTE | DDB_G0282335 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232430 | CDS | 5652642 | 240 | - | 0.375 |
DDB_G0282337 | DDB_G0282337 | DDB0232430 | CDS | 5654662 | 1692 | + | 0.290189 | |
DDB_G0282341 | DDB_G0282341 | belongs to the crotonase superfamily contains a predicted peroxisomal targeting signal | DDB0232430 | CDS | 5658262 | 750 | - | 0.264 |
DDB_G0282343 | DDB_G0282343 | DDB0232430 | CDS | 5660192 | 549 | + | 0.249545 | |
DDB_G0282351 | DDB_G0282351 | DDB0232430 | CDS | 5602431 | 1009 | - | 0.210109 | |
DDB_G0282355_TE | DDB_G0282355 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232430 | CDS | 5672383 | 1971 | + | 0.303399 |
DDB_G0282383 | DDB_G0282383 | DDB0232430 | CDS | 5685837 | 165 | - | 0.169697 | |
DDB_G0282385 | DDB_G0282385 | DDB0232430 | CDS | 5686594 | 2973 | - | 0.13959 | |
DDB_G0282387 | DDB_G0282387 | has similarity to mammalian exonuclease 3'-5' domain-like-containing protein 1 (EXDL1) | DDB0232430 | CDS | 5690073 | 1173 | + | 0.226769 |
DDB_G0282389 | DDB_G0282389 | DDB0232430 | CDS | 5691748 | 411 | + | 0.22871 | |
DDB_G0282391 | DDB_G0282391 | DDB0232430 | CDS | 5692688 | 2262 | - | 0.202034 | |
DDB_G0282393 | DDB_G0282393 | DDB0232430 | CDS | 5695519 | 699 | + | 0.276109 | |
DDB_G0282399 | DDB_G0282399 | DDB0232430 | CDS | 5704423 | 171 | - | 0.298246 | |
DDB_G0282401 | DDB_G0282401 | DDB0232430 | CDS | 5705279 | 177 | + | 0.288136 | |
DDB_G0282403 | DDB_G0282403 | DDB0232430 | CDS | 5705899 | 198 | + | 0.181818 | |
DDB_G0282405_RTE | DDB_G0282405 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5708573 | 1119 | + | 0.340483 |
DDB_G0282407 | DDB_G0282407 | DDB0232430 | CDS | 5710802 | 2262 | - | 0.376658 | |
DDB_G0282409 | DDB_G0282409 | DDB0232430 | CDS | 5714264 | 3627 | + | 0.302178 | |
DDB_G0282411 | DDB_G0282411 | DDB0232430 | CDS | 5721347 | 2376 | + | 0.244108 | |
DDB_G0282413 | DDB_G0282413 | DDB0232430 | CDS | 5724206 | 558 | + | 0.225806 | |
DDB_G0282415 | DDB_G0282415 | DDB0232430 | CDS | 5735049 | 537 | + | 0.240223 | |
DDB_G0282417 | DDB_G0282417 | DDB0232430 | CDS | 5736810 | 1587 | + | 0.289855 | |
DDB_G0282421 | DDB_G0282421 | DDB0232430 | CDS | 5745445 | 4128 | + | 0.2328 | |
DDB_G0282425 | DDB_G0282425 | bCommunity annotation:b DDB_G0282425 may well be related the yeast transcriptional regulator ADA3 which is widely conserved in fungi and animals. The gene is the first and only BLAST hit in Dicty using the mouse Ciona and Nematostella sequences as bait. The homology with the yeast or Ustilago sequences is much lower but DDB_G0282425 is still the first hit. When blasted out against the NCBI data base DDB_G0282425 hits many putative ADA3 orthologs. Sequences recognizable as ADA3 do not appear to occur in plants. Harry MacWilliams May 2010br | DDB0232430 | CDS | 5752284 | 2844 | - | 0.246484 |
DDB_G0282427 | DDB_G0282427 | shared a short region of similarity with histone-lysine N-methyltransferase H3 lysine-4 specific MLL3 contains a single HMG12 box | DDB0232430 | CDS | 5755702 | 2388 | + | 0.309045 |
DDB_G0282429 | DDB_G0282429 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | DDB0232430 | CDS | 5758659 | 939 | - | 0.312034 |
DDB_G0282431 | DDB_G0282431 | DDB0232430 | CDS | 5763247 | 1317 | + | 0.235383 | |
DDB_G0282433 | DDB_G0282433 | DDB0232430 | CDS | 5764726 | 423 | - | 0.238771 | |
DDB_G0282435 | DDB_G0282435 | DDB0232430 | CDS | 5765614 | 309 | - | 0.294498 | |
DDB_G0282437_ps | DDB_G0282437 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 5767462 | 672 | - | 0.309524 |
DDB_G0282439 | DDB_G0282439 | DDB0232430 | CDS | 5768407 | 303 | - | 0.290429 | |
DDB_G0282441 | DDB_G0282441 | DDB0232430 | CDS | 5769357 | 306 | - | 0.326797 | |
DDB_G0282443 | DDB_G0282443 | DDB0232430 | CDS | 5770557 | 315 | - | 0.250794 | |
DDB_G0282445 | DDB_G0282445 | DDB0232430 | CDS | 5771651 | 303 | - | 0.224422 | |
DDB_G0282447 | DDB_G0282447 | DDB0232430 | CDS | 5772493 | 282 | - | 0.294326 | |
DDB_G0282449 | DDB_G0282449 | DDB0232430 | CDS | 5773378 | 708 | - | 0.217514 | |
DDB_G0282451 | DDB_G0282451 | DDB0232430 | CDS | 5774365 | 507 | + | 0.246548 | |
DDB_G0282455 | DDB_G0282455 | DDB0232430 | CDS | 5781008 | 201 | + | 0.313433 | |
DDB_G0282463 | DDB_G0282463 | DDB0232430 | CDS | 5792759 | 2337 | + | 0.286264 | |
DDB_G0282465 | DDB_G0282465 | DDB0232430 | CDS | 5800686 | 429 | + | 0.153846 | |
DDB_G0282467 | DDB_G0282467 | catalyzes the reaction S-adenosyl-L-methionine 1-aminocyclopropane-1-carboxylate methylthioadenosine | DDB0232430 | CDS | 5805820 | 1452 | + | 0.239669 |
DDB_G0282471 | DDB_G0282471 | DDB0232430 | CDS | 5811380 | 4041 | + | 0.303885 | |
DDB_G0282477 | DDB_G0282477 | DDB0232430 | CDS | 5822316 | 267 | + | 0.318352 | |
DDB_G0282479 | DDB_G0282479 | DDB0232430 | CDS | 5826574 | 963 | - | 0.223261 | |
DDB_G0282481 | DDB_G0282481 | DDB0232430 | CDS | 5828096 | 468 | - | 0.196581 | |
DDB_G0282483 | DDB_G0282483 | DDB0232430 | CDS | 5829856 | 1128 | + | 0.338652 | |
DDB_G0282487 | DDB_G0282487 | DDB0232430 | CDS | 5834821 | 936 | + | 0.185897 | |
DDB_G0282491 | DDB_G0282491 | DDB0232430 | CDS | 5839851 | 2652 | - | 0.253771 | |
DDB_G0282495 | DDB_G0282495 | DDB0232430 | CDS | 5848284 | 939 | - | 0.265176 | |
DDB_G0282497 | DDB_G0282497 | DDB0232430 | CDS | 5849588 | 648 | - | 0.217593 | |
DDB_G0282499 | DDB_G0282499 | bCommunity annotation:b Transcriptional modulators of the E2F family fall into two groups. Both groups have othologs in animals and plants and thus appear to be ancient. The better known group represented by animal E2F1-3 and E2Fs a b and c of Arabidopsis consists of proteins which form heterodimers with the | DDB0232430 | CDS | 5850862 | 2808 | - | 0.188746 |
DDB_G0282501 | DDB_G0282501 | DDB0232430 | CDS | 5855098 | 3141 | + | 0.18943 | |
DDB_G0282507_RTE | DDB_G0282507 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5866236 | 1335 | - | 0.308614 |
DDB_G0282509_RTE | DDB_G0282509 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5869400 | 504 | - | 0.345238 |
DDB_G0282511 | DDB_G0282511 | DDB0232430 | CDS | 5870598 | 1005 | + | 0.19801 | |
DDB_G0282513 | DDB_G0282513 | DDB0232430 | CDS | 5872000 | 1812 | - | 0.174393 | |
DDB_G0282515 | DDB_G0282515 | DDB0232430 | CDS | 5873962 | 2295 | - | 0.203922 | |
DDB_G0282517 | DDB_G0282517 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232430 | CDS | 5877016 | 726 | - | 0.316804 |
DDB_G0282519 | DDB_G0282519 | DDB0232430 | CDS | 5880253 | 243 | + | 0.27572 | |
DDB_G0282521 | DDB_G0282521 | DDB0232430 | CDS | 5880742 | 717 | - | 0.245467 | |
DDB_G0282523 | DDB_G0282523 | DDB0232430 | CDS | 5885598 | 183 | + | 0.202186 | |
DDB_G0282525 | DDB_G0282525 | DDB0232430 | CDS | 5886297 | 1251 | + | 0.243006 | |
DDB_G0282531 | DDB_G0282531 | ortholog of human Tat DNase 1 (TATDN1) belongs to a large superfamily of metalloenzymes | DDB0232430 | CDS | 5890637 | 975 | - | 0.259487 |
DDB_G0282533 | DDB_G0282533 | DDB0232430 | CDS | 5893579 | 504 | + | 0.123016 | |
DDB_G0282535 | DDB_G0282535 | DDB0232430 | CDS | 5894376 | 1728 | - | 0.212384 | |
DDB_G0282541_RTE | DDB_G0282541 | Part of ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-C refer to GenBank AF298210 for partially assembled consensus element | DDB0232430 | CDS | 5902227 | 480 | - | 0.352083 |
DDB_G0282543_RTE | DDB_G0282543 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5905421 | 1125 | - | 0.343111 |
DDB_G0282549 | DDB_G0282549 | DDB0232430 | CDS | 5917328 | 924 | - | 0.212121 | |
DDB_G0282551 | DDB_G0282551 | weakly related to hssA2C7E family protein | DDB0232430 | CDS | 5918974 | 207 | - | 0.2657 |
DDB_G0282553_ps | DDB_G0282553 | putative pseudogene belongs to a family of small Dictyostelium-specific proteins | DDB0232430 | CDS | 5920217 | 126 | - | 0.293651 |
DDB_G0282555 | DDB_G0282555 | DDB0232430 | CDS | 5930270 | 1659 | - | 0.230862 | |
DDB_G0282557 | DDB_G0282557 | DDB0232430 | CDS | 5932394 | 1710 | - | 0.238596 | |
DDB_G0282561_RTE | DDB_G0282561 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5938105 | 243 | + | 0.226337 |
DDB_G0282563 | DDB_G0282563 | DDB0232430 | CDS | 5941283 | 1854 | - | 0.281553 | |
DDB_G0282565 | DDB_G0282565 | DDB0232430 | CDS | 5943856 | 1629 | + | 0.207489 | |
DDB_G0282567 | DDB_G0282567 | DDB0232430 | CDS | 5945975 | 828 | + | 0.210145 | |
DDB_G0282571 | DDB_G0282571 | DDB0232430 | CDS | 5952908 | 345 | + | 0.171014 | |
DDB_G0282573 | DDB_G0282573 | DDB0232430 | CDS | 5953713 | 1227 | + | 0.294214 | |
DDB_G0282575 | DDB_G0282575 | DDB0232430 | CDS | 5957238 | 3585 | + | 0.278661 | |
DDB_G0282577 | DDB_G0282577 | DDB0232430 | CDS | 5960962 | 3588 | - | 0.223523 | |
DDB_G0282583 | DDB_G0282583 | contains one RGS domain similar to human RGS1 (regulator of G-protein signalling) which inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits | DDB0232430 | CDS | 5972121 | 459 | - | 0.272331 |
DDB_G0282585 | DDB_G0282585 | DDB0232430 | CDS | 5975167 | 201 | - | 0.268657 | |
DDB_G0282587 | DDB_G0282587 | DDB0232430 | CDS | 5977758 | 525 | + | 0.241905 | |
DDB_G0282589 | DDB_G0282589 | DDB0232430 | CDS | 5978839 | 675 | - | 0.247407 | |
DDB_G0282593 | DDB_G0282593 | ortholog of human FAM50A a XAP5 protein found in the nucleus with potential DNA binding activity | DDB0232430 | CDS | 5983138 | 1089 | - | 0.275482 |
DDB_G0282597 | DDB_G0282597 | DDB0232430 | CDS | 5985770 | 3171 | + | 0.207821 | |
DDB_G0282599 | DDB_G0282599 | DDB0232430 | CDS | 5989441 | 1137 | - | 0.30431 | |
DDB_G0282603 | DDB_G0282603 | DDB0232430 | CDS | 5993046 | 600 | + | 0.261667 | |
DDB_G0282605 | DDB_G0282605 | DDB0232430 | CDS | 5993980 | 1659 | - | 0.265823 | |
DDB_G0282609 | DDB_G0282609 | DDB0232430 | CDS | 5999479 | 288 | - | 0.225694 | |
DDB_G0282611 | DDB_G0282611 | catalyzes the reactoin CTP (R)-4'-phosphopantothenate L-cysteine CMP diphosphate N-[(R)-4'-phosphopantothenoyl]-L-cysteine | DDB0232430 | CDS | 6001079 | 1170 | + | 0.260684 |
DDB_G0282613 | DDB_G0282613 | DDB0232430 | CDS | 6002359 | 591 | - | 0.189509 | |
DDB_G0282619 | DDB_G0282619 | DDB0232430 | CDS | 6007141 | 708 | + | 0.230226 | |
DDB_G0282621 | DDB_G0282621 | DDB0232430 | CDS | 6009133 | 321 | + | 0.277259 | |
DDB_G0282629 | DDB_G0282629 | DDB0232430 | CDS | 6026305 | 2700 | + | 0.228889 | |
DDB_G0282631 | DDB_G0282631 | DDB0232430 | CDS | 6029325 | 672 | - | 0.285714 | |
DDB_G0282633 | DDB_G0282633 | DDB0232430 | CDS | 6031309 | 2760 | + | 0.285507 | |
DDB_G0282635 | DDB_G0282635 | DDB0232430 | CDS | 6034361 | 492 | - | 0.252033 | |
DDB_G0282637 | DDB_G0282637 | DDB0232430 | CDS | 6035957 | 330 | + | 0.233333 | |
DDB_G0282639 | DDB_G0282639 | DDB0232430 | CDS | 6037460 | 7095 | + | 0.222833 | |
DDB_G0282641 | DDB_G0282641 | DDB0232430 | CDS | 6047385 | 3945 | + | 0.237009 | |
DDB_G0282643 | DDB_G0282643 | conserved hypothetical protein contains a putative signal peptide | DDB0232430 | CDS | 6051875 | 1137 | + | 0.294635 |
DDB_G0282645 | DDB_G0282645 | DDB0232430 | CDS | 6053393 | 516 | - | 0.20155 | |
DDB_G0282647 | DDB_G0282647 | DDB0232430 | CDS | 6054472 | 774 | + | 0.231266 | |
DDB_G0282649_ps | DDB_G0282649 | putative pseudogene Rab family protein | DDB0232430 | CDS | 6057374 | 894 | + | 0.193512 |
DDB_G0282653 | DDB_G0282653 | DDB0232430 | CDS | 6060135 | 633 | + | 0.233807 | |
DDB_G0282655 | DDB_G0282655 | DDB0232430 | CDS | 6063029 | 513 | - | 0.226121 | |
DDB_G0282657 | DDB_G0282657 | DDB0232430 | CDS | 6065769 | 525 | - | 0.289524 | |
DDB_G0282659_RTE | DDB_G0282659 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232430 | CDS | 6079285 | 642 | + | 0.274143 |
DDB_G0282661 | DDB_G0282661 | DDB0232430 | CDS | 6092418 | 804 | + | 0.208955 | |
DDB_G0282665_ps | DDB_G0282665 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 6093593 | 282 | + | 0.219858 |
DDB_G0282667 | DDB_G0282667 | DDB0232430 | CDS | 6096363 | 1581 | + | 0.267552 | |
DDB_G0282671_ps | DDB_G0282671 | putative pseudogene weakly similar to AGC protein kinases does not contain the consensus sequences required for kinase function | DDB0232430 | CDS | 6098622 | 765 | + | 0.257516 |
DDB_G0282673 | DDB_G0282673 | DDB0232430 | CDS | 6100946 | 1533 | + | 0.300065 | |
DDB_G0282675_ps | DDB_G0282675 | putative pseudogene very similar to Dictyostelium DDB_G0282777 a putative serinethreonine kinase | DDB0232430 | CDS | 6103495 | 2391 | - | 0.262652 |
DDB_G0282679 | DDB_G0282679 | DDB0232430 | CDS | 6110131 | 4380 | + | 0.237671 | |
DDB_G0282681_ps | DDB_G0282681 | putative pseudogene fragment similar to | DDB0232430 | CDS | 6115450 | 597 | + | 0.194305 |
DDB_G0282683 | DDB_G0282683 | DDB0232430 | CDS | 6123377 | 453 | + | 0.280353 | |
DDB_G0282685 | DDB_G0282685 | DDB0232430 | CDS | 6125852 | 1233 | - | 0.313058 | |
DDB_G0282689 | DDB_G0282689 | DDB0232430 | CDS | 6128420 | 2397 | - | 0.225699 | |
DDB_G0282695 | DDB_G0282695 | DDB0232430 | CDS | 6139156 | 1959 | + | 0.295559 | |
DDB_G0282699 | DDB_G0282699 | DDB0232430 | CDS | 6151208 | 1044 | - | 0.282567 | |
DDB_G0282701 | DDB_G0282701 | DDB0232430 | CDS | 6152994 | 1047 | - | 0.283668 | |
DDB_G0282703_TE | DDB_G0282703 | DDB0232430 | CDS | 6156398 | 537 | - | 0.327747 | |
DDB_G0282705 | DDB_G0282705 | DDB0232430 | CDS | 6158594 | 135 | - | 0.251852 | |
DDB_G0282707 | DDB_G0282707 | DDB0232430 | CDS | 6160620 | 3354 | - | 0.257603 | |
DDB_G0282711 | DDB_G0282711 | contains a plant homeodomain (PHD) finger a C4HC3 zinc-finger-like motif found in nuclear proteins thought to be involved in chromatin-mediated transcriptional regulation | DDB0232430 | CDS | 6179495 | 4086 | - | 0.263338 |
DDB_G0282713 | DDB_G0282713 | DDB0232430 | CDS | 6189456 | 1491 | + | 0.25285 | |
DDB_G0282715 | DDB_G0282715 | DDB0232430 | CDS | 6191274 | 2313 | - | 0.316904 | |
DDB_G0282719 | DDB_G0282719 | DDB0232430 | CDS | 6199706 | 1257 | + | 0.280032 | |
DDB_G0282721 | DDB_G0282721 | DDB0232430 | CDS | 6201456 | 1461 | + | 0.218344 | |
DDB_G0282729 | DDB_G0282729 | DDB0232430 | CDS | 6215725 | 3903 | + | 0.259288 | |
DDB_G0282737 | DDB_G0282737 | member of a Dictyostelium protein family that includes | DDB0232430 | CDS | 6225357 | 855 | + | 0.334503 |
DDB_G0282745 | DDB_G0282745 | DDB0232430 | CDS | 6234797 | 2394 | - | 0.225146 | |
DDB_G0282747 | DDB_G0282747 | similar to H. sapiens MAD2L2 a second protein in higher eukaryotes similar to S. cerevisiae MAD2 | DDB0232430 | CDS | 6239552 | 999 | + | 0.208208 |
DDB_G0282751_TE | DDB_G0282751 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232430 | CDS | 5676395 | 333 | + | 0.276276 |
DDB_G0282753_RTE | DDB_G0282753 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232430 | CDS | 5677651 | 3099 | - | 0.287512 |
DDB_G0282755_RTE | DDB_G0282755 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232430 | CDS | 5707254 | 1020 | + | 0.389216 |
DDB_G0282757 | DDB_G0282757 | DDB0232430 | CDS | 5762312 | 165 | + | 0.387879 | |
DDB_G0282759 | DDB_G0282759 | DDB0232430 | CDS | 5775152 | 1764 | - | 0.361111 | |
DDB_G0282761 | DDB_G0282761 | DDB0232430 | CDS | 5801585 | 2739 | - | 0.177437 | |
DDB_G0282765 | DDB_G0282765 | DDB0232430 | CDS | 5832783 | 915 | + | 0.254645 | |
DDB_G0282767 | DDB_G0282767 | DDB0232430 | CDS | 5858325 | 1062 | - | 0.328625 | |
DDB_G0282771_ps | DDB_G0282771 | putative pseudogene fragment similar to | DDB0232430 | CDS | 5861766 | 201 | - | 0.293532 |
DDB_G0282773 | DDB_G0282773 | DDB0232430 | CDS | 5884670 | 132 | + | 0.295455 | |
DDB_G0282777 | DDB_G0282777 | kinase domain similar to yeast cdc5 a serinethreonine kinase with multiple functions in mitosis and cytokinesis | DDB0232430 | CDS | 5908362 | 1920 | + | 0.266146 |
DDB_G0282779_ps | DDB_G0282779 | putative pseudogene similar to D. discoideum genes | DDB0232430 | CDS | 5911017 | 2427 | - | 0.261228 |
DDB_G0282781_ps | DDB_G0282781 | putative pseudogene similar to a family of genes including | DDB0232430 | CDS | 5913844 | 2568 | - | 0.167835 |
DDB_G0282783 | DDB_G0282783 | similar to a D. purpureum protein | DDB0232430 | CDS | 5921147 | 9054 | + | 0.230175 |
DDB_G0282785_RTE | DDB_G0282785 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 5936624 | 255 | + | 0.337255 |
DDB_G0282787_RTE | DDB_G0282787 | DDB0232430 | CDS | 5938746 | 1500 | - | 0.351333 | |
DDB_G0282791_ps | DDB_G0282791 | putative pseudogene small fragment similar to | DDB0232430 | CDS | 6046495 | 366 | + | 0.237705 |
DDB_G0282795 | DDB_G0282795 | DDB0232430 | CDS | 6067799 | 3396 | + | 0.250589 | |
DDB_G0282797_RTE | DDB_G0282797 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 6073164 | 3144 | - | 0.338422 |
DDB_G0282799_RTE | DDB_G0282799 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232430 | CDS | 6076598 | 1335 | - | 0.309363 |
DDB_G0282801 | DDB_G0282801 | DDB0232430 | CDS | 6081891 | 9243 | - | 0.236287 | |
DDB_G0282807_ps | DDB_G0282807 | putative pseudogene fragment similar to D. discoideum gene | DDB0232430 | CDS | 6147705 | 2562 | - | 0.240437 |
DDB_G0282809_ps | DDB_G0282809 | putative pseudogene similar to EGF repeat-containg proteins such as | DDB0232430 | CDS | 6165937 | 2988 | - | 0.248661 |
DDB_G0282815 | DDB_G0282815 | DDB0232430 | CDS | 6258530 | 855 | - | 0.330994 | |
DDB_G0282821 | DDB_G0282821 | DDB0232430 | CDS | 6255151 | 201 | - | 0.283582 | |
DDB_G0282823 | DDB_G0282823 | DDB0232430 | CDS | 6262357 | 2712 | - | 0.272493 | |
DDB_G0282827 | DDB_G0282827 | DDB0232430 | CDS | 6268123 | 1494 | - | 0.28581 | |
DDB_G0282833 | DDB_G0282833 | DDB0232430 | CDS | 6273796 | 957 | - | 0.347962 | |
DDB_G0282839 | DDB_G0282839 | DDB0232430 | CDS | 6282388 | 1104 | + | 0.238225 | |
DDB_G0282841 | DDB_G0282841 | DDB0232430 | CDS | 6284231 | 1569 | - | 0.307839 | |
DDB_G0282843 | DDB_G0282843 | DDB0232430 | CDS | 6287418 | 1170 | + | 0.223077 | |
DDB_G0282845 | DDB_G0282845 | DDB0232430 | CDS | 6289243 | 1224 | - | 0.258987 | |
DDB_G0282849 | DDB_G0282849 | DDB0232430 | CDS | 6293427 | 3189 | - | 0.29006 | |
DDB_G0282851 | DDB_G0282851 | DDB0232430 | CDS | 6297857 | 4146 | + | 0.263869 | |
DDB_G0282853 | DDB_G0282853 | similar to mammalian translationally controlled tumour protein (TCTP) and to S. cerevisiae TMA19 a protein associated with ribosomes | DDB0232430 | CDS | 6303739 | 525 | + | 0.369524 |
DDB_G0282855 | DDB_G0282855 | DDB0232430 | CDS | 6304937 | 1299 | + | 0.237875 | |
DDB_G0282857 | DDB_G0282857 | DDB0232430 | CDS | 6314029 | 1473 | - | 0.295995 | |
DDB_G0282859 | DDB_G0282859 | DDB0232430 | CDS | 6316518 | 1890 | + | 0.232804 | |
DDB_G0282861 | DDB_G0282861 | similar to mammalian translationally controlled tumour protein (TCTP) and to S. cerevisiae TMA19 a protein associated with ribosomes | DDB0232430 | CDS | 6318668 | 585 | - | 0.254701 |
DDB_G0282865 | DDB_G0282865 | DDB0232430 | CDS | 6320360 | 690 | - | 0.202899 | |
DDB_G0282867 | DDB_G0282867 | DDB0232430 | CDS | 6322173 | 1083 | - | 0.257618 | |
DDB_G0282873 | DDB_G0282873 | DDB0232430 | CDS | 6325570 | 2859 | - | 0.359566 | |
DDB_G0282875 | DDB_G0282875 | DDB0232430 | CDS | 6329217 | 729 | + | 0.242798 | |
DDB_G0282877 | DDB_G0282877 | DDB0232430 | CDS | 6330480 | 840 | + | 0.344048 | |
DDB_G0282879 | DDB_G0282879 | DDB0232430 | CDS | 6331837 | 861 | - | 0.24158 | |
DDB_G0282881 | DDB_G0282881 | DDB0232430 | CDS | 6333061 | 1296 | + | 0.354167 | |
DDB_G0282883 | DDB_G0282883 | DDB0232430 | CDS | 6337930 | 777 | + | 0.314028 | |
DDB_G0282885 | DDB_G0282885 | DDB0232430 | CDS | 6339466 | 1203 | + | 0.23192 | |
DDB_G0282893 | DDB_G0282893 | contains two predicted transmembrane domains the first may be a signal peptide almost identical to the downstream gene | DDB0232430 | CDS | 6349872 | 1188 | + | 0.267677 |
DDB_G0282895 | DDB_G0282895 | member of the TKL (tyrosine kinase-like) group contains three N-terminal MORN (Membrane Occupation and Recognition Nexus) repeats | DDB0232430 | CDS | 6249781 | 4905 | + | 0.262385 |
DDB_G0282901 | DDB_G0282901 | DDB0232430 | CDS | 6334464 | 711 | - | 0.216596 | |
DDB_G0282903 | DDB_G0282903 | similar to a D. purpureum gene contains 7 transmembrane domains | DDB0232430 | CDS | 6342424 | 2058 | + | 0.216715 |
DDB_G0282905 | DDB_G0282905 | contains one predicted transmembrane domain almost identical to the upstream gene | DDB0232430 | CDS | 6351923 | 1071 | + | 0.283847 |
DDB_G0282907_TE | DDB_G0282907 | DDB0232430 | CDS | 6356405 | 537 | + | 0.325885 | |
DDB_G0282917 | DDB_G0282917 | DDB0232431 | CDS | 3257 | 375 | - | 0.333333 | |
DDB_G0282919_TE | DDB_G0282919 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232431 | CDS | 101 | 821 | + | 0.303289 |
DDB_G0282935 | DDB_G0282935 | contains two putative transmembrane domains partial high similarity to D. purpureum protein | DDB0232431 | CDS | 17607 | 930 | - | 0.256989 |
DDB_G0282937 | DDB_G0282937 | DDB0232431 | CDS | 19492 | 312 | - | 0.294872 | |
DDB_G0282939 | DDB_G0282939 | DDB0232431 | CDS | 22195 | 1404 | - | 0.23433 | |
DDB_G0282941 | DDB_G0282941 | DDB0232431 | CDS | 24418 | 1827 | + | 0.307061 | |
DDB_G0282943 | DDB_G0282943 | DDB0232431 | CDS | 28010 | 3210 | + | 0.280685 | |
DDB_G0282945 | DDB_G0282945 | DDB0232431 | CDS | 31559 | 2010 | - | 0.280597 | |
DDB_G0282947 | DDB_G0282947 | DDB0232431 | CDS | 38803 | 3042 | - | 0.273504 | |
DDB_G0282951 | DDB_G0282951 | DDB0232431 | CDS | 45329 | 402 | + | 0.293532 | |
DDB_G0282953 | DDB_G0282953 | family member of conserved eukaryotic proteins of unknown function contains the conserved DUF1671 domain | DDB0232431 | CDS | 45934 | 1953 | - | 0.231439 |
DDB_G0282955 | DDB_G0282955 | DDB0232431 | CDS | 49492 | 903 | + | 0.221484 | |
DDB_G0282957 | DDB_G0282957 | DDB0232431 | CDS | 50957 | 207 | - | 0.251208 | |
DDB_G0282959 | DDB_G0282959 | DDB0232431 | CDS | 52235 | 4611 | + | 0.25591 | |
DDB_G0282961 | DDB_G0282961 | DDB0232431 | CDS | 57054 | 1716 | - | 0.277389 | |
DDB_G0282963 | DDB_G0282963 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats | DDB0232431 | CDS | 60445 | 5286 | + | 0.265796 |
DDB_G0282965 | DDB_G0282965 | DDB0232431 | CDS | 68065 | 972 | - | 0.246914 | |
DDB_G0282971 | DDB_G0282971 | DDB0232431 | CDS | 74287 | 2331 | + | 0.299013 | |
DDB_G0282973 | DDB_G0282973 | DDB0232431 | CDS | 78185 | 876 | + | 0.278539 | |
DDB_G0282975 | DDB_G0282975 | DDB0232431 | CDS | 80707 | 1101 | + | 0.305177 | |
DDB_G0282977 | DDB_G0282977 | DDB0232431 | CDS | 81934 | 3078 | - | 0.254061 | |
DDB_G0282983 | DDB_G0282983 | DDB0232431 | CDS | 99975 | 1746 | + | 0.231959 | |
DDB_G0282985 | DDB_G0282985 | DDB0232431 | CDS | 102023 | 2748 | - | 0.212518 | |
DDB_G0282991 | DDB_G0282991 | DDB0232431 | CDS | 109030 | 1020 | + | 0.227451 | |
DDB_G0282995 | DDB_G0282995 | DDB0232431 | CDS | 113431 | 1077 | + | 0.317549 | |
DDB_G0283003 | DDB_G0283003 | DDB0232431 | CDS | 141272 | 585 | + | 0.312821 | |
DDB_G0283007 | DDB_G0283007 | DDB0232431 | CDS | 147313 | 1230 | + | 0.305691 | |
DDB_G0283011 | DDB_G0283011 | DDB0232431 | CDS | 151994 | 360 | - | 0.286111 | |
DDB_G0283013 | DDB_G0283013 | DDB0232431 | CDS | 153182 | 6882 | + | 0.186574 | |
DDB_G0283015 | DDB_G0283015 | contains 2 putative transmembrane domains contains one putative coiled-coil domain | DDB0232431 | CDS | 161759 | 1599 | - | 0.220763 |
DDB_G0283017 | DDB_G0283017 | DDB0232431 | CDS | 164286 | 2676 | + | 0.246637 | |
DDB_G0283019 | DDB_G0283019 | contains two breast cancer type 2 repeats BRCA2 is a breast tumor suppressor with a potential function in the cellular response to DNA damage | DDB0232431 | CDS | 167136 | 408 | - | 0.264706 |
DDB_G0283025_ps | DDB_G0283025 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 171885 | 2268 | - | 0.27866 |
DDB_G0283031 | DDB_G0283031 | DDB0232431 | CDS | 177075 | 1167 | + | 0.151671 | |
DDB_G0283033 | DDB_G0283033 | DDB0232431 | CDS | 178285 | 2304 | - | 0.268229 | |
DDB_G0283039 | DDB_G0283039 | DDB0232431 | CDS | 196663 | 1341 | - | 0.222968 | |
DDB_G0283041 | DDB_G0283041 | DDB0232431 | CDS | 198610 | 633 | - | 0.276461 | |
DDB_G0283055 | DDB_G0283055 | very similar to the mammalian TBC1 domain family member 20 protein a potential multi-pass membrane protein | DDB0232431 | CDS | 20488 | 1203 | + | 0.261014 |
DDB_G0283057 | DDB_G0283057 | DDB0232431 | CDS | 34226 | 3150 | - | 0.281587 | |
DDB_G0283061 | DDB_G0283061 | DDB0232431 | CDS | 69391 | 1032 | - | 0.293605 | |
DDB_G0283063 | DDB_G0283063 | DDB0232431 | CDS | 115315 | 810 | - | 0.302469 | |
DDB_G0283065 | DDB_G0283065 | putative eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase putative protein serinethreonine kinase related to the GCN2 (general control non-derepressible) family of protein kinases that phosphorylate the alpha subunit of eIF2 | DDB0232431 | CDS | 122741 | 1914 | - | 0.242424 |
DDB_G0283067 | DDB_G0283067 | DDB0232431 | CDS | 138075 | 1203 | + | 0.287614 | |
DDB_G0283069 | DDB_G0283069 | DDB0232431 | CDS | 175065 | 237 | + | 0.350211 | |
DDB_G0283071 | DDB_G0283071 | DDB0232431 | CDS | 181322 | 618 | + | 0.194175 | |
DDB_G0283075 | DDB_G0283075 | ortholog of mammalian MORF4 and S. cerevisiae EAF3 a nonessential component of the NuA4 acetyltransferase complex | DDB0232431 | CDS | 188331 | 1140 | - | 0.25 |
DDB_G0283077 | DDB_G0283077 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 194597 | 1806 | + | 0.268549 |
DDB_G0283079_RTE | DDB_G0283079 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232431 | CDS | 199920 | 2053 | - | 0.293717 |
DDB_G0283087 | DDB_G0283087 | similar to butyrylcholinesterase and acetylcholinesterase precursor proteins contains a putative signal peptide | DDB0232431 | CDS | 203029 | 1638 | + | 0.286935 |
DDB_G0283089 | DDB_G0283089 | DDB0232431 | CDS | 205098 | 1434 | - | 0.24477 | |
DDB_G0283091 | DDB_G0283091 | DDB0232431 | CDS | 206705 | 1389 | - | 0.275018 | |
DDB_G0283093 | DDB_G0283093 | DDB0232431 | CDS | 208398 | 1344 | - | 0.274554 | |
DDB_G0283097 | DDB_G0283097 | DDB0232431 | CDS | 214573 | 1221 | + | 0.266994 | |
DDB_G0283099 | DDB_G0283099 | ortholog of the metazoan nipped-B protein which contains the armadillo-like (ARM-like) helical domain and two HEAT repeats the Drosophila protein plays a structural role in chromatin and is involved in sister chromatid cohesion | DDB0232431 | CDS | 217095 | 6192 | + | 0.258398 |
DDB_G0283101 | DDB_G0283101 | DDB0232431 | CDS | 235690 | 660 | + | 0.256061 | |
DDB_G0283103 | DDB_G0283103 | DDB0232431 | CDS | 237163 | 1443 | - | 0.261261 | |
DDB_G0283107 | DDB_G0283107 | DDB0232431 | CDS | 255521 | 1086 | - | 0.291897 | |
DDB_G0283117 | DDB_G0283117 | DDB0232431 | CDS | 267048 | 1032 | - | 0.243217 | |
DDB_G0283121 | DDB_G0283121 | bifunctional enzyme that catalyzes the reactions methylene-tetrahydrofolate NADP NADPH methenyl-Hsub4subF and NADPH methenyl-Hsub4subF methylene-tetrahydrofolate NADP | DDB0232431 | CDS | 275079 | 879 | + | 0.285552 |
DDB_G0283127 | DDB_G0283127 | DDB0232431 | CDS | 283814 | 1287 | - | 0.334887 | |
DDB_G0283129 | DDB_G0283129 | DDB0232431 | CDS | 286809 | 2652 | + | 0.274887 | |
DDB_G0283133_TE | DDB_G0283133 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232431 | CDS | 232444 | 2004 | - | 0.317864 |
DDB_G0283135 | DDB_G0283135 | DDB0232431 | CDS | 223712 | 246 | - | 0.349593 | |
DDB_G0283139 | DDB_G0283139 | mannose-6-phosphate receptors are involved in the transport of lysosomal enzymes from the Golgi complex and the cell surface to lysosomes contains a N-terminal predicted signal sequence and a C-terminal transmembrane domain | DDB0232431 | CDS | 228583 | 2916 | - | 0.250343 |
DDB_G0283143 | DDB_G0283143 | DDB0232431 | CDS | 243331 | 2940 | - | 0.270068 | |
DDB_G0283145 | DDB_G0283145 | DDB0232431 | CDS | 254487 | 771 | - | 0.32166 | |
DDB_G0283147 | DDB_G0283147 | DDB0232431 | CDS | 291263 | 3773 | - | 0.320435 | |
DDB_G0283155 | DDB_G0283155 | DDB0232431 | CDS | 297464 | 780 | + | 0.25641 | |
DDB_G0283159 | DDB_G0283159 | DDB0232431 | CDS | 301718 | 1971 | + | 0.221715 | |
DDB_G0283161 | DDB_G0283161 | DDB0232431 | CDS | 303938 | 405 | - | 0.192593 | |
DDB_G0283169 | DDB_G0283169 | DDB0232431 | CDS | 356370 | 603 | + | 0.258706 | |
DDB_G0283171 | DDB_G0283171 | DDB0232431 | CDS | 358763 | 330 | + | 0.206061 | |
DDB_G0283177 | DDB_G0283177 | DDB0232431 | CDS | 362729 | 1734 | + | 0.198962 | |
DDB_G0283179 | DDB_G0283179 | DDB0232431 | CDS | 366668 | 216 | - | 0.25463 | |
DDB_G0283185 | DDB_G0283185 | DDB0232431 | CDS | 376419 | 1344 | + | 0.145089 | |
DDB_G0283187 | DDB_G0283187 | catalyzes the reaction: A phosphoprotein Hsub2subO a protein phosphate conserved serinethreonine protein phosphatase family protein | DDB0232431 | CDS | 381819 | 939 | + | 0.308839 |
DDB_G0283189 | DDB_G0283189 | similar to DNA polymerase epsilon subunit A in yeast and vertebrates thought to be involved in DNA replication DNA repair and cell-cycle checkpoint control in eukaryotes | DDB0232431 | CDS | 385928 | 7143 | - | 0.297494 |
DDB_G0283191 | DDB_G0283191 | DDB0232431 | CDS | 394762 | 1695 | + | 0.277286 | |
DDB_G0283193 | DDB_G0283193 | DDB0232431 | CDS | 396519 | 1071 | - | 0.264239 | |
DDB_G0283195 | DDB_G0283195 | DDB0232431 | CDS | 400645 | 3024 | + | 0.236442 | |
DDB_G0283197 | DDB_G0283197 | DDB0232431 | CDS | 407180 | 1968 | + | 0.225102 | |
DDB_G0283199 | DDB_G0283199 | DDB0232431 | CDS | 409273 | 645 | - | 0.269767 | |
DDB_G0283201 | DDB_G0283201 | DDB0232431 | CDS | 413865 | 906 | + | 0.210817 | |
DDB_G0283209 | DDB_G0283209 | DDB0232431 | CDS | 364837 | 165 | - | 0.218182 | |
DDB_G0283211_ps | DDB_G0283211 | putative pseudogene belongs to the large D. discoideum zinc-containing alcohol dehydrogenase (ADH) family | DDB0232431 | CDS | 368141 | 768 | - | 0.272135 |
DDB_G0283213 | DDB_G0283213 | DDB0232431 | CDS | 309059 | 783 | - | 0.228608 | |
DDB_G0283215 | DDB_G0283215 | DDB0232431 | CDS | 311593 | 1518 | + | 0.254282 | |
DDB_G0283217_ps | DDB_G0283217 | putative pseudogene similar to a family of Dictyostelium putative mannose-6-phosphate receptors including | DDB0232431 | CDS | 313913 | 915 | + | 0.268852 |
DDB_G0283219_ps | DDB_G0283219 | putative pseudogene fusion fragment similar to parts of | DDB0232431 | CDS | 316554 | 531 | - | 0.312618 |
DDB_G0283221_ps | DDB_G0283221 | putative pseudogene fragment similar to | DDB0232431 | CDS | 317030 | 192 | - | 0.328125 |
DDB_G0283223_ps | DDB_G0283223 | putative pseudogene fragment similar to | DDB0232431 | CDS | 318683 | 696 | + | 0.239943 |
DDB_G0283227 | DDB_G0283227 | DDB0232431 | CDS | 319419 | 2913 | - | 0.240645 | |
DDB_G0283229 | DDB_G0283229 | DDB0232431 | CDS | 324812 | 2925 | - | 0.245128 | |
DDB_G0283231 | DDB_G0283231 | DDB0232431 | CDS | 329911 | 741 | - | 0.234818 | |
DDB_G0283233_ps | DDB_G0283233 | putative pseudogene similar to Dictyostelium genes | DDB0232431 | CDS | 331060 | 2760 | + | 0.238406 |
DDB_G0283235_ps | DDB_G0283235 | putative pseudogene similar to | DDB0232431 | CDS | 335133 | 513 | - | 0.235867 |
DDB_G0283237_ps | DDB_G0283237 | putative pseudogene similar to a family of Dictyostelium genes including | DDB0232431 | CDS | 336082 | 855 | + | 0.25848 |
DDB_G0283241 | DDB_G0283241 | DDB0232431 | CDS | 338450 | 642 | - | 0.23676 | |
DDB_G0283243 | DDB_G0283243 | DDB0232431 | CDS | 339770 | 2898 | + | 0.241201 | |
DDB_G0283245 | DDB_G0283245 | DDB0232431 | CDS | 343211 | 519 | - | 0.22158 | |
DDB_G0283251 | DDB_G0283251 | DDB0232431 | CDS | 377937 | 2190 | - | 0.2621 | |
DDB_G0283253 | DDB_G0283253 | DDB0232431 | CDS | 383852 | 318 | - | 0.289308 | |
DDB_G0283255 | DDB_G0283255 | DDB0232431 | CDS | 398240 | 1713 | + | 0.247519 | |
DDB_G0283259 | DDB_G0283259 | DDB0232431 | CDS | 295136 | 1002 | - | 0.328343 | |
DDB_G0283269 | DDB_G0283269 | has similarity to mammalian threonine aspartase 1 which belongs to the asparaginase 2 family | DDB0232431 | CDS | 428924 | 1770 | - | 0.233333 |
DDB_G0283271 | DDB_G0283271 | contains an N-terminal DOMON domain as it occurs in dopamine beta-monooxygenases the Dictyostelium protein is followed by a cytochrome b561 domain which contains 5 putative transmembrane regions in addition the protein contains a putative signal peptide | DDB0232431 | CDS | 436406 | 1146 | - | 0.362129 |
DDB_G0283275 | DDB_G0283275 | similar to bacterial 50S ribosomal L4L1e proteins | DDB0232431 | CDS | 442808 | 777 | + | 0.292149 |
DDB_G0283277_ps | DDB_G0283277 | putative pseudogene similar to CAZy family GH9 which catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 443932 | 1299 | - | 0.266359 |
DDB_G0283281 | DDB_G0283281 | catalyzes the reaction tryptamine secologanin 3-alpha(S)-strictosidine Hsub2subO in alkaloid biosynthesis | DDB0232431 | CDS | 447879 | 1179 | - | 0.261238 |
DDB_G0283285 | DDB_G0283285 | DDB0232431 | CDS | 458537 | 4368 | + | 0.278159 | |
DDB_G0283289 | DDB_G0283289 | DDB0232431 | CDS | 465144 | 2178 | + | 0.230946 | |
DDB_G0283291 | DDB_G0283291 | DDB0232431 | CDS | 467526 | 1092 | - | 0.271978 | |
DDB_G0283293 | DDB_G0283293 | catalyzes the reduction of glutamate to delta-1-pyrroline-5-carboxylate a critical step in the de novo biosynthesis of proline and ornithine expressed in pstO cells and in pstO cells and upper cup during culmination | DDB0232431 | CDS | 472326 | 1677 | + | 0.369112 |
DDB_G0283295 | DDB_G0283295 | DDB0232431 | CDS | 476937 | 165 | + | 0.29697 | |
DDB_G0283301 | DDB_G0283301 | DDB0232431 | CDS | 480042 | 1992 | + | 0.254016 | |
DDB_G0283303 | DDB_G0283303 | DDB0232431 | CDS | 497204 | 1404 | + | 0.264245 | |
DDB_G0283305 | DDB_G0283305 | DDB0232431 | CDS | 498765 | 1671 | - | 0.304608 | |
DDB_G0283309 | DDB_G0283309 | similar to the eIF-2B alphabetadelta subunits family | DDB0232431 | CDS | 511242 | 1041 | - | 0.397695 |
DDB_G0283311 | DDB_G0283311 | DDB0232431 | CDS | 512897 | 465 | + | 0.270968 | |
DDB_G0283313 | DDB_G0283313 | DDB0232431 | CDS | 513450 | 1542 | - | 0.295071 | |
DDB_G0283321 | DDB_G0283321 | DDB0232431 | CDS | 527883 | 1863 | - | 0.17284 | |
DDB_G0283325 | DDB_G0283325 | DDB0232431 | CDS | 424767 | 3960 | + | 0.255051 | |
DDB_G0283337 | DDB_G0283337 | DDB0232431 | CDS | 491931 | 3387 | - | 0.219368 | |
DDB_G0283339 | DDB_G0283339 | DDB0232431 | CDS | 501258 | 6369 | - | 0.28152 | |
DDB_G0283347 | DDB_G0283347 | DDB0232431 | CDS | 543684 | 1551 | - | 0.272083 | |
DDB_G0283351 | DDB_G0283351 | DDB0232431 | CDS | 550541 | 4812 | + | 0.209061 | |
DDB_G0283353 | DDB_G0283353 | DDB0232431 | CDS | 558631 | 93 | + | 0.354839 | |
DDB_G0283357 | DDB_G0283357 | DDB0232431 | CDS | 564906 | 3744 | + | 0.276175 | |
DDB_G0283361 | DDB_G0283361 | DDB0232431 | CDS | 572566 | 1557 | + | 0.245986 | |
DDB_G0283369 | DDB_G0283369 | DDB0232431 | CDS | 587429 | 6252 | - | 0.274152 | |
DDB_G0283373 | DDB_G0283373 | contains a predicted signal peptide contains one ERVALR sulphydryl oxidase domain similar to D. purpureum protein | DDB0232431 | CDS | 556576 | 1743 | + | 0.270797 |
DDB_G0283377 | DDB_G0283377 | DDB0232431 | CDS | 578428 | 1326 | + | 0.366516 | |
DDB_G0283379 | DDB_G0283379 | DDB0232431 | CDS | 579956 | 3594 | - | 0.175849 | |
DDB_G0283381 | DDB_G0283381 | contains a weak Spc7 kinetochore protein domain similar to D. purpureum proteinbrbr bCommunity annotation:b DDB_G0283381 appears to be the ortholog of spc7 of Saccharomyces pombe and spc105 of Saccharomyces cerevesiae. Spc105 is a kinetochore component (see Pagliuca et al Plos One 28 e7640m (2009)). Like the conserved kinetochore components spc25 nuf2 and ndc80 DDB_G0283381 is very strongly overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (spc25 30-fold nuf2 18-fold ndc80 16-fold DDB_G0283381 29-fold) (Doquang et al in preparation). This presumably reflects a cell cycle function as most cell cycle genes are overexpressed in this strain and most of the genes strongly overexpressed in the strain have identifiable cell cycle functions. Spc105 forms a complex with kre28 but I could not identify a corresponding gene in Dicty even by using Ashbya as an intermediate. Harry MacWilliams December 2009br | DDB0232431 | CDS | 594665 | 5541 | + | 0.242375 |
DDB_G0283383 | DDB_G0283383 | DDB0232431 | CDS | 603790 | 175 | - | 0.24 | |
DDB_G0283395 | DDB_G0283395 | almost identical to neighboring gene | DDB0232431 | CDS | 606034 | 189 | - | 0.296296 |
DDB_G0283397 | DDB_G0283397 | DDB0232431 | CDS | 606939 | 2757 | - | 0.283642 | |
DDB_G0283399 | DDB_G0283399 | DDB0232431 | CDS | 609993 | 504 | - | 0.18254 | |
DDB_G0283403 | DDB_G0283403 | DDB0232431 | CDS | 615804 | 2241 | + | 0.245872 | |
DDB_G0283407 | DDB_G0283407 | DDB0232431 | CDS | 632298 | 1368 | - | 0.214181 | |
DDB_G0283409 | DDB_G0283409 | DDB0232431 | CDS | 637844 | 387 | - | 0.281654 | |
DDB_G0283413 | DDB_G0283413 | DDB0232431 | CDS | 651190 | 912 | + | 0.267544 | |
DDB_G0283415 | DDB_G0283415 | DDB0232431 | CDS | 652443 | 738 | - | 0.247967 | |
DDB_G0283417 | DDB_G0283417 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232431 | CDS | 654013 | 693 | - | 0.215007 |
DDB_G0283421 | DDB_G0283421 | DDB0232431 | CDS | 663424 | 174 | + | 0.356322 | |
DDB_G0283423 | DDB_G0283423 | DDB0232431 | CDS | 673782 | 4578 | + | 0.189602 | |
DDB_G0283425 | DDB_G0283425 | DDB0232431 | CDS | 683015 | 3312 | - | 0.223732 | |
DDB_G0283427 | DDB_G0283427 | DDB0232431 | CDS | 687466 | 423 | + | 0.262411 | |
DDB_G0283429 | DDB_G0283429 | similar to proteins in bacteria and protozoa COG4271 predicted nucleotide-binding protein containing TIR -like domain (Transcription) | DDB0232431 | CDS | 691392 | 756 | - | 0.276455 |
DDB_G0283431 | DDB_G0283431 | DDB0232431 | CDS | 692545 | 342 | - | 0.122807 | |
DDB_G0283433_ps | DDB_G0283433 | putative pseudogene similar to a large family of D. discoideum proteins including | DDB0232431 | CDS | 694005 | 849 | + | 0.232038 |
DDB_G0283435 | DDB_G0283435 | DDB0232431 | CDS | 696044 | 747 | + | 0.170013 | |
DDB_G0283437 | DDB_G0283437 | DDB0232431 | CDS | 697659 | 621 | + | 0.281804 | |
DDB_G0283439 | DDB_G0283439 | similar to H. sapiens solute carrier family 29 member 1 (SLC29A2) putative ortholog of S. cerevisiae FUN2 | DDB0232431 | CDS | 699253 | 1293 | + | 0.324053 |
DDB_G0283441 | DDB_G0283441 | DDB0232431 | CDS | 702819 | 2916 | + | 0.284636 | |
DDB_G0283443 | DDB_G0283443 | DDB0232431 | CDS | 706025 | 1182 | - | 0.187817 | |
DDB_G0283445 | DDB_G0283445 | DDB0232431 | CDS | 707432 | 1284 | + | 0.221184 | |
DDB_G0283447 | DDB_G0283447 | DDB0232431 | CDS | 709169 | 2019 | + | 0.280832 | |
DDB_G0283449 | DDB_G0283449 | DDB0232431 | CDS | 711483 | 246 | - | 0.378049 | |
DDB_G0283451 | DDB_G0283451 | DDB0232431 | CDS | 712043 | 1215 | - | 0.33251 | |
DDB_G0283455 | DDB_G0283455 | DDB0232431 | CDS | 724620 | 288 | - | 0.284722 | |
DDB_G0283457 | DDB_G0283457 | DDB0232431 | CDS | 726060 | 813 | - | 0.172202 | |
DDB_G0283461 | DDB_G0283461 | DDB0232431 | CDS | 731858 | 195 | + | 0.271795 | |
DDB_G0283463 | DDB_G0283463 | DDB0232431 | CDS | 733335 | 141 | + | 0.312057 | |
DDB_G0283465 | DDB_G0283465 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 734816 | 174 | + | 0.316092 |
DDB_G0283467 | DDB_G0283467 | DDB0232431 | CDS | 735396 | 219 | - | 0.30137 | |
DDB_G0283469 | DDB_G0283469 | DDB0232431 | CDS | 737091 | 444 | + | 0.220721 | |
DDB_G0283471 | DDB_G0283471 | DDB0232431 | CDS | 738038 | 6009 | - | 0.192045 | |
DDB_G0283475 | DDB_G0283475 | DDB0232431 | CDS | 753547 | 7128 | + | 0.317761 | |
DDB_G0283477 | DDB_G0283477 | DDB0232431 | CDS | 763555 | 2520 | - | 0.198016 | |
DDB_G0283481 | DDB_G0283481 | similar to Dictystelium cell surface glycoproteins gp130 and cfrA B C and D (GP138A-D) | DDB0232431 | CDS | 772790 | 1749 | - | 0.238994 |
DDB_G0283485 | DDB_G0283485 | DDB0232431 | CDS | 641115 | 2292 | - | 0.253927 | |
DDB_G0283487 | DDB_G0283487 | DDB0232431 | CDS | 688705 | 2577 | + | 0.177726 | |
DDB_G0283493 | DDB_G0283493 | almost identical to neighboring gene | DDB0232431 | CDS | 605068 | 189 | - | 0.306878 |
DDB_G0283495 | DDB_G0283495 | DDB0232431 | CDS | 611003 | 2319 | + | 0.337214 | |
DDB_G0283499 | DDB_G0283499 | DDB0232431 | CDS | 660137 | 762 | - | 0.229659 | |
DDB_G0283501 | DDB_G0283501 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 665243 | 174 | + | 0.33908 |
DDB_G0283503 | DDB_G0283503 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 666044 | 174 | + | 0.33908 |
DDB_G0283505 | DDB_G0283505 | contains one putative transmembrane domain belongs to a family of small highly conserved genes unique to Dictyostelium discoideum | DDB0232431 | CDS | 666961 | 174 | + | 0.344828 |
DDB_G0283507 | DDB_G0283507 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 667839 | 174 | + | 0.333333 |
DDB_G0283509 | DDB_G0283509 | belongs to a family of small highly conserved genes unique to Dictyostelium discoideum | DDB0232431 | CDS | 668710 | 174 | + | 0.327586 |
DDB_G0283511 | DDB_G0283511 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells and in upper and lower cups during culmination | DDB0232431 | CDS | 669589 | 174 | + | 0.344828 |
DDB_G0283513 | DDB_G0283513 | belongs to a family of small highly conserved genes unique to Dictyostelium discoideum | DDB0232431 | CDS | 670441 | 174 | + | 0.333333 |
DDB_G0283515 | DDB_G0283515 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 671329 | 174 | + | 0.33908 |
DDB_G0283517 | DDB_G0283517 | DDB0232431 | CDS | 672171 | 174 | + | 0.316092 | |
DDB_G0283519 | DDB_G0283519 | DDB0232431 | CDS | 673055 | 174 | + | 0.356322 | |
DDB_G0283521 | DDB_G0283521 | DDB0232431 | CDS | 678402 | 3705 | - | 0.215385 | |
DDB_G0283523 | DDB_G0283523 | DDB0232431 | CDS | 701281 | 375 | + | 0.226667 | |
DDB_G0283527 | DDB_G0283527 | DDB0232431 | CDS | 732951 | 174 | - | 0.189655 | |
DDB_G0283529 | DDB_G0283529 | DDB0232431 | CDS | 760908 | 2349 | - | 0.180077 | |
DDB_G0283531 | DDB_G0283531 | DDB0232431 | CDS | 766653 | 822 | + | 0.304136 | |
DDB_G0283535 | DDB_G0283535 | similar to H. sapiens DMXL1 and DMXL2 and D. melanogaster DmX REMI mutant fails to aggregate see | DDB0232431 | CDS | 837650 | 8379 | - | 0.297291 |
DDB_G0283545 | DDB_G0283545 | DDB0232431 | CDS | 794803 | 2850 | + | 0.309474 | |
DDB_G0283549 | DDB_G0283549 | contains one C2 domain which is is a Ca2-dependent membrane-targeting module found in many cellular proteins involved in signal transduction or membrane trafficking | DDB0232431 | CDS | 803052 | 417 | + | 0.309353 |
DDB_G0283551 | DDB_G0283551 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity highly similar to neighboring gene | DDB0232431 | CDS | 810010 | 3975 | - | 0.255597 |
DDB_G0283553 | DDB_G0283553 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity highly similar to neighboring gene | DDB0232431 | CDS | 815506 | 4545 | - | 0.252805 |
DDB_G0283555 | DDB_G0283555 | contains Dictyostelium spore coat protein N-terminal domain and 7 follistatin-like domains similar to spore coat proteins CotA CotB and CotD expressed in prespore cells | DDB0232431 | CDS | 824798 | 1398 | - | 0.375536 |
DDB_G0283557 | DDB_G0283557 | DDB0232431 | CDS | 827565 | 1848 | + | 0.278139 | |
DDB_G0283559 | DDB_G0283559 | DDB0232431 | CDS | 830931 | 198 | - | 0.328283 | |
DDB_G0283561 | DDB_G0283561 | DDB0232431 | CDS | 831598 | 213 | + | 0.253521 | |
DDB_G0283565 | DDB_G0283565 | DDB0232431 | CDS | 833347 | 3024 | - | 0.305886 | |
DDB_G0283567 | DDB_G0283567 | DDB0232431 | CDS | 836774 | 270 | + | 0.292593 | |
DDB_G0283571 | DDB_G0283571 | DDB0232431 | CDS | 851425 | 318 | - | 0.27673 | |
DDB_G0283573 | DDB_G0283573 | DDB0232431 | CDS | 854108 | 231 | + | 0.363636 | |
DDB_G0283575 | DDB_G0283575 | catalyzes the reaction RX glutathione HX R-S-glutathione enriched in prespore cells | DDB0232431 | CDS | 855359 | 597 | + | 0.303183 |
DDB_G0283577 | DDB_G0283577 | DDB0232431 | CDS | 856410 | 3153 | - | 0.235014 | |
DDB_G0283585 | DDB_G0283585 | DDB0232431 | CDS | 785263 | 4275 | + | 0.340585 | |
DDB_G0283591 | DDB_G0283591 | DDB0232431 | CDS | 783267 | 747 | + | 0.239625 | |
DDB_G0283593 | DDB_G0283593 | DDB0232431 | CDS | 800982 | 1131 | - | 0.218391 | |
DDB_G0283595 | DDB_G0283595 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232431 | CDS | 805455 | 3873 | - | 0.251743 |
DDB_G0283623 | DDB_G0283623 | DDB0232431 | CDS | 873651 | 2988 | + | 0.251339 | |
DDB_G0283625 | DDB_G0283625 | contains a Mob1 motif however it does not cluster with Mob1 proteins | DDB0232431 | CDS | 882607 | 654 | + | 0.310398 |
DDB_G0283629 | DDB_G0283629 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232431 | CDS | 885727 | 1632 | - | 0.321691 |
DDB_G0283633 | DDB_G0283633 | DDB0232431 | CDS | 889575 | 1416 | - | 0.242232 | |
DDB_G0283639 | DDB_G0283639 | DDB0232431 | CDS | 895310 | 129 | + | 0.286822 | |
DDB_G0283643 | DDB_G0283643 | DDB0232431 | CDS | 896653 | 138 | + | 0.355072 | |
DDB_G0283645 | DDB_G0283645 | very similar to Dictyostelium cbpF cbpG and cbpC contains two EF-hands | DDB0232431 | CDS | 897818 | 516 | - | 0.302326 |
DDB_G0283647 | DDB_G0283647 | DDB0232431 | CDS | 907070 | 228 | - | 0.302632 | |
DDB_G0283649 | DDB_G0283649 | similar to the S. cerevisiae LOT6 a FMN-dependent NAD(P)H:quinone reductase that may be involved in quinone detoxification | DDB0232431 | CDS | 910617 | 600 | - | 0.301667 |
DDB_G0283651 | DDB_G0283651 | tyrosinases are copper monooxygenases that catalyzes the hydroxylation of monophenols and the oxidation of o-diphenols to o-quinols binds two copper ions by 3 conserved His residues there is an almost identical | DDB0232431 | CDS | 918296 | 2451 | - | 0.304774 |
DDB_G0283653 | DDB_G0283653 | tyrosinases are copper monooxygenases that catalyzes the hydroxylation of monophenols and the oxidation of o-diphenols to o-quinols binds two copper ions by 3 conserved His residues there is an almost identical | DDB0232431 | CDS | 921967 | 2463 | - | 0.310597 |
DDB_G0283655 | DDB_G0283655 | DDB0232431 | CDS | 925419 | 1524 | - | 0.224409 | |
DDB_G0283659_ps | DDB_G0283659 | putative pseudogene fragment similar to D. discoideum patatin gene family including | DDB0232431 | CDS | 938852 | 165 | - | 0.248485 |
DDB_G0283665_ps | DDB_G0283665 | putative pseudogene similar to Dictyostelium calcium binding proteins | DDB0232431 | CDS | 945236 | 228 | + | 0.285088 |
DDB_G0283667 | DDB_G0283667 | DDB0232431 | CDS | 946222 | 2400 | + | 0.212917 | |
DDB_G0283669 | DDB_G0283669 | conserved ubiquinol-cytochrome c oxidoreductase subunit a component of the mitochondrial inner membrane electron transport chain | DDB0232431 | CDS | 953002 | 201 | + | 0.368159 |
DDB_G0283675 | DDB_G0283675 | DDB0232431 | CDS | 961972 | 1179 | - | 0.296014 | |
DDB_G0283677 | DDB_G0283677 | DDB0232431 | CDS | 963963 | 882 | + | 0.217687 | |
DDB_G0283681 | DDB_G0283681 | similar to STAG (stromal antigen) proteins which are subunits of a protein complex required for sister chromatid cohesion in eukaryotes | DDB0232431 | CDS | 973798 | 4020 | - | 0.302488 |
DDB_G0283683 | DDB_G0283683 | DDB0232431 | CDS | 978468 | 1566 | - | 0.225415 | |
DDB_G0283687 | DDB_G0283687 | similar to CC1-like splicing factors characterized by an N-terminal arginine-rich low complexity domain followed by three RNA recognition domains similar to human RBM23 and RBM39 | DDB0232431 | CDS | 982205 | 2184 | + | 0.330586 |
DDB_G0283689 | DDB_G0283689 | DDB0232431 | CDS | 985671 | 543 | - | 0.28361 | |
DDB_G0283691 | DDB_G0283691 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D contains a predicted signal peptide | DDB0232431 | CDS | 986987 | 1278 | + | 0.261346 |
DDB_G0283693 | DDB_G0283693 | DDB0232431 | CDS | 990291 | 189 | + | 0.354497 | |
DDB_G0283695 | DDB_G0283695 | DDB0232431 | CDS | 990708 | 1047 | - | 0.221585 | |
DDB_G0283697 | DDB_G0283697 | DDB0232431 | CDS | 992255 | 2562 | + | 0.276347 | |
DDB_G0283703 | DDB_G0283703 | DDB0232431 | CDS | 1003190 | 282 | - | 0.287234 | |
DDB_G0283705 | DDB_G0283705 | DDB0232431 | CDS | 1004930 | 177 | + | 0.338983 | |
DDB_G0283707 | DDB_G0283707 | conserved protein in ciliates and plants contains 9 predicted transmembrane domains including one signal peptide there is an almost identical D. discoideum protein | DDB0232431 | CDS | 1005690 | 1524 | - | 0.377297 |
DDB_G0283711 | DDB_G0283711 | highly similar to other hssA2C7E family proteins | DDB0232431 | CDS | 1011158 | 258 | - | 0.325581 |
DDB_G0283713 | DDB_G0283713 | DDB0232431 | CDS | 1012257 | 261 | + | 0.329502 | |
DDB_G0283715 | DDB_G0283715 | DDB0232431 | CDS | 1012994 | 3216 | - | 0.294154 | |
DDB_G0283719 | DDB_G0283719 | DDB0232431 | CDS | 1023936 | 3963 | - | 0.217007 | |
DDB_G0283721 | DDB_G0283721 | almost identical to the upstream gene | DDB0232431 | CDS | 1029584 | 2190 | + | 0.245205 |
DDB_G0283723 | DDB_G0283723 | almost identical to the downstream gene | DDB0232431 | CDS | 1033128 | 2190 | + | 0.246119 |
DDB_G0283725_ps | DDB_G0283725 | putative pseudogene very similar to pyridoxal phosphate-dependent decarboxylase family genes | DDB0232431 | CDS | 1035645 | 1155 | + | 0.273593 |
DDB_G0283727 | DDB_G0283727 | DDB0232431 | CDS | 1038776 | 756 | + | 0.376984 | |
DDB_G0283729 | DDB_G0283729 | DDB0232431 | CDS | 1039785 | 1530 | - | 0.168627 | |
DDB_G0283731 | DDB_G0283731 | similar to D. purpureum protein contains a histidine rich region | DDB0232431 | CDS | 1041764 | 621 | - | 0.349436 |
DDB_G0283733 | DDB_G0283733 | DDB0232431 | CDS | 1042995 | 1137 | + | 0.278804 | |
DDB_G0283743 | DDB_G0283743 | DDB0232431 | CDS | 934848 | 2514 | + | 0.211615 | |
DDB_G0283745 | DDB_G0283745 | similar to transportin 3 which in human seems to function in nuclear protein import as nuclear transport receptor | DDB0232431 | CDS | 877706 | 2946 | - | 0.243381 |
DDB_G0283747 | DDB_G0283747 | DDB0232431 | CDS | 915081 | 2745 | + | 0.167577 | |
DDB_G0283749 | DDB_G0283749 | DDB0232431 | CDS | 929556 | 4416 | + | 0.217618 | |
DDB_G0283753 | DDB_G0283753 | DDB0232431 | CDS | 1050017 | 1668 | - | 0.285372 | |
DDB_G0283759 | DDB_G0283759 | DDB0232431 | CDS | 1232305 | 3240 | + | 0.274383 | |
DDB_G0283771 | DDB_G0283771 | bCommunity annotation: bDDB_G0283771 shows weak similarities to several kinesin family proteins. The gene is overexpressed sixfold in a Dictyostelium | DDB0232431 | CDS | 1079549 | 2142 | + | 0.280112 |
DDB_G0283773 | DDB_G0283773 | putative GTPase very conserved in protozoa and fungi | DDB0232431 | CDS | 1081883 | 1305 | - | 0.288123 |
DDB_G0283775 | DDB_G0283775 | DDB0232431 | CDS | 1083586 | 3657 | + | 0.178562 | |
DDB_G0283777 | DDB_G0283777 | DDB0232431 | CDS | 1087508 | 249 | - | 0.305221 | |
DDB_G0283781 | DDB_G0283781 | DDB0232431 | CDS | 1089062 | 1107 | + | 0.241192 | |
DDB_G0283783 | DDB_G0283783 | DDB0232431 | CDS | 1091245 | 450 | + | 0.326667 | |
DDB_G0283785 | DDB_G0283785 | contains 2 EGF-like domains a predicted signal sequence and one N-terminal transmembrane domain very similar to it's upstream and downstream neighbors | DDB0232431 | CDS | 1099059 | 3138 | + | 0.271192 |
DDB_G0283787 | DDB_G0283787 | contains 2 EGF-like domains a predicted signal sequence and one N-terminal transmembrane domain very similar to it's two upstream neighbors | DDB0232431 | CDS | 1103072 | 3195 | + | 0.281377 |
DDB_G0283791 | DDB_G0283791 | DDB0232431 | CDS | 1109469 | 1320 | - | 0.238636 | |
DDB_G0283793 | DDB_G0283793 | DDB0232431 | CDS | 1114386 | 2136 | - | 0.305243 | |
DDB_G0283797 | DDB_G0283797 | DDB0232431 | CDS | 1118346 | 1470 | - | 0.267347 | |
DDB_G0283799 | DDB_G0283799 | DDB0232431 | CDS | 1120333 | 1098 | - | 0.211293 | |
DDB_G0283803 | DDB_G0283803 | DDB0232431 | CDS | 1122911 | 582 | + | 0.298969 | |
DDB_G0283807 | DDB_G0283807 | DDB0232431 | CDS | 1128255 | 444 | + | 0.207207 | |
DDB_G0283815 | DDB_G0283815 | DDB0232431 | CDS | 1148242 | 1332 | - | 0.231982 | |
DDB_G0283817 | DDB_G0283817 | DDB0232431 | CDS | 1149949 | 882 | + | 0.314059 | |
DDB_G0283819 | DDB_G0283819 | DDB0232431 | CDS | 1153703 | 1524 | + | 0.349081 | |
DDB_G0283821 | DDB_G0283821 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis | DDB0232431 | CDS | 1155677 | 2826 | - | 0.295824 |
DDB_G0283823 | DDB_G0283823 | DDB0232431 | CDS | 1177277 | 600 | + | 0.273333 | |
DDB_G0283825 | DDB_G0283825 | DDB0232431 | CDS | 1178221 | 1056 | - | 0.24053 | |
DDB_G0283827 | DDB_G0283827 | DDB0232431 | CDS | 1180565 | 2718 | + | 0.307947 | |
DDB_G0283829 | DDB_G0283829 | similar to human ODR4 (odorant response abnormal protein 4) contains one putative transmembrane domain | DDB0232431 | CDS | 1183400 | 1371 | - | 0.190372 |
DDB_G0283831 | DDB_G0283831 | DDB0232431 | CDS | 1185329 | 771 | - | 0.276265 | |
DDB_G0283833 | DDB_G0283833 | DDB0232431 | CDS | 1187328 | 2856 | - | 0.238095 | |
DDB_G0283837 | DDB_G0283837 | proteins containing the actin depolymerisation factor (ADF)cofilin-like domain sever actin filaments and bind to actin monomers | DDB0232431 | CDS | 1195917 | 1860 | + | 0.22957 |
DDB_G0283843 | DDB_G0283843 | DDB0232431 | CDS | 1223477 | 531 | - | 0.306968 | |
DDB_G0283845 | DDB_G0283845 | DDB0232431 | CDS | 1227055 | 540 | + | 0.312963 | |
DDB_G0283847 | DDB_G0283847 | catalyzes the reaction: S-adenosyl-L-methionine phospholipid olefinic fatty acid S-adenosyl-L-homocysteine phospholipid cyclopropane fatty acid underexpressed in | DDB0232431 | CDS | 1228686 | 1293 | + | 0.254447 |
DDB_G0283849 | DDB_G0283849 | DDB0232431 | CDS | 1239874 | 552 | - | 0.282609 | |
DDB_G0283851 | DDB_G0283851 | DDB0232431 | CDS | 1253142 | 750 | - | 0.284 | |
DDB_G0283855 | DDB_G0283855 | DDB0232431 | CDS | 1060450 | 1644 | + | 0.242092 | |
DDB_G0283859 | DDB_G0283859 | DDB0232431 | CDS | 1066871 | 5037 | + | 0.289458 | |
DDB_G0283861 | DDB_G0283861 | DDB0232431 | CDS | 1072483 | 564 | + | 0.289007 | |
DDB_G0283863 | DDB_G0283863 | DDB0232431 | CDS | 1074074 | 1854 | - | 0.244337 | |
DDB_G0283869 | DDB_G0283869 | contains 3 EGF-like domains a predicted signal sequence and one N-terminal transmembrane domain very similar to it's two downstream neighbors | DDB0232431 | CDS | 1094707 | 3405 | + | 0.269016 |
DDB_G0283871 | DDB_G0283871 | DDB0232431 | CDS | 1126533 | 774 | + | 0.289406 | |
DDB_G0283879 | DDB_G0283879 | DDB0232431 | CDS | 1142351 | 591 | - | 0.184433 | |
DDB_G0283885 | DDB_G0283885 | member of a gene family comprising | DDB0232431 | CDS | 1166070 | 1587 | - | 0.21235 |
DDB_G0283887 | DDB_G0283887 | member of a gene family comprising | DDB0232431 | CDS | 1170844 | 1488 | - | 0.217742 |
DDB_G0283889 | DDB_G0283889 | DDB0232431 | CDS | 1174977 | 447 | - | 0.322148 | |
DDB_G0283893 | DDB_G0283893 | DDB0232431 | CDS | 1204398 | 17628 | - | 0.301849 | |
DDB_G0283897 | DDB_G0283897 | DDB0232431 | CDS | 1243225 | 2808 | + | 0.162037 | |
DDB_G0283901 | DDB_G0283901 | DDB0232431 | CDS | 1254332 | 1542 | - | 0.279507 | |
DDB_G0283911 | DDB_G0283911 | highly similar to neighboring gene | DDB0232431 | CDS | 1265347 | 1779 | - | 0.261383 |
DDB_G0283913 | DDB_G0283913 | large molecular weight protein that contains a hsp20 domain highly similar to neighboring gene | DDB0232431 | CDS | 1267681 | 2004 | - | 0.268962 |
DDB_G0283915 | DDB_G0283915 | DDB0232431 | CDS | 1270973 | 702 | + | 0.337607 | |
DDB_G0283919 | DDB_G0283919 | the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232431 | CDS | 1275553 | 3243 | + | 0.30589 |
DDB_G0283923 | DDB_G0283923 | DDB0232431 | CDS | 1301821 | 4350 | - | 0.223448 | |
DDB_G0283925 | DDB_G0283925 | DDB0232431 | CDS | 1306681 | 465 | - | 0.324731 | |
DDB_G0283927 | DDB_G0283927 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232431 | CDS | 1307685 | 1458 | - | 0.226337 |
DDB_G0283935 | DDB_G0283935 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232431 | CDS | 1333704 | 942 | + | 0.284501 |
DDB_G0283939 | DDB_G0283939 | DDB0232431 | CDS | 1338263 | 3156 | + | 0.290875 | |
DDB_G0283941 | DDB_G0283941 | DDB0232431 | CDS | 1341707 | 309 | - | 0.2589 | |
DDB_G0283943 | DDB_G0283943 | catalyzes the reaction aldehyde NADsupsup Hsub2subO an acid NADH Hsupsup | DDB0232431 | CDS | 1342529 | 1488 | - | 0.316532 |
DDB_G0283945 | DDB_G0283945 | DDB0232431 | CDS | 1345149 | 3078 | + | 0.196556 | |
DDB_G0283947 | DDB_G0283947 | DDB0232431 | CDS | 1349351 | 1101 | + | 0.297003 | |
DDB_G0283949 | DDB_G0283949 | DDB0232431 | CDS | 1350512 | 1398 | - | 0.268956 | |
DDB_G0283951 | DDB_G0283951 | contains a predicted signal peptide catalyzes the reaction sn-glycerol 3-phosphate a quinone glycerone phosphate a quinol | DDB0232431 | CDS | 1352908 | 1917 | + | 0.308816 |
DDB_G0283959 | DDB_G0283959 | DDB0232431 | CDS | 1374141 | 837 | + | 0.27957 | |
DDB_G0283961 | DDB_G0283961 | DDB0232431 | CDS | 1375647 | 813 | + | 0.281673 | |
DDB_G0283967 | DDB_G0283967 | DDB0232431 | CDS | 1387840 | 4905 | + | 0.198165 | |
DDB_G0283971 | DDB_G0283971 | contains an N-terminal ubiquitin domain very similar to D. purpureum protein | DDB0232431 | CDS | 1401996 | 2565 | - | 0.329045 |
DDB_G0283973 | DDB_G0283973 | DDB0232431 | CDS | 1405614 | 2154 | + | 0.32637 | |
DDB_G0283975 | DDB_G0283975 | DDB0232431 | CDS | 1408395 | 834 | + | 0.317746 | |
DDB_G0283977 | DDB_G0283977 | DDB0232431 | CDS | 1409294 | 2622 | - | 0.217391 | |
DDB_G0283979 | DDB_G0283979 | DDB0232431 | CDS | 1413537 | 3600 | + | 0.265833 | |
DDB_G0283985 | DDB_G0283985 | DDB0232431 | CDS | 1263489 | 1608 | + | 0.250622 | |
DDB_G0283989 | DDB_G0283989 | one of three paralogs in Dictyostelium (other genes: | DDB0232431 | CDS | 1284281 | 2694 | + | 0.311804 |
DDB_G0283991 | DDB_G0283991 | DDB0232431 | CDS | 1287653 | 1092 | + | 0.308608 | |
DDB_G0283993 | DDB_G0283993 | DDB0232431 | CDS | 1289307 | 3054 | + | 0.270138 | |
DDB_G0283995 | DDB_G0283995 | DDB0232431 | CDS | 1293218 | 2958 | + | 0.260649 | |
DDB_G0283997_ps | DDB_G0283997 | putative pseudogene similar to a family of D. discoideum protein family of unknown function including | DDB0232431 | CDS | 1298443 | 2412 | + | 0.238391 |
DDB_G0283999 | DDB_G0283999 | DDB0232431 | CDS | 1309513 | 1815 | - | 0.284848 | |
DDB_G0284005 | DDB_G0284005 | DDB0232431 | CDS | 1397618 | 285 | - | 0.280702 | |
DDB_G0284007 | DDB_G0284007 | DDB0232431 | CDS | 1398686 | 1059 | - | 0.240793 | |
DDB_G0284011 | DDB_G0284011 | DDB0232431 | CDS | 1429547 | 933 | - | 0.274384 | |
DDB_G0284015 | DDB_G0284015 | DDB0232431 | CDS | 1433731 | 2283 | - | 0.29873 | |
DDB_G0284019 | DDB_G0284019 | DDB0232431 | CDS | 1444241 | 2202 | - | 0.31653 | |
DDB_G0284021 | DDB_G0284021 | DDB0232431 | CDS | 1447496 | 573 | - | 0.280977 | |
DDB_G0284025 | DDB_G0284025 | DDB0232431 | CDS | 1440123 | 2226 | - | 0.269542 | |
DDB_G0284031 | DDB_G0284031 | DDB0232431 | CDS | 1458434 | 846 | + | 0.180851 | |
DDB_G0284037 | DDB_G0284037 | weakly similar to 26S proteasome regulatory subunit RPN11 (MPR1 protein) REMI mutant forms aberrant fruiting bodies (see | DDB0232431 | CDS | 1593040 | 2148 | + | 0.288175 |
DDB_G0284049 | DDB_G0284049 | DDB0232431 | CDS | 1467489 | 3561 | + | 0.243471 | |
DDB_G0284051 | DDB_G0284051 | DDB0232431 | CDS | 1471982 | 1527 | + | 0.333333 | |
DDB_G0284053 | DDB_G0284053 | DDB0232431 | CDS | 1473938 | 714 | + | 0.268908 | |
DDB_G0284055 | DDB_G0284055 | DDB0232431 | CDS | 1474815 | 1335 | - | 0.270412 | |
DDB_G0284057 | DDB_G0284057 | DDB0232431 | CDS | 1478033 | 372 | + | 0.233871 | |
DDB_G0284059 | DDB_G0284059 | DDB0232431 | CDS | 1478818 | 3843 | + | 0.287536 | |
DDB_G0284061 | DDB_G0284061 | DDB0232431 | CDS | 1483793 | 846 | + | 0.241135 | |
DDB_G0284063 | DDB_G0284063 | DDB0232431 | CDS | 1485717 | 825 | + | 0.197576 | |
DDB_G0284069 | DDB_G0284069 | DDB0232431 | CDS | 1498595 | 1281 | - | 0.250585 | |
DDB_G0284073 | DDB_G0284073 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D | DDB0232431 | CDS | 1506777 | 2643 | + | 0.23496 |
DDB_G0284077 | DDB_G0284077 | DDB0232431 | CDS | 1530962 | 1272 | + | 0.251572 | |
DDB_G0284079 | DDB_G0284079 | contains two ankyrin repeats and an RA domain which plays a role in RasGTP activation in mammals and mating in yeast highly similar to | DDB0232431 | CDS | 1538387 | 912 | + | 0.291667 |
DDB_G0284083 | DDB_G0284083 | DDB0232431 | CDS | 1548205 | 999 | + | 0.209209 | |
DDB_G0284085 | DDB_G0284085 | DDB0232431 | CDS | 1549462 | 1098 | + | 0.175774 | |
DDB_G0284087 | DDB_G0284087 | DDB0232431 | CDS | 1550807 | 3366 | + | 0.229352 | |
DDB_G0284091 | DDB_G0284091 | DDB0232431 | CDS | 1556685 | 723 | - | 0.337483 | |
DDB_G0284095 | DDB_G0284095 | DDB0232431 | CDS | 1559578 | 798 | - | 0.218045 | |
DDB_G0284097 | DDB_G0284097 | DDB0232431 | CDS | 1565830 | 1902 | - | 0.358044 | |
DDB_G0284099 | DDB_G0284099 | DDB0232431 | CDS | 1569018 | 1476 | - | 0.249322 | |
DDB_G0284105 | DDB_G0284105 | DDB0232431 | CDS | 1580531 | 1560 | - | 0.25641 | |
DDB_G0284109 | DDB_G0284109 | DDB0232431 | CDS | 1599639 | 375 | + | 0.293333 | |
DDB_G0284111 | DDB_G0284111 | DDB0232431 | CDS | 1601233 | 375 | + | 0.274667 | |
DDB_G0284115 | DDB_G0284115 | DDB0232431 | CDS | 1607949 | 423 | + | 0.276596 | |
DDB_G0284119 | DDB_G0284119 | contains 3 predicted transmembrane domains and an additional putative signal sequence member of a larger gene family in D. discoideum also present in other dictyostelids | DDB0232431 | CDS | 1614014 | 690 | - | 0.27971 |
DDB_G0284121 | DDB_G0284121 | DDB0232431 | CDS | 1615547 | 945 | - | 0.279365 | |
DDB_G0284125 | DDB_G0284125 | DDB0232431 | CDS | 1617796 | 1131 | - | 0.27763 | |
DDB_G0284127 | DDB_G0284127 | DDB0232431 | CDS | 1619168 | 1389 | + | 0.2455 | |
DDB_G0284131 | DDB_G0284131 | DDB0232431 | CDS | 1625572 | 1989 | + | 0.157366 | |
DDB_G0284133 | DDB_G0284133 | similar to P. pallidum protein weak similarity to PB1 domain in amino terminal region | DDB0232431 | CDS | 1629570 | 3153 | + | 0.290517 |
DDB_G0284135 | DDB_G0284135 | DDB0232431 | CDS | 1634829 | 2763 | + | 0.312704 | |
DDB_G0284137 | DDB_G0284137 | DDB0232431 | CDS | 1638105 | 1461 | - | 0.186858 | |
DDB_G0284139 | DDB_G0284139 | DDB0232431 | CDS | 1640056 | 1743 | - | 0.255307 | |
DDB_G0284143 | DDB_G0284143 | DDB0232431 | CDS | 1490360 | 384 | + | 0.255208 | |
DDB_G0284145 | DDB_G0284145 | DDB0232431 | CDS | 1523365 | 1317 | - | 0.2612 | |
DDB_G0284147 | DDB_G0284147 | DDB0232431 | CDS | 1532512 | 948 | - | 0.186709 | |
DDB_G0284149 | DDB_G0284149 | ortholog of yeast VID24 a peripheral membrane protein located at Vid (vacuole import and degradation) vesicles | DDB0232431 | CDS | 1533705 | 699 | - | 0.296137 |
DDB_G0284151 | DDB_G0284151 | DDB0232431 | CDS | 1536747 | 969 | + | 0.209494 | |
DDB_G0284153 | DDB_G0284153 | DDB0232431 | CDS | 1545923 | 1800 | - | 0.239444 | |
DDB_G0284155 | DDB_G0284155 | contains two PLDc domains has similarity to mammalian phospholipase D2 | DDB0232431 | CDS | 1561847 | 3390 | + | 0.270796 |
DDB_G0284157 | DDB_G0284157 | DDB0232431 | CDS | 1583322 | 3426 | + | 0.28955 | |
DDB_G0284161 | DDB_G0284161 | DDB0232431 | CDS | 1597279 | 312 | + | 0.275641 | |
DDB_G0284163 | DDB_G0284163 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon but the second exon is shorter | DDB0232431 | CDS | 1598186 | 192 | + | 0.322917 |
DDB_G0284165 | DDB_G0284165 | DDB0232431 | CDS | 1606151 | 186 | - | 0.263441 | |
DDB_G0284167 | DDB_G0284167 | DDB0232431 | CDS | 1610129 | 882 | - | 0.422902 | |
DDB_G0284169 | DDB_G0284169 | contains 3 predicted transmembrane domains and an additional putative signal sequence part of a larger gene family in D. discoideum also present in other dictyostelids | DDB0232431 | CDS | 1612603 | 621 | - | 0.322061 |
DDB_G0284173 | DDB_G0284173 | DDB0232431 | CDS | 1652572 | 786 | - | 0.198473 | |
DDB_G0284175 | DDB_G0284175 | similar to S. pombe mus81 in the 3' region also contains DNA polymerase B-like domain SAM domain and SWIM-type zinc finger domains | DDB0232431 | CDS | 1653717 | 2766 | + | 0.240781 |
DDB_G0284177 | DDB_G0284177 | DDB0232431 | CDS | 1658818 | 3171 | + | 0.268054 | |
DDB_G0284179 | DDB_G0284179 | DDB0232431 | CDS | 1643184 | 2079 | - | 0.132275 | |
DDB_G0284189 | DDB_G0284189 | DDB0232431 | CDS | 1669261 | 1044 | + | 0.288314 | |
DDB_G0284191 | DDB_G0284191 | DDB0232431 | CDS | 1670895 | 2205 | + | 0.307483 | |
DDB_G0284193 | DDB_G0284193 | DDB0232431 | CDS | 1673200 | 969 | + | 0.307534 | |
DDB_G0284195 | DDB_G0284195 | bCommunity annotation:b DDB_G0284195 is highly similar in the upstream half to cofactor of BRAC1 also known as COBRA1 which in mammals participates in a four-protein complex called NELF (negative elongation factor). NELF negatively regulates steroid-hormone induced gene regulation. Candidates for other components of the NELF complex are found in Dicty DDB_G0268678 is a clear NELF CD subunit DDB_G0286295 is a possible NELF A subunit DDB_G0276985 is a possible NELF RDBP subunit. Recent work shows that NELF participates in 3' end processing of histone mRNAs in association with the SLBP see Narita et al Mol. Cell 26 349-365 (2007).br DDB G0284195 is strongly (12-fold)overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (Doquang et al in preparation). Most genes with known roles in S-phase or mitosis are overexpressed in this strain. Several other proteins involved in histone mRNA processing are upregulated in the rblA disruptant these include DDB_G0 | DDB0232431 | CDS | 1676837 | 2565 | - | 0.283431 |
DDB_G0284199 | DDB_G0284199 | contains a predicted signal sequence similar to D. purpureum protein | DDB0232431 | CDS | 1682534 | 669 | - | 0.240658 |
DDB_G0284201 | DDB_G0284201 | very similar to RNA polymerase II transcription factor SIII subunit C elongin C or transcription elongation factor B polypeptide 1 (TCEB1) | DDB0232431 | CDS | 1684869 | 330 | + | 0.269697 |
DDB_G0284207 | DDB_G0284207 | DDB0232431 | CDS | 1688943 | 858 | + | 0.284382 | |
DDB_G0284209 | DDB_G0284209 | DDB0232431 | CDS | 1690478 | 876 | - | 0.280822 | |
DDB_G0284211_ps | DDB_G0284211 | putative pseudogene belonging to the short-chain dehydrogenasereductase (SDR) familybrbr bCommunity annotation:b probably a recent pseudogene of the short-chain dehydrogenase family including DDB0185894. The coding sequence share high level of homology with DDB0185894 before and after the stop codon resulting in a truncated and probably non functional protein if that gene is still transcribed. Christophe Anjard May 2007 | DDB0232431 | CDS | 1692886 | 738 | + | 0.298103 |
DDB_G0284213 | DDB_G0284213 | DDB0232431 | CDS | 1693957 | 2109 | - | 0.209578 | |
DDB_G0284217 | DDB_G0284217 | similar to H. sapiens CNOT7 and CNOT8 and S. cerevisiae POP2 which are components of the CCR4-NOT transcription complex | DDB0232431 | CDS | 1700271 | 1104 | - | 0.288043 |
DDB_G0284219 | DDB_G0284219 | member of the MAP65ASE1 family of microtubule associated proteins one of the the yeast homologs is an anaphase spindle elongation protein | DDB0232431 | CDS | 1702610 | 2298 | - | 0.222802 |
DDB_G0284223 | DDB_G0284223 | DDB0232431 | CDS | 1712491 | 1641 | - | 0.322364 | |
DDB_G0284227 | DDB_G0284227 | DDB0232431 | CDS | 1717119 | 4158 | + | 0.246513 | |
DDB_G0284229 | DDB_G0284229 | DDB0232431 | CDS | 1721453 | 222 | - | 0.297297 | |
DDB_G0284231 | DDB_G0284231 | DDB0232431 | CDS | 1721739 | 237 | - | 0.333333 | |
DDB_G0284233 | DDB_G0284233 | DDB0232431 | CDS | 1723068 | 186 | + | 0.333333 | |
DDB_G0284235 | DDB_G0284235 | DDB0232431 | CDS | 1723675 | 1296 | - | 0.206019 | |
DDB_G0284239 | DDB_G0284239 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 1731488 | 2031 | + | 0.356475 |
DDB_G0284241 | DDB_G0284241 | DDB0232431 | CDS | 1733961 | 1293 | + | 0.243619 | |
DDB_G0284243 | DDB_G0284243 | similar to yeast PTC1 type 2C protein phosphatase (PP2C) which is involved in mitochondrial inheritance tRNA splicing sporulation and cell separation | DDB0232431 | CDS | 1735866 | 1212 | - | 0.329208 |
DDB_G0284245 | DDB_G0284245 | contains a single N-terminal RRM domain which is similar to those in human splicing factors arginineserine-rich such as SFRS4 and SFRS6 however these proteins contain two N-terminal RRM domains | DDB0232431 | CDS | 1747466 | 1098 | - | 0.301457 |
DDB_G0284247 | DDB_G0284247 | DDB0232431 | CDS | 1749570 | 1854 | + | 0.228695 | |
DDB_G0284249 | DDB_G0284249 | putative metalloprotease of the peptidase M41 family which belong to a larger family of zinc metalloproteases includes the cell division protein FtsH and the yeast mitochondrial respiratory chain complexes assembly protein | DDB0232431 | CDS | 1751734 | 2295 | - | 0.31329 |
DDB_G0284251 | DDB_G0284251 | kinase domain similar to those of mitogen-activated protein kinases similar to the STE20 family | DDB0232431 | CDS | 1754346 | 1491 | - | 0.273642 |
DDB_G0284253 | DDB_G0284253 | similar to human EI24 (etoposide-induced protein 2.4 homolog) which may play a role in the cellular response to DNA damage andor p53-mediated apoptosis contains 6 putative transmembrane domains | DDB0232431 | CDS | 1758153 | 924 | - | 0.267316 |
DDB_G0284255 | DDB_G0284255 | DDB0232431 | CDS | 1777902 | 2874 | + | 0.292276 | |
DDB_G0284259 | DDB_G0284259 | DDB0232431 | CDS | 1787150 | 2724 | - | 0.335536 | |
DDB_G0284263 | DDB_G0284263 | conserved protein ortholog of human DNAJC11 | DDB0232431 | CDS | 1795281 | 1728 | - | 0.284144 |
DDB_G0284269 | DDB_G0284269 | DDB0232431 | CDS | 1803929 | 411 | + | 0.255474 | |
DDB_G0284271_ps | DDB_G0284271 | putative pseudogene fragment similar to EGF repeat-containing proteins | DDB0232431 | CDS | 1804849 | 915 | + | 0.257923 |
DDB_G0284273 | DDB_G0284273 | DDB0232431 | CDS | 1806777 | 1449 | + | 0.244997 | |
DDB_G0284275 | DDB_G0284275 | DDB0232431 | CDS | 1820423 | 1065 | + | 0.246948 | |
DDB_G0284277 | DDB_G0284277 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232431 | CDS | 1821556 | 870 | - | 0.314943 |
DDB_G0284279_ps | DDB_G0284279 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 1822941 | 3207 | - | 0.225444 |
DDB_G0284281 | DDB_G0284281 | DDB0232431 | CDS | 1827185 | 2940 | - | 0.25102 | |
DDB_G0284283 | DDB_G0284283 | DDB0232431 | CDS | 1832487 | 186 | + | 0.274194 | |
DDB_G0284285 | DDB_G0284285 | DDB0232431 | CDS | 1833130 | 396 | + | 0.282828 | |
DDB_G0284287 | DDB_G0284287 | DDB0232431 | CDS | 1834114 | 456 | - | 0.285088 | |
DDB_G0284289 | DDB_G0284289 | DDB0232431 | CDS | 1835474 | 2166 | - | 0.262696 | |
DDB_G0284303 | DDB_G0284303 | DDB0232431 | CDS | 1792427 | 423 | + | 0.248227 | |
DDB_G0284305_RTE | DDB_G0284305 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 1664505 | 1593 | + | 0.345888 |
DDB_G0284307 | DDB_G0284307 | conserved ortholog mammalian CAB39 (calcium-binding protein 39) and S. pombe Mo25 involved in cytokinesis | DDB0232431 | CDS | 1707062 | 1092 | + | 0.270147 |
DDB_G0284311 | DDB_G0284311 | DDB0232431 | CDS | 1711370 | 900 | + | 0.257778 | |
DDB_G0284315 | DDB_G0284315 | contains 6 putative transmembrane domains similar to D. purpureum protein | DDB0232431 | CDS | 1728697 | 930 | + | 0.329032 |
DDB_G0284321 | DDB_G0284321 | similar to PTBP1 PTB2 and ROD1 heterogeneous ribonucleoproteins that play a role in pre-mRNA splicing | DDB0232431 | CDS | 1760065 | 2679 | + | 0.267264 |
DDB_G0284325 | DDB_G0284325 | DDB0232431 | CDS | 1809449 | 2103 | + | 0.257252 | |
DDB_G0284337 | DDB_G0284337 | DDB0232431 | CDS | 1851676 | 3819 | + | 0.252946 | |
DDB_G0284343 | DDB_G0284343 | DDB0232431 | CDS | 1860277 | 1104 | - | 0.246377 | |
DDB_G0284351 | DDB_G0284351 | DDB0232431 | CDS | 1869385 | 735 | + | 0.287075 | |
DDB_G0284355 | DDB_G0284355 | DDB0232431 | CDS | 1873789 | 1908 | + | 0.208071 | |
DDB_G0284361 | DDB_G0284361 | DDB0232431 | CDS | 1888546 | 3129 | - | 0.270374 | |
DDB_G0284365 | DDB_G0284365 | DDB0232431 | CDS | 1895020 | 681 | + | 0.287812 | |
DDB_G0284367 | DDB_G0284367 | DDB0232431 | CDS | 1896160 | 816 | - | 0.313726 | |
DDB_G0284369 | DDB_G0284369 | DDB0232431 | CDS | 1898347 | 825 | - | 0.286061 | |
DDB_G0284371 | DDB_G0284371 | DDB0232431 | CDS | 1900513 | 825 | + | 0.266667 | |
DDB_G0284373 | DDB_G0284373 | DDB0232431 | CDS | 1901736 | 1089 | - | 0.240588 | |
DDB_G0284375 | DDB_G0284375 | DDB0232431 | CDS | 1905434 | 1059 | - | 0.266289 | |
DDB_G0284377 | DDB_G0284377 | DDB0232431 | CDS | 1910380 | 1563 | + | 0.213052 | |
DDB_G0284381 | DDB_G0284381 | DDB0232431 | CDS | 1916862 | 3270 | + | 0.307951 | |
DDB_G0284383 | DDB_G0284383 | DDB0232431 | CDS | 1920700 | 2409 | + | 0.288501 | |
DDB_G0284387 | DDB_G0284387 | DDB0232431 | CDS | 1929000 | 3231 | + | 0.263076 | |
DDB_G0284391 | DDB_G0284391 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232431 | CDS | 1935986 | 1761 | - | 0.27314 |
DDB_G0284393 | DDB_G0284393 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232431 | CDS | 1939162 | 1533 | - | 0.296804 |
DDB_G0284395 | DDB_G0284395 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232431 | CDS | 1942017 | 1614 | - | 0.296778 |
DDB_G0284397 | DDB_G0284397 | DDB0232431 | CDS | 1944417 | 381 | - | 0.333333 | |
DDB_G0284401 | DDB_G0284401 | conserved hypothetical Dictyostelium protein similar to bacterial ubiquinonemenaquinone biosynthesis methyltransferase ubiE | DDB0232431 | CDS | 1952708 | 879 | - | 0.287827 |
DDB_G0284413 | DDB_G0284413 | DDB0232431 | CDS | 1967001 | 483 | + | 0.300207 | |
DDB_G0284423 | DDB_G0284423 | DDB0232431 | CDS | 1976888 | 1080 | + | 0.201852 | |
DDB_G0284425 | DDB_G0284425 | DDB0232431 | CDS | 1978561 | 240 | + | 0.216667 | |
DDB_G0284427 | DDB_G0284427 | DDB0232431 | CDS | 1979111 | 1335 | - | 0.222472 | |
DDB_G0284429 | DDB_G0284429 | DDB0232431 | CDS | 1981059 | 864 | - | 0.261574 | |
DDB_G0284433 | DDB_G0284433 | DDB0232431 | CDS | 1985042 | 960 | + | 0.3375 | |
DDB_G0284437 | DDB_G0284437 | DDB0232431 | CDS | 1993267 | 987 | + | 0.233029 | |
DDB_G0284439 | DDB_G0284439 | DDB0232431 | CDS | 1994656 | 2079 | + | 0.259259 | |
DDB_G0284441 | DDB_G0284441 | DDB0232431 | CDS | 1997677 | 2505 | - | 0.264271 | |
DDB_G0284443 | DDB_G0284443 | DDB0232431 | CDS | 1858931 | 864 | + | 0.252315 | |
DDB_G0284445_RTE | DDB_G0284445 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 1878838 | 678 | - | 0.340708 |
DDB_G0284451_ps | DDB_G0284451 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 1880019 | 318 | + | 0.251572 |
DDB_G0284453 | DDB_G0284453 | DDB0232431 | CDS | 1903726 | 1056 | - | 0.251894 | |
DDB_G0284455 | DDB_G0284455 | DDB0232431 | CDS | 1906991 | 1917 | - | 0.245696 | |
DDB_G0284457 | DDB_G0284457 | DDB0232431 | CDS | 1974366 | 1104 | + | 0.241848 | |
DDB_G0284459 | DDB_G0284459 | DDB0232431 | CDS | 1986677 | 3675 | + | 0.32 | |
DDB_G0284461 | DDB_G0284461 | DDB0232431 | CDS | 2003252 | 1872 | - | 0.277778 | |
DDB_G0284475 | DDB_G0284475 | DDB0232431 | CDS | 2010250 | 7515 | - | 0.242182 | |
DDB_G0284477 | DDB_G0284477 | DDB0232431 | CDS | 2018714 | 3138 | + | 0.197259 | |
DDB_G0284479 | DDB_G0284479 | DDB0232431 | CDS | 2022587 | 780 | + | 0.346154 | |
DDB_G0284481 | DDB_G0284481 | DDB0232431 | CDS | 2027462 | 3087 | + | 0.288306 | |
DDB_G0284485 | DDB_G0284485 | DDB0232431 | CDS | 2034779 | 846 | - | 0.321513 | |
DDB_G0284487 | DDB_G0284487 | DDB0232431 | CDS | 2036413 | 1587 | + | 0.221172 | |
DDB_G0284491 | DDB_G0284491 | DDB0232431 | CDS | 2041403 | 3639 | - | 0.233855 | |
DDB_G0284493 | DDB_G0284493 | DDB0232431 | CDS | 2045896 | 1209 | + | 0.287014 | |
DDB_G0284497 | DDB_G0284497 | DDB0232431 | CDS | 2050510 | 615 | + | 0.294309 | |
DDB_G0284507 | DDB_G0284507 | putative ortholog of Rad51C which is involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks interacts with XRCC3 | DDB0232431 | CDS | 2070281 | 1146 | - | 0.233857 |
DDB_G0284511 | DDB_G0284511 | DDB0232431 | CDS | 2077506 | 798 | + | 0.29198 | |
DDB_G0284513 | DDB_G0284513 | DDB0232431 | CDS | 2079840 | 4377 | + | 0.275303 | |
DDB_G0284515 | DDB_G0284515 | DDB0232431 | CDS | 2085226 | 1506 | + | 0.241036 | |
DDB_G0284521 | DDB_G0284521 | DDB0232431 | CDS | 2100599 | 771 | - | 0.212711 | |
DDB_G0284523 | DDB_G0284523 | DDB0232431 | CDS | 2102761 | 813 | + | 0.228782 | |
DDB_G0284527 | DDB_G0284527 | DDB0232431 | CDS | 2115024 | 1488 | - | 0.296371 | |
DDB_G0284529 | DDB_G0284529 | DDB0232431 | CDS | 2118136 | 1485 | - | 0.303704 | |
DDB_G0284531 | DDB_G0284531 | DDB0232431 | CDS | 2120826 | 612 | - | 0.254902 | |
DDB_G0284537 | DDB_G0284537 | DDB0232431 | CDS | 2139831 | 906 | - | 0.291391 | |
DDB_G0284539 | DDB_G0284539 | DDB0232431 | CDS | 2152696 | 2997 | - | 0.242576 | |
DDB_G0284541 | DDB_G0284541 | DDB0232431 | CDS | 2025823 | 645 | + | 0.311628 | |
DDB_G0284547 | DDB_G0284547 | DDB0232431 | CDS | 2008237 | 219 | + | 0.255708 | |
DDB_G0284557 | DDB_G0284557 | catalyzes the reaction ATP D-gluconate ADP 6-phospho-D-gluconate | DDB0232431 | CDS | 2110678 | 603 | + | 0.238806 |
DDB_G0284559 | DDB_G0284559 | DDB0232431 | CDS | 2123220 | 1281 | + | 0.238095 | |
DDB_G0284561 | DDB_G0284561 | DDB0232431 | CDS | 2131768 | 2949 | + | 0.232282 | |
DDB_G0284565 | DDB_G0284565 | DDB0232431 | CDS | 2142583 | 4788 | - | 0.267126 | |
DDB_G0284569 | DDB_G0284569 | DDB0232431 | CDS | 2167100 | 2379 | + | 0.226566 | |
DDB_G0284575 | DDB_G0284575 | DDB0232431 | CDS | 2173651 | 1815 | - | 0.344353 | |
DDB_G0284577 | DDB_G0284577 | putative ortholog of H. sapiens CNOT2 and S. cerevisiae CDC36 component of the CCR4-NOT transcription complex | DDB0232431 | CDS | 2176004 | 1740 | - | 0.281034 |
DDB_G0284579 | DDB_G0284579 | DDB0232431 | CDS | 2163129 | 2295 | + | 0.334641 | |
DDB_G0284581 | DDB_G0284581 | DDB0232431 | CDS | 2180042 | 993 | + | 0.193353 | |
DDB_G0284587 | DDB_G0284587 | DDB0232431 | CDS | 2187151 | 1236 | + | 0.231392 | |
DDB_G0284591 | DDB_G0284591 | DDB0232431 | CDS | 2189321 | 3669 | - | 0.270373 | |
DDB_G0284599 | DDB_G0284599 | DDB0232431 | CDS | 2207693 | 1551 | + | 0.320438 | |
DDB_G0284603 | DDB_G0284603 | DDB0232431 | CDS | 2211789 | 1413 | + | 0.208068 | |
DDB_G0284605 | DDB_G0284605 | conserved plasma membrane calcium ATPases (PMCA) similar to Dictyostelium PAT1 contains 10 predicted transmembrane domains | DDB0232431 | CDS | 2214347 | 2784 | + | 0.354526 |
DDB_G0284609_RTE | DDB_G0284609 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 2220278 | 589 | + | 0.271647 |
DDB_G0284615 | DDB_G0284615 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232431 | CDS | 2228341 | 4296 | + | 0.233939 |
DDB_G0284617 | DDB_G0284617 | contains a weak RimK-like ATP-grasp domain which is found in the ribosomal S6 modification enzyme RimK | DDB0232431 | CDS | 2233409 | 1455 | - | 0.236426 |
DDB_G0284619 | DDB_G0284619 | DDB0232431 | CDS | 2237635 | 762 | - | 0.362205 | |
DDB_G0284623 | DDB_G0284623 | DDB0232431 | CDS | 2255880 | 219 | - | 0.305936 | |
DDB_G0284625 | DDB_G0284625 | conserved hypothetical Dictyostelium protein contains one EGF-like type 3 domain | DDB0232431 | CDS | 2257074 | 2667 | - | 0.241095 |
DDB_G0284627 | DDB_G0284627 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains an N-terminal transmembrane domain that might be a signal sequence | DDB0232431 | CDS | 2260399 | 1161 | - | 0.274763 |
DDB_G0284629 | DDB_G0284629 | conserved in Dictyostelids predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) there is a highly similar gene | DDB0232431 | CDS | 2262832 | 339 | + | 0.309735 |
DDB_G0284631 | DDB_G0284631 | conserved in Dictyostelids predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) there is a highly similar gene | DDB0232431 | CDS | 2263474 | 339 | - | 0.306785 |
DDB_G0284633 | DDB_G0284633 | DDB0232431 | CDS | 2264683 | 2184 | + | 0.277473 | |
DDB_G0284635 | DDB_G0284635 | DDB0232431 | CDS | 2267233 | 216 | - | 0.199074 | |
DDB_G0284637 | DDB_G0284637 | DDB0232431 | CDS | 2269967 | 1653 | + | 0.242589 | |
DDB_G0284639_ps | DDB_G0284639 | putative pseudogene nearly identical to the upstream | DDB0232431 | CDS | 2272052 | 1353 | + | 0.24612 |
DDB_G0284641 | DDB_G0284641 | DDB0232431 | CDS | 2274398 | 315 | + | 0.253968 | |
DDB_G0284643 | DDB_G0284643 | DDB0232431 | CDS | 2279720 | 1158 | + | 0.289292 | |
DDB_G0284645 | DDB_G0284645 | DDB0232431 | CDS | 2281332 | 651 | - | 0.394777 | |
DDB_G0284649 | DDB_G0284649 | DDB0232431 | CDS | 2287653 | 2103 | - | 0.258678 | |
DDB_G0284655_ps | DDB_G0284655 | putative pseudogene similar to the large D. discoideum family of FNIP repeat-containing proteins | DDB0232431 | CDS | 2294408 | 1284 | + | 0.288162 |
DDB_G0284657 | DDB_G0284657 | DDB0232431 | CDS | 2303787 | 2301 | + | 0.281617 | |
DDB_G0284661 | DDB_G0284661 | putative protein serinethreonine kinase CAMK group kinase domain similar to mammalian CAM kinase I | DDB0232431 | CDS | 2309177 | 1446 | - | 0.304288 |
DDB_G0284665 | DDB_G0284665 | DDB0232431 | CDS | 2318999 | 171 | - | 0.269006 | |
DDB_G0284671 | DDB_G0284671 | DDB0232431 | CDS | 2323961 | 918 | + | 0.401961 | |
DDB_G0284673_ps | DDB_G0284673 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 2325423 | 180 | - | 0.288889 |
DDB_G0284675 | DDB_G0284675 | DDB0232431 | CDS | 2326080 | 945 | - | 0.27619 | |
DDB_G0284679 | DDB_G0284679 | DDB0232431 | CDS | 2333236 | 1221 | - | 0.30303 | |
DDB_G0284681 | DDB_G0284681 | contains 2 SCP2 (sterol carrier protein) domains contains a predicted peroxisomal targeting signal | DDB0232431 | CDS | 2334842 | 735 | + | 0.327891 |
DDB_G0284683 | DDB_G0284683 | DDB0232431 | CDS | 2336209 | 2649 | - | 0.286523 | |
DDB_G0284687 | DDB_G0284687 | similar to protozoan and bacterial cardiolipin synthetases contains two PLDc domains | DDB0232431 | CDS | 2343826 | 1818 | + | 0.264026 |
DDB_G0284689 | DDB_G0284689 | DDB0232431 | CDS | 2350414 | 5040 | + | 0.22996 | |
DDB_G0284691 | DDB_G0284691 | DDB0232431 | CDS | 2357079 | 867 | + | 0.283737 | |
DDB_G0284693 | DDB_G0284693 | homolog of human COX6B1 and S. cerevisiae COX12 this protein is one of the polypeptide chains of cytochrome c oxidase the terminal oxidase in mitochondrial electron transport | DDB0232431 | CDS | 2358649 | 237 | - | 0.383966 |
DDB_G0284695 | DDB_G0284695 | DDB0232431 | CDS | 2359622 | 1353 | - | 0.27864 | |
DDB_G0284701 | DDB_G0284701 | DDB0232431 | CDS | 2371416 | 1314 | - | 0.269406 | |
DDB_G0284705 | DDB_G0284705 | DDB0232431 | CDS | 2378839 | 1305 | - | 0.308812 | |
DDB_G0284707 | DDB_G0284707 | belongs to a gene family conserved in amoeba similar to bacterial pentalenene synthase contains a putative metal-binding domain | DDB0232431 | CDS | 2388566 | 1086 | + | 0.325967 |
DDB_G0284721 | DDB_G0284721 | DDB0232431 | CDS | 2252387 | 2274 | + | 0.284081 | |
DDB_G0284727 | DDB_G0284727 | DDB0232431 | CDS | 2313169 | 2424 | + | 0.288779 | |
DDB_G0284731 | DDB_G0284731 | DDB0232431 | CDS | 2380797 | 1413 | + | 0.242746 | |
DDB_G0284733_TE | DDB_G0284733 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232431 | CDS | 2390943 | 231 | - | 0.277056 |
DDB_G0284737 | DDB_G0284737 | belongs to the haloacid dehalogenase (HAD) hydrolase IIA family similar to human PGP (phosphoglycolate phosphatase) and S. cerevisiae PHO13 (4-nitrophenylphosphatase) | DDB0232431 | CDS | 2397942 | 912 | - | 0.27193 |
DDB_G0284741 | DDB_G0284741 | DDB0232431 | CDS | 2402392 | 4188 | - | 0.298472 | |
DDB_G0284749 | DDB_G0284749 | DDB0232431 | CDS | 2426750 | 3780 | - | 0.234921 | |
DDB_G0284751 | DDB_G0284751 | DDB0232431 | CDS | 2431735 | 1161 | + | 0.228252 | |
DDB_G0284753 | DDB_G0284753 | DDB0232431 | CDS | 2432933 | 1395 | - | 0.276703 | |
DDB_G0284755 | DDB_G0284755 | DDB0232431 | CDS | 2435039 | 1422 | - | 0.262307 | |
DDB_G0284757 | DDB_G0284757 | related to the Ovarian Tumour (OTU) gene of Drosophila function is unknown but conserved cysteine and histidine and possibly the aspartate residues suggests that those not yet recognized as peptidases could possess cysteine protease activity | DDB0232431 | CDS | 2437158 | 2301 | - | 0.303346 |
DDB_G0284763 | DDB_G0284763 | DDB0232431 | CDS | 2448744 | 1185 | - | 0.31308 | |
DDB_G0284765 | DDB_G0284765 | contains a predicted signal peptide there are two similar genes in D. discoideum | DDB0232431 | CDS | 2450678 | 615 | - | 0.273171 |
DDB_G0284767 | DDB_G0284767 | weakly related to ABC transporters does not have transmembrane domains | DDB0232431 | CDS | 2452498 | 2274 | + | 0.228672 |
DDB_G0284773 | DDB_G0284773 | DDB0232431 | CDS | 2467019 | 1581 | + | 0.354839 | |
DDB_G0284777 | DDB_G0284777 | DDB0232431 | CDS | 2472579 | 963 | + | 0.303219 | |
DDB_G0284779 | DDB_G0284779 | DDB0232431 | CDS | 2475500 | 1680 | - | 0.255952 | |
DDB_G0284781 | DDB_G0284781 | DDB0232431 | CDS | 2477533 | 363 | - | 0.22314 | |
DDB_G0284783 | DDB_G0284783 | contains a glutamine-rich region similar to D. purpureum protein | DDB0232431 | CDS | 2479165 | 1812 | + | 0.175497 |
DDB_G0284787 | DDB_G0284787 | DDB0232431 | CDS | 2483195 | 261 | - | 0.218391 | |
DDB_G0284789_ps | DDB_G0284789 | putative pseudogene similar to gene | DDB0232431 | CDS | 2483989 | 1734 | + | 0.258362 |
DDB_G0284793 | DDB_G0284793 | belongs to the PLAC8 family (placenta-specific gene 8 protein) a family of cysteine-rich proteins with highly divergent low complexity amino terminal regions | DDB0232431 | CDS | 2488840 | 330 | - | 0.360606 |
DDB_G0284797_ps | DDB_G0284797 | putative pseudogene similar to | DDB0232431 | CDS | 2492140 | 309 | + | 0.281553 |
DDB_G0284801 | DDB_G0284801 | DDB0232431 | CDS | 2499782 | 600 | + | 0.263333 | |
DDB_G0284805 | DDB_G0284805 | DDB0232431 | CDS | 2500893 | 777 | - | 0.28314 | |
DDB_G0284807 | DDB_G0284807 | DDB0232431 | CDS | 2501891 | 2979 | - | 0.288016 | |
DDB_G0284811 | DDB_G0284811 | DDB0232431 | CDS | 2507767 | 882 | + | 0.31746 | |
DDB_G0284813 | DDB_G0284813 | DDB0232431 | CDS | 2508788 | 258 | - | 0.29845 | |
DDB_G0284815 | DDB_G0284815 | DDB0232431 | CDS | 2517388 | 903 | + | 0.172757 | |
DDB_G0284817 | DDB_G0284817 | DDB0232431 | CDS | 2518687 | 1641 | - | 0.311395 | |
DDB_G0284819 | DDB_G0284819 | DDB0232431 | CDS | 2520967 | 1002 | - | 0.243513 | |
DDB_G0284821 | DDB_G0284821 | DDB0232431 | CDS | 2523362 | 1245 | + | 0.258635 | |
DDB_G0284823 | DDB_G0284823 | DDB0232431 | CDS | 2525345 | 225 | + | 0.377778 | |
DDB_G0284825 | DDB_G0284825 | weakly similar to H. sapiens GARNL1 a RanGAP | DDB0232431 | CDS | 2526025 | 4923 | - | 0.299005 |
DDB_G0284829_TE | DDB_G0284829 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232431 | CDS | 2392075 | 1335 | - | 0.297378 |
DDB_G0284841 | DDB_G0284841 | DDB0232431 | CDS | 2510140 | 2640 | + | 0.273106 | |
DDB_G0284843 | DDB_G0284843 | DDB0232431 | CDS | 2515068 | 729 | + | 0.198903 | |
DDB_G0284847 | DDB_G0284847 | homolog of human SDF2 (stromal cell-derived factor 2) contains 3 MIR domains | DDB0232431 | CDS | 2556090 | 639 | - | 0.317684 |
DDB_G0284849 | DDB_G0284849 | DDB0232431 | CDS | 2557758 | 3561 | + | 0.298512 | |
DDB_G0284853 | DDB_G0284853 | large protein that has similarity to mammalian MYC binding protein 2 (MYCBP2) a putative E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins. | DDB0232431 | CDS | 2532768 | 12495 | + | 0.265146 |
DDB_G0284855 | DDB_G0284855 | DDB0232431 | CDS | 2546123 | 984 | + | 0.300813 | |
DDB_G0284871 | DDB_G0284871 | DDB0232431 | CDS | 2772764 | 1395 | - | 0.321147 | |
DDB_G0284873_RTE | DDB_G0284873 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 2562666 | 423 | - | 0.267139 |
DDB_G0284875 | DDB_G0284875 | DDB0232431 | CDS | 2563672 | 336 | + | 0.366071 | |
DDB_G0284881 | DDB_G0284881 | DDB0232431 | CDS | 2585806 | 612 | + | 0.26634 | |
DDB_G0284885 | DDB_G0284885 | DDB0232431 | CDS | 2588526 | 1503 | - | 0.208916 | |
DDB_G0284887 | DDB_G0284887 | DDB0232431 | CDS | 2599094 | 1245 | - | 0.254618 | |
DDB_G0284889 | DDB_G0284889 | DDB0232431 | CDS | 2600817 | 1215 | - | 0.25679 | |
DDB_G0284893 | DDB_G0284893 | DDB0232431 | CDS | 2604439 | 1080 | - | 0.235185 | |
DDB_G0284895 | DDB_G0284895 | contains an N-terminal SCP domain that occurs in prokaryotic and eukaryotic proteins proposed to be Ca chelating serine proteases also contains two C-terminal WSC domains which are putative carbohydrate binding domains | DDB0232431 | CDS | 2608632 | 2283 | + | 0.297854 |
DDB_G0284899 | DDB_G0284899 | DDB0232431 | CDS | 2613921 | 2838 | + | 0.231501 | |
DDB_G0284901 | DDB_G0284901 | similar to human ISOC2 (isochorismatase domain-containing protein 2 mitochondrial) contains a predicted peroxisomal targeting signal | DDB0232431 | CDS | 2617131 | 621 | - | 0.251208 |
DDB_G0284907 | DDB_G0284907 | DDB0232431 | CDS | 2626851 | 288 | - | 0.277778 | |
DDB_G0284909 | DDB_G0284909 | DDB0232431 | CDS | 2628238 | 1014 | + | 0.204142 | |
DDB_G0284913 | DDB_G0284913 | DDB0232431 | CDS | 2638616 | 4407 | + | 0.276152 | |
DDB_G0284915 | DDB_G0284915 | DDB0232431 | CDS | 2643291 | 696 | - | 0.310345 | |
DDB_G0284917 | DDB_G0284917 | DDB0232431 | CDS | 2644494 | 1533 | - | 0.305936 | |
DDB_G0284919 | DDB_G0284919 | similar to human DHRSX (dehydrogenasereductase SDR family member on chromosome X) and retinol dehydrogenase | DDB0232431 | CDS | 2646442 | 990 | - | 0.233333 |
DDB_G0284921 | DDB_G0284921 | DDB0232431 | CDS | 2648206 | 1515 | + | 0.307591 | |
DDB_G0284925 | DDB_G0284925 | this is one of four almost identical genes on C4 ( | DDB0232431 | CDS | 2654790 | 180 | - | 0.427778 |
DDB_G0284927 | DDB_G0284927 | this is one of four almost identical genes on C4 ( | DDB0232431 | CDS | 2652917 | 180 | - | 0.438889 |
DDB_G0284929 | DDB_G0284929 | DDB0232431 | CDS | 2657638 | 249 | + | 0.293173 | |
DDB_G0284931 | DDB_G0284931 | this is one of four almost identical genes on C4 ( | DDB0232431 | CDS | 2659079 | 174 | + | 0.431034 |
DDB_G0284933 | DDB_G0284933 | DDB0232431 | CDS | 2659670 | 3552 | - | 0.169482 | |
DDB_G0284935 | DDB_G0284935 | DDB0232431 | CDS | 2664011 | 1068 | + | 0.277154 | |
DDB_G0284937 | DDB_G0284937 | DDB0232431 | CDS | 2665360 | 1026 | + | 0.287524 | |
DDB_G0284939 | DDB_G0284939 | DDB0232431 | CDS | 2667885 | 396 | + | 0.282828 | |
DDB_G0284941 | DDB_G0284941 | DDB0232431 | CDS | 2668956 | 381 | + | 0.230971 | |
DDB_G0284943 | DDB_G0284943 | DDB0232431 | CDS | 2669585 | 2082 | - | 0.267531 | |
DDB_G0284949 | DDB_G0284949 | DDB0232431 | CDS | 2677540 | 132 | - | 0.310606 | |
DDB_G0284955 | DDB_G0284955 | DDB0232431 | CDS | 2684549 | 4602 | - | 0.27488 | |
DDB_G0284957 | DDB_G0284957 | DDB0232431 | CDS | 2694222 | 2280 | + | 0.249561 | |
DDB_G0284959 | DDB_G0284959 | ortholog of the conserved OPA3 in H. sapiens defects in OPA3 cause type III 3-methylglutaconic aciduria (MGA type III) also known as optic atrophy plus syndrome | DDB0232431 | CDS | 2698477 | 600 | + | 0.261667 |
DDB_G0284961 | DDB_G0284961 | DDB0232431 | CDS | 2699345 | 534 | - | 0.269663 | |
DDB_G0284963 | DDB_G0284963 | DDB0232431 | CDS | 2700406 | 1275 | + | 0.31451 | |
DDB_G0284965 | DDB_G0284965 | DDB0232431 | CDS | 2702978 | 852 | - | 0.219484 | |
DDB_G0284967 | DDB_G0284967 | DDB0232431 | CDS | 2704245 | 2547 | - | 0.206517 | |
DDB_G0284969 | DDB_G0284969 | DDB0232431 | CDS | 2719814 | 1764 | + | 0.272676 | |
DDB_G0284971 | DDB_G0284971 | DDB0232431 | CDS | 2726690 | 1029 | + | 0.199223 | |
DDB_G0284973 | DDB_G0284973 | DDB0232431 | CDS | 2731379 | 3468 | + | 0.238178 | |
DDB_G0284977 | DDB_G0284977 | DDB0232431 | CDS | 2738670 | 4227 | - | 0.287674 | |
DDB_G0284979 | DDB_G0284979 | DDB0232431 | CDS | 2743512 | 768 | - | 0.33724 | |
DDB_G0284981 | DDB_G0284981 | DDB0232431 | CDS | 2745658 | 1356 | + | 0.30826 | |
DDB_G0284991 | DDB_G0284991 | DDB0232431 | CDS | 2778336 | 3282 | + | 0.241316 | |
DDB_G0284993 | DDB_G0284993 | DDB0232431 | CDS | 2782082 | 129 | - | 0.209302 | |
DDB_G0284995 | DDB_G0284995 | DDB0232431 | CDS | 2782622 | 873 | + | 0.252005 | |
DDB_G0284997 | DDB_G0284997 | DDB0232431 | CDS | 2784039 | 1125 | - | 0.315556 | |
DDB_G0284999 | DDB_G0284999 | DDB0232431 | CDS | 2786060 | 834 | - | 0.306954 | |
DDB_G0285001 | DDB_G0285001 | DDB0232431 | CDS | 2788466 | 1755 | + | 0.249573 | |
DDB_G0285011 | DDB_G0285011 | similar to the fungi mitochondrial transferase caf17 a mitochondrial matrix protein involved in the incorporation of iron-sulfur clusters into mitochondrial aconitase-type proteins | DDB0232431 | CDS | 2814046 | 1227 | - | 0.295029 |
DDB_G0285013 | DDB_G0285013 | DDB0232431 | CDS | 2820652 | 915 | + | 0.253552 | |
DDB_G0285015_ps | DDB_G0285015 | putative pseudogene similar to a Dictyostelium family of genes including | DDB0232431 | CDS | 2822210 | 1053 | - | 0.185185 |
DDB_G0285019 | DDB_G0285019 | DDB0232431 | CDS | 2823631 | 3486 | - | 0.240964 | |
DDB_G0285021 | DDB_G0285021 | belongs to the complex I LYR family similar to human NDUFB9 (NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9) | DDB0232431 | CDS | 2830332 | 321 | - | 0.323988 |
DDB_G0285031 | DDB_G0285031 | DDB0232431 | CDS | 2836987 | 2388 | - | 0.215662 | |
DDB_G0285033 | DDB_G0285033 | belongs to the short-chain dehydrogenasereductase family | DDB0232431 | CDS | 2839925 | 786 | + | 0.307888 |
DDB_G0285035_RTE | DDB_G0285035 | DDB0232431 | CDS | 2841164 | 327 | + | 0.296636 | |
DDB_G0285037 | DDB_G0285037 | DDB0232431 | CDS | 2566569 | 183 | - | 0.262295 | |
DDB_G0285041 | DDB_G0285041 | similar to human ISOC2 (isochorismatase domain-containing protein 2 mitochondrial) contains a predicted peroxisomal targeting signal | DDB0232431 | CDS | 2620294 | 621 | - | 0.243156 |
DDB_G0285043 | DDB_G0285043 | this is one of four almost identical genes on C4 ( | DDB0232431 | CDS | 2656766 | 180 | + | 0.438889 |
DDB_G0285045 | DDB_G0285045 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232431 | CDS | 2573154 | 4140 | - | 0.257005 |
DDB_G0285047 | DDB_G0285047 | DDB0232431 | CDS | 2593257 | 1263 | - | 0.176564 | |
DDB_G0285049 | DDB_G0285049 | DDB0232431 | CDS | 2595117 | 1113 | - | 0.209344 | |
DDB_G0285055 | DDB_G0285055 | DDB0232431 | CDS | 2631798 | 5796 | - | 0.285714 | |
DDB_G0285057 | DDB_G0285057 | DDB0232431 | CDS | 2666993 | 516 | - | 0.261628 | |
DDB_G0285059 | DDB_G0285059 | DDB0232431 | CDS | 2696768 | 1104 | - | 0.181159 | |
DDB_G0285063 | DDB_G0285063 | similar to the H. sapiens HUWE1 an E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins. | DDB0232431 | CDS | 2707152 | 11379 | - | 0.321997 |
DDB_G0285065 | DDB_G0285065 | DDB0232431 | CDS | 2722034 | 1590 | - | 0.272956 | |
DDB_G0285073 | DDB_G0285073 | putative VPS9 ortholog a guanine nucleotide exchange factor involved in vesicle-mediated vacuolar protein transport | DDB0232431 | CDS | 2758636 | 2181 | + | 0.24851 |
DDB_G0285075_ps | DDB_G0285075 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 2776760 | 990 | + | 0.194949 |
DDB_G0285079 | DDB_G0285079 | DDB0232431 | CDS | 2802048 | 603 | + | 0.296849 | |
DDB_G0285081 | DDB_G0285081 | DDB0232431 | CDS | 2808780 | 4416 | + | 0.248188 | |
DDB_G0285083 | DDB_G0285083 | DDB0232431 | CDS | 2815942 | 3063 | + | 0.264447 | |
DDB_G0285085_ps | DDB_G0285085 | putative pseudogene fragment similar to | DDB0232431 | CDS | 2820125 | 1068 | + | 0.243446 |
DDB_G0285087 | DDB_G0285087 | DDB0232431 | CDS | 2827341 | 2205 | - | 0.177778 | |
DDB_G0285089_RTE | DDB_G0285089 | DDB0232431 | CDS | 2841636 | 2991 | + | 0.336342 | |
DDB_G0285091_RTE | DDB_G0285091 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232431 | CDS | 2847730 | 216 | - | 0.277778 |
DDB_G0285093 | DDB_G0285093 | DDB0232431 | CDS | 2568202 | 2958 | - | 0.23428 | |
DDB_G0285095 | DDB_G0285095 | DDB0232431 | CDS | 2804851 | 792 | - | 0.306818 | |
DDB_G0285097_RTE | DDB_G0285097 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 2848300 | 1119 | + | 0.341376 |
DDB_G0285103 | DDB_G0285103 | DDB0232431 | CDS | 2851187 | 816 | + | 0.253676 | |
DDB_G0285107 | DDB_G0285107 | DDB0232431 | CDS | 2855138 | 492 | + | 0.296748 | |
DDB_G0285109 | DDB_G0285109 | DDB0232431 | CDS | 2862240 | 975 | - | 0.25641 | |
DDB_G0285113 | DDB_G0285113 | similar to human MUDENG (MHD domain-containing death-inducing protein) which induces cell death in cytotoxic T-cells contains one MHD domain (mu homology domain) | DDB0232431 | CDS | 2865898 | 1758 | + | 0.30603 |
DDB_G0285115 | DDB_G0285115 | DDB0232431 | CDS | 2872325 | 639 | + | 0.219092 | |
DDB_G0285119 | DDB_G0285119 | DDB0232431 | CDS | 2877924 | 1566 | + | 0.275862 | |
DDB_G0285121 | DDB_G0285121 | DDB0232431 | CDS | 2881701 | 297 | + | 0.228956 | |
DDB_G0285123 | DDB_G0285123 | DDB0232431 | CDS | 2882150 | 2220 | + | 0.215315 | |
DDB_G0285125 | DDB_G0285125 | DDB0232431 | CDS | 2884598 | 1623 | - | 0.23167 | |
DDB_G0285127 | DDB_G0285127 | DDB0232431 | CDS | 2886739 | 1101 | - | 0.217984 | |
DDB_G0285129 | DDB_G0285129 | DDB0232431 | CDS | 2894961 | 792 | + | 0.257576 | |
DDB_G0285135 | DDB_G0285135 | DDB0232431 | CDS | 2903243 | 660 | - | 0.234848 | |
DDB_G0285143 | DDB_G0285143 | similar to | DDB0232431 | CDS | 2913006 | 1356 | - | 0.272861 |
DDB_G0285145 | DDB_G0285145 | DDB0232431 | CDS | 2915991 | 1305 | + | 0.2659 | |
DDB_G0285149 | DDB_G0285149 | similar to mammalian TNF receptor-associated factors 5 and 6 (TRAF5 TRAF6) | DDB0232431 | CDS | 2888446 | 1284 | - | 0.288162 |
DDB_G0285151 | DDB_G0285151 | DDB0232431 | CDS | 2868305 | 597 | + | 0.293132 | |
DDB_G0285153 | DDB_G0285153 | DDB0232431 | CDS | 2869433 | 939 | + | 0.234292 | |
DDB_G0285155 | DDB_G0285155 | DDB0232431 | CDS | 2891853 | 2406 | - | 0.190357 | |
DDB_G0285157 | DDB_G0285157 | DDB0232431 | CDS | 2898787 | 315 | + | 0.244444 | |
DDB_G0285167 | DDB_G0285167 | DDB0232431 | CDS | 2919389 | 975 | + | 0.222564 | |
DDB_G0285169 | DDB_G0285169 | DDB0232431 | CDS | 2928529 | 2820 | - | 0.197163 | |
DDB_G0285171_ps | DDB_G0285171 | putative pseudogene highly similar to | DDB0232431 | CDS | 2932277 | 516 | + | 0.300388 |
DDB_G0285173 | DDB_G0285173 | DDB0232431 | CDS | 2933402 | 2742 | - | 0.20496 | |
DDB_G0285177 | DDB_G0285177 | DDB0232431 | CDS | 2939040 | 1395 | - | 0.247312 | |
DDB_G0285179 | DDB_G0285179 | DDB0232431 | CDS | 2954586 | 918 | + | 0.27342 | |
DDB_G0285181 | DDB_G0285181 | DDB0232431 | CDS | 2955670 | 414 | - | 0.198068 | |
DDB_G0285183 | DDB_G0285183 | DDB0232431 | CDS | 2957139 | 3534 | + | 0.276174 | |
DDB_G0285185 | DDB_G0285185 | DDB0232431 | CDS | 2960975 | 993 | + | 0.233635 | |
DDB_G0285187 | DDB_G0285187 | DDB0232431 | CDS | 2962656 | 141 | - | 0.375887 | |
DDB_G0285189 | DDB_G0285189 | DDB0232431 | CDS | 2964201 | 462 | - | 0.264069 | |
DDB_G0285191 | DDB_G0285191 | DDB0232431 | CDS | 2965339 | 1785 | - | 0.317647 | |
DDB_G0285201 | DDB_G0285201 | DDB0232431 | CDS | 2968644 | 2385 | - | 0.255765 | |
DDB_G0285203 | DDB_G0285203 | DDB0232431 | CDS | 2941521 | 195 | + | 0.317949 | |
DDB_G0285207_ps | DDB_G0285207 | putative pseudogene highly similar to | DDB0232431 | CDS | 2927541 | 498 | + | 0.297189 |
DDB_G0285209 | DDB_G0285209 | DDB0232431 | CDS | 2951533 | 810 | + | 0.261728 | |
DDB_G0285215 | DDB_G0285215 | DDB0232431 | CDS | 2987082 | 1527 | - | 0.339227 | |
DDB_G0285219 | DDB_G0285219 | DDB0232431 | CDS | 2992421 | 831 | + | 0.311673 | |
DDB_G0285225 | DDB_G0285225 | DDB0232431 | CDS | 3013770 | 1701 | + | 0.218107 | |
DDB_G0285229 | DDB_G0285229 | DDB0232431 | CDS | 3018261 | 555 | - | 0.176577 | |
DDB_G0285233 | DDB_G0285233 | DDB0232431 | CDS | 2981196 | 1893 | - | 0.230851 | |
DDB_G0285235 | DDB_G0285235 | DDB0232431 | CDS | 2989642 | 192 | + | 0.25 | |
DDB_G0285237 | DDB_G0285237 | DDB0232431 | CDS | 2990906 | 705 | + | 0.28227 | |
DDB_G0285243 | DDB_G0285243 | has partial similarity to the S. cerevisiae SEN1 a putative helicase required for RNA polymerase II transcription termination and processing of RNAs | DDB0232431 | CDS | 2998910 | 6210 | + | 0.295169 |
DDB_G0285245 | DDB_G0285245 | DDB0232431 | CDS | 3006660 | 846 | - | 0.328605 | |
DDB_G0285249 | DDB_G0285249 | DDB0232431 | CDS | 3016456 | 828 | - | 0.190821 | |
DDB_G0285255 | DDB_G0285255 | DDB0232431 | CDS | 3020871 | 1140 | + | 0.225439 | |
DDB_G0285259 | DDB_G0285259 | DDB0232431 | CDS | 3024689 | 2052 | - | 0.240253 | |
DDB_G0285261 | DDB_G0285261 | DDB0232431 | CDS | 3027528 | 1266 | + | 0.239336 | |
DDB_G0285265 | DDB_G0285265 | contains one EF hand similar to calmodulin | DDB0232431 | CDS | 3032493 | 420 | - | 0.292857 |
DDB_G0285269 | DDB_G0285269 | DDB0232431 | CDS | 3037532 | 930 | + | 0.274194 | |
DDB_G0285271 | DDB_G0285271 | DDB0232431 | CDS | 3042778 | 3132 | + | 0.230204 | |
DDB_G0285273 | DDB_G0285273 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232431 | CDS | 3047069 | 474 | + | 0.308017 |
DDB_G0285275 | DDB_G0285275 | DDB0232431 | CDS | 3047966 | 831 | - | 0.306859 | |
DDB_G0285279 | DDB_G0285279 | DDB0232431 | CDS | 3050725 | 384 | - | 0.265625 | |
DDB_G0285281 | DDB_G0285281 | DDB0232431 | CDS | 3053971 | 774 | + | 0.232558 | |
DDB_G0285283 | DDB_G0285283 | DDB0232431 | CDS | 3058106 | 1854 | - | 0.319849 | |
DDB_G0285285 | DDB_G0285285 | DDB0232431 | CDS | 3060850 | 1323 | - | 0.253212 | |
DDB_G0285287 | DDB_G0285287 | putative ortholog of Rad51D which is involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks | DDB0232431 | CDS | 3062767 | 1065 | - | 0.23662 |
DDB_G0285289 | DDB_G0285289 | DDB0232431 | CDS | 3064118 | 849 | - | 0.332155 | |
DDB_G0285291 | DDB_G0285291 | DDB0232431 | CDS | 3065810 | 1239 | - | 0.34544 | |
DDB_G0285297 | DDB_G0285297 | DDB0232431 | CDS | 3039035 | 3198 | + | 0.262039 | |
DDB_G0285299 | DDB_G0285299 | DDB0232431 | CDS | 3070354 | 1635 | - | 0.310092 | |
DDB_G0285301 | DDB_G0285301 | DDB0232431 | CDS | 3019660 | 434 | - | 0.163594 | |
DDB_G0285305_RTE | DDB_G0285305 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3073434 | 2127 | + | 0.368594 |
DDB_G0285307_RTE | DDB_G0285307 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 3075949 | 1061 | + | 0.321395 |
DDB_G0285309 | DDB_G0285309 | DDB0232431 | CDS | 3077952 | 2850 | + | 0.2 | |
DDB_G0285315_RTE | DDB_G0285315 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3088593 | 1362 | - | 0.340675 |
DDB_G0285317_RTE | DDB_G0285317 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3090138 | 408 | - | 0.362745 |
DDB_G0285325_RTE | DDB_G0285325 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3091037 | 1953 | + | 0.348182 |
DDB_G0285329 | DDB_G0285329 | C-terminal half very similar to nucleotide binding protein 1 belongs to the highly conserved MrpNBP35 ATP-binding protein family | DDB0232431 | CDS | 3094412 | 1497 | - | 0.311289 |
DDB_G0285331 | DDB_G0285331 | DDB0232431 | CDS | 3096169 | 1137 | + | 0.221636 | |
DDB_G0285333 | DDB_G0285333 | DDB0232431 | CDS | 3097865 | 816 | - | 0.310049 | |
DDB_G0285335 | DDB_G0285335 | DDB0232431 | CDS | 3099238 | 1767 | - | 0.203169 | |
DDB_G0285337 | DDB_G0285337 | DDB0232431 | CDS | 3101144 | 1116 | - | 0.243728 | |
DDB_G0285341 | DDB_G0285341 | DDB0232431 | CDS | 3105820 | 1584 | + | 0.332071 | |
DDB_G0285345 | DDB_G0285345 | DDB0232431 | CDS | 3116252 | 228 | - | 0.364035 | |
DDB_G0285347 | DDB_G0285347 | DDB0232431 | CDS | 3118848 | 591 | - | 0.270728 | |
DDB_G0285351 | DDB_G0285351 | DDB0232431 | CDS | 3146811 | 1365 | - | 0.267399 | |
DDB_G0285355 | DDB_G0285355 | DDB0232431 | CDS | 3164414 | 591 | + | 0.203046 | |
DDB_G0285357 | DDB_G0285357 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | DDB0232431 | CDS | 3165268 | 1095 | - | 0.36895 |
DDB_G0285359 | DDB_G0285359 | DDB0232431 | CDS | 3166879 | 630 | - | 0.31746 | |
DDB_G0285361 | DDB_G0285361 | DDB0232431 | CDS | 3169327 | 984 | - | 0.322154 | |
DDB_G0285363 | DDB_G0285363 | DDB0232431 | CDS | 3170836 | 1047 | - | 0.3085 | |
DDB_G0285365 | DDB_G0285365 | DDB0232431 | CDS | 3173380 | 699 | + | 0.296137 | |
DDB_G0285369_ps | DDB_G0285369 | putative pseudogene similar to | DDB0232431 | CDS | 3174564 | 342 | + | 0.230994 |
DDB_G0285377 | DDB_G0285377 | DDB0232431 | CDS | 3204171 | 666 | - | 0.279279 | |
DDB_G0285379 | DDB_G0285379 | DDB0232431 | CDS | 3205403 | 315 | - | 0.209524 | |
DDB_G0285383 | DDB_G0285383 | DDB0232431 | CDS | 3210654 | 138 | - | 0.347826 | |
DDB_G0285385 | DDB_G0285385 | DDB0232431 | CDS | 3211353 | 912 | - | 0.172149 | |
DDB_G0285389 | DDB_G0285389 | putative ortholog of H. sapiens UXT (ubiquitously-expressed transcript) related to prefoldin alpha | DDB0232431 | CDS | 3107718 | 486 | - | 0.201646 |
DDB_G0285397 | DDB_G0285397 | DDB0232431 | CDS | 3149443 | 1437 | - | 0.230341 | |
DDB_G0285401 | DDB_G0285401 | DDB0232431 | CDS | 3154785 | 2763 | + | 0.305465 | |
DDB_G0285403 | DDB_G0285403 | DDB0232431 | CDS | 3157812 | 3108 | - | 0.320463 | |
DDB_G0285405 | DDB_G0285405 | DDB0232431 | CDS | 3175505 | 2772 | - | 0.240981 | |
DDB_G0285409 | DDB_G0285409 | DDB0232431 | CDS | 3184814 | 3579 | - | 0.222408 | |
DDB_G0285411 | DDB_G0285411 | DDB0232431 | CDS | 3189133 | 4317 | + | 0.217049 | |
DDB_G0285413 | DDB_G0285413 | DDB0232431 | CDS | 3199348 | 810 | + | 0.240741 | |
DDB_G0285421 | DDB_G0285421 | has a signal peptide followed by a transmembrane domain conserved in D. purpureum and P. pallidum | DDB0232431 | CDS | 3514189 | 3492 | + | 0.2626 |
DDB_G0285435 | DDB_G0285435 | DDB0232431 | CDS | 3216790 | 4929 | - | 0.313857 | |
DDB_G0285437 | DDB_G0285437 | DDB0232431 | CDS | 3223269 | 969 | + | 0.27451 | |
DDB_G0285439 | DDB_G0285439 | DDB0232431 | CDS | 3224754 | 2421 | + | 0.250723 | |
DDB_G0285441 | DDB_G0285441 | DDB0232431 | CDS | 3227919 | 216 | + | 0.402778 | |
DDB_G0285443 | DDB_G0285443 | DDB0232431 | CDS | 3229422 | 219 | + | 0.39726 | |
DDB_G0285445 | DDB_G0285445 | has the same domain composition as fbxA and | DDB0232431 | CDS | 3230059 | 3537 | - | 0.271699 |
DDB_G0285447 | DDB_G0285447 | conserved protein contains 2 putative transmembrane domains | DDB0232431 | CDS | 3236291 | 918 | - | 0.260349 |
DDB_G0285449 | DDB_G0285449 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232431 | CDS | 3237973 | 2241 | - | 0.253012 |
DDB_G0285459 | DDB_G0285459 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232431 | CDS | 3256332 | 786 | + | 0.282443 |
DDB_G0285463 | DDB_G0285463 | member of the TKL (tyrosine kinase-like) group and the CZAK (C-terminal domain of ZakA) family contains 7 putative transmembrane domains | DDB0232431 | CDS | 3259648 | 2076 | - | 0.308285 |
DDB_G0285467 | DDB_G0285467 | DDB0232431 | CDS | 3266519 | 1398 | + | 0.326896 | |
DDB_G0285469 | DDB_G0285469 | DDB0232431 | CDS | 3270785 | 222 | + | 0.193694 | |
DDB_G0285471 | DDB_G0285471 | belongs to the DUF836 family similar to S. cerevisiae glutaredoxin-like protein YDR286C | DDB0232431 | CDS | 3274352 | 327 | + | 0.217125 |
DDB_G0285473 | DDB_G0285473 | DDB0232431 | CDS | 3274945 | 510 | - | 0.186275 | |
DDB_G0285477 | DDB_G0285477 | DDB0232431 | CDS | 3279052 | 282 | - | 0.219858 | |
DDB_G0285481 | DDB_G0285481 | DDB0232431 | CDS | 3294537 | 1533 | - | 0.172864 | |
DDB_G0285483 | DDB_G0285483 | DDB0232431 | CDS | 3297334 | 4668 | + | 0.230291 | |
DDB_G0285485 | DDB_G0285485 | protein family conserved in protozoans fungi and invertebrate animals | DDB0232431 | CDS | 3302460 | 2070 | - | 0.282126 |
DDB_G0285487 | DDB_G0285487 | protein family conserved in protozoans fungi and invertebrate animals | DDB0232431 | CDS | 3305672 | 2205 | - | 0.273016 |
DDB_G0285489 | DDB_G0285489 | similar to human TRMT112 S. cerevisiae TRM112 (multifunctional methyltransferase subunit TRM112) | DDB0232431 | CDS | 3308405 | 387 | + | 0.250646 |
DDB_G0285491 | DDB_G0285491 | DDB0232431 | CDS | 3308999 | 807 | - | 0.262701 | |
DDB_G0285493 | DDB_G0285493 | DDB0232431 | CDS | 3310297 | 1125 | + | 0.255111 | |
DDB_G0285495 | DDB_G0285495 | DDB0232431 | CDS | 3311819 | 1488 | - | 0.252016 | |
DDB_G0285497 | DDB_G0285497 | DDB0232431 | CDS | 3313914 | 525 | + | 0.260952 | |
DDB_G0285499 | DDB_G0285499 | DDB0232431 | CDS | 3314745 | 5034 | + | 0.197855 | |
DDB_G0285501 | DDB_G0285501 | DDB0232431 | CDS | 3320640 | 969 | - | 0.307534 | |
DDB_G0285511 | DDB_G0285511 | DDB0232431 | CDS | 3331170 | 1683 | - | 0.322638 | |
DDB_G0285517 | DDB_G0285517 | DDB0232431 | CDS | 3338968 | 537 | + | 0.268156 | |
DDB_G0285519 | DDB_G0285519 | DDB0232431 | CDS | 3339980 | 867 | - | 0.267589 | |
DDB_G0285525 | DDB_G0285525 | phosphorylates dephospho-CoA to CoA in other organisms this activity is part of a bifunctional enzyme that also has pantetheine-phosphate adenylyltransferase activity in Dictyostelium the latter activity is encoded by | DDB0232431 | CDS | 3344366 | 624 | - | 0.245192 |
DDB_G0285529 | DDB_G0285529 | DDB0232431 | CDS | 3346712 | 1149 | + | 0.252393 | |
DDB_G0285531 | DDB_G0285531 | DDB0232431 | CDS | 3348010 | 1200 | + | 0.245833 | |
DDB_G0285535 | DDB_G0285535 | DDB0232431 | CDS | 3350719 | 1494 | - | 0.240295 | |
DDB_G0285539 | DDB_G0285539 | DDB0232431 | CDS | 3354945 | 1575 | + | 0.233016 | |
DDB_G0285541 | DDB_G0285541 | putative family member of integral membrane proteins that are found to increase tolerance to divalent metal ions such as cadmium zinc and cobalt contains 5 predicted transmembrane domains | DDB0232431 | CDS | 3356593 | 1305 | - | 0.314176 |
DDB_G0285543 | DDB_G0285543 | DDB0232431 | CDS | 3362096 | 2157 | + | 0.255911 | |
DDB_G0285545 | DDB_G0285545 | similar to H. sapiens solute carrier family 31 member 1 (SLC31A1) or high affinity copper uptake protein 1 contains 3 predicted transmembrane domains | DDB0232431 | CDS | 3364611 | 441 | - | 0.251701 |
DDB_G0285547_RTE | DDB_G0285547 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3366450 | 777 | + | 0.332046 |
DDB_G0285549 | DDB_G0285549 | DDB0232431 | CDS | 3370790 | 174 | + | 0.33908 | |
DDB_G0285551 | DDB_G0285551 | DDB0232431 | CDS | 3371635 | 180 | + | 0.316667 | |
DDB_G0285555 | DDB_G0285555 | highly similar to neighboring gene | DDB0232431 | CDS | 3373704 | 1698 | + | 0.287986 |
DDB_G0285557 | DDB_G0285557 | DDB0232431 | CDS | 3378778 | 840 | + | 0.207143 | |
DDB_G0285559 | DDB_G0285559 | DDB0232431 | CDS | 3380070 | 3711 | + | 0.221234 | |
DDB_G0285563 | DDB_G0285563 | DDB0232431 | CDS | 3385916 | 852 | - | 0.246479 | |
DDB_G0285565_ps | DDB_G0285565 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 3389420 | 1143 | + | 0.304462 |
DDB_G0285567 | DDB_G0285567 | DDB0232431 | CDS | 3392571 | 222 | - | 0.396396 | |
DDB_G0285569 | DDB_G0285569 | DDB0232431 | CDS | 3393304 | 219 | + | 0.406393 | |
DDB_G0285573_ps | DDB_G0285573 | putative pseudogene similar to short-chain dehydrogenasereductase (SDR) family proteins | DDB0232431 | CDS | 3394833 | 402 | + | 0.278607 |
DDB_G0285577 | DDB_G0285577 | DDB0232431 | CDS | 3396934 | 1275 | - | 0.219608 | |
DDB_G0285581 | DDB_G0285581 | DDB0232431 | CDS | 3402388 | 3645 | - | 0.249108 | |
DDB_G0285583 | DDB_G0285583 | DDB0232431 | CDS | 3409194 | 282 | - | 0.212766 | |
DDB_G0285585 | DDB_G0285585 | DDB0232431 | CDS | 3409926 | 2799 | - | 0.302608 | |
DDB_G0285587 | DDB_G0285587 | DDB0232431 | CDS | 3413814 | 1170 | - | 0.275214 | |
DDB_G0285595 | DDB_G0285595 | DDB0232431 | CDS | 3427765 | 573 | + | 0.249564 | |
DDB_G0285603 | DDB_G0285603 | DDB0232431 | CDS | 3435392 | 168 | + | 0.309524 | |
DDB_G0285605 | DDB_G0285605 | DDB0232431 | CDS | 3453352 | 1362 | - | 0.24743 | |
DDB_G0285607 | DDB_G0285607 | DDB0232431 | CDS | 3454900 | 1086 | - | 0.200737 | |
DDB_G0285609 | DDB_G0285609 | DDB0232431 | CDS | 3456501 | 2034 | - | 0.212881 | |
DDB_G0285611 | DDB_G0285611 | DDB0232431 | CDS | 3459087 | 1167 | + | 0.24593 | |
DDB_G0285613 | DDB_G0285613 | DDB0232431 | CDS | 3463966 | 1338 | + | 0.254111 | |
DDB_G0285617 | DDB_G0285617 | highly similar to | DDB0232431 | CDS | 3471998 | 1431 | + | 0.322851 |
DDB_G0285619 | DDB_G0285619 | DDB0232431 | CDS | 3474787 | 744 | + | 0.346774 | |
DDB_G0285621 | DDB_G0285621 | conserved Dictyostelium protein contains a putative signal sequence and one C-terminal transmembrane domain | DDB0232431 | CDS | 3475963 | 1665 | + | 0.282282 |
DDB_G0285623 | DDB_G0285623 | DDB0232431 | CDS | 3480410 | 801 | - | 0.273408 | |
DDB_G0285627 | DDB_G0285627 | DDB0232431 | CDS | 3486954 | 1422 | + | 0.268636 | |
DDB_G0285629 | DDB_G0285629 | DDB0232431 | CDS | 3488592 | 801 | - | 0.264669 | |
DDB_G0285631 | DDB_G0285631 | conserved Dictyostelium protein contains one putative transmembrane domain and an additional putative signal sequence | DDB0232431 | CDS | 3493674 | 1872 | - | 0.313034 |
DDB_G0285633 | DDB_G0285633 | DDB0232431 | CDS | 3496907 | 780 | + | 0.248718 | |
DDB_G0285635 | DDB_G0285635 | DDB0232431 | CDS | 3498174 | 3117 | - | 0.235804 | |
DDB_G0285639 | DDB_G0285639 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232431 | CDS | 3518236 | 462 | + | 0.25974 |
DDB_G0285645 | DDB_G0285645 | DDB0232431 | CDS | 3531932 | 957 | - | 0.256008 | |
DDB_G0285649 | DDB_G0285649 | the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232431 | CDS | 3536200 | 1197 | - | 0.345029 |
DDB_G0285651 | DDB_G0285651 | DDB0232431 | CDS | 3544377 | 183 | - | 0.278689 | |
DDB_G0285653 | DDB_G0285653 | DDB0232431 | CDS | 3545567 | 1605 | + | 0.270405 | |
DDB_G0285655 | DDB_G0285655 | DDB0232431 | CDS | 3547353 | 3402 | - | 0.288948 | |
DDB_G0285657 | DDB_G0285657 | DDB0232431 | CDS | 3551340 | 1260 | + | 0.246032 | |
DDB_G0285659 | DDB_G0285659 | DDB0232431 | CDS | 3553333 | 630 | + | 0.185714 | |
DDB_G0285663 | DDB_G0285663 | conserved protozoa protein that are putative permeases involved in the transport of lipids contains 10 putative transmembrane domains | DDB0232431 | CDS | 3554545 | 3456 | - | 0.308738 |
DDB_G0285665 | DDB_G0285665 | DDB0232431 | CDS | 3559921 | 3723 | - | 0.235831 | |
DDB_G0285667 | DDB_G0285667 | DDB0232431 | CDS | 3564751 | 3594 | - | 0.238175 | |
DDB_G0285669 | DDB_G0285669 | DDB0232431 | CDS | 3569277 | 3756 | - | 0.236954 | |
DDB_G0285671 | DDB_G0285671 | DDB0232431 | CDS | 3574096 | 555 | - | 0.212613 | |
DDB_G0285673 | DDB_G0285673 | DDB0232431 | CDS | 3575375 | 255 | - | 0.270588 | |
DDB_G0285675 | DDB_G0285675 | DDB0232431 | CDS | 3576296 | 774 | + | 0.21447 | |
DDB_G0285677 | DDB_G0285677 | DDB0232431 | CDS | 3577440 | 4140 | + | 0.251932 | |
DDB_G0285681 | DDB_G0285681 | DDB0232431 | CDS | 3584332 | 708 | - | 0.289548 | |
DDB_G0285685 | DDB_G0285685 | DDB0232431 | CDS | 3590065 | 1152 | + | 0.265625 | |
DDB_G0285687 | DDB_G0285687 | DDB0232431 | CDS | 3591605 | 1089 | - | 0.24977 | |
DDB_G0285689 | DDB_G0285689 | DDB0232431 | CDS | 3593584 | 1908 | - | 0.22065 | |
DDB_G0285691 | DDB_G0285691 | DDB0232431 | CDS | 3596207 | 975 | + | 0.212308 | |
DDB_G0285693 | DDB_G0285693 | DDB0232431 | CDS | 3597715 | 2736 | + | 0.240863 | |
DDB_G0285695 | DDB_G0285695 | conserved in Dictyostelium contains weak match to FNIP repeat regions | DDB0232431 | CDS | 3600764 | 1572 | - | 0.276081 |
DDB_G0285697 | DDB_G0285697 | DDB0232431 | CDS | 3603409 | 1389 | + | 0.36933 | |
DDB_G0285699 | DDB_G0285699 | DDB0232431 | CDS | 3605127 | 1839 | + | 0.269712 | |
DDB_G0285701 | DDB_G0285701 | DDB0232431 | CDS | 3607268 | 2649 | + | 0.177803 | |
DDB_G0285705 | DDB_G0285705 | contains a RING-finger that is a specialised type of Zn-finger domain which in some cases has been shown to be involved in ubiquitin E3 ligase activity contains 14 putative transmembrane domains | DDB0232431 | CDS | 3615364 | 3267 | + | 0.296602 |
DDB_G0285707 | DDB_G0285707 | DDB0232431 | CDS | 3619487 | 2613 | + | 0.202067 | |
DDB_G0285709 | DDB_G0285709 | DDB0232431 | CDS | 3622848 | 1554 | + | 0.341055 | |
DDB_G0285711 | DDB_G0285711 | the phox domain has been associated with diverse functions such as cell signalling vesicular trafficking protein sorting and lipid modification and the C2 domain is a Ca2-dependent membrane-targeting module found in many cellular proteins involved in signal transduction or membrane trafficking similar to D. purpureum protein | DDB0232431 | CDS | 3625722 | 990 | + | 0.256566 |
DDB_G0285715 | DDB_G0285715 | DDB0232431 | CDS | 3630133 | 873 | - | 0.234822 | |
DDB_G0285721 | DDB_G0285721 | DDB0232431 | CDS | 3632780 | 213 | + | 0.2723 | |
DDB_G0285723 | DDB_G0285723 | DDB0232431 | CDS | 3633398 | 2304 | - | 0.224392 | |
DDB_G0285729 | DDB_G0285729 | DDB0232431 | CDS | 3466396 | 1875 | + | 0.301333 | |
DDB_G0285735 | DDB_G0285735 | DDB0232431 | CDS | 3214213 | 2166 | + | 0.220683 | |
DDB_G0285737 | DDB_G0285737 | DDB0232431 | CDS | 3228708 | 222 | - | 0.396396 | |
DDB_G0285739 | DDB_G0285739 | DDB0232431 | CDS | 3251052 | 999 | - | 0.25025 | |
DDB_G0285743 | DDB_G0285743 | DDB0232431 | CDS | 3271863 | 2334 | - | 0.222793 | |
DDB_G0285745_ps | DDB_G0285745 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 3279817 | 3096 | - | 0.295866 |
DDB_G0285749 | DDB_G0285749 | DDB0232431 | CDS | 3360351 | 1407 | + | 0.180526 | |
DDB_G0285751 | DDB_G0285751 | DDB0232431 | CDS | 3367805 | 2289 | + | 0.187418 | |
DDB_G0285753_ps | DDB_G0285753 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 3388026 | 975 | + | 0.29641 |
DDB_G0285755_ps | DDB_G0285755 | putative pseudogene similar to cyclin-like F-box containing proteins | DDB0232431 | CDS | 3393941 | 645 | - | 0.317829 |
DDB_G0285757_ps | DDB_G0285757 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3406976 | 126 | + | 0.277778 |
DDB_G0285761 | DDB_G0285761 | contains a growth factor receptor domain contains a predicted signal peptide and a putative C-terminal transmembrane domain | DDB0232431 | CDS | 3436262 | 1560 | - | 0.364744 |
DDB_G0285763 | DDB_G0285763 | DDB0232431 | CDS | 3439404 | 1161 | + | 0.282515 | |
DDB_G0285765 | DDB_G0285765 | DDB0232431 | CDS | 3445107 | 2346 | - | 0.252771 | |
DDB_G0285767 | DDB_G0285767 | DDB0232431 | CDS | 3448354 | 4086 | + | 0.254772 | |
DDB_G0285769 | DDB_G0285769 | highly similar to agglutinin domain-containing protein | DDB0232431 | CDS | 3460993 | 1425 | - | 0.311579 |
DDB_G0285771 | DDB_G0285771 | DDB0232431 | CDS | 3478635 | 1413 | + | 0.257608 | |
DDB_G0285773 | DDB_G0285773 | conserved Dictyostelium protein contains one putative transmembrane domain | DDB0232431 | CDS | 3482506 | 1851 | - | 0.310103 |
DDB_G0285775 | DDB_G0285775 | conserved Dictyostelium protein contains one putative transmembrane domain | DDB0232431 | CDS | 3490502 | 1758 | - | 0.300341 |
DDB_G0285779 | DDB_G0285779 | DDB0232431 | CDS | 3507070 | 174 | - | 0.321839 | |
DDB_G0285781 | DDB_G0285781 | DDB0232431 | CDS | 3508114 | 468 | + | 0.288462 | |
DDB_G0285787 | DDB_G0285787 | DDB0232431 | CDS | 3526607 | 207 | - | 0.130435 | |
DDB_G0285791 | DDB_G0285791 | DDB0232431 | CDS | 3503514 | 771 | + | 0.203632 | |
DDB_G0285795_RTE | DDB_G0285795 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3658983 | 900 | + | 0.4 |
DDB_G0285797 | DDB_G0285797 | DDB0232431 | CDS | 3638134 | 16644 | + | 0.222603 | |
DDB_G0285799 | DDB_G0285799 | DDB0232431 | CDS | 3663997 | 1467 | + | 0.220859 | |
DDB_G0285801 | DDB_G0285801 | DDB0232431 | CDS | 3665650 | 1035 | + | 0.310145 | |
DDB_G0285803 | DDB_G0285803 | belongs to the GNAT family homolog of S. cerevisiae MAK3 (maintenance of killer protein 3) | DDB0232431 | CDS | 3673056 | 558 | + | 0.250896 |
DDB_G0285805 | DDB_G0285805 | DDB0232431 | CDS | 3681493 | 2529 | + | 0.232503 | |
DDB_G0285807 | DDB_G0285807 | DDB0232431 | CDS | 3686003 | 735 | + | 0.220408 | |
DDB_G0285811 | DDB_G0285811 | DDB0232431 | CDS | 3686858 | 660 | - | 0.295455 | |
DDB_G0285813 | DDB_G0285813 | belongs to the DUF812 family homolog of human CCDC22 (coiled-coil domain-containing protein 22) contains at least two coiled-coil domains | DDB0232431 | CDS | 3688403 | 1914 | + | 0.293103 |
DDB_G0285819_ps | DDB_G0285819 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3700169 | 531 | + | 0.350282 |
DDB_G0285823 | DDB_G0285823 | DDB0232431 | CDS | 3703536 | 1521 | + | 0.331361 | |
DDB_G0285825 | DDB_G0285825 | DDB0232431 | CDS | 3705430 | 468 | - | 0.273504 | |
DDB_G0285827 | DDB_G0285827 | DDB0232431 | CDS | 3706474 | 1002 | + | 0.251497 | |
DDB_G0285831 | DDB_G0285831 | DDB0232431 | CDS | 3709396 | 522 | + | 0.260536 | |
DDB_G0285833 | DDB_G0285833 | DDB0232431 | CDS | 3684831 | 246 | + | 0.268293 | |
DDB_G0285835_RTE | DDB_G0285835 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3661035 | 1953 | + | 0.343574 |
DDB_G0285837 | DDB_G0285837 | DDB0232431 | CDS | 3674059 | 6603 | - | 0.283356 | |
DDB_G0285839 | DDB_G0285839 | DDB0232431 | CDS | 3698143 | 1359 | + | 0.178808 | |
DDB_G0285841_RTE | DDB_G0285841 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3710715 | 539 | + | 0.369202 |
DDB_G0285851 | DDB_G0285851 | DDB0232431 | CDS | 3717914 | 708 | + | 0.305085 | |
DDB_G0285861 | DDB_G0285861 | DDB0232431 | CDS | 3733661 | 1101 | - | 0.234332 | |
DDB_G0285863 | DDB_G0285863 | DDB0232431 | CDS | 3736082 | 210 | + | 0.309524 | |
DDB_G0285865 | DDB_G0285865 | DDB0232431 | CDS | 3737676 | 2679 | + | 0.196342 | |
DDB_G0285867 | DDB_G0285867 | DDB0232431 | CDS | 3740816 | 189 | - | 0.222222 | |
DDB_G0285869 | DDB_G0285869 | DDB0232431 | CDS | 3741819 | 1299 | - | 0.282525 | |
DDB_G0285871 | DDB_G0285871 | DDB0232431 | CDS | 3745815 | 588 | - | 0.290816 | |
DDB_G0285873 | DDB_G0285873 | DDB0232431 | CDS | 3747167 | 552 | + | 0.199275 | |
DDB_G0285875 | DDB_G0285875 | DDB0232431 | CDS | 3748302 | 6714 | + | 0.260798 | |
DDB_G0285879 | DDB_G0285879 | DDB0232431 | CDS | 3762999 | 1614 | - | 0.228005 | |
DDB_G0285885_ps | DDB_G0285885 | putative pseudogene very similar to large conserved family of Dictyostelium EGF-like domain-containing proteins | DDB0232431 | CDS | 3776481 | 1125 | - | 0.251556 |
DDB_G0285887 | DDB_G0285887 | DDB0232431 | CDS | 3778774 | 825 | + | 0.242424 | |
DDB_G0285889 | DDB_G0285889 | DDB0232431 | CDS | 3780014 | 780 | + | 0.265385 | |
DDB_G0285893 | DDB_G0285893 | similar to other Dictyostelium hypothetical proteins contains a putative signal peptide | DDB0232431 | CDS | 3788417 | 1101 | + | 0.326975 |
DDB_G0285897 | DDB_G0285897 | DDB0232431 | CDS | 3798877 | 1701 | + | 0.280423 | |
DDB_G0285899 | DDB_G0285899 | catalyzes the reaction L-alanine 2-oxoglutarate pyruvate L-glutamate | DDB0232431 | CDS | 3800826 | 1605 | - | 0.332087 |
DDB_G0285901 | DDB_G0285901 | contains a Vps53-like N-terminal domain Vps53 complexes with Vps52 and Vps54 to form a multi-subunit complex which might be involved in regulating membrane trafficking events | DDB0232431 | CDS | 3805604 | 2517 | + | 0.294795 |
DDB_G0285903 | DDB_G0285903 | DDB0232431 | CDS | 3808445 | 792 | - | 0.27399 | |
DDB_G0285905 | DDB_G0285905 | DDB0232431 | CDS | 3809647 | 843 | - | 0.204033 | |
DDB_G0285907 | DDB_G0285907 | related to the Ovarian Tumour (OTU) gene of Drosophila function is unknown but conserved cysteine and histidine and possibly the aspartate residues suggests that those not yet recognized as peptidases could possess cysteine protease activity | DDB0232431 | CDS | 3810828 | 1614 | - | 0.254027 |
DDB_G0285909 | DDB_G0285909 | catalyzes the removal of a phosphate group attached to a tyrosine residue ortholog of S. cerevisiae SIW14 that plays a role in actin filament organization and endocytosis | DDB0232431 | CDS | 3812938 | 546 | + | 0.287546 |
DDB_G0285911 | DDB_G0285911 | DDB0232431 | CDS | 3814964 | 3186 | + | 0.27307 | |
DDB_G0285913 | DDB_G0285913 | DDB0232431 | CDS | 3818293 | 3525 | - | 0.217305 | |
DDB_G0285917 | DDB_G0285917 | DDB0232431 | CDS | 3827611 | 618 | - | 0.300971 | |
DDB_G0285919 | DDB_G0285919 | homolog of human TIPRL and S. cerevisiae TIP41 (TAP42-interacting protein 1) TIP41 interacts with TAP42 and negatively regulates the TOR signaling pathway TIPRL is a putative MAPK-activating protein | DDB0232431 | CDS | 3828991 | 825 | - | 0.255758 |
DDB_G0285923 | DDB_G0285923 | DDB0232431 | CDS | 3831998 | 2388 | - | 0.356784 | |
DDB_G0285927 | DDB_G0285927 | similar to mammalian AASDHPPT that transfers the 4'-phosphopantetheine moiety from coenzyme A to a serine residue of a broad range of acceptors | DDB0232431 | CDS | 3839546 | 891 | - | 0.216611 |
DDB_G0285929 | DDB_G0285929 | DDB0232431 | CDS | 3845153 | 246 | - | 0.292683 | |
DDB_G0285933 | DDB_G0285933 | DDB0232431 | CDS | 3854532 | 2721 | + | 0.247336 | |
DDB_G0285935 | DDB_G0285935 | DDB0232431 | CDS | 3859998 | 465 | - | 0.236559 | |
DDB_G0285941 | DDB_G0285941 | DDB0232431 | CDS | 3873726 | 1392 | - | 0.255747 | |
DDB_G0285943 | DDB_G0285943 | ortholg of mammalian transmembrane protein 87A (TMEM87A) contains seven transmembrane domains | DDB0232431 | CDS | 3726406 | 1737 | - | 0.279217 |
DDB_G0285945 | DDB_G0285945 | DDB0232431 | CDS | 3759550 | 126 | + | 0.380952 | |
DDB_G0285951_RTE | DDB_G0285951 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3715691 | 1080 | - | 0.414815 |
DDB_G0285953 | DDB_G0285953 | DDB0232431 | CDS | 3743951 | 1569 | + | 0.281708 | |
DDB_G0285955 | DDB_G0285955 | DDB0232431 | CDS | 3767530 | 6150 | + | 0.218537 | |
DDB_G0285959 | DDB_G0285959 | DDB0232431 | CDS | 3842242 | 2313 | + | 0.280588 | |
DDB_G0285965 | DDB_G0285965 | contains a AWS domain (Associated With SET) but not SET domain contains a signal peptide and a C-terminal transmembrane domain | DDB0232431 | CDS | 3879686 | 753 | - | 0.245684 |
DDB_G0285967 | DDB_G0285967 | tensin family protein (related to the tumor suppressor PTEN) contains a a lipid phosphatase domain and a C2-like domain and a C-terminal LIM domain (absent from PTEN) | DDB0232431 | CDS | 3881074 | 2997 | - | 0.265933 |
DDB_G0285969 | DDB_G0285969 | putative cysteine protease member of the DJ-1ThiJPfpI family which includes human PARK7 associated with Parkinson's disease | DDB0232431 | CDS | 3885433 | 618 | - | 0.305825 |
DDB_G0285973 | DDB_G0285973 | DDB0232431 | CDS | 3894503 | 1404 | + | 0.289174 | |
DDB_G0285975 | DDB_G0285975 | DDB0232431 | CDS | 3896573 | 2754 | + | 0.265432 | |
DDB_G0285979_ps | DDB_G0285979 | putative pseudogene similar to Dictyostelium genes | DDB0232431 | CDS | 3899815 | 834 | + | 0.226619 |
DDB_G0285981 | DDB_G0285981 | similar to the vertebrate loss of heterozygosity 11 chromosomal region 2 gene A | DDB0232431 | CDS | 3901446 | 2496 | + | 0.276843 |
DDB_G0285983 | DDB_G0285983 | DDB0232431 | CDS | 3904475 | 633 | - | 0.339652 | |
DDB_G0285985 | DDB_G0285985 | contains 7 predicted transmembrane domains very similar to D. purpureum protein | DDB0232431 | CDS | 3906524 | 936 | - | 0.258547 |
DDB_G0285987 | DDB_G0285987 | DDB0232431 | CDS | 3908514 | 1293 | - | 0.2529 | |
DDB_G0285989 | DDB_G0285989 | DDB0232431 | CDS | 3911476 | 3705 | + | 0.239676 | |
DDB_G0285991 | DDB_G0285991 | DDB0232431 | CDS | 3915272 | 882 | - | 0.25737 | |
DDB_G0286001 | DDB_G0286001 | DDB0232431 | CDS | 3920731 | 366 | + | 0.262295 | |
DDB_G0286003 | DDB_G0286003 | DDB0232431 | CDS | 3925023 | 3213 | + | 0.304077 | |
DDB_G0286017_ps | DDB_G0286017 | putative pseudogene similar to ubiquitin domain-containing proteins especially | DDB0232431 | CDS | 3946482 | 564 | - | 0.308511 |
DDB_G0286021 | DDB_G0286021 | DDB0232431 | CDS | 3953660 | 657 | + | 0.305936 | |
DDB_G0286023 | DDB_G0286023 | DDB0232431 | CDS | 3954952 | 264 | - | 0.32197 | |
DDB_G0286025 | DDB_G0286025 | similar to bacterial cellulase celA expressed in pstAB pstA and pstO cells | DDB0232431 | CDS | 3964324 | 1653 | + | 0.351482 |
DDB_G0286029_ps | DDB_G0286029 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3967753 | 345 | - | 0.194203 |
DDB_G0286039 | DDB_G0286039 | DDB0232431 | CDS | 3986273 | 1083 | - | 0.288089 | |
DDB_G0286043 | DDB_G0286043 | DDB0232431 | CDS | 3989629 | 1887 | + | 0.225755 | |
DDB_G0286045 | DDB_G0286045 | one of many putative Dictyostelium potassium channels contains 3 pentapeptide repeats | DDB0232431 | CDS | 3992727 | 2226 | + | 0.27044 |
DDB_G0286047 | DDB_G0286047 | DDB0232431 | CDS | 3995156 | 198 | + | 0.282828 | |
DDB_G0286053 | DDB_G0286053 | DDB0232431 | CDS | 4001619 | 744 | - | 0.327957 | |
DDB_G0286055 | DDB_G0286055 | conserved in Dictyostelids contains also a SCP-like extracellular domain | DDB0232431 | CDS | 4003428 | 1293 | + | 0.317092 |
DDB_G0286061 | DDB_G0286061 | DDB0232431 | CDS | 4010233 | 1629 | - | 0.327808 | |
DDB_G0286063 | DDB_G0286063 | DDB0232431 | CDS | 4014322 | 939 | - | 0.280085 | |
DDB_G0286065 | DDB_G0286065 | DDB0232431 | CDS | 4016707 | 1554 | + | 0.276062 | |
DDB_G0286067 | DDB_G0286067 | DDB0232431 | CDS | 4019113 | 3573 | + | 0.240974 | |
DDB_G0286071 | DDB_G0286071 | DDB0232431 | CDS | 4026106 | 339 | - | 0.233038 | |
DDB_G0286073 | DDB_G0286073 | DDB0232431 | CDS | 4028900 | 1638 | + | 0.281441 | |
DDB_G0286079 | DDB_G0286079 | DDB0232431 | CDS | 4034365 | 1554 | - | 0.346847 | |
DDB_G0286081 | DDB_G0286081 | DDB0232431 | CDS | 4036084 | 462 | - | 0.25974 | |
DDB_G0286083 | DDB_G0286083 | the SWIM domain is found in variety of prokaryotic and eukaryotic proteins it is predicted to have DNA-binding and protein-protein interaction functions in different contexts similar to D. purpureum protein | DDB0232431 | CDS | 4038588 | 486 | + | 0.244856 |
DDB_G0286085 | DDB_G0286085 | DDB0232431 | CDS | 4039412 | 1188 | - | 0.222222 | |
DDB_G0286087 | DDB_G0286087 | DDB0232431 | CDS | 4041102 | 189 | + | 0.354497 | |
DDB_G0286089 | DDB_G0286089 | DDB0232431 | CDS | 4041536 | 1113 | - | 0.253369 | |
DDB_G0286091 | DDB_G0286091 | DDB0232431 | CDS | 4045722 | 4077 | + | 0.201128 | |
DDB_G0286093 | DDB_G0286093 | DDB0232431 | CDS | 4055353 | 477 | - | 0.32914 | |
DDB_G0286097_RTE | DDB_G0286097 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 3948218 | 1335 | + | 0.307865 |
DDB_G0286101_RTE | DDB_G0286101 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3944436 | 860 | - | 0.40814 |
DDB_G0286103 | DDB_G0286103 | DDB0232431 | CDS | 3961629 | 480 | - | 0.245833 | |
DDB_G0286105 | DDB_G0286105 | DDB0232431 | CDS | 3980260 | 1230 | - | 0.233333 | |
DDB_G0286109 | DDB_G0286109 | similar to latrophilin-like receptor lrlA a G-protein-coupled receptor (GPCR) family protein contains four predicted transmembrane domains and is significantly shorter than lrlA | DDB0232431 | CDS | 3983688 | 603 | + | 0.28524 |
DDB_G0286113_ps | DDB_G0286113 | putative pseudogene fragment similar to | DDB0232431 | CDS | 4044149 | 603 | + | 0.233831 |
DDB_G0286115 | DDB_G0286115 | PIP5K catalyze the formation of phosphoinositol-45-bisphosphate via the phosphorylation of phosphatidylinositol-4-phosphate a precursor in the phosphinositide signaling pathway | DDB0232431 | CDS | 4051045 | 3816 | + | 0.277778 |
DDB_G0286129 | DDB_G0286129 | similar to mammalian F-boxWD repeat-containing protein 7 which is part to the E3 ubiquitin-protein ligase complex | DDB0232431 | CDS | 4060377 | 2220 | + | 0.263514 |
DDB_G0286133 | DDB_G0286133 | DDB0232431 | CDS | 4074134 | 996 | + | 0.257028 | |
DDB_G0286135 | DDB_G0286135 | DDB0232431 | CDS | 4075230 | 1239 | - | 0.256659 | |
DDB_G0286137 | DDB_G0286137 | ortholog of human HPS1 mutations in human HPS1 have been linked to Hermansky-Pudlak syndrome 1 | DDB0232431 | CDS | 4107413 | 3030 | + | 0.244884 |
DDB_G0286139 | DDB_G0286139 | DDB0232431 | CDS | 4110771 | 675 | - | 0.197037 | |
DDB_G0286141 | DDB_G0286141 | DDB0232431 | CDS | 4121354 | 291 | - | 0.329897 | |
DDB_G0286143 | DDB_G0286143 | DDB0232431 | CDS | 4126891 | 1035 | + | 0.28599 | |
DDB_G0286145 | DDB_G0286145 | DDB0232431 | CDS | 4130109 | 1128 | + | 0.25266 | |
DDB_G0286151 | DDB_G0286151 | similar to H. sapiens solute carrier family 2 facilitated glucose transporter member 1 (SLC2A1) | DDB0232431 | CDS | 4135325 | 1371 | + | 0.301969 |
DDB_G0286153 | DDB_G0286153 | DDB0232431 | CDS | 4137733 | 2769 | + | 0.216324 | |
DDB_G0286155_ps | DDB_G0286155 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 4140756 | 3867 | + | 0.221102 |
DDB_G0286157 | DDB_G0286157 | DDB0232431 | CDS | 4145918 | 1047 | + | 0.335244 | |
DDB_G0286161 | DDB_G0286161 | DDB0232431 | CDS | 4152139 | 1269 | + | 0.291568 | |
DDB_G0286163 | DDB_G0286163 | DDB0232431 | CDS | 4153623 | 1959 | - | 0.270036 | |
DDB_G0286165 | DDB_G0286165 | DDB0232431 | CDS | 4105304 | 1455 | + | 0.181443 | |
DDB_G0286167 | DDB_G0286167 | DDB0232431 | CDS | 4119612 | 1410 | - | 0.312057 | |
DDB_G0286173 | DDB_G0286173 | DDB0232431 | CDS | 4103161 | 1461 | + | 0.251882 | |
DDB_G0286175 | DDB_G0286175 | DDB0232431 | CDS | 4122107 | 1164 | - | 0.257732 | |
DDB_G0286177_ps | DDB_G0286177 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 4147632 | 2766 | + | 0.238612 |
DDB_G0286193 | DDB_G0286193 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 4160391 | 174 | - | 0.356322 |
DDB_G0286197 | DDB_G0286197 | DDB0232431 | CDS | 4164497 | 1557 | + | 0.344894 | |
DDB_G0286201_ps | DDB_G0286201 | putative pseudogene similar to a Dictyostelid family of oxidoreductases including | DDB0232431 | CDS | 4168246 | 846 | + | 0.239953 |
DDB_G0286203 | DDB_G0286203 | DDB0232431 | CDS | 4169821 | 1026 | + | 0.24269 | |
DDB_G0286205 | DDB_G0286205 | DDB0232431 | CDS | 4173358 | 1683 | + | 0.312537 | |
DDB_G0286207 | DDB_G0286207 | DDB0232431 | CDS | 4176726 | 1320 | + | 0.282576 | |
DDB_G0286209 | DDB_G0286209 | DDB0232431 | CDS | 4178618 | 2700 | + | 0.236667 | |
DDB_G0286211 | DDB_G0286211 | DDB0232431 | CDS | 4189884 | 2700 | + | 0.23963 | |
DDB_G0286213_ps | DDB_G0286213 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 4193633 | 594 | + | 0.215488 |
DDB_G0286215_ps | DDB_G0286215 | putative pseudogene fragment very similar to | DDB0232431 | CDS | 4194622 | 408 | - | 0.183824 |
DDB_G0286217_ps | DDB_G0286217 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 4195341 | 1722 | + | 0.263066 |
DDB_G0286219 | DDB_G0286219 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog highly similar to mammalian TBP-associated factor 172 (TAF-172BTAF1) and yeast MOT1 | DDB0232431 | CDS | 4198019 | 6018 | + | 0.302758 |
DDB_G0286223 | DDB_G0286223 | contains up to 13 WD40 repeats very similar to D. purpureum protein | DDB0232431 | CDS | 4210540 | 2304 | + | 0.291667 |
DDB_G0286225 | DDB_G0286225 | similar to D. purpureum protein contains an N-terminal signal sequence | DDB0232431 | CDS | 4213306 | 393 | - | 0.24173 |
DDB_G0286227 | DDB_G0286227 | DDB0232431 | CDS | 4214477 | 1329 | - | 0.24304 | |
DDB_G0286231 | DDB_G0286231 | DDB0232431 | CDS | 4221429 | 267 | + | 0.322097 | |
DDB_G0286235 | DDB_G0286235 | DDB0232431 | CDS | 4229393 | 900 | - | 0.222222 | |
DDB_G0286237 | DDB_G0286237 | DDB0232431 | CDS | 4231345 | 2271 | + | 0.231616 | |
DDB_G0286239 | DDB_G0286239 | DDB0232431 | CDS | 4234344 | 1080 | + | 0.316667 | |
DDB_G0286243 | DDB_G0286243 | DDB0232431 | CDS | 4239634 | 3012 | + | 0.285193 | |
DDB_G0286245 | DDB_G0286245 | DDB0232431 | CDS | 4243076 | 1338 | + | 0.190583 | |
DDB_G0286249 | DDB_G0286249 | DDB0232431 | CDS | 4245484 | 1125 | - | 0.205333 | |
DDB_G0286255_ps | DDB_G0286255 | putative pseudogene very similar to | DDB0232431 | CDS | 4255797 | 240 | - | 0.325 |
DDB_G0286259 | DDB_G0286259 | protein conserved in bacteria and plants D. discoideum contains a second highly similar protein ( | DDB0232431 | CDS | 4259863 | 537 | + | 0.258845 |
DDB_G0286261 | DDB_G0286261 | DDB0232431 | CDS | 4260842 | 1266 | + | 0.269352 | |
DDB_G0286263 | DDB_G0286263 | DDB0232431 | CDS | 4262351 | 1776 | + | 0.197072 | |
DDB_G0286265 | DDB_G0286265 | DDB0232431 | CDS | 4264645 | 648 | + | 0.310185 | |
DDB_G0286267 | DDB_G0286267 | DDB0232431 | CDS | 4265901 | 639 | + | 0.29108 | |
DDB_G0286269 | DDB_G0286269 | DDB0232431 | CDS | 4267268 | 3276 | - | 0.284188 | |
DDB_G0286271 | DDB_G0286271 | DDB0232431 | CDS | 4271583 | 1893 | + | 0.255151 | |
DDB_G0286277 | DDB_G0286277 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 4282916 | 1716 | + | 0.322844 |
DDB_G0286279 | DDB_G0286279 | DDB0232431 | CDS | 4287649 | 5016 | - | 0.203748 | |
DDB_G0286281 | DDB_G0286281 | DDB0232431 | CDS | 4293465 | 1311 | - | 0.156369 | |
DDB_G0286283 | DDB_G0286283 | DDB0232431 | CDS | 4297454 | 924 | + | 0.199134 | |
DDB_G0286285 | DDB_G0286285 | DDB0232431 | CDS | 4298472 | 231 | - | 0.281385 | |
DDB_G0286287 | DDB_G0286287 | DDB0232431 | CDS | 4298931 | 1293 | - | 0.234339 | |
DDB_G0286289 | DDB_G0286289 | DDB0232431 | CDS | 4300974 | 1836 | + | 0.26634 | |
DDB_G0286291 | DDB_G0286291 | DDB0232431 | CDS | 4305951 | 648 | - | 0.259259 | |
DDB_G0286295 | DDB_G0286295 | DDB0232431 | CDS | 4317522 | 2910 | + | 0.306873 | |
DDB_G0286297 | DDB_G0286297 | DDB0232431 | CDS | 4322636 | 354 | - | 0.251412 | |
DDB_G0286299 | DDB_G0286299 | lysin-rich threonine-rich repetitive protein sequence | DDB0232431 | CDS | 4324089 | 1356 | + | 0.368732 |
DDB_G0286305 | DDB_G0286305 | DDB0232431 | CDS | 4332234 | 1017 | - | 0.360865 | |
DDB_G0286307 | DDB_G0286307 | DDB0232431 | CDS | 4334492 | 696 | + | 0.267241 | |
DDB_G0286309 | DDB_G0286309 | DDB0232431 | CDS | 4335795 | 1026 | + | 0.337232 | |
DDB_G0286311 | DDB_G0286311 | DDB0232431 | CDS | 4337464 | 4422 | + | 0.313433 | |
DDB_G0286313 | DDB_G0286313 | DDB0232431 | CDS | 4342189 | 744 | - | 0.198925 | |
DDB_G0286315 | DDB_G0286315 | conserved protein contains a signal peptide and 11 transmembrane domains | DDB0232431 | CDS | 4343761 | 2028 | + | 0.296844 |
DDB_G0286317 | DDB_G0286317 | DDB0232431 | CDS | 4186251 | 2646 | + | 0.238473 | |
DDB_G0286321 | DDB_G0286321 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 4294974 | 1674 | - | 0.295699 |
DDB_G0286323 | DDB_G0286323 | DDB0232431 | CDS | 4348548 | 4242 | + | 0.244932 | |
DDB_G0286325_ps | DDB_G0286325 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 4171531 | 354 | + | 0.262712 |
DDB_G0286327 | DDB_G0286327 | DDB0232431 | CDS | 4175501 | 759 | + | 0.210804 | |
DDB_G0286329 | DDB_G0286329 | DDB0232431 | CDS | 4182511 | 2691 | + | 0.239316 | |
DDB_G0286331 | DDB_G0286331 | DDB0232431 | CDS | 4205671 | 2769 | + | 0.283135 | |
DDB_G0286333 | DDB_G0286333 | DDB0232431 | CDS | 4247436 | 1866 | + | 0.219185 | |
DDB_G0286341 | DDB_G0286341 | highly similar to bacterial glutathione S-transferase catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232431 | CDS | 4285901 | 975 | + | 0.300513 |
DDB_G0286343 | DDB_G0286343 | DDB0232431 | CDS | 4316449 | 282 | + | 0.230496 | |
DDB_G0286347 | DDB_G0286347 | DDB0232431 | CDS | 4346922 | 1293 | + | 0.225058 | |
DDB_G0286351 | DDB_G0286351 | similar to the cudA transcriptional regulator REMI mutant forms aberrant fruiting bodies (see | DDB0232431 | CDS | 4526380 | 1824 | - | 0.279057 |
DDB_G0286361 | DDB_G0286361 | DDB0232431 | CDS | 4357070 | 1545 | - | 0.248544 | |
DDB_G0286363 | DDB_G0286363 | DDB0232431 | CDS | 4359667 | 1233 | + | 0.301703 | |
DDB_G0286365 | DDB_G0286365 | DDB0232431 | CDS | 4361252 | 2802 | + | 0.210564 | |
DDB_G0286367 | DDB_G0286367 | DDB0232431 | CDS | 4364169 | 1488 | - | 0.190188 | |
DDB_G0286369 | DDB_G0286369 | DDB0232431 | CDS | 4366711 | 2475 | - | 0.192323 | |
DDB_G0286373 | DDB_G0286373 | DDB0232431 | CDS | 4372108 | 1011 | + | 0.228487 | |
DDB_G0286375 | DDB_G0286375 | DDB0232431 | CDS | 4381593 | 1650 | + | 0.276364 | |
DDB_G0286377 | DDB_G0286377 | DDB0232431 | CDS | 4383620 | 2157 | - | 0.251275 | |
DDB_G0286379 | DDB_G0286379 | DDB0232431 | CDS | 4386579 | 1125 | + | 0.265778 | |
DDB_G0286381 | DDB_G0286381 | DDB0232431 | CDS | 4388115 | 1494 | - | 0.305221 | |
DDB_G0286383 | DDB_G0286383 | DDB0232431 | CDS | 4391636 | 708 | + | 0.237288 | |
DDB_G0286387 | DDB_G0286387 | DDB0232431 | CDS | 4394653 | 1521 | - | 0.279421 | |
DDB_G0286393 | DDB_G0286393 | DDB0232431 | CDS | 4403606 | 843 | - | 0.339265 | |
DDB_G0286397 | DDB_G0286397 | DDB0232431 | CDS | 4407676 | 1281 | - | 0.225605 | |
DDB_G0286401 | DDB_G0286401 | DDB0232431 | CDS | 4410583 | 1149 | - | 0.238468 | |
DDB_G0286405 | DDB_G0286405 | DDB0232431 | CDS | 4419066 | 966 | - | 0.161491 | |
DDB_G0286407_ps | DDB_G0286407 | putative pseudogene similar to family of D. discoideum genes including | DDB0232431 | CDS | 4424245 | 213 | + | 0.248826 |
DDB_G0286409 | DDB_G0286409 | DDB0232431 | CDS | 4425235 | 936 | + | 0.252137 | |
DDB_G0286413 | DDB_G0286413 | DDB0232431 | CDS | 4443400 | 903 | + | 0.299003 | |
DDB_G0286417 | DDB_G0286417 | DDB0232431 | CDS | 4458209 | 3048 | - | 0.271982 | |
DDB_G0286421 | DDB_G0286421 | DDB0232431 | CDS | 4468376 | 231 | + | 0.30303 | |
DDB_G0286423 | DDB_G0286423 | DDB0232431 | CDS | 4468953 | 1521 | - | 0.275477 | |
DDB_G0286429 | DDB_G0286429 | DDB0232431 | CDS | 4478853 | 828 | + | 0.27657 | |
DDB_G0286431 | DDB_G0286431 | contains a predicted signal peptide conserved in Dictyostelium | DDB0232431 | CDS | 4480269 | 1596 | - | 0.275689 |
DDB_G0286435_ps | DDB_G0286435 | putative pseudogene similar to upstream EGF-like domain-containing proteins | DDB0232431 | CDS | 4482591 | 2133 | - | 0.241444 |
DDB_G0286437 | DDB_G0286437 | DDB0232431 | CDS | 4495367 | 2814 | - | 0.25693 | |
DDB_G0286439 | DDB_G0286439 | DDB0232431 | CDS | 4502152 | 213 | + | 0.220657 | |
DDB_G0286441 | DDB_G0286441 | DDB0232431 | CDS | 4511137 | 1749 | - | 0.276158 | |
DDB_G0286443 | DDB_G0286443 | DDB0232431 | CDS | 4513273 | 675 | - | 0.244444 | |
DDB_G0286445 | DDB_G0286445 | DDB0232431 | CDS | 4518430 | 840 | + | 0.230952 | |
DDB_G0286447 | DDB_G0286447 | DDB0232431 | CDS | 4520436 | 1566 | - | 0.292465 | |
DDB_G0286449 | DDB_G0286449 | DDB0232431 | CDS | 4523376 | 2082 | - | 0.207493 | |
DDB_G0286459 | DDB_G0286459 | contains one C1 domain (protein kinase C conserved region 1) which is involved in phorbol esterdiacylglycerol binding contains one coiled-coil domain | DDB0232431 | CDS | 4373322 | 4896 | - | 0.252247 |
DDB_G0286463 | DDB_G0286463 | DDB0232431 | CDS | 4380273 | 318 | + | 0.367925 | |
DDB_G0286465 | DDB_G0286465 | DDB0232431 | CDS | 4420447 | 3666 | + | 0.261866 | |
DDB_G0286467 | DDB_G0286467 | DDB0232431 | CDS | 4434479 | 3645 | + | 0.273251 | |
DDB_G0286469 | DDB_G0286469 | DDB0232431 | CDS | 4466916 | 1269 | - | 0.153664 | |
DDB_G0286475 | DDB_G0286475 | DDB0232431 | CDS | 4504352 | 156 | - | 0.25641 | |
DDB_G0286477 | DDB_G0286477 | DDB0232431 | CDS | 4505969 | 165 | + | 0.181818 | |
DDB_G0286479 | DDB_G0286479 | DDB0232431 | CDS | 4506469 | 3504 | - | 0.257991 | |
DDB_G0286481 | DDB_G0286481 | putative protein serinethreonine kinase similar to casein kinase II the alpha chain of a ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | DDB0232431 | CDS | 4514745 | 1818 | - | 0.264026 |
DDB_G0286485 | DDB_G0286485 | DDB0232431 | CDS | 4551311 | 1197 | + | 0.235589 | |
DDB_G0286487 | DDB_G0286487 | conserved protein ortholog of mammalian GPR108 contains a signal peptide and 7 transmembrane domains | DDB0232431 | CDS | 4553269 | 1350 | - | 0.275556 |
DDB_G0286489 | DDB_G0286489 | DDB0232431 | CDS | 4557644 | 2172 | + | 0.219613 | |
DDB_G0286493 | DDB_G0286493 | DDB0232431 | CDS | 4549634 | 156 | - | 0.275641 | |
DDB_G0286497_RTE | DDB_G0286497 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 4563823 | 360 | - | 0.330556 |
DDB_G0286503_RTE | DDB_G0286503 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232431 | CDS | 4566580 | 1558 | + | 0.290757 |
DDB_G0286505 | DDB_G0286505 | DDB0232431 | CDS | 4570772 | 1404 | + | 0.255698 | |
DDB_G0286507 | DDB_G0286507 | contains an RNA recognition motif (RRM) a putative RNA binding domain and a thioesterase domain | DDB0232431 | CDS | 4572284 | 1899 | - | 0.296998 |
DDB_G0286511 | DDB_G0286511 | similar to human ubiquitin-conjugating enzyme E2 J2 (UBE2J2) and yeast ubiquitin-conjugating 6 (UBC6) | DDB0232431 | CDS | 4575968 | 726 | - | 0.311295 |
DDB_G0286513 | DDB_G0286513 | DDB0232431 | CDS | 4577203 | 1683 | + | 0.236482 | |
DDB_G0286515 | DDB_G0286515 | DDB0232431 | CDS | 4579041 | 3036 | - | 0.244401 | |
DDB_G0286523 | DDB_G0286523 | DDB0232431 | CDS | 4588407 | 1884 | + | 0.306794 | |
DDB_G0286527_ps | DDB_G0286527 | putative pseudogene similar to a Dictyostelid family of putative SAM-dependent methyltransferases including | DDB0232431 | CDS | 4594246 | 561 | - | 0.247772 |
DDB_G0286531_RTE | DDB_G0286531 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232431 | CDS | 4596405 | 1318 | - | 0.383156 |
DDB_G0286533 | DDB_G0286533 | DDB0232431 | CDS | 4607142 | 2370 | + | 0.302532 | |
DDB_G0286537 | DDB_G0286537 | DDB0232431 | CDS | 4631120 | 1092 | - | 0.333333 | |
DDB_G0286539 | DDB_G0286539 | has limited similarity to mammalian p53 binding protein 1 (e.g. human TP53BP1) which plays a role in the response to DNA damagebrbr bCommunity annotation:b DDB G0286539 is similar (first blast hit both ways) to metazoan p53 binding protein. The homology is mostly within the BRCT domain but several additional small islands of homology are recognized by Blast2Sequences scattered along most of the length of the molecules. p53 binding protein aka 53BP1 is thought to mediate between sensors of double strand breaks and effectors of repair processes cell cycle arrest and apoptosis (see Fitzgerald et al Biochemical Society Transactions 37 897-904 (2009).br The Dicty gene is overexpressed fourfold (p2e-17)in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes whose products have roles in cell cycle progression are overexpressed in this strain this includes a number of genes for replication-coupled DNA repair (Doquang et al in preparation) and more specifical | DDB0232431 | CDS | 4632777 | 2724 | + | 0.270558 |
DDB_G0286543 | DDB_G0286543 | contains a RUN domain which is predicted to play a role in Ras-like GTPase signaling pathways | DDB0232431 | CDS | 4611232 | 4086 | + | 0.26603 |
DDB_G0286547_RTE | DDB_G0286547 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 4637483 | 2117 | - | 0.344355 |
DDB_G0286565 | DDB_G0286565 | DDB0232431 | CDS | 4641695 | 396 | + | 0.257576 | |
DDB_G0286567 | DDB_G0286567 | DDB0232431 | CDS | 4642679 | 1848 | + | 0.237554 | |
DDB_G0286569 | DDB_G0286569 | DDB0232431 | CDS | 4644643 | 345 | - | 0.173913 | |
DDB_G0286571 | DDB_G0286571 | DDB0232431 | CDS | 4645438 | 285 | + | 0.189474 | |
DDB_G0286575 | DDB_G0286575 | similar to retinol dehydrogenase and eukaryotic proteins of the short chain dehydrogenasesreductases family | DDB0232431 | CDS | 4647468 | 873 | + | 0.218786 |
DDB_G0286577 | DDB_G0286577 | DDB0232431 | CDS | 4648951 | 483 | + | 0.258799 | |
DDB_G0286581 | DDB_G0286581 | DDB0232431 | CDS | 4651768 | 915 | + | 0.285246 | |
DDB_G0286583 | DDB_G0286583 | DDB0232431 | CDS | 4653100 | 2169 | + | 0.262333 | |
DDB_G0286585 | DDB_G0286585 | DDB0232431 | CDS | 4657116 | 414 | + | 0.311594 | |
DDB_G0286587 | DDB_G0286587 | DDB0232431 | CDS | 4659532 | 414 | + | 0.318841 | |
DDB_G0286589 | DDB_G0286589 | DDB0232431 | CDS | 4670086 | 825 | - | 0.220606 | |
DDB_G0286591 | DDB_G0286591 | DDB0232431 | CDS | 4672737 | 2370 | - | 0.225738 | |
DDB_G0286593 | DDB_G0286593 | DDB0232431 | CDS | 4675755 | 1425 | + | 0.188772 | |
DDB_G0286595 | DDB_G0286595 | DDB0232431 | CDS | 4677268 | 1824 | - | 0.209978 | |
DDB_G0286597 | DDB_G0286597 | DDB0232431 | CDS | 4679470 | 525 | + | 0.260952 | |
DDB_G0286601 | DDB_G0286601 | DDB0232431 | CDS | 4687512 | 648 | - | 0.302469 | |
DDB_G0286603 | DDB_G0286603 | catalyzes the reaction L-glutamine D-fructose 6-phosphate L-glutamate D-glucosamine 6-phosphate | DDB0232431 | CDS | 4689118 | 1950 | - | 0.334359 |
DDB_G0286605 | DDB_G0286605 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232431 | CDS | 4695789 | 909 | - | 0.275028 |
DDB_G0286611 | DDB_G0286611 | DDB0232431 | CDS | 4704484 | 3666 | - | 0.267321 | |
DDB_G0286613 | DDB_G0286613 | DDB0232431 | CDS | 4708744 | 7692 | - | 0.303952 | |
DDB_G0286615 | DDB_G0286615 | DDB0232431 | CDS | 4721350 | 453 | - | 0.273731 | |
DDB_G0286619 | DDB_G0286619 | DDB0232431 | CDS | 4727396 | 1386 | - | 0.345599 | |
DDB_G0286625 | DDB_G0286625 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232431 | CDS | 4749168 | 1566 | - | 0.308429 |
DDB_G0286627 | DDB_G0286627 | putative protein serinethreonine kinase belongs to the STE group the kinase domain is similar to yeast BCK1 a mitogen-activated protein (MAP) kinase kinase kinase | DDB0232431 | CDS | 4756048 | 2016 | - | 0.251984 |
DDB_G0286629 | DDB_G0286629 | DDB0232431 | CDS | 4758841 | 312 | + | 0.224359 | |
DDB_G0286635 | DDB_G0286635 | DDB0232431 | CDS | 4764695 | 198 | - | 0.237374 | |
DDB_G0286637 | DDB_G0286637 | bifunctional enzyme catalyzes the reactions 510-methylenetetrahydrofolate 3-methyl-2-oxobutanoate tetrahydrofolate 2-dehydropantoate and (R)-pantoate NADP 2-dehydropantoate NADPH H | DDB0232431 | CDS | 4765267 | 2502 | - | 0.289369 |
DDB_G0286639 | DDB_G0286639 | DDB0232431 | CDS | 4771485 | 1107 | - | 0.307136 | |
DDB_G0286641 | DDB_G0286641 | putative GTPase that has high similarity to NOG1GTPBP4 GTPases which in S. cerevisiae associates with free 60S ribosomal subunits in the nucleolus this D. discoideumprotein is only about half the length and lacks the NOG1 C-terminal domain | DDB0232431 | CDS | 4774707 | 1044 | + | 0.198276 |
DDB_G0286649 | DDB_G0286649 | DDB0232431 | CDS | 4789671 | 867 | - | 0.314879 | |
DDB_G0286655 | DDB_G0286655 | DDB0232431 | CDS | 4795283 | 4173 | - | 0.22358 | |
DDB_G0286657 | DDB_G0286657 | contains a predicted signal peptide and two transmembrane domains highly similar to the neighboring gene | DDB0232431 | CDS | 4800131 | 303 | - | 0.306931 |
DDB_G0286659 | DDB_G0286659 | contains a predicted signal peptide and two transmembrane domains highly similar to the neighboring gene | DDB0232431 | CDS | 4800814 | 318 | - | 0.292453 |
DDB_G0286661 | DDB_G0286661 | bCommunity annotation:b DDB G0286661 is weakly similar to the histone chaperone chromatin-assembly factor caf1. DDB G0286661 and another caf1-related gene DDB_G0269800 are overexpressed in the Dicty rblA-null (fourfold and sevenfold respectively). Most genes associated with cell cycle progression are overexpressed in this strain. In addition DDB_G0269800 has a PIP (PCNA_interacting) domain (QKKLTSFF) as does human caf1. These observations support the idea that DDB_G0269800 is actually involved in replication-coupled chromatin assembly. br Harry MacWilliams September 2009 brbr bNote:b Do not confuse this gene with | DDB0232431 | CDS | 4801886 | 1485 | + | 0.261279 |
DDB_G0286667 | DDB_G0286667 | highly similar to | DDB0232431 | CDS | 4812413 | 267 | - | 0.348315 |
DDB_G0286669 | DDB_G0286669 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub | DDB0232431 | CDS | 4814848 | 2004 | - | 0.335329 |
DDB_G0286673 | DDB_G0286673 | DDB0232431 | CDS | 4821852 | 3297 | + | 0.234152 | |
DDB_G0286675 | DDB_G0286675 | DDB0232431 | CDS | 4825895 | 222 | - | 0.396396 | |
DDB_G0286677 | DDB_G0286677 | DDB0232431 | CDS | 4835533 | 4689 | + | 0.307955 | |
DDB_G0286679 | DDB_G0286679 | acyl carrier protein (ACP) is an essential cofactor in the synthesis of fatty acids in bacteria and plants in addition ACP is involved in many other reactions that require acyl transfer steps such as the synthesis of polyketide antibiotics phosphopantetheine is the prosthetic group of ACPs in some multienzyme complexes where it serves as a 'swinging arm' for the attachment of activated fatty acid and amino-acid groups | DDB0232431 | CDS | 4840734 | 258 | - | 0.232558 |
DDB_G0286681 | DDB_G0286681 | DDB0232431 | CDS | 4841268 | 2442 | - | 0.304668 | |
DDB_G0286683 | DDB_G0286683 | DDB0232431 | CDS | 4844701 | 618 | + | 0.190939 | |
DDB_G0286685 | DDB_G0286685 | DDB0232431 | CDS | 4845533 | 204 | - | 0.279412 | |
DDB_G0286687 | DDB_G0286687 | DDB0232431 | CDS | 4848740 | 132 | - | 0.19697 | |
DDB_G0286689 | DDB_G0286689 | DDB0232431 | CDS | 4852457 | 195 | + | 0.271795 | |
DDB_G0286691 | DDB_G0286691 | DDB0232431 | CDS | 4852997 | 408 | + | 0.25 | |
DDB_G0286695 | DDB_G0286695 | DDB0232431 | CDS | 4856852 | 735 | - | 0.285714 | |
DDB_G0286697 | DDB_G0286697 | DDB0232431 | CDS | 4858448 | 3414 | - | 0.227006 | |
DDB_G0286699 | DDB_G0286699 | DDB0232431 | CDS | 4862450 | 747 | + | 0.301205 | |
DDB_G0286701 | DDB_G0286701 | DDB0232431 | CDS | 4868445 | 1659 | + | 0.229656 | |
DDB_G0286707 | DDB_G0286707 | DDB0232431 | CDS | 4875042 | 2937 | + | 0.243105 | |
DDB_G0286713 | DDB_G0286713 | DDB0232431 | CDS | 4882439 | 693 | - | 0.277056 | |
DDB_G0286727 | DDB_G0286727 | similar to ChaC proteins thought to be associated with the putative ChaA calciumhydrogen cation transport protein in E. coli but with a PUA RNA binding domain fused at the carboxyl terminus | DDB0232431 | CDS | 4900621 | 969 | - | 0.330237 |
DDB_G0286729 | DDB_G0286729 | DDB0232431 | CDS | 4902848 | 786 | + | 0.328244 | |
DDB_G0286731 | DDB_G0286731 | DDB0232431 | CDS | 4904757 | 543 | + | 0.292818 | |
DDB_G0286735 | DDB_G0286735 | DDB0232431 | CDS | 4909097 | 2085 | + | 0.317026 | |
DDB_G0286737 | DDB_G0286737 | DDB0232431 | CDS | 4911744 | 1629 | + | 0.206262 | |
DDB_G0286739 | DDB_G0286739 | DDB0232431 | CDS | 4913488 | 591 | - | 0.182741 | |
DDB_G0286741 | DDB_G0286741 | DDB0232431 | CDS | 4914735 | 1260 | + | 0.307937 | |
DDB_G0286745 | DDB_G0286745 | DDB0232431 | CDS | 4920445 | 1449 | - | 0.285714 | |
DDB_G0286749 | DDB_G0286749 | DDB0232431 | CDS | 4924314 | 2643 | + | 0.259554 | |
DDB_G0286751 | DDB_G0286751 | DDB0232431 | CDS | 4927372 | 540 | - | 0.157407 | |
DDB_G0286755 | DDB_G0286755 | catalyzes the reaction NADPH 78-dihydrofolate NADP tetrahydrofolate in folate biosynthesis and formylTHF biosynthesis | DDB0232431 | CDS | 4931449 | 615 | - | 0.260163 |
DDB_G0286757 | DDB_G0286757 | DDB0232431 | CDS | 4933318 | 1227 | + | 0.321108 | |
DDB_G0286759 | DDB_G0286759 | similar to the mammalian KRTCAP2 (keratinocytes-associated protein 2) contains 4 putative transmembrane domains | DDB0232431 | CDS | 4935044 | 384 | - | 0.294271 |
DDB_G0286761 | DDB_G0286761 | DDB0232431 | CDS | 4936897 | 915 | + | 0.239344 | |
DDB_G0286763 | DDB_G0286763 | DDB0232431 | CDS | 4937865 | 1977 | - | 0.195245 | |
DDB_G0286765 | DDB_G0286765 | similar to BCS1 a mitochondrial chaperone required for assembly of cytochrome BC(1) complex expressed in pstA and pstO cells and in the upper and lower cups during culmination | DDB0232431 | CDS | 4940455 | 1725 | + | 0.276522 |
DDB_G0286767 | DDB_G0286767 | DDB0232431 | CDS | 4943773 | 255 | + | 0.313726 | |
DDB_G0286769 | DDB_G0286769 | DDB0232431 | CDS | 4945147 | 624 | - | 0.211538 | |
DDB_G0286775_ps | DDB_G0286775 | putative pseudogene fragment similar to gene | DDB0232431 | CDS | 4660931 | 444 | + | 0.198198 |
DDB_G0286779 | DDB_G0286779 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232431 | CDS | 4846920 | 195 | - | 0.230769 |
DDB_G0286781 | DDB_G0286781 | DDB0232431 | CDS | 4849724 | 195 | - | 0.282051 | |
DDB_G0286783 | DDB_G0286783 | DDB0232431 | CDS | 4929423 | 129 | - | 0.170543 | |
DDB_G0286787 | DDB_G0286787 | DDB0232431 | CDS | 4655553 | 639 | - | 0.214397 | |
DDB_G0286789 | DDB_G0286789 | DDB0232431 | CDS | 4662033 | 624 | + | 0.328526 | |
DDB_G0286791 | DDB_G0286791 | DDB0232431 | CDS | 4668476 | 1419 | + | 0.188865 | |
DDB_G0286793 | DDB_G0286793 | DDB0232431 | CDS | 4671665 | 576 | + | 0.291667 | |
DDB_G0286795 | DDB_G0286795 | DDB0232431 | CDS | 4684750 | 2076 | - | 0.186416 | |
DDB_G0286799 | DDB_G0286799 | DDB0232431 | CDS | 4720383 | 183 | - | 0.229508 | |
DDB_G0286801 | DDB_G0286801 | DDB0232431 | CDS | 4733206 | 282 | + | 0.255319 | |
DDB_G0286805 | DDB_G0286805 | DDB0232431 | CDS | 4742371 | 2757 | - | 0.261153 | |
DDB_G0286807 | DDB_G0286807 | DDB0232431 | CDS | 4751624 | 2067 | - | 0.195936 | |
DDB_G0286809 | DDB_G0286809 | DDB0232431 | CDS | 4768925 | 1560 | - | 0.253205 | |
DDB_G0286811 | DDB_G0286811 | DDB0232431 | CDS | 4773313 | 1191 | - | 0.25105 | |
DDB_G0286813_ps | DDB_G0286813 | putative pseudogene fragment similar to large EGF domain-containing proteins such as | DDB0232431 | CDS | 4811831 | 327 | + | 0.229358 |
DDB_G0286815_ps | DDB_G0286815 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 4826644 | 246 | + | 0.247967 |
DDB_G0286817 | DDB_G0286817 | DDB0232431 | CDS | 4863743 | 3132 | - | 0.24106 | |
DDB_G0286821 | DDB_G0286821 | DDB0232431 | CDS | 4918278 | 2088 | + | 0.198755 | |
DDB_G0286823_RTE | DDB_G0286823 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 4639700 | 1392 | - | 0.355603 |
DDB_G0286827_ps | DDB_G0286827 | putative pseudogene similar to | DDB0232431 | CDS | 4953029 | 363 | - | 0.261708 |
DDB_G0286829 | DDB_G0286829 | DDB0232431 | CDS | 4954349 | 585 | + | 0.217094 | |
DDB_G0286831 | DDB_G0286831 | DDB0232431 | CDS | 4955377 | 324 | - | 0.29321 | |
DDB_G0286833 | DDB_G0286833 | DDB0232431 | CDS | 4956036 | 987 | - | 0.316109 | |
DDB_G0286835 | DDB_G0286835 | DDB0232431 | CDS | 4957742 | 1602 | + | 0.182896 | |
DDB_G0286841 | DDB_G0286841 | member of the AGC kinase group similar to the kinase domains of MAST kinases (Microtubule-Associated SerineThreonine kinase) | DDB0232431 | CDS | 4966020 | 1389 | - | 0.218143 |
DDB_G0286845 | DDB_G0286845 | DDB0232431 | CDS | 4972112 | 885 | + | 0.277966 | |
DDB_G0286847 | DDB_G0286847 | DDB0232431 | CDS | 4973256 | 2538 | - | 0.215524 | |
DDB_G0286849 | DDB_G0286849 | similar to bacterial short-chain dehydrogenasereductase family proteins and human RDH8 (retinol dehydrogenase 8) | DDB0232431 | CDS | 4977120 | 870 | - | 0.28046 |
DDB_G0286853 | DDB_G0286853 | DDB0232431 | CDS | 4990193 | 714 | + | 0.277311 | |
DDB_G0286861 | DDB_G0286861 | DDB0232431 | CDS | 4978558 | 885 | + | 0.275706 | |
DDB_G0286863_RTE | DDB_G0286863 | DDB0232431 | CDS | 4996972 | 1293 | + | 0.288476 | |
DDB_G0286865 | DDB_G0286865 | DDB0232431 | CDS | 5001179 | 171 | - | 0.245614 | |
DDB_G0286867 | DDB_G0286867 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232431 | CDS | 5001922 | 4224 | - | 0.253788 |
DDB_G0286869 | DDB_G0286869 | DDB0232431 | CDS | 5007468 | 1266 | + | 0.259084 | |
DDB_G0286871 | DDB_G0286871 | DDB0232431 | CDS | 5008976 | 573 | + | 0.233857 | |
DDB_G0286873 | DDB_G0286873 | DDB0232431 | CDS | 5009906 | 1077 | + | 0.257196 | |
DDB_G0286877 | DDB_G0286877 | DDB0232431 | CDS | 5013005 | 4725 | - | 0.205291 | |
DDB_G0286879 | DDB_G0286879 | DDB0232431 | CDS | 5018337 | 561 | - | 0.210339 | |
DDB_G0286881 | DDB_G0286881 | DDB0232431 | CDS | 5019240 | 2853 | + | 0.278654 | |
DDB_G0286883 | DDB_G0286883 | DDB0232431 | CDS | 5022922 | 573 | - | 0.277487 | |
DDB_G0286885 | DDB_G0286885 | DDB0232431 | CDS | 5024349 | 1764 | + | 0.384354 | |
DDB_G0286887 | DDB_G0286887 | DDB0232431 | CDS | 5026472 | 372 | - | 0.271505 | |
DDB_G0286891 | DDB_G0286891 | DDB0232431 | CDS | 5031762 | 3546 | + | 0.227862 | |
DDB_G0286897 | DDB_G0286897 | DDB0232431 | CDS | 5040461 | 4215 | - | 0.308422 | |
DDB_G0286899 | DDB_G0286899 | DDB0232431 | CDS | 5047649 | 3129 | + | 0.230745 | |
DDB_G0286901 | DDB_G0286901 | DDB0232431 | CDS | 5050966 | 2181 | - | 0.200367 | |
DDB_G0286911 | DDB_G0286911 | DDB0232431 | CDS | 5061049 | 1503 | + | 0.29674 | |
DDB_G0286913 | DDB_G0286913 | DDB0232431 | CDS | 5070335 | 2940 | + | 0.187755 | |
DDB_G0286915 | DDB_G0286915 | DDB0232431 | CDS | 5073666 | 237 | - | 0.409283 | |
DDB_G0286917 | DDB_G0286917 | DDB0232431 | CDS | 5074484 | 1932 | + | 0.201346 | |
DDB_G0286921 | DDB_G0286921 | DDB0232431 | CDS | 5081040 | 1605 | - | 0.28162 | |
DDB_G0286923 | DDB_G0286923 | DDB0232431 | CDS | 5085448 | 1203 | - | 0.335827 | |
DDB_G0286925 | DDB_G0286925 | DDB0232431 | CDS | 5087989 | 990 | + | 0.363636 | |
DDB_G0286929 | DDB_G0286929 | DDB0232431 | CDS | 5090123 | 651 | + | 0.27957 | |
DDB_G0286931 | DDB_G0286931 | DDB0232431 | CDS | 5091515 | 15669 | + | 0.264535 | |
DDB_G0286933 | DDB_G0286933 | DDB0232431 | CDS | 5107749 | 2073 | + | 0.239267 | |
DDB_G0286935 | DDB_G0286935 | DDB0232431 | CDS | 5114045 | 1605 | + | 0.189408 | |
DDB_G0286937 | DDB_G0286937 | DDB0232431 | CDS | 5117554 | 126 | + | 0.222222 | |
DDB_G0286939 | DDB_G0286939 | DDB0232431 | CDS | 5118438 | 834 | + | 0.252998 | |
DDB_G0286941 | DDB_G0286941 | DDB0232431 | CDS | 5119924 | 2415 | + | 0.291511 | |
DDB_G0286943 | DDB_G0286943 | DDB0232431 | CDS | 5123987 | 156 | + | 0.275641 | |
DDB_G0286947 | DDB_G0286947 | DDB0232431 | CDS | 5126978 | 5022 | + | 0.258662 | |
DDB_G0286949 | DDB_G0286949 | DDB0232431 | CDS | 5132153 | 285 | + | 0.252632 | |
DDB_G0286951 | DDB_G0286951 | DDB0232431 | CDS | 5136274 | 3333 | + | 0.259826 | |
DDB_G0286955 | DDB_G0286955 | DDB0232431 | CDS | 5145533 | 1125 | - | 0.277333 | |
DDB_G0286957 | DDB_G0286957 | DDB0232431 | CDS | 5147352 | 249 | - | 0.39759 | |
DDB_G0286959 | DDB_G0286959 | DDB0232431 | CDS | 5154310 | 1710 | - | 0.261404 | |
DDB_G0286963 | DDB_G0286963 | DDB0232431 | CDS | 5110525 | 2316 | + | 0.269862 | |
DDB_G0286965 | DDB_G0286965 | DDB0232431 | CDS | 5117185 | 300 | + | 0.243333 | |
DDB_G0286969 | DDB_G0286969 | DDB0232431 | CDS | 5063512 | 6240 | + | 0.356731 | |
DDB_G0286973 | DDB_G0286973 | DDB0232431 | CDS | 5142082 | 1713 | - | 0.253357 | |
DDB_G0286975_ps | DDB_G0286975 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 5144135 | 969 | - | 0.283798 |
DDB_G0286977 | DDB_G0286977 | DDB0232431 | CDS | 5148727 | 1143 | - | 0.276465 | |
DDB_G0286979 | DDB_G0286979 | DDB0232431 | CDS | 5150412 | 1884 | - | 0.277601 | |
DDB_G0286981 | DDB_G0286981 | DDB0232431 | CDS | 5158045 | 5043 | + | 0.17906 | |
DDB_G0286983 | DDB_G0286983 | DDB0232431 | CDS | 5163425 | 1503 | - | 0.302728 | |
DDB_G0286987_RTE | DDB_G0286987 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 5166703 | 1335 | - | 0.307116 |
DDB_G0286989 | DDB_G0286989 | DDB0232431 | CDS | 5175729 | 402 | + | 0.310945 | |
DDB_G0286991 | DDB_G0286991 | DDB0232431 | CDS | 5177493 | 1380 | + | 0.33913 | |
DDB_G0286993 | DDB_G0286993 | DDB0232431 | CDS | 5169198 | 1524 | - | 0.211942 | |
DDB_G0286995 | DDB_G0286995 | DDB0232431 | CDS | 5179444 | 1834 | + | 0.23337 | |
DDB_G0286999 | DDB_G0286999 | DDB0232431 | CDS | 5181860 | 1561 | + | 0.305573 | |
DDB_G0287001 | DDB_G0287001 | member of the TKL (tyrosine kinase-like) group contains zinc-binding LIM domain | DDB0232431 | CDS | 5188585 | 1953 | - | 0.28213 |
DDB_G0287003 | DDB_G0287003 | DDB0232431 | CDS | 5191304 | 1254 | - | 0.334928 | |
DDB_G0287005 | DDB_G0287005 | similar to the H. sapiens eukaryotic translation initiation factor 3 subunit M (EIF3M) | DDB0232431 | CDS | 5193960 | 1206 | + | 0.27529 |
DDB_G0287013 | DDB_G0287013 | DDB0232431 | CDS | 5205106 | 1026 | - | 0.346979 | |
DDB_G0287015 | DDB_G0287015 | DDB0232431 | CDS | 5207077 | 414 | + | 0.345411 | |
DDB_G0287017 | DDB_G0287017 | belongs to the HAD-like hydrolase superfamily similar to human HDHD3 (haloacid dehalogenase-like hydrolase domain-containing protein 3) | DDB0232431 | CDS | 5207898 | 858 | - | 0.221445 |
DDB_G0287023 | DDB_G0287023 | DDB0232431 | CDS | 5202818 | 669 | + | 0.139013 | |
DDB_G0287025 | DDB_G0287025 | DDB0232431 | CDS | 5203841 | 984 | + | 0.251016 | |
DDB_G0287027 | DDB_G0287027 | DDB0232431 | CDS | 5209927 | 3015 | - | 0.242454 | |
DDB_G0287037 | DDB_G0287037 | DDB0232431 | CDS | 5215181 | 978 | + | 0.274029 | |
DDB_G0287039 | DDB_G0287039 | DDB0232431 | CDS | 5219424 | 1599 | - | 0.202001 | |
DDB_G0287041 | DDB_G0287041 | DDB0232431 | CDS | 5221229 | 1827 | + | 0.181719 | |
DDB_G0287043 | DDB_G0287043 | DDB0232431 | CDS | 5225371 | 1083 | + | 0.263158 | |
DDB_G0287047 | DDB_G0287047 | DDB0232431 | CDS | 5227447 | 249 | - | 0.405622 | |
DDB_G0287051 | DDB_G0287051 | DDB0232431 | CDS | 5231470 | 777 | + | 0.235521 | |
DDB_G0287059 | DDB_G0287059 | DDB0232431 | CDS | 5272697 | 2523 | - | 0.200159 | |
DDB_G0287061 | DDB_G0287061 | contains a Rab GTPase domain but due to its predicted molecular weight (1836 amino acids) it is not a small GTPase | DDB0232431 | CDS | 5278698 | 5511 | + | 0.245328 |
DDB_G0287063 | DDB_G0287063 | DDB0232431 | CDS | 5285069 | 1296 | + | 0.266975 | |
DDB_G0287065 | DDB_G0287065 | DDB0232431 | CDS | 5286829 | 480 | + | 0.258333 | |
DDB_G0287067 | DDB_G0287067 | DDB0232431 | CDS | 5289082 | 393 | - | 0.29771 | |
DDB_G0287069 | DDB_G0287069 | DDB0232431 | CDS | 5289970 | 1167 | + | 0.264782 | |
DDB_G0287071 | DDB_G0287071 | DDB0232431 | CDS | 5291519 | 1101 | + | 0.248865 | |
DDB_G0287073 | DDB_G0287073 | contains a single HMG12 box | DDB0232431 | CDS | 5293321 | 1053 | + | 0.296296 |
DDB_G0287075 | DDB_G0287075 | DDB0232431 | CDS | 5294660 | 1419 | - | 0.317829 | |
DDB_G0287077 | DDB_G0287077 | DDB0232431 | CDS | 5299968 | 1221 | + | 0.22932 | |
DDB_G0287079 | DDB_G0287079 | DDB0232431 | CDS | 5302047 | 1824 | + | 0.247259 | |
DDB_G0287081 | DDB_G0287081 | DDB0232431 | CDS | 5304055 | 840 | - | 0.24881 | |
DDB_G0287083 | DDB_G0287083 | DDB0232431 | CDS | 5305570 | 1755 | + | 0.211966 | |
DDB_G0287085 | DDB_G0287085 | there is a paralog of this gene | DDB0232431 | CDS | 5307684 | 948 | - | 0.257384 |
DDB_G0287089 | DDB_G0287089 | DDB0232431 | CDS | 5311879 | 489 | - | 0.255624 | |
DDB_G0287091 | DDB_G0287091 | DDB0232431 | CDS | 5313189 | 492 | - | 0.288618 | |
DDB_G0287093 | DDB_G0287093 | DDB0232431 | CDS | 5314330 | 471 | - | 0.248408 | |
DDB_G0287097 | DDB_G0287097 | contains 4 FNIP repeats conserved in Dictyostelium | DDB0232431 | CDS | 5338338 | 1497 | + | 0.263193 |
DDB_G0287099 | DDB_G0287099 | DDB0232431 | CDS | 5339911 | 669 | - | 0.227205 | |
DDB_G0287103 | DDB_G0287103 | similar to timeless which in Drosophila forms a complex at replication forks that plays a role in the DNA damage response and is phosphorylated by cyclin-dependent kinases brbr bCommunity annotation: bDDB G0287103 is induced 11-fold in a | DDB0232431 | CDS | 5268402 | 3981 | + | 0.262999 |
DDB_G0287105 | DDB_G0287105 | DDB0232431 | CDS | 5213175 | 1323 | - | 0.250189 | |
DDB_G0287107 | DDB_G0287107 | DDB0232431 | CDS | 5223614 | 1176 | - | 0.261054 | |
DDB_G0287111 | DDB_G0287111 | DDB0232431 | CDS | 5266193 | 765 | + | 0.235294 | |
DDB_G0287113 | DDB_G0287113 | DDB0232431 | CDS | 5275365 | 2301 | - | 0.280748 | |
DDB_G0287115 | DDB_G0287115 | DDB0232431 | CDS | 5287659 | 1137 | - | 0.284081 | |
DDB_G0287117_TE | DDB_G0287117 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232431 | CDS | 5315241 | 3150 | - | 0.275238 |
DDB_G0287123 | DDB_G0287123 | DDB0232431 | CDS | 5341430 | 5022 | + | 0.175627 | |
DDB_G0287129 | DDB_G0287129 | DDB0232431 | CDS | 5352426 | 420 | - | 0.292857 | |
DDB_G0287133 | DDB_G0287133 | DDB0232431 | CDS | 5355378 | 2250 | - | 0.211556 | |
DDB_G0287135 | DDB_G0287135 | DDB0232431 | CDS | 5361475 | 1197 | - | 0.185464 | |
DDB_G0287139 | DDB_G0287139 | DDB0232431 | CDS | 5368411 | 816 | + | 0.280637 | |
DDB_G0287145 | DDB_G0287145 | DDB0232431 | CDS | 5377683 | 213 | - | 0.211268 | |
DDB_G0287149 | DDB_G0287149 | similar to mammalian DNA polymerase kappa (POLK) and E. coli dinB a translesion DNA repair polymerase | DDB0232431 | CDS | 5382189 | 1554 | - | 0.240026 |
DDB_G0287151 | DDB_G0287151 | similar to retinol dehydrogenase and eukaryotic short chain dehydrogenasesreductases family proteins | DDB0232431 | CDS | 5393798 | 930 | - | 0.224731 |
DDB_G0287153 | DDB_G0287153 | DDB0232431 | CDS | 5400400 | 480 | + | 0.308333 | |
DDB_G0287155 | DDB_G0287155 | DDB0232431 | CDS | 5407048 | 495 | + | 0.161616 | |
DDB_G0287157 | DDB_G0287157 | DDB0232431 | CDS | 5407710 | 4575 | - | 0.261639 | |
DDB_G0287161 | DDB_G0287161 | DDB0232431 | CDS | 5415608 | 1059 | - | 0.266289 | |
DDB_G0287163 | DDB_G0287163 | DDB0232431 | CDS | 5419077 | 819 | - | 0.191697 | |
DDB_G0287165 | DDB_G0287165 | similar to spastin (spastic paraplegia 4 protein) a mammalian ATP-dependent microtubule severing protein | DDB0232431 | CDS | 5420537 | 1968 | + | 0.269817 |
DDB_G0287167 | DDB_G0287167 | DDB0232431 | CDS | 5422690 | 4314 | - | 0.248725 | |
DDB_G0287169 | DDB_G0287169 | DDB0232431 | CDS | 5428138 | 693 | - | 0.265512 | |
DDB_G0287171 | DDB_G0287171 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232431 | CDS | 5429343 | 5619 | + | 0.2399 |
DDB_G0287173_ps | DDB_G0287173 | putative pseudogene similar to protein kinases but does not contain the consensus sequences required for kinase function | DDB0232431 | CDS | 5444697 | 834 | - | 0.27458 |
DDB_G0287175_ps | DDB_G0287175 | putative pseudogene similar to a D. discoideum gene family including | DDB0232431 | CDS | 5376601 | 354 | + | 0.285311 |
DDB_G0287177 | DDB_G0287177 | DDB0232431 | CDS | 5445848 | 339 | - | 0.277286 | |
DDB_G0287179 | DDB_G0287179 | DDB0232431 | CDS | 5446279 | 294 | - | 0.20068 | |
DDB_G0287183_ps | DDB_G0287183 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 5446818 | 720 | + | 0.323611 |
DDB_G0287185 | DDB_G0287185 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232431 | CDS | 5448496 | 456 | - | 0.263158 |
DDB_G0287187 | DDB_G0287187 | DDB0232431 | CDS | 5359561 | 1791 | + | 0.156896 | |
DDB_G0287189 | DDB_G0287189 | DDB0232431 | CDS | 5363024 | 624 | - | 0.192308 | |
DDB_G0287191 | DDB_G0287191 | DDB0232431 | CDS | 5366531 | 219 | + | 0.493151 | |
DDB_G0287193 | DDB_G0287193 | DDB0232431 | CDS | 5388100 | 3177 | + | 0.251495 | |
DDB_G0287195 | DDB_G0287195 | DDB0232431 | CDS | 5391671 | 1593 | + | 0.244821 | |
DDB_G0287201 | DDB_G0287201 | DDB0232431 | CDS | 5401496 | 1863 | - | 0.243156 | |
DDB_G0287205 | DDB_G0287205 | DDB0232431 | CDS | 5405589 | 168 | - | 0.27381 | |
DDB_G0287207 | DDB_G0287207 | large protein (1685 amino acids) containing a Rab domain Rab small GTPases are usually around 200 amino acids in length | DDB0232431 | CDS | 5437470 | 5058 | + | 0.217477 |
DDB_G0287215 | DDB_G0287215 | DDB0232432 | CDS | 3070 | 1113 | - | 0.28841 | |
DDB_G0287217 | DDB_G0287217 | DDB0232432 | CDS | 5282 | 3435 | + | 0.2131 | |
DDB_G0287219 | DDB_G0287219 | conserved Dictyostelium protein similar to bacterial proteins contains a predicted signal peptide | DDB0232432 | CDS | 8994 | 408 | - | 0.291667 |
DDB_G0287221 | DDB_G0287221 | similar to TRIP12 (thyroid hormone receptor interactor 12) a component of PA700 an ATP-dependent multisubunit protein that activates the proteolytic activities of the 20S proteasome | DDB0232432 | CDS | 10149 | 6294 | - | 0.317445 |
DDB_G0287225 | DDB_G0287225 | DDB0232432 | CDS | 21182 | 2106 | + | 0.195632 | |
DDB_G0287235_ps | DDB_G0287235 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 35600 | 2313 | - | 0.242542 |
DDB_G0287237_ps | DDB_G0287237 | putative pseudogene contains a kinase domain that lacks a RD signature | DDB0232432 | CDS | 42818 | 972 | - | 0.255144 |
DDB_G0287239 | DDB_G0287239 | DDB0232432 | CDS | 52532 | 921 | - | 0.230185 | |
DDB_G0287241 | DDB_G0287241 | DDB0232432 | CDS | 58745 | 939 | + | 0.217252 | |
DDB_G0287243 | DDB_G0287243 | DDB0232432 | CDS | 60363 | 1077 | + | 0.275766 | |
DDB_G0287249_TE | DDB_G0287249 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232432 | CDS | 101 | 1535 | - | 0.225407 |
DDB_G0287251 | DDB_G0287251 | DDB0232432 | CDS | 19093 | 744 | - | 0.215054 | |
DDB_G0287257 | DDB_G0287257 | DDB0232432 | CDS | 49910 | 1513 | - | 0.356907 | |
DDB_G0287263 | DDB_G0287263 | DDB0232432 | CDS | 64505 | 213 | + | 0.267606 | |
DDB_G0287265 | DDB_G0287265 | DDB0232432 | CDS | 65084 | 1470 | - | 0.238776 | |
DDB_G0287267 | DDB_G0287267 | DDB0232432 | CDS | 67613 | 2187 | - | 0.306813 | |
DDB_G0287275 | DDB_G0287275 | DDB0232432 | CDS | 77605 | 4059 | + | 0.272974 | |
DDB_G0287277 | DDB_G0287277 | members of the NAD-dependent epimerasedehydratase family use nucleotide-sugar substrates for a variety of chemical reactions | DDB0232432 | CDS | 82214 | 1014 | - | 0.300789 |
DDB_G0287279 | DDB_G0287279 | belongs to the UPF0203 family similar to human TRIAP1 (TP53-regulated inhibitor of apoptosis 1) | DDB0232432 | CDS | 83567 | 243 | - | 0.255144 |
DDB_G0287281 | DDB_G0287281 | DDB0232432 | CDS | 84160 | 1254 | - | 0.261563 | |
DDB_G0287283 | DDB_G0287283 | DDB0232432 | CDS | 91412 | 153 | - | 0.24183 | |
DDB_G0287287 | DDB_G0287287 | DDB0232432 | CDS | 74321 | 2298 | - | 0.239774 | |
DDB_G0287289 | DDB_G0287289 | DDB0232432 | CDS | 86247 | 4419 | + | 0.283548 | |
DDB_G0287299 | DDB_G0287299 | DDB0232432 | CDS | 94597 | 1266 | + | 0.2109 | |
DDB_G0287303 | DDB_G0287303 | amino acid permeases are integral membrane proteins involved in the transport of amino acids into the cell contains 12 putative transmembrane domains | DDB0232432 | CDS | 104846 | 1998 | - | 0.278278 |
DDB_G0287305 | DDB_G0287305 | DDB0232432 | CDS | 110292 | 543 | - | 0.246777 | |
DDB_G0287309 | DDB_G0287309 | DDB0232432 | CDS | 112586 | 600 | + | 0.26 | |
DDB_G0287311_ps | DDB_G0287311 | putative pseudogene similar to D. discoideum genes | DDB0232432 | CDS | 113384 | 336 | - | 0.27381 |
DDB_G0287313 | DDB_G0287313 | DDB0232432 | CDS | 114376 | 2025 | + | 0.185185 | |
DDB_G0287315 | DDB_G0287315 | DDB0232432 | CDS | 120470 | 4677 | + | 0.297199 | |
DDB_G0287317 | DDB_G0287317 | DDB0232432 | CDS | 125370 | 1839 | - | 0.290375 | |
DDB_G0287319 | DDB_G0287319 | similar to human SLC35E2 (solute carrier family 35 member E2) contains 10 putative transmembrane domains | DDB0232432 | CDS | 129877 | 1047 | + | 0.30468 |
DDB_G0287321 | DDB_G0287321 | DDB0232432 | CDS | 131270 | 399 | - | 0.205514 | |
DDB_G0287323 | DDB_G0287323 | contains an N-terminal oxidoreductase domain and a partial C-terminal oxidoreductase domain the GfoIdhMocA family proteins utilize NADP or NAD | DDB0232432 | CDS | 133013 | 1293 | + | 0.28925 |
DDB_G0287325 | DDB_G0287325 | similar to mammalian EPS15 a clathrin adaptor that binds to the AP2 alpha subunit in mammalian cells | DDB0232432 | CDS | 137312 | 3591 | + | 0.310498 |
DDB_G0287329 | DDB_G0287329 | DDB0232432 | CDS | 143681 | 219 | - | 0.342466 | |
DDB_G0287331 | DDB_G0287331 | DDB0232432 | CDS | 144715 | 2136 | + | 0.267322 | |
DDB_G0287335 | DDB_G0287335 | has similarity to human cold inducible RNA binding protein (CIRBP) however it is considreably shorter | DDB0232432 | CDS | 148219 | 276 | + | 0.344203 |
DDB_G0287339 | DDB_G0287339 | DDB0232432 | CDS | 154225 | 2106 | + | 0.188509 | |
DDB_G0287341 | DDB_G0287341 | DDB0232432 | CDS | 157067 | 738 | + | 0.216802 | |
DDB_G0287343 | DDB_G0287343 | DDB0232432 | CDS | 158259 | 837 | - | 0.215054 | |
DDB_G0287347 | DDB_G0287347 | DDB0232432 | CDS | 162247 | 2343 | - | 0.216389 | |
DDB_G0287355 | DDB_G0287355 | DDB0232432 | CDS | 172169 | 126 | - | 0.412698 | |
DDB_G0287357 | DDB_G0287357 | DDB0232432 | CDS | 172540 | 2127 | - | 0.29149 | |
DDB_G0287359 | DDB_G0287359 | DDB0232432 | CDS | 175065 | 1446 | - | 0.280083 | |
DDB_G0287365 | DDB_G0287365 | DDB0232432 | CDS | 199757 | 3300 | - | 0.267576 | |
DDB_G0287367 | DDB_G0287367 | DDB0232432 | CDS | 204023 | 981 | + | 0.24261 | |
DDB_G0287369 | DDB_G0287369 | DDB0232432 | CDS | 205200 | 858 | - | 0.19697 | |
DDB_G0287373 | DDB_G0287373 | DDB0232432 | CDS | 217435 | 933 | - | 0.230439 | |
DDB_G0287375 | DDB_G0287375 | DDB0232432 | CDS | 219071 | 2973 | + | 0.215607 | |
DDB_G0287379 | DDB_G0287379 | DDB0232432 | CDS | 233763 | 3231 | + | 0.320644 | |
DDB_G0287381 | DDB_G0287381 | DDB0232432 | CDS | 237838 | 843 | + | 0.200475 | |
DDB_G0287383 | DDB_G0287383 | DDB0232432 | CDS | 239046 | 510 | + | 0.294118 | |
DDB_G0287385 | DDB_G0287385 | DDB0232432 | CDS | 239982 | 1125 | + | 0.249778 | |
DDB_G0287387 | DDB_G0287387 | DDB0232432 | CDS | 241597 | 879 | - | 0.196815 | |
DDB_G0287389 | DDB_G0287389 | DDB0232432 | CDS | 243540 | 2307 | + | 0.202427 | |
DDB_G0287395 | DDB_G0287395 | DDB0232432 | CDS | 250770 | 843 | + | 0.238434 | |
DDB_G0287397 | DDB_G0287397 | DDB0232432 | CDS | 251848 | 2013 | - | 0.273224 | |
DDB_G0287399 | DDB_G0287399 | DDB0232432 | CDS | 255717 | 1461 | - | 0.370979 | |
DDB_G0287403 | DDB_G0287403 | similar to | DDB0232432 | CDS | 259377 | 459 | - | 0.254902 |
DDB_G0287405 | DDB_G0287405 | conserved protein of unknown function contains 9 putative transmembrane domains | DDB0232432 | CDS | 260619 | 1533 | - | 0.307893 |
DDB_G0287407 | DDB_G0287407 | similar to nephrocystin 3 Grp94 neighboring nucleotidase and other TPR repeat-containing proteins | DDB0232432 | CDS | 263392 | 4992 | + | 0.313902 |
DDB_G0287409_RTE | DDB_G0287409 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232432 | CDS | 269267 | 1335 | + | 0.307865 |
DDB_G0287411 | DDB_G0287411 | DDB0232432 | CDS | 271707 | 2298 | - | 0.219756 | |
DDB_G0287413 | DDB_G0287413 | DDB0232432 | CDS | 274270 | 666 | + | 0.202703 | |
DDB_G0287415 | DDB_G0287415 | DDB0232432 | CDS | 275303 | 3039 | + | 0.303389 | |
DDB_G0287417 | DDB_G0287417 | DDB0232432 | CDS | 181547 | 1680 | + | 0.232738 | |
DDB_G0287421_RTE | DDB_G0287421 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232432 | CDS | 278825 | 561 | + | 0.342246 |
DDB_G0287423 | DDB_G0287423 | DDB0232432 | CDS | 96074 | 1515 | - | 0.264026 | |
DDB_G0287425 | DDB_G0287425 | DDB0232432 | CDS | 98175 | 1521 | - | 0.286654 | |
DDB_G0287427 | DDB_G0287427 | DDB0232432 | CDS | 107640 | 1023 | + | 0.256109 | |
DDB_G0287429 | DDB_G0287429 | DDB0232432 | CDS | 109242 | 810 | + | 0.216049 | |
DDB_G0287431_ps | DDB_G0287431 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 117395 | 1494 | - | 0.271754 |
DDB_G0287433 | DDB_G0287433 | DDB0232432 | CDS | 118782 | 222 | - | 0.220721 | |
DDB_G0287437 | DDB_G0287437 | DDB0232432 | CDS | 131874 | 663 | - | 0.227753 | |
DDB_G0287439 | DDB_G0287439 | DDB0232432 | CDS | 148729 | 888 | - | 0.269144 | |
DDB_G0287441 | DDB_G0287441 | contains six predicted transmembrane domains similar to a D. purpureum protein | DDB0232432 | CDS | 160889 | 969 | + | 0.275542 |
DDB_G0287445 | DDB_G0287445 | conserved protein ortholog of the human C11orf2 (Chromosome 11 Open Reading Frame 2) protein contains a putative Dor1 domain which in yeast is involved in vesicle targeting to the Golgi apparatus and complexes with a number of other trafficking proteins | DDB0232432 | CDS | 177577 | 2754 | + | 0.289397 |
DDB_G0287447 | DDB_G0287447 | ortholog of the bacterial epsilon subunit of DNA polymerase III a multisubunit enzyme responsible for most of the replicative synthesis in bacteria the contain the editing function and is a proofreading 3'-5' exonuclease the Dictyostelium gene is missing approximately 100 amino acids at the carboxyl terminus | DDB0232432 | CDS | 185922 | 1452 | + | 0.232782 |
DDB_G0287449 | DDB_G0287449 | DDB0232432 | CDS | 189973 | 903 | + | 0.272425 | |
DDB_G0287451_ps | DDB_G0287451 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232432 | CDS | 229012 | 624 | - | 0.232372 |
DDB_G0287453_ps | DDB_G0287453 | putative pseudogene fragment similar to EGF repeat-containing proteins | DDB0232432 | CDS | 280003 | 714 | - | 0.285714 |
DDB_G0287455_RTE | DDB_G0287455 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232432 | CDS | 282346 | 1666 | - | 0.264106 |
DDB_G0287457 | DDB_G0287457 | DDB0232432 | CDS | 209576 | 2334 | - | 0.191088 | |
DDB_G0287463 | DDB_G0287463 | DDB0232432 | CDS | 290618 | 1269 | - | 0.19937 | |
DDB_G0287465 | DDB_G0287465 | DDB0232432 | CDS | 292797 | 1356 | + | 0.272861 | |
DDB_G0287471 | DDB_G0287471 | contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232432 | CDS | 300793 | 1047 | - | 0.282713 |
DDB_G0287473_ps | DDB_G0287473 | putative pseudogene paramecium surface antigen repeat-containing protein family gene | DDB0232432 | CDS | 302500 | 1475 | - | 0.231186 |
DDB_G0287475 | DDB_G0287475 | DDB0232432 | CDS | 312971 | 810 | - | 0.233333 | |
DDB_G0287477 | DDB_G0287477 | conserved Dictyostelium protein contains one putative transmembrane domain and an additional putative signal sequence | DDB0232432 | CDS | 314532 | 1944 | - | 0.277263 |
DDB_G0287479 | DDB_G0287479 | DDB0232432 | CDS | 323189 | 1881 | - | 0.150984 | |
DDB_G0287489 | DDB_G0287489 | DDB0232432 | CDS | 294648 | 264 | - | 0.19697 | |
DDB_G0287491 | DDB_G0287491 | contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232432 | CDS | 308656 | 1077 | - | 0.299907 |
DDB_G0287493_ps | DDB_G0287493 | putative pseudogene paramecium surface antigen repeat-containing family protein | DDB0232432 | CDS | 310846 | 426 | - | 0.293427 |
DDB_G0287499 | DDB_G0287499 | DDB0232432 | CDS | 334918 | 1125 | - | 0.200889 | |
DDB_G0287501 | DDB_G0287501 | similar to polyketide synthases but missing more than half of the amino terminus | DDB0232432 | CDS | 336533 | 3795 | - | 0.253228 |
DDB_G0287503 | DDB_G0287503 | DDB0232432 | CDS | 327483 | 2048 | + | 0.132324 | |
DDB_G0287509 | DDB_G0287509 | similar to bacterial 14-dihydroxy-2-naphthoate octaprenyltransferase which catalyzes the reaction 14-dihydroxy-2-naphthoate polyprenylpyrophosphate demethylmenaquinone-8 pyrophosphate COsub2sub and similar to mammalian transitional epithelia response protein of unknown function | DDB0232432 | CDS | 341417 | 993 | - | 0.266868 |
DDB_G0287511 | DDB_G0287511 | DDB0232432 | CDS | 343078 | 3939 | - | 0.262503 | |
DDB_G0287517 | DDB_G0287517 | DDB0232432 | CDS | 360366 | 351 | - | 0.264957 | |
DDB_G0287519 | DDB_G0287519 | catalyzes the reaction acetoacetyl-CoA Hsub2subO CoA acetoacetate | DDB0232432 | CDS | 362168 | 1599 | - | 0.3596 |
DDB_G0287521 | DDB_G0287521 | ortholog of the conserved signal peptide peptidase-like 3 (SPPL3) contains 8 predicted transmembrane domains and an additional N-terminal signal sequence | DDB0232432 | CDS | 364712 | 1116 | - | 0.236559 |
DDB_G0287525 | DDB_G0287525 | DDB0232432 | CDS | 366594 | 255 | - | 0.215686 | |
DDB_G0287527 | DDB_G0287527 | DDB0232432 | CDS | 367089 | 357 | + | 0.235294 | |
DDB_G0287529 | DDB_G0287529 | DDB0232432 | CDS | 369718 | 1296 | - | 0.329475 | |
DDB_G0287533 | DDB_G0287533 | DDB0232432 | CDS | 373625 | 1149 | + | 0.260226 | |
DDB_G0287535 | DDB_G0287535 | DDB0232432 | CDS | 385388 | 1848 | + | 0.209957 | |
DDB_G0287541 | DDB_G0287541 | DDB0232432 | CDS | 397759 | 2010 | + | 0.21592 | |
DDB_G0287543 | DDB_G0287543 | very similar to H. sapiens B-cell receptor-associated protein 29 and 31 (BCAP2931) and S. cerevisiae endoplasmic reticulum transmembrane protein 1 and 3 (YET13) contains a putative signal peptide and two transmembrane domains | DDB0232432 | CDS | 400560 | 588 | + | 0.270408 |
DDB_G0287545 | DDB_G0287545 | DDB0232432 | CDS | 401763 | 1128 | + | 0.286348 | |
DDB_G0287547 | DDB_G0287547 | DDB0232432 | CDS | 403298 | 1140 | - | 0.219298 | |
DDB_G0287549 | DDB_G0287549 | DDB0232432 | CDS | 405148 | 387 | - | 0.322997 | |
DDB_G0287551 | DDB_G0287551 | DDB0232432 | CDS | 406658 | 1368 | + | 0.284357 | |
DDB_G0287555 | DDB_G0287555 | catalyzes the reaction L-cysteine Osub2sub 3-sulfinoalanine | DDB0232432 | CDS | 412142 | 798 | + | 0.275689 |
DDB_G0287559 | DDB_G0287559 | DDB0232432 | CDS | 419276 | 579 | - | 0.262522 | |
DDB_G0287561 | DDB_G0287561 | DDB0232432 | CDS | 420291 | 1248 | - | 0.321314 | |
DDB_G0287565_ps | DDB_G0287565 | putative pseudogene similar to a family of Zinc finger N-recognin domain-containing Dictyostelium proteins | DDB0232432 | CDS | 347764 | 930 | + | 0.267742 |
DDB_G0287571 | DDB_G0287571 | DDB0232432 | CDS | 367808 | 1500 | + | 0.222667 | |
DDB_G0287573 | DDB_G0287573 | DDB0232432 | CDS | 391871 | 1398 | - | 0.205293 | |
DDB_G0287575 | DDB_G0287575 | DDB0232432 | CDS | 393959 | 1830 | + | 0.248087 | |
DDB_G0287579_TE | DDB_G0287579 | DDB0232432 | CDS | 424020 | 381 | - | 0.32021 | |
DDB_G0287581 | DDB_G0287581 | putative extracellular protein contains a predicted N-terminal signal sequence | DDB0232432 | CDS | 433923 | 804 | + | 0.287313 |
DDB_G0287591 | DDB_G0287591 | DDB0232432 | CDS | 517253 | 2562 | - | 0.215847 | |
DDB_G0287599 | DDB_G0287599 | DDB0232432 | CDS | 452628 | 354 | + | 0.175141 | |
DDB_G0287601 | DDB_G0287601 | DDB0232432 | CDS | 453256 | 399 | - | 0.273183 | |
DDB_G0287603 | DDB_G0287603 | DDB0232432 | CDS | 453942 | 324 | - | 0.243827 | |
DDB_G0287609 | DDB_G0287609 | highly similar to cinB (94 | DDB0232432 | CDS | 464998 | 1014 | + | 0.272189 |
DDB_G0287611 | DDB_G0287611 | DDB0232432 | CDS | 466151 | 720 | - | 0.297222 | |
DDB_G0287613 | DDB_G0287613 | DDB0232432 | CDS | 467594 | 1011 | - | 0.237389 | |
DDB_G0287615 | DDB_G0287615 | DDB0232432 | CDS | 470940 | 2349 | + | 0.304811 | |
DDB_G0287617 | DDB_G0287617 | similar to Bax inhibitor 1 that may have a role in inhibition of apoptosis contains 7 transmembrane domains | DDB0232432 | CDS | 479630 | 765 | + | 0.284967 |
DDB_G0287621 | DDB_G0287621 | DDB0232432 | CDS | 483890 | 2637 | + | 0.293515 | |
DDB_G0287623 | DDB_G0287623 | DDB0232432 | CDS | 486671 | 1677 | - | 0.189028 | |
DDB_G0287625 | DDB_G0287625 | DDB0232432 | CDS | 489912 | 2937 | - | 0.244127 | |
DDB_G0287633 | DDB_G0287633 | weakly similar to S. cerevisiae SEM1 a short acidic protein which regulates exocyst function and pseudohyphal differentiation | DDB0232432 | CDS | 532724 | 231 | + | 0.324675 |
DDB_G0287639 | DDB_G0287639 | DDB0232432 | CDS | 538405 | 2037 | + | 0.258714 | |
DDB_G0287641 | DDB_G0287641 | DDB0232432 | CDS | 540812 | 609 | - | 0.298851 | |
DDB_G0287643 | DDB_G0287643 | DDB0232432 | CDS | 543713 | 897 | - | 0.326644 | |
DDB_G0287645 | DDB_G0287645 | similar to the human transmembrane protein 112 contains 5 putative transmembrane domains | DDB0232432 | CDS | 550085 | 2316 | + | 0.250432 |
DDB_G0287647 | DDB_G0287647 | DDB0232432 | CDS | 552795 | 1266 | - | 0.333333 | |
DDB_G0287651 | DDB_G0287651 | belongs to a large D. discoideum protein family of unknown function this protein is a putative guanylate cyclase family protein | DDB0232432 | CDS | 436285 | 4053 | + | 0.23168 |
DDB_G0287655 | DDB_G0287655 | DDB0232432 | CDS | 443153 | 1020 | + | 0.276471 | |
DDB_G0287663 | DDB_G0287663 | DDB0232432 | CDS | 477935 | 522 | - | 0.300766 | |
DDB_G0287665 | DDB_G0287665 | DDB0232432 | CDS | 501928 | 3654 | + | 0.288725 | |
DDB_G0287667 | DDB_G0287667 | DDB0232432 | CDS | 506343 | 2208 | + | 0.294837 | |
DDB_G0287671 | DDB_G0287671 | DDB0232432 | CDS | 512195 | 633 | + | 0.28278 | |
DDB_G0287673 | DDB_G0287673 | DDB0232432 | CDS | 513198 | 324 | + | 0.175926 | |
DDB_G0287675 | DDB_G0287675 | DDB0232432 | CDS | 515703 | 1314 | + | 0.177321 | |
DDB_G0287677 | DDB_G0287677 | similar to NAD-dependent epimerasedehydratase family proteins that use nucleotide-sugar substrates for a variety of chemical reactions contains a partial NmrA-like domain near the N-terminus | DDB0232432 | CDS | 541940 | 1005 | - | 0.313433 |
DDB_G0287679 | DDB_G0287679 | DDB0232432 | CDS | 545368 | 3369 | - | 0.290591 | |
DDB_G0287695 | DDB_G0287695 | DDB0232432 | CDS | 566252 | 2037 | + | 0.26215 | |
DDB_G0287697 | DDB_G0287697 | DDB0232432 | CDS | 569375 | 2262 | + | 0.259063 | |
DDB_G0287699 | DDB_G0287699 | DDB0232432 | CDS | 573108 | 2229 | + | 0.212651 | |
DDB_G0287701 | DDB_G0287701 | DDB0232432 | CDS | 575637 | 897 | + | 0.264214 | |
DDB_G0287703 | DDB_G0287703 | DDB0232432 | CDS | 576895 | 4362 | - | 0.251719 | |
DDB_G0287705 | DDB_G0287705 | DDB0232432 | CDS | 582459 | 1122 | - | 0.272727 | |
DDB_G0287709 | DDB_G0287709 | DDB0232432 | CDS | 584610 | 2652 | - | 0.245098 | |
DDB_G0287711 | DDB_G0287711 | belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family homolog of human AADAT (kynureninealpha-aminoadipate aminotransferase) and S. cerevisiae ARO8 (aromatic amino acid aminotransferase) | DDB0232432 | CDS | 588099 | 1323 | - | 0.281179 |
DDB_G0287713 | DDB_G0287713 | DDB0232432 | CDS | 594468 | 1425 | + | 0.226667 | |
DDB_G0287715 | DDB_G0287715 | DDB0232432 | CDS | 596372 | 147 | - | 0.244898 | |
DDB_G0287719 | DDB_G0287719 | DDB0232432 | CDS | 598885 | 180 | - | 0.222222 | |
DDB_G0287721 | DDB_G0287721 | DDB0232432 | CDS | 600318 | 1041 | + | 0.304515 | |
DDB_G0287723 | DDB_G0287723 | DDB0232432 | CDS | 601565 | 2796 | - | 0.341559 | |
DDB_G0287725 | DDB_G0287725 | DDB0232432 | CDS | 605033 | 1716 | + | 0.262238 | |
DDB_G0287727 | DDB_G0287727 | DDB0232432 | CDS | 609137 | 3261 | + | 0.272002 | |
DDB_G0287729 | DDB_G0287729 | DDB0232432 | CDS | 613467 | 2121 | + | 0.296558 | |
DDB_G0287731 | DDB_G0287731 | belongs to the PLAC8 family (placenta-specific gene 8 protein) a family of cysteine-rich proteins with highly divergent low complexity amino terminal regions | DDB0232432 | CDS | 616064 | 426 | - | 0.328638 |
DDB_G0287735 | DDB_G0287735 | catalyzes the reaction a 5'-ribonucleotide Hsub2subO a ribonucleoside phosphate | DDB0232432 | CDS | 620499 | 1380 | + | 0.266667 |
DDB_G0287737 | DDB_G0287737 | DDB0232432 | CDS | 635143 | 564 | - | 0.242908 | |
DDB_G0287741 | DDB_G0287741 | DDB0232432 | CDS | 638654 | 1284 | - | 0.288941 | |
DDB_G0287743 | DDB_G0287743 | DDB0232432 | CDS | 640479 | 600 | + | 0.14 | |
DDB_G0287745 | DDB_G0287745 | putative ortholog of human cdk5rap3LZAP an ARF binding protein involved in cell cycle regulation | DDB0232432 | CDS | 644291 | 1800 | - | 0.225556 |
DDB_G0287749 | DDB_G0287749 | DDB0232432 | CDS | 647248 | 387 | - | 0.307494 | |
DDB_G0287751 | DDB_G0287751 | DDB0232432 | CDS | 648202 | 1707 | + | 0.207967 | |
DDB_G0287753 | DDB_G0287753 | DDB0232432 | CDS | 656012 | 891 | + | 0.251403 | |
DDB_G0287757 | DDB_G0287757 | ortholog of the conserved IMPACT (Imprinted and ancient) protein a translational regulator that ensures constant high levels of translation under amino acid starvation | DDB0232432 | CDS | 661336 | 1038 | + | 0.233141 |
DDB_G0287759 | DDB_G0287759 | DDB0232432 | CDS | 662849 | 1140 | - | 0.261404 | |
DDB_G0287761 | DDB_G0287761 | DDB0232432 | CDS | 664647 | 1455 | - | 0.262543 | |
DDB_G0287763 | DDB_G0287763 | similar to D. melanogaster slv (saliva) and human RAG1AP1 RAG1AP1 facilitates gene activation of recombination activating gene 1 contains 2 MtN3_slv domains contains 7 putative transmembrane domains | DDB0232432 | CDS | 669499 | 663 | + | 0.239819 |
DDB_G0287765 | DDB_G0287765 | overexpressed in | DDB0232432 | CDS | 671692 | 1317 | - | 0.297646 |
DDB_G0287767_ps | DDB_G0287767 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 675515 | 135 | + | 0.222222 |
DDB_G0287771 | DDB_G0287771 | DDB0232432 | CDS | 677716 | 399 | + | 0.270677 | |
DDB_G0287783 | DDB_G0287783 | DDB0232432 | CDS | 687490 | 498 | + | 0.307229 | |
DDB_G0287787_ps | DDB_G0287787 | putative pseudogene similar to many different classes of protein kinases | DDB0232432 | CDS | 701445 | 2061 | - | 0.289665 |
DDB_G0287789_ps | DDB_G0287789 | putative pseudogene similar to | DDB0232432 | CDS | 703769 | 282 | - | 0.195035 |
DDB_G0287793 | DDB_G0287793 | similar to human GSTT2 (glutathione S-transferase theta-2) glutathione transferases participate in the detoxification of reactive electrophilic compounds by catalysing their conjugation to glutathione contains a predicted peroxisomal targeting signal | DDB0232432 | CDS | 710171 | 669 | + | 0.246637 |
DDB_G0287797 | DDB_G0287797 | DDB0232432 | CDS | 713390 | 2088 | - | 0.244732 | |
DDB_G0287799 | DDB_G0287799 | contains a putative N-end rule-based degradation signal which targets a protein for ubiquitin-dependent proteolysis | DDB0232432 | CDS | 715755 | 5445 | + | 0.279339 |
DDB_G0287805 | DDB_G0287805 | DDB0232432 | CDS | 739515 | 4788 | - | 0.266708 | |
DDB_G0287807 | DDB_G0287807 | DDB0232432 | CDS | 744839 | 1485 | - | 0.256566 | |
DDB_G0287809 | DDB_G0287809 | DDB0232432 | CDS | 746961 | 852 | - | 0.223005 | |
DDB_G0287811 | DDB_G0287811 | DDB0232432 | CDS | 748966 | 309 | + | 0.326861 | |
DDB_G0287813 | DDB_G0287813 | DDB0232432 | CDS | 756116 | 1182 | + | 0.319797 | |
DDB_G0287815 | DDB_G0287815 | weak ortholog of the conserved chromatin assembly factor 1 (CAF1) subunit Abr bNote:b Do not confuse this gene with | DDB0232432 | CDS | 758176 | 2199 | + | 0.295589 |
DDB_G0287821 | DDB_G0287821 | DDB0232432 | CDS | 765881 | 498 | - | 0.309237 | |
DDB_G0287825 | DDB_G0287825 | DDB0232432 | CDS | 771339 | 1386 | + | 0.277778 | |
DDB_G0287831 | DDB_G0287831 | DDB0232432 | CDS | 776635 | 1629 | + | 0.228361 | |
DDB_G0287833 | DDB_G0287833 | DDB0232432 | CDS | 779158 | 4344 | + | 0.267726 | |
DDB_G0287835 | DDB_G0287835 | DDB0232432 | CDS | 783822 | 402 | - | 0.149254 | |
DDB_G0287837 | DDB_G0287837 | DDB0232432 | CDS | 787959 | 738 | + | 0.188347 | |
DDB_G0287839 | DDB_G0287839 | DDB0232432 | CDS | 789237 | 1452 | + | 0.309917 | |
DDB_G0287841 | DDB_G0287841 | DDB0232432 | CDS | 797545 | 1236 | - | 0.267799 | |
DDB_G0287843 | DDB_G0287843 | DDB0232432 | CDS | 806278 | 1923 | - | 0.333853 | |
DDB_G0287845 | DDB_G0287845 | DDB0232432 | CDS | 809663 | 2763 | - | 0.175896 | |
DDB_G0287847 | DDB_G0287847 | DDB0232432 | CDS | 813389 | 2040 | + | 0.260294 | |
DDB_G0287851 | DDB_G0287851 | DDB0232432 | CDS | 822730 | 2889 | + | 0.317411 | |
DDB_G0287857 | DDB_G0287857 | DDB0232432 | CDS | 667105 | 1599 | - | 0.243277 | |
DDB_G0287859 | DDB_G0287859 | contains a putative N-end rule-based degradation signal which targets a protein for ubiquitin-dependent proteolysis | DDB0232432 | CDS | 694189 | 4743 | + | 0.292009 |
DDB_G0287863 | DDB_G0287863 | developmental expression pattern altered in GBF null cells highly repetitive protein serine and glycine rich contains a predicted signal peptide | DDB0232432 | CDS | 733543 | 5790 | + | 0.383765 |
DDB_G0287865 | DDB_G0287865 | DDB0232432 | CDS | 829648 | 189 | - | 0.21164 | |
DDB_G0287869 | DDB_G0287869 | DDB0232432 | CDS | 591245 | 948 | - | 0.300633 | |
DDB_G0287871 | DDB_G0287871 | DDB0232432 | CDS | 607163 | 171 | - | 0.169591 | |
DDB_G0287873 | DDB_G0287873 | DDB0232432 | CDS | 622124 | 6861 | - | 0.288005 | |
DDB_G0287875 | DDB_G0287875 | contains a calponin-like actin binding domain and a pleckstrin homology domain and two ras association domains | DDB0232432 | CDS | 630862 | 3636 | + | 0.300055 |
DDB_G0287877 | DDB_G0287877 | DDB0232432 | CDS | 641447 | 2784 | + | 0.195402 | |
DDB_G0287879 | DDB_G0287879 | DDB0232432 | CDS | 650440 | 1206 | + | 0.276949 | |
DDB_G0287885 | DDB_G0287885 | DDB0232432 | CDS | 670518 | 783 | + | 0.297573 | |
DDB_G0287889 | DDB_G0287889 | DDB0232432 | CDS | 749668 | 948 | - | 0.341772 | |
DDB_G0287893 | DDB_G0287893 | DDB0232432 | CDS | 784589 | 534 | - | 0.226592 | |
DDB_G0287897 | DDB_G0287897 | DDB0232432 | CDS | 803720 | 1821 | - | 0.267435 | |
DDB_G0287903 | DDB_G0287903 | DDB0232432 | CDS | 830599 | 210 | - | 0.285714 | |
DDB_G0287907 | DDB_G0287907 | DDB0232432 | CDS | 833038 | 753 | + | 0.229748 | |
DDB_G0287909 | DDB_G0287909 | DDB0232432 | CDS | 833953 | 3585 | - | 0.271409 | |
DDB_G0287911 | DDB_G0287911 | DDB0232432 | CDS | 838039 | 1467 | - | 0.250852 | |
DDB_G0287927 | DDB_G0287927 | DDB0232432 | CDS | 859603 | 1485 | + | 0.256566 | |
DDB_G0287929 | DDB_G0287929 | DDB0232432 | CDS | 861720 | 1377 | + | 0.302832 | |
DDB_G0287931 | DDB_G0287931 | DDB0232432 | CDS | 863622 | 507 | + | 0.220907 | |
DDB_G0287933 | DDB_G0287933 | DDB0232432 | CDS | 864291 | 1515 | - | 0.279208 | |
DDB_G0287935 | DDB_G0287935 | DDB0232432 | CDS | 867361 | 2139 | - | 0.295465 | |
DDB_G0287943 | DDB_G0287943 | DDB0232432 | CDS | 852371 | 1944 | - | 0.261317 | |
DDB_G0287947 | DDB_G0287947 | DDB0232432 | CDS | 874209 | 633 | - | 0.268562 | |
DDB_G0287949 | DDB_G0287949 | DDB0232432 | CDS | 875204 | 1155 | + | 0.27013 | |
DDB_G0287951 | DDB_G0287951 | carboxyl terminus is highly similar to Ataxin-7-like protein 3 the rest of the protein is extremely repetitive | DDB0232432 | CDS | 876413 | 4344 | - | 0.315838 |
DDB_G0287955 | DDB_G0287955 | DDB0232432 | CDS | 885768 | 1221 | + | 0.242424 | |
DDB_G0287957 | DDB_G0287957 | DDB0232432 | CDS | 889459 | 1623 | - | 0.162662 | |
DDB_G0287959 | DDB_G0287959 | putative copper transporter contains 3 predicted transmembrane domains | DDB0232432 | CDS | 893285 | 633 | + | 0.271722 |
DDB_G0287961 | DDB_G0287961 | DDB0232432 | CDS | 894476 | 5595 | - | 0.27328 | |
DDB_G0287963 | DDB_G0287963 | DDB0232432 | CDS | 892450 | 144 | - | 0.270833 | |
DDB_G0287967 | DDB_G0287967 | DDB0232432 | CDS | 902212 | 333 | + | 0.279279 | |
DDB_G0287971 | DDB_G0287971 | DDB0232432 | CDS | 914990 | 1539 | - | 0.246914 | |
DDB_G0287973 | DDB_G0287973 | DDB0232432 | CDS | 917728 | 1032 | + | 0.306202 | |
DDB_G0287975 | DDB_G0287975 | DDB0232432 | CDS | 919012 | 501 | - | 0.243513 | |
DDB_G0287979 | DDB_G0287979 | DDB0232432 | CDS | 922041 | 3255 | - | 0.242704 | |
DDB_G0287985 | DDB_G0287985 | DDB0232432 | CDS | 933669 | 912 | + | 0.3125 | |
DDB_G0287989 | DDB_G0287989 | DDB0232432 | CDS | 937712 | 1149 | - | 0.255004 | |
DDB_G0287991 | DDB_G0287991 | DDB0232432 | CDS | 939192 | 831 | - | 0.322503 | |
DDB_G0287999 | DDB_G0287999 | DDB0232432 | CDS | 948929 | 3615 | + | 0.237344 | |
DDB_G0288001 | DDB_G0288001 | related to fatty acyl-CoA synthetase catalyzes the reaction ATP a long-chain carboxylic acid CoA AMP diphosphate an acyl-CoA mediates the retrieval of fatty acids from endosomes to the cytoplasm | DDB0232432 | CDS | 953191 | 3816 | + | 0.280136 |
DDB_G0288003 | DDB_G0288003 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 957063 | 4110 | - | 0.251825 |
DDB_G0288005 | DDB_G0288005 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232432 | CDS | 962125 | 960 | - | 0.314583 |
DDB_G0288007 | DDB_G0288007 | DDB0232432 | CDS | 963824 | 5637 | - | 0.284016 | |
DDB_G0288009 | DDB_G0288009 | putative ortholog of human UPF0663 downregulated in multiple cancers | DDB0232432 | CDS | 970396 | 2718 | + | 0.292127 |
DDB_G0288011 | DDB_G0288011 | DDB0232432 | CDS | 974125 | 780 | + | 0.305128 | |
DDB_G0288013 | DDB_G0288013 | DDB0232432 | CDS | 975395 | 756 | - | 0.244709 | |
DDB_G0288017 | DDB_G0288017 | DDB0232432 | CDS | 978356 | 1377 | - | 0.315904 | |
DDB_G0288019 | DDB_G0288019 | DDB0232432 | CDS | 981451 | 720 | - | 0.306944 | |
DDB_G0288023 | DDB_G0288023 | DDB0232432 | CDS | 988438 | 1356 | - | 0.235251 | |
DDB_G0288029 | DDB_G0288029 | member of the aspartateglutamateuridylate kinase family similar to glutamate 5-kinase | DDB0232432 | CDS | 994876 | 891 | - | 0.243547 |
DDB_G0288031 | DDB_G0288031 | large protein with cysteine-containing leucine-rich repeats and a C-terminal villin headpiece contains an unknown domain (residues 300-620) found in different species and in several Dictyostelium proteins represented in Pfam-B domains PB008617 and PB046085 | DDB0232432 | CDS | 996657 | 6630 | + | 0.265309 |
DDB_G0288033 | DDB_G0288033 | DDB0232432 | CDS | 1003620 | 735 | - | 0.22585 | |
DDB_G0288035 | DDB_G0288035 | DDB0232432 | CDS | 1006610 | 204 | + | 0.303922 | |
DDB_G0288037 | DDB_G0288037 | DDB0232432 | CDS | 1008144 | 447 | - | 0.149888 | |
DDB_G0288039 | DDB_G0288039 | DDB0232432 | CDS | 1009340 | 771 | + | 0.268482 | |
DDB_G0288041 | DDB_G0288041 | DDB0232432 | CDS | 1011026 | 8853 | + | 0.276403 | |
DDB_G0288043 | DDB_G0288043 | DDB0232432 | CDS | 1021151 | 1041 | - | 0.283381 | |
DDB_G0288045 | DDB_G0288045 | DDB0232432 | CDS | 1024941 | 1809 | + | 0.254284 | |
DDB_G0288049_ps | DDB_G0288049 | putative pseudogene fragment of group of large D. discoideum proteins including | DDB0232432 | CDS | 1032772 | 351 | + | 0.17094 |
DDB_G0288051 | DDB_G0288051 | DDB0232432 | CDS | 1034769 | 1014 | - | 0.288955 | |
DDB_G0288055 | DDB_G0288055 | belongs to a family of conserved potassium transporters in bacteria yeast and plants overexpressed in | DDB0232432 | CDS | 929613 | 2151 | - | 0.317992 |
DDB_G0288057 | DDB_G0288057 | DDB0232432 | CDS | 983015 | 852 | - | 0.187793 | |
DDB_G0288059 | DDB_G0288059 | DDB0232432 | CDS | 1029614 | 630 | + | 0.284127 | |
DDB_G0288069 | DDB_G0288069 | DDB0232432 | CDS | 1045172 | 3249 | + | 0.271776 | |
DDB_G0288073 | DDB_G0288073 | DDB0232432 | CDS | 1051212 | 6114 | - | 0.292607 | |
DDB_G0288075 | DDB_G0288075 | DDB0232432 | CDS | 1059598 | 1896 | - | 0.262658 | |
DDB_G0288077_ps | DDB_G0288077 | almost identical to a small portion of scy1 a protein kinase | DDB0232432 | CDS | 1063204 | 171 | - | 0.292398 |
DDB_G0288079_ps | DDB_G0288079 | similar to DDB_G0277993 a protein of the importin family | DDB0232432 | CDS | 1063770 | 1194 | - | 0.326633 |
DDB_G0288081 | DDB_G0288081 | DDB0232432 | CDS | 1079984 | 399 | + | 0.305764 | |
DDB_G0288087 | DDB_G0288087 | DDB0232432 | CDS | 1082632 | 633 | - | 0.271722 | |
DDB_G0288089 | DDB_G0288089 | possible homolog of human GCFC (C21orf66) a putative transcription factor | DDB0232432 | CDS | 1084262 | 2832 | + | 0.234463 |
DDB_G0288091 | DDB_G0288091 | DDB0232432 | CDS | 1087651 | 834 | + | 0.323741 | |
DDB_G0288093 | DDB_G0288093 | contains a putative N-end rule-based degradation signal which targets a protein for ubiquitin-dependent proteolysis | DDB0232432 | CDS | 1089133 | 5268 | + | 0.278094 |
DDB_G0288095 | DDB_G0288095 | conserved in Dictyostelium and Polysphondylium contains a predicted signal peptide | DDB0232432 | CDS | 1094749 | 1521 | + | 0.322814 |
DDB_G0288097 | DDB_G0288097 | DDB0232432 | CDS | 1097291 | 1554 | + | 0.311454 | |
DDB_G0288099 | DDB_G0288099 | DDB0232432 | CDS | 1100340 | 765 | - | 0.256209 | |
DDB_G0288107 | DDB_G0288107 | the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232432 | CDS | 1124020 | 1182 | + | 0.267343 |
DDB_G0288109 | DDB_G0288109 | DDB0232432 | CDS | 1042048 | 2142 | + | 0.288049 | |
DDB_G0288111 | DDB_G0288111 | DDB0232432 | CDS | 1058090 | 717 | + | 0.217573 | |
DDB_G0288113_ps | DDB_G0288113 | similar to a large family of D. discoideum genes | DDB0232432 | CDS | 1061950 | 120 | + | 0.308333 |
DDB_G0288121 | DDB_G0288121 | DDB0232432 | CDS | 1069064 | 4308 | + | 0.246054 | |
DDB_G0288123 | DDB_G0288123 | DDB0232432 | CDS | 1076323 | 2790 | + | 0.25448 | |
DDB_G0288125 | DDB_G0288125 | DDB0232432 | CDS | 1099194 | 795 | - | 0.262893 | |
DDB_G0288129 | DDB_G0288129 | DDB0232432 | CDS | 1107652 | 2739 | + | 0.280029 | |
DDB_G0288133 | DDB_G0288133 | DDB0232432 | CDS | 1130852 | 798 | - | 0.421053 | |
DDB_G0288135 | DDB_G0288135 | DDB0232432 | CDS | 1132899 | 1545 | - | 0.206472 | |
DDB_G0288137 | DDB_G0288137 | DDB0232432 | CDS | 1135535 | 966 | + | 0.34265 | |
DDB_G0288139 | DDB_G0288139 | DDB0232432 | CDS | 1136855 | 753 | + | 0.247012 | |
DDB_G0288141 | DDB_G0288141 | DDB0232432 | CDS | 1137934 | 261 | - | 0.325671 | |
DDB_G0288143 | DDB_G0288143 | similar to lysozyme C proteins from insects contains an additional serine-rich C-terminal region | DDB0232432 | CDS | 1139463 | 564 | - | 0.320922 |
DDB_G0288147 | DDB_G0288147 | member of the tyrosine kinase-like (TKL) group similar to plant serinethreonine kinases contains a phorbol esterdiacylglycerol-binding domain | DDB0232432 | CDS | 1147360 | 4044 | + | 0.271513 |
DDB_G0288149 | DDB_G0288149 | DDB0232432 | CDS | 1152736 | 723 | + | 0.260028 | |
DDB_G0288151 | DDB_G0288151 | DDB0232432 | CDS | 1156915 | 1704 | - | 0.200117 | |
DDB_G0288153 | DDB_G0288153 | belongs to the thioredoxin family lacks redox-active cysteines compared with many homologs so may be catalytically inactive | DDB0232432 | CDS | 1158956 | 327 | - | 0.235474 |
DDB_G0288155 | DDB_G0288155 | DDB0232432 | CDS | 1159975 | 741 | - | 0.333333 | |
DDB_G0288157 | DDB_G0288157 | DDB0232432 | CDS | 1161244 | 732 | - | 0.266393 | |
DDB_G0288159 | DDB_G0288159 | DDB0232432 | CDS | 1166139 | 147 | + | 0.346939 | |
DDB_G0288161 | DDB_G0288161 | DDB0232432 | CDS | 1166708 | 2844 | - | 0.307665 | |
DDB_G0288165 | DDB_G0288165 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232432 | CDS | 1172053 | 1116 | - | 0.292115 |
DDB_G0288167 | DDB_G0288167 | DDB0232432 | CDS | 1174416 | 219 | + | 0.406393 | |
DDB_G0288175 | DDB_G0288175 | DDB0232432 | CDS | 1154137 | 2475 | + | 0.245253 | |
DDB_G0288185 | DDB_G0288185 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232432 | CDS | 1178682 | 276 | - | 0.362319 |
DDB_G0288189 | DDB_G0288189 | DDB0232432 | CDS | 1182370 | 1299 | + | 0.193995 | |
DDB_G0288191 | DDB_G0288191 | DDB0232432 | CDS | 1183802 | 2115 | - | 0.249645 | |
DDB_G0288193 | DDB_G0288193 | DDB0232432 | CDS | 1186484 | 1440 | + | 0.241667 | |
DDB_G0288199_ps | DDB_G0288199 | putative pseudogene xpr1 family gene | DDB0232432 | CDS | 1217412 | 1167 | + | 0.172237 |
DDB_G0288201 | DDB_G0288201 | DDB0232432 | CDS | 1230521 | 942 | - | 0.266454 | |
DDB_G0288203 | DDB_G0288203 | amino terminal region is similar to the interferon-related developmental regulator family contains one HEAT repeat similar to D. purpureum protein | DDB0232432 | CDS | 1233063 | 1383 | + | 0.292842 |
DDB_G0288207 | DDB_G0288207 | DDB0232432 | CDS | 1245352 | 492 | - | 0.223577 | |
DDB_G0288209 | DDB_G0288209 | ortholog of mitochondrial twinkle protein involved in mitochondrial DNA (mtDNA) metabolism defects in this gene cause progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal dominant type 3 | DDB0232432 | CDS | 1246731 | 2319 | + | 0.269082 |
DDB_G0288211 | DDB_G0288211 | DDB0232432 | CDS | 1249148 | 1485 | - | 0.238384 | |
DDB_G0288213 | DDB_G0288213 | DDB0232432 | CDS | 1254786 | 288 | - | 0.229167 | |
DDB_G0288215 | DDB_G0288215 | DDB0232432 | CDS | 1256711 | 2808 | - | 0.226496 | |
DDB_G0288219 | DDB_G0288219 | DDB0232432 | CDS | 1267913 | 1779 | - | 0.32715 | |
DDB_G0288221 | DDB_G0288221 | DDB0232432 | CDS | 1272181 | 1188 | + | 0.313131 | |
DDB_G0288227 | DDB_G0288227 | similar to the mammalian SET domain-containing protein 7 (SETD7) a histone methyltransferase that specifically monomethylates Lys-4 of histone H3 | DDB0232432 | CDS | 1280700 | 1194 | + | 0.303183 |
DDB_G0288231 | DDB_G0288231 | DDB0232432 | CDS | 1264761 | 3036 | + | 0.301713 | |
DDB_G0288233 | DDB_G0288233 | DDB0232432 | CDS | 1270786 | 633 | - | 0.238547 | |
DDB_G0288235 | DDB_G0288235 | DDB0232432 | CDS | 1177513 | 1008 | + | 0.172619 | |
DDB_G0288237 | DDB_G0288237 | DDB0232432 | CDS | 1188181 | 4467 | - | 0.283412 | |
DDB_G0288241 | DDB_G0288241 | DDB0232432 | CDS | 1240397 | 4431 | + | 0.296547 | |
DDB_G0288243 | DDB_G0288243 | DDB0232432 | CDS | 1278382 | 1209 | - | 0.263854 | |
DDB_G0288255 | DDB_G0288255 | very similar to bacterial ribosomal RNA large subunit methyltransferase Nalso known as radical SAM protein or Cfr family protein | DDB0232432 | CDS | 1294679 | 1224 | - | 0.287582 |
DDB_G0288263 | DDB_G0288263 | DDB0232432 | CDS | 1310716 | 1266 | - | 0.226698 | |
DDB_G0288265 | DDB_G0288265 | very similar to S. cerevisiae HSP10 A. thaliana CPN10 and human HSPE1 (HSP10)mitochondrial chaperonins | DDB0232432 | CDS | 1314543 | 309 | + | 0.291262 |
DDB_G0288271 | DDB_G0288271 | DDB0232432 | CDS | 1300715 | 1119 | - | 0.242181 | |
DDB_G0288277 | DDB_G0288277 | DDB0232432 | CDS | 1329697 | 2394 | - | 0.281537 | |
DDB_G0288279 | DDB_G0288279 | DDB0232432 | CDS | 1332303 | 747 | + | 0.253012 | |
DDB_G0288281 | DDB_G0288281 | DDB0232432 | CDS | 1341246 | 156 | + | 0.403846 | |
DDB_G0288283 | DDB_G0288283 | DDB0232432 | CDS | 1345783 | 783 | + | 0.305236 | |
DDB_G0288291 | DDB_G0288291 | contains 1 RRM (RNA recognition motif) domain similar to the RRM domain of eukaryotic peptidyl-prolyl cis-trans isomerase E | DDB0232432 | CDS | 1356313 | 372 | + | 0.266129 |
DDB_G0288293 | DDB_G0288293 | conserved protein contains 5 predicted transmembrane domains | DDB0232432 | CDS | 1357343 | 846 | + | 0.301418 |
DDB_G0288297 | DDB_G0288297 | DDB0232432 | CDS | 1360320 | 1422 | - | 0.174402 | |
DDB_G0288301 | DDB_G0288301 | DDB0232432 | CDS | 1364968 | 4233 | + | 0.282542 | |
DDB_G0288303 | DDB_G0288303 | DDB0232432 | CDS | 1375029 | 627 | - | 0.274322 | |
DDB_G0288309 | DDB_G0288309 | DDB0232432 | CDS | 1333499 | 540 | - | 0.222222 | |
DDB_G0288311 | DDB_G0288311 | DDB0232432 | CDS | 1334323 | 2226 | + | 0.1469 | |
DDB_G0288315 | DDB_G0288315 | conserved protein contains 8 predicted transmembrane domains and is similar to transmembrane proteins of unknown function in other species | DDB0232432 | CDS | 1343263 | 1746 | + | 0.299542 |
DDB_G0288317 | DDB_G0288317 | DDB0232432 | CDS | 1370056 | 4095 | + | 0.275214 | |
DDB_G0288325 | DDB_G0288325 | conserved uncharacterized transmembrane protein contains 2 predicted transmembrane domains | DDB0232432 | CDS | 1394062 | 231 | - | 0.320346 |
DDB_G0288329 | DDB_G0288329 | DDB0232432 | CDS | 1397987 | 654 | + | 0.292049 | |
DDB_G0288339 | DDB_G0288339 | DDB0232432 | CDS | 1405893 | 2724 | - | 0.179148 | |
DDB_G0288341 | DDB_G0288341 | DDB0232432 | CDS | 1409331 | 1149 | + | 0.261967 | |
DDB_G0288343 | DDB_G0288343 | DDB0232432 | CDS | 1412629 | 126 | + | 0.261905 | |
DDB_G0288345 | DDB_G0288345 | DDB0232432 | CDS | 1413915 | 1554 | + | 0.261261 | |
DDB_G0288351 | DDB_G0288351 | DDB0232432 | CDS | 1420134 | 1560 | + | 0.207051 | |
DDB_G0288353 | DDB_G0288353 | DDB0232432 | CDS | 1428760 | 507 | - | 0.220907 | |
DDB_G0288355 | DDB_G0288355 | possible ortholog of THOC5 which exists in the THO complex required for transcriptional elongation | DDB0232432 | CDS | 1430508 | 2505 | + | 0.266667 |
DDB_G0288357 | DDB_G0288357 | DDB0232432 | CDS | 1434151 | 312 | + | 0.221154 | |
DDB_G0288363 | DDB_G0288363 | belongs to the peptidase S8 family contains a predicted signal peptide contains one EGF-like domain | DDB0232432 | CDS | 1391586 | 2037 | + | 0.311733 |
DDB_G0288367 | DDB_G0288367 | DDB0232432 | CDS | 1434816 | 3597 | - | 0.2263 | |
DDB_G0288369 | DDB_G0288369 | DDB0232432 | CDS | 1416573 | 1035 | - | 0.269565 | |
DDB_G0288371 | DDB_G0288371 | weakly similar to S. cerevisiae VPS74 a protein of unknown function involved in vacuolar protein sorting | DDB0232432 | CDS | 1426752 | 789 | - | 0.244613 |
DDB_G0288379 | DDB_G0288379 | small cortactin protein a putative actin binding protein conserved in Dictyostelids | DDB0232432 | CDS | 1459573 | 291 | - | 0.32646 |
DDB_G0288381 | DDB_G0288381 | DDB0232432 | CDS | 1460823 | 1650 | - | 0.270303 | |
DDB_G0288385 | DDB_G0288385 | DDB0232432 | CDS | 1467682 | 1113 | - | 0.233603 | |
DDB_G0288389 | DDB_G0288389 | DDB0232432 | CDS | 1486099 | 450 | + | 0.224444 | |
DDB_G0288393 | DDB_G0288393 | DDB0232432 | CDS | 1488951 | 639 | + | 0.211268 | |
DDB_G0288395 | DDB_G0288395 | DDB0232432 | CDS | 1489692 | 339 | - | 0.247788 | |
DDB_G0288397 | DDB_G0288397 | DDB0232432 | CDS | 1490397 | 267 | - | 0.348315 | |
DDB_G0288399 | DDB_G0288399 | DDB0232432 | CDS | 1491224 | 222 | - | 0.301802 | |
DDB_G0288403 | DDB_G0288403 | DDB0232432 | CDS | 1499232 | 1455 | - | 0.243299 | |
DDB_G0288405 | DDB_G0288405 | DDB0232432 | CDS | 1502693 | 2202 | + | 0.265668 | |
DDB_G0288407 | DDB_G0288407 | DDB0232432 | CDS | 1505496 | 687 | - | 0.269287 | |
DDB_G0288411_ps | DDB_G0288411 | putative pseudogene similar to | DDB0232432 | CDS | 1506576 | 1704 | + | 0.231808 |
DDB_G0288417 | DDB_G0288417 | DDB0232432 | CDS | 1511045 | 384 | - | 0.335938 | |
DDB_G0288419 | DDB_G0288419 | DDB0232432 | CDS | 1511818 | 1455 | + | 0.383505 | |
DDB_G0288429 | DDB_G0288429 | belongs to the short-chain dehydrogenasesreductases (SDR) family | DDB0232432 | CDS | 1527197 | 993 | + | 0.281974 |
DDB_G0288433 | DDB_G0288433 | DDB0232432 | CDS | 1528754 | 825 | + | 0.232727 | |
DDB_G0288435 | DDB_G0288435 | DDB0232432 | CDS | 1530778 | 1554 | + | 0.328829 | |
DDB_G0288437 | DDB_G0288437 | DDB0232432 | CDS | 1535366 | 3909 | + | 0.300588 | |
DDB_G0288441 | DDB_G0288441 | DDB0232432 | CDS | 1540991 | 804 | + | 0.263682 | |
DDB_G0288443 | DDB_G0288443 | DDB0232432 | CDS | 1542340 | 975 | + | 0.260513 | |
DDB_G0288447 | DDB_G0288447 | DDB0232432 | CDS | 1482942 | 2028 | - | 0.236686 | |
DDB_G0288451_ps | DDB_G0288451 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 1513586 | 846 | + | 0.20331 |
DDB_G0288453 | DDB_G0288453 | DDB0232432 | CDS | 1521809 | 2913 | - | 0.270855 | |
DDB_G0288455_ps | DDB_G0288455 | putative pseudogene similar to | DDB0232432 | CDS | 1532524 | 1620 | + | 0.295679 |
DDB_G0288459 | DDB_G0288459 | DDB0232432 | CDS | 1551650 | 3717 | - | 0.304009 | |
DDB_G0288465 | DDB_G0288465 | converts pantetheine 4'-phosphate to 3'-dephospho-CoA in other organisms this activity is part of a bifunctional enzyme that also has dephospho-CoA kinase activity in Dictyostelium the latter activity is encoded by | DDB0232432 | CDS | 1558211 | 1230 | - | 0.233333 |
DDB_G0288467 | DDB_G0288467 | DDB0232432 | CDS | 1559882 | 531 | - | 0.293785 | |
DDB_G0288469 | DDB_G0288469 | DDB0232432 | CDS | 1563184 | 2883 | + | 0.226153 | |
DDB_G0288473 | DDB_G0288473 | DDB0232432 | CDS | 1569035 | 6093 | + | 0.278516 | |
DDB_G0288475 | DDB_G0288475 | DDB0232432 | CDS | 1575886 | 3360 | + | 0.34256 | |
DDB_G0288477 | DDB_G0288477 | DDB0232432 | CDS | 1580012 | 1914 | - | 0.3093 | |
DDB_G0288489 | DDB_G0288489 | DDB0232432 | CDS | 1599423 | 843 | + | 0.313167 | |
DDB_G0288493 | DDB_G0288493 | DDB0232432 | CDS | 1604662 | 480 | - | 0.30625 | |
DDB_G0288497 | DDB_G0288497 | DDB0232432 | CDS | 1611473 | 3741 | - | 0.190323 | |
DDB_G0288499 | DDB_G0288499 | DDB0232432 | CDS | 1594285 | 2853 | + | 0.222222 | |
DDB_G0288505_RTE | DDB_G0288505 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232432 | CDS | 1590688 | 908 | - | 0.409692 |
DDB_G0288513 | DDB_G0288513 | DDB0232432 | CDS | 1631607 | 1245 | + | 0.204819 | |
DDB_G0288515 | DDB_G0288515 | DDB0232432 | CDS | 1633091 | 786 | + | 0.198473 | |
DDB_G0288517 | DDB_G0288517 | DDB0232432 | CDS | 1633993 | 831 | + | 0.223827 | |
DDB_G0288519 | DDB_G0288519 | DDB0232432 | CDS | 1635029 | 1323 | - | 0.247166 | |
DDB_G0288521 | DDB_G0288521 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232432 | CDS | 1636790 | 1512 | + | 0.315476 |
DDB_G0288525 | DDB_G0288525 | DDB0232432 | CDS | 1644947 | 1674 | - | 0.247909 | |
DDB_G0288529 | DDB_G0288529 | DDB0232432 | CDS | 1628807 | 1587 | + | 0.267171 | |
DDB_G0288531 | DDB_G0288531 | DDB0232432 | CDS | 1649759 | 2196 | + | 0.255009 | |
DDB_G0288535 | DDB_G0288535 | DDB0232432 | CDS | 1660756 | 1395 | - | 0.235842 | |
DDB_G0288537 | DDB_G0288537 | DDB0232432 | CDS | 1662584 | 2541 | - | 0.277056 | |
DDB_G0288539 | DDB_G0288539 | DDB0232432 | CDS | 1648133 | 798 | - | 0.177945 | |
DDB_G0288547 | DDB_G0288547 | DDB0232432 | CDS | 1676407 | 1038 | - | 0.259152 | |
DDB_G0288549 | DDB_G0288549 | DDB0232432 | CDS | 1677926 | 822 | - | 0.244526 | |
DDB_G0288551 | DDB_G0288551 | conserved protein contains 5 PUF domains D. melanogaster pumilio binds through a PUF domain to the 3' UTR of target mRNAs | DDB0232432 | CDS | 1679413 | 2040 | + | 0.283333 |
DDB_G0288555 | DDB_G0288555 | DDB0232432 | CDS | 1681661 | 2182 | - | 0.192026 | |
DDB_G0288559 | DDB_G0288559 | DDB0232432 | CDS | 1685010 | 1650 | + | 0.303636 | |
DDB_G0288561_ps | DDB_G0288561 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 1686921 | 834 | - | 0.257794 |
DDB_G0288563 | DDB_G0288563 | DDB0232432 | CDS | 1689437 | 945 | - | 0.368254 | |
DDB_G0288567 | DDB_G0288567 | DDB0232432 | CDS | 1693029 | 522 | + | 0.16092 | |
DDB_G0288569 | DDB_G0288569 | DDB0232432 | CDS | 1693802 | 3495 | - | 0.303577 | |
DDB_G0288571 | DDB_G0288571 | DDB0232432 | CDS | 1698545 | 1134 | + | 0.251323 | |
DDB_G0288573 | DDB_G0288573 | DDB0232432 | CDS | 1700402 | 684 | + | 0.276316 | |
DDB_G0288575 | DDB_G0288575 | DDB0232432 | CDS | 1706213 | 369 | + | 0.306233 | |
DDB_G0288577 | DDB_G0288577 | DDB0232432 | CDS | 1717040 | 159 | + | 0.402516 | |
DDB_G0288579 | DDB_G0288579 | DDB0232432 | CDS | 1717737 | 369 | + | 0.325203 | |
DDB_G0288581 | DDB_G0288581 | DDB0232432 | CDS | 1718254 | 972 | - | 0.256173 | |
DDB_G0288583 | DDB_G0288583 | DDB0232432 | CDS | 1719547 | 708 | - | 0.258475 | |
DDB_G0288585 | DDB_G0288585 | DDB0232432 | CDS | 1720817 | 759 | + | 0.200264 | |
DDB_G0288587 | DDB_G0288587 | DDB0232432 | CDS | 1721620 | 714 | - | 0.22549 | |
DDB_G0288589 | DDB_G0288589 | DDB0232432 | CDS | 1722609 | 1338 | - | 0.272048 | |
DDB_G0288591 | DDB_G0288591 | DDB0232432 | CDS | 1726934 | 861 | + | 0.293844 | |
DDB_G0288593 | DDB_G0288593 | DDB0232432 | CDS | 1728286 | 2085 | - | 0.313669 | |
DDB_G0288595 | DDB_G0288595 | DDB0232432 | CDS | 1730911 | 1224 | + | 0.227124 | |
DDB_G0288597 | DDB_G0288597 | DDB0232432 | CDS | 1732418 | 1926 | - | 0.226895 | |
DDB_G0288599 | DDB_G0288599 | MBOAT family protein membrane proteins that contains a variety of acyltransferase enzymes most similar to S. cerevisiae glycerol uptake protein 1 (GUP1) contains 11 predicted transmembrane domains | DDB0232432 | CDS | 1734624 | 1695 | + | 0.315634 |
DDB_G0288601_ps | DDB_G0288601 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 1725951 | 189 | + | 0.227513 |
DDB_G0288615 | DDB_G0288615 | DDB0232432 | CDS | 1744822 | 285 | + | 0.287719 | |
DDB_G0288619 | DDB_G0288619 | DDB0232432 | CDS | 1748711 | 828 | - | 0.286232 | |
DDB_G0288625 | DDB_G0288625 | DDB0232432 | CDS | 1759888 | 2316 | - | 0.295337 | |
DDB_G0288627 | DDB_G0288627 | DDB0232432 | CDS | 1763068 | 1212 | + | 0.229373 | |
DDB_G0288629 | DDB_G0288629 | DDB0232432 | CDS | 1764970 | 792 | + | 0.285354 | |
DDB_G0288631 | DDB_G0288631 | DDB0232432 | CDS | 1767936 | 2103 | - | 0.262958 | |
DDB_G0288635 | DDB_G0288635 | DDB0232432 | CDS | 1774014 | 663 | - | 0.315234 | |
DDB_G0288637_ps | DDB_G0288637 | putative pseudogene similar to | DDB0232432 | CDS | 1772020 | 1164 | + | 0.268041 |
DDB_G0288639 | DDB_G0288639 | conserved protein DnaJ homolog subfamily C member 7 (DNAJC7) | DDB0232432 | CDS | 1756684 | 1620 | + | 0.334568 |
DDB_G0288641 | DDB_G0288641 | DDB0232432 | CDS | 1759110 | 639 | + | 0.242567 | |
DDB_G0288643 | DDB_G0288643 | DDB0232432 | CDS | 1766588 | 1185 | + | 0.24135 | |
DDB_G0288645 | DDB_G0288645 | DDB0232432 | CDS | 1776536 | 1650 | - | 0.277576 | |
DDB_G0288651 | DDB_G0288651 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232432 | CDS | 1782938 | 1353 | - | 0.317812 |
DDB_G0288653 | DDB_G0288653 | DDB0232432 | CDS | 1786499 | 453 | - | 0.181015 | |
DDB_G0288657 | DDB_G0288657 | DDB0232432 | CDS | 1789768 | 249 | - | 0.281125 | |
DDB_G0288661 | DDB_G0288661 | DDB0232432 | CDS | 1792404 | 924 | + | 0.208874 | |
DDB_G0288663 | DDB_G0288663 | DDB0232432 | CDS | 1793780 | 591 | + | 0.28934 | |
DDB_G0288665 | DDB_G0288665 | DDB0232432 | CDS | 1795019 | 594 | + | 0.311448 | |
DDB_G0288667 | DDB_G0288667 | DDB0232432 | CDS | 1796243 | 441 | - | 0.265306 | |
DDB_G0288669 | DDB_G0288669 | DDB0232432 | CDS | 1797088 | 930 | - | 0.230108 | |
DDB_G0288671 | DDB_G0288671 | catalyzes the reaction L-proline NAD(P)supsup 1-pyrroline-5-carboxylate NAD(P)H Hsupsup | DDB0232432 | CDS | 1798454 | 1656 | - | 0.341184 |
DDB_G0288673 | DDB_G0288673 | DDB0232432 | CDS | 1800597 | 972 | - | 0.236626 | |
DDB_G0288675 | DDB_G0288675 | DDB0232432 | CDS | 1808800 | 396 | - | 0.217172 | |
DDB_G0288683 | DDB_G0288683 | DDB0232432 | CDS | 1810485 | 2562 | + | 0.26815 | |
DDB_G0288687 | DDB_G0288687 | DDB0232432 | CDS | 1817419 | 1746 | + | 0.182131 | |
DDB_G0288689 | DDB_G0288689 | DDB0232432 | CDS | 1819614 | 1800 | - | 0.215556 | |
DDB_G0288693 | DDB_G0288693 | DDB0232432 | CDS | 1834141 | 1806 | + | 0.296788 | |
DDB_G0288695 | DDB_G0288695 | DDB0232432 | CDS | 1836785 | 2718 | - | 0.181015 | |
DDB_G0288697 | DDB_G0288697 | DDB0232432 | CDS | 1839851 | 1758 | - | 0.303185 | |
DDB_G0288707 | DDB_G0288707 | DDB0232432 | CDS | 1852460 | 2958 | - | 0.281947 | |
DDB_G0288713 | DDB_G0288713 | DDB0232432 | CDS | 1863605 | 609 | + | 0.208539 | |
DDB_G0288717 | DDB_G0288717 | DDB0232432 | CDS | 1867636 | 1647 | - | 0.333333 | |
DDB_G0288723 | DDB_G0288723 | DDB0232432 | CDS | 1876927 | 966 | - | 0.279503 | |
DDB_G0288725 | DDB_G0288725 | DDB0232432 | CDS | 1879264 | 3498 | - | 0.193253 | |
DDB_G0288727 | DDB_G0288727 | DDB0232432 | CDS | 1883551 | 435 | + | 0.25977 | |
DDB_G0288729 | DDB_G0288729 | ortholog of the mammalian reticulon-4-interacting protein 1 a zinc-containing alcohol dehydrogenase | DDB0232432 | CDS | 1887042 | 1059 | - | 0.249292 |
DDB_G0288731 | DDB_G0288731 | highly similar to mammalian myotubularin-related protein 2 in sequence and in domain architecture a dual-specific lipid phosphatase that dephosphorylates phosphatidylinositol 3-phosphate and phosphatidylinositol (35)-bi-phosphate | DDB0232432 | CDS | 1888714 | 3684 | + | 0.266015 |
DDB_G0288733_ps | DDB_G0288733 | putative pseudogene similar to a family of genes including | DDB0232432 | CDS | 1894171 | 375 | + | 0.352 |
DDB_G0288735 | DDB_G0288735 | very similar to acyl-coenzyme A oxidases but lacks the full domain | DDB0232432 | CDS | 1895573 | 1959 | + | 0.338948 |
DDB_G0288737 | DDB_G0288737 | DDB0232432 | CDS | 1864937 | 612 | + | 0.228758 | |
DDB_G0288739 | DDB_G0288739 | DDB0232432 | CDS | 1826054 | 1398 | - | 0.261087 | |
DDB_G0288745 | DDB_G0288745 | DDB0232432 | CDS | 1892916 | 642 | + | 0.291277 | |
DDB_G0288747 | DDB_G0288747 | contains one Myb DNA-binding domain similar to D. rerio DNA methyltransferase 1 associated protein 1 | DDB0232432 | CDS | 1912921 | 3129 | + | 0.282838 |
DDB_G0288751 | DDB_G0288751 | DDB0232432 | CDS | 1903969 | 3690 | + | 0.250677 | |
DDB_G0288757 | DDB_G0288757 | catalyzes the reaction ATP nicotinamide ribonucleotide diphosphate NAD | DDB0232432 | CDS | 1926304 | 579 | - | 0.229706 |
DDB_G0288761 | DDB_G0288761 | DDB0232432 | CDS | 1927278 | 129 | - | 0.24031 | |
DDB_G0288763 | DDB_G0288763 | DDB0232432 | CDS | 1933766 | 1119 | + | 0.304736 | |
DDB_G0288765 | DDB_G0288765 | DDB0232432 | CDS | 1935972 | 255 | + | 0.215686 | |
DDB_G0288767 | DDB_G0288767 | DDB0232432 | CDS | 1936647 | 609 | + | 0.275862 | |
DDB_G0288779 | DDB_G0288779 | DDB0232432 | CDS | 1950277 | 1482 | + | 0.212551 | |
DDB_G0288781 | DDB_G0288781 | DDB0232432 | CDS | 1951922 | 1371 | - | 0.340627 | |
DDB_G0288793 | DDB_G0288793 | DDB0232432 | CDS | 1973649 | 1521 | - | 0.26167 | |
DDB_G0288795 | DDB_G0288795 | putative protein serinethreonine kinase AGC group similar to the kinase domains of mammalian AKTPKB similar to yeast protein kinases GAD8 and SCH9 | DDB0232432 | CDS | 1975761 | 1926 | - | 0.317757 |
DDB_G0288801 | DDB_G0288801 | DDB0232432 | CDS | 1982434 | 2106 | - | 0.349003 | |
DDB_G0288805 | DDB_G0288805 | DDB0232432 | CDS | 1990254 | 2601 | + | 0.235679 | |
DDB_G0288811 | DDB_G0288811 | very similar to TBC1 domain family member 15 proteins and yeast GYP7 TBC domain-containing proteins in yeast are GTPase activator proteins | DDB0232432 | CDS | 2006806 | 2490 | + | 0.284739 |
DDB_G0288813 | DDB_G0288813 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 2010767 | 4197 | + | 0.245413 |
DDB_G0288815 | DDB_G0288815 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 2016292 | 4173 | + | 0.259286 |
DDB_G0288821 | DDB_G0288821 | DDB0232432 | CDS | 2033361 | 951 | - | 0.33123 | |
DDB_G0288825 | DDB_G0288825 | DDB0232432 | CDS | 2036092 | 2901 | - | 0.247156 | |
DDB_G0288827 | DDB_G0288827 | DDB0232432 | CDS | 2040745 | 2988 | + | 0.218541 | |
DDB_G0288829 | DDB_G0288829 | DDB0232432 | CDS | 2043960 | 252 | - | 0.297619 | |
DDB_G0288841 | DDB_G0288841 | DDB0232432 | CDS | 2053563 | 216 | + | 0.412037 | |
DDB_G0288847 | DDB_G0288847 | DDB0232432 | CDS | 2055893 | 450 | - | 0.295556 | |
DDB_G0288849 | DDB_G0288849 | contains a predicted signal peptide and a putative C-terminal transmembrane domain similar to S. cerevisiae ERO1 (endoplasmic oxidoreductin-1) which is required for the formation of disulfide bonds in the proteins in the endoplasmic reticulum | DDB0232432 | CDS | 2057527 | 1662 | - | 0.253309 |
DDB_G0288851 | DDB_G0288851 | DDB0232432 | CDS | 2060041 | 432 | + | 0.24537 | |
DDB_G0288853 | DDB_G0288853 | DDB0232432 | CDS | 2063858 | 1374 | + | 0.201601 | |
DDB_G0288861 | DDB_G0288861 | DDB0232432 | CDS | 1954614 | 2169 | + | 0.319963 | |
DDB_G0288865 | DDB_G0288865 | DDB0232432 | CDS | 1959111 | 486 | - | 0.257202 | |
DDB_G0288867 | DDB_G0288867 | DDB0232432 | CDS | 1970396 | 2844 | - | 0.182841 | |
DDB_G0288869 | DDB_G0288869 | contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one extracellular EGF-2 domain | DDB0232432 | CDS | 2021392 | 3024 | + | 0.257275 |
DDB_G0288871 | DDB_G0288871 | DDB0232432 | CDS | 2060725 | 240 | - | 0.320833 | |
DDB_G0288883 | DDB_G0288883 | DDB0232432 | CDS | 2083221 | 450 | - | 0.246667 | |
DDB_G0288885 | DDB_G0288885 | DDB0232432 | CDS | 2083996 | 918 | + | 0.308279 | |
DDB_G0288887 | DDB_G0288887 | DDB0232432 | CDS | 2086198 | 135 | - | 0.303704 | |
DDB_G0288889 | DDB_G0288889 | DDB0232432 | CDS | 2086808 | 1437 | - | 0.177453 | |
DDB_G0288895 | DDB_G0288895 | contains one BAR (BINAmphiphysinRvs) domain and SH3 domain | DDB0232432 | CDS | 2091691 | 1395 | - | 0.324014 |
DDB_G0288897 | DDB_G0288897 | DDB0232432 | CDS | 2093655 | 1050 | - | 0.202857 | |
DDB_G0288901 | DDB_G0288901 | DDB0232432 | CDS | 2103495 | 1563 | + | 0.221369 | |
DDB_G0288905 | DDB_G0288905 | DDB0232432 | CDS | 2106066 | 1797 | - | 0.188091 | |
DDB_G0288911 | DDB_G0288911 | contains a predicted signal sequence similar to a D. purpureum protein | DDB0232432 | CDS | 2112807 | 420 | + | 0.307143 |
DDB_G0288913 | DDB_G0288913 | DDB0232432 | CDS | 2113860 | 432 | + | 0.217593 | |
DDB_G0288915 | DDB_G0288915 | DDB0232432 | CDS | 2114788 | 3561 | - | 0.329683 | |
DDB_G0288917 | DDB_G0288917 | similar to retinol dehydrogenase and eukaryotic proteins of the short chain dehydrogenasesreductases family | DDB0232432 | CDS | 2119308 | 954 | + | 0.240042 |
DDB_G0288925 | DDB_G0288925 | DDB0232432 | CDS | 2134650 | 399 | - | 0.243108 | |
DDB_G0288929 | DDB_G0288929 | DDB0232432 | CDS | 2135701 | 1179 | + | 0.245123 | |
DDB_G0288931 | DDB_G0288931 | DDB0232432 | CDS | 2137477 | 564 | + | 0.281915 | |
DDB_G0288941 | DDB_G0288941 | DDB0232432 | CDS | 2158460 | 303 | + | 0.280528 | |
DDB_G0288943 | DDB_G0288943 | DDB0232432 | CDS | 2159616 | 1023 | + | 0.298143 | |
DDB_G0288945 | DDB_G0288945 | DDB0232432 | CDS | 2161054 | 186 | - | 0.258065 | |
DDB_G0288947 | DDB_G0288947 | DDB0232432 | CDS | 2162285 | 4416 | + | 0.279212 | |
DDB_G0288949 | DDB_G0288949 | DDB0232432 | CDS | 2101452 | 1392 | - | 0.236351 | |
DDB_G0288951 | DDB_G0288951 | DDB0232432 | CDS | 2077569 | 2955 | + | 0.226058 | |
DDB_G0288953 | DDB_G0288953 | DDB0232432 | CDS | 2080789 | 1446 | - | 0.276625 | |
DDB_G0288955 | DDB_G0288955 | contains multiple EGF-like domains contains contains a predicted signal sequece and a putative transmembrane domain | DDB0232432 | CDS | 2096747 | 3462 | - | 0.234258 |
DDB_G0288957 | DDB_G0288957 | DDB0232432 | CDS | 2140408 | 2229 | + | 0.236429 | |
DDB_G0288959 | DDB_G0288959 | DDB0232432 | CDS | 2143283 | 1257 | - | 0.247414 | |
DDB_G0288963 | DDB_G0288963 | similar to the conserved metallocarboxypeptidase D (CPD) a membrane bound protein the Dictyostelium protein is shorter and has only one M14 peptidase domain versus three such domains in the animal proteins and also does not seem to contain a transmembrane domain | DDB0232432 | CDS | 2155528 | 1500 | - | 0.266 |
DDB_G0288965 | DDB_G0288965 | DDB0232432 | CDS | 2174329 | 1749 | - | 0.256146 | |
DDB_G0288967 | DDB_G0288967 | DDB0232432 | CDS | 2179762 | 2721 | + | 0.246968 | |
DDB_G0288969 | DDB_G0288969 | DDB0232432 | CDS | 2182982 | 3108 | + | 0.223616 | |
DDB_G0288971 | DDB_G0288971 | DDB0232432 | CDS | 2186215 | 354 | - | 0.271186 | |
DDB_G0288973 | DDB_G0288973 | DDB0232432 | CDS | 2186905 | 1386 | + | 0.155844 | |
DDB_G0288981 | DDB_G0288981 | DDB0232432 | CDS | 2203346 | 441 | - | 0.206349 | |
DDB_G0288987 | DDB_G0288987 | DDB0232432 | CDS | 2206848 | 2130 | - | 0.239906 | |
DDB_G0288991 | DDB_G0288991 | DDB0232432 | CDS | 2210519 | 273 | - | 0.300366 | |
DDB_G0288997 | DDB_G0288997 | DDB0232432 | CDS | 2215599 | 609 | + | 0.229885 | |
DDB_G0288999_ps | DDB_G0288999 | putative pseudogene highly conserved family containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232432 | CDS | 2216611 | 453 | - | 0.267108 |
DDB_G0289007 | DDB_G0289007 | DDB0232432 | CDS | 2223594 | 1284 | + | 0.246106 | |
DDB_G0289009 | DDB_G0289009 | DDB0232432 | CDS | 2225715 | 708 | - | 0.185028 | |
DDB_G0289011 | DDB_G0289011 | similar to human C20orf24 (Rab5-interacting protein) contains 2 putative transmembrane domains | DDB0232432 | CDS | 2226660 | 342 | - | 0.263158 |
DDB_G0289015 | DDB_G0289015 | DDB0232432 | CDS | 2232832 | 1026 | - | 0.344055 | |
DDB_G0289017 | DDB_G0289017 | DDB0232432 | CDS | 2236776 | 4179 | - | 0.228045 | |
DDB_G0289019 | DDB_G0289019 | DDB0232432 | CDS | 2243747 | 2748 | - | 0.290393 | |
DDB_G0289023 | DDB_G0289023 | DDB0232432 | CDS | 2251614 | 1221 | + | 0.207207 | |
DDB_G0289027 | DDB_G0289027 | DDB0232432 | CDS | 2254543 | 513 | - | 0.302144 | |
DDB_G0289029 | DDB_G0289029 | conserved protein similar to S. cerevisiae IST1 (Increased Sodium Tolerance) that plays a role in the endosome to vacuole transport via the multivesicular body sorting pathway contains an N-terminal DUF292 domain | DDB0232432 | CDS | 2256321 | 1110 | - | 0.288288 |
DDB_G0289031 | DDB_G0289031 | ortholog of the conserved spastic paraplegia 21 (SPG21) also known as Maspardin defects in human SPG21 are the cause of the neurodegenerative disorder spastic paraplegia also known as Mast syndrome | DDB0232432 | CDS | 2258354 | 1155 | - | 0.256277 |
DDB_G0289033 | DDB_G0289033 | DDB0232432 | CDS | 2277325 | 4770 | - | 0.292243 | |
DDB_G0289039 | DDB_G0289039 | DDB0232432 | CDS | 2286110 | 1287 | + | 0.262626 | |
DDB_G0289041 | DDB_G0289041 | DDB0232432 | CDS | 2287957 | 2334 | + | 0.24036 | |
DDB_G0289043 | DDB_G0289043 | DDB0232432 | CDS | 2291494 | 5457 | + | 0.226315 | |
DDB_G0289045 | DDB_G0289045 | DDB0232432 | CDS | 2297386 | 654 | - | 0.266055 | |
DDB_G0289047 | DDB_G0289047 | highly similar to bacterial ClpB expressed in prespore cells | DDB0232432 | CDS | 2299492 | 2388 | - | 0.348827 |
DDB_G0289049_RTE | DDB_G0289049 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232432 | CDS | 2260286 | 3960 | + | 0.194697 |
DDB_G0289051 | DDB_G0289051 | DDB0232432 | CDS | 2275554 | 1257 | + | 0.290374 | |
DDB_G0289053 | DDB_G0289053 | similar to mammalian RNPS1 (RNA-binding protein with serine-rich domain 1) part of pre- and post-splicing multiprotein mRNP complexes | DDB0232432 | CDS | 2302813 | 1539 | - | 0.322287 |
DDB_G0289057 | DDB_G0289057 | DDB0232432 | CDS | 2307545 | 936 | + | 0.238248 | |
DDB_G0289059 | DDB_G0289059 | DDB0232432 | CDS | 2308883 | 996 | + | 0.252008 | |
DDB_G0289061 | DDB_G0289061 | DDB0232432 | CDS | 2310384 | 1002 | + | 0.257485 | |
DDB_G0289063 | DDB_G0289063 | DDB0232432 | CDS | 2312279 | 816 | + | 0.281863 | |
DDB_G0289065 | DDB_G0289065 | similar to yeast ERG28 an endoplasmic reticulum protein involved in ergosterol biosynthesis contains 4 putative transmembrane domains | DDB0232432 | CDS | 2314833 | 372 | + | 0.252688 |
DDB_G0289071_RTE | DDB_G0289071 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232432 | CDS | 2321624 | 458 | + | 0.395196 |
DDB_G0289077 | DDB_G0289077 | DDB0232432 | CDS | 2326670 | 3246 | - | 0.254775 | |
DDB_G0289081 | DDB_G0289081 | contains a NAD(P)-binding domain contains a predicted peroxisomal targeting signal | DDB0232432 | CDS | 2331738 | 3840 | - | 0.336198 |
DDB_G0289089 | DDB_G0289089 | DDB0232432 | CDS | 2339443 | 222 | - | 0.220721 | |
DDB_G0289091 | DDB_G0289091 | DDB0232432 | CDS | 2340065 | 2028 | - | 0.233235 | |
DDB_G0289093 | DDB_G0289093 | DDB0232432 | CDS | 2345850 | 1074 | + | 0.264432 | |
DDB_G0289095 | DDB_G0289095 | DDB0232432 | CDS | 2348039 | 1677 | + | 0.214669 | |
DDB_G0289097 | DDB_G0289097 | DDB0232432 | CDS | 2349881 | 1350 | - | 0.298519 | |
DDB_G0289099 | DDB_G0289099 | DDB0232432 | CDS | 2356325 | 2355 | + | 0.290021 | |
DDB_G0289101 | DDB_G0289101 | DDB0232432 | CDS | 2361177 | 261 | + | 0.291188 | |
DDB_G0289107_RTE | DDB_G0289107 | DDB0232432 | CDS | 2322480 | 1791 | + | 0.349525 | |
DDB_G0289109 | DDB_G0289109 | DDB0232432 | CDS | 2325208 | 735 | - | 0.382313 | |
DDB_G0289111 | DDB_G0289111 | DDB0232432 | CDS | 2353928 | 942 | + | 0.335456 | |
DDB_G0289113 | DDB_G0289113 | DDB0232432 | CDS | 2369676 | 3660 | + | 0.269126 | |
DDB_G0289123 | DDB_G0289123 | DDB0232432 | CDS | 2378873 | 5022 | - | 0.263839 | |
DDB_G0289125 | DDB_G0289125 | DDB0232432 | CDS | 2384391 | 768 | + | 0.22526 | |
DDB_G0289127 | DDB_G0289127 | DDB0232432 | CDS | 2385358 | 861 | - | 0.304297 | |
DDB_G0289129 | DDB_G0289129 | DDB0232432 | CDS | 2386701 | 885 | - | 0.310734 | |
DDB_G0289131 | DDB_G0289131 | DDB0232432 | CDS | 2388498 | 1101 | + | 0.167121 | |
DDB_G0289133 | DDB_G0289133 | DDB0232432 | CDS | 2389784 | 1341 | - | 0.221477 | |
DDB_G0289137 | DDB_G0289137 | DDB0232432 | CDS | 2392822 | 273 | - | 0.296703 | |
DDB_G0289141 | DDB_G0289141 | DDB0232432 | CDS | 2395095 | 5412 | + | 0.320584 | |
DDB_G0289143 | DDB_G0289143 | contains 11 putative transmembrane domains similar to D. purpureum protein | DDB0232432 | CDS | 2407681 | 1719 | + | 0.285049 |
DDB_G0289147 | DDB_G0289147 | DDB0232432 | CDS | 2417343 | 804 | - | 0.253731 | |
DDB_G0289159 | DDB_G0289159 | DDB0232432 | CDS | 2435887 | 333 | + | 0.225225 | |
DDB_G0289161 | DDB_G0289161 | DDB0232432 | CDS | 2436601 | 477 | - | 0.287212 | |
DDB_G0289163 | DDB_G0289163 | DDB0232432 | CDS | 2437452 | 297 | - | 0.191919 | |
DDB_G0289167 | DDB_G0289167 | similar to bacterial short-chain dehydrogenasereductase family proteins and human RDH8 (retinol dehydrogenase 8) | DDB0232432 | CDS | 2441551 | 972 | - | 0.244856 |
DDB_G0289171 | DDB_G0289171 | DDB0232432 | CDS | 2439587 | 1059 | - | 0.260623 | |
DDB_G0289183 | DDB_G0289183 | DDB0232432 | CDS | 2445521 | 2337 | - | 0.307231 | |
DDB_G0289185 | DDB_G0289185 | DDB0232432 | CDS | 2448283 | 3081 | + | 0.212918 | |
DDB_G0289191 | DDB_G0289191 | DDB0232432 | CDS | 2454071 | 837 | + | 0.216249 | |
DDB_G0289195 | DDB_G0289195 | DDB0232432 | CDS | 2456763 | 891 | + | 0.260382 | |
DDB_G0289199 | DDB_G0289199 | DDB0232432 | CDS | 2458510 | 1899 | - | 0.282254 | |
DDB_G0289203 | DDB_G0289203 | DDB0232432 | CDS | 2464468 | 444 | + | 0.286036 | |
DDB_G0289205 | DDB_G0289205 | DDB0232432 | CDS | 2467250 | 4203 | + | 0.305972 | |
DDB_G0289209 | DDB_G0289209 | DDB0232432 | CDS | 2478124 | 927 | - | 0.242718 | |
DDB_G0289211 | DDB_G0289211 | contains a central large T4 RNA ligase RnlA-like domain a property shared by a related gene | DDB0232432 | CDS | 2485943 | 1392 | + | 0.26796 |
DDB_G0289213 | DDB_G0289213 | DDB0232432 | CDS | 2487904 | 1593 | + | 0.209667 | |
DDB_G0289215 | DDB_G0289215 | DDB0232432 | CDS | 2489574 | 1527 | - | 0.206287 | |
DDB_G0289217 | DDB_G0289217 | DDB0232432 | CDS | 2491401 | 1482 | + | 0.274629 | |
DDB_G0289219_ps | DDB_G0289219 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 2493243 | 234 | - | 0.226496 |
DDB_G0289221 | DDB_G0289221 | DDB0232432 | CDS | 2494619 | 2382 | + | 0.274139 | |
DDB_G0289225_ps | DDB_G0289225 | putative pseudogene partial similar to IPTTIG domain-containing proteins e.g | DDB0232432 | CDS | 2497743 | 1587 | - | 0.271582 |
DDB_G0289227 | DDB_G0289227 | DDB0232432 | CDS | 2500724 | 2433 | - | 0.21866 | |
DDB_G0289231 | DDB_G0289231 | member of the peptidase S28 family of serine proteases a group containing lysosomal Pro-X carboxypeptidase dipeptidyl-peptidase II and thymus-specific serine peptidase | DDB0232432 | CDS | 2519340 | 1542 | + | 0.275616 |
DDB_G0289233 | DDB_G0289233 | similar to human and S. cerevisiae VAC14 (vacuole morphology and inheritance protein 14) contains 3 HEAT repeats | DDB0232432 | CDS | 2521042 | 2343 | - | 0.24968 |
DDB_G0289235 | DDB_G0289235 | DDB0232432 | CDS | 2524160 | 2523 | + | 0.266746 | |
DDB_G0289243 | DDB_G0289243 | bCommunity annotation:b The computer has already noticed that this gene is similar to the widely-conserved folliculin interacting protein FNIP. Dicty in fact has a homolog of folliculin (DDB_G0281111) which the computer has also identified. In mammals folliculin is a tumor suppressor protein mutation of which in the Birt-Hogg-Dube syndrome leads to renal and pulmonary cysts renal cancer and noncancerous tumors of the hair follicles. Folliculin participates in a complex with FNIP1 and FNIP2 which | DDB0232432 | CDS | 2504135 | 2916 | - | 0.258573 |
DDB_G0289245 | DDB_G0289245 | DDB0232432 | CDS | 2518176 | 165 | - | 0.387879 | |
DDB_G0289249 | DDB_G0289249 | DDB0232432 | CDS | 2541277 | 1887 | + | 0.294648 | |
DDB_G0289251 | DDB_G0289251 | belongs to the PLAC8 family (placenta-specific gene 8 protein) a family of cysteine-rich proteins with highly divergent low complexity amino terminal regions similar to D. purpureum protein | DDB0232432 | CDS | 2543934 | 417 | + | 0.280576 |
DDB_G0289255 | DDB_G0289255 | DDB0232432 | CDS | 2550795 | 132 | + | 0.265152 | |
DDB_G0289259 | DDB_G0289259 | similar to bacterial fungal and plant proteins from the short-chain dehydrogenasereductase family | DDB0232432 | CDS | 2556391 | 879 | - | 0.265074 |
DDB_G0289261_ps | DDB_G0289261 | putative pseudogene similar to family of Endotoxin_N-terminal domain-containing proteins including | DDB0232432 | CDS | 2538517 | 1782 | - | 0.274972 |
DDB_G0289263 | DDB_G0289263 | DDB0232432 | CDS | 2557966 | 2799 | - | 0.246874 | |
DDB_G0289265 | DDB_G0289265 | has similarity to flavin containing monoamine oxidases contains one amino oxidase domain | DDB0232432 | CDS | 2564981 | 1395 | - | 0.341935 |
DDB_G0289267 | DDB_G0289267 | DDB0232432 | CDS | 2568808 | 219 | + | 0.30137 | |
DDB_G0289269 | DDB_G0289269 | DDB0232432 | CDS | 2569964 | 483 | + | 0.329193 | |
DDB_G0289273 | DDB_G0289273 | DDB0232432 | CDS | 2572028 | 3111 | - | 0.270653 | |
DDB_G0289275 | DDB_G0289275 | DDB0232432 | CDS | 2576362 | 1002 | - | 0.281437 | |
DDB_G0289279_RTE | DDB_G0289279 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 2578513 | 934 | + | 0.334047 |
DDB_G0289285 | DDB_G0289285 | putative secreted protein contains a predicted signal sequence similar to D. purpureum protein | DDB0232432 | CDS | 2598434 | 1101 | + | 0.300636 |
DDB_G0289287 | DDB_G0289287 | DDB0232432 | CDS | 2600762 | 3828 | + | 0.161181 | |
DDB_G0289293 | DDB_G0289293 | DDB0232432 | CDS | 2607143 | 399 | + | 0.305764 | |
DDB_G0289295 | DDB_G0289295 | DDB0232432 | CDS | 2607639 | 186 | + | 0.397849 | |
DDB_G0289303 | DDB_G0289303 | DDB0232432 | CDS | 2604715 | 1350 | - | 0.295556 | |
DDB_G0289307_ps | DDB_G0289307 | putative pseudogene highly similar to | DDB0232432 | CDS | 2609390 | 933 | - | 0.424437 |
DDB_G0289309 | DDB_G0289309 | carboxyl terminus is highly similar to that of cup (calcium up-regulated) genes but the rest of the protein shares little similarity | DDB0232432 | CDS | 2616286 | 3024 | - | 0.18287 |
DDB_G0289311 | DDB_G0289311 | DDB0232432 | CDS | 2622270 | 2025 | - | 0.222222 | |
DDB_G0289315 | DDB_G0289315 | DDB0232432 | CDS | 2619812 | 861 | - | 0.163763 | |
DDB_G0289321 | DDB_G0289321 | DDB0232432 | CDS | 2637678 | 2571 | + | 0.28238 | |
DDB_G0289333 | DDB_G0289333 | DDB0232432 | CDS | 2646115 | 1866 | - | 0.343516 | |
DDB_G0289335 | DDB_G0289335 | DDB0232432 | CDS | 2652694 | 2064 | - | 0.28876 | |
DDB_G0289337 | DDB_G0289337 | DDB0232432 | CDS | 2656525 | 4587 | + | 0.240026 | |
DDB_G0289341 | DDB_G0289341 | C-terminal half has similarity to yeast E3 SUMO-protein ligase MMS21 (NSE2) which acts in a DNA repair pathway for removal of UV-induced DNA damagebrbr bCommunity annotation:b DDB_G0289341 is similar (best Blast hit both ways) to nse2 an E3 sumo protein ligase which acts in a complex with SMC5 and SMC6 in homologous recombination and telomere maintenance (see Murray and Carr Nature Reviews Molecular Cell Biology 9 177-182 (2008)). Both of these processes are associated with chromosomal replication. DDB_G0289341 is overexpressed threefold in a Dicty strain in which the retinoblastoma-like gene rblA is disrupted ( | DDB0232432 | CDS | 2662531 | 756 | + | 0.292328 |
DDB_G0289345 | DDB_G0289345 | DDB0232432 | CDS | 2666970 | 1257 | + | 0.284805 | |
DDB_G0289347 | DDB_G0289347 | DDB0232432 | CDS | 2668661 | 738 | - | 0.227642 | |
DDB_G0289349 | DDB_G0289349 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity also contains an N-terminal transmembrane domain | DDB0232432 | CDS | 2670443 | 1479 | + | 0.279919 |
DDB_G0289351 | DDB_G0289351 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and 4 extracellular EGF domains | DDB0232432 | CDS | 2672362 | 3669 | + | 0.292178 |
DDB_G0289355 | DDB_G0289355 | DDB0232432 | CDS | 2681578 | 1893 | + | 0.216587 | |
DDB_G0289357 | DDB_G0289357 | DDB0232432 | CDS | 2685876 | 1671 | + | 0.285458 | |
DDB_G0289359 | DDB_G0289359 | DDB0232432 | CDS | 2687826 | 165 | - | 0.278788 | |
DDB_G0289363 | DDB_G0289363 | DDB0232432 | CDS | 2707148 | 372 | - | 0.287634 | |
DDB_G0289369 | DDB_G0289369 | contains an AN1-type at the amino terminus and a UBX domain found in ubiquitin-regulatory proteins at the carboxyl terminus | DDB0232432 | CDS | 2722171 | 1263 | + | 0.243864 |
DDB_G0289377 | DDB_G0289377 | DDB0232432 | CDS | 2645520 | 189 | - | 0.333333 | |
DDB_G0289381 | DDB_G0289381 | DDB0232432 | CDS | 2697784 | 2541 | + | 0.237308 | |
DDB_G0289385 | DDB_G0289385 | DDB0232432 | CDS | 2714901 | 6525 | + | 0.235709 | |
DDB_G0289387_RTE | DDB_G0289387 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232432 | CDS | 2728693 | 1094 | + | 0.297075 |
DDB_G0289397 | DDB_G0289397 | DDB0232432 | CDS | 2739034 | 1200 | - | 0.3925 | |
DDB_G0289399 | DDB_G0289399 | contains 3 laminin-type EGF-like domains contains one IPTTIG domain that has an immunoglobulin-like fold contains one predicted C-terminal transmembrane domain | DDB0232432 | CDS | 2743899 | 2010 | + | 0.289055 |
DDB_G0289401 | DDB_G0289401 | DDB0232432 | CDS | 2748299 | 780 | - | 0.255128 | |
DDB_G0289403 | DDB_G0289403 | DDB0232432 | CDS | 2749137 | 966 | - | 0.315735 | |
DDB_G0289405_ps | DDB_G0289405 | putative pseudogene very similar to parts of DDB_G0289409 | DDB0232432 | CDS | 2751258 | 471 | + | 0.301486 |
DDB_G0289407 | DDB_G0289407 | almost identical to | DDB0232432 | CDS | 2752168 | 2412 | - | 0.274461 |
DDB_G0289409 | DDB_G0289409 | DDB0232432 | CDS | 2755696 | 11793 | + | 0.287628 | |
DDB_G0289411 | DDB_G0289411 | DDB0232432 | CDS | 2771756 | 444 | - | 0.335586 | |
DDB_G0289413 | DDB_G0289413 | DDB0232432 | CDS | 2773421 | 1524 | + | 0.17126 | |
DDB_G0289415 | DDB_G0289415 | DDB0232432 | CDS | 2775105 | 2037 | - | 0.307806 | |
DDB_G0289419_ps | DDB_G0289419 | putative pseudogene fragment very similar to | DDB0232432 | CDS | 2780778 | 594 | - | 0.239057 |
DDB_G0289421 | DDB_G0289421 | has limited similarity to mammalian Mis18-alpha and beta (MIS18A MIS18B) that are required for normal chromosome segregation during mitosisbrbr bCommunity annotation:b DDB G0289421 is weakly similar (first Blast hit both ways) to Mis18-alpha and Mis18-beta. In mammals these two closely related proteins are necessary for loading histone H3 variant CENP-A onto centromeric chromatin at the telophaseG1 boundary (see Fujita et al Developmental Cell 12 17-30 (2007). Knockdown of Mis18-alpha Mis18-beta or the third component of this complex (M18BP1) leads to misalignment of mitotic chromosomes presumably at the following mitosis and apparently without activation of the spindle checkpoint.br In Dicty there appears to be only one Mis18 and neither M18BP1 nor CENP-A itself is identifiable. DDB_G0289421 nonetheless appears to be a cell cycle gene: it is overexpressed threefold (p5e-11) in a strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes with known functions in S- | DDB0232432 | CDS | 2784742 | 1599 | - | 0.285178 |
DDB_G0289423 | DDB_G0289423 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | DDB0232432 | CDS | 2794822 | 3246 | + | 0.279421 |
DDB_G0289427 | DDB_G0289427 | DDB0232432 | CDS | 2779634 | 270 | - | 0.244444 | |
DDB_G0289433_ps | DDB_G0289433 | putative pseudogene almost identical to | DDB0232432 | CDS | 2741182 | 1998 | + | 0.29029 |
DDB_G0289437 | DDB_G0289437 | DDB0232432 | CDS | 2750374 | 420 | - | 0.209524 | |
DDB_G0289439 | DDB_G0289439 | DDB0232432 | CDS | 2778983 | 405 | + | 0.367901 | |
DDB_G0289441_RTE | DDB_G0289441 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232432 | CDS | 2730874 | 211 | + | 0.393365 |
DDB_G0289443 | DDB_G0289443 | small Dictyostelium protein family expressed in pstO cells and in upper cup during culmination | DDB0232432 | CDS | 2802474 | 240 | - | 0.320833 |
DDB_G0289453 | DDB_G0289453 | possible homolog of human LSM11 a U7 snRNA-associated Sm-like protein | DDB0232432 | CDS | 2807299 | 774 | - | 0.277778 |
DDB_G0289455 | DDB_G0289455 | DDB0232432 | CDS | 2808377 | 1071 | + | 0.278245 | |
DDB_G0289457 | DDB_G0289457 | DDB0232432 | CDS | 2809612 | 750 | - | 0.217333 | |
DDB_G0289459 | DDB_G0289459 | DDB0232432 | CDS | 2812938 | 582 | - | 0.223368 | |
DDB_G0289461 | DDB_G0289461 | putative ortholog of H. sapiens CNOT6 and S. cerevisiae CCR4 component of the CCR4-NOT transcription complex | DDB0232432 | CDS | 2814027 | 1722 | - | 0.260163 |
DDB_G0289465 | DDB_G0289465 | DDB0232432 | CDS | 2818342 | 2496 | + | 0.23758 | |
DDB_G0289469 | DDB_G0289469 | similar to D. purpureum and P. pallidum protein C-terminal region similar to ribosomal protein S15P family | DDB0232432 | CDS | 2826905 | 1824 | + | 0.307018 |
DDB_G0289473 | DDB_G0289473 | ortholog of the conserved plasma membrane calcium ATPases (PMCA) such as Dictyostelium PAT1 contains at least 8 predicted transmembrane domains | DDB0232432 | CDS | 2830601 | 3234 | - | 0.310761 |
DDB_G0289491 | DDB_G0289491 | DDB0232432 | CDS | 2849682 | 174 | - | 0.229885 | |
DDB_G0289493 | DDB_G0289493 | DDB0232432 | CDS | 2850667 | 378 | - | 0.293651 | |
DDB_G0289495 | DDB_G0289495 | DDB0232432 | CDS | 2851858 | 3594 | + | 0.258486 | |
DDB_G0289497 | DDB_G0289497 | bCommunity annotation:b DDB_G0289497 has been alleged to be a member of the dickkopf family (Guder et al 2006 Development 133 901-911 ). Mammals have four dickkopf genes (Dkk1 Dkk2 Dkk3 and Dkk4) of which Dkk1 2 and 4 have been shown to be secreted antagonists of wingless signalling. Heterologous expression of any of these in vertebrate embryos leads to a reduction of posterior structures with accompanying enhancement of the head hence the name dickkopf which literally means fathead in German (Glinka et al 1998 Nature 391 357-362). The Dictyostelium gene is most similar to Dkk3 which is somewhat divergent from the others (see Niehrs 2006 Oncogene 25 7469-7481). Members of the Dkk3 subfamily have signal peptides (as does DDB_G0289497) and are probably secreted proteins. | DDB0232432 | CDS | 2856146 | 246 | + | 0.378049 |
DDB_G0289503_ps | DDB_G0289503 | putative pseudogene almost identical to neighboring gene | DDB0232432 | CDS | 2868325 | 5166 | - | 0.258227 |
DDB_G0289517 | DDB_G0289517 | DDB0232432 | CDS | 2901066 | 2139 | - | 0.266947 | |
DDB_G0289519 | DDB_G0289519 | DDB0232432 | CDS | 2904697 | 1626 | - | 0.278598 | |
DDB_G0289527 | DDB_G0289527 | DDB0232432 | CDS | 2912060 | 231 | + | 0.264069 | |
DDB_G0289529 | DDB_G0289529 | DDB0232432 | CDS | 2862639 | 5034 | - | 0.265395 | |
DDB_G0289537 | DDB_G0289537 | DDB0232432 | CDS | 2908181 | 1749 | + | 0.227559 | |
DDB_G0289539 | DDB_G0289539 | DDB0232432 | CDS | 2914742 | 1590 | + | 0.296226 | |
DDB_G0289545 | DDB_G0289545 | DDB0232432 | CDS | 2926893 | 3675 | - | 0.163265 | |
DDB_G0289547 | DDB_G0289547 | DDB0232432 | CDS | 2930859 | 1164 | + | 0.28866 | |
DDB_G0289549 | DDB_G0289549 | DDB0232432 | CDS | 2932427 | 270 | + | 0.285185 | |
DDB_G0289551 | DDB_G0289551 | DDB0232432 | CDS | 2933097 | 2163 | - | 0.306981 | |
DDB_G0289557 | DDB_G0289557 | DDB0232432 | CDS | 2946489 | 2328 | - | 0.226804 | |
DDB_G0289561 | DDB_G0289561 | DDB0232432 | CDS | 2951390 | 2777 | + | 0.218581 | |
DDB_G0289567_ps | DDB_G0289567 | putative pseudogene fragment similar to FNIP repeat containing proteins | DDB0232432 | CDS | 2957193 | 498 | + | 0.259036 |
DDB_G0289571 | DDB_G0289571 | DDB0232432 | CDS | 2958707 | 2739 | + | 0.262505 | |
DDB_G0289573 | DDB_G0289573 | DDB0232432 | CDS | 2973076 | 372 | - | 0.266129 | |
DDB_G0289575 | DDB_G0289575 | DDB0232432 | CDS | 2971496 | 1149 | + | 0.288077 | |
DDB_G0289577 | DDB_G0289577 | DDB0232432 | CDS | 2964470 | 2190 | + | 0.257078 | |
DDB_G0289579 | DDB_G0289579 | DDB0232432 | CDS | 2967354 | 456 | + | 0.300439 | |
DDB_G0289581 | DDB_G0289581 | DDB0232432 | CDS | 2997750 | 741 | - | 0.237517 | |
DDB_G0289583 | DDB_G0289583 | ortholog of human SDCCAG1 (serologically defined colon cancer antigen 1) a conserved eukaryotic protein of unknown function | DDB0232432 | CDS | 2992157 | 3807 | - | 0.276333 |
DDB_G0289585 | DDB_G0289585 | leucine-rich repeat protein with filaminABP280 at the carboxyl terminus | DDB0232432 | CDS | 2989530 | 1497 | - | 0.297261 |
DDB_G0289587 | DDB_G0289587 | belongs to the RRN3 family similar to human and S. cerevisiae RRN3 (RNA polymerase I-specific transcription initiation factor RRN3) | DDB0232432 | CDS | 2981034 | 2121 | + | 0.290429 |
DDB_G0289591 | DDB_G0289591 | DDB0232432 | CDS | 2974797 | 2421 | + | 0.173895 | |
DDB_G0289603 | DDB_G0289603 | DDB0232432 | CDS | 3013032 | 3603 | - | 0.189564 | |
DDB_G0289607 | DDB_G0289607 | DDB0232432 | CDS | 3018845 | 504 | - | 0.238095 | |
DDB_G0289609 | DDB_G0289609 | contains two CBS domains expressed in pstAO cells and in upper cup during culmination | DDB0232432 | CDS | 3019826 | 438 | - | 0.296804 |
DDB_G0289615 | DDB_G0289615 | DDB0232432 | CDS | 3032158 | 2073 | + | 0.242161 | |
DDB_G0289617 | DDB_G0289617 | DDB0232432 | CDS | 3034658 | 774 | + | 0.158915 | |
DDB_G0289619_ps | DDB_G0289619 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3042065 | 771 | + | 0.267185 |
DDB_G0289621 | DDB_G0289621 | DDB0232432 | CDS | 3043521 | 714 | + | 0.317927 | |
DDB_G0289625 | DDB_G0289625 | DDB0232432 | CDS | 3045458 | 615 | + | 0.252033 | |
DDB_G0289627 | DDB_G0289627 | DDB0232432 | CDS | 3046500 | 2223 | - | 0.304094 | |
DDB_G0289629 | DDB_G0289629 | DDB0232432 | CDS | 3049902 | 2181 | - | 0.279688 | |
DDB_G0289631_ps | DDB_G0289631 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 3054610 | 615 | + | 0.265041 |
DDB_G0289635 | DDB_G0289635 | DDB0232432 | CDS | 3008595 | 3279 | - | 0.174748 | |
DDB_G0289637 | DDB_G0289637 | DDB0232432 | CDS | 3035690 | 3093 | + | 0.259295 | |
DDB_G0289641 | DDB_G0289641 | DDB0232432 | CDS | 3039503 | 1542 | + | 0.219844 | |
DDB_G0289643 | DDB_G0289643 | DDB0232432 | CDS | 3052862 | 849 | - | 0.254417 | |
DDB_G0289647_ps | DDB_G0289647 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3056743 | 1062 | - | 0.193032 |
DDB_G0289649 | DDB_G0289649 | DDB0232432 | CDS | 3058125 | 168 | - | 0.25 | |
DDB_G0289669 | DDB_G0289669 | DDB0232432 | CDS | 3069414 | 1626 | - | 0.264453 | |
DDB_G0289671 | DDB_G0289671 | similar to human ABHD13 (Abhydrolase domain-containing protein 13) and S. pombe bem46 contains one putative transmembrane domain | DDB0232432 | CDS | 3072697 | 864 | + | 0.280093 |
DDB_G0289673 | DDB_G0289673 | DDB0232432 | CDS | 3074556 | 2979 | + | 0.249413 | |
DDB_G0289679 | DDB_G0289679 | DDB0232432 | CDS | 3090972 | 288 | - | 0.354167 | |
DDB_G0289681 | DDB_G0289681 | DDB0232432 | CDS | 3092553 | 864 | - | 0.212963 | |
DDB_G0289683 | DDB_G0289683 | DDB0232432 | CDS | 3093903 | 2787 | + | 0.175099 | |
DDB_G0289685 | DDB_G0289685 | DDB0232432 | CDS | 3096922 | 2607 | + | 0.169544 | |
DDB_G0289687 | DDB_G0289687 | DDB0232432 | CDS | 3103046 | 2694 | + | 0.199332 | |
DDB_G0289689 | DDB_G0289689 | DDB0232432 | CDS | 3108150 | 2832 | - | 0.248588 | |
DDB_G0289691 | DDB_G0289691 | DDB0232432 | CDS | 3111862 | 672 | - | 0.206845 | |
DDB_G0289693 | DDB_G0289693 | DDB0232432 | CDS | 3113883 | 360 | - | 0.305556 | |
DDB_G0289695 | DDB_G0289695 | DDB0232432 | CDS | 3114892 | 501 | - | 0.265469 | |
DDB_G0289697 | DDB_G0289697 | DDB0232432 | CDS | 3115871 | 1359 | + | 0.314202 | |
DDB_G0289701 | DDB_G0289701 | has similarity to nuclear pore protein 214 contains a Wd40-like region and a moesin C-terminal domain | DDB0232432 | CDS | 3121180 | 5115 | - | 0.324145 |
DDB_G0289703 | DDB_G0289703 | DDB0232432 | CDS | 3127157 | 2931 | + | 0.247015 | |
DDB_G0289705 | DDB_G0289705 | DDB0232432 | CDS | 3136742 | 6009 | + | 0.305542 | |
DDB_G0289707 | DDB_G0289707 | DDB0232432 | CDS | 3143077 | 1071 | + | 0.267974 | |
DDB_G0289713 | DDB_G0289713 | DDB0232432 | CDS | 3151658 | 1668 | + | 0.251199 | |
DDB_G0289715 | DDB_G0289715 | DDB0232432 | CDS | 3153407 | 846 | - | 0.326241 | |
DDB_G0289717 | DDB_G0289717 | contains one B-box zinc-finger domain and 7 FNIP repeats contains one coiled-coil domain | DDB0232432 | CDS | 3156042 | 1977 | - | 0.231158 |
DDB_G0289719 | DDB_G0289719 | DDB0232432 | CDS | 3159163 | 4260 | + | 0.28662 | |
DDB_G0289729 | DDB_G0289729 | DDB0232432 | CDS | 3173059 | 534 | - | 0.237828 | |
DDB_G0289731 | DDB_G0289731 | DDB0232432 | CDS | 3175755 | 1404 | - | 0.294872 | |
DDB_G0289733 | DDB_G0289733 | similar to fungal and plant proteins contains 4 putative transmembrane domains | DDB0232432 | CDS | 3177932 | 561 | - | 0.28877 |
DDB_G0289735 | DDB_G0289735 | DDB0232432 | CDS | 3179530 | 1626 | + | 0.245387 | |
DDB_G0289737 | DDB_G0289737 | DDB0232432 | CDS | 3181881 | 4692 | + | 0.249787 | |
DDB_G0289739 | DDB_G0289739 | DDB0232432 | CDS | 3188713 | 414 | - | 0.272947 | |
DDB_G0289741 | DDB_G0289741 | DDB0232432 | CDS | 3189387 | 3300 | - | 0.213333 | |
DDB_G0289743 | DDB_G0289743 | DDB0232432 | CDS | 3193439 | 1002 | + | 0.215569 | |
DDB_G0289745_ps | DDB_G0289745 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 3194481 | 285 | - | 0.221053 |
DDB_G0289749 | DDB_G0289749 | member of the peptidase S28 family of serine proteases a group containing lysosomal Pro-X carboxypeptidase dipeptidyl-peptidase II and thymus-specific serine peptidase | DDB0232432 | CDS | 3208495 | 1542 | - | 0.346952 |
DDB_G0289751 | DDB_G0289751 | DDB0232432 | CDS | 3211024 | 1194 | + | 0.259631 | |
DDB_G0289753 | DDB_G0289753 | DDB0232432 | CDS | 3213101 | 2283 | + | 0.242225 | |
DDB_G0289755 | DDB_G0289755 | DDB0232432 | CDS | 3219108 | 3510 | + | 0.27037 | |
DDB_G0289757 | DDB_G0289757 | DDB0232432 | CDS | 3223411 | 1173 | + | 0.238704 | |
DDB_G0289759 | DDB_G0289759 | DDB0232432 | CDS | 3225323 | 1719 | + | 0.270506 | |
DDB_G0289761 | DDB_G0289761 | DDB0232432 | CDS | 3227434 | 5901 | - | 0.239451 | |
DDB_G0289765 | DDB_G0289765 | DDB0232432 | CDS | 3243093 | 297 | - | 0.262626 | |
DDB_G0289767 | DDB_G0289767 | DDB0232432 | CDS | 3244131 | 192 | - | 0.291667 | |
DDB_G0289769 | DDB_G0289769 | DDB0232432 | CDS | 3246114 | 1446 | + | 0.239281 | |
DDB_G0289771 | DDB_G0289771 | belongs to the major facilitator superfamily similar to human SLC43A3 (solute carrier family 43 member 3) contains 12 putative transmembrane domains | DDB0232432 | CDS | 3247669 | 1539 | - | 0.250162 |
DDB_G0289773 | DDB_G0289773 | DDB0232432 | CDS | 3250091 | 1101 | - | 0.260672 | |
DDB_G0289777_ps | DDB_G0289777 | putative pseudogene fragment similar to FNIP repeat containing proteins | DDB0232432 | CDS | 3258199 | 996 | - | 0.210843 |
DDB_G0289781 | DDB_G0289781 | DDB0232432 | CDS | 3268015 | 1821 | - | 0.213619 | |
DDB_G0289783_ps | DDB_G0289783 | putative pseudogene similar to a family of small D. discoideum genes including | DDB0232432 | CDS | 3079913 | 180 | - | 0.277778 |
DDB_G0289787 | DDB_G0289787 | DDB0232432 | CDS | 3105859 | 1590 | - | 0.284906 | |
DDB_G0289789 | DDB_G0289789 | DDB0232432 | CDS | 3131180 | 3711 | + | 0.162759 | |
DDB_G0289793_RTE | DDB_G0289793 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232432 | CDS | 3060165 | 1020 | - | 0.385294 |
DDB_G0289795 | DDB_G0289795 | DDB0232432 | CDS | 3100083 | 1872 | + | 0.223291 | |
DDB_G0289797_ps | DDB_G0289797 | putative pseudogene small fragment of D. discoideum gene | DDB0232432 | CDS | 3215546 | 522 | + | 0.258621 |
DDB_G0289799_ps | DDB_G0289799 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3216855 | 756 | + | 0.251323 |
DDB_G0289801_ps | DDB_G0289801 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3234217 | 1794 | + | 0.238016 |
DDB_G0289805_RTE | DDB_G0289805 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 3259385 | 4881 | + | 0.314075 |
DDB_G0289807 | DDB_G0289807 | DDB0232432 | CDS | 3270257 | 2403 | - | 0.265501 | |
DDB_G0289809_ps | DDB_G0289809 | putative pseudogene similar to | DDB0232432 | CDS | 3273269 | 303 | - | 0.290429 |
DDB_G0289817_ps | DDB_G0289817 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3280631 | 1827 | - | 0.231527 |
DDB_G0289819 | DDB_G0289819 | DDB0232432 | CDS | 3283950 | 3210 | - | 0.250156 | |
DDB_G0289825 | DDB_G0289825 | DDB0232432 | CDS | 3292116 | 450 | + | 0.217778 | |
DDB_G0289829 | DDB_G0289829 | DDB0232432 | CDS | 3294597 | 13773 | + | 0.253467 | |
DDB_G0289831 | DDB_G0289831 | contains a HDc domain (metal-dependent phosphohydrolases with conserved | DDB0232432 | CDS | 3320745 | 657 | + | 0.210046 |
DDB_G0289833 | DDB_G0289833 | DDB0232432 | CDS | 3325551 | 561 | + | 0.279857 | |
DDB_G0289835 | DDB_G0289835 | DDB0232432 | CDS | 3326670 | 708 | + | 0.276836 | |
DDB_G0289837 | DDB_G0289837 | DDB0232432 | CDS | 3338795 | 1320 | + | 0.234091 | |
DDB_G0289839 | DDB_G0289839 | DDB0232432 | CDS | 3349145 | 2481 | - | 0.232568 | |
DDB_G0289841_ps | DDB_G0289841 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3351960 | 360 | - | 0.294444 |
DDB_G0289843_ps | DDB_G0289843 | putative pseudogene very similar to | DDB0232432 | CDS | 3352483 | 303 | + | 0.316832 |
DDB_G0289845_ps | DDB_G0289845 | putative pseudogene similar to Dictyostelium genes | DDB0232432 | CDS | 3355012 | 3663 | - | 0.205296 |
DDB_G0289849 | DDB_G0289849 | DDB0232432 | CDS | 3275554 | 1533 | - | 0.21983 | |
DDB_G0289851_ps | DDB_G0289851 | putative pseudogene similar to a larger gene family including | DDB0232432 | CDS | 3287942 | 780 | - | 0.219231 |
DDB_G0289853 | DDB_G0289853 | DDB0232432 | CDS | 3274098 | 861 | - | 0.259001 | |
DDB_G0289855_ps | DDB_G0289855 | putative pseudogene fragment similar to FNIP repeat containing proteins | DDB0232432 | CDS | 3277922 | 621 | - | 0.249597 |
DDB_G0289857 | DDB_G0289857 | DDB0232432 | CDS | 3279027 | 861 | - | 0.259001 | |
DDB_G0289861 | DDB_G0289861 | DDB0232432 | CDS | 3321520 | 2409 | - | 0.268991 | |
DDB_G0289863 | DDB_G0289863 | DDB0232432 | CDS | 3327630 | 4173 | - | 0.288521 | |
DDB_G0289865 | DDB_G0289865 | DDB0232432 | CDS | 3333090 | 2580 | - | 0.156589 | |
DDB_G0289869 | DDB_G0289869 | DDB0232432 | CDS | 3345167 | 3852 | + | 0.22352 | |
DDB_G0289871 | DDB_G0289871 | DDB0232432 | CDS | 3353422 | 999 | - | 0.298298 | |
DDB_G0289887 | DDB_G0289887 | DDB0232432 | CDS | 3364902 | 927 | - | 0.20712 | |
DDB_G0289889 | DDB_G0289889 | DDB0232432 | CDS | 3366559 | 663 | - | 0.236802 | |
DDB_G0289891 | DDB_G0289891 | DDB0232432 | CDS | 3367899 | 873 | - | 0.254296 | |
DDB_G0289895 | DDB_G0289895 | DDB0232432 | CDS | 3370229 | 3180 | - | 0.199686 | |
DDB_G0289897 | DDB_G0289897 | DDB0232432 | CDS | 3373542 | 2934 | - | 0.190866 | |
DDB_G0289899 | DDB_G0289899 | DDB0232432 | CDS | 3376818 | 432 | - | 0.275463 | |
DDB_G0289901 | DDB_G0289901 | highly repetitive protein serine and glycine rich contains a predicted signal peptide | DDB0232432 | CDS | 3379595 | 3432 | + | 0.456002 |
DDB_G0289903 | DDB_G0289903 | DDB0232432 | CDS | 3385552 | 3060 | - | 0.186601 | |
DDB_G0289905 | DDB_G0289905 | DDB0232432 | CDS | 3389153 | 870 | + | 0.265517 | |
DDB_G0289907 | DDB_G0289907 | DDB0232432 | CDS | 3390166 | 4527 | - | 0.279435 | |
DDB_G0289909 | DDB_G0289909 | DDB0232432 | CDS | 3396878 | 3282 | - | 0.240402 | |
DDB_G0289911_ps | DDB_G0289911 | putative pseudogene fragment similar to | DDB0232432 | CDS | 3408321 | 330 | - | 0.30303 |
DDB_G0289913 | DDB_G0289913 | DDB0232432 | CDS | 3412058 | 894 | + | 0.229306 | |
DDB_G0289915 | DDB_G0289915 | DDB0232432 | CDS | 3412976 | 951 | - | 0.218717 | |
DDB_G0289917 | DDB_G0289917 | similar to neighboring gene | DDB0232432 | CDS | 3415174 | 2907 | + | 0.318885 |
DDB_G0289921 | DDB_G0289921 | DDB0232432 | CDS | 3426110 | 3708 | + | 0.263484 | |
DDB_G0289933 | DDB_G0289933 | DDB0232432 | CDS | 3455388 | 1629 | - | 0.274401 | |
DDB_G0289937 | DDB_G0289937 | DDB0232432 | CDS | 3460667 | 2694 | + | 0.224944 | |
DDB_G0289939 | DDB_G0289939 | DDB0232432 | CDS | 3468286 | 2919 | + | 0.224049 | |
DDB_G0289941 | DDB_G0289941 | DDB0232432 | CDS | 3478416 | 1446 | + | 0.296681 | |
DDB_G0289943 | DDB_G0289943 | DDB0232432 | CDS | 3479964 | 4653 | - | 0.27939 | |
DDB_G0289945 | DDB_G0289945 | DDB0232432 | CDS | 3488380 | 741 | + | 0.219973 | |
DDB_G0289947 | DDB_G0289947 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 3490340 | 4692 | + | 0.27728 |
DDB_G0289949 | DDB_G0289949 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 3495799 | 4452 | + | 0.287511 |
DDB_G0289951 | DDB_G0289951 | DDB0232432 | CDS | 3502780 | 297 | - | 0.212121 | |
DDB_G0289953 | DDB_G0289953 | DDB0232432 | CDS | 3505573 | 2313 | - | 0.26243 | |
DDB_G0289955 | DDB_G0289955 | DDB0232432 | CDS | 3508916 | 594 | - | 0.311448 | |
DDB_G0289957 | DDB_G0289957 | DDB0232432 | CDS | 3510343 | 225 | - | 0.244444 | |
DDB_G0289961 | DDB_G0289961 | ortholog of mammalian lunapark (LNP) that may be involved in limb and central nervous system development contains two transmembrane domains | DDB0232432 | CDS | 3444195 | 1359 | + | 0.256806 |
DDB_G0289963 | DDB_G0289963 | DDB0232432 | CDS | 3511088 | 1584 | + | 0.243687 | |
DDB_G0289965 | DDB_G0289965 | DDB0232432 | CDS | 3377583 | 876 | - | 0.200913 | |
DDB_G0289969 | DDB_G0289969 | DDB0232432 | CDS | 3396462 | 216 | + | 0.333333 | |
DDB_G0289973 | DDB_G0289973 | DDB0232432 | CDS | 3409130 | 1653 | - | 0.199637 | |
DDB_G0289975 | DDB_G0289975 | similar to neighboring gene | DDB0232432 | CDS | 3419568 | 3099 | + | 0.247822 |
DDB_G0289977_ps | DDB_G0289977 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 3430004 | 1452 | - | 0.174242 |
DDB_G0289979 | DDB_G0289979 | has similarity to mammalian tensin a cytoplasmic phosphoprotein | DDB0232432 | CDS | 3435700 | 2715 | - | 0.299079 |
DDB_G0289985 | DDB_G0289985 | similar to human protein KIAA0195 a transmembrane protein contains 8 putative transmembrane domains | DDB0232432 | CDS | 3471284 | 5832 | - | 0.290123 |
DDB_G0289987 | DDB_G0289987 | DDB0232432 | CDS | 3515224 | 3111 | + | 0.309547 | |
DDB_G0289989 | DDB_G0289989 | DDB0232432 | CDS | 3520850 | 168 | + | 0.166667 | |
DDB_G0289991 | DDB_G0289991 | DDB0232432 | CDS | 3521273 | 1203 | - | 0.284289 | |
DDB_G0289993 | DDB_G0289993 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub | DDB0232432 | CDS | 3523290 | 2103 | - | 0.269615 |
DDB_G0289995 | DDB_G0289995 | DDB0232432 | CDS | 3525827 | 1377 | - | 0.276688 | |
DDB_G0289997 | DDB_G0289997 | DDB0232432 | CDS | 3527673 | 456 | - | 0.203947 | |
DDB_G0289999 | DDB_G0289999 | DDB0232432 | CDS | 3529568 | 879 | - | 0.25711 | |
DDB_G0290001 | DDB_G0290001 | DDB0232432 | CDS | 3530853 | 855 | - | 0.260819 | |
DDB_G0290003 | DDB_G0290003 | DDB0232432 | CDS | 3519269 | 174 | + | 0.178161 | |
DDB_G0290005 | DDB_G0290005 | similar to myotubularin a dual-specific lipid phosphatase that dephosphorylates phosphatidylinositol 3-phosphate and phosphatidylinositol (35)-bi-phosphate | DDB0232432 | CDS | 3532204 | 3975 | - | 0.27195 |
DDB_G0290007 | DDB_G0290007 | DDB0232432 | CDS | 3538386 | 591 | - | 0.233503 | |
DDB_G0290013 | DDB_G0290013 | DDB0232432 | CDS | 3541529 | 168 | + | 0.196429 | |
DDB_G0290017 | DDB_G0290017 | DDB0232432 | CDS | 3543307 | 531 | - | 0.271186 | |
DDB_G0290019 | DDB_G0290019 | DDB0232432 | CDS | 3544279 | 3753 | + | 0.229683 | |
DDB_G0290021 | DDB_G0290021 | DDB0232432 | CDS | 3549059 | 2955 | + | 0.171912 | |
DDB_G0290025 | DDB_G0290025 | contains one UBA-like domain and one DCUN1 domain homolog of human DCUN1D1 and S. cerevisiae DCN1 (defective in cullin neddylation protein 1) defects in DCUN1D1 may be a cause of squamous cell carcinomas | DDB0232432 | CDS | 3556440 | 750 | + | 0.261333 |
DDB_G0290027 | DDB_G0290027 | DDB0232432 | CDS | 3557818 | 264 | + | 0.265152 | |
DDB_G0290029 | DDB_G0290029 | DDB0232432 | CDS | 3560404 | 1209 | - | 0.292804 | |
DDB_G0290031 | DDB_G0290031 | belongs to the ribosomal protein S8e family ortholog of human TINP1 (TGF-beta-inducible nuclear protein 1) and S. cerevisiae NSA2 NSA2 (NOP seven associated 2) is involved in the biogenesis of the 60S ribosomal subunit | DDB0232432 | CDS | 3562515 | 783 | + | 0.342273 |
DDB_G0290035 | DDB_G0290035 | DDB0232432 | CDS | 3574815 | 3498 | + | 0.242996 | |
DDB_G0290037 | DDB_G0290037 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 3583640 | 4218 | - | 0.252015 |
DDB_G0290039 | DDB_G0290039 | DDB0232432 | CDS | 3601688 | 3279 | - | 0.191217 | |
DDB_G0290041 | DDB_G0290041 | DDB0232432 | CDS | 3605172 | 234 | - | 0.311966 | |
DDB_G0290043 | DDB_G0290043 | DDB0232432 | CDS | 3605816 | 1656 | - | 0.209541 | |
DDB_G0290045_ps | DDB_G0290045 | putative pseudogene fragment similar to UNC93-like protein MFSD11 family members | DDB0232432 | CDS | 3608057 | 288 | + | 0.322917 |
DDB_G0290047_ps | DDB_G0290047 | putative pseudogene fragment similar to | DDB0232432 | CDS | 3609197 | 285 | - | 0.140351 |
DDB_G0290051 | DDB_G0290051 | putative pseudogene similar to a large gene family encoding FNIP repeat-containing proteins including | DDB0232432 | CDS | 3563896 | 1875 | - | 0.245867 |
DDB_G0290057 | DDB_G0290057 | DDB0232432 | CDS | 3570445 | 1620 | - | 0.223457 | |
DDB_G0290059_ps | DDB_G0290059 | putative pseudogene similar to Dictyostelium genes | DDB0232432 | CDS | 3578349 | 4047 | - | 0.255004 |
DDB_G0290061 | DDB_G0290061 | DDB0232432 | CDS | 3588988 | 4158 | - | 0.263107 | |
DDB_G0290063 | DDB_G0290063 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain enriched in gametes | DDB0232432 | CDS | 3595858 | 4200 | - | 0.267381 |
DDB_G0290065 | DDB_G0290065 | DDB0232432 | CDS | 3610142 | 226 | - | 0.252212 | |
DDB_G0290073 | DDB_G0290073 | DDB0232432 | CDS | 3614348 | 2481 | - | 0.261588 | |
DDB_G0290075 | DDB_G0290075 | protein phosphatase 2C is a serinethreonine specific protein phosphatase with broad substrate specificity and dependent on divalent cations (mainly manganese and magnesium) for its activity | DDB0232432 | CDS | 3618710 | 1620 | - | 0.297531 |
DDB_G0290083 | DDB_G0290083 | DDB0232432 | CDS | 3631373 | 612 | - | 0.269608 | |
DDB_G0290085 | DDB_G0290085 | DDB0232432 | CDS | 3636614 | 4683 | + | 0.26009 | |
DDB_G0290089 | DDB_G0290089 | involved in fatty acid biosynthesis catalyzes the conversion of malonyl-CoA to acetyl-CoA | DDB0232432 | CDS | 3648784 | 1350 | - | 0.221481 |
DDB_G0290093 | DDB_G0290093 | DDB0232432 | CDS | 3653634 | 651 | - | 0.25192 | |
DDB_G0290095 | DDB_G0290095 | DDB0232432 | CDS | 3611605 | 2532 | + | 0.189573 | |
DDB_G0290097 | DDB_G0290097 | DDB0232432 | CDS | 3634285 | 1608 | + | 0.174129 | |
DDB_G0290101 | DDB_G0290101 | putative pseudogene similar to a large gene family encoding FNIP repeat-containing proteins including | DDB0232432 | CDS | 3664675 | 1980 | + | 0.239899 |
DDB_G0290105 | DDB_G0290105 | DDB0232432 | CDS | 3654997 | 674 | - | 0.327893 | |
DDB_G0290107 | DDB_G0290107 | contains 9 putative transmembrane domains conserved in Polysphondylium pallidum and D. purpureum | DDB0232432 | CDS | 3660841 | 1782 | - | 0.255331 |
DDB_G0290109 | DDB_G0290109 | DDB0232432 | CDS | 3667946 | 2235 | + | 0.22774 | |
DDB_G0290113 | DDB_G0290113 | DDB0232432 | CDS | 3675019 | 2826 | + | 0.225407 | |
DDB_G0290119_ps | DDB_G0290119 | putative pseudogene FNIP repeat family protein | DDB0232432 | CDS | 3679131 | 1260 | + | 0.216667 |
DDB_G0290125 | DDB_G0290125 | DDB0232432 | CDS | 3685883 | 2517 | - | 0.196663 | |
DDB_G0290127 | DDB_G0290127 | DDB0232432 | CDS | 3689897 | 1950 | + | 0.212308 | |
DDB_G0290129_RTE | DDB_G0290129 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232432 | CDS | 3694123 | 518 | + | 0.401544 |
DDB_G0290133 | DDB_G0290133 | DDB0232432 | CDS | 3697750 | 267 | + | 0.254682 | |
DDB_G0290135 | DDB_G0290135 | DDB0232432 | CDS | 3699370 | 129 | - | 0.186047 | |
DDB_G0290137 | DDB_G0290137 | DDB0232432 | CDS | 3700826 | 785 | + | 0.17707 | |
DDB_G0290139 | DDB_G0290139 | DDB0232432 | CDS | 3695903 | 1431 | + | 0.331936 | |
DDB_G0290143 | DDB_G0290143 | DDB0232432 | CDS | 3704919 | 651 | - | 0.302611 | |
DDB_G0290145 | DDB_G0290145 | DDB0232432 | CDS | 3707194 | 3378 | - | 0.204263 | |
DDB_G0290147 | DDB_G0290147 | DDB0232432 | CDS | 3711190 | 345 | + | 0.292754 | |
DDB_G0290151 | DDB_G0290151 | DDB0232432 | CDS | 3703699 | 840 | + | 0.22619 | |
DDB_G0290153 | DDB_G0290153 | DDB0232432 | CDS | 3712218 | 1545 | - | 0.318447 | |
DDB_G0290155 | DDB_G0290155 | DDB0232432 | CDS | 3702246 | 877 | + | 0.163056 | |
DDB_G0290167 | DDB_G0290167 | DDB0232432 | CDS | 3729972 | 159 | - | 0.245283 | |
DDB_G0290175 | DDB_G0290175 | contains a predicted signal peptide and a C-teminal transmembrane domain small gene family in D. discoideum and D. purpureum | DDB0232432 | CDS | 3738710 | 1260 | - | 0.251587 |
DDB_G0290177 | DDB_G0290177 | contains an N-terminal signal sequence and a C-terminal transmembrane domain underexpressed in | DDB0232432 | CDS | 3740464 | 1170 | - | 0.346154 |
DDB_G0290181 | DDB_G0290181 | similar to S.cerevisiae RRP5 and animal PDCD11 (Programmed cell death protein 11) | DDB0232432 | CDS | 3746723 | 2730 | - | 0.25641 |
DDB_G0290183 | DDB_G0290183 | DDB0232432 | CDS | 3749810 | 1344 | + | 0.238095 | |
DDB_G0290189 | DDB_G0290189 | DDB0232432 | CDS | 3766463 | 930 | + | 0.263441 | |
DDB_G0290191 | DDB_G0290191 | DDB0232432 | CDS | 3774102 | 471 | + | 0.248408 | |
DDB_G0290193 | DDB_G0290193 | DDB0232432 | CDS | 3774767 | 3828 | - | 0.269854 | |
DDB_G0290195 | DDB_G0290195 | DDB0232432 | CDS | 3779790 | 333 | - | 0.237237 | |
DDB_G0290197 | DDB_G0290197 | similar to plant and fungi NADH dehydrogenases such as S. cerevisiae NDE1 and NDE2 the external mitochondrial NADH dehydrogenases that catalyze the oxidation of cytosolic NADH | DDB0232432 | CDS | 3781653 | 1965 | + | 0.293639 |
DDB_G0290199 | DDB_G0290199 | DDB0232432 | CDS | 3783788 | 651 | - | 0.241167 | |
DDB_G0290201 | DDB_G0290201 | DDB0232432 | CDS | 3784827 | 1467 | + | 0.236537 | |
DDB_G0290203 | DDB_G0290203 | DDB0232432 | CDS | 3792983 | 801 | + | 0.252185 | |
DDB_G0290205 | DDB_G0290205 | DDB0232432 | CDS | 3794310 | 738 | + | 0.258808 | |
DDB_G0290211 | DDB_G0290211 | DDB0232432 | CDS | 3798435 | 3669 | + | 0.271191 | |
DDB_G0290215 | DDB_G0290215 | DDB0232432 | CDS | 3805894 | 3354 | + | 0.233751 | |
DDB_G0290219 | DDB_G0290219 | DDB0232432 | CDS | 3812159 | 1095 | - | 0.251142 | |
DDB_G0290223 | DDB_G0290223 | DDB0232432 | CDS | 3816109 | 555 | + | 0.32973 | |
DDB_G0290225 | DDB_G0290225 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity enriched in gametes | DDB0232432 | CDS | 3824091 | 1212 | - | 0.287954 |
DDB_G0290229 | DDB_G0290229 | catalyzes the reaction CTP choline phosphate diphosphate CDPcholine | DDB0232432 | CDS | 3830807 | 1251 | + | 0.295763 |
DDB_G0290231 | DDB_G0290231 | DDB0232432 | CDS | 3832338 | 1356 | - | 0.233038 | |
DDB_G0290235 | DDB_G0290235 | DDB0232432 | CDS | 3838039 | 123 | - | 0.284553 | |
DDB_G0290239 | DDB_G0290239 | DDB0232432 | CDS | 3786795 | 930 | + | 0.203226 | |
DDB_G0290241_RTE | DDB_G0290241 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 3764090 | 1506 | + | 0.294821 |
DDB_G0290247 | DDB_G0290247 | DDB0232432 | CDS | 3789362 | 2946 | + | 0.191785 | |
DDB_G0290249 | DDB_G0290249 | DDB0232432 | CDS | 3821076 | 2871 | - | 0.223267 | |
DDB_G0290251_ps | DDB_G0290251 | putative pseudogene related to the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232432 | CDS | 3826055 | 1125 | - | 0.286222 |
DDB_G0290255 | DDB_G0290255 | DDB0232432 | CDS | 3846563 | 391 | + | 0.140665 | |
DDB_G0290273 | DDB_G0290273 | DDB0232432 | CDS | 3847142 | 1959 | + | 0.135784 | |
DDB_G0290275 | DDB_G0290275 | DDB0232432 | CDS | 3849199 | 951 | - | 0.209253 | |
DDB_G0290283 | DDB_G0290283 | DDB0232432 | CDS | 3859451 | 3438 | - | 0.232984 | |
DDB_G0290285 | DDB_G0290285 | DDB0232432 | CDS | 3865328 | 2463 | + | 0.279334 | |
DDB_G0290289 | DDB_G0290289 | DDB0232432 | CDS | 3884030 | 5952 | + | 0.243112 | |
DDB_G0290291 | DDB_G0290291 | similar to MAPEG (membrane associated proteins in eicosanoid and glutathione metabolism) family which includes microsomal glutathione S-transferase II and 5-lipoxygenase activating protein expressed in prespore cells | DDB0232432 | CDS | 3893526 | 450 | - | 0.337778 |
DDB_G0290295 | DDB_G0290295 | DDB0232432 | CDS | 3920410 | 636 | - | 0.286164 | |
DDB_G0290299 | DDB_G0290299 | DDB0232432 | CDS | 3922756 | 363 | - | 0.289256 | |
DDB_G0290301 | DDB_G0290301 | DDB0232432 | CDS | 3923457 | 3717 | - | 0.29244 | |
DDB_G0290305 | DDB_G0290305 | DDB0232432 | CDS | 3936242 | 1716 | + | 0.287296 | |
DDB_G0290307 | DDB_G0290307 | contains three RRM domains homolog of ELAVL1 (embryonic lethal abnormal vision-like 1) | DDB0232432 | CDS | 3938585 | 1380 | + | 0.300725 |
DDB_G0290309 | DDB_G0290309 | DDB0232432 | CDS | 3940357 | 486 | - | 0.228395 | |
DDB_G0290311 | DDB_G0290311 | DDB0232432 | CDS | 3942085 | 1086 | - | 0.300184 | |
DDB_G0290313 | DDB_G0290313 | DDB0232432 | CDS | 3944329 | 1656 | + | 0.221014 | |
DDB_G0290319 | DDB_G0290319 | DDB0232432 | CDS | 3952440 | 456 | + | 0.27193 | |
DDB_G0290321 | DDB_G0290321 | DDB0232432 | CDS | 3953111 | 2394 | - | 0.190894 | |
DDB_G0290323 | DDB_G0290323 | DDB0232432 | CDS | 3955755 | 2274 | - | 0.174142 | |
DDB_G0290329 | DDB_G0290329 | DDB0232432 | CDS | 3968559 | 906 | - | 0.335541 | |
DDB_G0290333 | DDB_G0290333 | belongs to the peptidase S53 family similar to P. polycephalum physarolisin contains a predicted signal peptide | DDB0232432 | CDS | 3973178 | 1797 | + | 0.413467 |
DDB_G0290335 | DDB_G0290335 | DDB0232432 | CDS | 3975307 | 1080 | + | 0.203704 | |
DDB_G0290337 | DDB_G0290337 | DDB0232432 | CDS | 3983670 | 2439 | + | 0.275933 | |
DDB_G0290341 | DDB_G0290341 | similar to S. cerevisiae SFT2 contains 4 putative transmembrane domains similar to D. purpureum protein | DDB0232432 | CDS | 3989030 | 621 | - | 0.259259 |
DDB_G0290347 | DDB_G0290347 | DDB0232432 | CDS | 4001426 | 1203 | - | 0.23857 | |
DDB_G0290349 | DDB_G0290349 | DDB0232432 | CDS | 3868716 | 2133 | + | 0.263479 | |
DDB_G0290351 | DDB_G0290351 | DDB0232432 | CDS | 3890601 | 2304 | + | 0.249132 | |
DDB_G0290359 | DDB_G0290359 | the N-terminal half of the protein is very similar to human EFR3A (Protein EFR3 homolog A) similar to D. purpureum protein | DDB0232432 | CDS | 3850328 | 2790 | - | 0.260215 |
DDB_G0290361_ps | DDB_G0290361 | putative pseudogene similar to a D. discoideum gene family including the just upstream | DDB0232432 | CDS | 3871677 | 1176 | + | 0.27551 |
DDB_G0290369 | DDB_G0290369 | DDB0232432 | CDS | 3976953 | 5661 | + | 0.242183 | |
DDB_G0290371 | DDB_G0290371 | DDB0232432 | CDS | 3991148 | 930 | + | 0.272043 | |
DDB_G0290373 | DDB_G0290373 | DDB0232432 | CDS | 3993062 | 4971 | - | 0.206196 | |
DDB_G0290375_RTE | DDB_G0290375 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232432 | CDS | 4004269 | 1032 | + | 0.325581 |
DDB_G0290379 | DDB_G0290379 | DDB0232432 | CDS | 4011706 | 1023 | - | 0.252199 | |
DDB_G0290381 | DDB_G0290381 | DDB0232432 | CDS | 4013215 | 2118 | + | 0.259207 | |
DDB_G0290383 | DDB_G0290383 | DDB0232432 | CDS | 4017007 | 330 | + | 0.221212 | |
DDB_G0290387 | DDB_G0290387 | similar to D. purpureum proteins small gene family in both species | DDB0232432 | CDS | 4019200 | 927 | + | 0.307443 |
DDB_G0290391 | DDB_G0290391 | DDB0232432 | CDS | 4027524 | 927 | - | 0.289105 | |
DDB_G0290393 | DDB_G0290393 | similar to yeast ERG28 an endoplasmic reticulum protein involved in ergosterol biosynthesis contains 3 putative transmembrane domains | DDB0232432 | CDS | 4028814 | 372 | - | 0.290323 |
DDB_G0290395 | DDB_G0290395 | DDB0232432 | CDS | 4029574 | 1143 | - | 0.343832 | |
DDB_G0290399 | DDB_G0290399 | DDB0232432 | CDS | 4034032 | 3270 | - | 0.195107 | |
DDB_G0290401 | DDB_G0290401 | phosphorylates (R)-pantothenate to (R)-4'-phosphopantothenate | DDB0232432 | CDS | 4038671 | 2058 | + | 0.270651 |
DDB_G0290403 | DDB_G0290403 | DDB0232432 | CDS | 4041398 | 495 | + | 0.282828 | |
DDB_G0290409 | DDB_G0290409 | DDB0232432 | CDS | 4048204 | 1410 | + | 0.284397 | |
DDB_G0290411 | DDB_G0290411 | DDB0232432 | CDS | 4050217 | 726 | - | 0.30303 | |
DDB_G0290415 | DDB_G0290415 | DDB0232432 | CDS | 4053731 | 3303 | + | 0.277929 | |
DDB_G0290419 | DDB_G0290419 | DDB0232432 | CDS | 4062441 | 315 | - | 0.273016 | |
DDB_G0290421 | DDB_G0290421 | DDB0232432 | CDS | 4063431 | 2082 | - | 0.246878 | |
DDB_G0290423 | DDB_G0290423 | DDB0232432 | CDS | 4067949 | 1743 | + | 0.242111 | |
DDB_G0290425 | DDB_G0290425 | DDB0232432 | CDS | 4070123 | 1191 | + | 0.279597 | |
DDB_G0290427 | DDB_G0290427 | DDB0232432 | CDS | 4113138 | 963 | - | 0.311526 | |
DDB_G0290429 | DDB_G0290429 | DDB0232432 | CDS | 4115465 | 396 | + | 0.275253 | |
DDB_G0290431 | DDB_G0290431 | DDB0232432 | CDS | 4116429 | 1458 | + | 0.222222 | |
DDB_G0290433 | DDB_G0290433 | DDB0232432 | CDS | 4118281 | 4869 | - | 0.326556 | |
DDB_G0290435 | DDB_G0290435 | DDB0232432 | CDS | 4124662 | 2559 | + | 0.19109 | |
DDB_G0290437 | DDB_G0290437 | DDB0232432 | CDS | 4128169 | 327 | + | 0.287462 | |
DDB_G0290441 | DDB_G0290441 | DDB0232432 | CDS | 4134020 | 1353 | + | 0.195861 | |
DDB_G0290443 | DDB_G0290443 | DDB0232432 | CDS | 4111634 | 975 | - | 0.215385 | |
DDB_G0290447_RTE | DDB_G0290447 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 4006163 | 406 | + | 0.283251 |
DDB_G0290449 | DDB_G0290449 | DDB0232432 | CDS | 4015567 | 924 | - | 0.238095 | |
DDB_G0290457 | DDB_G0290457 | DDB0232432 | CDS | 4077605 | 1323 | - | 0.244142 | |
DDB_G0290459 | DDB_G0290459 | DDB0232432 | CDS | 4079741 | 1215 | + | 0.185185 | |
DDB_G0290461 | DDB_G0290461 | DDB0232432 | CDS | 4081599 | 636 | + | 0.232704 | |
DDB_G0290463 | DDB_G0290463 | DDB0232432 | CDS | 4082312 | 318 | - | 0.163522 | |
DDB_G0290465 | DDB_G0290465 | conserved hypothetical 695 aa Dictyostelium protein centrosomal component | DDB0232432 | CDS | 4083295 | 2088 | + | 0.28592 |
DDB_G0290471 | DDB_G0290471 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats does not contain the consensus sequences required for kinase function | DDB0232432 | CDS | 4105828 | 1059 | - | 0.234183 |
DDB_G0290473 | DDB_G0290473 | DDB0232432 | CDS | 4107607 | 1965 | - | 0.205089 | |
DDB_G0290475 | DDB_G0290475 | DDB0232432 | CDS | 4110262 | 339 | + | 0.271386 | |
DDB_G0290487 | DDB_G0290487 | DDB0232432 | CDS | 4140984 | 2082 | + | 0.161383 | |
DDB_G0290489 | DDB_G0290489 | DDB0232432 | CDS | 4143852 | 1467 | + | 0.179959 | |
DDB_G0290491 | DDB_G0290491 | DDB0232432 | CDS | 4146073 | 381 | - | 0.272966 | |
DDB_G0290495 | DDB_G0290495 | DDB0232432 | CDS | 4151099 | 702 | - | 0.230769 | |
DDB_G0290497 | DDB_G0290497 | DDB0232432 | CDS | 4152368 | 1875 | - | 0.231467 | |
DDB_G0290503 | DDB_G0290503 | DDB0232432 | CDS | 4159418 | 4479 | - | 0.20384 | |
DDB_G0290505 | DDB_G0290505 | DDB0232432 | CDS | 4164699 | 1908 | - | 0.226415 | |
DDB_G0290507 | DDB_G0290507 | DDB0232432 | CDS | 4167405 | 2142 | - | 0.203081 | |
DDB_G0290513 | DDB_G0290513 | DDB0232432 | CDS | 4175909 | 3162 | + | 0.183744 | |
DDB_G0290519 | DDB_G0290519 | DDB0232432 | CDS | 4199032 | 144 | + | 0.263889 | |
DDB_G0290521 | DDB_G0290521 | DDB0232432 | CDS | 4200324 | 1293 | - | 0.354988 | |
DDB_G0290523 | DDB_G0290523 | DDB0232432 | CDS | 4204192 | 1035 | - | 0.261836 | |
DDB_G0290525 | DDB_G0290525 | DDB0232432 | CDS | 4212337 | 1275 | - | 0.20549 | |
DDB_G0290527 | DDB_G0290527 | DDB0232432 | CDS | 4214740 | 2307 | - | 0.21023 | |
DDB_G0290531 | DDB_G0290531 | DDB0232432 | CDS | 4228089 | 297 | + | 0.309764 | |
DDB_G0290533 | DDB_G0290533 | DDB0232432 | CDS | 4229551 | 885 | + | 0.273446 | |
DDB_G0290535 | DDB_G0290535 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232432 | CDS | 4232732 | 1488 | - | 0.346102 |
DDB_G0290537 | DDB_G0290537 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232432 | CDS | 4235159 | 1485 | + | 0.333333 |
DDB_G0290539 | DDB_G0290539 | DDB0232432 | CDS | 4236850 | 714 | - | 0.219888 | |
DDB_G0290541 | DDB_G0290541 | DDB0232432 | CDS | 4238133 | 1398 | - | 0.316881 | |
DDB_G0290543 | DDB_G0290543 | DDB0232432 | CDS | 4242895 | 837 | - | 0.25687 | |
DDB_G0290545 | DDB_G0290545 | DDB0232432 | CDS | 4245577 | 2238 | + | 0.224754 | |
DDB_G0290547 | DDB_G0290547 | DDB0232432 | CDS | 4248317 | 444 | - | 0.34009 | |
DDB_G0290549 | DDB_G0290549 | DDB0232432 | CDS | 4250883 | 1152 | + | 0.197917 | |
DDB_G0290553 | DDB_G0290553 | DDB0232432 | CDS | 4265295 | 1506 | - | 0.233732 | |
DDB_G0290555 | DDB_G0290555 | DDB0232432 | CDS | 4267110 | 1527 | + | 0.264571 | |
DDB_G0290557 | DDB_G0290557 | DDB0232432 | CDS | 4269452 | 2061 | + | 0.280932 | |
DDB_G0290559 | DDB_G0290559 | DDB0232432 | CDS | 4272924 | 2013 | - | 0.232489 | |
DDB_G0290561_ps | DDB_G0290561 | putative pseudogene similar to a family of genes including | DDB0232432 | CDS | 4275359 | 1089 | - | 0.199265 |
DDB_G0290565_ps | DDB_G0290565 | DDB0232432 | CDS | 4282644 | 1452 | - | 0.220386 | |
DDB_G0290567_ps | DDB_G0290567 | putative pseudogene similar to Dictyostelium genes | DDB0232432 | CDS | 4284701 | 1191 | - | 0.248531 |
DDB_G0290569_ps | DDB_G0290569 | putative pseudogene very similar to FNIP-domain containing protein coding genes | DDB0232432 | CDS | 4288392 | 1953 | - | 0.229903 |
DDB_G0290571 | DDB_G0290571 | contains 7 FNIP domains conserved in Dictyostelium similar to D. purpureum protein | DDB0232432 | CDS | 4292030 | 2154 | - | 0.221913 |
DDB_G0290573 | DDB_G0290573 | DDB0232432 | CDS | 4295576 | 1344 | - | 0.25744 | |
DDB_G0290575 | DDB_G0290575 | DDB0232432 | CDS | 4299544 | 1419 | + | 0.34179 | |
DDB_G0290579 | DDB_G0290579 | DDB0232432 | CDS | 4310280 | 336 | + | 0.244048 | |
DDB_G0290583 | DDB_G0290583 | DDB0232432 | CDS | 4319294 | 168 | - | 0.333333 | |
DDB_G0290585 | DDB_G0290585 | DDB0232432 | CDS | 4319962 | 171 | - | 0.25731 | |
DDB_G0290587 | DDB_G0290587 | DDB0232432 | CDS | 4322112 | 2199 | - | 0.331514 | |
DDB_G0290589 | DDB_G0290589 | DDB0232432 | CDS | 4325235 | 192 | - | 0.25 | |
DDB_G0290591 | DDB_G0290591 | DDB0232432 | CDS | 4327797 | 6255 | - | 0.264748 | |
DDB_G0290593 | DDB_G0290593 | DDB0232432 | CDS | 4335292 | 435 | + | 0.344828 | |
DDB_G0290595 | DDB_G0290595 | DDB0232432 | CDS | 4337348 | 687 | + | 0.257642 | |
DDB_G0290597 | DDB_G0290597 | DDB0232432 | CDS | 4338558 | 1113 | + | 0.286613 | |
DDB_G0290599 | DDB_G0290599 | DDB0232432 | CDS | 4343609 | 192 | - | 0.260417 | |
DDB_G0290603 | DDB_G0290603 | DDB0232432 | CDS | 4352727 | 1866 | - | 0.339228 | |
DDB_G0290605 | DDB_G0290605 | DDB0232432 | CDS | 4356438 | 1155 | + | 0.27619 | |
DDB_G0290607_ps | DDB_G0290607 | putative pseudogene similar to FNIP domain-containing proteins | DDB0232432 | CDS | 4360447 | 726 | + | 0.241047 |
DDB_G0290613 | DDB_G0290613 | DDB0232432 | CDS | 4370850 | 2274 | + | 0.207124 | |
DDB_G0290619 | DDB_G0290619 | DDB0232432 | CDS | 4380155 | 2163 | - | 0.283403 | |
DDB_G0290621 | DDB_G0290621 | DDB0232432 | CDS | 4383355 | 2904 | - | 0.22865 | |
DDB_G0290623 | DDB_G0290623 | DDB0232432 | CDS | 4387215 | 2436 | + | 0.2578 | |
DDB_G0290625 | DDB_G0290625 | DDB0232432 | CDS | 4389816 | 1641 | - | 0.193784 | |
DDB_G0290627 | DDB_G0290627 | DDB0232432 | CDS | 4392045 | 1833 | - | 0.233497 | |
DDB_G0290629 | DDB_G0290629 | DDB0232432 | CDS | 4394537 | 2913 | - | 0.252317 | |
DDB_G0290631 | DDB_G0290631 | DDB0232432 | CDS | 4398765 | 558 | - | 0.297491 | |
DDB_G0290633 | DDB_G0290633 | DDB0232432 | CDS | 4403175 | 1824 | + | 0.22807 | |
DDB_G0290635 | DDB_G0290635 | DDB0232432 | CDS | 4405679 | 3762 | + | 0.249867 | |
DDB_G0290637 | DDB_G0290637 | similar to | DDB0232432 | CDS | 4321079 | 366 | - | 0.308743 |
DDB_G0290639 | DDB_G0290639 | DDB0232432 | CDS | 4378104 | 1851 | + | 0.219341 | |
DDB_G0290641 | DDB_G0290641 | DDB0232432 | CDS | 4179788 | 17406 | + | 0.258704 | |
DDB_G0290645 | DDB_G0290645 | DDB0232432 | CDS | 4303636 | 1074 | + | 0.199255 | |
DDB_G0290647 | DDB_G0290647 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | DDB0232432 | CDS | 4170905 | 2784 | + | 0.30819 |
DDB_G0290649 | DDB_G0290649 | conserved RNA binding motif protein ortholog of mammalian RBM22 and similar to yeast ECM2 a pre-mRNA splicing factor | DDB0232432 | CDS | 4202596 | 1224 | + | 0.258987 |
DDB_G0290651 | DDB_G0290651 | DDB0232432 | CDS | 4206508 | 2913 | + | 0.283556 | |
DDB_G0290653 | DDB_G0290653 | DDB0232432 | CDS | 4220163 | 5154 | - | 0.28832 | |
DDB_G0290655 | DDB_G0290655 | DDB0232432 | CDS | 4241124 | 126 | + | 0.301587 | |
DDB_G0290657 | DDB_G0290657 | DDB0232432 | CDS | 4241742 | 225 | + | 0.328889 | |
DDB_G0290663 | DDB_G0290663 | DDB0232432 | CDS | 4305581 | 2754 | + | 0.172476 | |
DDB_G0290667 | DDB_G0290667 | DDB0232432 | CDS | 4313752 | 1107 | - | 0.226739 | |
DDB_G0290673 | DDB_G0290673 | DDB0232432 | CDS | 4340691 | 1059 | + | 0.17186 | |
DDB_G0290675 | DDB_G0290675 | DDB0232432 | CDS | 4342512 | 756 | + | 0.268519 | |
DDB_G0290677 | DDB_G0290677 | DDB0232432 | CDS | 4347032 | 5175 | + | 0.182222 | |
DDB_G0290679 | DDB_G0290679 | DDB0232432 | CDS | 4358106 | 1911 | + | 0.239142 | |
DDB_G0290681_ps | DDB_G0290681 | putative pseudogene similar to FNIP domain-containing proteins | DDB0232432 | CDS | 4365656 | 1485 | + | 0.250505 |
DDB_G0290683_ps | DDB_G0290683 | putative pseudogene similar to FNIP domain-containing proteins | DDB0232432 | CDS | 4368520 | 1164 | + | 0.239691 |
DDB_G0290689 | DDB_G0290689 | homolog of E. coli rppH very similar to | DDB0232432 | CDS | 4419333 | 552 | - | 0.278986 |
DDB_G0290691 | DDB_G0290691 | DDB0232432 | CDS | 4421497 | 1581 | - | 0.25933 | |
DDB_G0290695 | DDB_G0290695 | DDB0232432 | CDS | 4432334 | 1095 | - | 0.273973 | |
DDB_G0290697 | DDB_G0290697 | DDB0232432 | CDS | 4431661 | 276 | + | 0.318841 | |
DDB_G0290711_ps | DDB_G0290711 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232432 | CDS | 4483031 | 1929 | - | 0.270607 |
DDB_G0290713_RTE | DDB_G0290713 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 4485678 | 594 | + | 0.321549 |
DDB_G0290715 | DDB_G0290715 | DDB0232432 | CDS | 4435379 | 2469 | + | 0.203321 | |
DDB_G0290721 | DDB_G0290721 | similar to bacterial aminotransferase class-III proteins which are pyridoxal-phosphate-dependent enzymes | DDB0232432 | CDS | 4489219 | 1485 | - | 0.346128 |
DDB_G0290727 | DDB_G0290727 | DDB0232432 | CDS | 4504173 | 2274 | + | 0.223395 | |
DDB_G0290739_ps | DDB_G0290739 | putative pseudogene fragment very similar to several other genes e.g. | DDB0232432 | CDS | 4533356 | 348 | + | 0.117816 |
DDB_G0290747_ps | DDB_G0290747 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232432 | CDS | 4517745 | 3564 | + | 0.250281 |
DDB_G0290749_RTE | DDB_G0290749 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 4537600 | 1174 | - | 0.291312 |
DDB_G0290753 | DDB_G0290753 | contains a C2 calciumlipid-binding region (CaLB) | DDB0232432 | CDS | 4566125 | 588 | + | 0.289116 |
DDB_G0290755 | DDB_G0290755 | contains a C2 calciumlipid-binding region (CaLB) | DDB0232432 | CDS | 4567289 | 546 | + | 0.291209 |
DDB_G0290763 | DDB_G0290763 | DDB0232432 | CDS | 4563065 | 2667 | + | 0.170229 | |
DDB_G0290767 | DDB_G0290767 | DDB0232432 | CDS | 4586394 | 837 | + | 0.210275 | |
DDB_G0290771 | DDB_G0290771 | DDB0232432 | CDS | 4578736 | 5247 | - | 0.27673 | |
DDB_G0290773 | DDB_G0290773 | DDB0232432 | CDS | 4584906 | 414 | - | 0.251208 | |
DDB_G0290777 | DDB_G0290777 | DDB0232432 | CDS | 4587507 | 3095 | - | 0.187399 | |
DDB_G0290785 | DDB_G0290785 | DDB0232432 | CDS | 4596636 | 1551 | - | 0.294004 | |
DDB_G0290797 | DDB_G0290797 | DDB0232432 | CDS | 4615081 | 393 | + | 0.236641 | |
DDB_G0290799 | DDB_G0290799 | conserved protein brbr bCommunity annotation:b DDB_G0290799 is highly conserved throughout the eukaryotes. It contains a YjeF domain which in other systems has been implicated in the regulation of RNA stability specifically of genes involved in eukaryotic cell cycle regulation [see Anantharaman and Aravind BMC Genomics 5:45 (2004)]. A budding yeast homolog YKL151C is expressed at MG1 after temperature-sensitive cdc28 synchronization (see a target | DDB0232432 | CDS | 4616309 | 921 | + | 0.299674 |
DDB_G0290801 | DDB_G0290801 | DDB0232432 | CDS | 4618085 | 756 | + | 0.260582 | |
DDB_G0290803 | DDB_G0290803 | DDB0232432 | CDS | 4619234 | 1104 | - | 0.247283 | |
DDB_G0290805 | DDB_G0290805 | DDB0232432 | CDS | 4624322 | 1275 | - | 0.238431 | |
DDB_G0290807_ps | DDB_G0290807 | putative pseudogenes fragment similar to a family of D. discoideum genes including | DDB0232432 | CDS | 4626001 | 579 | - | 0.264249 |
DDB_G0290811 | DDB_G0290811 | DDB0232432 | CDS | 4626993 | 387 | - | 0.387597 | |
DDB_G0290815 | DDB_G0290815 | DDB0232432 | CDS | 4628184 | 7365 | - | 0.281874 | |
DDB_G0290817_ps | DDB_G0290817 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 4642551 | 1287 | + | 0.212898 |
DDB_G0290819 | DDB_G0290819 | DDB0232432 | CDS | 4644346 | 126 | + | 0.253968 | |
DDB_G0290821 | DDB_G0290821 | DDB0232432 | CDS | 4644529 | 1194 | - | 0.252931 | |
DDB_G0290823 | DDB_G0290823 | DDB0232432 | CDS | 4646192 | 1224 | - | 0.251634 | |
DDB_G0290827 | DDB_G0290827 | DDB0232432 | CDS | 4603659 | 753 | - | 0.200531 | |
DDB_G0290835 | DDB_G0290835 | DDB0232432 | CDS | 4620639 | 3231 | - | 0.244197 | |
DDB_G0290837 | DDB_G0290837 | DDB0232432 | CDS | 4637184 | 2280 | + | 0.307456 | |
DDB_G0290839 | DDB_G0290839 | DDB0232432 | CDS | 4590906 | 1278 | - | 0.21518 | |
DDB_G0290841 | DDB_G0290841 | DDB0232432 | CDS | 4662421 | 4242 | + | 0.269448 | |
DDB_G0290843 | DDB_G0290843 | DDB0232432 | CDS | 4667305 | 168 | - | 0.196429 | |
DDB_G0290847 | DDB_G0290847 | DDB0232432 | CDS | 4672145 | 957 | + | 0.236155 | |
DDB_G0290855 | DDB_G0290855 | DDB0232432 | CDS | 4670841 | 357 | + | 0.280112 | |
DDB_G0290857 | DDB_G0290857 | DDB0232432 | CDS | 4682925 | 1560 | + | 0.286538 | |
DDB_G0290859 | DDB_G0290859 | member of the AGC kinase group similar to NDR (nuclear Dbf2-related) and RSK (ribosomal S6 kinase) family members | DDB0232432 | CDS | 4688665 | 1260 | + | 0.307143 |
DDB_G0290863 | DDB_G0290863 | DDB0232432 | CDS | 4694739 | 1020 | - | 0.22549 | |
DDB_G0290865_ps | DDB_G0290865 | putative pseudogene fragment similar to | DDB0232432 | CDS | 4696122 | 519 | - | 0.267823 |
DDB_G0290871 | DDB_G0290871 | DDB0232432 | CDS | 4698932 | 210 | + | 0.204762 | |
DDB_G0290877 | DDB_G0290877 | DDB0232432 | CDS | 4704549 | 2475 | - | 0.288081 | |
DDB_G0290879 | DDB_G0290879 | DDB0232432 | CDS | 4708116 | 531 | + | 0.220339 | |
DDB_G0290881 | DDB_G0290881 | DDB0232432 | CDS | 4709313 | 492 | + | 0.243902 | |
DDB_G0290883 | DDB_G0290883 | highly similar (93 | DDB0232432 | CDS | 4710716 | 1383 | + | 0.261027 |
DDB_G0290885 | DDB_G0290885 | conserved Dictyostelium protein contains a putative signal sequence underexpressed in | DDB0232432 | CDS | 4714181 | 543 | - | 0.303867 |
DDB_G0290887 | DDB_G0290887 | conserved Dictyostelium protein contains a putative signal sequence | DDB0232432 | CDS | 4716370 | 543 | - | 0.311234 |
DDB_G0290893 | DDB_G0290893 | DDB0232432 | CDS | 4676692 | 5457 | + | 0.230346 | |
DDB_G0290895_ps | DDB_G0290895 | putative pseudogene similar to the family of FNIP repeat-containing genes such as | DDB0232432 | CDS | 4690806 | 1434 | + | 0.226639 |
DDB_G0290897_ps | DDB_G0290897 | putative pseudogene similar to | DDB0232432 | CDS | 4712501 | 1170 | + | 0.286325 |
DDB_G0290903 | DDB_G0290903 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232432 | CDS | 4735255 | 228 | - | 0.337719 |
DDB_G0290905 | DDB_G0290905 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232432 | CDS | 4735853 | 228 | + | 0.324561 |
DDB_G0290907 | DDB_G0290907 | DDB0232432 | CDS | 4736810 | 192 | - | 0.296875 | |
DDB_G0290911 | DDB_G0290911 | DDB0232432 | CDS | 4739761 | 150 | - | 0.253333 | |
DDB_G0290915 | DDB_G0290915 | DDB0232432 | CDS | 4742302 | 1170 | + | 0.22906 | |
DDB_G0290923 | DDB_G0290923 | DDB0232432 | CDS | 4757036 | 4101 | + | 0.18971 | |
DDB_G0290931 | DDB_G0290931 | DDB0232432 | CDS | 4768327 | 1536 | - | 0.251302 | |
DDB_G0290933_ps | DDB_G0290933 | putative pseudogene fragment similar to TRAF-type zinc finger-containing proteins including | DDB0232432 | CDS | 4770388 | 339 | - | 0.20944 |
DDB_G0290941_ps | DDB_G0290941 | putative pseudogene N-terminal fragment of RING zinc finger- and TRAF-type zinc finger-containing proteins including | DDB0232432 | CDS | 4785018 | 567 | - | 0.231041 |
DDB_G0290945 | DDB_G0290945 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232432 | CDS | 4734513 | 258 | + | 0.333333 |
DDB_G0290947 | DDB_G0290947 | DDB0232432 | CDS | 4749424 | 4317 | - | 0.28214 | |
DDB_G0290953_TE | DDB_G0290953 | DDB0232432 | CDS | 4796402 | 432 | + | 0.314815 | |
DDB_G0290955_TE | DDB_G0290955 | ORF1 encoding a protein of unknown function of the putative DNA transposon Tdd-5 refer to AF298206 for full-length consensus element | DDB0232432 | CDS | 4798680 | 889 | - | 0.31946 |
DDB_G0290965 | DDB_G0290965 | DDB0232432 | CDS | 4802105 | 1728 | - | 0.23669 | |
DDB_G0290967 | DDB_G0290967 | DDB0232432 | CDS | 4806120 | 1563 | - | 0.272553 | |
DDB_G0290969 | DDB_G0290969 | DDB0232432 | CDS | 4808227 | 1179 | - | 0.189992 | |
DDB_G0290971 | DDB_G0290971 | DDB0232432 | CDS | 4814825 | 1338 | - | 0.27429 | |
DDB_G0290973 | DDB_G0290973 | similar to Polysphondylium pallidum protein contains at least two predicted coiled-coil domains | DDB0232432 | CDS | 4816558 | 5334 | - | 0.250469 |
DDB_G0290975 | DDB_G0290975 | highly similar to cinB (99 | DDB0232432 | CDS | 4829775 | 1014 | + | 0.270217 |
DDB_G0290977 | DDB_G0290977 | DDB0232432 | CDS | 4841153 | 1599 | + | 0.245779 | |
DDB_G0290983 | DDB_G0290983 | DDB0232432 | CDS | 4844885 | 4008 | - | 0.221307 | |
DDB_G0290985 | DDB_G0290985 | DDB0232432 | CDS | 4854167 | 2370 | + | 0.28481 | |
DDB_G0290989 | DDB_G0290989 | DDB0232432 | CDS | 4859470 | 3462 | - | 0.253611 | |
DDB_G0290991 | DDB_G0290991 | DDB0232432 | CDS | 4863621 | 1368 | - | 0.233918 | |
DDB_G0290993 | DDB_G0290993 | DDB0232432 | CDS | 4865936 | 603 | - | 0.303483 | |
DDB_G0290995 | DDB_G0290995 | DDB0232432 | CDS | 4867138 | 909 | - | 0.246425 | |
DDB_G0290999 | DDB_G0290999 | DDB0232432 | CDS | 4872338 | 2757 | - | 0.219804 | |
DDB_G0291001 | DDB_G0291001 | DDB0232432 | CDS | 4875486 | 219 | - | 0.324201 | |
DDB_G0291003 | DDB_G0291003 | DDB0232432 | CDS | 4876763 | 2598 | - | 0.299461 | |
DDB_G0291005 | DDB_G0291005 | DDB0232432 | CDS | 4879944 | 909 | + | 0.214521 | |
DDB_G0291011 | DDB_G0291011 | DDB0232432 | CDS | 4886164 | 2919 | - | 0.258993 | |
DDB_G0291013 | DDB_G0291013 | DDB0232432 | CDS | 4889905 | 1149 | + | 0.302872 | |
DDB_G0291015 | DDB_G0291015 | possible homolog of human LSM10 a U7 snRNA-associated Sm-like protein | DDB0232432 | CDS | 4891178 | 414 | - | 0.23913 |
DDB_G0291017_ps | DDB_G0291017 | putative pseudogene fragment similar to | DDB0232432 | CDS | 4893398 | 495 | - | 0.284848 |
DDB_G0291019 | DDB_G0291019 | DDB0232432 | CDS | 4894200 | 1023 | - | 0.234604 | |
DDB_G0291023 | DDB_G0291023 | DDB0232432 | CDS | 4906011 | 1734 | - | 0.27797 | |
DDB_G0291025 | DDB_G0291025 | DDB0232432 | CDS | 4915458 | 2445 | + | 0.251534 | |
DDB_G0291027 | DDB_G0291027 | DDB0232432 | CDS | 4918030 | 4254 | - | 0.271979 | |
DDB_G0291029 | DDB_G0291029 | catalyzes the reaction SOsub4subsup2-sup ATP APS pyrophosphate | DDB0232432 | CDS | 4928744 | 1767 | - | 0.367289 |
DDB_G0291033 | DDB_G0291033 | DDB0232432 | CDS | 4933146 | 2238 | - | 0.298481 | |
DDB_G0291035_ps | DDB_G0291035 | putative pseudogene similar to genes of the RING zinc finger family such as the | DDB0232432 | CDS | 4832043 | 339 | - | 0.218289 |
DDB_G0291041_ps | DDB_G0291041 | putative pseudogene fragment similar to a D. discoideum gene family including | DDB0232432 | CDS | 4805100 | 306 | - | 0.238562 |
DDB_G0291045 | DDB_G0291045 | DDB0232432 | CDS | 4923512 | 4269 | - | 0.271024 | |
DDB_G0291051_ps | DDB_G0291051 | putative pseudogene fragment similar to | DDB0232432 | CDS | 4829057 | 204 | + | 0.245098 |
DDB_G0291053_ps | DDB_G0291053 | putative pseudogene similar gene the | DDB0232432 | CDS | 4830916 | 492 | - | 0.315041 |
DDB_G0291055 | DDB_G0291055 | homolog of human SFT2D1 (SFT2 domain-containing protein 1) contains 4 putative transmembrane domains | DDB0232432 | CDS | 4835830 | 477 | + | 0.295597 |
DDB_G0291057 | DDB_G0291057 | DDB0232432 | CDS | 4836534 | 1035 | - | 0.211594 | |
DDB_G0291059 | DDB_G0291059 | contains two ankyrin repeats and two K homology (KH) domains similar to high density lipoprotein-binding protein (vigilin) | DDB0232432 | CDS | 4839561 | 1155 | + | 0.303896 |
DDB_G0291061 | DDB_G0291061 | DDB0232432 | CDS | 4868366 | 234 | + | 0.294872 | |
DDB_G0291065 | DDB_G0291065 | DDB0232432 | CDS | 4936261 | 7389 | + | 0.280282 | |
DDB_G0291067_RTE | DDB_G0291067 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 4945727 | 1063 | - | 0.292568 |
DDB_G0291069_RTE | DDB_G0291069 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232432 | CDS | 4946964 | 645 | - | 0.294574 |
DDB_G0291071 | DDB_G0291071 | DDB0232432 | CDS | 4948671 | 1275 | - | 0.278431 | |
DDB_G0291073 | DDB_G0291073 | DDB0232432 | CDS | 4950352 | 963 | - | 0.187954 | |
DDB_G0291083 | DDB_G0291083 | DDB0232432 | CDS | 4954952 | 606 | - | 0.20132 | |
DDB_G0291087_ps | DDB_G0291087 | putative pseudogene very similar to | DDB0232432 | CDS | 4958200 | 177 | + | 0.338983 |
DDB_G0291089 | DDB_G0291089 | DDB0232432 | CDS | 4970973 | 249 | + | 0.297189 | |
DDB_G0291099 | DDB_G0291099 | DDB0232432 | CDS | 4996259 | 1752 | + | 0.260274 | |
DDB_G0291101 | DDB_G0291101 | DDB0232432 | CDS | 4998499 | 426 | + | 0.241784 | |
DDB_G0291103 | DDB_G0291103 | DDB0232432 | CDS | 4999483 | 327 | + | 0.275229 | |
DDB_G0291107 | DDB_G0291107 | DDB0232432 | CDS | 4952079 | 1350 | - | 0.295556 | |
DDB_G0291109 | DDB_G0291109 | DDB0232432 | CDS | 4968619 | 1329 | - | 0.239278 | |
DDB_G0291111 | DDB_G0291111 | DDB0232432 | CDS | 4977011 | 3294 | - | 0.245598 | |
DDB_G0291115 | DDB_G0291115 | DDB0232432 | CDS | 5000155 | 5757 | - | 0.265763 | |
DDB_G0291119 | DDB_G0291119 | DDB0232432 | CDS | 5015686 | 1308 | + | 0.248471 | |
DDB_G0291131 | DDB_G0291131 | DDB0232432 | CDS | 5027479 | 2148 | + | 0.363128 | |
DDB_G0291133 | DDB_G0291133 | putative protein tyrosine kinase similar to S. pombe wee1 inhibitor of mitosis through phosphorylation of cdc2 | DDB0232432 | CDS | 5030354 | 2337 | + | 0.26059 |
DDB_G0291135 | DDB_G0291135 | DDB0232432 | CDS | 5033227 | 1185 | + | 0.263291 | |
DDB_G0291137 | DDB_G0291137 | DDB0232432 | CDS | 5040435 | 558 | + | 0.344086 | |
DDB_G0291139 | DDB_G0291139 | DDB0232432 | CDS | 5041464 | 906 | - | 0.236203 | |
DDB_G0291141 | DDB_G0291141 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 15 putative transmembrane domains | DDB0232432 | CDS | 5043001 | 2313 | + | 0.278859 |
DDB_G0291143 | DDB_G0291143 | DDB0232432 | CDS | 5045979 | 810 | - | 0.21358 | |
DDB_G0291147 | DDB_G0291147 | DDB0232432 | CDS | 5049086 | 2817 | + | 0.242457 | |
DDB_G0291149 | DDB_G0291149 | DDB0232432 | CDS | 5052148 | 1569 | - | 0.251115 | |
DDB_G0291151 | DDB_G0291151 | DDB0232432 | CDS | 5054416 | 1134 | + | 0.250441 | |
DDB_G0291153_ps | DDB_G0291153 | putative pseudogene similar gene the | DDB0232432 | CDS | 5057151 | 522 | - | 0.310345 |
DDB_G0291155 | DDB_G0291155 | DDB0232432 | CDS | 5058540 | 936 | - | 0.317308 | |
DDB_G0291159 | DDB_G0291159 | DDB0232432 | CDS | 5062119 | 855 | + | 0.263158 | |
DDB_G0291161 | DDB_G0291161 | DDB0232432 | CDS | 5063347 | 4944 | - | 0.303803 | |
DDB_G0291165 | DDB_G0291165 | DDB0232432 | CDS | 5083069 | 228 | + | 0.201754 | |
DDB_G0291167 | DDB_G0291167 | DDB0232432 | CDS | 5083393 | 681 | - | 0.251101 | |
DDB_G0291169 | DDB_G0291169 | DDB0232432 | CDS | 5089340 | 894 | + | 0.279642 | |
DDB_G0291171 | DDB_G0291171 | DDB0232432 | CDS | 5090921 | 882 | + | 0.297052 | |
DDB_G0291175 | DDB_G0291175 | DDB0232432 | CDS | 5097563 | 3102 | + | 0.297872 | |
DDB_G0291181 | DDB_G0291181 | DDB0232432 | CDS | 5105448 | 1080 | + | 0.327778 | |
DDB_G0291187 | DDB_G0291187 | similar to A. thaliana PCS1 (phytochelatin synthase 1) catalyzes the reaction glutathione (Glu(-Cys))(n)-Gly Gly (Glu(-Cys))(n1)-Gly | DDB0232432 | CDS | 5037394 | 1881 | - | 0.290803 |
DDB_G0291189 | DDB_G0291189 | DDB0232432 | CDS | 5084851 | 696 | + | 0.238506 | |
DDB_G0291191 | DDB_G0291191 | DDB0232432 | CDS | 5086072 | 1059 | - | 0.367328 | |
DDB_G0291195 | DDB_G0291195 | DDB0232432 | CDS | 5092325 | 792 | + | 0.294192 | |
DDB_G0291203 | DDB_G0291203 | similar to D. purpureum protein contains a region conserved with eukaryotic transmembrane receptors (lung_7-TM_R: PF06814) contains 7 putative transmembrane domains | DDB0232432 | CDS | 5116417 | 1593 | + | 0.254237 |
DDB_G0291205 | DDB_G0291205 | DDB0232432 | CDS | 5120775 | 2727 | + | 0.268794 | |
DDB_G0291209_ps | DDB_G0291209 | putative pseudogene highly similar to a D. discoideum gene family including | DDB0232433 | CDS | 2814 | 336 | - | 0.330357 |
DDB_G0291213_RTE | DDB_G0291213 | ORF2 encoding reverse transcriptase (RT) and integrase (IN) proteins of long terminal repeat retrotransposon Skipper refer to AF049230 for consensus element | DDB0232433 | CDS | 4067 | 939 | - | 0.331203 |
DDB_G0291215_TE | DDB_G0291215 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-B refer to AF298202 for full-length consensus element | DDB0232433 | CDS | 8948 | 651 | + | 0.222734 |
DDB_G0291217_RTE | DDB_G0291217 | ORF2 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232433 | CDS | 11026 | 858 | - | 0.38345 |
DDB_G0291219_TE | DDB_G0291219 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-B refer to AF298202 for full-length consensus element | DDB0232433 | CDS | 10525 | 291 | + | 0.206186 |
DDB_G0291221_RTE | DDB_G0291221 | ORF1 protein of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232433 | CDS | 1271 | 1008 | - | 0.371032 |
DDB_G0291223_RTE | DDB_G0291223 | fused fragments of the DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232433 | CDS | 6464 | 903 | + | 0.388704 |
DDB_G0291257_TE | DDB_G0291257 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232433 | CDS | 14558 | 1413 | - | 0.225053 |
DDB_G0291259 | DDB_G0291259 | DDB0232433 | CDS | 18892 | 1632 | + | 0.307598 | |
DDB_G0291261 | DDB_G0291261 | protein conserved in bacteria and plants D. discoideum contains a second highly similar protein ( | DDB0232433 | CDS | 21629 | 558 | + | 0.283154 |
DDB_G0291263 | DDB_G0291263 | DDB0232433 | CDS | 22760 | 4752 | + | 0.258207 | |
DDB_G0291277 | DDB_G0291277 | DDB0232433 | CDS | 44334 | 633 | - | 0.306477 | |
DDB_G0291279 | DDB_G0291279 | contains 11 putative transmembrane domains similar to feline leukemia virus subgroup C receptor-related proteins | DDB0232433 | CDS | 45543 | 1575 | + | 0.333333 |
DDB_G0291281 | DDB_G0291281 | DDB0232433 | CDS | 48286 | 372 | + | 0.282258 | |
DDB_G0291285 | DDB_G0291285 | DDB0232433 | CDS | 53775 | 2280 | + | 0.217105 | |
DDB_G0291289 | DDB_G0291289 | DDB0232433 | CDS | 59612 | 4179 | + | 0.216559 | |
DDB_G0291299 | DDB_G0291299 | DDB0232433 | CDS | 80308 | 1407 | - | 0.294243 | |
DDB_G0291301 | DDB_G0291301 | at the N-terminus similar to peroxisomal sarcosine oxidases (PSO) at the C-terminus similar to L-amino-acid oxidases (LAO) | DDB0232433 | CDS | 87606 | 3243 | + | 0.362319 |
DDB_G0291308 | DDB_G0291308 | DDB0232433 | CDS | 107010 | 5058 | - | 0.205417 | |
DDB_G0291310 | DDB_G0291310 | DDB0232433 | CDS | 112763 | 1143 | + | 0.314086 | |
DDB_G0291314 | DDB_G0291314 | highly similar to plant HSP101 expressed in prespore cells | DDB0232433 | CDS | 116087 | 2661 | + | 0.34611 |
DDB_G0291316 | DDB_G0291316 | DDB0232433 | CDS | 118975 | 675 | - | 0.262222 | |
DDB_G0291318 | DDB_G0291318 | has similarity to yeast mrp10 the mitochondrial ribosome 37 S subunit component | DDB0232433 | CDS | 120345 | 276 | + | 0.304348 |
DDB_G0291322 | DDB_G0291322 | DDB0232433 | CDS | 123984 | 2631 | + | 0.199164 | |
DDB_G0291324 | DDB_G0291324 | DDB0232433 | CDS | 126721 | 699 | - | 0.270386 | |
DDB_G0291326 | DDB_G0291326 | DDB0232433 | CDS | 127766 | 231 | - | 0.264069 | |
DDB_G0291328 | DDB_G0291328 | DDB0232433 | CDS | 128308 | 744 | - | 0.322581 | |
DDB_G0291332 | DDB_G0291332 | DDB0232433 | CDS | 131894 | 951 | - | 0.278654 | |
DDB_G0291334 | DDB_G0291334 | DDB0232433 | CDS | 133565 | 486 | + | 0.193416 | |
DDB_G0291336 | DDB_G0291336 | DDB0232433 | CDS | 134282 | 834 | - | 0.2494 | |
DDB_G0291338 | DDB_G0291338 | DDB0232433 | CDS | 135540 | 657 | + | 0.219178 | |
DDB_G0291340 | DDB_G0291340 | DDB0232433 | CDS | 136448 | 1263 | - | 0.346793 | |
DDB_G0291344 | DDB_G0291344 | similar to butyrylcholinesterase and acetylcholinesterase precursor proteins contains a putative signal peptide | DDB0232433 | CDS | 143653 | 1581 | + | 0.29475 |
DDB_G0291348 | DDB_G0291348 | DDB0232433 | CDS | 160343 | 2316 | + | 0.239206 | |
DDB_G0291350 | DDB_G0291350 | putative protein serinethreonine kinase similar to mammalian MPSK (myristoylated and palmitoylated serinethreonine kinase) a kinase involved in transcriptional regulation and protein phosphorylation may be an intermediary in the TGF-beta signaling pathway | DDB0232433 | CDS | 162730 | 1110 | - | 0.245045 |
DDB_G0291354 | DDB_G0291354 | DDB0232433 | CDS | 169469 | 2817 | - | 0.270501 | |
DDB_G0291364 | DDB_G0291364 | DDB0232433 | CDS | 183283 | 519 | + | 0.368015 | |
DDB_G0291366 | DDB_G0291366 | belongs to the thioredoxin family similar to A. thaliana PRXIIF (peroxiredoxin IIF) lacks redox-active cysteine compared with many homologs so may be catalytically inactive | DDB0232433 | CDS | 184226 | 549 | - | 0.275046 |
DDB_G0291370 | DDB_G0291370 | DDB0232433 | CDS | 192185 | 1206 | - | 0.354063 | |
DDB_G0291374 | DDB_G0291374 | ortholog of the H. sapiens TEX261 (testis expressed 261) contains a putative N-terminal signal sequence and 3 to 4 additional transmembrane domains | DDB0232433 | CDS | 199740 | 624 | - | 0.25641 |
DDB_G0291382 | DDB_G0291382 | DDB0232433 | CDS | 224492 | 456 | - | 0.230263 | |
DDB_G0291384 | DDB_G0291384 | DDB0232433 | CDS | 226725 | 1878 | + | 0.256124 | |
DDB_G0291386 | DDB_G0291386 | DDB0232433 | CDS | 229175 | 1392 | + | 0.297414 | |
DDB_G0291388 | DDB_G0291388 | DDB0232433 | CDS | 231261 | 219 | - | 0.324201 | |
DDB_G0291392 | DDB_G0291392 | similar to spore coat protein PspB expressed in prespore cells | DDB0232433 | CDS | 246726 | 1407 | - | 0.372424 |
DDB_G0291394 | DDB_G0291394 | DDB0232433 | CDS | 249853 | 921 | + | 0.304017 | |
DDB_G0291396 | DDB_G0291396 | contains a dilute domain found at the carboxyl terminus of non-muscle myosin V | DDB0232433 | CDS | 252157 | 2907 | + | 0.257998 |
DDB_G0291400 | DDB_G0291400 | DDB0232433 | CDS | 255522 | 1827 | - | 0.262726 | |
DDB_G0291402 | DDB_G0291402 | DDB0232433 | CDS | 257921 | 447 | - | 0.306488 | |
DDB_G0291406 | DDB_G0291406 | DDB0232433 | CDS | 260638 | 12408 | + | 0.230819 | |
DDB_G0291408 | DDB_G0291408 | conserved protein in Dictyostelium fungi and bacteria | DDB0232433 | CDS | 273229 | 582 | - | 0.28866 |
DDB_G0291410 | DDB_G0291410 | DDB0232433 | CDS | 274574 | 858 | + | 0.30303 | |
DDB_G0291414 | DDB_G0291414 | DDB0232433 | CDS | 278393 | 270 | + | 0.266667 | |
DDB_G0291416 | DDB_G0291416 | DDB0232433 | CDS | 279007 | 702 | - | 0.270655 | |
DDB_G0291418 | DDB_G0291418 | DDB0232433 | CDS | 280209 | 1392 | + | 0.214799 | |
DDB_G0291420 | DDB_G0291420 | DDB0232433 | CDS | 286253 | 216 | - | 0.319444 | |
DDB_G0291422 | DDB_G0291422 | DDB0232433 | CDS | 286642 | 324 | - | 0.265432 | |
DDB_G0291424 | DDB_G0291424 | DDB0232433 | CDS | 289088 | 2709 | + | 0.276486 | |
DDB_G0291426 | DDB_G0291426 | DDB0232433 | CDS | 292100 | 870 | - | 0.297701 | |
DDB_G0291428 | DDB_G0291428 | contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232433 | CDS | 293845 | 1053 | + | 0.303894 |
DDB_G0291430 | DDB_G0291430 | DDB0232433 | CDS | 295544 | 2067 | + | 0.196904 | |
DDB_G0291432 | DDB_G0291432 | DDB0232433 | CDS | 297698 | 1665 | - | 0.252252 | |
DDB_G0291436 | DDB_G0291436 | DDB0232433 | CDS | 302806 | 1263 | + | 0.231987 | |
DDB_G0291442 | DDB_G0291442 | DDB0232433 | CDS | 319912 | 216 | - | 0.240741 | |
DDB_G0291444 | DDB_G0291444 | DDB0232433 | CDS | 320738 | 1344 | + | 0.287946 | |
DDB_G0291446 | DDB_G0291446 | DDB0232433 | CDS | 322306 | 420 | - | 0.214286 | |
DDB_G0291450 | DDB_G0291450 | DDB0232433 | CDS | 326534 | 3219 | - | 0.192917 | |
DDB_G0291452 | DDB_G0291452 | DDB0232433 | CDS | 330303 | 1851 | - | 0.226364 | |
DDB_G0291462 | DDB_G0291462 | DDB0232433 | CDS | 366300 | 1095 | - | 0.189954 | |
DDB_G0291464 | DDB_G0291464 | DDB0232433 | CDS | 369674 | 3414 | - | 0.289104 | |
DDB_G0291466 | DDB_G0291466 | DDB0232433 | CDS | 376634 | 1329 | - | 0.222724 | |
DDB_G0291468 | DDB_G0291468 | DDB0232433 | CDS | 378403 | 1608 | + | 0.264303 | |
DDB_G0291470 | DDB_G0291470 | DDB0232433 | CDS | 380554 | 1032 | + | 0.247093 | |
DDB_G0291472 | DDB_G0291472 | DDB0232433 | CDS | 381635 | 1221 | - | 0.290745 | |
DDB_G0291474 | DDB_G0291474 | DDB0232433 | CDS | 387688 | 3480 | + | 0.266092 | |
DDB_G0291476 | DDB_G0291476 | DDB0232433 | CDS | 396540 | 726 | + | 0.316804 | |
DDB_G0291478 | DDB_G0291478 | DDB0232433 | CDS | 405733 | 1263 | - | 0.257324 | |
DDB_G0291480 | DDB_G0291480 | DDB0232433 | CDS | 408654 | 1506 | - | 0.225764 | |
DDB_G0291484 | DDB_G0291484 | DDB0232433 | CDS | 412297 | 756 | - | 0.23545 | |
DDB_G0291486 | DDB_G0291486 | similar to CUGBP proteins and Bruno-like proteins human CUGBP1 regulates splicing and translation of various RNAs contains 3 RRM domains | DDB0232433 | CDS | 413873 | 1470 | + | 0.348299 |
DDB_G0291488 | DDB_G0291488 | DDB0232433 | CDS | 417129 | 1131 | - | 0.177719 | |
DDB_G0291492 | DDB_G0291492 | DDB0232433 | CDS | 423677 | 1077 | - | 0.246054 | |
DDB_G0291494 | DDB_G0291494 | DDB0232433 | CDS | 430069 | 834 | + | 0.293765 | |
DDB_G0291496 | DDB_G0291496 | DDB0232433 | CDS | 435835 | 1074 | + | 0.259777 | |
DDB_G0291508 | DDB_G0291508 | DDB0232433 | CDS | 452441 | 150 | + | 0.24 | |
DDB_G0291510 | DDB_G0291510 | ortholog of the human GTPase activating RapranGAP protein GARNL3 contains a Rapran-GAP domain and a citron-like domain | DDB0232433 | CDS | 452902 | 3096 | - | 0.266796 |
DDB_G0291516 | DDB_G0291516 | highly similar to | DDB0232433 | CDS | 469339 | 2898 | + | 0.277433 |
DDB_G0291518 | DDB_G0291518 | DDB0232433 | CDS | 473275 | 240 | + | 0.225 | |
DDB_G0291522 | DDB_G0291522 | DDB0232433 | CDS | 478316 | 528 | + | 0.147727 | |
DDB_G0291524 | DDB_G0291524 | very similar to human NAGA an alpha-N-acetylgalactosaminidase which catalyzes the hydrolysis of terminal non-reducing N-acetyl-D-galactosamine residues in N-acetyl-alpha-D-galactosaminides | DDB0232433 | CDS | 479074 | 1401 | - | 0.292648 |
DDB_G0291530 | DDB_G0291530 | DDB0232433 | CDS | 485007 | 1167 | + | 0.238218 | |
DDB_G0291532 | DDB_G0291532 | DDB0232433 | CDS | 486511 | 858 | + | 0.244755 | |
DDB_G0291534 | DDB_G0291534 | DDB0232433 | CDS | 487852 | 1113 | + | 0.261456 | |
DDB_G0291538 | DDB_G0291538 | similar to bacterial acetyltransferases homolog of E. coli maa (maltose O-acetyltransferase) contains a predicted peroxisomal targeting signal | DDB0232433 | CDS | 533329 | 546 | + | 0.322344 |
DDB_G0291540 | DDB_G0291540 | DDB0232433 | CDS | 530842 | 1677 | - | 0.202743 | |
DDB_G0291542_ps | DDB_G0291542 | putative pseudogene fragment similar to D. discoideum gene | DDB0232433 | CDS | 523707 | 240 | - | 0.191667 |
DDB_G0291544 | DDB_G0291544 | DDB0232433 | CDS | 518857 | 2382 | + | 0.232158 | |
DDB_G0291546 | DDB_G0291546 | DDB0232433 | CDS | 515184 | 2898 | + | 0.23706 | |
DDB_G0291548 | DDB_G0291548 | DDB0232433 | CDS | 512943 | 1863 | + | 0.247987 | |
DDB_G0291552_ps | DDB_G0291552 | putative pseudogene similar to D. discoideum gene | DDB0232433 | CDS | 511252 | 609 | - | 0.243021 |
DDB_G0291554 | DDB_G0291554 | DDB0232433 | CDS | 506713 | 2334 | + | 0.340189 | |
DDB_G0291558 | DDB_G0291558 | DDB0232433 | CDS | 503745 | 420 | - | 0.202381 | |
DDB_G0291560_ps | DDB_G0291560 | DDB0232433 | CDS | 501788 | 585 | + | 0.355556 | |
DDB_G0291564 | DDB_G0291564 | DDB0232433 | CDS | 555673 | 147 | + | 0.210884 | |
DDB_G0291572 | DDB_G0291572 | DDB0232433 | CDS | 564716 | 1050 | - | 0.28 | |
DDB_G0291574 | DDB_G0291574 | DDB0232433 | CDS | 566754 | 732 | - | 0.29235 | |
DDB_G0291576 | DDB_G0291576 | conserved hypothetical protein contains a putative N-terminal signal sequence | DDB0232433 | CDS | 569331 | 939 | + | 0.217252 |
DDB_G0291578 | DDB_G0291578 | member of a small Dictyostelium gene family missing the carboxyl half compared to related proteins | DDB0232433 | CDS | 571007 | 486 | + | 0.195473 |
DDB_G0291580 | DDB_G0291580 | DDB0232433 | CDS | 571564 | 1047 | + | 0.221585 | |
DDB_G0291582_ps | DDB_G0291582 | DDB0232433 | CDS | 573502 | 492 | + | 0.203252 | |
DDB_G0291586_ps | DDB_G0291586 | putative pseudogene very similar to a small D. discoideum gene family including | DDB0232433 | CDS | 576491 | 645 | + | 0.229457 |
DDB_G0291592 | DDB_G0291592 | DDB0232433 | CDS | 584708 | 1248 | + | 0.252404 | |
DDB_G0291598 | DDB_G0291598 | DDB0232433 | CDS | 590338 | 1779 | + | 0.289488 | |
DDB_G0291602 | DDB_G0291602 | DDB0232433 | CDS | 594807 | 549 | + | 0.233151 | |
DDB_G0291604 | DDB_G0291604 | similar to polyketide synthases but only about one third of the size | DDB0232433 | CDS | 595950 | 3030 | + | 0.184158 |
DDB_G0291608 | DDB_G0291608 | DDB0232433 | CDS | 235528 | 2760 | + | 0.306522 | |
DDB_G0291610_ps | DDB_G0291610 | putative pseudogene similar to a family of genes including | DDB0232433 | CDS | 426330 | 1116 | + | 0.252688 |
DDB_G0291612 | DDB_G0291612 | DDB0232433 | CDS | 497249 | 1509 | + | 0.206759 | |
DDB_G0291616 | DDB_G0291616 | DDB0232433 | CDS | 575206 | 1050 | + | 0.214286 | |
DDB_G0291618 | DDB_G0291618 | DDB0232433 | CDS | 582226 | 456 | - | 0.208333 | |
DDB_G0291620_RTE | DDB_G0291620 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 606324 | 3168 | - | 0.348485 |
DDB_G0291626 | DDB_G0291626 | DDB0232433 | CDS | 368247 | 216 | - | 0.157407 | |
DDB_G0291628 | DDB_G0291628 | DDB0232433 | CDS | 387018 | 189 | + | 0.243386 | |
DDB_G0291632 | DDB_G0291632 | DDB0232433 | CDS | 427952 | 1527 | + | 0.300589 | |
DDB_G0291638 | DDB_G0291638 | DDB0232433 | CDS | 476401 | 282 | + | 0.195035 | |
DDB_G0291640 | DDB_G0291640 | DDB0232433 | CDS | 496074 | 303 | - | 0.270627 | |
DDB_G0291642_ps | DDB_G0291642 | putative pseudogene similar to a D. discoideum gene family including | DDB0232433 | CDS | 524418 | 1047 | - | 0.239733 |
DDB_G0291644 | DDB_G0291644 | DDB0232433 | CDS | 526360 | 1560 | - | 0.189744 | |
DDB_G0291646 | DDB_G0291646 | DDB0232433 | CDS | 583710 | 390 | - | 0.230769 | |
DDB_G0291650 | DDB_G0291650 | DDB0232433 | CDS | 82693 | 3204 | + | 0.335206 | |
DDB_G0291654 | DDB_G0291654 | DDB0232433 | CDS | 138933 | 867 | - | 0.294118 | |
DDB_G0291658 | DDB_G0291658 | DDB0232433 | CDS | 186929 | 1194 | + | 0.278057 | |
DDB_G0291664 | DDB_G0291664 | highly similar to | DDB0232433 | CDS | 338918 | 2880 | + | 0.291319 |
DDB_G0291670 | DDB_G0291670 | DDB0232433 | CDS | 364638 | 1602 | + | 0.310861 | |
DDB_G0291672 | DDB_G0291672 | DDB0232433 | CDS | 408084 | 255 | + | 0.298039 | |
DDB_G0291674 | DDB_G0291674 | similar to bacterial short-chain dehydrogenasereductase family proteins and human RDH8 (retinol dehydrogenase 8) | DDB0232433 | CDS | 431044 | 951 | - | 0.281809 |
DDB_G0291676 | DDB_G0291676 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232433 | CDS | 432569 | 903 | - | 0.282392 |
DDB_G0291678_ps | DDB_G0291678 | putative pseudogene similar to | DDB0232433 | CDS | 509192 | 969 | + | 0.223942 |
DDB_G0291680_ps | DDB_G0291680 | putative pseudogene very similar to | DDB0232433 | CDS | 528420 | 759 | + | 0.225296 |
DDB_G0291682_ps | DDB_G0291682 | putative pseudogene similar to Dictyostelium genes | DDB0232433 | CDS | 533918 | 1101 | - | 0.202543 |
DDB_G0291686_RTE | DDB_G0291686 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 599555 | 876 | - | 0.310502 |
DDB_G0291688_RTE | DDB_G0291688 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 601031 | 3405 | - | 0.318943 |
DDB_G0291692_RTE | DDB_G0291692 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 610016 | 942 | - | 0.412951 |
DDB_G0291694 | DDB_G0291694 | DDB0232433 | CDS | 613952 | 2553 | - | 0.276146 | |
DDB_G0291696_RTE | DDB_G0291696 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 611564 | 1335 | + | 0.307116 |
DDB_G0291700 | DDB_G0291700 | DDB0232433 | CDS | 663460 | 2265 | - | 0.325386 | |
DDB_G0291704 | DDB_G0291704 | DDB0232433 | CDS | 645330 | 1107 | - | 0.265583 | |
DDB_G0291706 | DDB_G0291706 | DDB0232433 | CDS | 643919 | 726 | + | 0.274105 | |
DDB_G0291712 | DDB_G0291712 | DDB0232433 | CDS | 646777 | 1392 | - | 0.181034 | |
DDB_G0291716 | DDB_G0291716 | DDB0232433 | CDS | 726193 | 2322 | - | 0.251938 | |
DDB_G0291718 | DDB_G0291718 | DDB0232433 | CDS | 724492 | 1395 | + | 0.267384 | |
DDB_G0291720 | DDB_G0291720 | DDB0232433 | CDS | 721305 | 1278 | - | 0.311424 | |
DDB_G0291722 | DDB_G0291722 | DDB0232433 | CDS | 719367 | 1344 | - | 0.233631 | |
DDB_G0291724_ps | DDB_G0291724 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232433 | CDS | 718700 | 303 | + | 0.39934 |
DDB_G0291726 | DDB_G0291726 | DDB0232433 | CDS | 716979 | 690 | - | 0.356522 | |
DDB_G0291730 | DDB_G0291730 | DDB0232433 | CDS | 712314 | 1374 | - | 0.235808 | |
DDB_G0291732 | DDB_G0291732 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232433 | CDS | 711008 | 927 | + | 0.326861 |
DDB_G0291740 | DDB_G0291740 | DDB0232433 | CDS | 678305 | 1125 | - | 0.274667 | |
DDB_G0291742_ps | DDB_G0291742 | putative pseudogene similar to D. discoideum gene | DDB0232433 | CDS | 680092 | 480 | - | 0.283333 |
DDB_G0291744 | DDB_G0291744 | DDB0232433 | CDS | 681611 | 3126 | - | 0.18682 | |
DDB_G0291748 | DDB_G0291748 | DDB0232433 | CDS | 685440 | 741 | + | 0.264507 | |
DDB_G0291754 | DDB_G0291754 | DDB0232433 | CDS | 693935 | 726 | - | 0.311295 | |
DDB_G0291758 | DDB_G0291758 | DDB0232433 | CDS | 697440 | 1194 | + | 0.273869 | |
DDB_G0291760 | DDB_G0291760 | DDB0232433 | CDS | 701991 | 867 | + | 0.283737 | |
DDB_G0291764 | DDB_G0291764 | related to ribonucleotide reductase small subunit missing about 25 | DDB0232433 | CDS | 704842 | 774 | + | 0.239018 |
DDB_G0291766 | DDB_G0291766 | DDB0232433 | CDS | 707563 | 1053 | + | 0.255461 | |
DDB_G0291768 | DDB_G0291768 | DDB0232433 | CDS | 730635 | 1692 | - | 0.278369 | |
DDB_G0291770_ps | DDB_G0291770 | putative pseudogene similar to D. discoideum gene | DDB0232433 | CDS | 673796 | 1026 | - | 0.287524 |
DDB_G0291772 | DDB_G0291772 | DDB0232433 | CDS | 699835 | 1206 | + | 0.280265 | |
DDB_G0291774 | DDB_G0291774 | DDB0232433 | CDS | 703802 | 924 | - | 0.306277 | |
DDB_G0291778 | DDB_G0291778 | DDB0232433 | CDS | 709621 | 240 | + | 0.241667 | |
DDB_G0291782 | DDB_G0291782 | DDB0232433 | CDS | 739204 | 3027 | + | 0.248761 | |
DDB_G0291784_ps | DDB_G0291784 | putative pseudogene similar to a small family of D. discoideum genes | DDB0232433 | CDS | 743770 | 1230 | - | 0.270732 |
DDB_G0291786 | DDB_G0291786 | DDB0232433 | CDS | 736206 | 552 | + | 0.182971 | |
DDB_G0291790_ps | DDB_G0291790 | putative pseudogene similar to D. discoideum genes | DDB0232433 | CDS | 747483 | 1176 | + | 0.244898 |
DDB_G0291792 | DDB_G0291792 | DDB0232433 | CDS | 749614 | 2970 | + | 0.260269 | |
DDB_G0291796 | DDB_G0291796 | DDB0232433 | CDS | 757607 | 2541 | + | 0.284534 | |
DDB_G0291798 | DDB_G0291798 | DDB0232433 | CDS | 762390 | 3693 | + | 0.294611 | |
DDB_G0291800 | DDB_G0291800 | GFA enzymes catalyze the condensation of formaldehyde and glutathione to S-hydroxymethylglutathione all known members of this family contain 5 strongly conserved cysteine residues | DDB0232433 | CDS | 768935 | 390 | - | 0.274359 |
DDB_G0291806 | DDB_G0291806 | DDB0232433 | CDS | 777729 | 2871 | - | 0.254615 | |
DDB_G0291808 | DDB_G0291808 | DDB0232433 | CDS | 781062 | 2577 | - | 0.197128 | |
DDB_G0291810 | DDB_G0291810 | DDB0232433 | CDS | 784328 | 1974 | - | 0.346505 | |
DDB_G0291812 | DDB_G0291812 | DDB0232433 | CDS | 791270 | 3564 | + | 0.241863 | |
DDB_G0291816 | DDB_G0291816 | DDB0232433 | CDS | 805833 | 1002 | - | 0.313373 | |
DDB_G0291818 | DDB_G0291818 | DDB0232433 | CDS | 808065 | 1977 | + | 0.264036 | |
DDB_G0291820 | DDB_G0291820 | DDB0232433 | CDS | 810431 | 942 | - | 0.314225 | |
DDB_G0291824 | DDB_G0291824 | DDB0232433 | CDS | 827281 | 1878 | - | 0.300319 | |
DDB_G0291826 | DDB_G0291826 | DDB0232433 | CDS | 830929 | 162 | + | 0.388889 | |
DDB_G0291828 | DDB_G0291828 | DDB0232433 | CDS | 832120 | 945 | - | 0.262434 | |
DDB_G0291836 | DDB_G0291836 | DDB0232433 | CDS | 812338 | 2850 | + | 0.236842 | |
DDB_G0291842 | DDB_G0291842 | putative protein tyrosine kinase similar to S. pombe WEE1 inhibitor of mitosis through phosphorylation of cdc2 | DDB0232433 | CDS | 822502 | 1059 | - | 0.351275 |
DDB_G0291844 | DDB_G0291844 | DDB0232433 | CDS | 838751 | 1998 | - | 0.20971 | |
DDB_G0291852 | DDB_G0291852 | DDB0232433 | CDS | 775774 | 1071 | - | 0.259571 | |
DDB_G0291854 | DDB_G0291854 | DDB0232433 | CDS | 787015 | 2022 | - | 0.300692 | |
DDB_G0291860 | DDB_G0291860 | has a short region of similarity with CARD3 (caspase recruitment domain family member 3) | DDB0232433 | CDS | 846677 | 2394 | - | 0.24269 |
DDB_G0291872 | DDB_G0291872 | DDB0232433 | CDS | 855161 | 2688 | + | 0.273438 | |
DDB_G0291874 | DDB_G0291874 | DDB0232433 | CDS | 858095 | 336 | - | 0.235119 | |
DDB_G0291878_RTE | DDB_G0291878 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 861379 | 2322 | + | 0.353144 |
DDB_G0291880_RTE | DDB_G0291880 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 874531 | 684 | + | 0.337719 |
DDB_G0291882_RTE | DDB_G0291882 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 875439 | 684 | + | 0.337719 |
DDB_G0291884_RTE | DDB_G0291884 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 878204 | 3180 | + | 0.350629 |
DDB_G0291886_ps | DDB_G0291886 | similar to | DDB0232433 | CDS | 881755 | 2151 | + | 0.248257 |
DDB_G0291888 | DDB_G0291888 | DDB0232433 | CDS | 886219 | 1416 | + | 0.214689 | |
DDB_G0291892 | DDB_G0291892 | DDB0232433 | CDS | 899533 | 861 | + | 0.227642 | |
DDB_G0291896 | DDB_G0291896 | weakly similar to mammalian NASP (Nuclear Autoantigenic Sperm Protein) a histone chaperone required for DNA replication normal cell cycle progression and cell proliferationbrbr bCommunity annotation:b DDB G0291896 is similar (first blast hit both ways) to the N1N2 protein of Xenopus in humans known as NASP (nuclear autoantigenic sperm protein) a histone chaperone found in all dividing cells and implicated in chromatin assembly (see Wang et al NAR 36 5763-5772 (2008). NASP is required for cell cycle progression and is upregulated in a variety of cancers (see Alekseev et al Reproductive Biology and Endocrinology 7 45 2009).br DDB_G0291896 is overexpressed threefold (p2e-72) in a Dicty strain in which the retinoblastoma-like protein rblA has been disrupted. Most genes with functions in cell cycle progression are overexpressed in this strain and most overexpressed genes have identifiable cell cycle functions (Doquang et al. in preparation) these include other genes involved in chromatin as | DDB0232433 | CDS | 904350 | 1503 | + | 0.314039 |
DDB_G0291898 | DDB_G0291898 | DDB0232433 | CDS | 909614 | 165 | + | 0.345455 | |
DDB_G0291900 | DDB_G0291900 | DDB0232433 | CDS | 911015 | 780 | + | 0.264103 | |
DDB_G0291902 | DDB_G0291902 | DDB0232433 | CDS | 911883 | 1011 | - | 0.229476 | |
DDB_G0291904 | DDB_G0291904 | DDB0232433 | CDS | 915091 | 1791 | + | 0.244556 | |
DDB_G0291906 | DDB_G0291906 | DDB0232433 | CDS | 917876 | 3711 | + | 0.261385 | |
DDB_G0291908 | DDB_G0291908 | DDB0232433 | CDS | 921791 | 1020 | - | 0.204902 | |
DDB_G0291912 | DDB_G0291912 | DDB0232433 | CDS | 931229 | 1251 | - | 0.282174 | |
DDB_G0291914 | DDB_G0291914 | DDB0232433 | CDS | 933442 | 351 | - | 0.230769 | |
DDB_G0291918 | DDB_G0291918 | putative protein serinethreonine kinase CAMK group kinase domain is similar to those of mammalian death-associated protein kinases (DAPK) | DDB0232433 | CDS | 943654 | 2010 | + | 0.287065 |
DDB_G0291920 | DDB_G0291920 | DDB0232433 | CDS | 946580 | 1380 | + | 0.136232 | |
DDB_G0291924 | DDB_G0291924 | DDB0232433 | CDS | 952138 | 939 | + | 0.15442 | |
DDB_G0291926 | DDB_G0291926 | weakly similar ro S. cerevisiae Arc1 a protein that binds tRNA and methionyl- and glutamyl-tRNA synthetases delivering tRNA to them stimulating catalysis and ensuring their localization to the cytoplasm | DDB0232433 | CDS | 959253 | 1092 | - | 0.282967 |
DDB_G0291930_ps | DDB_G0291930 | putative pseudogene similar to a family of Dictyostelium genes including | DDB0232433 | CDS | 906094 | 2850 | - | 0.155789 |
DDB_G0291934 | DDB_G0291934 | DDB0232433 | CDS | 937759 | 2727 | - | 0.164283 | |
DDB_G0291936 | DDB_G0291936 | DDB0232433 | CDS | 962283 | 810 | + | 0.197531 | |
DDB_G0291938 | DDB_G0291938 | DDB0232433 | CDS | 964334 | 1158 | + | 0.221071 | |
DDB_G0291940_RTE | DDB_G0291940 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 872034 | 2310 | + | 0.352381 |
DDB_G0291942 | DDB_G0291942 | DDB0232433 | CDS | 898616 | 477 | + | 0.274633 | |
DDB_G0291946 | DDB_G0291946 | DDB0232433 | CDS | 934204 | 1722 | - | 0.233449 | |
DDB_G0291948 | DDB_G0291948 | belongs to the UPF0539 family similar to human C7orf59 | DDB0232433 | CDS | 936889 | 264 | - | 0.268939 |
DDB_G0291952 | DDB_G0291952 | DDB0232433 | CDS | 841885 | 480 | + | 0.310417 | |
DDB_G0291954_RTE | DDB_G0291954 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 860099 | 756 | + | 0.420635 |
DDB_G0291956_RTE | DDB_G0291956 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 864825 | 237 | + | 0.337553 |
DDB_G0291958_RTE | DDB_G0291958 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 866031 | 3828 | + | 0.309039 |
DDB_G0291960_RTE | DDB_G0291960 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 870523 | 720 | + | 0.398611 |
DDB_G0291962_RTE | DDB_G0291962 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 876601 | 1080 | + | 0.412963 |
DDB_G0291964_RTE | DDB_G0291964 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 893019 | 4221 | - | 0.309879 |
DDB_G0291966 | DDB_G0291966 | DDB0232433 | CDS | 948054 | 939 | - | 0.345048 | |
DDB_G0291968 | DDB_G0291968 | DDB0232433 | CDS | 966638 | 1950 | + | 0.168205 | |
DDB_G0291984 | DDB_G0291984 | DDB0232433 | CDS | 1206606 | 3669 | + | 0.334696 | |
DDB_G0291992 | DDB_G0291992 | no known homologs REMI mutant forms aberrant fruiting bodies (see | DDB0232433 | CDS | 1056383 | 900 | - | 0.244444 |
DDB_G0292000 | DDB_G0292000 | DDB0232433 | CDS | 992955 | 1779 | - | 0.232153 | |
DDB_G0292006 | DDB_G0292006 | DDB0232433 | CDS | 1004992 | 966 | + | 0.247412 | |
DDB_G0292008 | DDB_G0292008 | DDB0232433 | CDS | 1010717 | 2406 | + | 0.201579 | |
DDB_G0292010 | DDB_G0292010 | DDB0232433 | CDS | 1014321 | 2334 | + | 0.288346 | |
DDB_G0292012 | DDB_G0292012 | belongs to the GNAT family conserved in fungi | DDB0232433 | CDS | 1016886 | 1158 | + | 0.239206 |
DDB_G0292016 | DDB_G0292016 | DDB0232433 | CDS | 1027245 | 2757 | + | 0.305767 | |
DDB_G0292018_ps | DDB_G0292018 | putative pseudogene similar to | DDB0232433 | CDS | 1030321 | 135 | + | 0.251852 |
DDB_G0292020 | DDB_G0292020 | DDB0232433 | CDS | 1032623 | 2541 | - | 0.258166 | |
DDB_G0292024 | DDB_G0292024 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232433 | CDS | 1039810 | 501 | + | 0.339321 |
DDB_G0292028 | DDB_G0292028 | DDB0232433 | CDS | 1046109 | 2799 | + | 0.310468 | |
DDB_G0292030 | DDB_G0292030 | DDB0232433 | CDS | 1049058 | 1038 | - | 0.226397 | |
DDB_G0292032 | DDB_G0292032 | DDB0232433 | CDS | 1051056 | 4944 | + | 0.218649 | |
DDB_G0292038 | DDB_G0292038 | conserved in bacteria predicted to have a structural domain found in several acyl-CoA acyltransferase enzymes contains a predicted peroxisomal targeting signal | DDB0232433 | CDS | 1062124 | 813 | + | 0.250923 |
DDB_G0292042 | DDB_G0292042 | DDB0232433 | CDS | 1066047 | 2346 | - | 0.322677 | |
DDB_G0292044 | DDB_G0292044 | DDB0232433 | CDS | 1069821 | 1617 | + | 0.246753 | |
DDB_G0292046 | DDB_G0292046 | DDB0232433 | CDS | 1071921 | 9723 | + | 0.246735 | |
DDB_G0292048 | DDB_G0292048 | DDB0232433 | CDS | 1082258 | 774 | + | 0.237726 | |
DDB_G0292054 | DDB_G0292054 | DDB0232433 | CDS | 1101689 | 1212 | + | 0.331683 | |
DDB_G0292056 | DDB_G0292056 | DDB0232433 | CDS | 1115547 | 5472 | + | 0.272844 | |
DDB_G0292058 | DDB_G0292058 | contains a weak tweety (tty) domain which is of unknown function | DDB0232433 | CDS | 1121898 | 1662 | - | 0.316486 |
DDB_G0292060_RTE | DDB_G0292060 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1125152 | 849 | + | 0.365135 |
DDB_G0292062_RTE | DDB_G0292062 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1126179 | 1362 | + | 0.339941 |
DDB_G0292070 | DDB_G0292070 | DDB0232433 | CDS | 1148827 | 2484 | - | 0.296699 | |
DDB_G0292076 | DDB_G0292076 | DDB0232433 | CDS | 1156278 | 984 | + | 0.284553 | |
DDB_G0292078 | DDB_G0292078 | DDB0232433 | CDS | 1157682 | 168 | - | 0.261905 | |
DDB_G0292080 | DDB_G0292080 | DDB0232433 | CDS | 1159633 | 972 | + | 0.359053 | |
DDB_G0292084_ps | DDB_G0292084 | putative pseudogene similar to D. discoideum gene | DDB0232433 | CDS | 1161454 | 501 | - | 0.411178 |
DDB_G0292086_ps | DDB_G0292086 | putative pseudogene similar to D. discoideum gene | DDB0232433 | CDS | 1166334 | 351 | + | 0.310541 |
DDB_G0292088 | DDB_G0292088 | DDB0232433 | CDS | 1166986 | 336 | - | 0.327381 | |
DDB_G0292090_ps | DDB_G0292090 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232433 | CDS | 1167971 | 507 | - | 0.422091 |
DDB_G0292092 | DDB_G0292092 | DDB0232433 | CDS | 1169702 | 369 | + | 0.311653 | |
DDB_G0292094 | DDB_G0292094 | DDB0232433 | CDS | 1170735 | 1038 | - | 0.300578 | |
DDB_G0292096 | DDB_G0292096 | contains a cytidine and deoxycytidylate deaminase zinc-binding region contains a carbohydrate-binding domain contains a predicted signal peptide | DDB0232433 | CDS | 1176701 | 966 | - | 0.421325 |
DDB_G0292098 | DDB_G0292098 | DDB0232433 | CDS | 1180007 | 3129 | + | 0.259508 | |
DDB_G0292106 | DDB_G0292106 | DDB0232433 | CDS | 1191356 | 903 | + | 0.293466 | |
DDB_G0292108 | DDB_G0292108 | DDB0232433 | CDS | 1192584 | 2490 | - | 0.278715 | |
DDB_G0292110 | DDB_G0292110 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232433 | CDS | 1201167 | 1053 | + | 0.253561 |
DDB_G0292114 | DDB_G0292114 | DDB0232433 | CDS | 1217707 | 627 | - | 0.236045 | |
DDB_G0292116 | DDB_G0292116 | belongs to the short-chain dehydrogenasesreductases family similar to human HSDL2 (Hydroxysteroid dehydrogenase-like protein 2) | DDB0232433 | CDS | 1219275 | 849 | - | 0.328622 |
DDB_G0292124 | DDB_G0292124 | DDB0232433 | CDS | 1228678 | 3513 | - | 0.24936 | |
DDB_G0292128 | DDB_G0292128 | DDB0232433 | CDS | 1233335 | 5919 | - | 0.281298 | |
DDB_G0292132 | DDB_G0292132 | members of the multi antimicrobial extrusion (MATE) family function as drugsodium antiporters and are found in bacteria archaea and eukaryotes these proteins are predicted to have 12 alpha-helical transmembrane regions | DDB0232433 | CDS | 1244360 | 2007 | - | 0.269058 |
DDB_G0292138 | DDB_G0292138 | DDB0232433 | CDS | 1250981 | 552 | + | 0.309783 | |
DDB_G0292140 | DDB_G0292140 | DDB0232433 | CDS | 1256247 | 1566 | - | 0.295658 | |
DDB_G0292144 | DDB_G0292144 | DDB0232433 | CDS | 1267882 | 1059 | - | 0.234183 | |
DDB_G0292146 | DDB_G0292146 | DDB0232433 | CDS | 1271733 | 1137 | + | 0.208443 | |
DDB_G0292148 | DDB_G0292148 | DDB0232433 | CDS | 1273206 | 1569 | - | 0.262588 | |
DDB_G0292154 | DDB_G0292154 | DDB0232433 | CDS | 1006156 | 4152 | - | 0.221821 | |
DDB_G0292158 | DDB_G0292158 | DDB0232433 | CDS | 1139831 | 717 | + | 0.241283 | |
DDB_G0292160 | DDB_G0292160 | DDB0232433 | CDS | 1263546 | 525 | + | 0.306667 | |
DDB_G0292162 | DDB_G0292162 | DDB0232433 | CDS | 1269573 | 1251 | - | 0.211831 | |
DDB_G0292166 | DDB_G0292166 | DDB0232433 | CDS | 968881 | 3309 | + | 0.187972 | |
DDB_G0292170 | DDB_G0292170 | DDB0232433 | CDS | 1113786 | 696 | + | 0.195402 | |
DDB_G0292172_RTE | DDB_G0292172 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 1128211 | 1065 | - | 0.292019 |
DDB_G0292174_RTE | DDB_G0292174 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 1130560 | 1335 | + | 0.307116 |
DDB_G0292178_ps | DDB_G0292178 | putative pseudogene similar to D. discoideum gene | DDB0232433 | CDS | 1163265 | 432 | - | 0.31713 |
DDB_G0292186 | DDB_G0292186 | DDB0232433 | CDS | 1196812 | 3402 | + | 0.255144 | |
DDB_G0292188 | DDB_G0292188 | conserved hypothetical Dictyostelium protein contains a weak von Willebrand factor type A domain | DDB0232433 | CDS | 1253197 | 4386 | - | 0.331509 |
DDB_G0292190 | DDB_G0292190 | DDB0232433 | CDS | 1259597 | 2835 | - | 0.257143 | |
DDB_G0292192 | DDB_G0292192 | DDB0232433 | CDS | 1275799 | 1689 | - | 0.253996 | |
DDB_G0292194 | DDB_G0292194 | DDB0232433 | CDS | 1279409 | 1680 | + | 0.250595 | |
DDB_G0292196 | DDB_G0292196 | DDB0232433 | CDS | 1282462 | 1959 | - | 0.235835 | |
DDB_G0292198_RTE | DDB_G0292198 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1298736 | 565 | - | 0.318584 |
DDB_G0292202 | DDB_G0292202 | DDB0232433 | CDS | 1065129 | 777 | + | 0.253539 | |
DDB_G0292208 | DDB_G0292208 | DDB0232433 | CDS | 1336984 | 327 | - | 0.33945 | |
DDB_G0292210 | DDB_G0292210 | DDB0232433 | CDS | 1335430 | 564 | - | 0.235816 | |
DDB_G0292214 | DDB_G0292214 | DDB0232433 | CDS | 1330581 | 2280 | - | 0.291667 | |
DDB_G0292226 | DDB_G0292226 | DDB0232433 | CDS | 1323250 | 1092 | + | 0.244505 | |
DDB_G0292228 | DDB_G0292228 | DDB0232433 | CDS | 1321609 | 120 | - | 0.233333 | |
DDB_G0292230 | DDB_G0292230 | DDB0232433 | CDS | 1311188 | 9000 | + | 0.296667 | |
DDB_G0292232 | DDB_G0292232 | DDB0232433 | CDS | 1340609 | 210 | - | 0.285714 | |
DDB_G0292234 | DDB_G0292234 | DDB0232433 | CDS | 1341999 | 5478 | - | 0.301387 | |
DDB_G0292236 | DDB_G0292236 | conserved hypothetical protein contains a putative signal peptide | DDB0232433 | CDS | 1348680 | 1002 | + | 0.241517 |
DDB_G0292240 | DDB_G0292240 | DDB0232433 | CDS | 1358978 | 1140 | + | 0.317544 | |
DDB_G0292246 | DDB_G0292246 | DDB0232433 | CDS | 1370987 | 891 | + | 0.274972 | |
DDB_G0292248 | DDB_G0292248 | DDB0232433 | CDS | 1372308 | 945 | - | 0.284656 | |
DDB_G0292252 | DDB_G0292252 | DDB0232433 | CDS | 1302637 | 3771 | - | 0.222222 | |
DDB_G0292254 | DDB_G0292254 | DDB0232433 | CDS | 1308810 | 447 | - | 0.239374 | |
DDB_G0292256 | DDB_G0292256 | DDB0232433 | CDS | 1339608 | 219 | + | 0.360731 | |
DDB_G0292258 | DDB_G0292258 | DDB0232433 | CDS | 1307362 | 741 | + | 0.236167 | |
DDB_G0292260_RTE | DDB_G0292260 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 1373916 | 3793 | + | 0.321645 |
DDB_G0292272_TE | DDB_G0292272 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232433 | CDS | 1379067 | 2148 | - | 0.304935 |
DDB_G0292274_ps | DDB_G0292274 | DDB0232433 | CDS | 1381886 | 1044 | + | 0.228927 | |
DDB_G0292280_ps | DDB_G0292280 | putative pseudogene similar to a protein family including | DDB0232433 | CDS | 1383635 | 771 | + | 0.263294 |
DDB_G0292282 | DDB_G0292282 | DDB0232433 | CDS | 1385822 | 1779 | + | 0.226532 | |
DDB_G0292284 | DDB_G0292284 | DDB0232433 | CDS | 1387934 | 1557 | + | 0.226076 | |
DDB_G0292286 | DDB_G0292286 | DDB0232433 | CDS | 1390052 | 3726 | + | 0.27241 | |
DDB_G0292288 | DDB_G0292288 | DDB0232433 | CDS | 1393939 | 1008 | - | 0.318452 | |
DDB_G0292290 | DDB_G0292290 | DDB0232433 | CDS | 1396696 | 2310 | + | 0.237662 | |
DDB_G0292292 | DDB_G0292292 | DDB0232433 | CDS | 1399162 | 1989 | - | 0.23278 | |
DDB_G0292298 | DDB_G0292298 | DDB0232433 | CDS | 1424473 | 501 | - | 0.307385 | |
DDB_G0292302 | DDB_G0292302 | DDB0232433 | CDS | 1428528 | 2319 | - | 0.330746 | |
DDB_G0292312 | DDB_G0292312 | DDB0232433 | CDS | 1454104 | 1593 | - | 0.287508 | |
DDB_G0292320 | DDB_G0292320 | DDB0232433 | CDS | 1479615 | 786 | + | 0.270992 | |
DDB_G0292322 | DDB_G0292322 | DDB0232433 | CDS | 1481023 | 873 | - | 0.250859 | |
DDB_G0292330 | DDB_G0292330 | DDB0232433 | CDS | 1495780 | 543 | + | 0.224678 | |
DDB_G0292332 | DDB_G0292332 | DDB0232433 | CDS | 1500852 | 561 | + | 0.210339 | |
DDB_G0292334 | DDB_G0292334 | DDB0232433 | CDS | 1502579 | 2331 | - | 0.277134 | |
DDB_G0292336 | DDB_G0292336 | DDB0232433 | CDS | 1512244 | 1236 | - | 0.223301 | |
DDB_G0292338_RTE | DDB_G0292338 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1524225 | 3096 | - | 0.348514 |
DDB_G0292340 | DDB_G0292340 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232433 | CDS | 1444957 | 5022 | - | 0.202708 |
DDB_G0292342 | DDB_G0292342 | DDB0232433 | CDS | 1441126 | 1017 | + | 0.212389 | |
DDB_G0292350 | DDB_G0292350 | DDB0232433 | CDS | 1496951 | 3675 | + | 0.270204 | |
DDB_G0292352_TE | DDB_G0292352 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232433 | CDS | 1508214 | 1770 | - | 0.314689 |
DDB_G0292354 | DDB_G0292354 | putative protein serinethreonine kinase TTBK family similar to casein kinase similar to mammalian tau-tubulin kinase (TTBK) which phosphorylates the microtubule-associated protein tau implicated in Alzheimer's disease | DDB0232433 | CDS | 1420214 | 1488 | + | 0.30578 |
DDB_G0292360 | DDB_G0292360 | DDB0232433 | CDS | 1482971 | 192 | + | 0.28125 | |
DDB_G0292362 | DDB_G0292362 | putative ortholog of mammalian thimet oligopeptidase THOP1 involved in cytoplasmic peptide degradation including neuropeptides and S. cerevisiae PRD1 involved in degradation of mitochondrial proteins and of presequence peptides cleaved from imported proteins | DDB0232433 | CDS | 1486590 | 2022 | + | 0.32542 |
DDB_G0292364_TE | DDB_G0292364 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232433 | CDS | 1506515 | 942 | - | 0.235669 |
DDB_G0292366 | DDB_G0292366 | DDB0232433 | CDS | 1514365 | 906 | - | 0.339956 | |
DDB_G0292368 | DDB_G0292368 | DDB0232433 | CDS | 1516008 | 714 | + | 0.312325 | |
DDB_G0292370_RTE | DDB_G0292370 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 1516913 | 531 | - | 0.306968 |
DDB_G0292372_RTE | DDB_G0292372 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1518919 | 2856 | - | 0.34979 |
DDB_G0292374_RTE | DDB_G0292374 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1522623 | 1086 | - | 0.413444 |
DDB_G0292376_RTE | DDB_G0292376 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1527937 | 1080 | - | 0.414815 |
DDB_G0292394 | DDB_G0292394 | DDB0232433 | CDS | 1536171 | 3378 | - | 0.214032 | |
DDB_G0292396 | DDB_G0292396 | DDB0232433 | CDS | 1540535 | 3366 | + | 0.258467 | |
DDB_G0292408 | DDB_G0292408 | DDB0232433 | CDS | 1560005 | 642 | + | 0.221184 | |
DDB_G0292410 | DDB_G0292410 | similar to H. sapiens zinc finger CCCH-type containing 15 and M. musculus immediate early response erythropoietin 4 | DDB0232433 | CDS | 1561008 | 1122 | - | 0.336898 |
DDB_G0292412 | DDB_G0292412 | similar to S. cerevisiae and S. pombe TRK1 and TRK2 potassium transporters contains 9 predicted transmembrane domains | DDB0232433 | CDS | 1563103 | 1947 | - | 0.260401 |
DDB_G0292414 | DDB_G0292414 | DDB0232433 | CDS | 1566054 | 2439 | - | 0.222222 | |
DDB_G0292416 | DDB_G0292416 | DDB0232433 | CDS | 1569201 | 2793 | - | 0.257787 | |
DDB_G0292422 | DDB_G0292422 | contains two RNA recognition motifs (RRMs) which are putative RNA binding domains | DDB0232433 | CDS | 1580488 | 2064 | - | 0.265988 |
DDB_G0292424 | DDB_G0292424 | DDB0232433 | CDS | 1593747 | 1017 | + | 0.285152 | |
DDB_G0292428 | DDB_G0292428 | DDB0232433 | CDS | 1601647 | 1203 | - | 0.240233 | |
DDB_G0292430 | DDB_G0292430 | DDB0232433 | CDS | 1609068 | 1323 | - | 0.249433 | |
DDB_G0292432 | DDB_G0292432 | DDB0232433 | CDS | 1610862 | 1815 | - | 0.293113 | |
DDB_G0292434 | DDB_G0292434 | DDB0232433 | CDS | 1618538 | 771 | + | 0.311284 | |
DDB_G0292438 | DDB_G0292438 | DDB0232433 | CDS | 1631231 | 816 | + | 0.230392 | |
DDB_G0292440 | DDB_G0292440 | DDB0232433 | CDS | 1632296 | 1068 | - | 0.282772 | |
DDB_G0292442 | DDB_G0292442 | phosphorylates NAD to NADP | DDB0232433 | CDS | 1638801 | 2574 | - | 0.266123 |
DDB_G0292444 | DDB_G0292444 | DDB0232433 | CDS | 1653442 | 1302 | - | 0.208141 | |
DDB_G0292446 | DDB_G0292446 | DDB0232433 | CDS | 1655640 | 3909 | + | 0.294705 | |
DDB_G0292448 | DDB_G0292448 | DDB0232433 | CDS | 1659633 | 1044 | - | 0.234674 | |
DDB_G0292450 | DDB_G0292450 | DDB0232433 | CDS | 1660973 | 1719 | + | 0.201862 | |
DDB_G0292452_RTE | DDB_G0292452 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232433 | CDS | 1664228 | 2160 | + | 0.371759 |
DDB_G0292454 | DDB_G0292454 | DDB0232433 | CDS | 1666854 | 1032 | + | 0.246124 | |
DDB_G0292458 | DDB_G0292458 | DDB0232433 | CDS | 1671355 | 1767 | + | 0.273345 | |
DDB_G0292462 | DDB_G0292462 | DDB0232433 | CDS | 1678244 | 972 | + | 0.322016 | |
DDB_G0292464 | DDB_G0292464 | homolog of human DGCR14 believed to play a role in velocardiofacialDiGeorge syndrome (VCFSDGS) | DDB0232433 | CDS | 1679719 | 1584 | + | 0.277778 |
DDB_G0292468 | DDB_G0292468 | DDB0232433 | CDS | 1683880 | 2076 | + | 0.27553 | |
DDB_G0292472 | DDB_G0292472 | DDB0232433 | CDS | 1689735 | 1653 | + | 0.238355 | |
DDB_G0292474 | DDB_G0292474 | DDB0232433 | CDS | 1692117 | 930 | - | 0.247312 | |
DDB_G0292476 | DDB_G0292476 | similar to human PRSS16 (thymus-specific serine protease) contains a putative signal peptide | DDB0232433 | CDS | 1697908 | 1458 | + | 0.266804 |
DDB_G0292478 | DDB_G0292478 | DDB0232433 | CDS | 1704175 | 3804 | + | 0.298896 | |
DDB_G0292480 | DDB_G0292480 | DDB0232433 | CDS | 1708601 | 2154 | + | 0.303621 | |
DDB_G0292482 | DDB_G0292482 | DDB0232433 | CDS | 1711273 | 552 | + | 0.246377 | |
DDB_G0292484 | DDB_G0292484 | DDB0232433 | CDS | 1712190 | 1335 | + | 0.225468 | |
DDB_G0292492 | DDB_G0292492 | DDB0232433 | CDS | 1734904 | 678 | + | 0.193215 | |
DDB_G0292494 | DDB_G0292494 | similar to human TTC39A and TTC39B matches PFAM outer membrane protein IML2 mitochondrialtetratricopeptide repeat protein 39 | DDB0232433 | CDS | 1739944 | 2388 | - | 0.220268 |
DDB_G0292498 | DDB_G0292498 | DDB0232433 | CDS | 1745775 | 153 | - | 0.326797 | |
DDB_G0292500 | DDB_G0292500 | DDB0232433 | CDS | 1746019 | 741 | - | 0.186235 | |
DDB_G0292502 | DDB_G0292502 | DDB0232433 | CDS | 1747364 | 558 | + | 0.236559 | |
DDB_G0292506 | DDB_G0292506 | DDB0232433 | CDS | 1755318 | 1935 | - | 0.327132 | |
DDB_G0292516_RTE | DDB_G0292516 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 1532417 | 1335 | + | 0.307865 |
DDB_G0292518 | DDB_G0292518 | DDB0232433 | CDS | 1553006 | 261 | + | 0.348659 | |
DDB_G0292520 | DDB_G0292520 | DDB0232433 | CDS | 1591188 | 747 | + | 0.322624 | |
DDB_G0292524 | DDB_G0292524 | dymeclin ortholog involoved in Dyggve-Melchior-Clausen syndrome | DDB0232433 | CDS | 1597521 | 2796 | - | 0.24535 |
DDB_G0292526 | DDB_G0292526 | DDB0232433 | CDS | 1607713 | 177 | - | 0.214689 | |
DDB_G0292528 | DDB_G0292528 | DDB0232433 | CDS | 1616689 | 897 | - | 0.331104 | |
DDB_G0292530 | DDB_G0292530 | DDB0232433 | CDS | 1625548 | 2967 | + | 0.276373 | |
DDB_G0292532_ps | DDB_G0292532 | DDB0232433 | CDS | 1629116 | 1386 | - | 0.26912 | |
DDB_G0292534 | DDB_G0292534 | DDB0232433 | CDS | 1633774 | 180 | + | 0.316667 | |
DDB_G0292536_ps | DDB_G0292536 | putative pseudogene carbohydratepurine kinase domain-containing protein similar to | DDB0232433 | CDS | 1634108 | 201 | - | 0.268657 |
DDB_G0292540_RTE | DDB_G0292540 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 1700323 | 867 | - | 0.311419 |
DDB_G0292542 | DDB_G0292542 | DDB0232433 | CDS | 1702357 | 318 | - | 0.31761 | |
DDB_G0292546 | DDB_G0292546 | DDB0232433 | CDS | 1752243 | 741 | - | 0.210526 | |
DDB_G0292548_RTE | DDB_G0292548 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1759374 | 684 | - | 0.333333 |
DDB_G0292550 | DDB_G0292550 | DDB0232433 | CDS | 1642791 | 4194 | - | 0.223891 | |
DDB_G0292556 | DDB_G0292556 | DDB0232433 | CDS | 1877443 | 4584 | + | 0.220986 | |
DDB_G0292568 | DDB_G0292568 | DDB0232433 | CDS | 1778529 | 1044 | - | 0.29023 | |
DDB_G0292570 | DDB_G0292570 | DDB0232433 | CDS | 1784981 | 522 | - | 0.254789 | |
DDB_G0292572_ps | DDB_G0292572 | putative pseudogene fragment similar to D. discoideum gene | DDB0232433 | CDS | 1789760 | 309 | + | 0.242718 |
DDB_G0292574 | DDB_G0292574 | DDB0232433 | CDS | 1791327 | 870 | + | 0.270115 | |
DDB_G0292576_ps | DDB_G0292576 | putative pseudogene fragment very similar to | DDB0232433 | CDS | 1792509 | 1263 | - | 0.223278 |
DDB_G0292578 | DDB_G0292578 | DDB0232433 | CDS | 1796405 | 3402 | - | 0.237507 | |
DDB_G0292580_ps | DDB_G0292580 | putative pseudogene similar to D. discoideum gene | DDB0232433 | CDS | 1800000 | 609 | - | 0.205255 |
DDB_G0292582_ps | DDB_G0292582 | putative pseudogene similar to | DDB0232433 | CDS | 1801613 | 333 | - | 0.228228 |
DDB_G0292586 | DDB_G0292586 | DDB0232433 | CDS | 1803595 | 1368 | + | 0.29386 | |
DDB_G0292590 | DDB_G0292590 | DDB0232433 | CDS | 1817104 | 2292 | - | 0.202007 | |
DDB_G0292598 | DDB_G0292598 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232433 | CDS | 1825370 | 204 | + | 0.29902 |
DDB_G0292602 | DDB_G0292602 | DDB0232433 | CDS | 1827272 | 879 | - | 0.31058 | |
DDB_G0292610 | DDB_G0292610 | DDB0232433 | CDS | 1838484 | 768 | - | 0.356771 | |
DDB_G0292612 | DDB_G0292612 | DDB0232433 | CDS | 1840465 | 1503 | + | 0.132402 | |
DDB_G0292614 | DDB_G0292614 | DDB0232433 | CDS | 1842218 | 282 | - | 0.251773 | |
DDB_G0292616 | DDB_G0292616 | DDB0232433 | CDS | 1845104 | 2310 | + | 0.224675 | |
DDB_G0292624 | DDB_G0292624 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | DDB0232433 | CDS | 1864394 | 942 | + | 0.298301 |
DDB_G0292626 | DDB_G0292626 | belongs to the RAS-like GTPase superfamily similar to bacterial GTP-binding protein YchF similar to D. purpureum protein | DDB0232433 | CDS | 1866598 | 1230 | + | 0.293496 |
DDB_G0292628 | DDB_G0292628 | DDB0232433 | CDS | 1868427 | 540 | + | 0.194444 | |
DDB_G0292630 | DDB_G0292630 | DDB0232433 | CDS | 1870947 | 642 | + | 0.285047 | |
DDB_G0292634 | DDB_G0292634 | DDB0232433 | CDS | 1874997 | 495 | + | 0.230303 | |
DDB_G0292636 | DDB_G0292636 | DDB0232433 | CDS | 1875598 | 483 | - | 0.281574 | |
DDB_G0292638 | DDB_G0292638 | DDB0232433 | CDS | 1888191 | 999 | - | 0.293293 | |
DDB_G0292640 | DDB_G0292640 | DDB0232433 | CDS | 1889950 | 1107 | + | 0.231256 | |
DDB_G0292642 | DDB_G0292642 | DDB0232433 | CDS | 1892855 | 2712 | - | 0.297935 | |
DDB_G0292644 | DDB_G0292644 | DDB0232433 | CDS | 1897455 | 792 | + | 0.291667 | |
DDB_G0292646 | DDB_G0292646 | DDB0232433 | CDS | 1898644 | 879 | - | 0.195677 | |
DDB_G0292648 | DDB_G0292648 | has similarity to the mammalian coiled-coil domain-containing protein 12 (CCDC12) the cwf18 family is involved in mRNA splicing which has been isolated as a subcomplex of the splicosome in Schizosaccharomyces pombe | DDB0232433 | CDS | 1901580 | 978 | + | 0.202454 |
DDB_G0292650 | DDB_G0292650 | DDB0232433 | CDS | 1902913 | 774 | + | 0.267442 | |
DDB_G0292652 | DDB_G0292652 | DDB0232433 | CDS | 1905792 | 612 | + | 0.243464 | |
DDB_G0292656 | DDB_G0292656 | DDB0232433 | CDS | 1913079 | 2379 | - | 0.211433 | |
DDB_G0292658 | DDB_G0292658 | DDB0232433 | CDS | 1915721 | 1035 | - | 0.226087 | |
DDB_G0292660 | DDB_G0292660 | DDB0232433 | CDS | 1917310 | 450 | - | 0.248889 | |
DDB_G0292662 | DDB_G0292662 | DDB0232433 | CDS | 1918021 | 1152 | + | 0.246528 | |
DDB_G0292664 | DDB_G0292664 | DDB0232433 | CDS | 1919877 | 531 | + | 0.354049 | |
DDB_G0292666 | DDB_G0292666 | DDB0232433 | CDS | 1920980 | 1563 | - | 0.264875 | |
DDB_G0292668 | DDB_G0292668 | DDB0232433 | CDS | 1923247 | 3288 | + | 0.218066 | |
DDB_G0292672_ps | DDB_G0292672 | putative pseudogene fragment similar to the neighboring gene | DDB0232433 | CDS | 1927372 | 756 | - | 0.190476 |
DDB_G0292674 | DDB_G0292674 | DDB0232433 | CDS | 1929551 | 3237 | - | 0.216559 | |
DDB_G0292680 | DDB_G0292680 | DDB0232433 | CDS | 1939703 | 1920 | + | 0.301562 | |
DDB_G0292682 | DDB_G0292682 | DDB0232433 | CDS | 1942435 | 3882 | + | 0.279495 | |
DDB_G0292684 | DDB_G0292684 | DDB0232433 | CDS | 1946830 | 672 | - | 0.160714 | |
DDB_G0292692 | DDB_G0292692 | DDB0232433 | CDS | 1955631 | 882 | + | 0.246032 | |
DDB_G0292694 | DDB_G0292694 | DDB0232433 | CDS | 1956745 | 2355 | - | 0.227176 | |
DDB_G0292698 | DDB_G0292698 | DDB0232433 | CDS | 1997307 | 921 | - | 0.365907 | |
DDB_G0292700 | DDB_G0292700 | DDB0232433 | CDS | 1999329 | 894 | - | 0.241611 | |
DDB_G0292704 | DDB_G0292704 | DDB0232433 | CDS | 1843458 | 321 | - | 0.286604 | |
DDB_G0292710 | DDB_G0292710 | contains one PPIase cyclophilin-type domain and one RRM (RNA recognition motif) domain homolog of human PPIL4 and S. pombe cyp6 PPIase is an enzyme that accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232433 | CDS | 1995447 | 1470 | - | 0.278912 |
DDB_G0292712_RTE | DDB_G0292712 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 1777391 | 275 | + | 0.323636 |
DDB_G0292714 | DDB_G0292714 | DDB0232433 | CDS | 1780390 | 4446 | + | 0.234818 | |
DDB_G0292718_ps | DDB_G0292718 | putative pseudogene fragment similar to | DDB0232433 | CDS | 1794964 | 234 | - | 0.269231 |
DDB_G0292720_ps | DDB_G0292720 | putative pseudogene fragment similar to | DDB0232433 | CDS | 1795540 | 294 | + | 0.309524 |
DDB_G0292722 | DDB_G0292722 | DDB0232433 | CDS | 1834902 | 1026 | - | 0.246589 | |
DDB_G0292726_RTE | DDB_G0292726 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 1910704 | 1335 | - | 0.307865 |
DDB_G0292728 | DDB_G0292728 | DDB0232433 | CDS | 2001708 | 464 | + | 0.258621 | |
DDB_G0292734 | DDB_G0292734 | putative eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase putative protein serinethreonine kinase related to the GCN2 (general control non-derepressible) family of protein kinases that phosphorylate the alpha subunit of eIF2 | DDB0232433 | CDS | 2002272 | 888 | + | 0.324324 |
DDB_G0292738 | DDB_G0292738 | DDB0232433 | CDS | 2081220 | 900 | + | 0.277778 | |
DDB_G0292740 | DDB_G0292740 | related to H. sapiens BCSC-1 (LOH11CR2A) a possible tumor suppressor gene | DDB0232433 | CDS | 2078010 | 2733 | + | 0.279546 |
DDB_G0292742 | DDB_G0292742 | contains a dilute domain found at the carboxyl terminus of non-muscle myosin V | DDB0232433 | CDS | 2074742 | 2640 | + | 0.267803 |
DDB_G0292746 | DDB_G0292746 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity also contains a PH domain involved in intracellular signaling | DDB0232433 | CDS | 2069434 | 2898 | + | 0.327467 |
DDB_G0292748 | DDB_G0292748 | DDB0232433 | CDS | 2066863 | 1068 | - | 0.309925 | |
DDB_G0292750 | DDB_G0292750 | DDB0232433 | CDS | 2064418 | 2055 | + | 0.254988 | |
DDB_G0292752 | DDB_G0292752 | DDB0232433 | CDS | 2063367 | 465 | + | 0.329032 | |
DDB_G0292754 | DDB_G0292754 | DDB0232433 | CDS | 2058466 | 294 | + | 0.380952 | |
DDB_G0292756 | DDB_G0292756 | DDB0232433 | CDS | 2057283 | 516 | + | 0.257752 | |
DDB_G0292764 | DDB_G0292764 | DDB0232433 | CDS | 2050588 | 408 | - | 0.306373 | |
DDB_G0292766 | DDB_G0292766 | DDB0232433 | CDS | 2041426 | 861 | - | 0.221835 | |
DDB_G0292774 | DDB_G0292774 | DDB0232433 | CDS | 2013605 | 1098 | + | 0.270492 | |
DDB_G0292776 | DDB_G0292776 | DDB0232433 | CDS | 2016449 | 627 | + | 0.255183 | |
DDB_G0292780 | DDB_G0292780 | DDB0232433 | CDS | 2019712 | 1416 | - | 0.293785 | |
DDB_G0292796_RTE | DDB_G0292796 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 2083172 | 3144 | - | 0.33874 |
DDB_G0292798_RTE | DDB_G0292798 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 2086606 | 1032 | - | 0.323643 |
DDB_G0292802 | DDB_G0292802 | DDB0232433 | CDS | 2089930 | 3645 | - | 0.19369 | |
DDB_G0292818 | DDB_G0292818 | DDB0232433 | CDS | 2182883 | 633 | + | 0.240126 | |
DDB_G0292822 | DDB_G0292822 | DDB0232433 | CDS | 2100987 | 1800 | + | 0.3 | |
DDB_G0292824 | DDB_G0292824 | DDB0232433 | CDS | 2103859 | 1794 | + | 0.299889 | |
DDB_G0292826 | DDB_G0292826 | DDB0232433 | CDS | 2106426 | 1785 | + | 0.29916 | |
DDB_G0292828 | DDB_G0292828 | DDB0232433 | CDS | 2109065 | 1872 | + | 0.269231 | |
DDB_G0292832 | DDB_G0292832 | DDB0232433 | CDS | 2127296 | 798 | - | 0.285714 | |
DDB_G0292834 | DDB_G0292834 | DDB0232433 | CDS | 2130562 | 1710 | - | 0.29883 | |
DDB_G0292836 | DDB_G0292836 | similar to minor histocompatibility antigen H13 belongs to the peptidase A22B family | DDB0232433 | CDS | 2133981 | 1065 | - | 0.276995 |
DDB_G0292842_ps | DDB_G0292842 | putative pseudogene very similar to | DDB0232433 | CDS | 2138630 | 438 | - | 0.33105 |
DDB_G0292844 | DDB_G0292844 | DDB0232433 | CDS | 2139605 | 639 | - | 0.312989 | |
DDB_G0292846 | DDB_G0292846 | DDB0232433 | CDS | 2145680 | 1107 | + | 0.290876 | |
DDB_G0292848 | DDB_G0292848 | DDB0232433 | CDS | 2146988 | 2919 | - | 0.310038 | |
DDB_G0292852 | DDB_G0292852 | ortholog of human LACE1 an AFG1-like ATPase and similar to yeast AFG1 family of proteins contains a P-loop motif and are predicted to be ATPases | DDB0232433 | CDS | 2099022 | 1584 | + | 0.279672 |
DDB_G0292854 | DDB_G0292854 | DDB0232433 | CDS | 2154718 | 2121 | - | 0.27157 | |
DDB_G0292856 | DDB_G0292856 | DDB0232433 | CDS | 2162983 | 2796 | + | 0.202074 | |
DDB_G0292858 | DDB_G0292858 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity also contains 10 predicted transmembrane domains | DDB0232433 | CDS | 2166120 | 3570 | - | 0.291036 |
DDB_G0292860 | DDB_G0292860 | DDB0232433 | CDS | 2170773 | 1173 | - | 0.306905 | |
DDB_G0292866 | DDB_G0292866 | DDB0232433 | CDS | 2176999 | 2601 | - | 0.247597 | |
DDB_G0292874 | DDB_G0292874 | DDB0232433 | CDS | 2190855 | 678 | - | 0.241888 | |
DDB_G0292876 | DDB_G0292876 | DDB0232433 | CDS | 2191825 | 1821 | + | 0.278418 | |
DDB_G0292880 | DDB_G0292880 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232433 | CDS | 2200299 | 1833 | + | 0.286961 |
DDB_G0292882 | DDB_G0292882 | DDB0232433 | CDS | 2208837 | 1020 | - | 0.32549 | |
DDB_G0292884 | DDB_G0292884 | DDB0232433 | CDS | 2211021 | 2628 | + | 0.325723 | |
DDB_G0292886 | DDB_G0292886 | DDB0232433 | CDS | 2214235 | 1485 | + | 0.249158 | |
DDB_G0292888 | DDB_G0292888 | DDB0232433 | CDS | 2216174 | 657 | + | 0.258752 | |
DDB_G0292890 | DDB_G0292890 | DDB0232433 | CDS | 2218813 | 366 | + | 0.229508 | |
DDB_G0292892 | DDB_G0292892 | DDB0232433 | CDS | 2219566 | 327 | + | 0.302752 | |
DDB_G0292894 | DDB_G0292894 | deaminates L-ornithine to L-proline this family also contains mu-crystallin the major component of the eye lens in several Australian marsupials | DDB0232433 | CDS | 2220707 | 1107 | - | 0.296296 |
DDB_G0292900 | DDB_G0292900 | DDB0232433 | CDS | 2233950 | 1497 | + | 0.273881 | |
DDB_G0292902 | DDB_G0292902 | the SWIM domain is found in variety of prokaryotic and eukaryotic proteins it is predicted to have DNA-binding and protein-protein interaction functions in different contexts | DDB0232433 | CDS | 2238007 | 1857 | - | 0.234249 |
DDB_G0292906 | DDB_G0292906 | DDB0232433 | CDS | 2252539 | 372 | - | 0.290323 | |
DDB_G0292914 | DDB_G0292914 | DDB0232433 | CDS | 2269065 | 723 | + | 0.262794 | |
DDB_G0292916 | DDB_G0292916 | DDB0232433 | CDS | 2269986 | 327 | - | 0.217125 | |
DDB_G0292918 | DDB_G0292918 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232433 | CDS | 2271200 | 1728 | - | 0.333333 |
DDB_G0292920 | DDB_G0292920 | tensin family protein (related to the tumor suppressor PTEN) contains a a lipid phosphatase domain and a C2-like domain | DDB0232433 | CDS | 2274050 | 1362 | - | 0.259912 |
DDB_G0292922 | DDB_G0292922 | DDB0232433 | CDS | 2276495 | 447 | + | 0.232662 | |
DDB_G0292928 | DDB_G0292928 | DDB0232433 | CDS | 2282811 | 483 | - | 0.233954 | |
DDB_G0292930 | DDB_G0292930 | DDB0232433 | CDS | 2283488 | 2304 | + | 0.258681 | |
DDB_G0292932 | DDB_G0292932 | DDB0232433 | CDS | 2286339 | 2307 | - | 0.192458 | |
DDB_G0292934 | DDB_G0292934 | DDB0232433 | CDS | 2295609 | 2343 | - | 0.198037 | |
DDB_G0292936 | DDB_G0292936 | DDB0232433 | CDS | 2298560 | 2460 | - | 0.199593 | |
DDB_G0292938_RTE | DDB_G0292938 | DDB0232433 | CDS | 2258753 | 324 | + | 0.327161 | |
DDB_G0292940 | DDB_G0292940 | DDB0232433 | CDS | 2158048 | 219 | - | 0.232877 | |
DDB_G0292946 | DDB_G0292946 | similar to D. purpureum protein contains a putative signal sequence and one central transmembrane domain | DDB0232433 | CDS | 2228053 | 1254 | + | 0.254386 |
DDB_G0292950 | DDB_G0292950 | DDB0232433 | CDS | 2289490 | 2325 | - | 0.205591 | |
DDB_G0292952 | DDB_G0292952 | DDB0232433 | CDS | 2292229 | 2727 | - | 0.19802 | |
DDB_G0292954_TE | DDB_G0292954 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232433 | CDS | 2301581 | 714 | + | 0.323529 |
DDB_G0292960 | DDB_G0292960 | DDB0232433 | CDS | 2129207 | 1173 | + | 0.225916 | |
DDB_G0292962 | DDB_G0292962 | DDB0232433 | CDS | 2140644 | 642 | - | 0.309969 | |
DDB_G0292964 | DDB_G0292964 | DDB0232433 | CDS | 2142125 | 1101 | - | 0.273388 | |
DDB_G0292966 | DDB_G0292966 | DDB0232433 | CDS | 2143669 | 810 | - | 0.341975 | |
DDB_G0292968 | DDB_G0292968 | similar to beta-1-31-4-endoglucanase expressed in pstAO cells and in upper cup during culmination | DDB0232433 | CDS | 2151110 | 2268 | - | 0.315256 |
DDB_G0292970 | DDB_G0292970 | DDB0232433 | CDS | 2176472 | 210 | - | 0.3 | |
DDB_G0292972 | DDB_G0292972 | similar to hypothetical bacterial protein contains a weak SIR2 domain | DDB0232433 | CDS | 2196528 | 3504 | + | 0.321347 |
DDB_G0292976 | DDB_G0292976 | similar to D. purpureum protein contains seven predicted transmembrane domains | DDB0232433 | CDS | 2224445 | 1644 | + | 0.212287 |
DDB_G0292978 | DDB_G0292978 | DDB0232433 | CDS | 2236386 | 1326 | + | 0.282805 | |
DDB_G0292988 | DDB_G0292988 | DDB0232433 | CDS | 2312391 | 5034 | - | 0.319031 | |
DDB_G0292990 | DDB_G0292990 | DDB0232433 | CDS | 2303391 | 2040 | - | 0.194608 | |
DDB_G0293014 | DDB_G0293014 | similar to human PRSS16 (thymus-specific serine protease) contains a putative signal peptide | DDB0232433 | CDS | 2331143 | 1461 | + | 0.321013 |
DDB_G0293016 | DDB_G0293016 | DDB0232433 | CDS | 2333163 | 270 | + | 0.233333 | |
DDB_G0293020 | DDB_G0293020 | DDB0232433 | CDS | 2337693 | 963 | + | 0.261682 | |
DDB_G0293022_ps | DDB_G0293022 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232433 | CDS | 2342209 | 150 | - | 0.326667 |
DDB_G0293026 | DDB_G0293026 | highly similar to | DDB0232433 | CDS | 2343104 | 498 | - | 0.289157 |
DDB_G0293028 | DDB_G0293028 | DDB0232433 | CDS | 2344265 | 513 | + | 0.378168 | |
DDB_G0293032 | DDB_G0293032 | DDB0232433 | CDS | 2351624 | 4698 | - | 0.270115 | |
DDB_G0293034 | DDB_G0293034 | DDB0232433 | CDS | 2371825 | 942 | - | 0.33121 | |
DDB_G0293038 | DDB_G0293038 | DDB0232433 | CDS | 2375925 | 372 | + | 0.362903 | |
DDB_G0293040 | DDB_G0293040 | DDB0232433 | CDS | 2376674 | 2187 | + | 0.221765 | |
DDB_G0293042 | DDB_G0293042 | DDB0232433 | CDS | 2379108 | 1251 | - | 0.28697 | |
DDB_G0293044 | DDB_G0293044 | DDB0232433 | CDS | 2381806 | 2151 | - | 0.273826 | |
DDB_G0293046 | DDB_G0293046 | DDB0232433 | CDS | 2389862 | 513 | - | 0.269006 | |
DDB_G0293048 | DDB_G0293048 | DDB0232433 | CDS | 2398022 | 291 | - | 0.298969 | |
DDB_G0293050 | DDB_G0293050 | DDB0232433 | CDS | 2399122 | 873 | - | 0.272623 | |
DDB_G0293054 | DDB_G0293054 | DDB0232433 | CDS | 2404735 | 1392 | + | 0.217672 | |
DDB_G0293056 | DDB_G0293056 | DDB0232433 | CDS | 2406225 | 2109 | - | 0.209578 | |
DDB_G0293058 | DDB_G0293058 | DDB0232433 | CDS | 2409869 | 3030 | + | 0.176898 | |
DDB_G0293060 | DDB_G0293060 | DDB0232433 | CDS | 2413794 | 1158 | + | 0.330743 | |
DDB_G0293062 | DDB_G0293062 | conserved in plants and bacteria predicted to have a structural domain found in several acyl-CoA acyltransferase enzymes | DDB0232433 | CDS | 2415200 | 246 | + | 0.313008 |
DDB_G0293064 | DDB_G0293064 | DDB0232433 | CDS | 2418202 | 1722 | - | 0.334495 | |
DDB_G0293066 | DDB_G0293066 | conserved in Dictyostelium contains one putative transmembrane domain | DDB0232433 | CDS | 2420535 | 2868 | - | 0.279637 |
DDB_G0293068 | DDB_G0293068 | DDB0232433 | CDS | 2425522 | 858 | + | 0.276224 | |
DDB_G0293070 | DDB_G0293070 | putative ortholog of H. sapiens TEP1 a component of the telomerase ribonucleoprotein complex involved in replication of chromosome termini | DDB0232433 | CDS | 2426564 | 7293 | - | 0.319896 |
DDB_G0293072 | DDB_G0293072 | DDB0232433 | CDS | 2434758 | 1701 | - | 0.258083 | |
DDB_G0293074 | DDB_G0293074 | belongs to the amino acidauxin permease family similar to human SLC36A4 disruption reduces extracellular GABA levels | DDB0232433 | CDS | 2437739 | 1368 | - | 0.313596 |
DDB_G0293078 | DDB_G0293078 | DDB0232433 | CDS | 2446845 | 825 | - | 0.26303 | |
DDB_G0293082 | DDB_G0293082 | DDB0232433 | CDS | 2450060 | 1092 | - | 0.282051 | |
DDB_G0293090 | DDB_G0293090 | DDB0232433 | CDS | 2463701 | 6024 | + | 0.336155 | |
DDB_G0293098 | DDB_G0293098 | DDB0232433 | CDS | 2491651 | 1050 | + | 0.194286 | |
DDB_G0293100 | DDB_G0293100 | DDB0232433 | CDS | 2506785 | 615 | - | 0.279675 | |
DDB_G0293102 | DDB_G0293102 | DDB0232433 | CDS | 2508062 | 1260 | - | 0.22619 | |
DDB_G0293106 | DDB_G0293106 | DDB0232433 | CDS | 2517023 | 2454 | - | 0.236756 | |
DDB_G0293108 | DDB_G0293108 | DDB0232433 | CDS | 2520283 | 1434 | - | 0.279637 | |
DDB_G0293112 | DDB_G0293112 | DDB0232433 | CDS | 2526722 | 195 | + | 0.323077 | |
DDB_G0293114 | DDB_G0293114 | DDB0232433 | CDS | 2527421 | 1230 | - | 0.296748 | |
DDB_G0293116 | DDB_G0293116 | DDB0232433 | CDS | 2529994 | 456 | + | 0.333333 | |
DDB_G0293118 | DDB_G0293118 | DDB0232433 | CDS | 2535539 | 1539 | + | 0.306043 | |
DDB_G0293120 | DDB_G0293120 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232433 | CDS | 2546935 | 6618 | - | 0.294349 |
DDB_G0293122 | DDB_G0293122 | similar to human GSTT2 (glutathione S-transferase theta-2) glutathione transferases participate in the detoxification of reactive electrophilic compounds by catalysing their conjugation to glutathione | DDB0232433 | CDS | 2554630 | 660 | - | 0.237879 |
DDB_G0293126 | DDB_G0293126 | DDB0232433 | CDS | 2565278 | 660 | - | 0.277273 | |
DDB_G0293128 | DDB_G0293128 | DDB0232433 | CDS | 2567187 | 6678 | + | 0.28227 | |
DDB_G0293132 | DDB_G0293132 | DDB0232433 | CDS | 2577800 | 2301 | + | 0.269013 | |
DDB_G0293134 | DDB_G0293134 | DDB0232433 | CDS | 2580338 | 1245 | - | 0.194378 | |
DDB_G0293138 | DDB_G0293138 | bCommunity annotation:b DDB_G0293138 is related (first blast hit both ways) to a gene which is called src1 in budding yeast. DDB_G0293138 is threefold upregulated in vegetative cells of a Dicty strain in which the retinoblastoma-like gene rblA has been disrubpted. Many genes with roles in cell cycle progression are upregulated in this strain. The gene also shows the developmental trajectory typical of cell cycle genes (see DictyExpress) in both Dd and Dp. The Dp promoter contains an element recognized by smyd3 a chromatin modifier which is rblA-repressed in Dicty and implicated as an oncogene in vertebrates. The Dp element (TTTCCCTCC) is close to conserved in Dd (TTTCCCTCT). All of these suggest that DDB_G0293138 is a cell cycle gene in amebae. In both Dp and Dd there is also expression in late development which is rblA-independent in Dd suggesting a possible cell-cycle independent role during terminal differentiation.Harry MacWilliams March 2010br | DDB0232433 | CDS | 2586745 | 2829 | + | 0.278897 |
DDB_G0293140_RTE | DDB_G0293140 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 2365100 | 1497 | + | 0.352705 |
DDB_G0293142_RTE | DDB_G0293142 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 2479985 | 1335 | + | 0.307116 |
DDB_G0293144_RTE | DDB_G0293144 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 2482983 | 1335 | + | 0.307865 |
DDB_G0293150 | DDB_G0293150 | DDB0232433 | CDS | 2585552 | 201 | + | 0.243781 | |
DDB_G0293152_RTE | DDB_G0293152 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 2591529 | 3127 | - | 0.301567 |
DDB_G0293154 | DDB_G0293154 | this gene belongs to the trx family of genes and is located next to | DDB0232433 | CDS | 2334087 | 153 | - | 0.30719 |
DDB_G0293156_ps | DDB_G0293156 | putative pseudogene related to the TKL (tyrosine kinase-like) group of protein kinases contains a partial kinase domain | DDB0232433 | CDS | 2336989 | 324 | + | 0.327161 |
DDB_G0293158_RTE | DDB_G0293158 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 2340052 | 558 | - | 0.34767 |
DDB_G0293160_RTE | DDB_G0293160 | DDB0232433 | CDS | 2340864 | 789 | + | 0.377693 | |
DDB_G0293162 | DDB_G0293162 | highly similar to | DDB0232433 | CDS | 2346747 | 498 | - | 0.291165 |
DDB_G0293164 | DDB_G0293164 | DDB0232433 | CDS | 2357058 | 1167 | + | 0.261354 | |
DDB_G0293166 | DDB_G0293166 | DDB0232433 | CDS | 2359312 | 918 | + | 0.249455 | |
DDB_G0293170 | DDB_G0293170 | DDB0232433 | CDS | 2392178 | 3165 | + | 0.222749 | |
DDB_G0293172_ps | DDB_G0293172 | putative pseudogene similar to | DDB0232433 | CDS | 2470132 | 1785 | + | 0.239776 |
DDB_G0293174 | DDB_G0293174 | DDB0232433 | CDS | 2473465 | 3810 | + | 0.246194 | |
DDB_G0293176 | DDB_G0293176 | DDB0232433 | CDS | 2485971 | 5169 | + | 0.285935 | |
DDB_G0293178 | DDB_G0293178 | DDB0232433 | CDS | 2497885 | 1020 | - | 0.177451 | |
DDB_G0293184 | DDB_G0293184 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis contains RhoGAP domain found in the Rho family of small G proteins unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232433 | CDS | 2540484 | 3561 | + | 0.281382 |
DDB_G0293186 | DDB_G0293186 | DDB0232433 | CDS | 2544546 | 1266 | - | 0.314376 | |
DDB_G0293188 | DDB_G0293188 | DDB0232433 | CDS | 2553978 | 345 | - | 0.226087 | |
DDB_G0293190 | DDB_G0293190 | DDB0232433 | CDS | 2583503 | 1002 | - | 0.277445 | |
DDB_G0293200_ps | DDB_G0293200 | putative pseudogene similar to D. discoideum genes | DDB0232433 | CDS | 2729012 | 1152 | + | 0.259549 |
DDB_G0293202 | DDB_G0293202 | has similarity to mammalian TNF receptor-associated factors 5 and 6 (TRAF5 TRAF6) | DDB0232433 | CDS | 2718912 | 1314 | - | 0.313546 |
DDB_G0293204 | DDB_G0293204 | one of three paralogs in Dictyostelium (other genes: | DDB0232433 | CDS | 2716007 | 2745 | - | 0.28816 |
DDB_G0293206 | DDB_G0293206 | DDB0232433 | CDS | 2715182 | 549 | - | 0.202186 | |
DDB_G0293208 | DDB_G0293208 | similar to | DDB0232433 | CDS | 2710326 | 468 | - | 0.247863 |
DDB_G0293212 | DDB_G0293212 | DDB0232433 | CDS | 2696303 | 2541 | + | 0.275482 | |
DDB_G0293216 | DDB_G0293216 | DDB0232433 | CDS | 2689035 | 3537 | - | 0.240317 | |
DDB_G0293222 | DDB_G0293222 | DDB0232433 | CDS | 2682288 | 918 | - | 0.242919 | |
DDB_G0293234 | DDB_G0293234 | ortholog of the conserved non-catalytic N-acetyltransferase that catalyzes the transfer of an acetyl group to the N-terminal residue of a protein that contains a Met-Glu Met-Asp Met-Asn or Met-Met N-terminus ortholog of S. cerevisiae MDM20 the N-terminal acetyltransferase B (NatB) complex subunit | DDB0232433 | CDS | 2661843 | 2814 | - | 0.27221 |
DDB_G0293236 | DDB_G0293236 | DDB0232433 | CDS | 2653194 | 1320 | + | 0.265909 | |
DDB_G0293240 | DDB_G0293240 | DDB0232433 | CDS | 2643748 | 1617 | + | 0.22449 | |
DDB_G0293242 | DDB_G0293242 | DDB0232433 | CDS | 2642031 | 1446 | + | 0.309129 | |
DDB_G0293244 | DDB_G0293244 | DDB0232433 | CDS | 2638704 | 1941 | + | 0.297269 | |
DDB_G0293250 | DDB_G0293250 | contains 4 predicted transmembrane domains similar to D. purpureum gene | DDB0232433 | CDS | 2630267 | 429 | - | 0.286713 |
DDB_G0293252 | DDB_G0293252 | contains 2 RRM1 domains a SWAPSurp domain and a C-terminal ENTHVHS domain putative RNA splicing factor similar to D. purpureum gene | DDB0232433 | CDS | 2627689 | 2010 | + | 0.332836 |
DDB_G0293256 | DDB_G0293256 | DDB0232433 | CDS | 2616152 | 207 | - | 0.173913 | |
DDB_G0293258 | DDB_G0293258 | similar to myotubularin a dual-specific lipid phosphatase that dephosphorylates phosphatidylinositol 3-phosphate and phosphatidylinositol (35)-bi-phosphate | DDB0232433 | CDS | 2612161 | 3579 | + | 0.230791 |
DDB_G0293260 | DDB_G0293260 | DDB0232433 | CDS | 2610415 | 498 | - | 0.184739 | |
DDB_G0293262 | DDB_G0293262 | contains a predicted signal peptide similar to | DDB0232433 | CDS | 2609479 | 450 | - | 0.286667 |
DDB_G0293268 | DDB_G0293268 | DDB0232433 | CDS | 2601693 | 210 | + | 0.314286 | |
DDB_G0293270_RTE | DDB_G0293270 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 2595773 | 1209 | - | 0.336642 |
DDB_G0293272_RTE | DDB_G0293272 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 2726875 | 1335 | - | 0.305618 |
DDB_G0293274 | DDB_G0293274 | contains 2 FNIP domains contains 1 B-box zinc finger domain | DDB0232433 | CDS | 2721106 | 1623 | - | 0.28589 |
DDB_G0293276 | DDB_G0293276 | member of the AGC kinase group similar to kinase domains of AktPKB and MAST (microtubule-associated serinethreonine kinase) family members | DDB0232433 | CDS | 2701490 | 1551 | - | 0.246937 |
DDB_G0293278 | DDB_G0293278 | DDB0232433 | CDS | 2700382 | 156 | - | 0.198718 | |
DDB_G0293280_RTE | DDB_G0293280 | part of ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-C refer to GenBank AF298210 (DDB_G0293280) for a partially assembled consensus element | DDB0232433 | CDS | 2730183 | 686 | + | 0.370262 |
DDB_G0293282_ps | DDB_G0293282 | putative pseudogene similar to Dictyostelium genes | DDB0232433 | CDS | 2723111 | 2118 | - | 0.260623 |
DDB_G0293284 | DDB_G0293284 | DDB0232433 | CDS | 2698963 | 912 | - | 0.240132 | |
DDB_G0293290 | DDB_G0293290 | DDB0232433 | CDS | 2658870 | 2364 | - | 0.232657 | |
DDB_G0293292 | DDB_G0293292 | putative protein serinethreonine kinase N-terminal kinase domain similar to vertebrate Nek kinases which are involved in regulation of mitosis C-terminal kinase domain weakly similar to ULK (Unc-51-like kinase) | DDB0232433 | CDS | 2647324 | 4116 | + | 0.234208 |
DDB_G0293294 | DDB_G0293294 | DDB0232433 | CDS | 2636918 | 1506 | + | 0.2417 | |
DDB_G0293296 | DDB_G0293296 | DDB0232433 | CDS | 2634996 | 1413 | + | 0.206653 | |
DDB_G0293300 | DDB_G0293300 | DDB0232433 | CDS | 2733345 | 3654 | + | 0.281883 | |
DDB_G0293302 | DDB_G0293302 | DDB0232433 | CDS | 2737579 | 1959 | + | 0.18632 | |
DDB_G0293304 | DDB_G0293304 | DDB0232433 | CDS | 2739726 | 786 | - | 0.21374 | |
DDB_G0293308 | DDB_G0293308 | DDB0232433 | CDS | 2743223 | 3438 | + | 0.287086 | |
DDB_G0293310 | DDB_G0293310 | DDB0232433 | CDS | 2747762 | 180 | - | 0.266667 | |
DDB_G0293312 | DDB_G0293312 | DDB0232433 | CDS | 2748675 | 231 | + | 0.272727 | |
DDB_G0293314 | DDB_G0293314 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232433 | CDS | 2749397 | 288 | - | 0.378472 |
DDB_G0293316 | DDB_G0293316 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232433 | CDS | 2750083 | 252 | + | 0.321429 |
DDB_G0293318 | DDB_G0293318 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232433 | CDS | 2750911 | 243 | - | 0.366255 |
DDB_G0293320 | DDB_G0293320 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232433 | CDS | 2751543 | 246 | + | 0.304878 |
DDB_G0293322 | DDB_G0293322 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232433 | CDS | 2752374 | 273 | - | 0.377289 |
DDB_G0293324 | DDB_G0293324 | DDB0232433 | CDS | 2755452 | 210 | - | 0.319048 | |
DDB_G0293326 | DDB_G0293326 | DDB0232433 | CDS | 2756536 | 276 | - | 0.387681 | |
DDB_G0293328 | DDB_G0293328 | DDB0232433 | CDS | 2760211 | 396 | + | 0.39899 | |
DDB_G0293330 | DDB_G0293330 | DDB0232433 | CDS | 2764080 | 402 | - | 0.253731 | |
DDB_G0293332 | DDB_G0293332 | DDB0232433 | CDS | 2765016 | 699 | + | 0.194564 | |
DDB_G0293334 | DDB_G0293334 | DDB0232433 | CDS | 2765769 | 1533 | - | 0.210046 | |
DDB_G0293336 | DDB_G0293336 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232433 | CDS | 2753047 | 252 | + | 0.313492 |
DDB_G0293342_RTE | DDB_G0293342 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 2768512 | 684 | - | 0.342105 |
DDB_G0293344_RTE | DDB_G0293344 | Part of ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-C refer to GenBank AF298210 for partially assembled consensus element | DDB0232433 | CDS | 2772108 | 420 | + | 0.366667 |
DDB_G0293346 | DDB_G0293346 | DDB0232433 | CDS | 2774066 | 3084 | + | 0.260052 | |
DDB_G0293348_RTE | DDB_G0293348 | DDB0232433 | CDS | 2777877 | 669 | + | 0.28849 | |
DDB_G0293350_RTE | DDB_G0293350 | DDB0232433 | CDS | 2778739 | 3444 | + | 0.334204 | |
DDB_G0293352_ps | DDB_G0293352 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232433 | CDS | 2782815 | 408 | + | 0.335784 |
DDB_G0293354 | DDB_G0293354 | catalyzes the reaction (3S)-3-hydroxyacyl-CoA trans-2(or 3)-enoyl-CoA Hsub2subO | DDB0232433 | CDS | 2784930 | 894 | - | 0.32774 |
DDB_G0293356 | DDB_G0293356 | highly similar to other short proteins expressed in the prestalk region expressed in pstO cells | DDB0232433 | CDS | 2786412 | 258 | - | 0.383721 |
DDB_G0293362 | DDB_G0293362 | DDB0232433 | CDS | 2790501 | 267 | + | 0.430712 | |
DDB_G0293366 | DDB_G0293366 | DDB0232433 | CDS | 2795992 | 531 | + | 0.382298 | |
DDB_G0293370 | DDB_G0293370 | DDB0232433 | CDS | 2797816 | 318 | + | 0.289308 | |
DDB_G0293378 | DDB_G0293378 | DDB0232433 | CDS | 2818966 | 1650 | + | 0.287273 | |
DDB_G0293380 | DDB_G0293380 | bCommunity annotation:b DDB G0293380 contains a conserved domain which is best matched by COG0116 N6 adenine-specific DNA methylase (E-value 5e-14). The similarity to PRK11783 rRNA methyltransferase is lower (9e-11). The blast matches list both putative RNA methylases and putative N6 adenine-specific DNA methylases. Thus although it does not now appear to be possible to assign DDB_G0293380 conclusively to either category the case for a DNA methylase currently looks a bit stronger.br DDB_G0293380 is overexpressed fivefold (p0.008) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes with functions necessary for cell cycle progression are overexpressed in this strain and most of the overexpressed genes have identifiable cell cycle functions. A tempting interpretation is that the product of DDB_G0293380 is involved in a DNA methylation pathway which is coupled with DNA replication. Harry MacWilliams December 2009br | DDB0232433 | CDS | 2824551 | 1686 | + | 0.242586 |
DDB_G0293382 | DDB_G0293382 | identical to | DDB0232433 | CDS | 2791219 | 477 | + | 0.417191 |
DDB_G0293384 | DDB_G0293384 | DDB0232433 | CDS | 2826651 | 930 | + | 0.17957 | |
DDB_G0293386 | DDB_G0293386 | DDB0232433 | CDS | 2792033 | 2073 | - | 0.232996 | |
DDB_G0293388 | DDB_G0293388 | putative ATP-dependent metalloprotease FtsH similar to S. cerevisiae YME1 that plays a role in mitochondrial protein metabolism | DDB0232433 | CDS | 2798298 | 2304 | - | 0.327691 |
DDB_G0293390 | DDB_G0293390 | DDB0232433 | CDS | 2828734 | 1392 | + | 0.155891 | |
DDB_G0293392 | DDB_G0293392 | conserved protein mammalian orthologs are predicted Zn-dependent hydrolases of the beta-lactamase fold | DDB0232433 | CDS | 2830538 | 1110 | + | 0.282883 |
DDB_G0293400_RTE | DDB_G0293400 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 2839313 | 561 | - | 0.344029 |
DDB_G0293402 | DDB_G0293402 | DDB0232433 | CDS | 2841033 | 1032 | - | 0.205426 | |
DDB_G0293404 | DDB_G0293404 | poorly characterized but highly conserved protein may function as a tRNA m5C methyltransferase chaperone | DDB0232433 | CDS | 2846362 | 456 | - | 0.265351 |
DDB_G0293406 | DDB_G0293406 | DDB0232433 | CDS | 2852833 | 3429 | - | 0.230679 | |
DDB_G0293410 | DDB_G0293410 | identical to | DDB0232433 | CDS | 2842898 | 477 | - | 0.417191 |
DDB_G0293412 | DDB_G0293412 | DDB0232433 | CDS | 2844115 | 2010 | + | 0.30199 | |
DDB_G0293414 | DDB_G0293414 | DDB0232433 | CDS | 2847823 | 4851 | + | 0.288394 | |
DDB_G0293418 | DDB_G0293418 | DDB0232433 | CDS | 2859059 | 195 | + | 0.328205 | |
DDB_G0293420 | DDB_G0293420 | DDB0232433 | CDS | 2859525 | 1341 | + | 0.211037 | |
DDB_G0293422 | DDB_G0293422 | DDB0232433 | CDS | 2865868 | 210 | - | 0.266667 | |
DDB_G0293424 | DDB_G0293424 | DDB0232433 | CDS | 2868585 | 267 | + | 0.337079 | |
DDB_G0293426 | DDB_G0293426 | DDB0232433 | CDS | 2868959 | 1482 | - | 0.306343 | |
DDB_G0293428 | DDB_G0293428 | DDB0232433 | CDS | 2864640 | 825 | - | 0.288485 | |
DDB_G0293430 | DDB_G0293430 | DDB0232433 | CDS | 2872733 | 159 | + | 0.283019 | |
DDB_G0293432_TE | DDB_G0293432 | DDB0232433 | CDS | 2873447 | 429 | - | 0.307692 | |
DDB_G0293440 | DDB_G0293440 | DDB0232433 | CDS | 2897244 | 1152 | - | 0.250868 | |
DDB_G0293442 | DDB_G0293442 | DDB0232433 | CDS | 2899455 | 1164 | - | 0.317869 | |
DDB_G0293444 | DDB_G0293444 | DDB0232433 | CDS | 2901323 | 1368 | - | 0.296784 | |
DDB_G0293446_ps | DDB_G0293446 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232433 | CDS | 2886461 | 4002 | + | 0.247626 |
DDB_G0293448 | DDB_G0293448 | DDB0232433 | CDS | 2875111 | 1431 | - | 0.245982 | |
DDB_G0293452_TE | DDB_G0293452 | DDB0232433 | CDS | 2904523 | 231 | - | 0.277056 | |
DDB_G0293454 | DDB_G0293454 | DDB0232433 | CDS | 2905541 | 510 | - | 0.24902 | |
DDB_G0293456 | DDB_G0293456 | DDB0232433 | CDS | 2907748 | 441 | + | 0.258503 | |
DDB_G0293460 | DDB_G0293460 | DDB0232433 | CDS | 2919081 | 1275 | + | 0.287843 | |
DDB_G0293464 | DDB_G0293464 | DDB0232433 | CDS | 2906126 | 1332 | - | 0.283784 | |
DDB_G0293474 | DDB_G0293474 | DDB0232433 | CDS | 2927015 | 717 | + | 0.217573 | |
DDB_G0293478 | DDB_G0293478 | weakly similar to cudA contains the motifs believed to be required for DNA binding: LSS and RCVSK (RVVSK in CudA) | DDB0232433 | CDS | 2942975 | 1524 | - | 0.256562 |
DDB_G0293480 | DDB_G0293480 | DDB0232433 | CDS | 2945490 | 264 | + | 0.299242 | |
DDB_G0293482_RTE | DDB_G0293482 | DDB0232433 | CDS | 2933475 | 1188 | - | 0.311448 | |
DDB_G0293486_RTE | DDB_G0293486 | DDB0232433 | CDS | 2934812 | 876 | - | 0.300228 | |
DDB_G0293488 | DDB_G0293488 | DDB0232433 | CDS | 2946961 | 729 | + | 0.326475 | |
DDB_G0293490_RTE | DDB_G0293490 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 2948897 | 1775 | + | 0.347606 |
DDB_G0293492 | DDB_G0293492 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide | DDB0232433 | CDS | 2951996 | 642 | + | 0.356698 |
DDB_G0293494 | DDB_G0293494 | DDB0232433 | CDS | 2959996 | 786 | - | 0.183206 | |
DDB_G0293498 | DDB_G0293498 | contains a UBX domain found in ubiquitin-regulatory proteins | DDB0232433 | CDS | 2964407 | 1248 | + | 0.33734 |
DDB_G0293500 | DDB_G0293500 | DDB0232433 | CDS | 2965853 | 1173 | - | 0.225064 | |
DDB_G0293504 | DDB_G0293504 | belongs to the nucleotidyltransferase superfamily contains one poly A polymerase head domain | DDB0232433 | CDS | 2968920 | 1677 | - | 0.285033 |
DDB_G0293506_ps | DDB_G0293506 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232433 | CDS | 2971375 | 345 | - | 0.255072 |
DDB_G0293508 | DDB_G0293508 | DDB0232433 | CDS | 2972530 | 3108 | + | 0.287323 | |
DDB_G0293512 | DDB_G0293512 | DDB0232433 | CDS | 2978200 | 1527 | - | 0.301899 | |
DDB_G0293514 | DDB_G0293514 | DDB0232433 | CDS | 2984590 | 492 | + | 0.292683 | |
DDB_G0293516_RTE | DDB_G0293516 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 2985588 | 549 | + | 0.35337 |
DDB_G0293518_ps | DDB_G0293518 | putative pseudogene similar to a D. discoideum gene family including | DDB0232433 | CDS | 2980192 | 282 | + | 0.336879 |
DDB_G0293534 | DDB_G0293534 | DDB0232433 | CDS | 3002117 | 3000 | + | 0.242333 | |
DDB_G0293542 | DDB_G0293542 | DDB0232433 | CDS | 2989503 | 921 | - | 0.283388 | |
DDB_G0293548 | DDB_G0293548 | DDB0232433 | CDS | 3018651 | 1998 | - | 0.23974 | |
DDB_G0293550 | DDB_G0293550 | DDB0232433 | CDS | 3022571 | 3657 | + | 0.184851 | |
DDB_G0293552 | DDB_G0293552 | DDB0232433 | CDS | 3026375 | 2034 | - | 0.326942 | |
DDB_G0293562 | DDB_G0293562 | DDB0232433 | CDS | 3048907 | 1584 | + | 0.289141 | |
DDB_G0293566 | DDB_G0293566 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide | DDB0232433 | CDS | 3051866 | 651 | + | 0.3149 |
DDB_G0293570 | DDB_G0293570 | contains a RUN domain which is predicted to play a role in Ras-like GTPase signaling pathways | DDB0232433 | CDS | 3056692 | 4062 | + | 0.239783 |
DDB_G0293572 | DDB_G0293572 | DDB0232433 | CDS | 3061098 | 390 | - | 0.207692 | |
DDB_G0293574 | DDB_G0293574 | DDB0232433 | CDS | 3063340 | 210 | + | 0.2 | |
DDB_G0293578 | DDB_G0293578 | DDB0232433 | CDS | 3070057 | 1986 | - | 0.288016 | |
DDB_G0293580 | DDB_G0293580 | catalyzes the reaction Hsub2subO dCTP NH3 dUTP in de novo biosynthesis of pyrimidine deoxyribonucleotides | DDB0232433 | CDS | 3073231 | 525 | - | 0.289524 |
DDB_G0293582 | DDB_G0293582 | DDB0232433 | CDS | 3074914 | 744 | + | 0.264785 | |
DDB_G0293586 | DDB_G0293586 | contains one LisH domain contains 3 predicted coiled-coil domains | DDB0232433 | CDS | 3081583 | 6045 | - | 0.305045 |
DDB_G0293590 | DDB_G0293590 | DDB0232433 | CDS | 3095576 | 4521 | - | 0.297722 | |
DDB_G0293592 | DDB_G0293592 | DDB0232433 | CDS | 3100713 | 483 | + | 0.277433 | |
DDB_G0293594 | DDB_G0293594 | DDB0232433 | CDS | 3101875 | 492 | + | 0.264228 | |
DDB_G0293596 | DDB_G0293596 | DDB0232433 | CDS | 3106575 | 2379 | + | 0.338377 | |
DDB_G0293598 | DDB_G0293598 | DDB0232433 | CDS | 3109284 | 2007 | - | 0.209766 | |
DDB_G0293600_ps | DDB_G0293600 | putative pseudogene fragment similar to the neighboring genes | DDB0232433 | CDS | 3111920 | 1092 | - | 0.250916 |
DDB_G0293604 | DDB_G0293604 | DDB0232433 | CDS | 3126896 | 897 | - | 0.248606 | |
DDB_G0293606 | DDB_G0293606 | DDB0232433 | CDS | 3128846 | 1056 | - | 0.300189 | |
DDB_G0293610 | DDB_G0293610 | conserved protein in ciliates and plants contains 9 predicted transmembrane domains including one signal peptide there is an almost identical D. discoideum protein | DDB0232433 | CDS | 3135284 | 1524 | + | 0.343832 |
DDB_G0293612 | DDB_G0293612 | DDB0232433 | CDS | 3141895 | 2775 | + | 0.184144 | |
DDB_G0293614 | DDB_G0293614 | ortholog of S. cerevisiae DIS3 and H. sapiens KIAA1008 component of the nucleolar exosome involved in RNA processing | DDB0232433 | CDS | 3144728 | 3021 | - | 0.300232 |
DDB_G0293616 | DDB_G0293616 | DDB0232433 | CDS | 3148125 | 222 | - | 0.198198 | |
DDB_G0293620 | DDB_G0293620 | DDB0232433 | CDS | 3157149 | 1728 | - | 0.234375 | |
DDB_G0293622 | DDB_G0293622 | DDB0232433 | CDS | 3159608 | 2976 | + | 0.290995 | |
DDB_G0293624 | DDB_G0293624 | DDB0232433 | CDS | 3162861 | 372 | + | 0.193548 | |
DDB_G0293626 | DDB_G0293626 | DDB0232433 | CDS | 3164445 | 1830 | + | 0.271038 | |
DDB_G0293628 | DDB_G0293628 | DDB0232433 | CDS | 3167249 | 4926 | + | 0.252944 | |
DDB_G0293630_RTE | DDB_G0293630 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232433 | CDS | 3176971 | 3435 | - | 0.346725 |
DDB_G0293632_RTE | DDB_G0293632 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank GenBank AF298209 for consensus full-length element | DDB0232433 | CDS | 3180508 | 1365 | - | 0.311355 |
DDB_G0293636 | DDB_G0293636 | similar to the conserved survival of motor neuron-related splicing factor 30 (SMNDC1 SPF30) the tudor domain is found in many proteins that colocalize with ribonucleoprotein or single-strand DNA-associated complexes | DDB0232433 | CDS | 3190337 | 975 | - | 0.251282 |
DDB_G0293638 | DDB_G0293638 | DDB0232433 | CDS | 3191821 | 861 | - | 0.28223 | |
DDB_G0293640 | DDB_G0293640 | DDB0232433 | CDS | 3195274 | 447 | + | 0.331096 | |
DDB_G0293644 | DDB_G0293644 | DDB0232433 | CDS | 3198630 | 1374 | + | 0.279476 | |
DDB_G0293648 | DDB_G0293648 | DDB0232433 | CDS | 3208622 | 252 | + | 0.329365 | |
DDB_G0293652 | DDB_G0293652 | DDB0232433 | CDS | 3211810 | 1968 | - | 0.186484 | |
DDB_G0293658 | DDB_G0293658 | DDB0232433 | CDS | 3221806 | 1245 | - | 0.258635 | |
DDB_G0293660 | DDB_G0293660 | DDB0232433 | CDS | 3223447 | 198 | - | 0.181818 | |
DDB_G0293662 | DDB_G0293662 | DDB0232433 | CDS | 3224777 | 1992 | + | 0.240462 | |
DDB_G0293664 | DDB_G0293664 | DDB0232433 | CDS | 3227956 | 4284 | + | 0.247666 | |
DDB_G0293666 | DDB_G0293666 | similar to terpene cyclases (C1) of the class 1 family of isoprenoid biosynthesis enzymes which are found in bacteria fungi and plants | DDB0232433 | CDS | 3235366 | 939 | - | 0.251331 |
DDB_G0293668 | DDB_G0293668 | DDB0232433 | CDS | 3238981 | 909 | + | 0.20242 | |
DDB_G0293670 | DDB_G0293670 | DDB0232433 | CDS | 3241196 | 792 | + | 0.224747 | |
DDB_G0293672 | DDB_G0293672 | DDB0232433 | CDS | 3242621 | 285 | + | 0.249123 | |
DDB_G0293674 | DDB_G0293674 | DDB0232433 | CDS | 3243242 | 1893 | + | 0.310618 | |
DDB_G0293676 | DDB_G0293676 | DDB0232433 | CDS | 3246015 | 267 | + | 0.400749 | |
DDB_G0293678 | DDB_G0293678 | DDB0232433 | CDS | 3246808 | 1710 | + | 0.293567 | |
DDB_G0293680 | DDB_G0293680 | DDB0232433 | CDS | 3248934 | 336 | - | 0.267857 | |
DDB_G0293682 | DDB_G0293682 | DDB0232433 | CDS | 3251577 | 1578 | + | 0.222433 | |
DDB_G0293684_RTE | DDB_G0293684 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 3066410 | 1335 | - | 0.306367 |
DDB_G0293688 | DDB_G0293688 | DDB0232433 | CDS | 3133176 | 162 | + | 0.203704 | |
DDB_G0293690_RTE | DDB_G0293690 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 3138091 | 1335 | + | 0.307116 |
DDB_G0293692_RTE | DDB_G0293692 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 3009712 | 1335 | + | 0.307116 |
DDB_G0293694 | DDB_G0293694 | DDB0232433 | CDS | 2998070 | 543 | + | 0.294659 | |
DDB_G0293696 | DDB_G0293696 | small Dictyostelium protein family absent from other organisms very similar to neighboring gene | DDB0232433 | CDS | 3006120 | 240 | + | 0.341667 |
DDB_G0293698 | DDB_G0293698 | small Dictyostelium protein family absent from other organisms very similar to neighboring gene | DDB0232433 | CDS | 3007121 | 240 | + | 0.3375 |
DDB_G0293704 | DDB_G0293704 | DDB0232433 | CDS | 3034210 | 708 | - | 0.223164 | |
DDB_G0293708 | DDB_G0293708 | DDB0232433 | CDS | 3054649 | 333 | + | 0.318318 | |
DDB_G0293712 | DDB_G0293712 | DDB0232433 | CDS | 3080260 | 564 | + | 0.281915 | |
DDB_G0293714 | DDB_G0293714 | DDB0232433 | CDS | 3102749 | 504 | + | 0.281746 | |
DDB_G0293716_ps | DDB_G0293716 | putative pseudogene similar to D. discoideum gene | DDB0232433 | CDS | 3103876 | 651 | + | 0.262673 |
DDB_G0293718 | DDB_G0293718 | DDB0232433 | CDS | 3104858 | 483 | + | 0.318841 | |
DDB_G0293720 | DDB_G0293720 | DDB0232433 | CDS | 3113521 | 4311 | - | 0.24913 | |
DDB_G0293722 | DDB_G0293722 | DDB0232433 | CDS | 3118866 | 4311 | - | 0.257017 | |
DDB_G0293724 | DDB_G0293724 | DDB0232433 | CDS | 3124039 | 2088 | - | 0.312739 | |
DDB_G0293726_RTE | DDB_G0293726 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 3139824 | 201 | + | 0.263682 |
DDB_G0293728 | DDB_G0293728 | DDB0232433 | CDS | 3153008 | 375 | + | 0.296 | |
DDB_G0293730 | DDB_G0293730 | the TIM betaalpha-barrel domain is found in phospholipase C (PLC) like phosphodiesterases | DDB0232433 | CDS | 3154705 | 2205 | + | 0.278912 |
DDB_G0293732_RTE | DDB_G0293732 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 3173111 | 477 | - | 0.30608 |
DDB_G0293734_RTE | DDB_G0293734 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 3182350 | 984 | + | 0.332317 |
DDB_G0293736_RTE | DDB_G0293736 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 3185294 | 1854 | + | 0.298813 |
DDB_G0293744 | DDB_G0293744 | DDB0232433 | CDS | 3261758 | 2538 | + | 0.179275 | |
DDB_G0293746 | DDB_G0293746 | low level of similarity to mammalian PLK (polo-like kinase) unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232433 | CDS | 3265690 | 1188 | + | 0.223906 |
DDB_G0293748 | DDB_G0293748 | DDB0232433 | CDS | 3267287 | 4056 | + | 0.235454 | |
DDB_G0293754 | DDB_G0293754 | DDB0232433 | CDS | 3282657 | 537 | + | 0.18622 | |
DDB_G0293756 | DDB_G0293756 | DDB0232433 | CDS | 3283369 | 3300 | - | 0.23 | |
DDB_G0293760 | DDB_G0293760 | DDB0232433 | CDS | 3291080 | 345 | + | 0.269565 | |
DDB_G0293762 | DDB_G0293762 | highly similar to | DDB0232433 | CDS | 3293162 | 3414 | + | 0.269772 |
DDB_G0293764_RTE | DDB_G0293764 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 3297716 | 1953 | - | 0.346646 |
DDB_G0293770 | DDB_G0293770 | DDB0232433 | CDS | 3303029 | 6324 | - | 0.306293 | |
DDB_G0293774 | DDB_G0293774 | DDB0232433 | CDS | 3310894 | 1518 | - | 0.267457 | |
DDB_G0293776 | DDB_G0293776 | DDB0232433 | CDS | 3312862 | 234 | + | 0.264957 | |
DDB_G0293778_ps | DDB_G0293778 | putative pseudogene similar to Dictyostelium genes | DDB0232433 | CDS | 3316597 | 423 | + | 0.243499 |
DDB_G0293782 | DDB_G0293782 | DDB0232433 | CDS | 3259115 | 2292 | + | 0.172775 | |
DDB_G0293786 | DDB_G0293786 | DDB0232433 | CDS | 3287474 | 834 | - | 0.194245 | |
DDB_G0293788 | DDB_G0293788 | DDB0232433 | CDS | 3313981 | 384 | - | 0.325521 | |
DDB_G0293790_ps | DDB_G0293790 | DDB0232433 | CDS | 3314676 | 231 | - | 0.324675 | |
DDB_G0293792 | DDB_G0293792 | DDB0232433 | CDS | 3318747 | 1311 | + | 0.294432 | |
DDB_G0293794 | DDB_G0293794 | DDB0232433 | CDS | 3321471 | 1062 | + | 0.277778 | |
DDB_G0293796 | DDB_G0293796 | DDB0232433 | CDS | 3323921 | 144 | + | 0.291667 | |
DDB_G0293798 | DDB_G0293798 | DDB0232433 | CDS | 3324262 | 495 | + | 0.313131 | |
DDB_G0293800 | DDB_G0293800 | atypical protein kinase GTE group contains ankyrin repeats a bromodomain and a BTPPOZ domain | DDB0232433 | CDS | 3334534 | 2421 | + | 0.297811 |
DDB_G0293802 | DDB_G0293802 | DDB0232433 | CDS | 3338059 | 2151 | - | 0.30172 | |
DDB_G0293804 | DDB_G0293804 | DDB0232433 | CDS | 3341293 | 1341 | - | 0.255034 | |
DDB_G0293806 | DDB_G0293806 | DDB0232433 | CDS | 3343109 | 741 | + | 0.233468 | |
DDB_G0293808 | DDB_G0293808 | DDB0232433 | CDS | 3352978 | 273 | - | 0.340659 | |
DDB_G0293810 | DDB_G0293810 | conserved hypothetical Dictyostelium protein contains no functional domains | DDB0232433 | CDS | 3353625 | 156 | + | 0.237179 |
DDB_G0293812 | DDB_G0293812 | conserved in D. purpureum and P. pallidum contains 12 putative transmembrane domains C-terminal region similar to new-glue protein | DDB0232433 | CDS | 3355348 | 2343 | + | 0.311993 |
DDB_G0293814 | DDB_G0293814 | DDB0232433 | CDS | 3361018 | 846 | - | 0.199764 | |
DDB_G0293816 | DDB_G0293816 | DDB0232433 | CDS | 3362954 | 936 | - | 0.221154 | |
DDB_G0293818_RTE | DDB_G0293818 | DDB0232433 | CDS | 3326857 | 3318 | + | 0.331525 | |
DDB_G0293820 | DDB_G0293820 | DDB0232433 | CDS | 3332058 | 819 | - | 0.318681 | |
DDB_G0293822 | DDB_G0293822 | DDB0232433 | CDS | 3344068 | 1332 | - | 0.234234 | |
DDB_G0293826 | DDB_G0293826 | DDB0232433 | CDS | 3348949 | 3786 | + | 0.243529 | |
DDB_G0293828 | DDB_G0293828 | DDB0232433 | CDS | 3358255 | 2283 | + | 0.261936 | |
DDB_G0293830 | DDB_G0293830 | DDB0232433 | CDS | 3365828 | 1110 | + | 0.24955 | |
DDB_G0293832 | DDB_G0293832 | DDB0232433 | CDS | 3367295 | 1038 | - | 0.262042 | |
DDB_G0293836 | DDB_G0293836 | no homologs in other organisms contains a predicted signal peptide and a possible C-terminal transmembrane domain | DDB0232433 | CDS | 3369650 | 1572 | + | 0.254453 |
DDB_G0293838 | DDB_G0293838 | has similarity to the mammalian adiponectin receptor protein 1 contains 6 predicted transmembrane domains | DDB0232433 | CDS | 3371531 | 1119 | + | 0.206434 |
DDB_G0293842 | DDB_G0293842 | DDB0232433 | CDS | 3375777 | 612 | - | 0.156863 | |
DDB_G0293846 | DDB_G0293846 | DDB0232433 | CDS | 3380322 | 3216 | + | 0.145522 | |
DDB_G0293852_RTE | DDB_G0293852 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232433 | CDS | 3384170 | 222 | - | 0.351351 |
DDB_G0293854 | DDB_G0293854 | DDB0232433 | CDS | 3388739 | 255 | + | 0.305882 | |
DDB_G0293856 | DDB_G0293856 | DDB0232433 | CDS | 3389682 | 1830 | - | 0.257377 | |
DDB_G0293858 | DDB_G0293858 | DDB0232433 | CDS | 3392240 | 2403 | - | 0.226384 | |
DDB_G0293860 | DDB_G0293860 | DDB0232433 | CDS | 3395178 | 813 | + | 0.195572 | |
DDB_G0293862 | DDB_G0293862 | DDB0232433 | CDS | 3396260 | 750 | - | 0.309333 | |
DDB_G0293864 | DDB_G0293864 | DDB0232433 | CDS | 3398572 | 1527 | + | 0.251473 | |
DDB_G0293866 | DDB_G0293866 | bCommunity annotation:b DDB_G0293866 has both N and C-terminal domains similar to aprataxin and contains a poly-ADP ribose binding domain. Aprataxin is suspected to play a role in several different DNA repair pathways specifically by resolving abortive ligation intermediates [see Ahe et. al Nature 443 713-6 (2006) Rass et al. JBC 282 9469-9474 (2007).]br DDB_GO293866 is 5-fold overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (Doquang et al in preparation). Genes whose products are involved in replication-coupled DNA repair are generally overexpressed 3 to 6-fold in this strain while genes in replication-independent repair pathways are overexpressed by smaller factors if at all. In mammalian cells aprataxin interacts with XRCC1 and Ligase3 which are involved in (replication-independent) excision repair. The corresponding Dictyostelium genes are overexpressed less than twofold in the rblA-disruptant. Harry MacWilliams September 2009br | DDB0232433 | CDS | 3400165 | 1692 | - | 0.22695 |
DDB_G0293868 | DDB_G0293868 | DDB0232433 | CDS | 3402442 | 1638 | - | 0.230159 | |
DDB_G0293870 | DDB_G0293870 | DDB0232433 | CDS | 3406393 | 186 | + | 0.258065 | |
DDB_G0293878 | DDB_G0293878 | DDB0232433 | CDS | 3413755 | 4326 | + | 0.258437 | |
DDB_G0293880 | DDB_G0293880 | DDB0232433 | CDS | 3418217 | 987 | - | 0.281662 | |
DDB_G0293884 | DDB_G0293884 | DDB0232433 | CDS | 3421920 | 1542 | + | 0.218547 | |
DDB_G0293890 | DDB_G0293890 | DDB0232433 | CDS | 3429586 | 222 | + | 0.387387 | |
DDB_G0293892_RTE | DDB_G0293892 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232433 | CDS | 3384527 | 675 | + | 0.333333 |
DDB_G0293894_RTE | DDB_G0293894 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 3431147 | 441 | + | 0.408163 |
DDB_G0293906 | DDB_G0293906 | DDB0232433 | CDS | 3432681 | 318 | + | 0.27673 | |
DDB_G0293908_ps | DDB_G0293908 | putative pseudogene similar to | DDB0232433 | CDS | 3436293 | 900 | - | 0.195556 |
DDB_G0293910 | DDB_G0293910 | DDB0232433 | CDS | 3449223 | 318 | + | 0.27673 | |
DDB_G0293916 | DDB_G0293916 | DDB0232433 | CDS | 3471747 | 3510 | + | 0.241311 | |
DDB_G0293920 | DDB_G0293920 | DDB0232433 | CDS | 3481501 | 2586 | + | 0.322892 | |
DDB_G0293922 | DDB_G0293922 | DDB0232433 | CDS | 3484508 | 1146 | + | 0.222513 | |
DDB_G0293924 | DDB_G0293924 | DDB0232433 | CDS | 3490466 | 2661 | + | 0.282601 | |
DDB_G0293926 | DDB_G0293926 | DDB0232433 | CDS | 3504658 | 1497 | - | 0.225785 | |
DDB_G0293930 | DDB_G0293930 | similar to human ZDHHC16 (zinc finger DHHC domain-containing protein 16) contains 4 putative transmembrane domains | DDB0232433 | CDS | 3510935 | 960 | - | 0.258333 |
DDB_G0293934 | DDB_G0293934 | DDB0232433 | CDS | 3520311 | 5142 | - | 0.280436 | |
DDB_G0293938 | DDB_G0293938 | DDB0232433 | CDS | 3532350 | 1788 | + | 0.266779 | |
DDB_G0293940 | DDB_G0293940 | DDB0232433 | CDS | 3536699 | 1017 | + | 0.261554 | |
DDB_G0293942 | DDB_G0293942 | DDB0232433 | CDS | 3553305 | 4677 | + | 0.245884 | |
DDB_G0293944 | DDB_G0293944 | DDB0232433 | CDS | 3558157 | 390 | - | 0.197436 | |
DDB_G0293946 | DDB_G0293946 | conserved protein similar to S. cerevisiae EMI5 a mitochondrial protein which is involved in meiotic-specific transcription and sporulation | DDB0232433 | CDS | 3558856 | 426 | + | 0.230047 |
DDB_G0293948 | DDB_G0293948 | DDB0232433 | CDS | 3559692 | 2361 | + | 0.203727 | |
DDB_G0293950 | DDB_G0293950 | DDB0232433 | CDS | 3562548 | 972 | + | 0.26749 | |
DDB_G0293954 | DDB_G0293954 | DDB0232433 | CDS | 3570187 | 576 | - | 0.277778 | |
DDB_G0293956 | DDB_G0293956 | DDB0232433 | CDS | 3572844 | 354 | - | 0.30226 | |
DDB_G0293958 | DDB_G0293958 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232433 | CDS | 3460612 | 4779 | + | 0.208203 |
DDB_G0293964_RTE | DDB_G0293964 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 3574884 | 3180 | + | 0.35 |
DDB_G0293970 | DDB_G0293970 | DDB0232433 | CDS | 3434517 | 375 | - | 0.298667 | |
DDB_G0293974 | DDB_G0293974 | DDB0232433 | CDS | 3466413 | 1710 | - | 0.173099 | |
DDB_G0293976 | DDB_G0293976 | DDB0232433 | CDS | 3485736 | 1347 | - | 0.200445 | |
DDB_G0293980 | DDB_G0293980 | DDB0232433 | CDS | 3518793 | 993 | + | 0.277946 | |
DDB_G0293982 | DDB_G0293982 | DDB0232433 | CDS | 3537923 | 13014 | - | 0.256954 | |
DDB_G0293988 | DDB_G0293988 | DDB0232433 | CDS | 3583283 | 2928 | - | 0.244194 | |
DDB_G0293990 | DDB_G0293990 | DDB0232433 | CDS | 3578831 | 966 | - | 0.219462 | |
DDB_G0293992 | DDB_G0293992 | contains one C2 domain which is is a Ca2-dependent membrane-targeting module found in many cellular proteins involved in signal transduction or membrane trafficking | DDB0232433 | CDS | 3588432 | 477 | + | 0.255765 |
DDB_G0293998 | DDB_G0293998 | DDB0232433 | CDS | 3596687 | 459 | + | 0.300654 | |
DDB_G0294002_RTE | DDB_G0294002 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank GenBank AF298209 for consensus full-length element | DDB0232433 | CDS | 3600862 | 1365 | - | 0.311355 |
DDB_G0294004 | DDB_G0294004 | DDB0232433 | CDS | 3589297 | 2220 | - | 0.185135 | |
DDB_G0294006_ps | DDB_G0294006 | putative pseudogene small fragment similar to | DDB0232433 | CDS | 3593501 | 561 | - | 0.187166 |
DDB_G0294008_ps | DDB_G0294008 | putative pseudogene similar to Dictyostelium genes | DDB0232433 | CDS | 3598311 | 423 | + | 0.243499 |
DDB_G0294010_TE | DDB_G0294010 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232433 | CDS | 3599142 | 1149 | - | 0.227154 |
DDB_G0294290 | DDB_G0294290 | shares a short region of similarity with the nucleotide excision repair protein ERCC5XPG | DDB0232429 | CDS | 10462 | 2934 | + | 0.214724 |
DDB_G0294292 | DDB_G0294292 | similar to S. cerevisiae Lgs1 a putative GTPase involved in 60S ribosomal subunit biogenesis | DDB0232429 | CDS | 8123 | 2025 | + | 0.304198 |
DDB_G0294294 | DDB_G0294294 | DDB0232429 | CDS | 5771 | 327 | + | 0.324159 | |
DDB_G0294296_TE | DDB_G0294296 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232429 | CDS | 2782 | 1683 | - | 0.224005 |
DDB_G0294437_RTE | DDB_G0294437 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232429 | CDS | 4973434 | 4290 | + | 0.285548 |
DDB_G0294553 | DDB_G0294553 | DDB0232428 | CDS | 2805074 | 1380 | - | 0.278986 | |
DDB_G0294555 | DDB_G0294555 | DDB0232433 | CDS | 100153 | 1659 | + | 0.246534 | |
DDB_G0294557 | DDB_G0294557 | similar to the cortexillins actin-bundling proteins of the alpha-actininspectrin superfamily | DDB0232430 | CDS | 517463 | 1470 | - | 0.317687 |
DDB_G0294559 | DDB_G0294559 | DDB0232431 | CDS | 1421546 | 1047 | - | 0.281757 | |
DDB_G0294563 | DDB_G0294563 | EGF domain similar to the EGF-like repeats found in subtilisin-like serine peptidase tenascin X and WIF (Wnt inhibitory factor) | DDB0232431 | CDS | 2282608 | 2265 | - | 0.236645 |
DDB_G0294567 | DDB_G0294567 | DDB0232430 | CDS | 2439525 | 696 | + | 0.271552 | |
DDB_G0294569 | DDB_G0294569 | DDB0232429 | CDS | 1099522 | 540 | - | 0.225926 | |
DDB_G0294571 | DDB_G0294571 | DDB0232432 | CDS | 4610784 | 612 | - | 0.28268 | |
DDB_G0294573 | DDB_G0294573 | similar to | DDB0232433 | CDS | 3288367 | 360 | - | 0.261111 |
DDB_G0294575 | DDB_G0294575 | DDB0232430 | CDS | 156515 | 4926 | + | 0.204425 | |
DDB_G0294577 | DDB_G0294577 | DDB0232430 | CDS | 6055905 | 672 | + | 0.235119 | |
DDB_G0294583 | DDB_G0294583 | DDB0232429 | CDS | 1122814 | 705 | + | 0.229787 | |
DDB_G0294585 | DDB_G0294585 | contains a domain found in the family of Major Royal Jelly Proteins constituting 82-90 | DDB0232430 | CDS | 3552325 | 4941 | - | 0.277069 |
DDB_G0294587 | DDB_G0294587 | DDB0232429 | CDS | 920601 | 3547 | + | 0.31435 | |
DDB_G0294589 | DDB_G0294589 | DDB0232431 | CDS | 4603487 | 882 | + | 0.276644 | |
DDB_G0294591 | DDB_G0294591 | contains three putative transmembrane domains not similar to any other protein | DDB0232432 | CDS | 1587124 | 1209 | + | 0.257237 |
DDB_G0294593 | DDB_G0294593 | DDB0232431 | CDS | 470714 | 624 | - | 0.219551 | |
DDB_G0294595 | DDB_G0294595 | multi-domain protein the TPR superhelical structures present a surface that is well suited to binding large substrates such as proteins and nucleic acids | DDB0232431 | CDS | 1785353 | 1542 | + | 0.217899 |
DDB_G0294597 | DDB_G0294597 | DDB0232428 | CDS | 3979902 | 1323 | - | 0.294785 | |
DDB_G0294603 | DDB_G0294603 | DDB0232432 | CDS | 4577727 | 525 | - | 0.259048 | |
DDB_G0294605 | DDB_G0294605 | conserved hypothetical Dictyostelium protein identical to | DDB0232430 | CDS | 3695606 | 141 | - | 0.496454 |
DDB_G0294607_ps | DDB_G0294607 | putative pseudogene conserved hypothetical protein | DDB0232430 | CDS | 3694386 | 258 | + | 0.344961 |
DDB_G0294611 | DDB_G0294611 | DDB0232432 | CDS | 2837078 | 1836 | - | 0.314815 | |
DDB_G0294617 | DDB_G0294617 | DDB0232430 | CDS | 200995 | 738 | - | 0.223577 | |
DDB_G0294619 | DDB_G0294619 | DDB0232430 | CDS | 2827799 | 1398 | - | 0.183119 | |
DDB_G0294621 | DDB_G0294621 | contains three Sel1-like repeats which are related to tetratricopeptide (TPR) repeats | DDB0232431 | CDS | 86151 | 1854 | + | 0.304207 |
DDB_G0294625_ps | DDB_G0294625 | putative pseudogene conserved Dictyostelium protein family | DDB0232433 | CDS | 1607077 | 243 | - | 0.308642 |
DDB_G0294627 | DDB_G0294627 | DDB0232433 | CDS | 1606038 | 609 | - | 0.308703 | |
DDB_G0294629 | DDB_G0294629 | DDB0232433 | CDS | 1603469 | 1785 | - | 0.285154 | |
DDB_G0294631 | DDB_G0294631 | similar to Entamoeba histolytica XP_650568 contains no conserved functional domains | DDB0232431 | CDS | 4158602 | 765 | - | 0.267974 |
DDB_G0294633 | DDB_G0294633 | contains two ankyrin repeats which are among the most common protein-protein interaction motifs | DDB0232429 | CDS | 6456944 | 3039 | - | 0.273445 |
DDB_G0294635 | DDB_G0294635 | DDB0232430 | CDS | 2232590 | 2457 | + | 0.265364 | |
DDB_G0295473 | DDB_G0295473 | glycine-rich 52 amino acid protein | DDB0232430 | CDS | 1548383 | 159 | + | 0.446541 |
DDB_G0295475 | DDB_G0295475 | DDB0232433 | CDS | 418715 | 1710 | - | 0.283626 | |
DDB_G0295479 | DDB_G0295479 | similar to polyketide synthases but only 179 amino acids long other polyketide synthase genes encode proteins of about 3000 amino acids | DDB0232432 | CDS | 4104623 | 537 | + | 0.232775 |
DDB_G0295481_ps | DDB_G0295481 | putative pseudogene fragment very similar to Dictyostelium ppiD | DDB0232431 | CDS | 944514 | 243 | + | 0.283951 |
DDB_G0295483 | DDB_G0295483 | similar to H. sapiens C13orf18 RUN domains are predicted to play roles in Ras-like GTPase signaling pathways | DDB0232433 | CDS | 636558 | 4197 | + | 0.250655 |
DDB_G0295485 | DDB_G0295485 | DDB0232431 | CDS | 3666930 | 5076 | - | 0.310481 | |
DDB_G0295661 | DDB_G0295661 | there is an identical copy of this gene on chromosome 2 | DDB0232432 | CDS | 4559095 | 1755 | - | 0.317949 |
DDB_G0295665 | DDB_G0295665 | DDB0232432 | CDS | 4561968 | 564 | + | 0.271277 | |
DDB_G0295669 | DDB_G0295669 | isochorismatase (also: 23 dihydro-23 dihydroxybenzoate synthase) catalyses the conversion of isochorismate Hsub2subO to 23-dihydroxybenzoate and pyruvate conserved in bacteria fungi amoeba and plants | DDB0232433 | CDS | 769784 | 552 | - | 0.318841 |
DDB_G0295671 | DDB_G0295671 | DDB0232431 | CDS | 4703129 | 1083 | - | 0.237304 | |
DDB_G0295675 | DDB_G0295675 | DDB0232432 | CDS | 2700736 | 2478 | + | 0.282486 | |
DDB_G0295679 | DDB_G0295679 | DDB0232430 | CDS | 22082 | 3372 | + | 0.273725 | |
DDB_G0295681 | DDB_G0295681 | DDB0232430 | CDS | 32370 | 336 | + | 0.357143 | |
DDB_G0295683 | DDB_G0295683 | DDB0232433 | CDS | 1769740 | 4770 | + | 0.291614 | |
DDB_G0295685 | DDB_G0295685 | highly similar to other Dictyostelium small proteins antibodies against this protein inhibits aggregation | DDB0232429 | CDS | 833213 | 270 | - | 0.325926 |
DDB_G0295689 | DDB_G0295689 | contains a predicted signal peptide and two transmembrane domains has no known homologs | DDB0232432 | CDS | 188514 | 405 | + | 0.301235 |
DDB_G0295691 | DDB_G0295691 | shares a region of similarity with proteins of unknown functions contains eight predicted transmembrane domains | DDB0232433 | CDS | 883760 | 1164 | + | 0.256873 |
DDB_G0295693 | DDB_G0295693 | similar to | DDB0232432 | CDS | 4571270 | 969 | - | 0.177503 |
DDB_G0295695 | DDB_G0295695 | conserved Dictyostelium protein similar to bacterial proteins contains a predicted signal peptide | DDB0232428 | CDS | 4586186 | 369 | + | 0.281843 |
DDB_G0295701 | DDB_G0295701 | contains a predicted signal peptide contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232432 | CDS | 304647 | 1002 | - | 0.287425 |
DDB_G0295705 | DDB_G0295705 | DDB0232433 | CDS | 621820 | 2340 | - | 0.191026 | |
DDB_G0295713 | DDB_G0295713 | DDB0232430 | CDS | 4417290 | 2115 | - | 0.249645 | |
DDB_G0295715 | DDB_G0295715 | DDB0232430 | CDS | 5300180 | 4668 | + | 0.322408 | |
DDB_G0295717 | DDB_G0295717 | DDB0232431 | CDS | 2373104 | 2466 | - | 0.242092 | |
DDB_G0295719 | DDB_G0295719 | DDB0232431 | CDS | 2369310 | 1851 | + | 0.415451 | |
DDB_G0295723 | DDB_G0295723 | DDB0232430 | CDS | 283984 | 2316 | - | 0.294041 | |
DDB_G0295725 | DDB_G0295725 | DDB0232430 | CDS | 312009 | 1077 | - | 0.321263 | |
DDB_G0295727 | DDB_G0295727 | amino terminus is similar to spore coat proteins cotESP65 and cotDSP75 serine and glycine rich the central region contains repeats of the sequence GTSTT or GRSTT contains a predicted signal peptide and at least 18 transmembrane domains | DDB0232430 | CDS | 416548 | 6258 | + | 0.446948 |
DDB_G0295731 | DDB_G0295731 | DDB0232430 | CDS | 2424448 | 1680 | + | 0.192857 | |
DDB_G0295733 | DDB_G0295733 | DDB0232431 | CDS | 4157569 | 480 | - | 0.277083 | |
DDB_G0295735 | DDB_G0295735 | DDB0232432 | CDS | 1928245 | 1809 | + | 0.210061 | |
DDB_G0295737 | DDB_G0295737 | DDB0232432 | CDS | 3359151 | 2817 | - | 0.29535 | |
DDB_G0295739 | DDB_G0295739 | DDB0232432 | CDS | 3772467 | 999 | - | 0.309309 | |
DDB_G0295741 | DDB_G0295741 | contains a C-terminal FR47-like N-acyltransferase-like domain has similarity to H. sapiens glycine N-acyltransferase-like protein 1 (GLYATL1) | DDB0232433 | CDS | 842775 | 909 | - | 0.246425 |
DDB_G0295743 | DDB_G0295743 | DDB0232432 | CDS | 2586654 | 2175 | - | 0.262989 | |
DDB_G0295745 | DDB_G0295745 | DDB0232432 | CDS | 2584317 | 192 | - | 0.223958 | |
DDB_G0295747 | DDB_G0295747 | DDB0232432 | CDS | 2582433 | 1590 | - | 0.215094 | |
DDB_G0295749 | DDB_G0295749 | highly similar to | DDB0232432 | CDS | 2579548 | 1714 | - | 0.280047 |
DDB_G0295751 | DDB_G0295751 | conserved D. discoideum protein | DDB0232428 | CDS | 3269066 | 252 | - | 0.373016 |
DDB_G0295753 | DDB_G0295753 | very similar to Dictyostelium mcfN and to human SLC25A3 and S. cerevisiae MIR1 which transports inorganic phosphate from the cytosol to the mitochondrion matrix | DDB0232432 | CDS | 2590095 | 900 | + | 0.342222 |
DDB_G0295757 | DDB_G0295757 | DDB0232428 | CDS | 2506114 | 10143 | + | 0.292714 | |
DDB_G0295759 | DDB_G0295759 | DDB0232432 | CDS | 2606597 | 267 | - | 0.303371 | |
DDB_G0295763 | DDB_G0295763 | DDB0232428 | CDS | 3613525 | 1980 | + | 0.150505 | |
DDB_G0295767 | DDB_G0295767 | DDB0232430 | CDS | 5185447 | 99 | + | 0.525253 | |
DDB_G0295769 | DDB_G0295769 | DDB0232430 | CDS | 5184689 | 99 | + | 0.373737 | |
DDB_G0295771 | DDB_G0295771 | DDB0232430 | CDS | 5795939 | 4542 | + | 0.217305 | |
DDB_G0295773 | DDB_G0295773 | similar to the eukaryotic transmembrane protein 85 (TMEM85) contains two putative transmembrane domains | DDB0232429 | CDS | 6907430 | 594 | + | 0.281145 |
DDB_G0295775 | DDB_G0295775 | has similarity to the plant importin alpha chain subunit of a protein transporter | DDB0232429 | CDS | 5276826 | 999 | - | 0.231231 |
DDB_G0295777 | DDB_G0295777 | DDB0232432 | CDS | 428287 | 927 | - | 0.186624 | |
DDB_G0295779 | DDB_G0295779 | DDB0232432 | CDS | 1450193 | 528 | - | 0.327652 | |
DDB_G0295781 | DDB_G0295781 | weakly similar to S. cerevisiae DUG3 involved in degradation of glutathione (GSH) and other peptides containing a gamma-glu-X bond in an alternative pathway to GSH degradation by gamma-glutamyl transpeptidase | DDB0232431 | CDS | 4542261 | 1125 | - | 0.330667 |
DDB_G0295783 | DDB_G0295783 | DDB0232431 | CDS | 4538199 | 156 | - | 0.24359 | |
DDB_G0295785 | DDB_G0295785 | DDB0232431 | CDS | 4536016 | 1086 | + | 0.252302 | |
DDB_G0295789 | DDB_G0295789 | shares a short region of similarity with GRP1 (general receptor for phosphoinositides 1)-associated scaffold protein contains one transmembrane domain | DDB0232431 | CDS | 3213388 | 480 | - | 0.279167 |
DDB_G0295791 | DDB_G0295791 | DDB0232433 | CDS | 1765779 | 2322 | - | 0.216193 | |
DDB_G0295793 | DDB_G0295793 | DDB0232433 | CDS | 2856788 | 1974 | + | 0.340426 | |
DDB_G0295797 | DDB_G0295797 | DDB0232433 | CDS | 1762213 | 1338 | + | 0.286248 | |
DDB_G0295799 | DDB_G0295799 | DDB0232433 | CDS | 1763747 | 753 | - | 0.289509 | |
DDB_G0295801 | DDB_G0295801 | DDB0232433 | CDS | 1765213 | 408 | + | 0.308824 | |
DDB_G0295803 | DDB_G0295803 | DDB0232433 | CDS | 1775198 | 486 | + | 0.162551 | |
DDB_G0295807 | DDB_G0295807 | DDB0232429 | CDS | 986307 | 912 | - | 0.302632 | |
DDB_G0295809 | DDB_G0295809 | DDB0232429 | CDS | 985804 | 303 | - | 0.214521 | |
DDB_G0295811 | DDB_G0295811 | DDB0232430 | CDS | 1753571 | 912 | - | 0.288377 | |
DDB_G0295813 | DDB_G0295813 | DDB0232432 | CDS | 2607950 | 396 | - | 0.29798 | |
DDB_G0295815_ps | DDB_G0295815 | putative pseudogene very similar to | DDB0232432 | CDS | 2608554 | 204 | - | 0.348039 |
DDB_G0295817 | DDB_G0295817 | DDB0232429 | CDS | 151328 | 2187 | - | 0.186557 | |
DDB_G0295819 | DDB_G0295819 | DDB0232429 | CDS | 472505 | 1428 | - | 0.215686 | |
DDB_G0295821 | DDB_G0295821 | DDB0232429 | CDS | 1423166 | 2958 | + | 0.218053 | |
DDB_G0295823 | DDB_G0295823 | DDB0232431 | CDS | 3559137 | 111 | + | 0.369369 | |
DDB_G0295827 | DDB_G0295827 | DDB0232429 | CDS | 3933601 | 1719 | + | 0.276323 | |
DDB_G0295829 | DDB_G0295829 | DDB0232428 | CDS | 1266897 | 3072 | + | 0.198568 | |
DDB_G0295833 | DDB_G0295833 | there is a second copy of this gene | DDB0232429 | CDS | 2544712 | 915 | - | 0.243716 |
DDB_G0295839 | DDB_G0295839 | DDB0232430 | CDS | 41608 | 843 | + | 0.257414 | |
DDB_G0295841 | DDB_G0295841 | DDB0232433 | CDS | 1614536 | 2094 | + | 0.206781 | |
DDB_G0295843 | DDB_G0295843 | contains a partial serinethreonine protein kinase catalytic domain that is similar to eukaryotic translation initiation factor 2-alpha kinase however the domain does not have the catalytic aspartate conserved. | DDB0232433 | CDS | 2093907 | 1827 | - | 0.300493 |
DDB_G0295845 | DDB_G0295845 | DDB0232429 | CDS | 1309841 | 711 | - | 0.299578 | |
DDB_G0295847 | DDB_G0295847 | DDB0232428 | CDS | 585586 | 4029 | - | 0.275503 | |
DDB_G0295849 | DDB_G0295849 | DDB0232430 | CDS | 5349087 | 1470 | + | 0.353061 | |
DDB_G0302530 | DDB_G0302530 | DDB0232430 | CDS | 2010240 | 3444 | - | 0.23374 | |
DDB_G0302543 | DDB_G0302543 | DDB0232429 | CDS | 4133180 | 2571 | - | 0.285103 | |
DDB_G0302588 | DDB_G0302588 | DDB0232428 | CDS | 1056562 | 10701 | - | 0.305766 | |
DDB_G0302676 | DDB_G0302676 | DDB0232430 | CDS | 2829765 | 522 | - | 0.258621 | |
DDB_G0304475 | DDB_G0304475 | DDB0232430 | CDS | 168687 | 1329 | + | 0.320542 | |
DDB_G0304561 | DDB_G0304561 | similar to solute carrier family 35 member E4 (SLC35E4) proteins contains 10 predicted transmembrane domains | DDB0232431 | CDS | 2797226 | 1476 | + | 0.278455 |
DDB_G0304683 | DDB_G0304683 | DDB0232433 | CDS | 1860016 | 2583 | - | 0.258227 | |
DDB_G0304886 | DDB_G0304886 | DDB0232431 | CDS | 5267330 | 372 | + | 0.317204 | |
DDB_G0305367 | DDB_G0305367 | DDB0232429 | CDS | 7708598 | 1356 | - | 0.247788 | |
DDB_G0305372 | DDB_G0305372 | DDB0232429 | CDS | 6432588 | 1170 | - | 0.259829 | |
DDB_G0305463_RTE | DDB_G0305463 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232429 | CDS | 4980794 | 1581 | + | 0.295383 |
DDB_G0305465 | DDB_G0305465 | DDB0232429 | CDS | 4978458 | 516 | + | 0.312016 | |
DDB_G0305520 | DDB_G0305520 | belongs to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8214671 | 4092 | + | 0.217498 |
DDB_G0305538 | DDB_G0305538 | very similar to neighboring genes that belong to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8239430 | 4189 | + | 0.226307 |
DDB_G0305545 | DDB_G0305545 | DDB0232430 | CDS | 1726391 | 933 | + | 0.237942 | |
DDB_G0305565_TE | DDB_G0305565 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232430 | CDS | 2683915 | 3690 | - | 0.264228 |
DDB_G0305569 | DDB_G0305569 | DDB0232428 | CDS | 4921654 | 693 | + | 0.300144 | |
DDB_G0305706_RTE | DDB_G0305706 | ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 184608 | 1847 | + | 0.400108 |
DDB_G0305708_RTE | DDB_G0305708 | ORF1 protein fragment of DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232428 | CDS | 174742 | 652 | - | 0.366564 |
DDB_G0305714_RTE | DDB_G0305714 | ORF2 protein encoding reverse transcriptase (RT) and integrase (IN) of long terminal repeat retrotransposon Skipper refer to Genbank AF049230 for full-length element | DDB0232430 | CDS | 2688175 | 3723 | + | 0.32823 |
DDB_G0305791_ps | DDB_G0305791 | putative pseudogene EGF-like domain-containing protein | DDB0232429 | CDS | 8098024 | 3598 | + | 0.23652 |
DDB_G0306367 | DDB_G0306367 | similar to Dictystelium cfrA B C and D (GP138A-D) | DDB0232428 | CDS | 2395862 | 1653 | + | 0.203267 |
DDB_G0306370_RTE | DDB_G0306370 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232428 | CDS | 2398639 | 3798 | + | 0.322275 |
DDB_G0306976 | DDB_G0306976 | DDB0232430 | CDS | 2609748 | 3567 | + | 0.216148 | |
DDB_G0306979 | DDB_G0306979 | conserved Dictyostelium protein contains 2 EGF-like domains contains both a predicted N-terminal signal sequence and C-terminal transmembrane domain | DDB0232430 | CDS | 2613814 | 3411 | + | 0.274993 |
DDB_G0307042 | DDB_G0307042 | DDB0232431 | CDS | 4491401 | 2778 | - | 0.257019 | |
DDB_G0307043 | DDB_G0307043 | DDB0232431 | CDS | 4487639 | 2757 | - | 0.228509 | |
DDB_G0307284 | DDB_G0307284 | DDB0232429 | CDS | 7949669 | 906 | + | 0.222958 | |
DDB_G0307694 | DDB_G0307694 | DDB0232428 | CDS | 3656011 | 2181 | - | 0.185695 | |
DDB_G0307697 | DDB_G0307697 | DDB0232428 | CDS | 3653375 | 2028 | - | 0.277613 | |
DDB_G0307754_RTE | DDB_G0307754 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2849483 | 468 | - | 0.344017 |
DDB_G0307769_RTE | DDB_G0307769 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232428 | CDS | 2849081 | 285 | - | 0.242105 |
DDB_G0346536 | DDB_G0346536 | DDB0232432 | CDS | 3206289 | 1596 | - | 0.231203 | |
DDB_G0346538 | DDB_G0346538 | DDB0232432 | CDS | 3204528 | 1599 | - | 0.232645 | |
DDB_G0346831 | DDB_G0346831 | DDB0232428 | CDS | 4895305 | 2262 | + | 0.229443 | |
DDB_G0346833 | DDB_G0346833 | DDB0232428 | CDS | 4898040 | 1848 | + | 0.207251 | |
DDB_G0346922 | DDB_G0346922 | DDB0232432 | CDS | 102942 | 1521 | - | 0.277449 | |
DDB_G0346924 | DDB_G0346924 | DDB0232432 | CDS | 100675 | 1521 | - | 0.275477 | |
DDB_G0347202 | DDB_G0347202 | DDB0232428 | CDS | 4201625 | 609 | - | 0.27422 | |
DDB_G0347333 | DDB_G0347333 | DDB0232428 | CDS | 4009790 | 444 | - | 0.265766 | |
DDB_G0347550 | DDB_G0347550 | DDB0232432 | CDS | 4718494 | 1497 | + | 0.279893 | |
DDB_G0347551 | DDB_G0347551 | DDB0232432 | CDS | 4720437 | 1845 | + | 0.211382 | |
DDB_G0347657 | DDB_G0347657 | DDB0232432 | CDS | 3251908 | 1257 | + | 0.215593 | |
DDB_G0347658 | DDB_G0347658 | DDB0232432 | CDS | 3253562 | 1257 | + | 0.351631 | |
DDB_G0347686 | DDB_G0347686 | DDB0232428 | CDS | 2750055 | 2184 | + | 0.266941 | |
DDB_G0347687 | DDB_G0347687 | DDB0232428 | CDS | 2752444 | 537 | - | 0.299814 | |
DDB_G0347783 | DDB_G0347783 | DDB0232431 | CDS | 989598 | 174 | + | 0.281609 | |
DDB_G0347826 | DDB_G0347826 | DDB0232429 | CDS | 299937 | 1980 | - | 0.189394 | |
DDB_G0347828 | DDB_G0347828 | DDB0232429 | CDS | 302268 | 441 | - | 0.315193 | |
DDB_G0347907 | DDB_G0347907 | DDB0232430 | CDS | 5473812 | 786 | + | 0.254453 | |
DDB_G0347908 | DDB_G0347908 | DDB0232430 | CDS | 5474915 | 2082 | + | 0.20317 | |
DDB_G0348143 | DDB_G0348143 | DDB0232432 | CDS | 514890 | 93 | + | 0.408602 | |
DDB_G0348179 | DDB_G0348179 | DDB0232428 | CDS | 1390845 | 105 | + | 0.361905 | |
DDB_G0348183 | DDB_G0348183 | DDB0232432 | CDS | 4073745 | 2241 | + | 0.279786 | |
DDB_G0348184 | DDB_G0348184 | DDB0232432 | CDS | 4076581 | 900 | + | 0.26 | |
DDB_G0348373 | DDB_G0348373 | DDB0232431 | CDS | 2073118 | 135 | - | 0.281481 | |
DDB_G0348374 | DDB_G0348374 | DDB0232431 | CDS | 2071986 | 195 | - | 0.333333 | |
DDB_G0348427_ps | DDB_G0348427 | putative pseudogene similar to D. discoideum genes | DDB0232428 | CDS | 4054671 | 765 | - | 0.230065 |
DDB_G0348428 | DDB_G0348428 | DDB0232428 | CDS | 4055932 | 2043 | - | 0.184533 | |
DDB_G0348565 | DDB_G0348565 | DDB0232429 | CDS | 7861958 | 948 | - | 0.2827 | |
DDB_G0348639 | DDB_G0348639 | DDB0232429 | CDS | 188685 | 210 | - | 0.290476 | |
DDB_G0348640_ps | DDB_G0348640 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 185586 | 2028 | - | 0.233235 |
DDB_G0348736_ps | DDB_G0348736 | putative pseudogene similar to the large family of EGF repeat-containing proteins including neighboring gene | DDB0232429 | CDS | 2184460 | 2204 | - | 0.236842 |
DDB_G0348834 | DDB_G0348834 | DDB0232431 | CDS | 3284415 | 4749 | + | 0.217098 | |
DDB_G0348835 | DDB_G0348835 | DDB0232431 | CDS | 3289563 | 4740 | + | 0.221097 | |
DDB_G0348861 | DDB_G0348861 | DDB0232429 | CDS | 1185450 | 90 | - | 0.344444 | |
DDB_G0348868 | DDB_G0348868 | DDB0232432 | CDS | 2648590 | 117 | - | 0.418803 | |
DDB_G0348940 | DDB_G0348940 | DDB0232429 | CDS | 7403620 | 1473 | + | 0.220638 | |
DDB_G0348941_ps | DDB_G0348941 | putative pseudogene fragment similar to D. discoideum genes | DDB0232429 | CDS | 7405279 | 1084 | + | 0.307196 |
DDB_G0349030 | DDB_G0349030 | DDB0232428 | CDS | 3163747 | 834 | - | 0.255396 | |
DDB_G0349042 | DDB_G0349042 | DDB0232432 | CDS | 1339549 | 1050 | - | 0.287619 | |
DDB_G0349043 | DDB_G0349043 | DDB0232432 | CDS | 1336627 | 1767 | - | 0.271647 | |
DDB_G0349057 | DDB_G0349057 | DDB0232430 | CDS | 4157794 | 804 | - | 0.254975 | |
DDB_G0349073_ps | DDB_G0349073 | putative pseudogene fragment similar to a D. discoideum gene family including | DDB0232431 | CDS | 241054 | 1427 | - | 0.28171 |
DDB_G0349118 | DDB_G0349118 | DDB0232429 | CDS | 7074945 | 162 | - | 0.209877 | |
DDB_G0349136 | DDB_G0349136 | DDB0232433 | CDS | 1350474 | 3105 | + | 0.260225 | |
DDB_G0349138 | DDB_G0349138 | DDB0232433 | CDS | 1354305 | 492 | + | 0.243902 | |
DDB_G0349203 | DDB_G0349203 | DDB0232430 | CDS | 5409867 | 2754 | + | 0.200073 | |
DDB_G0349205 | DDB_G0349205 | DDB0232430 | CDS | 5413178 | 5190 | + | 0.267245 | |
DDB_G0349222 | DDB_G0349222 | DDB0232430 | CDS | 598613 | 444 | - | 0.231982 | |
DDB_G0349279 | DDB_G0349279 | DDB0232428 | CDS | 530163 | 816 | - | 0.208333 | |
DDB_G0349281 | DDB_G0349281 | DDB0232428 | CDS | 529188 | 267 | - | 0.318352 | |
DDB_G0349319 | DDB_G0349319 | DDB0232432 | CDS | 4344171 | 903 | + | 0.219269 | |
DDB_G0349321 | DDB_G0349321 | DDB0232432 | CDS | 4345695 | 702 | + | 0.274929 | |
DDB_G0349347 | DDB_G0349347 | DDB0232433 | CDS | 3330793 | 354 | - | 0.282486 | |
DDB_G0349375 | DDB_G0349375 | DDB0232429 | CDS | 5604371 | 612 | + | 0.267974 | |
DDB_G0349377 | DDB_G0349377 | DDB0232429 | CDS | 5605276 | 774 | + | 0.273902 | |
DDB_G0349390 | DDB_G0349390 | DDB0232429 | CDS | 7161840 | 171 | + | 0.222222 | |
DDB_G0349426 | DDB_G0349426 | DDB0232430 | CDS | 6135302 | 453 | - | 0.271523 | |
DDB_G0349427 | DDB_G0349427 | DDB0232430 | CDS | 6132903 | 1845 | - | 0.175068 | |
DDB_G0349444 | DDB_G0349444 | putative pseudogene similar to a large gene family encoding FNIP repeat-containing proteins including | DDB0232432 | CDS | 3645353 | 1455 | - | 0.195876 |
DDB_G0349476_ps | DDB_G0349476 | putative pseudogene fragment similar to D. discoideum genes | DDB0232429 | CDS | 1884778 | 3639 | - | 0.209673 |
DDB_G0349487 | DDB_G0349487 | DDB0232429 | CDS | 6914688 | 618 | - | 0.307443 | |
DDB_G0349488 | DDB_G0349488 | DDB0232429 | CDS | 6912714 | 1473 | - | 0.297352 | |
DDB_G0349497_ps | DDB_G0349497 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 2205077 | 1859 | + | 0.236686 |
DDB_G0349499 | DDB_G0349499 | DDB0232429 | CDS | 2207279 | 4164 | + | 0.25048 | |
DDB_G0349518 | DDB_G0349518 | DDB0232429 | CDS | 5616700 | 81 | - | 0.209877 | |
DDB_G0349530 | DDB_G0349530 | DDB0232431 | CDS | 1603328 | 2448 | - | 0.33701 | |
DDB_G0349537 | DDB_G0349537 | DDB0232430 | CDS | 5666499 | 396 | + | 0.330808 | |
DDB_G0349761_RTE | DDB_G0349761 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232430 | CDS | 2634953 | 2856 | + | 0.348039 |
DDB_G0349834_ps | DDB_G0349834 | putative pseudogene fragment similar to gene | DDB0232429 | CDS | 4523885 | 403 | - | 0.188586 |
DDB_G0350235 | DDB_G0350235 | DDB0232428 | CDS | 3983950 | 465 | - | 0.236559 | |
DG1037 | DDB_G0287925 | DDB0232432 | CDS | 857146 | 1815 | + | 0.251791 | |
DG1091 | DDB_G0289175 | DDB0232432 | CDS | 2479410 | 5478 | - | 0.220701 | |
DG1098 | DDB_G0293192 | DDB0232433 | CDS | 2617515 | 6132 | + | 0.21396 | |
DG1105 | DDB_G0277843 | DDB0232430 | CDS | 1006468 | 4749 | - | 0.336281 | |
DG1112 | DDB_G0276463 | DDB0232429 | CDS | 6915740 | 3174 | - | 0.26528 | |
DG1113 | DDB_G0280959 | DDB0232430 | CDS | 4213401 | 3474 | - | 0.250144 | |
DG1122 | DDB_G0277397 | DDB0232429 | CDS | 7998660 | 2142 | + | 0.249767 | |
DG1124 | DDB_G0274577 | DDB0232429 | CDS | 3892978 | 3849 | - | 0.28423 | |
DG2033 | DDB_G0278965 | DDB0232430 | CDS | 1480041 | 5043 | + | 0.223478 | |
DG2044 | DDB_G0285423 | DDB0232431 | CDS | 3504616 | 1833 | + | 0.228587 | |
Dd5P1 | DDB_G0279927 | DDB0232430 | CDS | 2713196 | 2823 | + | 0.295785 | |
Dd5P2 | DDB_G0284187 | DDB0232431 | CDS | 1813905 | 5403 | - | 0.294281 | |
Dd5P3 | DDB_G0292392 | DDB0232433 | CDS | 1583730 | 4140 | - | 0.320773 | |
Dd5P4 | DDB_G0267462 | inositol 5-phosphatase similar to the human protein OCRL which when defect causes Lowe syndrome involved in Dictyostelium growth development and phagocytosis | DDB0232428 | CDS | 1752059 | 2364 | + | 0.26692 |
H1 | DDB_G0285319 | linker histone H1H5 family protein plays a role in formation of 30 nm chromatin fiber | DDB0232431 | CDS | 3145643 | 543 | + | 0.401473 |
H2AX | DDB_G0279667 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H2B | DDB0232430 | CDS | 2410613 | 465 | + | 0.427957 |
H2AZ | DDB_G0286747 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H2B | DDB0232431 | CDS | 4922308 | 432 | - | 0.293981 |
H2Av1 | DDB_G0289187 | DDB0232432 | CDS | 2451919 | 783 | + | 0.246488 | |
H2Av2 | DDB_G0289193 | DDB0232432 | CDS | 2455467 | 861 | + | 0.339141 | |
H2Av3 | DDB_G0289197 | DDB0232432 | CDS | 2457890 | 378 | + | 0.195767 | |
H2Bv1 | DDB_G0293758 | DDB0232433 | CDS | 3289579 | 681 | - | 0.330396 | |
H2Bv2 | DDB_G0276273 | DDB0232429 | CDS | 6631152 | 1425 | + | 0.247018 | |
H2Bv3 | DDB_G0286509 | DDB0232431 | CDS | 4575107 | 465 | + | 0.393548 | |
H3a | DDB_G0267402 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H4 | DDB0232428 | CDS | 1520754 | 420 | + | 0.414286 |
H3b | DDB_G0270838 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H4 | DDB0232428 | CDS | 4846006 | 411 | - | 0.403893 |
H3c | DDB_G0271092 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H4 | DDB0232428 | CDS | 4845008 | 411 | - | 0.347932 |
H3v1 | DDB_G0291185 | DDB0232432 | CDS | 5034573 | 1860 | - | 0.374731 | |
H3v2 | DDB_G0277979 | DDB0232430 | CDS | 91596 | 270 | - | 0.32963 | |
H4a | DDB_G0277183 | one of two identical H4 proteins (other is | DDB0232429 | CDS | 7697697 | 327 | - | 0.425076 |
H4b | DDB_G0276863 | one of two identical H4 proteins (other is | DDB0232429 | CDS | 7515236 | 327 | + | 0.40367 |
I6KA | DDB_G0278739 | mediates chemotaxis via pleckstrin homology (PH) domain-PtdIns(345)P3 interactions | DDB0232430 | CDS | 1187328 | 2151 | - | 0.23245 |
X69101 | DDB_G0294501 | DDB0232433 | CDS | 3385382 | 116 | + | 0.362069 | |
aarA | DDB_G0288877 | component of actin-associated intercellular junctions and involved in cell-cell adhesion signal transduction and stalk formation during development binds to Ctnna the Dictyostelium alpha-catenin related protein | DDB0232432 | CDS | 2168858 | 2274 | - | 0.255937 |
aass | DDB_G0284835 | bifunctional enzyme: lysine-ketoglutarate reductase (lysine alpha-ketoglutarate NADPH saccharopine) and saccharopine dehydrogenase (catalyzes the reaction saccharopine L-glutamate 2-aminoadipate 6-semialdehyde NADH Hsupsup) there is a related monofunctional saccharopine reductase | DDB0232431 | CDS | 2456087 | 2730 | + | 0.342125 |
aatA | DDB_G0268664 | catalyzes the reaction oxaloacetate L-glutamate L-aspartate | DDB0232428 | CDS | 1889432 | 1281 | + | 0.387978 |
aatB | DDB_G0282493 | catalyzes the reaction oxaloacetate L-glutamate L-aspartate | DDB0232430 | CDS | 5845721 | 1317 | - | 0.389522 |
abcA1 | DDB_G0291994 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 1093282 | 2634 | + | 0.319286 |
abcA10 | DDB_G0283387 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232431 | CDS | 620087 | 2664 | + | 0.267643 |
abcA11 | DDB_G0275453 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232429 | CDS | 6103616 | 2505 | + | 0.227944 |
abcA2 | DDB_G0267438 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232428 | CDS | 758875 | 4866 | + | 0.30374 |
abcA3 | DDB_G0293436 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 2880255 | 5109 | + | 0.267371 |
abcA4 | DDB_G0274121 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232429 | CDS | 3872948 | 4848 | - | 0.249587 |
abcA5 | DDB_G0274119 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232429 | CDS | 4156981 | 4989 | - | 0.274805 |
abcA6 | DDB_G0291245 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 313947 | 4896 | - | 0.278595 |
abcA7 | DDB_G0271140 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232429 | CDS | 196707 | 2520 | + | 0.280952 |
abcA8 | DDB_G0271138 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232429 | CDS | 193220 | 2514 | - | 0.26253 |
abcA9 | DDB_G0291980 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 1089711 | 2538 | - | 0.289992 |
abcB1 | DDB_G0293416 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 2861187 | 2730 | - | 0.279487 |
abcB2 | DDB_G0293438 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 2891271 | 4194 | - | 0.313782 |
abcB3 | DDB_G0291714 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 667903 | 4299 | + | 0.32682 |
abcB4 | DDB_G0279915 | half transporter consisting of one ABC domain and one transmembrane domain serves as an anchor for the calcium-dependent cell-cell adhesion protein CadA | DDB0232430 | CDS | 2759596 | 2304 | - | 0.296875 |
abcB5 | DDB_G0292554 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 1786504 | 2094 | - | 0.294651 |
abcB6 | DDB_G0282931 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232431 | CDS | 9046 | 2037 | - | 0.300442 |
abcB7 | DDB_G0269720 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232428 | CDS | 3410490 | 2475 | - | 0.21697 |
abcC1 | DDB_G0280541 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232430 | CDS | 3500769 | 4080 | - | 0.265931 |
abcC10 | DDB_G0280977 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232430 | CDS | 4347748 | 4005 | + | 0.29613 |
abcC12 | DDB_G0280973 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232430 | CDS | 4340141 | 3972 | - | 0.296324 |
abcC13 | DDB_G0280539 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232430 | CDS | 3484694 | 4053 | - | 0.25586 |
abcC14 | DDB_G0287589 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 520445 | 3954 | - | 0.250379 |
abcC15 | DDB_G0280459 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232430 | CDS | 3386881 | 4311 | + | 0.247506 |
abcC2 | DDB_G0280055 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232430 | CDS | 3230743 | 4155 | - | 0.283754 |
abcC3 | DDB_G0287691 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 792495 | 4239 | + | 0.338759 |
abcC5 | DDB_G0286559 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232431 | CDS | 4828905 | 4383 | - | 0.281314 |
abcC6 | DDB_G0287593 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 525231 | 4056 | - | 0.256657 |
abcC7 | DDB_G0291243 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 391713 | 3987 | - | 0.251818 |
abcC8 | DDB_G0284867 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232431 | CDS | 2579815 | 4782 | - | 0.31765 |
abcC9 | DDB_G0285165 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232431 | CDS | 2942482 | 4038 | + | 0.23477 |
abcD1 | DDB_G0279917 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232430 | CDS | 2772102 | 2205 | - | 0.247166 |
abcD2 | DDB_G0293194 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 2712310 | 2226 | + | 0.32929 |
abcD3 | DDB_G0279919 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232430 | CDS | 2769281 | 2253 | - | 0.246338 |
abcE1 | DDB_G0290483 | DDB0232432 | CDS | 4209815 | 1812 | - | 0.34989 | |
abcF1 | DDB_G0285997 | DDB0232431 | CDS | 3922084 | 2127 | - | 0.381758 | |
abcF2 | DDB_G0284047 | DDB0232431 | CDS | 1542455 | 1782 | - | 0.335578 | |
abcF3 | DDB_G0275637 | DDB0232429 | CDS | 6056870 | 1959 | - | 0.325166 | |
abcF4 | DDB_G0267436 | DDB0232428 | CDS | 1263019 | 3429 | + | 0.31846 | |
abcG1 | DDB_G0269214 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232428 | CDS | 2895800 | 2382 | + | 0.289253 |
abcG10 | DDB_G0292986 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 2306939 | 4401 | + | 0.310384 |
abcG11 | DDB_G0269212 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232428 | CDS | 3029557 | 4329 | + | 0.319704 |
abcG12 | DDB_G0274115 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232429 | CDS | 4432128 | 1917 | + | 0.299426 |
abcG14 | DDB_G0269210 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232428 | CDS | 3002229 | 4320 | + | 0.313194 |
abcG15 | DDB_G0267432 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232428 | CDS | 752355 | 4428 | + | 0.317073 |
abcG16 | DDB_G0289331 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 2688872 | 4587 | + | 0.276651 |
abcG17-1 | DDB_G0273073 | full transporter consisting of two ABC domains and two transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 2630264 | 4431 | - | 0.298127 |
abcG17-2 | DDB_G0273781 | full transporter consisting of two ABC domains and two transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 3396905 | 4431 | + | 0.298127 |
abcG18 | DDB_G0275687 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232429 | CDS | 5754874 | 4431 | - | 0.292033 |
abcG19 | DDB_G0269208 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232428 | CDS | 4493232 | 4350 | - | 0.303678 |
abcG2 | DDB_G0275689 | full transporter consisting of two ABC domains and two transmembrane domains involved in pH maintenance | DDB0232429 | CDS | 5760590 | 3987 | - | 0.329069 |
abcG20 | DDB_G0267430 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232428 | CDS | 609146 | 2193 | + | 0.27679 |
abcG21 | DDB_G0269206 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232428 | CDS | 4486597 | 4350 | - | 0.317471 |
abcG22 | DDB_G0270826 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232428 | CDS | 3432396 | 1848 | + | 0.319805 |
abcG23 | DDB_G0269026 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232428 | CDS | 2337236 | 2106 | - | 0.257835 |
abcG24 | DDB_G0282103 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232430 | CDS | 5372934 | 3480 | - | 0.323563 |
abcG3 | DDB_G0287461 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 284599 | 4182 | - | 0.308943 |
abcG4 | DDB_G0289657 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232432 | CDS | 3066245 | 2397 | - | 0.254068 |
abcG5 | DDB_G0281391 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232430 | CDS | 4586992 | 4530 | - | 0.295806 |
abcG6 | DDB_G0281389 | full transporter consisting of two ABC domains and two transmembrane domains expressed in prespore cells | DDB0232430 | CDS | 4592822 | 4605 | - | 0.291857 |
abcG7 | DDB_G0289655 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232432 | CDS | 3062303 | 2448 | - | 0.226307 |
abcG8 | DDB_G0274117 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232429 | CDS | 4435257 | 1881 | + | 0.290803 |
abcG9 | DDB_G0293450 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 2911255 | 4347 | + | 0.326202 |
abcG_ps1 | DDB_G0287785 | putative pseudogene similar to abcG family proteins | DDB0232432 | CDS | 699242 | 207 | - | 0.309179 |
abcG_ps2 | DDB_G0293466 | putative pseudogene fragment similar to abcG family proteins including | DDB0232433 | CDS | 2916261 | 189 | + | 0.365079 |
abcH1 | DDB_G0292384 | DDB0232433 | CDS | 1754062 | 801 | + | 0.280899 | |
abcH2 | DDB_G0267428 | DDB0232428 | CDS | 1443157 | 1542 | + | 0.230869 | |
abcH3 | DDB_G0275697 | DDB0232429 | CDS | 5590467 | 3357 | - | 0.233244 | |
abcH4 | DDB_G0283479 | DDB0232431 | CDS | 768532 | 2649 | - | 0.254058 | |
abhd | DDB_G0289723 | DDB0232432 | CDS | 3165541 | 1188 | - | 0.289562 | |
abiA | DDB_G0267956 | similar to Abi2 Abl-interactor 2 | DDB0232428 | CDS | 1177308 | 999 | - | 0.377377 |
abkA | DDB_G0288749 | atypical protein serinethreonine kinase contains ABC1 kinase (protein kinase-like) domain yeast ABC1 essential for the electron transfer in the BC(1) complex E.coli homolog required for ubiquinone biosynthesis | DDB0232432 | CDS | 1916080 | 1698 | - | 0.246761 |
abkB | DDB_G0281799 | atypical protein serinethreonine kinase contains ABC1 kinase (protein kinase-like) domain yeast ABC1 essential for the electron transfer in the BC(1) complex E.coli homolog required for ubiquinone biosynthesis | DDB0232430 | CDS | 4693676 | 2007 | - | 0.255107 |
abkC | DDB_G0267774 | atypical protein serinethreonine kinase contains ABC1 kinase (protein kinase-like) domain yeast ABC1 essential for the electron transfer in the BC(1) complex E.coli homolog required for ubiquinone biosynthesis | DDB0232428 | CDS | 825289 | 2070 | - | 0.246377 |
abkD | DDB_G0284897 | atypical protein serinethreonine kinase contains ABC1 kinase (protein kinase-like) domain yeast ABC1 essential for the electron transfer in the BC(1) complex E.coli homolog required for ubiquinone biosynthesis | DDB0232431 | CDS | 2611033 | 2088 | - | 0.273946 |
abnA | DDB_G0270884 | very similar to Acanthamoeba actobindin contains two actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domains | DDB0232428 | CDS | 2941556 | 279 | - | 0.37276 |
abnB | DDB_G0269518 | very similar to Acanthamoeba actobindin contains two actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domains | DDB0232428 | CDS | 2942536 | 273 | - | 0.380952 |
abnC | DDB_G0269520 | very similar to Acanthamoeba actobindin contains two actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domains | DDB0232428 | CDS | 2943585 | 273 | + | 0.380952 |
abpA | DDB_G0268632 | DDB0232428 | CDS | 2137156 | 2586 | + | 0.361562 | |
abpB | DDB_G0279081 | DDB0232430 | CDS | 1621394 | 888 | - | 0.393018 | |
abpC | DDB_G0269100 | 120 kDa F-actin binding protein also often called filamin involved in actin cytoskeleton organization motility and development enriched in prestalk cells | DDB0232428 | CDS | 4554019 | 2574 | - | 0.408702 |
abpD | DDB_G0287291 | actin binding protein that is developmentally and cAMP-regulated associates with intracellular membranes | DDB0232432 | CDS | 222824 | 5217 | + | 0.242285 |
abpE-1 | DDB_G0273447 | involved in pseudopod formation contains an N-terminal ADFcofilin-like actin binding domain and a c-terminal SH3 domain there is a second copy of this gene | DDB0232429 | CDS | 2984113 | 1446 | - | 0.364454 |
abpE-2 | DDB_G0273517 | involved in pseudopod formation contains an N-terminal ADFcofilin-like actin binding domain and a c-terminal SH3 domain there is a second copy of this gene | DDB0232429 | CDS | 3046146 | 1446 | + | 0.364454 |
abpF | DDB_G0291229 | actin-binding protein that localizes to the centrosome expression enhanced in myosin II knock-out cells purified protein makes ring-like structures in vitro (from K. R. Niebling's Thesis (1993) James Spudich Lab Standford U.) | DDB0232433 | CDS | 145941 | 7095 | - | 0.297252 |
acaA | DDB_G0281545 | twelve transmembrane domain adenylyl cyclase expressed during aggregation essential for streaming in early development | DDB0232430 | CDS | 4958602 | 4224 | + | 0.264205 |
acad8 | DDB_G0288647 | ortholog of the H. sapiens ACAD8 that has very high activity toward isobutyryl-CoA and might be an isobutyryl-CoA dehydrogenase that functions in valine catabolism | DDB0232432 | CDS | 1779747 | 1251 | - | 0.384492 |
acadsb | DDB_G0282967 | mammalian ACADSB has highest activity toward short branched chain acyl-CoA derivative such as (s)-2-methylbutyryl-CoA isobutyryl-CoA and 2-methylhexanoyl-CoA as well as toward short straight chain butyryl-CoA and hexanoyl-CoA in human defects in ACADSB cause shortbranched-chain acyl-CoA dehydrogenase deficiency (SBCADD) also called 2-methylbutyryl-CoA dehydrogenase deficiency or 2-methylbutyryl glycinuria | DDB0232431 | CDS | 70875 | 1242 | + | 0.329308 |
acapA | DDB_G0279649 | plays a role in cytokinesis cell migration and actin cytoskeleton dynamics hydrolyzes GTP bound to ArfA in vitro | DDB0232430 | CDS | 2363863 | 4002 | + | 0.31959 |
acapB | DDB_G0276395 | similar to mammalian Acap3 hydrolyzes GTP bound to ArfA in vitro | DDB0232429 | CDS | 6763233 | 2532 | + | 0.265798 |
acat | DDB_G0271544 | acetyl-CoA C-acetyltransferase catalyzes the reaction 2 acetyl-CoA CoA acetoacetyl-CoA | DDB0232429 | CDS | 605879 | 2445 | - | 0.383231 |
acbA | DDB_G0270658 | precursor of SDF-2 similar to diazepam binding inhibitor enriched in prespore cells | DDB0232428 | CDS | 3673860 | 255 | + | 0.396078 |
acbd6 | DDB_G0290237 | DDB0232432 | CDS | 3838664 | 867 | + | 0.260669 | |
accA | DDB_G0288387 | catalizes the reactions BCCP-biotin-COsub2sub acetyl-CoA ATP malonyl-CoA BCCP-biotin phosphate ADP bandb BCCP-biotin COsub2sub ATP phosphate ADP BCCP-biotin-COsub2sub | DDB0232432 | CDS | 1474122 | 6849 | - | 0.327201 |
acgA | DDB_G0274569 | DDB0232429 | CDS | 3977236 | 2577 | + | 0.261156 | |
acly | DDB_G0278345 | catalyzes the reaction ADP phosphate acetyl-CoA oxaloacetate ATP citrate CoA | DDB0232430 | CDS | 726196 | 1869 | + | 0.361691 |
acmsd | DDB_G0286525 | catalyzes the reaction: 2-amino-3-(3-oxoprop-1-en-1-yl)but-2-enedioate 2-aminomuconate semialdehyde CO2 | DDB0232431 | CDS | 4592587 | 1080 | + | 0.340741 |
acn9 | DDB_G0275645 | ortholog of the conserved ACN9 in S. cerevisiae localized to the mitochondrial intermembrane space and required for acetate utilization and gluconeogenesis | DDB0232429 | CDS | 5859116 | 408 | + | 0.191176 |
aco | DDB_G0277497 | bNomenclature conflict:b Do not confuse this gene with acoA the acyl-CoA oxidase or aco1 and aco2 the aconitases | DDB0232429 | CDS | 8019782 | 1107 | + | 0.29991 |
aco1 | DDB_G0279159 | catalyzes the reaction citrate cis-aconitate Hsub2subO highly similar to iron responsive element binding protein expressed in pstAB cells and in upper cup and stalk during culminationbr bNomenclature conflict:b Do not confuse this gene with aco the oxidoreductase or acoA the acyl-CoA oxidase | DDB0232430 | CDS | 1708174 | 2685 | - | 0.353073 |
aco2 | DDB_G0278779 | catalyzes the reaction citrate cis-aconitate Hsub2subObr bNomenclature conflict:b Do not confuse this gene with aco the oxidoreductase or acoA the acyl-CoA oxidase | DDB0232430 | CDS | 1168705 | 2316 | - | 0.40285 |
acoA | DDB_G0283261 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2subbr bNomenclature conflict:b Do not confuse this gene with aco the oxidoreductase or aco1 and aco2 the aconitases | DDB0232431 | CDS | 449907 | 2064 | + | 0.307655 |
acp1 | DDB_G0267484 | conserved low molecular weight phosphotyrosine protein phosphatase acts on tyrosine phosphorylated proteins low-MW aryl phosphates and natural and synthetic acyl phosphates | DDB0232428 | CDS | 208100 | 540 | + | 0.303704 |
acpA | DDB_G0267374 | 32 kDa subunit of heterodimeric actin capping protein cap3234 34 kDa subunit is encoded by acpB contributes to the dynactin complex | DDB0232428 | CDS | 1647348 | 819 | + | 0.32967 |
acpB | DDB_G0272104 | 34 kDa subunit of heterodimeric actin capping protein cap3234 32 kDa subunit is encoded by acpA contributes to the dynactin complex | DDB0232429 | CDS | 1562720 | 846 | + | 0.35461 |
acrA | DDB_G0267376 | contains a cyclase domain 7 transmembrane helices a histidine kinase domain and two receiver domains | DDB0232428 | CDS | 1738891 | 6372 | + | 0.274796 |
acsA | DDB_G0277815 | catalyzes the reaction ATP acetate CoA AMP diphosphate acetyl-CoA | DDB0232429 | CDS | 8448576 | 2025 | - | 0.342716 |
act1 | DDB_G0289553 | has 94 | DDB0232432 | CDS | 2938326 | 1131 | - | 0.365164 |
act10 | DDB_G0289811 | has 94 | DDB0232432 | CDS | 3337403 | 1131 | + | 0.415561 |
act11 | DDB_G0288879 | has 94 | DDB0232432 | CDS | 2167534 | 1131 | + | 0.421751 |
act12 | DDB_G0274129 | has 94 | DDB0232429 | CDS | 4718776 | 1131 | - | 0.386384 |
act13 | DDB_G0274599 | has 94 | DDB0232429 | CDS | 4495093 | 1131 | - | 0.41733 |
act14 | DDB_G0274137 | has 94 | DDB0232429 | CDS | 4418543 | 1131 | + | 0.418214 |
act15 | DDB_G0272520 | has 94 | DDB0232429 | CDS | 1781191 | 1131 | + | 0.414677 |
act16 | DDB_G0272248 | has 94 | DDB0232429 | CDS | 1607842 | 1131 | - | 0.392573 |
act17 | DDB_G0274131 | has 80 | DDB0232429 | CDS | 4723516 | 1125 | + | 0.357333 |
act18 | DDB_G0289489 | has 83 | DDB0232432 | CDS | 2886806 | 1143 | + | 0.343832 |
act19 | DDB_G0274727 | has 94 | DDB0232429 | CDS | 4053689 | 1131 | + | 0.399646 |
act2 | DDB_G0274133 | has 94 | DDB0232429 | CDS | 4722018 | 1131 | + | 0.386384 |
act20 | DDB_G0274285 | has 94 | DDB0232429 | CDS | 4047769 | 1131 | - | 0.400531 |
act21 | DDB_G0274561 | has 94 | DDB0232429 | CDS | 4052062 | 1131 | - | 0.399646 |
act22 | DDB_G0275023 | has 94 | DDB0232429 | CDS | 5343575 | 1131 | + | 0.376658 |
act23 | DDB_G0268744 | DDB0232428 | CDS | 2031686 | 1077 | + | 0.36676 | |
act24 | DDB_G0289505 | has 80 | DDB0232432 | CDS | 2876728 | 1134 | + | 0.347443 |
act24_ps | DDB_G0293368 | putative pseudogene contains an incomplete actin domain similar to | DDB0232433 | CDS | 2797121 | 126 | - | 0.31746 |
act25 | DDB_G0289507 | has 74 | DDB0232432 | CDS | 2878511 | 1158 | + | 0.337651 |
act26 | DDB_G0269902 | has 64 | DDB0232428 | CDS | 3826453 | 1128 | + | 0.300532 |
act27 | DDB_G0289533 | has 61 | DDB0232432 | CDS | 2880348 | 1119 | + | 0.328865 |
act28 | DDB_G0289511 | contributes to DdPPK2 activity also described as member of the polyphosphate kinase PPK3 family | DDB0232432 | CDS | 2883081 | 1062 | + | 0.335217 |
act29 | DDB_G0286893 | has 56 | DDB0232431 | CDS | 5035700 | 1164 | - | 0.265464 |
act3 | DDB_G0289487 | has 92 | DDB0232432 | CDS | 2884652 | 1131 | + | 0.358974 |
act30_ps | DDB_G0289525 | putative pseudogene contains an actin domain | DDB0232432 | CDS | 2874594 | 1098 | + | 0.343352 |
act31 | DDB_G0269476 | DDB0232428 | CDS | 2844541 | 1068 | + | 0.293071 | |
act32 | DDB_G0269544 | DDB0232428 | CDS | 2967350 | 1179 | - | 0.274809 | |
act33 | DDB_G0287981 | similar to macronuclear actin 1 of ciliates also similar to A. thaliana ACT11 | DDB0232432 | CDS | 925837 | 1245 | - | 0.236948 |
act34_ps | DDB_G0272446 | putative pseudogene contains an incomplete actin domain | DDB0232429 | CDS | 1603869 | 756 | - | 0.366402 |
act35_ps | DDB_G0280749 | putative pseudogene contains a partial actin domain | DDB0232430 | CDS | 3674980 | 336 | + | 0.348214 |
act36_ps | DDB_G0289509 | putative pseudogene contains a partial actin domain | DDB0232432 | CDS | 2881811 | 408 | + | 0.338235 |
act37_ps | DDB_G0280679 | putative pseudogene contains a partial actin domain | DDB0232430 | CDS | 3624484 | 204 | - | 0.377451 |
act38_ps | DDB_G0280883 | putative pseudogene contains a partial actin domain | DDB0232430 | CDS | 3832477 | 267 | + | 0.370787 |
act39_ps | DDB_G0290243 | putative pseudogene contains a partial actin domain | DDB0232432 | CDS | 3768414 | 369 | - | 0.319783 |
act4 | DDB_G0289005 | has 94 | DDB0232432 | CDS | 2234318 | 1131 | - | 0.419982 |
act5 | DDB_G0289663 | has 94 | DDB0232432 | CDS | 3186992 | 1131 | - | 0.419098 |
act6 | DDB_G0274135 | has 94 | DDB0232429 | CDS | 4055916 | 1131 | + | 0.397878 |
act7 | DDB_G0280545 | has 94 | DDB0232430 | CDS | 3684122 | 1131 | + | 0.376658 |
act8 | DDB_G0269234 | has 94 | DDB0232428 | CDS | 4602557 | 1131 | + | 0.425287 |
act9 | DDB_G0274601 | has 94 | DDB0232429 | CDS | 4455464 | 1131 | + | 0.419098 |
acy1 | DDB_G0270562 | catalyzes the reaction: N-acyl-L-amino acid H2O carboxylate L-amino acid (EC 3.5.1.14) | DDB0232428 | CDS | 3048022 | 1227 | - | 0.302363 |
ada | DDB_G0287371 | catalyzes the reaction Hsub2subO adenosine NHsub3sub inosine in salvage pathways of nucleosides contains two tandem repeats of the adenosine deaminase domain | DDB0232432 | CDS | 206705 | 2319 | + | 0.287193 |
ada2 | DDB_G0280079 | C-terminal half has similarity to the histone acetyltransferase complex component of Zea mays brbr bCommunity annotationb: DDB_G0280079 codes for a protein with significant homologies to the transcriptional ADAptor subunit ADA2 of budding yeast. Yeast ADA2 participates in several complexes together with the histone acetyl transferase GCN5 which also has an ortholog in Dicty. DDB_GO280079 appears likely to be cell-cycle regulated in Dicty as it is threefold overexpressed in a strain in which the Dicty Rb ortholog rblA has been disrupted.In addition DDB_G0280079 shows a developmental trajectory similar to those of most genes involved in cell cycle progression (see DictyExpress). Finally the promoter contains an element (GCGCCCAAA) which is highly enriched in the promoters of Dictyostelium cell cycle genes. Harry MacWilliams June 2010br | DDB0232430 | CDS | 2899122 | 2745 | - | 0.27796 |
adamts | DDB_G0279795 | DDB0232430 | CDS | 2560881 | 2175 | + | 0.288276 | |
adcA | DDB_G0292924 | contains an arrestin domain found in beta-arrestin which functions in regulation of beta-adrenergic receptors br bNomenclature conflictb: Do not confuse adcA (arrestin domain-containing protein) with dcd3A (alkaline dihydroceramidase) | DDB0232433 | CDS | 2277184 | 1743 | - | 0.365462 |
adcB | DDB_G0274395 | DDB0232429 | CDS | 4691677 | 1854 | - | 0.288565 | |
adcC | DDB_G0271022 | DDB0232428 | CDS | 4136186 | 1965 | + | 0.294656 | |
adcD | DDB_G0286693 | DDB0232431 | CDS | 4853622 | 2358 | - | 0.242578 | |
adcE | DDB_G0267584 | DDB0232428 | CDS | 373253 | 1695 | - | 0.276106 | |
adcF | DDB_G0289229 | DDB0232432 | CDS | 2510064 | 3093 | - | 0.201423 | |
adh5 | DDB_G0281865 | ortholog of H. sapiens ADH5 and other mammalian ADHs zinc-containing dimeric enzyme responsible for the oxidation of long-chain alcohols and omega-hydroxy fatty acids | DDB0232430 | CDS | 5043162 | 1140 | - | 0.385088 |
adhfe1 | DDB_G0290111 | DDB0232432 | CDS | 3671708 | 1644 | + | 0.317518 | |
adi1 | DDB_G0291376 | DDB0232433 | CDS | 203637 | 444 | - | 0.259009 | |
adk | DDB_G0286057 | catalyzes the reaction ATP adenosine ADP AMP | DDB0232431 | CDS | 4005558 | 1023 | + | 0.396872 |
adkA | DDB_G0283805 | catalyzes the reaction AMP ATP ADP ADP in de novo DNA synthesis | DDB0232431 | CDS | 1124176 | 831 | - | 0.32491 |
adkB | DDB_G0292730 | catalyzes the reaction AMP ATP ADP ADP in de novo DNA synthesis predicted to be nuclear | DDB0232433 | CDS | 2003598 | 699 | - | 0.291846 |
adprh | DDB_G0289675 | conserved enzyme catalyzes the reaction: N(omega)-(ADP-D-ribosyl)-L-arginine H(2)O ADP-ribose L-arginine reverses the reaction of mono-ADP-ribosylation | DDB0232432 | CDS | 3077727 | 1179 | - | 0.31637 |
adprt1A | DDB_G0278741 | putative ortholog of PARP1 catalyzes ADP-ribosylation a posttranslational protein modification in which the ADP-ribose moiety of NAD is transferred onto specific amino acid side chains of cell surface secreted cytosolic or nuclear proteins | DDB0232430 | CDS | 1394183 | 2817 | - | 0.323039 |
adprt1B | DDB_G0279195 | highly similar to adprt1A catalyzes ADP-ribosylation a posttranslational protein modification in which the ADP-ribose moiety of NAD is transferred onto specific amino acid side chains of cell surface secreted cytosolic or nuclear proteins | DDB0232430 | CDS | 1744004 | 2415 | - | 0.298137 |
adprt2 | DDB_G0292820 | putative ortholog of PARP2 catalyzes ADP-ribosylation a posttranslational protein modification in which the ADP-ribose moiety of NAD is transferred onto specific amino acid side chains of cell surface secreted cytosolic or nuclear proteins | DDB0232433 | CDS | 2124835 | 2103 | + | 0.324774 |
adprt3 | DDB_G0291788 | catalyzes ADP-ribosylation a posttranslational protein modification in which the ADP-ribose moiety of NAD is transferred onto specific amino acid side chains of cell surface secreted cytosolic or nuclear proteins | DDB0232433 | CDS | 795337 | 7611 | + | 0.327027 |
adprt4 | DDB_G0267468 | catalyzes ADP-ribosylation a posttranslational protein modification in which the ADP-ribose moiety of NAD is transferred onto specific amino acid side chains of cell surface secreted cytosolic or nuclear proteins | DDB0232428 | CDS | 243053 | 1935 | + | 0.281137 |
adrm1-1 | DDB_G0272624 | interacts with the phg2 kinase pathway plays a role in the transition from growth to differentiationbr there is a second copy of this gene | DDB0232429 | CDS | 2270218 | 864 | - | 0.311343 |
adrm1-2 | DDB_G0274093 | interacts with the phg2 kinase pathway plays a role in the transition from growth to differentiationbr there is a second copy of this gene | DDB0232429 | CDS | 3759990 | 864 | + | 0.311343 |
agl | DDB_G0287569 | DDB0232432 | CDS | 354336 | 4827 | - | 0.311995 | |
agnA | DDB_G0276299 | DDB0232429 | CDS | 6579134 | 2940 | - | 0.345578 | |
agnB | DDB_G0290377 | DDB0232432 | CDS | 4008116 | 2703 | - | 0.290788 | |
agnC | DDB_G0271870 | DDB0232429 | CDS | 975850 | 3627 | + | 0.326441 | |
agnD | DDB_G0281955 | DDB0232430 | CDS | 5166543 | 3888 | + | 0.35571 | |
agnE | DDB_G0289367 | DDB0232432 | CDS | 2710003 | 3603 | - | 0.251457 | |
agnF | DDB_G0281959 | DDB0232430 | CDS | 5171485 | 498 | + | 0.303213 | |
agpA | DDB_G0269848 | belongs to the acyltransferase superfamily contains 2 predicted transmembrane domains | DDB0232428 | CDS | 3711642 | 1095 | + | 0.269406 |
agpB | DDB_G0288523 | DDB0232432 | CDS | 1643762 | 1038 | + | 0.310212 | |
agpC | DDB_G0288863 | DDB0232432 | CDS | 1956943 | 1299 | - | 0.294842 | |
agps | DDB_G0286183 | catalyses the reaction: 1-acyl-glycerone 3-phosphate a long-chain alcohol 1-alkyl-glycerone 3-phosphate a long-chain acid anion in ether lipid biosynthesis mutations in the human ortholog AGPS causes peroxisomal disorders | DDB0232431 | CDS | 4303510 | 1836 | + | 0.345316 |
agtA | DDB_G0283005 | likely catalyzes the alpha addition of galactose to Fuc-Gal-GlcNAc-HyPro143-Skp1 (FpaAFpaB) | DDB0232431 | CDS | 143819 | 1947 | - | 0.214689 |
agxt | DDB_G0289923 | ortholog of the conserved AGXT defects in the human AGXT cause primary hyperoxaluria type I | DDB0232432 | CDS | 3442183 | 1224 | + | 0.356209 |
ahhA | DDB_G0282009 | highly similar to mammalian adducin 1 expressed in pstO cells and in pstAB pstO and stalk cells during culmination underexpressed in dstA- cells | DDB0232430 | CDS | 5237565 | 807 | - | 0.32342 |
ahsa | DDB_G0269712 | DDB0232428 | CDS | 3388870 | 1152 | - | 0.332465 | |
aif | DDB_G0288247 | involved in caspase-independent mitochondrial cell death similar to H. sapiens AIFM1 the mitochondrial Apoptosis-Inducing Factor 1 | DDB0232432 | CDS | 1306170 | 1599 | - | 0.317699 |
aifB | DDB_G0285005 | similar to H. sapiens AIFM2 a caspase-independent mitochondrial effector of apoptotic cell death | DDB0232431 | CDS | 2794340 | 1164 | - | 0.287801 |
aifC | DDB_G0285003 | similar to H. sapiens AIFM2 a caspase-independent mitochondrial effector of apoptotic cell death | DDB0232431 | CDS | 2790283 | 1227 | - | 0.235534 |
aifD | DDB_G0286241 | similar to H. sapiens AIFM2 a caspase-independent mitochondrial effector of apoptotic cell death | DDB0232431 | CDS | 4236868 | 1194 | + | 0.329983 |
aip1 | DDB_G0278733 | conserved protein containing WD40 repeats involved in actin-dependent processes such as endocytosis cytokinesis and motility interacts genetically with nhe1 and suppresses nhe1- mutant phenotypes | DDB0232430 | CDS | 1283399 | 1794 | + | 0.377926 |
ak1 | DDB_G0292150 | atypical protein serinethreonine kinase contains an N-terminal ArfGap domain and a C-terminal Alpha kinase domain | DDB0232433 | CDS | 1289254 | 4059 | + | 0.319783 |
alaS | DDB_G0277823 | catalyzes the reaction ATP L-alanine tRNAAla AMP diphosphate L-alanyl-tRNAAla | DDB0232430 | CDS | 919657 | 2841 | - | 0.377684 |
alfA | DDB_G0274391 | Dictyostelium enzyme that hydrolyses O- and S-glycosyl compounds with a preference for cleaving the alpha1-6-O-fucolsyl bonds in fucosylated oligosaccharides secreted during development | DDB0232429 | CDS | 4784888 | 1386 | - | 0.305916 |
alg1 | DDB_G0286011 | CAZy family GT33 catalyzes N-linked mannosylation | DDB0232431 | CDS | 3960039 | 1482 | + | 0.279352 |
alg10 | DDB_G0277817 | CAZy family GT59 catalyzes N-linked glucosylation | DDB0232429 | CDS | 8459161 | 1458 | - | 0.198903 |
alg11 | DDB_G0292118 | CAZy family GT4 catalyzes N-linked mannosylation | DDB0232433 | CDS | 1220852 | 1518 | + | 0.28722 |
alg12 | DDB_G0267884 | CAZy family GT22 catalyzes N-linked mannosylation | DDB0232428 | CDS | 1032061 | 1941 | - | 0.24781 |
alg2 | DDB_G0272730 | CAZy family GT4 catalyzes N-linked mannosylation | DDB0232429 | CDS | 2218228 | 1263 | - | 0.292162 |
alg3 | DDB_G0268238 | CAZy family GT58 catalyzes N-linked mannosylation | DDB0232428 | CDS | 1736097 | 1341 | - | 0.219239 |
alg6 | DDB_G0283841 | CAZy family GT57 catalyzes N-linked glucosylation | DDB0232431 | CDS | 1202486 | 1557 | + | 0.242775 |
alg8 | DDB_G0275261 | CAZy family GT57 catalyzes N-linked glucosylation | DDB0232429 | CDS | 5068593 | 1878 | - | 0.198083 |
alg9 | DDB_G0279349 | CAZy family GT22 catalyzes N-linked mannosylation | DDB0232430 | CDS | 1972184 | 1950 | + | 0.232308 |
alkB | DDB_G0285575 | DDB0232431 | CDS | 3395637 | 1182 | + | 0.307953 | |
allB1 | DDB_G0282199 | catalyzes the reaction Hsub2subO allantoin allantoate | DDB0232430 | CDS | 5513834 | 1950 | + | 0.318462 |
allB2 | DDB_G0270162 | catalyzes the reaction Hsub2subO allantoin allantoate expressed in upper cup cells during culmination | DDB0232428 | CDS | 4345093 | 1533 | + | 0.262231 |
allC | DDB_G0280267 | catalyzes the reaction allantoate Hsub2subO (S)-ureidoglycolate urea in allantoin degradation | DDB0232430 | CDS | 3183979 | 1110 | + | 0.336036 |
alp | DDB_G0278495 | catalyzes the reaction a phosphate monoester Hsub2subO an alcohol phosphate exhibits a punctate pattern in immunoflourescence that most likely represents vesicles enzymatic activity is developmentally regulated in a cell type-specific manner | DDB0232430 | CDS | 968065 | 1680 | - | 0.380952 |
alrA | DDB_G0293850 | involved in regulation of aggregate size member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232433 | CDS | 3404974 | 894 | + | 0.325503 |
alrB | DDB_G0285053 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2618768 | 936 | - | 0.318376 |
alrC | DDB_G0268058 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232428 | CDS | 1371493 | 966 | - | 0.258799 |
alrD | DDB_G0285027 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2833891 | 873 | - | 0.266896 |
alrE | DDB_G0285025 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2832495 | 870 | - | 0.301149 |
alrF | DDB_G0285023 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2831142 | 918 | - | 0.238562 |
alr_ps | DDB_G0268562 | putative pseudogene similar to aldo-keto reductases alrA-F | DDB0232428 | CDS | 1373976 | 462 | - | 0.248918 |
alxA | DDB_G0275451 | similar to mammalian Alix which interacts with ALG-2 (apoptosis-linked gene 2) contains 1 BRO1 (Bro1-rhophilin) domain 3 coiled-coil regions 1 proline-rich region and a conserved recognition sequence for Src-type tyrosine kinases | DDB0232429 | CDS | 5948745 | 2385 | - | 0.30021 |
alyA | DDB_G0275123 | DDB0232429 | CDS | 5002742 | 546 | - | 0.377289 | |
alyB | DDB_G0275119 | DDB0232429 | CDS | 5005709 | 546 | - | 0.380952 | |
alyC | DDB_G0275121 | DDB0232429 | CDS | 5004280 | 546 | - | 0.368132 | |
alyD-1 | DDB_G0273197 | DDB0232429 | CDS | 2696096 | 783 | - | 0.360153 | |
alyD-2 | DDB_G0273731 | member of a new lysozyme class there is a second copy of this gene | DDB0232429 | CDS | 3334723 | 783 | + | 0.360153 |
alyL | DDB_G0286229 | amoeba lysozyme family protein (aly) but divergent compared to alyA-D | DDB0232431 | CDS | 4218365 | 1719 | + | 0.401396 |
amd1 | DDB_G0275567 | catalyzes the removal of the carboxylate group of S-adenosylmethionine to form S-adenosyl-5'-3-methylpropylamine which then acts as the n-propylamine group donor in the synthesis of the polyamines spermidine and sperminebr bNomenclature conflict: b Do not confuse this gene with amdA encoding AMP deaminase | DDB0232429 | CDS | 5517792 | 1140 | + | 0.35614 |
amdA | DDB_G0292266 | required for spore formation inhibits the formation of aspidocytes catalyzes the reaction AMP Hsub2subO IMP NHsub3subbr bNomenclature conflict: b Do not confuse this gene with amd1 encoding S-adenosylmethionine decarboxylase | DDB0232433 | CDS | 1491265 | 2373 | - | 0.313527 |
amdhd1 | DDB_G0269854 | catalyzes the reaction (S)-3-(5-oxo-45-dihydro-3H-imidazol-4-yl)propanoate H2O N-formimidoyl-L-glutamate H | DDB0232428 | CDS | 3737738 | 1281 | - | 0.34192 |
amfr | DDB_G0279345 | ortholog of the long isoform (isoform 2) of the human autocrine motility factor receptor a RING finger-dependent ubiquitin protein ligase (E3) of the endoplasmic reticulum that is involved in tumor invasion and metastasis contains four putative transmembrane domains and an additional signal sequence | DDB0232430 | CDS | 1961529 | 2040 | - | 0.258824 |
amiB | DDB_G0282375 | novel protein required for aggregation putative poorly conserved ortholog of the mediator of RNA polymerase II transcription subunit 13 | DDB0232430 | CDS | 6170766 | 8037 | + | 0.286425 |
ampA | DDB_G0275695 | DDB0232429 | CDS | 5588037 | 855 | - | 0.366082 | |
ampA_ps | DDB_G0267806 | putative pseudogene fragment similar to D. discoideum gene | DDB0232428 | CDS | 902491 | 129 | - | 0.302326 |
amtA | DDB_G0277503 | DDB0232429 | CDS | 8112427 | 1392 | - | 0.35704 | |
amtB | DDB_G0277889 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | DDB0232430 | CDS | 276805 | 1296 | + | 0.364198 |
amtC | DDB_G0267424 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | DDB0232428 | CDS | 1034624 | 1296 | + | 0.350309 |
amyA | DDB_G0281547 | DDB0232430 | CDS | 4671220 | 1413 | - | 0.357396 | |
anapc1 | DDB_G0285349 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232431 | CDS | 3135215 | 6810 | - | 0.22467 |
anapc10 | DDB_G0268992 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232428 | CDS | 2080758 | 567 | + | 0.257496 |
anapc11 | DDB_G0286909 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232431 | CDS | 5059870 | 264 | - | 0.348485 |
anapc2 | DDB_G0276377 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232429 | CDS | 6676259 | 2724 | - | 0.216593 |
anapc3 | DDB_G0288223 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232432 | CDS | 1273822 | 2913 | - | 0.278064 |
anapc4 | DDB_G0285223 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232431 | CDS | 3010019 | 2514 | + | 0.234686 |
anapc5 | DDB_G0280113 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232430 | CDS | 2955422 | 3054 | - | 0.225606 |
anapc6 | DDB_G0286233 | putative ortholog of cdc16 a conserved protein containing several TPRs (tetratrico peptide repeats) | DDB0232431 | CDS | 4222260 | 2598 | - | 0.234411 |
anapc7 | DDB_G0292470 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232433 | CDS | 1686299 | 1743 | + | 0.243259 |
anapc8 | DDB_G0272775 | DDB0232429 | CDS | 2162746 | 1779 | - | 0.323215 | |
ancA | DDB_G0267454 | ortholog of human SLC25A4 which catalyzes the exchange of ADP and ATP across the mitochondrial inner membrane contains six predicted transmembrane domains brbrbCommunity annotation:b Overview of the | DDB0232428 | CDS | 424007 | 930 | + | 0.387097 |
ankrd39 | DDB_G0287345 | DDB0232432 | CDS | 159445 | 525 | - | 0.266667 | |
aoxA | DDB_G0280819 | DDB0232430 | CDS | 1437954 | 1014 | - | 0.282051 | |
ap1b1 | DDB_G0279141 | highly similar to AP-1 complex subunit beta-1 (AP1B1) and AP-2 complex subunit beta-1 (AP2B1) which play a role in clathrin-dependent protein sorting | DDB0232430 | CDS | 1680228 | 2829 | - | 0.331212 |
ap1g1 | DDB_G0281957 | DDB0232430 | CDS | 5194623 | 2688 | + | 0.324777 | |
ap1s1 | DDB_G0279359 | DDB0232430 | CDS | 1984933 | 471 | + | 0.26327 | |
ap1s2 | DDB_G0295711 | DDB0232433 | CDS | 619891 | 465 | - | 0.260215 | |
ap2a1-1 | DDB_G0273439 | there is a second copy of this gene | DDB0232429 | CDS | 3000942 | 2970 | - | 0.305387 |
ap2a1-2 | DDB_G0273501 | there is a second copy of this gene | DDB0232429 | CDS | 3027162 | 2970 | + | 0.306061 |
ap2s1 | DDB_G0289721 | DDB0232432 | CDS | 3163717 | 429 | - | 0.261072 | |
ap3b-1 | DDB_G0272578 | there is a second copy of this gene | DDB0232429 | CDS | 2374895 | 3327 | - | 0.285843 |
ap3b-2 | DDB_G0274003 | there is a second copy of this gene | DDB0232429 | CDS | 3652959 | 3327 | + | 0.285843 |
ap3d1 | DDB_G0279537 | DDB0232430 | CDS | 2224744 | 3432 | - | 0.338287 | |
ap3s1 | DDB_G0275405 | DDB0232429 | CDS | 5412017 | 516 | - | 0.226744 | |
ap4b1 | DDB_G0283319 | putative ortholog of H. sapiens AP4B1 member of a complex that mediates protein sorting | DDB0232431 | CDS | 525048 | 2517 | + | 0.247517 |
ap4e1 | DDB_G0280427 | DDB0232430 | CDS | 3335352 | 3243 | - | 0.254702 | |
ap4s1 | DDB_G0284905 | DDB0232431 | CDS | 2625777 | 420 | - | 0.240476 | |
apeA | DDB_G0277701 | AP-endonuclease catalyses the exonucleolytic cleavage of damaged double stranded DNA in the 3'- to 5'-direction to yield nucleoside 5'-phosphates | DDB0232429 | CDS | 8367690 | 1086 | + | 0.323204 |
apeh | DDB_G0292456 | DDB0232433 | CDS | 1668118 | 2295 | - | 0.290632 | |
aph1 | DDB_G0267976 | component of the gamma-secretase complex which executes the intramembrane proteolysis of type I integral membrane proteins | DDB0232428 | CDS | 1217963 | 987 | - | 0.26849 |
aplA | DDB_G0284043 | DDB0232431 | CDS | 1521553 | 1569 | + | 0.303378 | |
aplB | DDB_G0286651 | DDB0232431 | CDS | 4791776 | 1005 | + | 0.371144 | |
aplC | DDB_G0286561 | DDB0232431 | CDS | 4793559 | 474 | + | 0.303797 | |
aplD | DDB_G0293010 | DDB0232433 | CDS | 2590611 | 432 | + | 0.252315 | |
aplE | DDB_G0279705 | DDB0232430 | CDS | 2469013 | 666 | - | 0.280781 | |
aplF | DDB_G0277703 | DDB0232429 | CDS | 8369439 | 603 | + | 0.278607 | |
aplG | DDB_G0269616 | DDB0232428 | CDS | 3148640 | 618 | + | 0.281553 | |
aplH | DDB_G0282153 | DDB0232430 | CDS | 5460939 | 591 | - | 0.348562 | |
aplJ | DDB_G0268890 | DDB0232428 | CDS | 2331887 | 645 | - | 0.275969 | |
aplK | DDB_G0279713 | DDB0232430 | CDS | 2474053 | 735 | - | 0.251701 | |
aplL | DDB_G0274967 | DDB0232429 | CDS | 4684532 | 684 | - | 0.225146 | |
aplM | DDB_G0291113 | DDB0232432 | CDS | 4994396 | 1251 | - | 0.242206 | |
aplN | DDB_G0284339 | DDB0232431 | CDS | 1855900 | 882 | + | 0.263039 | |
aplO | DDB_G0286653 | DDB0232431 | CDS | 4794405 | 555 | + | 0.27027 | |
aplP | DDB_G0292508 | DDB0232433 | CDS | 1757953 | 486 | - | 0.279835 | |
aplQ | DDB_G0281659 | DDB0232430 | CDS | 4774706 | 312 | + | 0.285256 | |
aplR | DDB_G0270248 | DDB0232428 | CDS | 4516591 | 489 | + | 0.276074 | |
apl_ps | DDB_G0288605 | putative pseudogene fragment similar to the family of saposin domain-containing amoebapore-like proteins | DDB0232432 | CDS | 1708038 | 288 | + | 0.25 |
apm1 | DDB_G0289247 | shares 69 | DDB0232432 | CDS | 2536641 | 1287 | + | 0.317793 |
apm2 | DDB_G0277139 | DDB0232429 | CDS | 7788092 | 1320 | + | 0.325758 | |
apm3 | DDB_G0277901 | DDB0232430 | CDS | 792608 | 1266 | + | 0.300948 | |
apm4 | DDB_G0276945 | DDB0232429 | CDS | 7532909 | 1593 | - | 0.272442 | |
apnA | DDB_G0279923 | breaks the C-O-P bond 5' to an apurinic or apyrimidinic site in DNA brbr bCommunity annotation:b ApnA has a canonical PCNA-interacting domain also known as a PIP sequence in this case QtsItdFF. For a discussion of PIP domains (see Supplementary table 1 in | DDB0232430 | CDS | 2784977 | 1629 | - | 0.259055 |
apnB | DDB_G0277247 | breaks the C-O-P bond 3' to an apurinic or apyrimidinic site in DNA | DDB0232429 | CDS | 7816486 | 1050 | + | 0.281905 |
aprA | DDB_G0281663 | secreted protein that exists in a 150 kDa complex repressor of cell proliferation | DDB0232430 | CDS | 4787137 | 1485 | + | 0.334007 |
aprt | DDB_G0270174 | catalyzes the reaction AMP pyrophosphate PRPP adenine in nucleoside salvage pathways | DDB0232428 | CDS | 4368158 | 600 | + | 0.29 |
aqpA | DDB_G0267378 | similar to aquaporin family of water-channel proteins expressed in prespore cells | DDB0232428 | CDS | 1385036 | 840 | + | 0.365476 |
aqpB | DDB_G0279443 | belongs to the MIP (major intrinsic protein) family contains 6 putative transmembrane domains | DDB0232430 | CDS | 2058202 | 1719 | + | 0.37929 |
aqr | DDB_G0274797 | ortholog of the mammalian aquarius (AQR) protein an intron-binding spliceosomal protein required to link pre-mRNA splicing and snoRNP (small nucleolar ribonucleoprotein) biogenesis | DDB0232429 | CDS | 3881369 | 4464 | - | 0.225134 |
arcA | DDB_G0277825 | component of the Dictyostelium Arp2Arp3 complex | DDB0232430 | CDS | 304397 | 1110 | - | 0.396396 |
arcB | DDB_G0282813 | 34 kDa component of the Dictyostelium Arp2Arp3 complexbr bNomenclature conflict:b Do not confuse this gene with arpE (actin related protein 5) | DDB0232430 | CDS | 6271490 | 882 | + | 0.34127 |
arcC | DDB_G0292804 | component of the Dictyostelium Arp2Arp3 complex | DDB0232433 | CDS | 2116342 | 525 | + | 0.361905 |
arcD | DDB_G0269102 | 20 kDa component of the Dictyostelium Arp2Arp3 complex | DDB0232428 | CDS | 3892076 | 510 | + | 0.307843 |
arcE | DDB_G0288319 | component of the Dictyostelium Arp2Arp3 complex | DDB0232432 | CDS | 1410951 | 417 | - | 0.366906 |
arfA | DDB_G0289173 | DDB0232432 | CDS | 2516577 | 549 | + | 0.35337 | |
arfrp1 | DDB_G0283631 | DDB0232431 | CDS | 888563 | 651 | + | 0.271889 | |
argB | DDB_G0274811 | catalyzes the reaction ATP N-acetyl-L-glutamate ADP N-acetyl-L-glutamate 5-phosphate | DDB0232429 | CDS | 3967434 | 3339 | + | 0.321953 |
argC | DDB_G0286257 | contains both N-acetyl-gamma-glutamyl-phosphate reductase and acetylglutamate kinase activities catalyzes the reactions N-acetyl-L-glutamate 5-semialdehyde NADPsupsup phosphate N-acetyl-L-glutamyl 5-phosphate NADPH Hsupsup bandb ATP N-acetyl-L-glutamate ADP N-acetyl-L-glutamate 5-phosphate | DDB0232431 | CDS | 4256396 | 2544 | - | 0.331368 |
argD | DDB_G0269526 | catalyzes the reaction Nsub2sub-acetyl-L-ornithine 2-oxoglutarate N-acetyl-L-glutamate 5-semialdehyde L-glutamate | DDB0232428 | CDS | 2946561 | 1362 | - | 0.316446 |
argE | DDB_G0267380 | DDB0232428 | CDS | 414980 | 1344 | + | 0.345982 | |
argJ | DDB_G0291916 | catalyzes the reactions acetyl-CoA L-glutamate CoA N-acetyl-L-glutamate bandb Nsub2sub-acetyl-L-ornithine L-glutamate L-ornithine N-acetyl-L-glutamate | DDB0232433 | CDS | 940721 | 1329 | - | 0.311512 |
argS1 | DDB_G0272867 | catalyzes the reaction ATP L-arginine tRNAArg AMP diphosphate L-arginyl-tRNAArg | DDB0232429 | CDS | 2065311 | 1770 | + | 0.332203 |
argS2 | DDB_G0287803 | catalyzes the reaction ATP L-arginine tRNAArg AMP diphosphate L-arginyl-tRNAArg | DDB0232432 | CDS | 724797 | 2217 | + | 0.280108 |
arkA | DDB_G0289555 | suppressor of spalten (spnA) mutant member of the TKL (tyrosine kinase-like) group and ARK (ankyrin repeat-containing kinase) family | DDB0232432 | CDS | 2941850 | 4383 | + | 0.300707 |
arl1 | DDB_G0288163 | DDB0232432 | CDS | 1170444 | 552 | - | 0.304348 | |
arl2 | DDB_G0281307 | DDB0232430 | CDS | 4073757 | 555 | + | 0.261261 | |
arl5 | DDB_G0271942 | DDB0232429 | CDS | 1019381 | 552 | - | 0.293478 | |
arl8 | DDB_G0283525 | DDB0232431 | CDS | 729167 | 558 | + | 0.284946 | |
armc8 | DDB_G0270626 | DDB0232428 | CDS | 3447052 | 2109 | + | 0.288288 | |
arpA | DDB_G0288937 | centrosome-associated actin homolog contributes to the dynactin complex contributes to DdPPK2 activity also described as member of the polyphosphate kinase PPK3 family | DDB0232432 | CDS | 2149735 | 1152 | - | 0.329861 |
arpB | DDB_G0272106 | component of the Dictyostelium Arp2Arp3 complex contributes to DdPPK2 activity also described as member of the polyphosphate kinase PPK3 family | DDB0232429 | CDS | 1646887 | 1179 | - | 0.398643 |
arpC | DDB_G0283755 | component of the Dictyostelium Arp2Arp3 complex | DDB0232431 | CDS | 1135639 | 1257 | - | 0.381862 |
arpD | DDB_G0280887 | ortholog of A. thaliana ARP4 and very similar to the mammalian actin-like protein 6A which is involved in transcriptional activation and repression of select genes by chromatin remodelling | DDB0232430 | CDS | 3833482 | 1323 | + | 0.297808 |
arpE | DDB_G0291728 | ortholog of the conserved actin related protein ARP5 in mammalian named ACTR5 the yeast protein is a nuclear actin-related protein involved in chromatin remodelingbr bNomenclature conflict:b Do not confuse this gene with arcB the 34 kDa component of the Arp2Arp3 complex. | DDB0232433 | CDS | 714429 | 2055 | + | 0.287591 |
arpF | DDB_G0287007 | ortholog of the conserved actin related protein ARP6 in mammalian called ACTR6 a putative component of a chromatin-remodeling complex | DDB0232431 | CDS | 5196102 | 1473 | + | 0.260014 |
arpG | DDB_G0287779 | similar to the actin related protein ARP8 in mammalian called ACTR8 a putative component of a chromatin-remodeling complex | DDB0232432 | CDS | 683410 | 2622 | - | 0.272311 |
arpH | DDB_G0287739 | similar to mammalian and yeast actin related protein 10 part of the dynactin complex | DDB0232432 | CDS | 636584 | 1428 | - | 0.238095 |
arpin | DDB_G0291009 | DDB0232432 | CDS | 4884944 | 675 | - | 0.278519 | |
arrA | DDB_G0282457 | DDB0232430 | CDS | 5783278 | 594 | - | 0.210438 | |
arrB | DDB_G0274445 | DDB0232429 | CDS | 4578208 | 540 | - | 0.244444 | |
arrC | DDB_G0271792 | DDB0232429 | CDS | 729816 | 603 | + | 0.26534 | |
arrD | DDB_G0289069 | DDB0232432 | CDS | 2306273 | 651 | + | 0.265745 | |
arrE | DDB_G0280479 | DDB0232430 | CDS | 3427999 | 594 | - | 0.287879 | |
arrF | DDB_G0289435 | DDB0232432 | CDS | 2746763 | 573 | + | 0.273997 | |
arrG_ps | DDB_G0280697 | putative pseudogene ADP-ribosylation factor family protein | DDB0232430 | CDS | 3643332 | 381 | + | 0.270341 |
arrH | DDB_G0288015 | bCommunity annotations: b The arrH arrJ and arrK genes and no others of the arrX group are strongly (6 to 30-fold) overexpressed in a Dictyostelium strain in which the retinoblastoma-like gene rblA has been disrupted. Most of the genes overexpressed in this strain are associated with cell cycle progression and this suggests that the main role of the corresponding proteins is in S-phase or mitosis. Human Arf1 has been reported to be essential for Golgi complex fragmentation during mitosis (Tang et al JBC 283 6085-94 (2008) Xiang et al JBC 282 21829-37 (2007). It thus seems possible that ArrH ArrJ and ArrK are involved in this process in Dicty. Harry MacWilliams September 2009brbr We have found very similar results including human C. elegans and D. melanogaster sequences in the set of proteins used for the tree. See Weeks G Gaudet P and Insall RH. (2005) The small GTPase superfamily. in Dictyostelium Genomics. Horizon Bioscience. Pascale Gaudet October 2009br | DDB0232432 | CDS | 977719 | 570 | + | 0.282456 |
arrI_ps | DDB_G0280687 | putative pseudogene ADP-ribosylation factor family protein | DDB0232430 | CDS | 3629662 | 234 | + | 0.286325 |
arrJ | DDB_G0280621 | DDB0232430 | CDS | 3577717 | 567 | + | 0.282187 | |
arrJ_ps | DDB_G0280683 | putative pseudogene ADP-ribosylation factor family protein | DDB0232430 | CDS | 3626750 | 207 | + | 0.246377 |
arrK | DDB_G0280633 | DDB0232430 | CDS | 3586248 | 567 | + | 0.280423 | |
arrL | DDB_G0278057 | DDB0232430 | CDS | 206243 | 588 | + | 0.267007 | |
arsA | DDB_G0293528 | homologous to bacterial genes that are involved in the transport of arsenate selenate and other anionic compounds outside the cell | DDB0232433 | CDS | 3193289 | 990 | - | 0.285859 |
arsB | DDB_G0289879 | has two putative transmembrane domains bacterial homolog associates with ArsA to transport arsenate selenate and other anionic compounds outside the cell | DDB0232432 | CDS | 3431951 | 1692 | + | 0.253546 |
arv1 | DDB_G0290221 | ortholog of in S. cerevisiae ARV1 that transports glycosylphosphatidylinositol intermediates into the ER lumen required for normal intracellular sterol distribution and for sphingolipid metabolism and required for viability in the absence of ARE2 (ACAT-related enzyme 2) | DDB0232432 | CDS | 3814762 | 741 | + | 0.264507 |
ascc2 | DDB_G0280455 | ortholog of human ASCC2 part of the TRIP4 complex that enhances activation of NF-kappa-B SRF and AP1 | DDB0232430 | CDS | 3375530 | 2826 | + | 0.284501 |
ascc3 | DDB_G0290389 | ortholog of human ASCC3 part of the TRIP4 complex that enhances activation of NF-kappa-B SRF and AP1 | DDB0232432 | CDS | 4020336 | 6588 | - | 0.307377 |
ascc3l | DDB_G0270042 | putative RNA helicase involved in the second step of RNA splicing ortholog of human ASCC3L1 and yeast BRR2 | DDB0232428 | CDS | 4082408 | 6714 | - | 0.320077 |
asf1 | DDB_G0285513 | DDB0232431 | CDS | 3334165 | 465 | - | 0.301075 | |
aslA-1 | DDB_G0273213 | highly similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA expressed in pstAB cells and in upper and lower cups during culmination there is a second copy of this gene | DDB0232429 | CDS | 2719022 | 1956 | - | 0.244376 |
aslB | DDB_G0274939 | highly similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA | DDB0232429 | CDS | 4557935 | 2067 | + | 0.353169 |
aslC-1 | DDB_G0273225 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 2736552 | 1968 | + | 0.265752 |
aslC-2 | DDB_G0273697 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 3293184 | 1968 | - | 0.265752 |
aslD-1 | DDB_G0273211 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 2715892 | 1941 | - | 0.261721 |
aslD-2 | DDB_G0273717 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 3313863 | 1941 | + | 0.261721 |
aslE | DDB_G0272300 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA | DDB0232429 | CDS | 1684996 | 1977 | - | 0.257461 |
aslE_ps-1 | DDB_G0273303 | putative pseudogene AMP-dependent synthetase and ligase family protein there is a second copy of this gene | DDB0232429 | CDS | 2718060 | 120 | - | 0.216667 |
aslE_ps-2 | DDB_G0273715 | putative pseudogene AMP-dependent synthetase and ligase family protein there is a second copy of this gene | DDB0232429 | CDS | 3313316 | 120 | + | 0.216667 |
aslF | DDB_G0272216 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA | DDB0232429 | CDS | 1682586 | 2046 | - | 0.258065 |
aslG-1 | DDB_G0273215 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 2725007 | 1944 | - | 0.242798 |
aslG-2 | DDB_G0273709 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 3304775 | 1944 | + | 0.242798 |
aslG_ps-1 | DDB_G0273359 | putative pseudogene AMP-dependent synthetase and ligase family protein there is a second copy of this gene | DDB0232429 | CDS | 2722019 | 1821 | - | 0.24547 |
aslG_ps-2 | DDB_G0273711 | putative pseudogene AMP-dependent synthetase and ligase family protein there is a second copy of this gene | DDB0232429 | CDS | 3307762 | 1821 | + | 0.24547 |
aslH | DDB_G0267506 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA | DDB0232428 | CDS | 248894 | 2055 | + | 0.254015 |
aslI-1 | DDB_G0273227 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 2738884 | 1959 | + | 0.256253 |
aslI-2 | DDB_G0273695 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 3290882 | 1959 | - | 0.256253 |
aslI_ps-1 | DDB_G0273363 | putative pseudogene acetyl-CoA synthetase family protein there is a second copy of this gene | DDB0232429 | CDS | 2741497 | 1053 | + | 0.25736 |
aslI_ps-2 | DDB_G0273693 | putative pseudogene acetyl-CoA synthetase family protein there is a second copy of this gene | DDB0232429 | CDS | 3288753 | 1053 | - | 0.25736 |
aslJ-1 | DDB_G0273305 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 2743505 | 1938 | + | 0.258514 |
aslJ-2 | DDB_G0273691 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 3286264 | 1938 | - | 0.258514 |
aslJ_ps | DDB_G0271518 | putative pseudogene similar to D. discoideum gene | DDB0232429 | CDS | 497016 | 426 | - | 0.288732 |
aslK-1 | DDB_G0273229 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 2746225 | 1935 | + | 0.264083 |
aslK-2 | DDB_G0273689 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 3283546 | 1935 | - | 0.264083 |
aslL-1 | DDB_G0273365 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 2750963 | 1935 | + | 0.265633 |
aslL-2 | DDB_G0273687 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 3278808 | 1935 | - | 0.265633 |
aslM | DDB_G0267544 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA | DDB0232428 | CDS | 307708 | 1923 | - | 0.24805 |
aslN | DDB_G0268272 | similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA | DDB0232428 | CDS | 304919 | 1923 | - | 0.23921 |
aslO-1 | DDB_G0273223 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 2733819 | 2130 | + | 0.259624 |
aslO-2 | DDB_G0273699 | similar to bacterial acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA there is a second copy of this gene | DDB0232429 | CDS | 3295736 | 2130 | - | 0.259624 |
asnB | DDB_G0275515 | catalyzes the reaction Hsub2subO L-glutamine L-aspartate ATP - L-glutamate L-asparagine pyrophosphate AMP | DDB0232429 | CDS | 6051213 | 1944 | + | 0.269547 |
asnS1 | DDB_G0275263 | catalyzes the reaction ATP L-asparagine tRNAAsn AMP diphosphate L-asparaginyl-tRNAAsn expression is repressed in low calcium | DDB0232429 | CDS | 5075841 | 1962 | - | 0.356269 |
asnS2 | DDB_G0268100 | catalyzes the reaction ATP L-asparagine tRNAAsn AMP diphosphate L-asparaginyl-tRNAAsn similar to bacterial Asn-tRNA-ligases | DDB0232428 | CDS | 1453036 | 1383 | - | 0.315257 |
asns | DDB_G0286059 | catalyzes the reaction Hsub2subO L-glutamine L-aspartate ATP - L-glutamate L-asparagine pyrophosphate AMP | DDB0232431 | CDS | 4007481 | 1674 | - | 0.367981 |
aspA | DDB_G0271924 | catalyzes the reaction L-asparagine Hsub2subO L-aspartate NHsub3sub | DDB0232429 | CDS | 1048524 | 1308 | + | 0.316514 |
aspS1 | DDB_G0272236 | catalyzes the reaction ATP L-aspartate tRNAAsp AMP diphosphate L-aspartyl-tRNAAsp | DDB0232429 | CDS | 1722204 | 1731 | + | 0.367995 |
aspS2 | DDB_G0272304 | catalyzes the reaction ATP L-aspartate tRNAAsp AMP diphosphate L-aspartyl-tRNAAsp | DDB0232429 | CDS | 1720046 | 1710 | + | 0.201754 |
ate1 | DDB_G0269024 | ortholog of the conserved arginine-tRNA-protein transferase ATE1 involved in the post-translational conjugation of arginine to the amino termini of acceptor proteins which are then subject to degradation via the ubiquitin pathway catalyzes rhe reaction L-arginyl-tRNA protein tRNA L-arginyl-protein | DDB0232428 | CDS | 2333199 | 1890 | + | 0.230688 |
atg1 | DDB_G0292390 | Dictyostelium homolog of yeast atg1 belongs to the ULK (Unc-51-like kinase) family of kinases required for macroautophagy | DDB0232433 | CDS | 1694801 | 2007 | + | 0.255605 |
atg10 | DDB_G0268840 | DDB0232428 | CDS | 2216150 | 693 | + | 0.186147 | |
atg101 | DDB_G0288287 | DDB0232432 | CDS | 1352566 | 561 | - | 0.263815 | |
atg12 | DDB_G0282929 | DDB0232431 | CDS | 160759 | 375 | - | 0.269333 | |
atg17 | DDB_G0295673 | DDB0232430 | CDS | 5509670 | 1467 | - | 0.216769 | |
atg18 | DDB_G0285375 | ortholog of the conserved fungi ATG18 and very similar to the mammalian WIPI2 and WIPI1 proteins contains 2 WD-40 repeats | DDB0232431 | CDS | 3197399 | 1119 | - | 0.2958 |
atg3 | DDB_G0277319 | DDB0232429 | CDS | 7690557 | 1017 | - | 0.302852 | |
atg4-1 | DDB_G0273443 | ortholog of the conserved ATG4 cysteine protease involved in autophagy there is a second copy of this gene | DDB0232429 | CDS | 2936962 | 2238 | - | 0.272118 |
atg4-2 | DDB_G0273553 | ortholog of the conserved ATG4 cysteine protease involved in autophagy there is a second copy of this gene | DDB0232429 | CDS | 3092131 | 2238 | + | 0.272118 |
atg5 | DDB_G0289881 | Dictyostelium homolog of yeast atg5 conjugated to atg12 | DDB0232432 | CDS | 3433996 | 1197 | + | 0.230576 |
atg6A | DDB_G0269244 | homolog of S. cerevisiae ATG6 and H. sapiens beclin (BECN1) involved in autophagy and apoptosis | DDB0232428 | CDS | 4264499 | 4107 | + | 0.226199 |
atg6B | DDB_G0288021 | homolog of S. cerevisiae ATG6 and H. sapiens beclin (BECN1) involved in autophagy and apoptosis | DDB0232432 | CDS | 985635 | 2568 | + | 0.308022 |
atg7 | DDB_G0271096 | DDB0232429 | CDS | 20345 | 2124 | - | 0.285782 | |
atg8 | DDB_G0286191 | DDB0232431 | CDS | 4321108 | 369 | - | 0.319783 | |
atg9 | DDB_G0285323 | Dictyostelium homolog of yeast atg9 involved in phagocytosis growth development and the response to pathogen bacteria contains 6 predicted transmembrane domains | DDB0232431 | CDS | 3194807 | 2100 | + | 0.279048 |
athl1 | DDB_G0287109 | DDB0232431 | CDS | 5232785 | 2142 | - | 0.294118 | |
atox1 | DDB_G0284221 | DDB0232431 | CDS | 1705613 | 204 | - | 0.289216 | |
atp12 | DDB_G0292678 | DDB0232433 | CDS | 1937753 | 993 | - | 0.257805 | |
atp5C1 | DDB_G0292306 | DDB0232433 | CDS | 1438508 | 921 | + | 0.373507 | |
atp5D | DDB_G0269038 | delta subunit of the central stalk of mitochondrial F1F0 ATP synthase the enzyme complex responsible for ATP synthesis | DDB0232428 | CDS | 1816266 | 513 | - | 0.360624 |
atp5O | DDB_G0283283 | DDB0232431 | CDS | 456147 | 891 | + | 0.342312 | |
atp5b | DDB_G0269916 | DDB0232428 | CDS | 3855247 | 1956 | + | 0.396728 | |
atp5e | DDB_G0276241 | epsilon subunit of the F1 sector of mitochondrial F1F0 ATP synthase the enzyme complex responsible for ATP synthesis | DDB0232429 | CDS | 6417198 | 225 | - | 0.337778 |
atp7a | DDB_G0284141 | DDB0232431 | CDS | 1486936 | 2958 | - | 0.315416 | |
atp9b | DDB_G0270870 | P-type ATPase (E1-E2) ortholog of human ATP9B and yeast NEO1 which is involved in transport from the Golgi to the ER | DDB0232428 | CDS | 2777615 | 3588 | + | 0.298495 |
atr1 | DDB_G0291380 | atypical PIKK family protein kinase similar to protein kinase ATR which modulates cell cycle progression and DNA repair in other organisms ATR phosphorylates Rad17 histone H2AX p53 and Nbs1 | DDB0232433 | CDS | 214264 | 9474 | - | 0.259552 |
atxn10 | DDB_G0268880 | similar to the human ataxin-10 (ATXN10) defects in the gene cause spinocerebellar ataxia 10 (SCA10) contains an armadillo-like helical domain (ARM-like) | DDB0232428 | CDS | 2306169 | 1830 | - | 0.22623 |
atxn2 | DDB_G0269682 | similar to the human ataxin-2 (ATXN2) defects in the gene cause spinocerebellar ataxia 2 (SCA2) | DDB0232428 | CDS | 3309660 | 3312 | - | 0.352657 |
auh | DDB_G0289471 | catalyzes the reaction: (S)-3-hydroxy-3-methylglutaryl-CoA trans-3-methylglutaconyl-CoA H2O ortholog of the human AUH protein that was identified as an RNA-binding protein that binds to clustered 5'-AUUUA-3' motifs (EC 4.2.1.18) | DDB0232432 | CDS | 2829282 | 912 | - | 0.309211 |
aurK | DDB_G0279343 | putative protein serinethreonine kinase Aur family associates with the mitotic spindle and plays a key role in mitosis the single Dictyostelium aurora kinase has properties of both aurora A and B kinases in other organisms | DDB0232430 | CDS | 1959552 | 1155 | - | 0.30303 |
bcaA | DDB_G0285509 | catalyzes the reaction 2-keto-3-methyl-valerate L-glutamate L-iso-leucine | DDB0232431 | CDS | 3329709 | 1137 | + | 0.35708 |
bcs1lA | DDB_G0289135 | conserved mitochondrial chaperone necessary for the assembly of mitochondrial respiratory chain complex III Dictyostelium has a second BCS1-like protein | DDB0232432 | CDS | 2391473 | 1266 | + | 0.304897 |
bcs1lB | DDB_G0291910 | conserved mitochondrial chaperone necessary for the assembly of mitochondrial respiratory chain complex III Dictyostelium has a second BCS1-like protein | DDB0232433 | CDS | 923283 | 1377 | + | 0.304285 |
bdp1 | DDB_G0283405 | TFIIIB subunit interacts with the non LTR retrotransposon TRE5-Abrbr bCommunity annotation:b Bdp1 is a subunit of TFIIIB a factor necessary for the initiation of transcription by RNA polIII and thus for the production of tRNA and several other small RNAs. TFIIIB is overexpressed in a wide variety of cancers see White Oncogene 23 3208-3216 (2004). In healthy cells TFIIIB interacts with and is inhibited by the tumor-suppressor Rb. Interestingly bdp1 is overexpressed (threefold p6e-10) in a Dicty strain in which the rb-like gene rblA has been disrupted. The TFIIIB-Rb antagonism thus predates the development of organisms that have tumors. The function of this interaction remains to be explained. Harry MacWilliams September 2009 | DDB0232431 | CDS | 618312 | 1374 | - | 0.275837 |
bkdA | DDB_G0286335 | catalyzes the reaction 3-methyl-2-oxobutanoate lipoamide S-(2-methylpropanoyl)-dihydrolipoamide COsub2sub E1 component of branched-chain keto acid dehydrogenase | DDB0232431 | CDS | 4250107 | 1326 | + | 0.337858 |
bkdB | DDB_G0268020 | catalyzes the reaction 3-methyl-2-oxobutanoate lipoamide S-(2-methylpropanoyl)-dihydrolipoamide COsub2sub E1 component of branched-chain keto acid dehydrogenase | DDB0232428 | CDS | 1317002 | 1113 | + | 0.334232 |
bkdC | DDB_G0281797 | multimeric enzyme (24-mer) transfers 2-methylpropanoyl 3-methylbutanoyl or S-2-methylbutanoyl groups to coenzyme A E2 component of branched-chain keto acid dehydrogenase | DDB0232430 | CDS | 4689130 | 1554 | + | 0.30888 |
blm | DDB_G0292130 | E. coli ATP-dependent DNA helicase RecQ is involved in genome maintenance this is the ortholog of the H. sapiens Bloom syndrome protein defects in BLM cause genetic instability including a high level of sister chromatid exchanges associated with a greatly increased predisposition to a wide range of cancers | DDB0232433 | CDS | 1240457 | 3780 | + | 0.286243 |
bloc1s1 | DDB_G0280077 | ortholog of human BLOC1S1 component of the BLOC-1 complex that is required for normal biogenesis of lysosome-related organelles | DDB0232430 | CDS | 2898485 | 408 | + | 0.264706 |
bloc1s2 | DDB_G0278387 | ortholog of human BLOC1S2 a component of the BLOC-1 complex that is required for normal biogenesis of lysosome-related organelles | DDB0232430 | CDS | 811383 | 705 | - | 0.289362 |
bloc1s4 | DDB_G0280403 | ortholog of human BLOC1S4 a component of the BLOC-1 complex | DDB0232430 | CDS | 3309264 | 789 | + | 0.285171 |
bloc1s5 | DDB_G0281859 | similar to human MUTED and mouse Muted which is involved in the development of lysosome-related organelles contains one putative coiled-coil domain | DDB0232430 | CDS | 5036440 | 477 | + | 0.222222 |
bloc1s6 | DDB_G0290921 | ortholog of human BLOC1S6 a component of the BLOC-1 complex mutations in human BLOC1S6 have been linked to Hermansky-Pudlak syndrome 9 | DDB0232432 | CDS | 4755734 | 624 | - | 0.213141 |
bloc1s7 | DDB_G0283001 | ortholog of human SNAPINBLOC1S7 a component of the BLOC-1 complex that is required for normal biogenesis of lysosome-related organelles | DDB0232431 | CDS | 139924 | 669 | - | 0.275037 |
bms1l | DDB_G0287891 | DDB0232432 | CDS | 751626 | 3618 | + | 0.298784 | |
bopA | DDB_G0270830 | similar to mouse BOP a zinc finger protein | DDB0232428 | CDS | 3361680 | 2091 | - | 0.247728 |
bre1 | DDB_G0274241 | very similar in the C-terminal RING Zn finger domain belongs to the BRE1 family | DDB0232429 | CDS | 4227111 | 3243 | - | 0.258094 |
brf1 | DDB_G0281215 | general transcription factor required for the initiation of transcription by RNA polymerase III TFIIIB subunit interacts with the non LTR retrotransposon TRE5-A | DDB0232430 | CDS | 4228761 | 2121 | - | 0.309288 |
btg | DDB_G0285069 | interacts with RblA to control cell fate commitment during development homolog of mammalian BTG2 | DDB0232431 | CDS | 2748189 | 1272 | + | 0.327044 |
bub1 | DDB_G0292676 | probable mitotic checkpoint serinethreonine-protein kinase a component of the mitotic checkpoint that delays anaphase until all chromosomes are properly attached to the mitotic spindle. | DDB0232433 | CDS | 1933350 | 3921 | + | 0.285896 |
bub2 | DDB_G0268794 | putative ortholog of S. cerevisiae BUB2 a mitotic checkpoint protein | DDB0232428 | CDS | 2123318 | 1101 | + | 0.269755 |
bub3 | DDB_G0292134 | ortholog of BUB3 a mitotic checkpoint protein in human a kinetochore protein that interacts with BUB1 | DDB0232433 | CDS | 1247461 | 996 | - | 0.346386 |
bud13 | DDB_G0288703 | ortholog of BUD13 which is involved in mRNA splicing in yeast | DDB0232432 | CDS | 1846726 | 1428 | - | 0.270308 |
bud31 | DDB_G0270360 | a very conserved protein known as G10 protein or BUD31 which in human is suggested to be a nuclear transcription factor and in S. pombe and S. cerevisiae has been shown to be a splicing factor | DDB0232428 | CDS | 4710295 | 666 | - | 0.27027 |
bud32 | DDB_G0279977 | belongs to the Bud32 family highly similar in sequence and length to yeast BUD32 and mammalian PRPK (p53-related protein kinase) | DDB0232430 | CDS | 2805237 | 759 | + | 0.264822 |
bxdc1 | DDB_G0292216 | ortholog of S. cerevisiae RPF2 and H. sapiens BXDC1 a nucleolar protein involved in the assembly of the large ribosomal subunit | DDB0232433 | CDS | 1328996 | 924 | - | 0.29329 |
bxdc2 | DDB_G0287937 | ortholog of the H. sapiens BXDC2 and S. cerevisiae BRX1 a nucleolar protein involved in the assembly of the large ribosomal subunit | DDB0232432 | CDS | 871082 | 981 | - | 0.313965 |
bxdc5 | DDB_G0285829 | ortholog of S. cerevisiae RPF1 and H. sapiens BXDC5 a nucleolar protein involved in the assembly of the large ribosomal subunit | DDB0232431 | CDS | 3708077 | 954 | - | 0.292453 |
bysl | DDB_G0288565 | conserved protein in H. sapiens required for processing of 20S pre-rRNA precursor and biogenesis of 40S ribosomal subunits and possibly for trophinin-dependent regulation of cell adhesion | DDB0232432 | CDS | 1691217 | 1428 | - | 0.308123 |
bzpC | DDB_G0279439 | DDB0232430 | CDS | 2050082 | 2415 | - | 0.256729 | |
bzpD | DDB_G0278379 | DDB0232430 | CDS | 795514 | 2505 | + | 0.284631 | |
bzpE | DDB_G0269338 | DDB0232428 | CDS | 2564023 | 1257 | - | 0.220366 | |
bzpF | DDB_G0279529 | DDB0232430 | CDS | 2206682 | 1896 | - | 0.245253 | |
bzpG | DDB_G0282749 | DDB0232430 | CDS | 6241172 | 1119 | - | 0.247542 | |
bzpH | DDB_G0277681 | DDB0232429 | CDS | 8349001 | 1530 | - | 0.264052 | |
bzpI | DDB_G0290173 | DDB0232432 | CDS | 3736207 | 2226 | - | 0.298293 | |
bzpJ | DDB_G0274993 | DDB0232429 | CDS | 4824947 | 2364 | + | 0.258883 | |
bzpK | DDB_G0282049 | DDB0232430 | CDS | 5331009 | 1953 | + | 0.217102 | |
bzpL | DDB_G0284023 | DDB0232431 | CDS | 1449089 | 1593 | - | 0.252354 | |
bzpM | DDB_G0282047 | DDB0232430 | CDS | 5328852 | 1767 | + | 0.224109 | |
bzpN | DDB_G0286411 | DDB0232431 | CDS | 4426368 | 3000 | - | 0.301667 | |
bzpO | DDB_G0290169 | DDB0232432 | CDS | 3730693 | 2151 | - | 0.251511 | |
bzpP | DDB_G0290303 | DDB0232432 | CDS | 3929845 | 2496 | + | 0.314503 | |
bzpQ | DDB_G0288705 | DDB0232432 | CDS | 1849253 | 2931 | + | 0.282497 | |
bzpR | DDB_G0290165 | DDB0232432 | CDS | 3726519 | 2694 | - | 0.250557 | |
bzpS | DDB_G0290171 | DDB0232432 | CDS | 3733307 | 2532 | - | 0.232622 | |
cad2 | DDB_G0275439 | similar to cadA (cad1) a calcium-binding cell-cell adhesion molecule | DDB0232429 | CDS | 5977948 | 606 | - | 0.334983 |
cad3 | DDB_G0285817 | very similar to cadA (cad1) a calcium-binding cell-cell adhesion molecule | DDB0232431 | CDS | 3695620 | 642 | - | 0.366044 |
cadA | DDB_G0285793 | calcium-dependent cell-cell adhesion protein lacks a signal sequence and is transported through the contractile vacuole to the plasma membrane for either secretion or cell surface presentation abcb4 has been identified as the anchor on the membranebr bNomenclature conflict:b Do not confuse the cadA gene encoding a calcium-dependent cell adhesion molecule with the cadA locus associated with resistance to cadmium ( | DDB0232431 | CDS | 3656149 | 642 | + | 0.333333 |
cafA | DDB_G0277827 | bNomenclature conflict:b Do not confuse this gene with the subunits ( | DDB0232430 | CDS | 292760 | 510 | - | 0.290196 |
cahA | DDB_G0269106 | DDB0232428 | CDS | 4712273 | 831 | + | 0.34657 | |
cak1-1 | DDB_G0273059 | protein serinethreonine kinase CK1 family similar to human CK1 and yeast YCK may play a role in DNA repair there is a second copy of this gene | DDB0232429 | CDS | 2688821 | 1281 | + | 0.320062 |
cak1-2 | DDB_G0273737 | protein serinethreonine kinase CK1 family similar to human CK1 and yeast YCK may play a role in DNA repair there is a second copy of this gene | DDB0232429 | CDS | 3341355 | 1281 | - | 0.320062 |
calA | DDB_G0279407 | calcium-dependent regulatory protein involved in cytokinesis regulated by cytosolic Ca2 fluxes allowing differential binding to target CaM binding proteins (CaMBPs) binds several proteins among them nuclear NumA and Cdk5 | DDB0232430 | CDS | 2244074 | 459 | - | 0.35512 |
calB | DDB_G0269104 | DDB0232428 | CDS | 2981116 | 450 | + | 0.275556 | |
canA | DDB_G0276883 | catalytic subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase | DDB0232429 | CDS | 7189408 | 1872 | + | 0.320513 |
cand1 | DDB_G0274167 | highly conserved protein interacts with TATA binding protein (TBP) and with the SCF (Skp1-Cul1-F-box) ubiquitin ligase complex | DDB0232429 | CDS | 4865578 | 3717 | - | 0.335217 |
cap | DDB_G0288769 | component of the endo-lysosomal system links with actin cytoskeleton br bNomenclature conflict:b Do not confuse this gene with capA the cAMP-binding protein | DDB0232432 | CDS | 1946096 | 1395 | + | 0.354839 |
capA-1 | DDB_G0272560 | there is a second copy of this gene | DDB0232429 | CDS | 2353564 | 1893 | - | 0.43159 |
capA-2 | DDB_G0274023 | there is a second copy of this gene | DDB0232429 | CDS | 3677221 | 1893 | + | 0.43159 |
capB | DDB_G0277501 | bCommunity annotation:b I used an mRNAseq read fitter which is particular friendly to splice variants (in preparation) to determine the developmental time course of the two curated splice variants of capB using the raw data of Dicty Express (courteously provided by G. Shaulsky and A Parikh). Both variants increase in mid to late development splvarB shows in addition a strong peak in veg cells. The curves for the two variants should add up to the curve for the common sequences and this is approximately true during development suggesting that variants A and B account for most of the developmental transcription. In the growth phase however A and B add up to less than the total suggesting that an additional variant exists which is expressed largely or entirely in the growth phase. Harry MacWilliams October 2010br | DDB0232429 | CDS | 8096571 | 1626 | + | 0.389914 |
captA | DDB_G0271794 | catalyzes the reaction CDP-choline 12-diacylglycerol CMP a phosphatidylcholine putative ortholog of human CEPT1 | DDB0232429 | CDS | 747447 | 1146 | + | 0.260035 |
captB | DDB_G0278947 | catalyzes the reaction CDP-choline 12-diacylglycerol CMP a phosphatidylcholine putative ortholog of human CHPT1 | DDB0232430 | CDS | 1290736 | 1230 | + | 0.307317 |
captC | DDB_G0276763 | catalyzes the reaction CDP-choline 12-diacylglycerol CMP a phosphatidylcholine most similar to plant genes REMI mutant forms aberrant fruiting bodies see | DDB0232429 | CDS | 7210164 | 1200 | + | 0.27 |
captD | DDB_G0275235 | catalyzes the reaction CDP-choline 12-diacylglycerol CMP a phosphatidylcholine | DDB0232429 | CDS | 4940204 | 1140 | + | 0.3 |
carA-1 | DDB_G0273397 | high affinity cAMP receptor belongs to the serpentineG-protein coupled receptor family there is a second copy of this gene | DDB0232429 | CDS | 2964374 | 1179 | - | 0.307888 |
carA-2 | DDB_G0273533 | high affinity cAMP receptor belongs to the serpentineG-protein coupled receptor family there is a second copy of this gene | DDB0232429 | CDS | 3066091 | 1179 | + | 0.307888 |
carB | DDB_G0288179 | low affinity cAMP receptor belongs to the serpentineG-protein coupled receptor family | DDB0232432 | CDS | 1252723 | 1128 | + | 0.289007 |
carC | DDB_G0277829 | high affinity cAMP receptor belongs to the serpentineG-protein coupled receptor family | DDB0232430 | CDS | 504442 | 1473 | + | 0.271555 |
carD | DDB_G0277831 | low affinity cAMP receptor belongs to the serpentineG-protein coupled receptor family | DDB0232430 | CDS | 498291 | 1332 | + | 0.261261 |
carmil | DDB_G0292386 | DDB0232433 | CDS | 1735919 | 3153 | - | 0.326673 | |
cas1 | DDB_G0269226 | DDB0232428 | CDS | 3476704 | 2112 | - | 0.338542 | |
casK | DDB_G0276885 | CK2 family protein kinase a ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | DDB0232429 | CDS | 7370887 | 1014 | + | 0.310651 |
catA | DDB_G0274595 | catalyzes the reaction 2Hsub2subOsub2sub catalase 2Hsub2subO Osub2sub expressed throughout development expression restricted to prestalk cells during post-aggregationbr bNomenclature conflict:b Do not confuse the acrA gene encoding the late development adenylate cyclase ACR with the genetic locus acrA corresponding to the catA catalase that confers resistance to acriflavin ( | DDB0232429 | CDS | 3823148 | 1491 | + | 0.380952 |
catB | DDB_G0269108 | catalyzes the reaction 2Hsub2subOsub2sub catalase 2Hsub2subO Osub2sub only expressed in post-aggregative development in prespore cells regulated by the MADS-box transcription factor SrfA during development | DDB0232428 | CDS | 3244376 | 2079 | + | 0.351611 |
cax1 | DDB_G0279301 | contains 13 transmembrane domains transports Ca2 or other cations using the gradient of H or Na generated by energy-coupled primary transporters | DDB0232430 | CDS | 1901303 | 2340 | + | 0.29188 |
cbfA | DDB_G0279409 | nuclear DNA-binding protein binds to C-module of retrotransposon DRE general transcriptional regulator | DDB0232430 | CDS | 2308619 | 3003 | - | 0.30303 |
cbfB | DDB_G0293470 | similar to Dictyostelium cbfA contains a jmjC domain | DDB0232433 | CDS | 2928133 | 4425 | - | 0.250847 |
cbhA | DDB_G0268446 | DDB0232428 | CDS | 1540789 | 1374 | + | 0.372635 | |
cblA-1 | DDB_G0273141 | homolog of the metazoan cbl proteins contains a tyrosine kinase binding domain (TBK) at the amino terminus connected to a RING finger regulates STAT signaling via PTP3 there is a second copy of this gene | DDB0232429 | CDS | 2863138 | 1998 | - | 0.214715 |
cblA-2 | DDB_G0273609 | homolog of the metazoan cbl proteins contains a tyrosine kinase binding domain (TBK) at the amino terminus connected to a RING finger regulates STAT signaling via PTP3 there is a second copy of this gene | DDB0232429 | CDS | 3166651 | 1998 | + | 0.214715 |
cbp2 | DDB_G0267456 | DDB0232428 | CDS | 872490 | 507 | - | 0.315582 | |
cbpA | DDB_G0276759 | contains four EF hands regulates reorganization of the actin cytoskeleton during cell aggregation | DDB0232429 | CDS | 7265714 | 471 | - | 0.339703 |
cbpB | DDB_G0283533 | DDB0232431 | CDS | 829856 | 423 | + | 0.283688 | |
cbpC | DDB_G0283613 | DDB0232431 | CDS | 904975 | 501 | - | 0.287425 | |
cbpD1 | DDB_G0283153 | contains four EF-hands expressed in post-aggregation stage of development | DDB0232431 | CDS | 347658 | 489 | - | 0.292434 |
cbpD2 | DDB_G0283083 | contains four EF-hands expressed in post-aggregation stage of development | DDB0232431 | CDS | 279175 | 948 | - | 0.299578 |
cbpD3_ps | DDB_G0285475 | putative pseudogene very similar to Dicyostelium cbpD1 and cbpD2 but missing their conserved N-terminal 15 amino acids | DDB0232431 | CDS | 3277201 | 438 | - | 0.289954 |
cbpE | DDB_G0274099 | DDB0232429 | CDS | 4580344 | 543 | - | 0.32965 | |
cbpF | DDB_G0283611 | DDB0232431 | CDS | 899345 | 525 | - | 0.312381 | |
cbpG | DDB_G0283609 | DDB0232431 | CDS | 901731 | 510 | - | 0.296078 | |
cbpH | DDB_G0288623 | DDB0232432 | CDS | 1770590 | 498 | - | 0.238956 | |
cbpI | DDB_G0272827 | expressed in prespore cells contains only 3 EF hands and does not bind calcium | DDB0232429 | CDS | 2048952 | 492 | - | 0.270325 |
cbpJ | DDB_G0270210 | Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232428 | CDS | 4415136 | 585 | - | 0.232479 |
cbpK | DDB_G0274359 | putative Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232429 | CDS | 3815183 | 570 | - | 0.303509 |
cbpL | DDB_G0288785 | putative Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232432 | CDS | 1964055 | 576 | + | 0.258681 |
cbpM | DDB_G0286371 | putative Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232431 | CDS | 4370399 | 552 | - | 0.277174 |
cbpP | DDB_G0277909 | DDB0232430 | CDS | 179912 | 1404 | - | 0.456553 | |
ccbl | DDB_G0287269 | catalyzes the reaction L-kynurenine 2-oxoglutarate 4-(2-aminophenyl)-24-dioxobutanoate L-glutamate | DDB0232432 | CDS | 47854 | 1308 | - | 0.33104 |
ccdc124 | DDB_G0289893 | DDB0232432 | CDS | 3369167 | 744 | + | 0.310484 | |
ccdc130 | DDB_G0281599 | DDB0232430 | CDS | 4696808 | 978 | + | 0.216769 | |
ccdc25 | DDB_G0269786 | DDB0232428 | CDS | 3556678 | 621 | + | 0.278583 | |
ccdc53 | DDB_G0267948 | DDB0232428 | CDS | 1170991 | 1065 | - | 0.36338 | |
ccdc94 | DDB_G0279481 | conserved hypothetical protein containing domain of unknown function DUF572 ortholog of human CCDC94 and yeast YJU2CWF16 believed to be involved in mRNA splicing | DDB0232430 | CDS | 2120888 | 975 | + | 0.246154 |
cchl | DDB_G0275895 | catalyzes the covalent attachment of a heme group on two cysteine residues of cytochrome c and c1 defects in the human gene causes syndromic microphthalmia 7 (MCOPS7) syndrome an X-linked dominant disorder characterized by unilateral or bilateral microphthalmia and linear skin defects | DDB0232429 | CDS | 5939682 | 636 | + | 0.292453 |
ccs | DDB_G0291031 | copper chaperone that specifically delivers Cu to sod1 copperzinc superoxide dismutase | DDB0232432 | CDS | 4931620 | 951 | - | 0.270242 |
cct2 | DDB_G0291358 | DDB0232433 | CDS | 177191 | 1599 | - | 0.358349 | |
cct3 | DDB_G0281741 | DDB0232430 | CDS | 4903167 | 1593 | + | 0.37602 | |
cct4 | DDB_G0292872 | DDB0232433 | CDS | 2188382 | 1602 | - | 0.373908 | |
cct5 | DDB_G0281849 | DDB0232430 | CDS | 5012149 | 1617 | + | 0.343847 | |
cct6 | DDB_G0277493 | DDB0232429 | CDS | 8001157 | 1620 | - | 0.340741 | |
cct7 | DDB_G0291225 | DDB0232433 | CDS | 201367 | 1668 | + | 0.41307 | |
cct8 | DDB_G0276233 | DDB0232429 | CDS | 6265977 | 1614 | - | 0.366791 | |
cda | DDB_G0288933 | catalyzes the reactions cytidine Hsub2subO uridine NHsub3sub and Hsub2subO deoxycytidine NHsub3sub deoxyuridine | DDB0232432 | CDS | 2144804 | 444 | - | 0.351351 |
cdc123 | DDB_G0276129 | ortholog of S. cerevisiae cdc123 involved in the nutritional control of the cell cycle | DDB0232429 | CDS | 6244624 | 1155 | - | 0.249351 |
cdc20 | DDB_G0285601 | ortholog of CDC20 a cell-cycle regulated activator of anaphase-promoting complexcyclosome (APCC) which is required for metaphaseanaphase transition directs ubiquitination of mitotic cyclins | DDB0232431 | CDS | 3433247 | 1500 | + | 0.346 |
cdc25 | DDB_G0283617 | similar to mammalian dual specificity protein phosphatases cdc25B and cdc25C involved in the G2M transition through dephosphorylation of cdc2 at Tyr15 and Thr14 | DDB0232431 | CDS | 1053164 | 3162 | - | 0.256799 |
cdc26 | DDB_G0293230 | cdc26 ortholog missing about half of the carboxyl terminus | DDB0232433 | CDS | 2676069 | 210 | + | 0.304762 |
cdc40 | DDB_G0289501 | conserved splicing factor S. cerevisiae cdc40 is important for catalytic step II of pre-mRNA splicing and plays a role in cell cycle progression | DDB0232432 | CDS | 2860682 | 1788 | + | 0.319351 |
cdc45 | DDB_G0267748 | ortholog of the conserved CDC45 or CDC45L protein in S. cerevisiae and S. pombe required for initiation of chromosomal DNA replication | DDB0232428 | CDS | 776324 | 1935 | - | 0.30491 |
cdc5l | DDB_G0279311 | contains two Myb DNA-binding domains ortholog of human CDC5L and yeast CEF1 may play a role in transcriptional activation and in mRNA splicing | DDB0232430 | CDS | 1918418 | 2403 | - | 0.28506 |
cdc6 | DDB_G0275983 | bCommunity annotation:b ortholog of cdc6 long known to be a critical member of the DNA pre-replication complex and more recently implicated in control of mitosis (see | DDB0232429 | CDS | 6146641 | 1317 | + | 0.247532 |
cdc7 | DDB_G0292152 | similar to S. cerevisiae cell division control protein 7 (CDC7) a serinethreonine kinase required for mitosis and meiosis | DDB0232433 | CDS | 1294776 | 3186 | + | 0.23666 |
cdc73 | DDB_G0274885 | component of the conserved Paf1 complex a multifunctional complex involved in histone methylation and plays a role in RNA elongation and processing defects in human CDC73 cause hyperparathyroidism-jaw tumor syndrome (HPT-JT) parathyroid carcinoma and hyperparathyroidism (FIHP) | DDB0232429 | CDS | 4342175 | 1599 | - | 0.290807 |
cdcD | DDB_G0288065 | highly conserved protein CDC48 in yeasts | DDB0232432 | CDS | 1118593 | 2382 | + | 0.398825 |
cdh1 | DDB_G0287259 | ortholog of FZR1CDH1 that regulates the ubiquitin ligase activity of the anaphase promoting complexcyclosome (APCC) which directs ubiquitination of cyclins resulting in mitotic exit related to cdc20 | DDB0232432 | CDS | 54882 | 2265 | - | 0.284768 |
cdipt | DDB_G0284857 | similar to human CDIPT and S. cerevisiae PIS1 (phosphatidylinositol synthase) catalyzes the reaction CDP-diacylglycerol myo-inositol CMP phosphatidyl-1D-myo-inositol contains 4 putative transmembrane domains | DDB0232431 | CDS | 2547724 | 624 | + | 0.298077 |
cdk1 | DDB_G0272813 | similar to CDK1 and CDK2 cell cycle CAK (CDK-activating kinase) kinases predicted to activate SG2 cyclins cyclin A B and D | DDB0232429 | CDS | 2216835 | 891 | + | 0.331089 |
cdk10 | DDB_G0268480 | putative cell division cycle 2 (CDC2)-like protein kinase has similarity to PITSLRE proteins and other cyclin-dependent kinase 2 kinases | DDB0232428 | CDS | 294048 | 1101 | - | 0.256131 |
cdk11 | DDB_G0283279 | very similar to human CDL1 (PITSLRE serinethreonine-protein kinase CDC2L1) which appears to play multiple roles in cell cycle progression cytokinesis and apoptosis predicted to interact with | DDB0232431 | CDS | 446640 | 1077 | - | 0.338904 |
cdk5 | DDB_G0288677 | CMGC group protein kinase highly similar to mammalian cdk5 localizes to the nucleus and shuttles to the cytoplasm during late mitosis binds calmodulin PsaA | DDB0232432 | CDS | 1885785 | 879 | + | 0.302617 |
cdk7 | DDB_G0285417 | putative ortholog of CDK7 and CTK1 which phosphorylates the C-terminal repeated domain of the RNA polymerase II large subunit predicted to be activated by | DDB0232431 | CDS | 3627427 | 1083 | + | 0.307479 |
cdk8 | DDB_G0267442 | controls RNA polymerase II activity by phosphorylating the carboxy terminal domain (CTD) of the largest subunit predicted to interact with | DDB0232428 | CDS | 1582311 | 1143 | - | 0.314961 |
cdk9-1 | DDB_G0273207 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases there is a second copy of this gene | DDB0232429 | CDS | 2708039 | 2085 | + | 0.282974 |
cdk9-2 | DDB_G0273721 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases there is a second copy of this gene | DDB0232429 | CDS | 3321422 | 2085 | - | 0.282974 |
cdsA | DDB_G0269742 | catalyzes the reaction: CTP phosphatidate diphosphate CDP-diacylglycerol provides CDP-diacylglycerol an important precursor for the synthesis of phospholipids contains 8 putative transmembrane domains | DDB0232428 | CDS | 3466584 | 1440 | + | 0.289583 |
celA | DDB_G0271134 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232429 | CDS | 58680 | 2118 | - | 0.36119 |
celB | DDB_G0269112 | DDB0232428 | CDS | 3166724 | 1599 | - | 0.368355 | |
cenA | DDB_G0288427 | similar to human Centrin 2 EF-hand protein localizes to the centromer from which it dissociates during mitosis | DDB0232432 | CDS | 1525659 | 456 | + | 0.245614 |
cenB | DDB_G0279151 | centrin required for nuclear and centrosome stability localizes to the nucleus in interphase but not during mitosis and is involved in the centrosome cycle | DDB0232430 | CDS | 1697579 | 453 | - | 0.258278 |
cepA | DDB_G0292142 | DDB0232433 | CDS | 1258240 | 1041 | + | 0.232469 | |
cepB | DDB_G0282485 | DDB0232430 | CDS | 5831395 | 1119 | - | 0.291332 | |
cepC | DDB_G0290509 | DDB0232432 | CDS | 4173965 | 1413 | - | 0.219391 | |
cepD | DDB_G0283111 | DDB0232431 | CDS | 261195 | 1959 | - | 0.244002 | |
cepE | DDB_G0275495 | DDB0232429 | CDS | 6003763 | 2400 | - | 0.307083 | |
cepF | DDB_G0270150 | similar to the conserved ZW10 kinetochore-associated protein an essential component of the mitotic checkpoint but the Dictyosteium potein localizes exclusively to the corona of the centrosome however the proteins may share the function of dyneindynactin targeting in interphase | DDB0232428 | CDS | 4316335 | 2670 | + | 0.201124 |
cepG | DDB_G0278809 | DDB0232430 | CDS | 1225451 | 3894 | + | 0.248074 | |
cepH | DDB_G0285313 | DDB0232431 | CDS | 3082073 | 5757 | - | 0.266806 | |
cepJ | DDB_G0268616 | DDB0232428 | CDS | 1809151 | 6042 | - | 0.295763 | |
cepK | DDB_G0293544 | localizes to the corona of the centrosome and to centromeres affects cell growth and chemotactic motility and is involved in the interaction with the nuclear envelope | DDB0232433 | CDS | 2990987 | 6333 | - | 0.225959 |
cf45-1 | DDB_G0269248 | component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) | DDB0232428 | CDS | 3267307 | 894 | + | 0.388143 |
cf50-1 | DDB_G0273175 | component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) there is a second copy of this gene | DDB0232429 | CDS | 2522303 | 912 | + | 0.349781 |
cf50-2 | DDB_G0273875 | component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) there is a second copy of this gene | DDB0232429 | CDS | 3508572 | 912 | - | 0.349781 |
cf60 | DDB_G0284363 | regulates aggregate size and number component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) similar to histidine acid phosphatase but does not possess phosphatase activity | DDB0232431 | CDS | 1892663 | 1251 | - | 0.347722 |
cfaA | DDB_G0277809 | DDB0232429 | CDS | 8442320 | 702 | + | 0.287749 | |
cfaB | DDB_G0277811 | DDB0232429 | CDS | 8443492 | 519 | + | 0.290944 | |
cfaC | DDB_G0276475 | DDB0232429 | CDS | 7023841 | 660 | + | 0.324242 | |
cfaD | DDB_G0281605 | related to cysteine protease C1A but has no detectable peptidase activity autocrine secreted factor that slows cell proliferation and thus has the properties of a chalone generates two products a 65 kDa and a 27 kDa peptide | DDB0232430 | CDS | 4701100 | 1596 | - | 0.379073 |
cfrA | DDB_G0290257 | DDB0232432 | CDS | 3901077 | 2193 | + | 0.279982 | |
cfrB | DDB_G0290259 | DDB0232432 | CDS | 3906804 | 2205 | + | 0.277551 | |
cfrC | DDB_G0290261 | DDB0232432 | CDS | 3911024 | 2241 | + | 0.277108 | |
cfrD | DDB_G0290265 | DDB0232432 | CDS | 3914845 | 2259 | + | 0.27977 | |
cfr_ps1 | DDB_G0290271 | putative pseudogene highly similar to cfr (Cell Fusion Related) genes (cell surface glycoprotein GP138) | DDB0232432 | CDS | 3898353 | 2238 | + | 0.262735 |
cfr_ps2 | DDB_G0290269 | putative pseudogene highly similar to cfr (Cell Fusion Related) genes (cell surface glycoprotein GP138) | DDB0232432 | CDS | 3918589 | 543 | + | 0.290976 |
cfr_ps3 | DDB_G0274529 | putative pseudogene highly similar to cfr (Cell Fusion Related) genes (cell surface glycoprotein GP138) | DDB0232429 | CDS | 4268033 | 2598 | - | 0.293303 |
chcA | DDB_G0277221 | DDB0232429 | CDS | 7717198 | 5085 | + | 0.369911 | |
chdA | DDB_G0284171 | CHD gene family protein containing a chromodomain a helicase domain and a DNA-binding domain similar to H. sapiens chromodomain-helicase-DNA-binding protein 2 (CHD-2) (SwissProt: O14647) chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232431 | CDS | 1645755 | 5754 | - | 0.310219 |
chdB | DDB_G0280705 | CHD gene family protein containing a chromodomain a C terminal helicase domain and a DNA-binding domain chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232430 | CDS | 3648861 | 7122 | - | 0.267762 |
chdC | DDB_G0293012 | CHD gene family protein containing a chromodomain a helicase domain and a DNA-binding domain chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232433 | CDS | 2321154 | 9216 | + | 0.312174 |
chdh | DDB_G0287229 | catalyzes the reaction: choline acceptor betaine aldehyde reduced acceptor ortholog of the mammalian CHDH contains a putative signal sequence | DDB0232432 | CDS | 24322 | 1770 | - | 0.327684 |
chid1 | DDB_G0290417 | DDB0232432 | CDS | 4060970 | 1158 | - | 0.244387 | |
chlA | DDB_G0290825 | catalyzes the chlorination step in DIF-1 biosynthesis belongs to the FAD-dependent oxidoreductase family belongs to the tryptophan halogenase family | DDB0232432 | CDS | 4647665 | 1812 | - | 0.313466 |
chtB | DDB_G0290617 | DDB0232432 | CDS | 4375423 | 2166 | + | 0.211911 | |
chtC | DDB_G0290959 | similar to heat shock protein Hsp20 domain-containing protein but does not contain a Hsp20 domain | DDB0232432 | CDS | 4833259 | 1956 | + | 0.249489 |
chtf18 | DDB_G0272758 | in S. cerevisiae essential for the fidelity of chromosome transmission and component of the RFC complexbrbr bCommunity annotation:b CTF18 ( | DDB0232429 | CDS | 2108163 | 2814 | + | 0.264748 |
ciao1 | DDB_G0269728 | ortholog of the conserved CIA1 (S. cerevisiae) or CIAO1 (Mammals) which in yeast is essential for assembly of cytosolic and nuclear iron-sulfur proteins contains 7 WD40 repeats | DDB0232428 | CDS | 3427650 | 1002 | + | 0.284431 |
cigA | DDB_G0288245 | DDB0232432 | CDS | 1317088 | 2445 | + | 0.274847 | |
cigB | DDB_G0290067 | DDB0232432 | CDS | 3642812 | 2235 | - | 0.229978 | |
cinB | DDB_G0291121 | DDB0232432 | CDS | 5056007 | 1014 | + | 0.269231 | |
cinC | DDB_G0287685 | translocates peptidyl-tRNA from the aminoacyl site to the peptidyl site on the ribosome during protein synthesis induced by cycloheximide knockdown has significantly reduced ability for protein synthesis | DDB0232432 | CDS | 689907 | 2562 | + | 0.358314 |
cinD-1 | DDB_G0273061 | ortholog of Saccharomyces cerevisiae Mbf1 protein expressed at high level in vegetative celly and decreases sharply in early development induced by cycloheximide there is a second copy of this gene | DDB0232429 | CDS | 2640075 | 315 | + | 0.336508 |
cinD-2 | DDB_G0273775 | ortholog of Saccharomyces cerevisiae Mbf1 protein expressed at high level in vegetative celly and decreases sharply in early development induced by cycloheximide there is a second copy of this gene | DDB0232429 | CDS | 3390843 | 315 | - | 0.336508 |
cirh1a | DDB_G0293462 | DDB0232433 | CDS | 2920900 | 1389 | + | 0.24982 | |
cks1 | DDB_G0271642 | ortholog of the conserved CKS1 protein which binds to the catalytic subunit of cyclin dependent kinases and is essential for their biological function | DDB0232429 | CDS | 614231 | 249 | + | 0.317269 |
clasp | DDB_G0271286 | DDB0232429 | CDS | 155520 | 2700 | - | 0.248889 | |
clc | DDB_G0277403 | clathrin is composed of three heavy chain subunits (ChcA) and three light chain subunits (Clc)br bNomenclature conflict:b Do not confuse this gene with clcA encoding a conserved chloride channel | DDB0232429 | CDS | 8123072 | 585 | - | 0.302564 |
clcA | DDB_G0294096 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers br bNomenclature conflict:b Do not confuse this gene with clc also known as clcA encoding the clathrin light chain | DDB0232429 | CDS | 435997 | 2592 | + | 0.328318 |
clcB | DDB_G0276865 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232429 | CDS | 7525349 | 2448 | - | 0.280637 |
clcC | DDB_G0276229 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232429 | CDS | 6228081 | 2274 | + | 0.311785 |
clcD | DDB_G0278639 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232430 | CDS | 535599 | 3003 | - | 0.360972 |
clcE | DDB_G0286491 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232431 | CDS | 4560350 | 2985 | + | 0.283417 |
clcF | DDB_G0293130 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232433 | CDS | 2574912 | 2430 | + | 0.295885 |
cldA | DDB_G0278895 | DDB0232430 | CDS | 1348299 | 3942 | - | 0.28691 | |
cldB | DDB_G0276091 | DDB0232429 | CDS | 6345319 | 4338 | - | 0.263947 | |
clkA | DDB_G0281179 | similar to cyclin-like kinases (CLK) putative dual specifity kinase | DDB0232430 | CDS | 4167312 | 2799 | + | 0.215077 |
clmA | DDB_G0278685 | clathrin adaptor protein that regulates contractile vacuole size and involved in the response to osmotic stress interacts with Vamp7B and retrieves Vamp7B from the contractile vacuole ortholog of H. sapiens SNAP91 | DDB0232430 | CDS | 852176 | 2088 | - | 0.293582 |
cln3 | DDB_G0291157 | ortholog of Cln3 responsible for Batten's disease a juvenile neurological disorder | DDB0232432 | CDS | 5060161 | 1266 | - | 0.313586 |
cln5 | DDB_G0275299 | ortholog of Cln5 implicated in neuronal ceroid lipofuscinoses neurodegenerative disorders | DDB0232429 | CDS | 5272269 | 969 | + | 0.298246 |
clp1 | DDB_G0285507 | ortholog of the conserved CLP1 protein S. cerevisiae CLP1 is involved in both the endonucleolytic cleavage and polyadenylation steps of mRNA 3'-end maturation Mammalian CLP1 is a subunit of cleavage complex IIA which is required for cleavage but not for polyadenylation of pre-mRNA | DDB0232431 | CDS | 3327387 | 1380 | - | 0.322464 |
cluA | DDB_G0292806 | a 150 kD protein responsible for distribution of mitochondria in the cell and cytokinesis in the null mutant mitochondria are clustered in the cell center | DDB0232433 | CDS | 2247666 | 3963 | - | 0.354529 |
clybl | DDB_G0284067 | DDB0232431 | CDS | 1497378 | 1083 | + | 0.279778 | |
cmbB | DDB_G0288131 | calmodulin-binding protein comprised of tandem repeats of newly identified IP22 motifs which occur in mimivirus and Dictyostelium IP22 motifs may play a role in cell motility and chemotaxis | DDB0232432 | CDS | 1162843 | 1242 | - | 0.309984 |
cmbC | DDB_G0269116 | conserved Dictyostelium protein similar to bacterial proteins contains a predicted signal peptide | DDB0232428 | CDS | 4695724 | 405 | - | 0.325926 |
cmbC_ps1 | DDB_G0283131 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 290287 | 246 | + | 0.333333 |
cmbC_ps2 | DDB_G0270796 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232428 | CDS | 4716417 | 336 | + | 0.297619 |
cmbl | DDB_G0285591 | DDB0232431 | CDS | 3421735 | 768 | - | 0.303385 | |
cmfA | DDB_G0275007 | DDB0232429 | CDS | 5236396 | 2100 | + | 0.339048 | |
cmfB | DDB_G0289157 | DDB0232432 | CDS | 2432359 | 1533 | + | 0.395303 | |
cmr | DDB_G0279711 | similar to comitin a lectin and actin binding protein linking the actin cytoskeleton to the Golgi apparatus | DDB0232430 | CDS | 2473335 | 408 | + | 0.294118 |
cnbA | DDB_G0267446 | regulatory subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase contains an EF-hand calcium binding motif | DDB0232428 | CDS | 816934 | 1041 | - | 0.26513 |
cnbB | DDB_G0285999 | contains 3 EF-hands similar to calcineurin B (cnbA) the regulatory subunit of the Ca2calmodulin-dependent serinethreonine protein phosphatase | DDB0232431 | CDS | 3918232 | 552 | + | 0.269928 |
cniA | DDB_G0270698 | similar to human CNIH S. pombe erv14 human and Drosophila cornichon act in the selective transport and maturation of TGFalpha family proteins contains 3 predicted transmembrane domains | DDB0232428 | CDS | 3944438 | 444 | + | 0.252252 |
cniB | DDB_G0279785 | similar to human CNIH4 and S. pombe erv14 contains 3 predicted transmembrane domains | DDB0232430 | CDS | 2547350 | 423 | - | 0.241135 |
cnrB | DDB_G0283115 | identified as a suppressor of smlA null mutant cnr2 contains six predicted transmembrane domains | DDB0232431 | CDS | 264436 | 1860 | - | 0.277419 |
cnrC | DDB_G0269764 | identified as a suppressor of smlA null mutant cnr3 has a predicted signal anchor sequence | DDB0232428 | CDS | 3515795 | 1464 | + | 0.28347 |
cnrD | DDB_G0275209 | identified as a suppressor of smlA null mutant cnr4 contains a Cue domain which may be involved in binding ubiquitin-conjugating enzymes | DDB0232429 | CDS | 5044037 | 1089 | + | 0.314968 |
cnrF | DDB_G0276119 | DDB0232429 | CDS | 6259472 | 2961 | + | 0.280986 | |
cnrG | DDB_G0287483 | identified as a suppressor of smlA null mutant cnr6 contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232432 | CDS | 306749 | 984 | - | 0.273374 |
cnrI | DDB_G0269768 | DDB0232428 | CDS | 3520960 | 1704 | + | 0.349765 | |
cnrJ | DDB_G0277309 | DDB0232429 | CDS | 7641137 | 2076 | + | 0.318401 | |
cnrK | DDB_G0292120 | DDB0232433 | CDS | 1222744 | 3645 | - | 0.266941 | |
cnrM | DDB_G0288307 | DDB0232432 | CDS | 1376942 | 4920 | - | 0.293089 | |
cnrN | DDB_G0287969 | identified as a suppressor of smlA null mutant cnr14 phosphatase involved in late-aggregation events including the regulation of fruiting body size as well as cAMP and PI3K signaling | DDB0232432 | CDS | 912043 | 1920 | + | 0.25625 |
cnrO | DDB_G0278101 | DDB0232430 | CDS | 272535 | 399 | - | 0.280702 | |
cnrP | DDB_G0279327 | ortholog of importin 9 a nuclear transport receptor that is thought to mediate docking of the importinsubstrate complex to the nuclear pore complex identified as a suppressor of smlA null mutant cnr16 | DDB0232430 | CDS | 1941566 | 3333 | - | 0.311131 |
cnxA | DDB_G0271144 | Ca2-binding protein with chaperone activity in the endoplasmic reticulum plays a role in phagocytosis | DDB0232429 | CDS | 216838 | 1611 | - | 0.377405 |
coaA | DDB_G0293898 | DDB0232433 | CDS | 3517422 | 441 | + | 0.387755 | |
cofA | DDB_G0277833 | DDB0232430 | CDS | 608653 | 414 | - | 0.391304 | |
cofB | DDB_G0291970 | coding region identical to cofA the 15 kDa actin severing protein | DDB0232433 | CDS | 1044327 | 414 | - | 0.391304 |
cofC-1 | DDB_G0272568 | a new member of the cofilin family specifically expressed during aggregation there is a second copy of this gene | DDB0232429 | CDS | 2310809 | 432 | - | 0.24537 |
cofC-2 | DDB_G0274059 | a new member of the cofilin family specifically expressed during aggregation there is a second copy of this gene | DDB0232429 | CDS | 3720546 | 432 | + | 0.24537 |
cofD-1 | DDB_G0272646 | very similar to cofC and similar to cofA a 15 kDa protein with actin filament severing activity contains an actin-binding cofilintropomyosin type domain there is a second copy of this gene | DDB0232429 | CDS | 2311642 | 417 | - | 0.28777 |
cofD-2 | DDB_G0274057 | very similar to cofC and similar to cofA a 15 kDa protein with actin filament severing activity contains an actin-binding cofilintropomyosin type domain there is a second copy of this gene | DDB0232429 | CDS | 3719728 | 417 | + | 0.28777 |
cofE | DDB_G0283367 | similar to cofA a 15 kDa protein with actin filament severing activity contains an actin-binding cofilintropomyosin type domain | DDB0232431 | CDS | 586631 | 408 | - | 0.267157 |
cofF | DDB_G0274589 | similar to cofilins contains an actin-binding cofilintropomyosin type domain | DDB0232429 | CDS | 3865902 | 369 | + | 0.205962 |
cog1 | DDB_G0277691 | similar to COG1 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | DDB0232429 | CDS | 8323828 | 4350 | + | 0.24092 |
cog2 | DDB_G0281163 | highly similar to COG2 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | DDB0232430 | CDS | 4125474 | 2715 | + | 0.21547 |
cog3 | DDB_G0281511 | highly similar to COG3 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | DDB0232430 | CDS | 4648103 | 2778 | - | 0.221022 |
cog4 | DDB_G0267960 | highly similar to COG4 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | DDB0232428 | CDS | 1187972 | 2736 | - | 0.240863 |
cog5 | DDB_G0289535 | highly similar to COG5 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | DDB0232432 | CDS | 2897974 | 2697 | + | 0.229885 |
cog6 | DDB_G0292784 | highly similar to COG6 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | DDB0232433 | CDS | 2027082 | 2022 | - | 0.273986 |
cog7 | DDB_G0286705 | highly similar to COG7 component of the conserved oligomeric Golgi complex which is composed of eight different subunits Defects in human COG7 are the cause of congenital disorder of glycosylation type 2E (CDG2E) | DDB0232431 | CDS | 4871672 | 2991 | - | 0.252424 |
cog8 | DDB_G0271388 | similar to COG8 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | DDB0232429 | CDS | 199855 | 2340 | - | 0.235897 |
colA | DDB_G0292696 | collagen-binding surface protein Cna-like B-type domain-containing large protein | DDB0232433 | CDS | 1959495 | 33312 | - | 0.32826 |
colA_ps1 | DDB_G0290367 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232432 | CDS | 3904303 | 330 | - | 0.336364 |
colA_ps2 | DDB_G0290293 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232432 | CDS | 3899689 | 312 | - | 0.355769 |
colA_ps3 | DDB_G0279833 | putative pseudogene very small fragment similar to the large colossin A gene | DDB0232430 | CDS | 2605850 | 210 | + | 0.27619 |
colA_ps4 | DDB_G0281591 | putative pseudogene very small fragment similar to the large colossin A gene | DDB0232430 | CDS | 4683631 | 123 | + | 0.357724 |
colA_ps5 | DDB_G0291594 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232433 | CDS | 587234 | 171 | - | 0.321637 |
colA_ps6 | DDB_G0293024 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232433 | CDS | 2342348 | 210 | - | 0.361905 |
colA_ps7 | DDB_G0348674 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232429 | CDS | 400170 | 1104 | - | 0.315217 |
colA_ps8 | DDB_G0272915 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232429 | CDS | 1915268 | 276 | + | 0.351449 |
colA_ps9 | DDB_G0277587 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232429 | CDS | 8233577 | 249 | - | 0.349398 |
colB | DDB_G0274221 | DDB0232429 | CDS | 4737491 | 11292 | + | 0.309245 | |
colC | DDB_G0281507 | DDB0232430 | CDS | 4643635 | 2946 | + | 0.341819 | |
colD | DDB_G0284983 | DDB0232431 | CDS | 2752867 | 2778 | + | 0.311375 | |
comA | DDB_G0289599 | connects the actin cytoskeleton to the Golgi apparatus bundles actin filaments which is inhibited by mannose | DDB0232432 | CDS | 3003747 | 558 | - | 0.370968 |
comB | DDB_G0281825 | DDB0232430 | CDS | 5112758 | 6324 | - | 0.278937 | |
comC | DDB_G0271692 | similar to Mus musculus MEGF11 PROTEIN (KIAA1781) contains 14 EGF domains | DDB0232429 | CDS | 758362 | 4506 | - | 0.282512 |
comD | DDB_G0283345 | similar to drug resistance transporters contains 14 transmembrane domains | DDB0232431 | CDS | 539820 | 3528 | + | 0.291667 |
comE | DDB_G0281571 | DDB0232430 | CDS | 4677792 | 5121 | - | 0.220465 | |
comF-1 | DDB_G0273257 | REMI mutant fails to aggregate contains a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 2775403 | 3321 | + | 0.298705 |
comF-2 | DDB_G0273669 | contains a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 3252529 | 3321 | - | 0.298705 |
comG | DDB_G0292270 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232433 | CDS | 1403334 | 1413 | + | 0.339703 |
comH | DDB_G0280547 | isolated in a screen for communication mutants similar to Emericella nidulans NsdD has 20 amino acids between the two CX2C motifs | DDB0232430 | CDS | 3604056 | 396 | + | 0.444444 |
commd1 | DDB_G0292074 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232433 | CDS | 1155156 | 564 | - | 0.210993 |
commd10 | DDB_G0275249 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232429 | CDS | 5027832 | 636 | - | 0.212264 |
commd2 | DDB_G0284879 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232431 | CDS | 2578442 | 603 | - | 0.220564 |
commd3 | DDB_G0283795 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232431 | CDS | 1117216 | 588 | - | 0.231293 |
commd4 | DDB_G0277089 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232429 | CDS | 7487396 | 534 | - | 0.243446 |
commd5 | DDB_G0274791 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232429 | CDS | 3853864 | 618 | - | 0.254045 |
commd6 | DDB_G0286077 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232431 | CDS | 4032914 | 231 | + | 0.25974 |
commd7 | DDB_G0275055 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232429 | CDS | 5070972 | 630 | + | 0.228571 |
commd8 | DDB_G0292688 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232433 | CDS | 1952596 | 618 | + | 0.205502 |
copA | DDB_G0267982 | contains five WD40 repeats alpha subunit of the coatomer complex essential for the secretory pathway | DDB0232428 | CDS | 1232234 | 3666 | + | 0.331969 |
copB | DDB_G0284735 | beta subunit of the coatomer complex essential for the secretory pathway colocalizes with comitin at the Golgi | DDB0232431 | CDS | 2394561 | 2739 | + | 0.316174 |
copB2 | DDB_G0278285 | contains six WD40 repeats beta prime subunit of the coatomer complex essential for the secretory pathway | DDB0232430 | CDS | 618891 | 3018 | - | 0.333996 |
copD | DDB_G0268702 | delta subunit of the coatomer complex involved in intracellular protein transport ortholog of human ARCN1 (COPD) | DDB0232428 | CDS | 1941102 | 1623 | + | 0.311152 |
copE | DDB_G0267950 | DDB0232428 | CDS | 1172814 | 903 | + | 0.272425 | |
copG | DDB_G0289371 | DDB0232432 | CDS | 2724036 | 2697 | + | 0.309974 | |
copZa | DDB_G0289523 | zeta subunit of the coatomer complex essential for the secretory pathway there is another gene encoding a zeta subunit | DDB0232432 | CDS | 2913451 | 528 | - | 0.242424 |
copZb | DDB_G0293086 | zeta subunit of the coatomer complex involved in intracellular protein transport there is another gene encoding a zeta subunit | DDB0232433 | CDS | 2460151 | 537 | + | 0.266294 |
coq1 | DDB_G0280293 | adds prenyl units to all-trans-polyprenyl diphosphate similar to S. cerevisiae COQ1 which catalyzes the first step in ubiquinone (coenzyme Q) biosynthesis | DDB0232430 | CDS | 3214568 | 1371 | + | 0.278629 |
coq10-1 | DDB_G0273089 | ortholog of the conserved COQ10 a Coenzyme Q (ubiquinone) binding protein in S. cerevisiae there is a second copy of this gene | DDB0232429 | CDS | 2604150 | 618 | - | 0.257282 |
coq10-2 | DDB_G0273803 | ortholog of the conserved COQ10 a Coenzyme Q (ubiquinone) binding protein in S. cerevisiae there is a second copy of this gene | DDB0232429 | CDS | 3426934 | 618 | + | 0.257282 |
coq2 | DDB_G0281241 | catalyzes the reaction solanesyl diphosphate 4-hydroxybenzoate diphosphate nonaprenyl-4-hydroxybenzoate in ubiquinone biosynthesis | DDB0232430 | CDS | 4263598 | 1392 | + | 0.239224 |
coq3 | DDB_G0279037 | similar to S. cevevisiae and R. norvegicus coq3 which catalyze two O-methylation steps in ubiquinone biosynthesis | DDB0232430 | CDS | 1539737 | 966 | - | 0.233954 |
coq4 | DDB_G0292620 | similar to S. cerevisiae COQ4 a protein of unknown function required for ubiquinone biosynthesis | DDB0232433 | CDS | 1849018 | 861 | + | 0.269454 |
coq5 | DDB_G0280237 | S-adenosyl-L-methionine (SAM)-dependent methyltransferase methylates quinones: in E. coli: demethylmenaquinone and 2-octaprenyl-6-methoxy-14-benzoquinone and in S. cerevisiae: 2-hexaprenyl-6-methoxy-14-benzoquinone the substrates of this enzyme in Dictyostelium are not known. | DDB0232430 | CDS | 3148507 | 945 | + | 0.286772 |
coq6 | DDB_G0291440 | similar to S. cerevisiae COQ6 a putative flavin-dependent monooxygenase involved in ubiquinone (Coenzyme Q) biosynthesis | DDB0232433 | CDS | 308878 | 1488 | + | 0.252016 |
coq7 | DDB_G0280475 | ortholog of the conserved COQ7 a protein which in S. cerevisiae is required for ubiquinone (coenzyme Q) biosynthesis | DDB0232430 | CDS | 3414983 | 654 | - | 0.313456 |
coq9 | DDB_G0274457 | ortholog of the conserved COQ9 a protein which in S. cerevisiae is required for ubiquinone (coenzyme Q) biosynthesis | DDB0232429 | CDS | 4525163 | 924 | - | 0.243506 |
corA | DDB_G0267382 | actin binding protein regulating actin nucleation involved in cytokinesis and cell motility | DDB0232428 | CDS | 943374 | 1338 | - | 0.400598 |
corB | DDB_G0269388 | ortholog of human coronin-7 (CORO7) long protein corresponding to two coronin equivalents regulates F-actin depolymerization and is thus involved in substrate adhesion phagocytosis and cell motility | DDB0232428 | CDS | 2678066 | 2889 | + | 0.32918 |
cosA | DDB_G0272861 | belongs to the costars family similar to the C terminal region of mammalian striated muscle activator of Rho signaling | DDB0232429 | CDS | 2071499 | 249 | - | 0.349398 |
cotA | DDB_G0276941 | DDB0232429 | CDS | 7449284 | 1803 | + | 0.415973 | |
cotB | DDB_G0276761 | DDB0232429 | CDS | 7194376 | 1614 | + | 0.384758 | |
cotC | DDB_G0277141 | DDB0232429 | CDS | 7902745 | 1275 | - | 0.364706 | |
cotD | DDB_G0283149 | DDB0232431 | CDS | 411746 | 1668 | + | 0.413669 | |
cotE | DDB_G0277903 | contains cysteine-rich and mucin-like repeats contains a signal peptide such that the first 17 amino acids are cleaved from the mature protein expressed in late culmination | DDB0232430 | CDS | 412650 | 1395 | + | 0.417204 |
cox10 | DDB_G0288169 | ortholog of COX10 which catalyzes the first step in the conversion of protoheme to the heme A prosthetic group required for cytochrome c oxidase activity contains seven transmembrane domains | DDB0232432 | CDS | 1175200 | 1350 | - | 0.302222 |
cox11 | DDB_G0289353 | ortholog of COX11 the mitochondrial inner membrane protein required for delivering copper to subunit 1 of cytochrome c oxidase. | DDB0232432 | CDS | 2677137 | 939 | + | 0.27263 |
cox17 | DDB_G0288831 | DDB0232432 | CDS | 2045007 | 183 | - | 0.338798 | |
cox19 | DDB_G0288903 | DDB0232432 | CDS | 2105412 | 321 | + | 0.292835 | |
coxA | DDB_G0281549 | ortholog of COX15 required for the hydroxylation of heme O to form heme A a component of cytochrome c oxidase | DDB0232430 | CDS | 4977091 | 1449 | - | 0.31539 |
cpiA | DDB_G0291834 | similar to animal and plant cystatin A1 member of the stefin family of cysteine protease inhibitors | DDB0232433 | CDS | 838074 | 285 | + | 0.4 |
cpiB | DDB_G0280439 | similar to animal and plant cystatin A2 member of the stefin family of cysteine protease inhibitors | DDB0232430 | CDS | 3355162 | 288 | - | 0.291667 |
cpiC | DDB_G0277001 | similar to animal and plant cystatin A3 member of the stefin cystatin family of cysteine protease inhibitors | DDB0232429 | CDS | 7261455 | 282 | - | 0.304965 |
cplA | DDB_G0269200 | DDB0232428 | CDS | 4755270 | 1950 | - | 0.353846 | |
cpnA | DDB_G0293008 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232433 | CDS | 2395700 | 1803 | + | 0.321131 |
cpnB-1 | DDB_G0272875 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain there is a second copy of this gene | DDB0232429 | CDS | 2314701 | 1596 | - | 0.296366 |
cpnB-2 | DDB_G0274051 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain there is a second copy of this gene | DDB0232429 | CDS | 3715266 | 1596 | + | 0.296366 |
cpnC | DDB_G0284791 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232431 | CDS | 2486260 | 1620 | - | 0.296914 |
cpnD | DDB_G0267688 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232428 | CDS | 578409 | 1593 | - | 0.299435 |
cpnE | DDB_G0290529 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232432 | CDS | 4217898 | 1740 | - | 0.275862 |
cpnF | DDB_G0291498 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232433 | CDS | 437512 | 1653 | - | 0.255898 |
cprA | DDB_G0290957 | DDB0232432 | CDS | 4812963 | 1032 | + | 0.312984 | |
cprB | DDB_G0279799 | DDB0232430 | CDS | 2569081 | 1131 | - | 0.322723 | |
cprC | DDB_G0283867 | DDB0232431 | CDS | 1092858 | 1014 | + | 0.302761 | |
cprD | DDB_G0278721 | DDB0232430 | CDS | 1179274 | 1329 | - | 0.392024 | |
cprE | DDB_G0272815 | DDB0232429 | CDS | 2212329 | 1035 | - | 0.357488 | |
cprF | DDB_G0279185 | DDB0232430 | CDS | 1757140 | 1305 | - | 0.387739 | |
cprG | DDB_G0279187 | DDB0232430 | CDS | 1740048 | 1383 | + | 0.42227 | |
cprH | DDB_G0278401 | belongs to the peptidase family C1 sub-family C1A (papain family clan CA) repressed after Legionella pneumophila infection | DDB0232430 | CDS | 822687 | 1014 | + | 0.309665 |
cpras1 | DDB_G0277381 | DDB0232429 | CDS | 7946446 | 2529 | - | 0.316726 | |
cpras2 | DDB_G0293376 | contains a circularly permuted GTPase domain with the conserved motifs G1-G2 lying downstream of the G3-G4-G5 motifs large protein of unknown function whose domain composition is not conserved a closely related ortholog is found in D. purpureum | DDB0232433 | CDS | 2805934 | 11802 | - | 0.295543 |
cpsf1 | DDB_G0281585 | ortholog of the human CPSF1 and yeast YTH1 the 160 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs human CPSF1 involved in the RNA recognition step of the polyadenylation reaction | DDB0232430 | CDS | 4665204 | 4887 | - | 0.252507 |
cpsf2 | DDB_G0270392 | ortholog of the human CPSF2 and yeast CFT2 the 100 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs | DDB0232428 | CDS | 4749183 | 2355 | + | 0.292144 |
cpsf3 | DDB_G0274799 | ortholog of the human CPSF3 and yeast YSH1 the 73 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs | DDB0232429 | CDS | 3904161 | 2325 | - | 0.308387 |
cpsf4 | DDB_G0270148 | ortholog of the human CPSF4 and yeast YTH1 the 30 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs human CPSF4 binds RNA polymers with a preference for poly(U) | DDB0232428 | CDS | 4311820 | 1119 | + | 0.324397 |
crip | DDB_G0270314 | ortholog of human CRIP1 contains 1 zinc-binding LIM domain LIM domains are found in proteins with differing functions including gene expression and cytoskeleton organisation and development | DDB0232428 | CDS | 4620271 | 264 | + | 0.382576 |
crlA | DDB_G0280983 | involved in negative regulation of growth belongs to the serpentineG-protein coupled receptor family | DDB0232430 | CDS | 4253816 | 1110 | - | 0.234234 |
crlB | DDB_G0289395 | belongs to the serpentineG-protein coupled receptor family | DDB0232432 | CDS | 2737271 | 1329 | + | 0.243792 |
crlC | DDB_G0283619 | belongs to the serpentineG-protein coupled receptor family | DDB0232431 | CDS | 927333 | 1086 | - | 0.281768 |
crlD | DDB_G0283579 | similar to serpentineG-protein coupled receptors contains 7 putative transmembrane domains | DDB0232431 | CDS | 861957 | 1413 | + | 0.194621 |
crlE | DDB_G0286301 | similar to serpentineG-protein coupled receptors contains 7 putative transmembrane domains | DDB0232431 | CDS | 4326009 | 993 | + | 0.2286 |
crlF | DDB_G0290185 | similar to serpentineG-protein coupled receptors contains 7 putative transmembrane domains | DDB0232432 | CDS | 3754060 | 957 | - | 0.267503 |
crlG | DDB_G0279599 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a putative signal peptide | DDB0232430 | CDS | 2212555 | 1548 | + | 0.19832 |
crop | DDB_G0278799 | DDB0232430 | CDS | 1204493 | 1083 | - | 0.304709 | |
crsA | DDB_G0282607 | catalyzes the reaction acyl-CoA sphingosine CoA N-acylsphingosine in ceramide synthesis ortholog of S. cerevisiae LAG1 and H. sapiens TRH1 | DDB0232430 | CDS | 5996864 | 1026 | - | 0.273879 |
crtA | DDB_G0283539 | Ca2-binding protein with chaperone activity in the endoplasmic reticulum plays a role in phagocytosis | DDB0232431 | CDS | 820858 | 1275 | - | 0.374902 |
crtf | DDB_G0278077 | DDB0232430 | CDS | 235235 | 2631 | - | 0.298366 | |
crtp1 | DDB_G0276943 | similar to Plasmodium falciparum CRT which confers resistance to chloroquine localizes to intracellular vesicle membranes contains 10 predicted transmembrane domains | DDB0232429 | CDS | 7516807 | 1422 | + | 0.322082 |
crtp2 | DDB_G0277321 | similar to Plasmodium falciparum CRT which confers resistance to chloroquine contains 10 predicted transmembrane domains | DDB0232429 | CDS | 7694600 | 1455 | + | 0.272165 |
crtp3 | DDB_G0270204 | similar to Plasmodium falciparum CRT which confers resistance to chloroquine contains 10 predicted transmembrane domains | DDB0232428 | CDS | 4401703 | 1437 | + | 0.281141 |
cryS | DDB_G0285419 | DDB0232431 | CDS | 3375645 | 1653 | - | 0.329704 | |
csaA | DDB_G0289073 | DDB0232432 | CDS | 2342795 | 1545 | - | 0.350809 | |
csbA | DDB_G0272833 | DDB0232429 | CDS | 2107219 | 309 | - | 0.317152 | |
csbB | DDB_G0272562 | DDB0232429 | CDS | 2105702 | 312 | - | 0.298077 | |
csbC | DDB_G0272756 | DDB0232429 | CDS | 2103930 | 306 | - | 0.316993 | |
csbD_ps | DDB_G0273057 | putative pseudogene similar to csbA csbB and csbC | DDB0232429 | CDS | 2187983 | 421 | + | 0.270784 |
cshA | DDB_G0267426 | DDB0232428 | CDS | 1569279 | 1479 | - | 0.335362 | |
csn1 | DDB_G0283587 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232431 | CDS | 822737 | 1377 | - | 0.284677 |
csn2 | DDB_G0289361 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232432 | CDS | 2705143 | 1350 | + | 0.28 |
csn3 | DDB_G0291848 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232433 | CDS | 766772 | 1257 | - | 0.287192 |
csn4 | DDB_G0293844 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232433 | CDS | 3378445 | 1182 | + | 0.302876 |
csn5 | DDB_G0284597 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232431 | CDS | 2205667 | 999 | - | 0.304304 |
csn6 | DDB_G0293180 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232433 | CDS | 2499532 | 930 | + | 0.283871 |
csn7 | DDB_G0271282 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232429 | CDS | 160979 | 780 | - | 0.275641 |
csn8 | DDB_G0275471 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232429 | CDS | 6094205 | 591 | - | 0.265651 |
csnk2b | DDB_G0284601 | ortholog of the CK2 beta chain the regulatory subunit of the ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | DDB0232431 | CDS | 2209637 | 807 | - | 0.281289 |
cspA | DDB_G0277835 | DDB0232430 | CDS | 604573 | 1056 | + | 0.305871 | |
cspB | DDB_G0292808 | DDB0232433 | CDS | 2157251 | 177 | - | 0.38983 | |
cstf1 | DDB_G0278769 | component of the CSTF complex which in mammalian is required for polyadenylation and 3'-end cleavage of pre-mRNAs | DDB0232430 | CDS | 1141749 | 1521 | + | 0.302433 |
cstf2 | DDB_G0280529 | component of the CSTF complex which in mammalian is required for polyadenylation and 3'-end cleavage of pre-mRNAs | DDB0232430 | CDS | 3461453 | 1626 | + | 0.305043 |
cstf3 | DDB_G0286645 | component of the CSTF complex which in mammalian is required for polyadenylation and 3'-end cleavage of pre-mRNAs | DDB0232431 | CDS | 4781245 | 3198 | + | 0.329894 |
ctaA | DDB_G0293004 | DDB0232433 | CDS | 2385585 | 3897 | - | 0.308442 | |
ctbsA | DDB_G0274233 | very similar to H. sapiens di-N-acetylchitobiase (CBTS) a hydrolase involved in the degradation of asparagine-linked glycoproteins contains a putative N-terminal signal sequence | DDB0232429 | CDS | 4699494 | 1158 | + | 0.310881 |
ctbsB | DDB_G0276795 | similar to H. sapiens di-N-acetylchitobiase (CBTS) a hydrolase involved in the degradation of asparagine-linked glycoproteins contains a putative N-terminal signal sequence | DDB0232429 | CDS | 7316822 | 1122 | + | 0.294118 |
ctdspl2 | DDB_G0290365 | DDB0232432 | CDS | 3881786 | 1704 | + | 0.297535 | |
ctnA | DDB_G0274597 | component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) | DDB0232429 | CDS | 3807703 | 777 | + | 0.396396 |
ctnB | DDB_G0279797 | DDB0232430 | CDS | 2623695 | 765 | - | 0.396078 | |
ctnC | DDB_G0276479 | DDB0232429 | CDS | 6927901 | 669 | + | 0.313901 | |
ctnnA | DDB_G0285939 | cateninvinculin family protein binds to aardvark the Dictyostelium beta-catenin related protein required for the formation of a polarized epithelium at the culminant tip and thus for stalk formation during culmination | DDB0232431 | CDS | 3870921 | 2529 | + | 0.356267 |
ctnnbl1 | DDB_G0292778 | DDB0232433 | CDS | 2017543 | 1578 | + | 0.225602 | |
ctns | DDB_G0279445 | ortholog of cytonisin (CTNS) in human mutations in the gene causes cystinosis a disease resulting from defective lysosomal transport of cystine the classical nephropathic form is characterized by renal failure at age 10 contains 7 transmembrane domains | DDB0232430 | CDS | 2059799 | 855 | + | 0.239766 |
ctps | DDB_G0280567 | catalyzes the reaction L-glutamine Hsub2subO UTP ATP - CTP phosphate ADP L-glutamate in de novo biosynthesis of pyrimidine ribonucleotides | DDB0232430 | CDS | 3510967 | 1710 | - | 0.350292 |
ctr9 | DDB_G0277841 | component of the conserved Paf1 complex a multifunctional complex involved in histone methylation and plays a role in RNA elongation and processing REMI mutant forms aberrant fruiting bodies see | DDB0232430 | CDS | 746082 | 3321 | + | 0.308341 |
ctrA | DDB_G0291227 | similar to mammalian SLC7A1-4 (solute carrier family 7 members 1 to 4) multi-pass membrane protein contains 15 predicted transmembrane domains | DDB0232433 | CDS | 403181 | 1689 | - | 0.335702 |
ctrB | DDB_G0279983 | similar to mammalian SLC7A1-4 (solute carrier family 7 members 1 to 4) multi-pass membrane protein contains 14 predicted transmembrane domains | DDB0232430 | CDS | 2813758 | 2301 | + | 0.308127 |
ctrC | DDB_G0291201 | similar to mammalian SLC7A1-4 (solute carrier family 7 members 1 to 4) multi-pass membrane protein contains 15 predicted transmembrane domains | DDB0232432 | CDS | 5112561 | 1641 | - | 0.343693 |
ctsB | DDB_G0283921 | member of the papain cysteine protease family which has a wide range of specificities | DDB0232431 | CDS | 1297288 | 936 | + | 0.353632 |
ctsD | DDB_G0279411 | DDB0232430 | CDS | 2104523 | 1152 | + | 0.390625 | |
ctsZ | DDB_G0283401 | member of the papain cysteine protease family which has a wide range of specificities | DDB0232431 | CDS | 613897 | 891 | + | 0.367003 |
ctu1 | DDB_G0282921 | ortholog of S. pombe ctu1 (cytosolic thiouridylase subunit 1) with ctu2 required for thiolation of the uridine at the wobble position of Lys(UUU) and Glu(UUC) tRNAs | DDB0232431 | CDS | 190346 | 1083 | - | 0.272391 |
ctu2 | DDB_G0268714 | ortholog of S. pombe ctu2 (cytosolic thiouridylase subunit 2) with ctu1 required for thiolation of the uridine at the wobble position of Lys(UUU) and Glu(UUC) tRNAs | DDB0232428 | CDS | 1986771 | 1572 | - | 0.246819 |
ctxA | DDB_G0289483 | member of the alpha-actininspectrin superfamily dimerizes with cortexillin II involved in cytokinesis and development and associates with the actin cytoskeleton | DDB0232432 | CDS | 2847194 | 1335 | - | 0.347566 |
ctxB | DDB_G0276893 | member of the alpha-actininspectrin superfamily dimerizes with cortexillin I involved in cytokinesis and development and associates with the actin cytoskeleton | DDB0232429 | CDS | 7304770 | 1326 | - | 0.3454 |
cudA | DDB_G0284465 | required for culmination expressed in prespore and pstA cells exists as a homodimer | DDB0232431 | CDS | 2091815 | 2409 | - | 0.275633 |
culA | DDB_G0291972 | very similar to mammalian cullin 1 (CUL1) involved in ubiquitin-mediated protein degradation which in Dictyostelium controls PKA function and regulates cell differentiation | DDB0232433 | CDS | 977829 | 2313 | - | 0.285776 |
culB | DDB_G0267384 | similar to mammalian cullin 1 and 2 (CUL1 CUL2) involved in ubiquitin-mediated protein degradation regulates prestalk cell differentiation in Dictyostelium | DDB0232428 | CDS | 551012 | 2316 | - | 0.255613 |
culC | DDB_G0284903 | very similar to mammalian cullin 3 (CUL3) acts as scaffold for ubiquitin ligases (E3) involved in ubiquitin-mediated protein degradation | DDB0232431 | CDS | 2621558 | 2310 | - | 0.290476 |
culD | DDB_G0292794 | very similar to mammalian cullin 4 (CUL4A and CUL4B) acts as scaffold for ubiquitin ligases (E3) involved in ubiquitin-mediated protein degradation | DDB0232433 | CDS | 2047275 | 2409 | - | 0.28352 |
culE | DDB_G0278991 | similar to mammalian cullin 1 2 and 5 (CUL1 CUL2 CUL5) acts as scaffold for ubiquitin ligases (E3) involved in ubiquitin-mediated protein degradation | DDB0232430 | CDS | 1485914 | 2253 | - | 0.316467 |
cupA | DDB_G0267466 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells downstream ORF is potentially part of this gene | DDB0232428 | CDS | 1122624 | 1272 | + | 0.290094 |
cupB | DDB_G0289815 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells cells overexpressing antisense mRNA fail to aggregate | DDB0232432 | CDS | 3313764 | 2310 | + | 0.3 |
cupC | DDB_G0289283 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells | DDB0232432 | CDS | 2612450 | 2310 | - | 0.305195 |
cupD | DDB_G0293536 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells | DDB0232433 | CDS | 3204161 | 1905 | - | 0.303412 |
cupF | DDB_G0289813 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells | DDB0232432 | CDS | 3317807 | 2310 | + | 0.303463 |
cupG | DDB_G0289883 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells | DDB0232432 | CDS | 3463581 | 2307 | - | 0.302557 |
cupH | DDB_G0290563 | DDB0232432 | CDS | 4277976 | 2307 | + | 0.303424 | |
cupI | DDB_G0272242 | DDB0232429 | CDS | 1729711 | 2076 | - | 0.319364 | |
cupJ | DDB_G0277959 | DDB0232430 | CDS | 64771 | 1968 | + | 0.287602 | |
cutA | DDB_G0283621 | DDB0232431 | CDS | 908845 | 1551 | + | 0.359768 | |
cutc | DDB_G0287539 | DDB0232432 | CDS | 396188 | 843 | - | 0.269276 | |
cwc15-1 | DDB_G0273383 | ortholog of S. pombe Cwf15 and S. cerevisiae Cwc15 thought to be non-essential components of an mRNA splicing complex there is a second copy of this gene | DDB0232429 | CDS | 2839698 | 807 | - | 0.266419 |
cwc15-2 | DDB_G0273631 | ortholog of S. pombe Cwf15 and S. cerevisiae Cwc15 thought to be non-essential components of an mRNA splicing complex there is a second copy of this gene | DDB0232429 | CDS | 3191201 | 807 | + | 0.268897 |
cwc2 | DDB_G0284563 | similar to S. pombe and S. cerevisiae CWC2 which are involved in pre-mRNA splicing | DDB0232431 | CDS | 2134830 | 1587 | - | 0.308129 |
cxdA | DDB_G0281393 | DDB0232430 | CDS | 4421049 | 447 | + | 0.355705 | |
cxeA | DDB_G0269118 | DDB0232428 | CDS | 3937103 | 363 | + | 0.336088 | |
cxfA | DDB_G0282097 | DDB0232430 | CDS | 5368452 | 282 | - | 0.375887 | |
cxgE | DDB_G0277837 | DDB0232430 | CDS | 85494 | 162 | - | 0.358025 | |
cxgS | DDB_G0277839 | DDB0232430 | CDS | 84465 | 168 | - | 0.327381 | |
cyb5A | DDB_G0276033 | cytochrome b5 is a membrane bound hemoprotein that functions as an electron carrier for several membrane bound oxygenases contains a single C-terminal transmembrane domain | DDB0232429 | CDS | 6550267 | 402 | + | 0.355721 |
cyb5B | DDB_G0277079 | cytochrome b5 is a membrane bound hemoprotein that functions as an electron carrier for several membrane bound oxygenases contains a single C-terminal transmembrane domain | DDB0232429 | CDS | 7471494 | 450 | - | 0.3 |
cyb5C | DDB_G0278753 | cytochrome b5 proteins are membrane bound hemoproteins that function as an electron carrier for several membrane bound oxygenases however this protein seems truncated at the C-terminus and does not contain any transmembrane domain | DDB0232430 | CDS | 1118934 | 276 | - | 0.275362 |
cyb5r1 | DDB_G0285399 | catalyzes the reaction NADH 2 ferricytochrome b5 NAD() H() 2 ferrocytochrome involved in desaturation and elongation of fatty acids cholesterol biosynthesis and drug metabolism | DDB0232431 | CDS | 3151723 | 861 | + | 0.341463 |
cybA | DDB_G0267460 | homolog of the mammalian flavocytochrome B small subunit p22phox essential for spore formation | DDB0232428 | CDS | 364761 | 357 | - | 0.327731 |
cyc1 | DDB_G0292594 | ortholog of the heme-containing component of the cytochrome b-c1 complex (CYC1) which accepts electrons from Rieske protein and transfers electrons to cytochrome c in the mitochondrial respiratory chain | DDB0232433 | CDS | 1821453 | 828 | + | 0.390097 |
cycA | DDB_G0279085 | weakly similar to cyclin A predicted to interact with the cyclin-dependent kinase CDK12 ( | DDB0232430 | CDS | 1598641 | 1767 | + | 0.254669 |
cycB | DDB_G0275493 | similar to metazoan cyclin B predicted to interact with the cyclin-dependent kinase CDK12 ( | DDB0232429 | CDS | 6000211 | 1311 | - | 0.363844 |
cycC | DDB_G0274139 | similar to metazoan cyclin C predicted to interact with cyclin-dependent kinase | DDB0232429 | CDS | 4921649 | 768 | + | 0.247396 |
cycD | DDB_G0277439 | similar to metazoan and plant type-cyclins of the cell cycle group (G1 subgroup) highest similarity to algal cyclin D predicted to interact with the cyclin-dependent kinase CDK12 ( | DDB0232429 | CDS | 8066558 | 2085 | + | 0.242686 |
cycH | DDB_G0268668 | similar to metazoan cyclin H predicted to interact with cyclin-dependent kinase | DDB0232428 | CDS | 1891354 | 861 | - | 0.190476 |
cycK | DDB_G0286617 | similar to metazoan cyclin K predicted to interact with the cyclin-dependent kinase | DDB0232431 | CDS | 4722525 | 1218 | - | 0.297209 |
cycL | DDB_G0285553 | similar to metazoan and higher plants cyclin Lania-6 predicted to interact with | DDB0232431 | CDS | 3372094 | 822 | - | 0.284672 |
cyp508A1-1 | DDB_G0273045 | there is a second copy of this gene | DDB0232429 | CDS | 2451402 | 1455 | - | 0.265292 |
cyp508A1-2 | DDB_G0273943 | there is a second copy of this gene | DDB0232429 | CDS | 3578372 | 1455 | + | 0.265292 |
cyp508A2-1 | DDB_G0272604 | there is a second copy of this gene | DDB0232429 | CDS | 2449037 | 1482 | - | 0.27193 |
cyp508A2-2 | DDB_G0273945 | there is a second copy of this gene | DDB0232429 | CDS | 3580950 | 1482 | + | 0.27193 |
cyp508A3-1 | DDB_G0273047 | there is a second copy of this gene | DDB0232429 | CDS | 2454253 | 1440 | - | 0.23125 |
cyp508A3-2 | DDB_G0273941 | there is a second copy of this gene | DDB0232429 | CDS | 3575667 | 1440 | + | 0.23125 |
cyp508A4 | DDB_G0284535 | DDB0232431 | CDS | 2137636 | 1506 | + | 0.288181 | |
cyp508B1 | DDB_G0282419 | DDB0232430 | CDS | 5743012 | 1455 | - | 0.258419 | |
cyp508B2_ps | DDB_G0293080 | putative pseudogene related to the cytochrome P450 family | DDB0232433 | CDS | 2448065 | 1254 | - | 0.186603 |
cyp508C1 | DDB_G0292792 | DDB0232433 | CDS | 2044931 | 1488 | - | 0.22043 | |
cyp508D1 | DDB_G0292790 | DDB0232433 | CDS | 2042922 | 1449 | + | 0.26432 | |
cyp508E1_ps | DDB_G0270904 | putative pseudogene related to the cytochrome P450 family | DDB0232428 | CDS | 3249734 | 591 | - | 0.22335 |
cyp51 | DDB_G0279403 | E-class P450 group IV catalyzes the first step following cyclization in sterol biosynthesis most prevalent cytochrome P450 across species | DDB0232430 | CDS | 1970490 | 1401 | + | 0.363312 |
cyp513A1 | DDB_G0282183 | DDB0232430 | CDS | 5453620 | 1530 | - | 0.255556 | |
cyp513A2_ps | DDB_G0290981 | putative pseudogene related to the cytochrome P450 family | DDB0232432 | CDS | 4843316 | 924 | + | 0.239177 |
cyp513A3 | DDB_G0270354 | DDB0232428 | CDS | 4697435 | 1479 | + | 0.254226 | |
cyp513B1 | DDB_G0287087 | DDB0232431 | CDS | 5309664 | 1464 | - | 0.262295 | |
cyp513C1 | DDB_G0291105 | DDB0232432 | CDS | 5007182 | 1488 | - | 0.280914 | |
cyp513D1 | DDB_G0279763 | DDB0232430 | CDS | 2528127 | 1560 | - | 0.241667 | |
cyp513E1 | DDB_G0282353 | DDB0232430 | CDS | 5664216 | 1515 | - | 0.227063 | |
cyp513E2_ps | DDB_G0282347 | putative pseudogene related to the cytochrome P450 family | DDB0232430 | CDS | 5668014 | 1308 | - | 0.191132 |
cyp513E3_ps | DDB_G0282349 | putative pseudogene related to the cytochrome P450 family | DDB0232430 | CDS | 5669895 | 672 | - | 0.16369 |
cyp513F1 | DDB_G0278679 | DDB0232430 | CDS | 805261 | 1515 | - | 0.214521 | |
cyp513G1_ps | DDB_G0279631 | putative pseudogene related to the cytochrome P450 family | DDB0232430 | CDS | 2338838 | 2052 | - | 0.216374 |
cyp514A1 | DDB_G0290743 | DDB0232432 | CDS | 4534228 | 1728 | - | 0.24537 | |
cyp514A1_ps | DDB_G0288119 | similar to parts of CYP514A1 a cytochrome P450 family protein | DDB0232432 | CDS | 1068215 | 423 | - | 0.236407 |
cyp514A2 | DDB_G0294561 | DDB0232432 | CDS | 3895673 | 1503 | + | 0.245509 | |
cyp514A4 | DDB_G0290707 | DDB0232432 | CDS | 4469976 | 1509 | + | 0.241219 | |
cyp515A1 | DDB_G0272704 | DDB0232429 | CDS | 1915942 | 1485 | - | 0.22963 | |
cyp515A2_ps | DDB_G0272959 | putative pseudogene related to the cytochrome P450 family | DDB0232429 | CDS | 1913151 | 756 | - | 0.244709 |
cyp515B1 | DDB_G0282283 | DDB0232430 | CDS | 5497711 | 1482 | + | 0.250337 | |
cyp516A1 | DDB_G0292168 | DDB0232433 | CDS | 1087783 | 1464 | + | 0.267076 | |
cyp516B1 | DDB_G0271778 | DDB0232429 | CDS | 895254 | 1479 | + | 0.319811 | |
cyp517A1 | DDB_G0283929 | DDB0232431 | CDS | 1320998 | 1452 | + | 0.274793 | |
cyp517A2 | DDB_G0284647 | DDB0232431 | CDS | 2285672 | 1533 | - | 0.241357 | |
cyp517A3_ps | DDB_G0271224 | putative pseudogene related to the cytochrome P450 family | DDB0232429 | CDS | 264272 | 915 | - | 0.286339 |
cyp517A4 | DDB_G0283933 | DDB0232431 | CDS | 1331360 | 1452 | + | 0.270661 | |
cyp518A1 | DDB_G0277545 | DDB0232429 | CDS | 8037641 | 1485 | - | 0.243098 | |
cyp518A2_ps-1 | DDB_G0273349 | putative pseudogene related to the cytochrome P450 family there is a second copy of this gene | DDB0232429 | CDS | 2661937 | 216 | - | 0.268519 |
cyp518A2_ps-2 | DDB_G0273757 | putative pseudogene related to the cytochrome P450 family there is a second copy of this gene | DDB0232429 | CDS | 3369078 | 216 | + | 0.268519 |
cyp518B1 | DDB_G0275197 | DDB0232429 | CDS | 5201034 | 1473 | + | 0.228785 | |
cyp519A1 | DDB_G0274623 | DDB0232429 | CDS | 4728670 | 1593 | + | 0.273697 | |
cyp519B1 | DDB_G0284089 | DDB0232431 | CDS | 1554448 | 1530 | - | 0.241176 | |
cyp519C1 | DDB_G0272556 | DDB0232429 | CDS | 1842421 | 1575 | - | 0.229841 | |
cyp519C2_ps | DDB_G0280617 | putative pseudogene related to the cytochrome P450 family | DDB0232430 | CDS | 3573818 | 294 | - | 0.27551 |
cyp519D1 | DDB_G0291448 | DDB0232433 | CDS | 323966 | 1701 | - | 0.240447 | |
cyp519E1 | DDB_G0286419 | DDB0232431 | CDS | 4464134 | 1521 | - | 0.272847 | |
cyp519H1_ps | DDB_G0279031 | putative pseudogene related to the cytochrome P450 family | DDB0232430 | CDS | 1533206 | 930 | + | 0.266667 |
cyp520A1 | DDB_G0292496 | DDB0232433 | CDS | 1743792 | 1611 | + | 0.259466 | |
cyp520B1 | DDB_G0291702 | DDB0232433 | CDS | 657386 | 1446 | + | 0.239281 | |
cyp521A1 | DDB_G0293738 | DDB0232433 | CDS | 3236989 | 1476 | + | 0.250677 | |
cyp522A1 | DDB_G0282769 | DDB0232430 | CDS | 5859831 | 1470 | - | 0.257823 | |
cyp524A1 | DDB_G0269016 | DDB0232428 | CDS | 2256023 | 1599 | + | 0.372108 | |
cyp525A1 | DDB_G0272652 | DDB0232429 | CDS | 2253643 | 1806 | - | 0.183832 | |
cyp554A1 | DDB_G0284923 | DDB0232431 | CDS | 2649920 | 1509 | - | 0.222001 | |
cyp555A1 | DDB_G0286743 | DDB0232431 | CDS | 4916138 | 1455 | - | 0.187629 | |
cyp556A1 | DDB_G0284345 | DDB0232431 | CDS | 1862286 | 1974 | + | 0.238095 | |
cypB | DDB_G0269120 | DDB0232428 | CDS | 3371521 | 594 | - | 0.33165 | |
cypD | DDB_G0280401 | DDB0232430 | CDS | 3316821 | 525 | - | 0.321905 | |
cypE | DDB_G0269216 | cyclosporin A-sensitive peptidylprolyl cis-trans isomerase binds the SKIP ortholog snwA in a cyclosporin-independent manner | DDB0232428 | CDS | 3461467 | 471 | - | 0.295117 |
cyrA | DDB_G0281951 | similar to prestalk protein precursor contains three slime mold repeats and 4 EGF-like domains extracellular protein cleaved into a 45 and 40 kDa fragments found in the slime sheath interacts extracellularly with calmodulin the cyrA EGFL1 peptide regulates chemotactic cell motility | DDB0232430 | CDS | 5210687 | 1746 | - | 0.292669 |
cysA | DDB_G0269122 | catalyzes the reaction cystathionine Hsub2subO 2-oxobutanoate L-cysteine NHsub3sub | DDB0232428 | CDS | 2903199 | 1164 | - | 0.367698 |
cysB | DDB_G0267386 | catalyzes the reaction homocysteine L-serine Hsub2subO cystathionine | DDB0232428 | CDS | 1329298 | 1497 | + | 0.378758 |
cysK | DDB_G0292840 | catalyzes the reaction O-acetyl-L-serine Hsub2subS L-cysteine acetate | DDB0232433 | CDS | 2136817 | 1137 | + | 0.333333 |
cysS | DDB_G0287159 | catalyzes the reaction ATP L-cysteine tRNACys AMP diphosphate L-cysteinyl-tRNACys | DDB0232431 | CDS | 5412959 | 1983 | - | 0.328795 |
cytC | DDB_G0275537 | DDB0232429 | CDS | 5724705 | 342 | + | 0.380117 | |
d2hgdh | DDB_G0270500 | mitochondrial enzyme catalyzes the oxidation of D-2-hydroxyglutarate to alpha-ketoglutarate ortholog of the H. sapiens D2HGDH which when defect causes D-2-hydroxyglutaric aciduria a rare recessive neurometabolic disorder | DDB0232428 | CDS | 2682747 | 1587 | - | 0.289225 |
dafE | DDB_G0267388 | DDB0232428 | CDS | 286362 | 1545 | - | 0.256311 | |
dagA | DDB_G0285161 | DDB0232431 | CDS | 2973018 | 2097 | - | 0.314258 | |
dak | DDB_G0278191 | catalyzes the reaction ATP deoxyadenosine ADP dAMP | DDB0232430 | CDS | 426271 | 738 | + | 0.285908 |
darA | DDB_G0288771 | putative ortholog of the mammalian guanine nucleotide exchange factor smgGDS a GEF that acts on a broad spectrum of small GTPases (rap1 rac1 cdc42) in Dictyostelium darlin contains 11 armadillo-like repeats it binds to racE and racC but the GEF activity could not be detected using racE as a substrate the darA null mutant is aggregation defective when developed in buffer but the development is normal in the presence of bacteria | DDB0232432 | CDS | 1994269 | 2301 | - | 0.269013 |
dcc1 | DDB_G0271400 | similar to human DSCC1 and S. cerevisiae DCC1 involved in sister chromatid cohesion establishment | DDB0232429 | CDS | 227992 | 1131 | - | 0.241379 |
dcd1A | DDB_G0270296 | wealky similar to acid ceramidase which catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine | DDB0232428 | CDS | 4598954 | 1326 | + | 0.297888 |
dcd1B | DDB_G0292768 | wealky similar to acid ceramidase which catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine | DDB0232433 | CDS | 2039368 | 1503 | - | 0.293413 |
dcd2A | DDB_G0293538 | ceramidase bearing more similarity with neural and alkaline ceramidases however pH optimum of the enzyme is 3 | DDB0232433 | CDS | 3091013 | 2145 | + | 0.336597 |
dcd2B | DDB_G0268374 | DDB0232428 | CDS | 1007048 | 2157 | + | 0.325452 | |
dcd3A | DDB_G0288359 | catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine regulated by the MADS-box transcription factor SrfA during developmentbr bNomenclature conflictb: Do not confuse dcd3A (alkaline dihydroceramidase adcA) with adcA (arrestin domain-containing protein) | DDB0232432 | CDS | 1387850 | 867 | + | 0.310265 |
dcd3B | DDB_G0269574 | catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine | DDB0232428 | CDS | 3041058 | 858 | - | 0.311189 |
dclre1 | DDB_G0277755 | putative ortholog of yeast PSO2 gene required for double-strand break repair also related to the NHEJ DNA repair protein Artemis | DDB0232429 | CDS | 8451915 | 2763 | + | 0.247557 |
dcp2 | DDB_G0283315 | ortholog of the conserved mRNA-decapping enzyme 2 necessary for the degradation of mRNAs | DDB0232431 | CDS | 515744 | 1863 | + | 0.31723 |
dcp2_ps | DDB_G0283809 | putative pseudogene similar to | DDB0232431 | CDS | 1130346 | 258 | - | 0.325581 |
dcsA | DDB_G0269124 | CAZy family GT2 catalyzes the reaction UDP-glucose (14-beta-D-glucosyl)n UDP (14-beta-D-glucosyl)n1 | DDB0232428 | CDS | 3500588 | 3180 | - | 0.35912 |
dct | DDB_G0283767 | DDB0232431 | CDS | 1132285 | 1065 | + | 0.383099 | |
dcx | DDB_G0277115 | contains two doublecortin domains involved in microtubule stabilization and bundling functionally interacts with lis1 in cAMP signalling | DDB0232429 | CDS | 7567785 | 927 | - | 0.318231 |
ddcA | DDB_G0269856 | similar to diaminopimelate decarboxylase which catalyzes the reaction meso-26-diaminoheptanedioate L-lysine COsub2sub | DDB0232428 | CDS | 3743580 | 1266 | + | 0.267773 |
ddcB | DDB_G0276067 | similar to diaminopimelate decarboxylase which catalyzes the reaction meso-26-diaminoheptanedioate L-lysine COsub2sub | DDB0232429 | CDS | 6448691 | 1296 | + | 0.30787 |
ddi1 | DDB_G0288187 | conserved protein that in S. cerevisiae is a DNA damage-inducible v-SNARE binding protein | DDB0232432 | CDS | 1180046 | 1353 | - | 0.318551 |
ddiA | DDB_G0281293 | DDB0232430 | CDS | 4362245 | 672 | - | 0.352679 | |
ddiA_ps | DDB_G0278419 | putative pseudogene similar to the ribonuclease T2 | DDB0232430 | CDS | 863855 | 315 | + | 0.304762 |
ddj1 | DDB_G0280037 | DDB0232430 | CDS | 3103912 | 1236 | - | 0.394013 | |
ddo-1 | DDB_G0273783 | catalyzes the oxidation of neutral and basic D-amino acids into their corresponding keto acids there is a second copy of this gene | DDB0232429 | CDS | 3402431 | 1041 | + | 0.31316 |
ddo-2 | DDB_G0273291 | catalyzes the oxidation of neutral and basic D-amino acids into their corresponding keto acids there is a second copy of this gene | DDB0232429 | CDS | 2628315 | 1041 | - | 0.31316 |
dduA | DDB_G0282559 | downregulated in the uninfected | DDB0232430 | CDS | 5934889 | 1296 | - | 0.278549 |
dduB | DDB_G0271234 | downregulated in the uninfected | DDB0232429 | CDS | 252762 | 3606 | + | 0.267887 |
dduC | DDB_G0292604 | downregulated in the uninfected | DDB0232433 | CDS | 1828931 | 372 | + | 0.276882 |
dduD | DDB_G0278875 | contains a signal peptide member of a Dictyostelium protein family that includes DG1041 downregulated in the uninfected | DDB0232430 | CDS | 1323127 | 2934 | - | 0.296524 |
dduE | DDB_G0284357 | underexpressed in | DDB0232431 | CDS | 1881383 | 2076 | - | 0.276493 |
dduF | DDB_G0284549 | contains a predicted signal peptide (cleavage site not optimal) downregulated in the uninfected | DDB0232431 | CDS | 2024271 | 777 | + | 0.36036 |
ddx1 | DDB_G0269966 | ortholog of ATP-dependent RNA helicase DDX1 contains an SPRY domain which is of unknown function | DDB0232428 | CDS | 3941617 | 2298 | + | 0.302002 |
ddx10 | DDB_G0284017 | DDB0232431 | CDS | 1436851 | 2637 | + | 0.277209 | |
ddx17 | DDB_G0293168 | conserved RNA helicase very similar to mammalian DDX17 (p72) and DDX5 (p68) and yeast DBP2 | DDB0232433 | CDS | 2360817 | 2358 | - | 0.370229 |
ddx18 | DDB_G0282741 | DDB0232430 | CDS | 6230156 | 1809 | - | 0.334439 | |
ddx20 | DDB_G0277527 | ortholog of H. sapiens DDX20Gemin 3 a component of Cajal bodies (CBs) and Gems nuclear organelles responsible for spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis | DDB0232429 | CDS | 8128317 | 2550 | - | 0.22902 |
ddx24 | DDB_G0281841 | DDB0232430 | CDS | 5000989 | 2823 | + | 0.30039 | |
ddx27 | DDB_G0281711 | DDB0232430 | CDS | 4866495 | 2352 | + | 0.305697 | |
ddx3 | DDB_G0283661 | conserved RNA helicase very similar to mammalian DDX3X and DDX3Y and yeast DBP1 | DDB0232431 | CDS | 939305 | 2139 | - | 0.370266 |
ddx31 | DDB_G0271708 | DDB0232429 | CDS | 830367 | 2727 | + | 0.26696 | |
ddx3_ps | DDB_G0283657 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 937904 | 180 | + | 0.355556 |
ddx41 | DDB_G0287361 | conserved RNA helicase ortholog of D. melanogaster DEAD box protein abstrakt which is required during post-transcriptional gene expression | DDB0232432 | CDS | 183547 | 2016 | - | 0.315476 |
ddx42 | DDB_G0288501 | conserved putative RNA helicase very similar to mammalian DDX42 | DDB0232432 | CDS | 1607944 | 2961 | + | 0.274232 |
ddx47 | DDB_G0280147 | DDB0232430 | CDS | 3015956 | 1641 | - | 0.312614 | |
ddx49 | DDB_G0270396 | DDB0232428 | CDS | 4752654 | 1527 | + | 0.27112 | |
ddx5 | DDB_G0293036 | DDB0232433 | CDS | 2373448 | 2094 | + | 0.258835 | |
ddx51 | DDB_G0293740 | DDB0232433 | CDS | 3249527 | 1692 | - | 0.229905 | |
ddx52 | DDB_G0274325 | ortholog of H. sapiens DDX52 and S. cerevisiae ROK1 (Rescuer Of Kem1) ROK1 required for 18S rRNA synthesis | DDB0232429 | CDS | 3957548 | 2007 | + | 0.271051 |
ddx55 | DDB_G0291588 | ortholog of H. sapiens DDX55 and S. cerevisiae SBP4 (Suppressor of PAB1) SBP4 required for synthesis of 60S ribosomal subunits | DDB0232433 | CDS | 577637 | 1992 | - | 0.270582 |
ddx56 | DDB_G0280407 | ortholog of H. sapiens DDX56 and S. cerevisiae DBP9 (Dead Box Protein 9) involved in biogenesis of the 60S ribosomal subunit | DDB0232430 | CDS | 3312082 | 2058 | + | 0.266764 |
ddx6 | DDB_G0291804 | ortholog of H. sapiens DDX6 and S. cerevisiae DHH1 (DExDH-box Helicase) | DDB0232433 | CDS | 773358 | 1272 | + | 0.367925 |
denr | DDB_G0279677 | conserved protein contains a translation initiation factor SUI1 domain | DDB0232430 | CDS | 2428511 | 675 | - | 0.29037 |
derl1 | DDB_G0288833 | component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins contains 5 putative transmembrane domains | DDB0232432 | CDS | 2045678 | 729 | - | 0.292181 |
derl2 | DDB_G0285131 | component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins contains 5 putative transmembrane domains | DDB0232431 | CDS | 2896240 | 765 | - | 0.28366 |
desA | DDB_G0269738 | DDB0232428 | CDS | 3455193 | 1086 | + | 0.30663 | |
detA | DDB_G0277075 | similar to human DET1 localizes to the nucleus but excluded from the heterochromatin interacts with RepE and is involved in cell type specification during development | DDB0232429 | CDS | 7457975 | 4389 | + | 0.286853 |
dgat1 | DDB_G0271342 | catalyzes the reaction: acyl-CoA 12-diacylglycerol CoA triacylglycerol similar to mammalian DGAT1 contains 9 predicted transmembrane domains | DDB0232429 | CDS | 73360 | 1854 | - | 0.296117 |
dgat2 | DDB_G0290279 | conserved diglyceride acyltransferase most similar to U. ramanniana DGAT2B and H. sapiens DGAT2 catalyzing the reaction: acyl-CoA 12-diacylglycerol CoA triacylglycerol | DDB0232432 | CDS | 3856720 | 993 | - | 0.300101 |
dgcA | DDB_G0283453 | Dictyostelium diguanylate cyclase synthesizes cyclic-di-GMP from 2 molecules of GTP expressed at the slug and fruiting body tip responsible for stalk differentiation | DDB0232431 | CDS | 715640 | 1566 | - | 0.210089 |
dgk | DDB_G0280843 | catalyzes the reaction ATP deoxyguanosine ADP dGMP | DDB0232430 | CDS | 1424429 | 858 | - | 0.226107 |
dgkA | DDB_G0277223 | dgkA corresponds to a previously reported myosin II heavy chain kinase designated myosin heavy chain-protein kinase C (MHC-PKC) recent research shows the protein does not contain a protein kinase domain but a diacylglycerol kinase domain | DDB0232429 | CDS | 7741603 | 2664 | + | 0.28003 |
dgtA | DDB_G0288321 | CAZy family GT2 catalyzes the reaction UDP-glucose dolichyl phosphate UDP dolichyl beta-D-glucosyl phosphate | DDB0232432 | CDS | 1385100 | 984 | + | 0.272358 |
dgtB | DDB_G0286519 | CAZy family GT2 catalytic subunit forms a complex with DPM1 and DPM2 catalyzes the reaction GDP-mannose dolichyl phosphate GDP dolichyl D-mannosyl phosphate | DDB0232431 | CDS | 4586343 | 765 | - | 0.299346 |
dhak | DDB_G0269274 | catalyzes the reaction ATP glycerone ADP glycerone phosphate | DDB0232428 | CDS | 2438501 | 1947 | - | 0.249615 |
dhcA | DDB_G0276355 | DDB0232429 | CDS | 6681538 | 14193 | - | 0.337631 | |
dhkA | DDB_G0280961 | two-component histidine kinase which first autophosphorylates a histidine and then transfers the phosphate onto an aspartate before the signal is transduced also known as histidyl-aspartyl phosphorelay | DDB0232430 | CDS | 4220018 | 6453 | + | 0.284054 |
dhkB | DDB_G0277845 | DDB0232430 | CDS | 525688 | 5910 | - | 0.298646 | |
dhkC | DDB_G0274191 | DDB0232429 | CDS | 4805683 | 3678 | + | 0.259652 | |
dhkD | DDB_G0282289 | DDB0232430 | CDS | 5632424 | 4641 | - | 0.280112 | |
dhkE | DDB_G0269204 | DDB0232428 | CDS | 2700289 | 5100 | - | 0.217451 | |
dhkF | DDB_G0276143 | DDB0232429 | CDS | 6523775 | 3330 | - | 0.25976 | |
dhkG | DDB_G0284045 | DDB0232431 | CDS | 1509861 | 10299 | - | 0.239441 | |
dhkH | DDB_G0279913 | DDB0232430 | CDS | 2725463 | 4137 | + | 0.263718 | |
dhkI-1 | DDB_G0273475 | there is a second copy of this gene | DDB0232429 | CDS | 2926565 | 5211 | - | 0.257148 |
dhkI-2 | DDB_G0295835 | there is a second copy of this gene | DDB0232429 | CDS | 3099906 | 5199 | + | 0.25755 |
dhkJ | DDB_G0277883 | DDB0232430 | CDS | 102264 | 6189 | + | 0.320407 | |
dhkK | DDB_G0277887 | DDB0232430 | CDS | 942210 | 3642 | - | 0.280066 | |
dhkL | DDB_G0282927 | DDB0232431 | CDS | 127874 | 5130 | + | 0.280507 | |
dhkM | DDB_G0282377 | DDB0232430 | CDS | 5726442 | 7167 | + | 0.242919 | |
dhps | DDB_G0285725 | catalyzes the first step in the formation of deoxyhypusine: [eIF5A]-lysine spermidine [eIF5A]-deoxyhypusine propane-13-diamine an essential post-translational modification only found in mature eIF5A factor the second reaction is catalyzed by Dohh | DDB0232431 | CDS | 3636502 | 1131 | + | 0.318302 |
dhx15 | DDB_G0285213 | DDB0232431 | CDS | 2984261 | 2184 | + | 0.330128 | |
dhx16 | DDB_G0285937 | DEADDEAH box helicases are involved in various aspects of RNA metabolism including nuclear pre-mRNA splicing | DDB0232431 | CDS | 3866187 | 3321 | + | 0.311352 |
dhx33 | DDB_G0270110 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | DDB0232428 | CDS | 4244035 | 2193 | + | 0.272686 |
dhx35 | DDB_G0269306 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | DDB0232428 | CDS | 2485989 | 2151 | - | 0.272431 |
dhx37 | DDB_G0287351 | ortholog of H. sapiens DHX37 and S. cerevisiae ECM16 an RNA helicase involved in ribosomal biosynthesis | DDB0232432 | CDS | 165026 | 4386 | - | 0.287278 |
dhx57 | DDB_G0267516 | putative RNA helicase contains an RWD domain (RING finger and WD repeat) | DDB0232428 | CDS | 263217 | 4356 | - | 0.278007 |
dhx8 | DDB_G0291183 | conserved RNA helicase S. cerevisiae ortholog PRP22 mediates ATP-dependent mRNA release from the spliceosome and unwinds RNA duplexes | DDB0232432 | CDS | 5107365 | 3483 | - | 0.335343 |
dhx9 | DDB_G0275313 | ortholog of the human DHX9 that unwinds double-stranded DNA and RNA in a 3' to 5' direction | DDB0232429 | CDS | 5331812 | 4419 | - | 0.27857 |
dia1 | DDB_G0285431 | specifically expressed during the transition from growth to development serine-rich protein possibly anchored to the plasma membranebr bNomenclature conflict:b Do not confuse this gene with forF often called Ddia1 encoding a diaphanous formin | DDB0232431 | CDS | 3246902 | 1368 | - | 0.315058 |
dia2 | DDB_G0291253 | lysine and leucine rich protein specifically expressed during the transition from growth to development located in the ER in vegetative cells and in prespore vesicles during development | DDB0232433 | CDS | 434272 | 456 | - | 0.276316 |
dicA | DDB_G0280849 | DDB0232430 | CDS | 3856978 | 1965 | - | 0.337405 | |
dicB | DDB_G0267470 | forms a discoidin-inducing complex (DIC) with dicA1 pdsA and an unknown protein dicB alone does not induce discoidin expression | DDB0232428 | CDS | 298527 | 1824 | + | 0.311952 |
dimA | DDB_G0278971 | DDB0232430 | CDS | 1459749 | 3693 | - | 0.286759 | |
dimB | DDB_G0291372 | required for expression of prestalk genes in response to DIF-1 optimal binding to DNA sequences containing CACA | DDB0232433 | CDS | 197774 | 1809 | + | 0.310669 |
dimt1l | DDB_G0283789 | essential protein that dimethylates two adjacent adenosines in the loop of a conserved hairpin near the 3'-end of 18S rRNA in the 40S particle in S. cerevisiae | DDB0232431 | CDS | 1107655 | 945 | + | 0.285714 |
dio3 | DDB_G0275741 | contains a selenocysteine (U) residue at position 113 similar to animal Type III iodothyronine deiodinase (DIO3) catalyzes the reaction 33'5'-triiodo-L-thyronine iodide A H() L-thyroxine AH(2) | DDB0232429 | CDS | 5884722 | 774 | + | 0.299742 |
dlcA | DDB_G0284589 | dynein is a multisubunit microtubule-dependent motor enzyme that acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules belongs to the T-complex testis-specific protein 1 family | DDB0232431 | CDS | 2178851 | 336 | + | 0.285714 |
dlcB | DDB_G0274815 | DDB0232429 | CDS | 3974977 | 276 | - | 0.235507 | |
dlcC | DDB_G0285855 | dynein is a multisubunit microtubule-dependent motor enzyme that acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules belongs to the roadblockLC7 family | DDB0232431 | CDS | 3725623 | 294 | + | 0.234694 |
dlpA | DDB_G0268592 | involved in cytokinesis stabilizes actin filaments expressed in pstAB cells and in upper cup during culmination | DDB0232428 | CDS | 1676402 | 7986 | + | 0.326321 |
dlpB | DDB_G0285931 | DDB0232431 | CDS | 3850259 | 2427 | - | 0.309848 | |
dlpC | DDB_G0271628 | DDB0232429 | CDS | 572266 | 2715 | + | 0.295028 | |
dlrA | DDB_G0290485 | DDB0232432 | CDS | 4410371 | 2457 | - | 0.299959 | |
dmpA | DDB_G0275065 | DDB0232429 | CDS | 5096698 | 5061 | - | 0.303102 | |
dmtA | DDB_G0289329 | DDB0232432 | CDS | 2694067 | 1092 | - | 0.271978 | |
dnaja1 | DDB_G0291568 | conserved molecular chaperone DnaJ homolog subfamily A member 1 | DDB0232433 | CDS | 558877 | 1380 | + | 0.365942 |
dnaja5 | DDB_G0286579 | conserved eukaryotic protein of unknown function contains DNAJ domain and two C2H2-like Zinc finger domains | DDB0232431 | CDS | 4649529 | 1902 | - | 0.268665 |
dnajc13 | DDB_G0286293 | very similar to the mammalian DnaJ homolog subfamily C member 13 required in D. melanogaster (Rme-8) for receptor-mediated endocytosis 8 | DDB0232431 | CDS | 4307439 | 7779 | - | 0.331919 |
dnajc19 | DDB_G0283735 | putative component of the PAM complex required for the ATP-dependent translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix defects in DNAJC19 in human cause dilated cardiomyopathy with ataxia (DCMA) contains one putative N-terminal signal sequence | DDB0232431 | CDS | 1046052 | 342 | + | 0.304094 |
dnajc3 | DDB_G0286251 | DnaJ (Hsp40) homolog subfamily C member 3 which in H. sapiens is a interferon-induced double-stranded RNA-activated protein kinase inhibitor | DDB0232431 | CDS | 4252375 | 1509 | + | 0.319417 |
dnapkcs | DDB_G0281167 | atypical PIKK family protein kinase similar to human DNA-PKcs required for the repair of DNA double-strand breaks belongs to the PIKK family of protein kinases | DDB0232430 | CDS | 4132807 | 12900 | + | 0.265504 |
dnase2 | DDB_G0290577 | mammals have two lysosomal DNase II enzymes while Dictyosyelium has just one DNase II catalyzes endonucleolytic cleavage of preferably double-stranded DNA to nucleoside 3'-phosphates and 3'-phosphooligonucleotide end-products. | DDB0232432 | CDS | 4301494 | 1128 | - | 0.29344 |
dng1 | DDB_G0284411 | DDB0232431 | CDS | 1965235 | 975 | + | 0.322051 | |
dnmA | DDB_G0288047 | methylates cytosines in DNA belongs to the dnmt2 subfamily which has weak methylase activity | DDB0232432 | CDS | 1026957 | 1140 | - | 0.240351 |
dnpep | DDB_G0286149 | DDB0232431 | CDS | 4132917 | 1455 | - | 0.327148 | |
docA | DDB_G0291974 | DDB0232433 | CDS | 1105862 | 6666 | + | 0.30348 | |
docB | DDB_G0270404 | DDB0232428 | CDS | 4785053 | 6531 | - | 0.287858 | |
docC | DDB_G0292004 | bCommunity annotation:b DDB G0292004 (DockC) is threefold overexpressed in a dicty strain lacking the retinoblastoma-like gene rblA (Doquang et al in preparation). Most genes involved in cell cycle progression but relatively few other genes are upregulated in this strain suggesting that DockC has a role in the cell cycle possibly in cytokinesis. DockA B and D are not regulated by rblA. Harry MacWilliams May 2009br A c-terminal GFP fusion localizes to mitochondria. Rod-shaped and round mitochondria are seen in different cells. Cells with round mitochondria tend to be brighter suggesting that docC might influence the rod to round transition. Harry MacWilliams February 2011br | DDB0232433 | CDS | 999481 | 5211 | + | 0.264824 |
docD | DDB_G0284725 | DDB0232431 | CDS | 2297325 | 5775 | + | 0.29316 | |
dohh-1 | DDB_G0272634 | ortholog of H. sapiens DOHH that catalyzes the hydroxylation of the N(6)-(4-aminobutyl)-L-lysine intermediate to form hypusine an essential post-translational modification only found in mature eIF5A factor the first reaction is catalyzed by Dhps there is a second copy of this gene | DDB0232429 | CDS | 2283023 | 948 | - | 0.314346 |
dohh-2 | DDB_G0274079 | ortholog of H. sapiens DOHH that catalyzes the hydroxylation of the N(6)-(4-aminobutyl)-L-lysine intermediate to form hypusine an essential post-translational modification only found in mature eIF5A factor the first reaction is catalyzed by Dhps there is a second copy of this gene | DDB0232429 | CDS | 3747735 | 948 | + | 0.314346 |
dokA | DDB_G0274101 | DDB0232429 | CDS | 4563185 | 5016 | + | 0.297648 | |
dolpp1 | DDB_G0274591 | catalyzes the reaction dolichyl diphosphate Hsub2subO dolichyl phosphate phosphate contains 4 putative transmembrane domains | DDB0232429 | CDS | 3864574 | 690 | - | 0.249275 |
dotA | DDB_G0271626 | H3K79 methyltransferase in Dictyostelium involved in development and DNA repair similar to S. cerevisiae DOT1 which functions in gene silencing at telomeres and DNA repair and is cell cycle regulated Dictyostelium Dot1 however is not cell cycle dependent | DDB0232429 | CDS | 563064 | 5538 | + | 0.267786 |
dph1 | DDB_G0284257 | ortholog to the conserved DPH1 which in S. cerevisiae is required for synthesis of diphthamide a modified histidine residue of translation elongation factor 2 | DDB0232431 | CDS | 1781348 | 1419 | - | 0.319239 |
dph2 | DDB_G0295687 | similar to the conserved DPH2 which in S. cerevisiae is required for synthesis of diphthamide a modified histidine residue of translation elongation factor 2 | DDB0232430 | CDS | 2638120 | 1767 | + | 0.24335 |
dph3 | DDB_G0277061 | C-terminal half very similar to the conserved DPH3 the predicted Dictyostelium protein contains an additional repetitive N-terminal part that is not present in other species | DDB0232429 | CDS | 7407171 | 528 | - | 0.238636 |
dph4 | DDB_G0292980 | DDB0232433 | CDS | 2253222 | 513 | + | 0.224172 | |
dph5 | DDB_G0276115 | ortholog to the conserved DPH5 a methyltransferase which in S. cerevisiae is required for synthesis of diphthamide a modified histidine residue of translation elongation factor 2 | DDB0232429 | CDS | 6268498 | 822 | + | 0.306569 |
dpiA | DDB_G0274315 | DDB0232429 | CDS | 3943086 | 786 | - | 0.25827 | |
dpm2-1 | DDB_G0272588 | highly conserved protein involved in GPI biosynthesis forms a complex with DPM1 and DPM3 regulates the biosynthesis of dolichol-phosphate-mannose there is a second copy of this gene | DDB0232429 | CDS | 2396788 | 240 | + | 0.2625 |
dpm2-2 | DDB_G0273981 | highly conserved protein involved in GPI biosynthesis forms a complex with DPM1 and DPM3 regulates the biosynthesis of dolichol-phosphate-mannose there is a second copy of this gene | DDB0232429 | CDS | 3634594 | 240 | - | 0.2625 |
dpm3 | DDB_G0277435 | highly conserved protein involved in GPI biosynthesis stabilizer subunit of the dolichol-phosphate-mannose synthase complex with DPM1 and DPM2 | DDB0232429 | CDS | 8070416 | 279 | + | 0.247312 |
dpoA | DDB_G0274387 | involved in regulation of inositol (145) trisphosphate levels | DDB0232429 | CDS | 4862329 | 2283 | - | 0.306176 |
dpp3-1 | DDB_G0273471 | catalyzes the release of an N-terminal dipeptide from a peptide comprising four or more residues with broad specificity highly selective for Arg-Arg-2-naphthylamide at pH 9.2 there is a second copy of this gene | DDB0232429 | CDS | 2917844 | 2076 | + | 0.315029 |
dpp3-2 | DDB_G0273563 | catalyzes the release of an N-terminal dipeptide from a peptide comprising four or more residues with broad specificity highly selective for Arg-Arg-2-naphthylamide at pH 9.2 there is a second copy of this gene | DDB0232429 | CDS | 3111479 | 2076 | - | 0.315029 |
dr1 | DDB_G0269638 | DDB0232428 | CDS | 3204015 | 537 | - | 0.312849 | |
drap1 | DDB_G0292510 | DDB0232433 | CDS | 1574061 | 1653 | - | 0.255898 | |
drcA | DDB_G0293840 | belongs to the glutathione S-transferase superfamily catalzyes the first step in the breakdown of differentiation-inducing factor 1 | DDB0232433 | CDS | 3374878 | 828 | + | 0.270531 |
drg1 | DDB_G0289317 | ortholog of human DRG1 which may be involved in cell proliferation differentiation and death highly conserved in eukaryotes belongs to the GTP1OBG family | DDB0232432 | CDS | 2634493 | 1113 | - | 0.337826 |
drg2 | DDB_G0279451 | ortholog of human DRG2 which may be involved in cell proliferation differentiation and death highly conserved in eukaryotes belongs to the GTP1OBG family | DDB0232430 | CDS | 2066556 | 1095 | - | 0.305023 |
drkA | DDB_G0289791 | DDB0232432 | CDS | 3144874 | 1929 | + | 0.276827 | |
drkB | DDB_G0289709 | DDB0232432 | CDS | 3147575 | 2073 | + | 0.2904 | |
drkC | DDB_G0281899 | tyrosine kinase member of the TKL (tyrosine kinase-like) group and the DRK (Dictyostelium receptor-like kinase) subfamily involved in phagocytosis and late phagosomelysosome fusion enriched in S cells in slugs | DDB0232430 | CDS | 5088116 | 2250 | - | 0.305778 |
drkD | DDB_G0281557 | member of the TKL (tyrosine kinase-like) group and the DRK (Dictyostelium receptor-like kinase) subfamily contains a leucine-rich repeat (LRR) region | DDB0232430 | CDS | 4777368 | 3867 | + | 0.334885 |
drnA-1 | DDB_G0273051 | similar to the mammalian Dicer protein an RNase III protein that converts long dsRNA (double-stranded RNA) into siRNA (small interfering RNA) there is a second copy of this gene | DDB0232429 | CDS | 2284317 | 3612 | - | 0.251661 |
drnA-2 | DDB_G0274077 | similar to the mammalian Dicer protein an RNase III protein that converts long dsRNA (double-stranded RNA) into siRNA (small interfering RNA) there is a second copy of this gene | DDB0232429 | CDS | 3743727 | 3612 | + | 0.251661 |
drnA_ps | DDB_G0270602 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232428 | CDS | 3271877 | 177 | - | 0.242938 |
drnB | DDB_G0268410 | similar to the mammalian Dicer protein an RNase III protein that converts long dsRNA (double-stranded RNA) into siRNA (small interfering RNA) in Dictyostelium involved in RNA interference and microRNA processing | DDB0232428 | CDS | 1225333 | 4158 | + | 0.28836 |
drpp20 | DDB_G0289139 | DDB0232432 | CDS | 2393417 | 687 | + | 0.254731 | |
drpp20_ps | DDB_G0289083 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 2336464 | 339 | - | 0.221239 |
drpp21 | DDB_G0290281 | ortholog of RPR2 a subunit of nuclear RNase P which cleaves tRNA precursors to generate mature 5' ends | DDB0232432 | CDS | 3858234 | 675 | - | 0.185185 |
drpp25 | DDB_G0281409 | DDB0232430 | CDS | 4439811 | 1110 | + | 0.381982 | |
drpp30 | DDB_G0269980 | DDB0232428 | CDS | 3962023 | 1101 | + | 0.288828 | |
drpp40 | DDB_G0279961 | DDB0232430 | CDS | 2762286 | 1275 | + | 0.225882 | |
dscA-1 | DDB_G0273063 | there is a second copy of this gene | DDB0232429 | CDS | 2474613 | 762 | - | 0.383202 |
dscA-2 | DDB_G0273919 | there is a second copy of this gene | DDB0232429 | CDS | 3556412 | 762 | + | 0.383202 |
dscC-1 | DDB_G0273065 | there is a second copy of this gene | DDB0232429 | CDS | 2511465 | 762 | - | 0.370079 |
dscC-2 | DDB_G0273885 | there is a second copy of this gene | DDB0232429 | CDS | 3519560 | 762 | + | 0.370079 |
dscD-1 | DDB_G0273067 | there is a second copy of this gene | DDB0232429 | CDS | 2509980 | 762 | - | 0.374016 |
dscD-2 | DDB_G0273887 | there is a second copy of this gene | DDB0232429 | CDS | 3521045 | 762 | + | 0.374016 |
dscE | DDB_G0292552 | DDB0232433 | CDS | 1899844 | 774 | - | 0.320413 | |
dsc_ps1 | DDB_G0348645 | putative pseudogene short fragment similar to D. discoideum discoidin gene family including | DDB0232429 | CDS | 2506006 | 150 | - | 0.346667 |
dsc_ps2 | DDB_G0348648 | putative pseudogene short fragment similar to D. discoideum discoidin gene family including | DDB0232429 | CDS | 3525631 | 150 | + | 0.346667 |
dst1 | DDB_G0274593 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232429 | CDS | 3862026 | 2214 | + | 0.289521 |
dst2 | DDB_G0267730 | putative protein serinethreonine kinase the kinase domain is similar to mitogen-activated protein kinases and other STE20-like kinases stress-responsive kinase | DDB0232428 | CDS | 719427 | 3429 | + | 0.33275 |
dst3 | DDB_G0291267 | putative protein serinethreonine kinase the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232433 | CDS | 35064 | 1689 | - | 0.351095 |
dst4 | DDB_G0288071 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232432 | CDS | 1048762 | 1458 | - | 0.325789 |
dstA | DDB_G0281381 | DDB0232430 | CDS | 4448074 | 2124 | + | 0.31403 | |
dstB | DDB_G0268638 | DDB0232428 | CDS | 1834587 | 3447 | - | 0.267479 | |
dstC | DDB_G0293532 | DDB0232433 | CDS | 3253627 | 2796 | - | 0.331545 | |
dstD | DDB_G0275167 | DDB0232429 | CDS | 5102751 | 2436 | + | 0.300493 | |
dtd | DDB_G0291273 | hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr) in yeast substrate specifity may be broader | DDB0232433 | CDS | 40029 | 456 | + | 0.300439 |
dtfA | DDB_G0289389 | DDB0232432 | CDS | 2732174 | 4209 | - | 0.248278 | |
dtymk | DDB_G0290033 | catalyzes the reaction dTMP ATP dTDP ADP in de novo biosynthesis of pyrimidine deoxyribonucleotides | DDB0232432 | CDS | 3573621 | 669 | - | 0.258595 |
dupA | DDB_G0277071 | contains both a kinase domain and a phosphatase domain similar to MAP kinase phosphatase in plants and dual-specificty phosphatase 19 in mammals regulates the MAP Kinase response to Legionella pneumophila infection in Dictyostelium | DDB0232429 | CDS | 7439874 | 7365 | - | 0.295995 |
dus1l | DDB_G0278803 | ortholog of S. cerevisiae DUS1 and the animal DUS1L catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of tRNAs | DDB0232430 | CDS | 1208252 | 1308 | + | 0.323395 |
dus2l | DDB_G0283877 | ortholog of S. cerevisiae SMM1 and the animal DUS2L catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of tRNAs | DDB0232431 | CDS | 1134008 | 1209 | + | 0.276261 |
dus3l | DDB_G0292686 | ortholog of S. cerevisiae DUS3 and the animal DUS3L catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of tRNAs | DDB0232433 | CDS | 1949203 | 2016 | + | 0.291171 |
dus4l | DDB_G0291360 | ortholog of S. cerevisiae DUS4 and the animal DUS4L catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of tRNAs | DDB0232433 | CDS | 180987 | 1035 | - | 0.282126 |
dut | DDB_G0293374 | catalyses the reaction Hsub2subO dUTP pyrophosphate dUMP in de novo biosynthesis of pyrimidine deoxyribonucleotides | DDB0232433 | CDS | 2804871 | 540 | - | 0.327778 |
dutA | DDB_G0294515 | untranslatable RNA overexpression of dutA segments suppresses the culmination mutant phenotype of STATa (dstA) revealing an inhibitory role of dutA in culmination accordingly dutA expression ceases with the onset of culmination dutA segment overexpression is also correlated with increased tyrosine phosphorylation of STATa | DDB0232431 | CDS | 2979542 | 1060 | + | 0.162264 |
dwwA | DDB_G0281827 | homologous to human KIBRA protein a Dendrin binding protein | DDB0232430 | CDS | 5135547 | 1707 | + | 0.27065 |
dymA | DDB_G0277849 | DDB0232430 | CDS | 252381 | 2562 | - | 0.330211 | |
dymB | DDB_G0277851 | DDB0232430 | CDS | 1081009 | 2763 | - | 0.279045 | |
dynA | DDB_G0280435 | DDB0232430 | CDS | 3347902 | 4620 | - | 0.303896 | |
dynB | DDB_G0285503 | DDB0232431 | CDS | 3322100 | 1293 | + | 0.269142 | |
dynC | DDB_G0277561 | DDB0232429 | CDS | 8131744 | 714 | - | 0.246499 | |
dynD | DDB_G0280175 | DDB0232430 | CDS | 3050941 | 1821 | - | 0.27732 | |
dynE | DDB_G0278579 | DDB0232430 | CDS | 1102831 | 597 | + | 0.269682 | |
dynF | DDB_G0290757 | DDB0232432 | CDS | 4567986 | 570 | - | 0.27193 | |
dync1li1 | DDB_G0292904 | DDB0232433 | CDS | 2245112 | 1515 | - | 0.280528 | |
dyrk1 | DDB_G0277485 | DDB0232429 | CDS | 7981156 | 2511 | + | 0.249303 | |
dyrk2 | DDB_G0293750 | DDB0232433 | CDS | 3272270 | 2748 | + | 0.306405 | |
e2f | DDB_G0284129 | bCommunity annotation: b Dicty's single E2F is likely to be an | DDB0232431 | CDS | 1622284 | 2592 | + | 0.296682 |
eIF1 | DDB_G0274239 | EIF1SUI1 ortholog the eukaryotic initiation factor 1 involved in recognition of the initiator codon | DDB0232429 | CDS | 4232211 | 333 | - | 0.336336 |
eIF1a | DDB_G0278205 | EIF1AX (eukaryotic initiation factor 1A X-linked) and EIF1AY (eukaryotic initiation factor 1A Y-linked) homolog | DDB0232430 | CDS | 473374 | 426 | - | 0.335681 |
eIF2a | DDB_G0284267 | EIF2A ortholog the eukaryotic initiation factor 2A that binds Met-tRNA | DDB0232431 | CDS | 1799493 | 1827 | - | 0.363437 |
eIF4e | DDB_G0268574 | EIF4E ortholog the eukaryotic initiation factor 4E recognizes and binds the RNA cap during protein synthesis | DDB0232428 | CDS | 1556730 | 753 | + | 0.310757 |
eIF4e3 | DDB_G0270406 | EIF4E3 ortholog the eukaryotic initiation factor 4E member 3 recognizes and binds the RNA cap during protein synthesis | DDB0232428 | CDS | 4795840 | 2442 | - | 0.28706 |
eIF4g | DDB_G0275395 | homolog of mammalian EIF4G123 and S. cerevisiae TIF4631 component of the protein complex eIF4F involved in the recognition of the mRNA cap | DDB0232429 | CDS | 5358648 | 4134 | - | 0.350508 |
eIF5 | DDB_G0286753 | EIF5 ortholog the eukaryotic initiation factor 5 catalyzes the hydrolysis of GTP bound to the 40S ribosomal initiation complex | DDB0232431 | CDS | 4930004 | 1182 | + | 0.337563 |
eIF5b | DDB_G0278815 | EIF5B ortholog the eukaryotic initiation factor 5B promotes the binding of tRNA to the ribosome | DDB0232430 | CDS | 1232003 | 3138 | - | 0.360102 |
eIF6 | DDB_G0276493 | prevents 60S and 40S ribosomal subunits to form the 80S ribosome by binding to the 60S subunit in Dictyosteliium nutrition uptake stimulates gene expression | DDB0232429 | CDS | 6856691 | 735 | - | 0.361905 |
eRF3 | DDB_G0277919 | DDB0232430 | CDS | 855258 | 1674 | - | 0.390681 | |
eb1 | DDB_G0283607 | DDB0232431 | CDS | 912876 | 1521 | + | 0.326759 | |
ebp | DDB_G0269414 | similar to mammalian EBP (and EBPL) EBP catalyzes the conversion of Delta(8)-sterols to their corresponding Delta(7)-isomers defects in hEBP cause chondrodysplasia punctata X-linked dominant type 2 a rare disorder of defective cholesterol biosynthesis | DDB0232428 | CDS | 2725897 | 660 | - | 0.330303 |
ecd | DDB_G0287829 | ortholog of the eukaryotic SGT1 or ECD a putative transcription coactivator | DDB0232432 | CDS | 773675 | 2460 | - | 0.222764 |
ech1 | DDB_G0282261 | very conserved among prokaryotes and eukaryotes isomerizes 3-trans5-cis-dienoyl-CoA to 2-trans4-trans-dienoyl-CoA | DDB0232430 | CDS | 5585355 | 882 | - | 0.293651 |
echs1 | DDB_G0285071 | conserved protein catalyzes the reaction (3S)-3-hydroxyacyl-CoA trans-2(or 3)-enoyl-CoA Hsub2subO | DDB0232431 | CDS | 2750152 | 834 | + | 0.333333 |
ecmA | DDB_G0277853 | DDB0232430 | CDS | 558488 | 5133 | + | 0.365089 | |
ecmB | DDB_G0269132 | composed of approx. 35 copies of a 24-amino-acid cysteine-rich repeat expression is decreased in | DDB0232428 | CDS | 4826715 | 3162 | - | 0.373182 |
ecmC | DDB_G0286663 | forms a heterodimer sheathin 62 also forms a heterotrimer sheathin 68 with ecmB and ecmE | DDB0232431 | CDS | 4806034 | 831 | - | 0.299639 |
ecmD | DDB_G0286647 | forms a 68 kDa heterodimer with ecmB sheathin 55 and a homodimer sheathin 53 | DDB0232431 | CDS | 4787507 | 822 | - | 0.309002 |
ecmF | DDB_G0291291 | similar to staA and other short proteins expressed in the prestalk region expressed in pstA cells | DDB0232433 | CDS | 69233 | 387 | + | 0.299742 |
ecmG | DDB_G0292224 | expressed in pstAO cells expression is decreased in | DDB0232433 | CDS | 1325480 | 366 | + | 0.325137 |
ecmH | DDB_G0292220 | expression is decreased in | DDB0232433 | CDS | 1327483 | 369 | + | 0.284553 |
ecmI | DDB_G0292222 | expression is decreased in | DDB0232433 | CDS | 1326474 | 366 | + | 0.284153 |
ecmJ | DDB_G0274189 | expression is decreased in | DDB0232429 | CDS | 4809755 | 366 | - | 0.281421 |
ecmK | DDB_G0287819 | DDB0232432 | CDS | 764642 | 498 | - | 0.307229 | |
ecmL | DDB_G0280245 | DDB0232430 | CDS | 3158659 | 474 | - | 0.303797 | |
eco1 | DDB_G0279959 | ortholog of S. cerevisiae ECO1 an acetyltransferase required for the establishment of sister chromatid cohesion during DNA replicationbrbr bCommunity annotation: b The involvement of DDB_G0279959 in Dicty cell cycle progression is supported by its 7-fold overexpression in a Dictyostelium | DDB0232430 | CDS | 2758242 | 1326 | + | 0.291855 |
efa1B | DDB_G0284035 | DDB0232431 | CDS | 1535647 | 651 | + | 0.391705 | |
efa1G | DDB_G0282979 | component of the eukaryotic translation elongation factor EF-1 which plays a role in attaching aminoacyl-tRNAs to the ribosome | DDB0232431 | CDS | 88701 | 1233 | + | 0.400649 |
efaAI | DDB_G0269134 | elongation factor 1 alpha one of two genes coding for the same protein binds and bundles F-actin expressed in prespore cells | DDB0232428 | CDS | 2795744 | 1362 | - | 0.432452 |
efaAII | DDB_G0269136 | elongation factor 1 alpha one of two genes coding for the same protein binds and bundles F-actin | DDB0232428 | CDS | 2431765 | 1362 | - | 0.417768 |
efbA | DDB_G0288373 | translocates peptidyl-tRNA from the aminoacyl site to the peptidyl site on the ribosome during protein synthesis null mutants still synthesis protein suggesting that EF-2b (cinC) is the real translation elongation gector | DDB0232432 | CDS | 1470619 | 2520 | + | 0.418651 |
eftud1 | DDB_G0279689 | DDB0232430 | CDS | 2446020 | 3495 | - | 0.303577 | |
eftud2 | DDB_G0283359 | highly conserved U5 small nuclear ribonucleoprotein subunit that is similar to elongation factor Tu ortholog of yeast SNU114 and human EFTUD2 | DDB0232431 | CDS | 569125 | 3057 | - | 0.328099 |
egeA | DDB_G0272002 | DDB0232429 | CDS | 1164190 | 765 | - | 0.300654 | |
egeB | DDB_G0269164 | highly similar to EgeA required for aggregation | DDB0232428 | CDS | 4173872 | 1278 | + | 0.309859 |
eif2b1 | DDB_G0288961 | DDB0232432 | CDS | 2146739 | 966 | + | 0.295031 | |
eif2b2 | DDB_G0291271 | DDB0232433 | CDS | 38541 | 1167 | - | 0.288775 | |
eif2b3 | DDB_G0290693 | EIF2B3 ortholog the eukaryotic initiation factor 2B gamma subunit guanyl nucleotide exchange factor for eIF2 defects are linked to leukoencephalopathy with vanishing white matter | DDB0232432 | CDS | 4424632 | 1323 | + | 0.265306 |
eif2b4 | DDB_G0290759 | ortholog of human EIF2B4 delta subunit of the translation initiation factor eIF2B the guanine-nucleotide exchange factor for eIF2 | DDB0232432 | CDS | 4569158 | 1860 | + | 0.317204 |
eif2b5 | DDB_G0283163 | EIF2B5 ortholog the eukaryotic initiation factor 2B epsilon subunit guanyl nucleotide exchange factor for eIF2 defects are linked to leukoencephalopathy with vanishing white matter | DDB0232431 | CDS | 349612 | 2124 | - | 0.303672 |
eif2s1 | DDB_G0271862 | EIF2S1 ortholog the eukaryotic initiation factor 2 alpha subunit in human binds to the 40S ribosome and to the mRNA for form a preinitiation complex contains an S1 RNA-binding domain characteristic of eIF2alpha | DDB0232429 | CDS | 944209 | 1026 | + | 0.334308 |
eif2s2 | DDB_G0282035 | EIF2S2 ortholog the eukaryotic initiation factor 2 beta subunit in human binds to the 40S ribosome and to the mRNA for form a preinitiation complex complex composed of 3 subunits | DDB0232430 | CDS | 5298628 | 954 | - | 0.348008 |
eif2s3 | DDB_G0278967 | DDB0232430 | CDS | 1529248 | 1383 | - | 0.348518 | |
eif3A | DDB_G0272078 | EIF3A ortholog the eukaryotic initiation factor theta subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232429 | CDS | 1223494 | 3093 | + | 0.38086 |
eif3B | DDB_G0283597 | EIF3B ortholog the eukaryotic initiation factor eta subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232431 | CDS | 847464 | 2013 | + | 0.350224 |
eif3C | DDB_G0279109 | EIF3C ortholog the eukaryotic initiation factor p110 subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232430 | CDS | 1642949 | 2811 | - | 0.37211 |
eif3D | DDB_G0274627 | EIF3S7 and S. pombe Moe1 ortholog the eukaryotic initiation factor zeta subunit in human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232429 | CDS | 4665266 | 1584 | - | 0.339015 |
eif3E | DDB_G0293052 | EIF3E ortholog the eukaryotic initiation factor p48 subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232433 | CDS | 2402071 | 1578 | + | 0.32763 |
eif3F | DDB_G0293254 | EIF3S5 ortholog the eukaryotic initiation factor epsilon subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232433 | CDS | 2626118 | 855 | - | 0.326316 |
eif3G | DDB_G0279549 | EIF3G ortholog the eukaryotic initiation factor delta subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232430 | CDS | 2241015 | 702 | - | 0.331909 |
eif3H | DDB_G0281153 | EIF3H ortholog the eukaryotic initiation factor gamma subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232430 | CDS | 4106976 | 960 | + | 0.276042 |
eif3I | DDB_G0285683 | EIF3I ortholog the eukaryotic initiation factor beta subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232431 | CDS | 3586013 | 996 | - | 0.348394 |
eif3J | DDB_G0287333 | EIF3J ortholog the eukaryotic initiation factor alpha subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232432 | CDS | 147100 | 660 | - | 0.263636 |
eif3K | DDB_G0291404 | EIF3SK ortholog the eukaryotic initiation factor 3 subunit in human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232433 | CDS | 259277 | 741 | + | 0.311741 |
eif3L | DDB_G0272076 | EIF3L ortholog has been shown in human to bind EIF3E | DDB0232429 | CDS | 1220684 | 1836 | - | 0.316993 |
eif5a | DDB_G0284861 | DDB0232431 | CDS | 2766075 | 480 | + | 0.395833 | |
elmoA | DDB_G0278051 | associates with myosin II and negatively regulates actin polymerization thus involved in the coordination of phagocytosis and cell migration | DDB0232430 | CDS | 194635 | 2934 | - | 0.249489 |
elmoB | DDB_G0280179 | DDB0232430 | CDS | 3058313 | 855 | + | 0.252632 | |
elmoC | DDB_G0282949 | DDB0232431 | CDS | 42516 | 1857 | - | 0.268713 | |
elmoD | DDB_G0280943 | DDB0232430 | CDS | 3852474 | 3804 | + | 0.253943 | |
elmoE | DDB_G0279657 | DDB0232430 | CDS | 2378488 | 5034 | - | 0.275129 | |
elmoF | DDB_G0267548 | DDB0232428 | CDS | 313115 | 3558 | - | 0.262788 | |
eloA | DDB_G0292896 | fatty acid elongase with substrate specificity for monounsaturated fatty acids in particular elongates 16:1 | DDB0232433 | CDS | 2229613 | 816 | - | 0.261029 |
eloB | DDB_G0281821 | DDB0232430 | CDS | 5029047 | 807 | - | 0.30855 | |
elof1 | DDB_G0287203 | ortholog of the conserved elongation factor 1 a transcription elongation factor that contains a conserved zinc finger domain implicated in chromatin structure maintenance in actively transcribed regions in S. cerevisiae | DDB0232431 | CDS | 5404659 | 243 | - | 0.366255 |
elp | DDB_G0287987 | similar to elongation factor 2 (EF-2) but lacks the EF-Tu binding domain 2 and EF-G domain EF-2 translocates peptidyl-tRNA from the aminoacyl site to the peptidyl site on the ribosome during protein synthesis | DDB0232432 | CDS | 934832 | 2520 | + | 0.271429 |
elp1 | DDB_G0284075 | similar to S. cerevisiae IKI3 subunit of the RNA polymerase II elongator complex and mammalian IKAP proteins | DDB0232431 | CDS | 1525708 | 4173 | + | 0.306255 |
elp2 | DDB_G0275651 | similar to S. cerevisiae ELP2 subunit of the RNA polymerase II elongator complex | DDB0232429 | CDS | 5847867 | 2706 | - | 0.318182 |
elp3 | DDB_G0290103 | similar to ELP3 the histone acetyltransferase subunit of the subunit of the RNA polymerase II elongator complex | DDB0232432 | CDS | 3656306 | 1680 | + | 0.335119 |
elp4 | DDB_G0278783 | similar to ELP4 subunit of the RNA polymerase II elongator complex | DDB0232430 | CDS | 1174736 | 1320 | + | 0.303788 |
emg1 | DDB_G0272732 | ortholog of S. cerevisiae and H. sapiens EMG1 involved in 40S ribosome biogenesis | DDB0232429 | CDS | 2220282 | 1017 | + | 0.298918 |
empA | DDB_G0288053 | DDB0232432 | CDS | 1036458 | 618 | - | 0.289644 | |
empB | DDB_G0293540 | DDB0232433 | CDS | 3021203 | 630 | + | 0.314286 | |
empC | DDB_G0278969 | DDB0232430 | CDS | 1473189 | 645 | - | 0.311628 | |
empD | DDB_G0277923 | DDB0232430 | CDS | 15087 | 666 | + | 0.303303 | |
enlA | DDB_G0276103 | N-terminal similarity to talin C-terminal similarity to fimbrins actin binding protein plays a role in cytokinesis and substrate adhesionbr bNomenclature conflict:b This gene has been erroneously referred to as | DDB0232429 | CDS | 6301145 | 4512 | + | 0.341534 |
enoA | DDB_G0283137 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO enriched in gametes | DDB0232431 | CDS | 225309 | 1305 | - | 0.36092 |
enoB | DDB_G0268214 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO | DDB0232428 | CDS | 1697493 | 1332 | - | 0.327327 |
epnA | DDB_G0291512 | epsin interacts dynamically with clathrin-coated pits at the plamid membrane and plays a role in cytokinesis and spore morphology regulates Hip1r phosphorylation with its ENTH domain | DDB0232433 | CDS | 459846 | 2061 | + | 0.319748 |
epnA_ps1 | DDB_G0271978 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232429 | CDS | 1096689 | 198 | - | 0.30303 |
epnA_ps2 | DDB_G0349475 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 1881173 | 749 | - | 0.300401 |
eppA | DDB_G0283327 | putative substrate for erkB highly repetitive protein contains a possible eggshell domain first identified in the human parasite Schistosome mansoni | DDB0232431 | CDS | 431083 | 1209 | + | 0.404467 |
eral1 | DDB_G0288609 | DDB0232432 | CDS | 1740020 | 1197 | - | 0.3066 | |
ercc1 | DDB_G0267682 | ortholog of H. sapiens ERCC1 and S. cerevisiae RAD10 nucleotide excision repair genes defects in ERCC1 cause cerebro-oculo-facio-skeletal syndrome type 4 (COFS4) | DDB0232428 | CDS | 559492 | 1545 | + | 0.291909 |
ercc6 | DDB_G0281441 | ortholog of S. cerevisiae RAD26 and H. sapiens ERCC6 (CSB) involved in Cockayne syndrome chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232430 | CDS | 4502255 | 4968 | - | 0.273752 |
ercc8 | DDB_G0276481 | ortholog of S. cerevisiae RAD26 and H. sapiens ERCC8 (CSA) involved in Cockayne syndrome | DDB0232429 | CDS | 6778627 | 1542 | + | 0.284695 |
erf1 | DDB_G0288613 | class I release factor of the translation termination machinery in eukaryotes with the universal genetic code predicted to recognizes all stop codons (UAA UAG and UGA) | DDB0232432 | CDS | 1753244 | 1326 | - | 0.361991 |
erg2 | DDB_G0270356 | DDB0232428 | CDS | 4699501 | 702 | + | 0.297721 | |
erg24 | DDB_G0284407 | catalyzes the reaction 44-dimethyl-5-alpha-cholesta-824-dien-3-beta-ol NADP() 44-dimethyl-5-alpha-cholesta-81424-trien-3-beta-ol NADPH | DDB0232431 | CDS | 1962362 | 1389 | + | 0.398848 |
ergic3 | DDB_G0292002 | conserved protein that might be involved in transport between endoplasmic reticulum and Golgi contains two putative transmembrane domains | DDB0232433 | CDS | 996494 | 1152 | - | 0.31684 |
erh | DDB_G0274565 | DDB0232429 | CDS | 3998159 | 303 | - | 0.30363 | |
eriA | DDB_G0283113 | similar to C. elegans eri-1 RNA exonuclease that acts as a negative regulator of RNA interference (RNAi) contains one exonuclease domainbrbr bCommunity annotation:b EriA codes for a multifunctional RNA exonuclease which has been identified with negative regulation of RNAi and in processing the 5.8s ribosomal RNA. The gene is nearly 8-fold overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA is disrupted. Other genes overexpressed in this strain include virtually all those with unique or major functions in S-phase or mitosis. Neither RNAi nor ribosomal processing obviously fits into this class. However it has recently been shown in mammalian cells that eriA under the pseudonym 3'hExo stably associates with histone pre-mRNAs and participates in a complex that determines the site of their cleavage (see Yang et al Mol Cell Biol 29 4045-4056 (2009). Another protein in this complex is the histone stem-loop binding protein DDB_G0277383 which is threefold upregulated in t | DDB0232431 | CDS | 263707 | 663 | + | 0.273002 |
erkA | DDB_G0286353 | DDB0232431 | CDS | 4355028 | 1590 | + | 0.303774 | |
erkB | DDB_G0283903 | DDB0232431 | CDS | 1385123 | 1110 | - | 0.323423 | |
esd | DDB_G0283037 | very similar to human ESD and to S. cerevisiae S-formylglutathione hydrolase (YJL068C) which seems to be involved in formaldehyde detoxification | DDB0232431 | CDS | 192516 | 858 | + | 0.264569 |
esf2 | DDB_G0293576 | DDB0232433 | CDS | 3063826 | 891 | - | 0.258137 | |
espl1 | DDB_G0290325 | caspase-like protease also called separin (ESP1) which plays a central role in sister chromosome segregation in yeastbrbr bCommunity annotation:b espl1 is highly similar to separase (aka separin) a widely-conserved peptidase which cleaves the rad21ssc1 non-SMC subunit of cohesin rings remaining at the centromere at metaphase allowing the sister chromatids to separate. Consistent with this homology espl1 is overexpressed fourfold (p6e-14) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes with roles in S-phase or mitosis are overexpressed in this strain and most of the overexpressed genes have identifiable cell cycle functions. espl1 also shows the developmental time course most typical of cell cycle genes.br The separase inhibitor securin conserved between yeast and humans which is broken down at the metaphaseanaphase junction under control of the spindle checkpoint is not recognizable in Dicty. Securin is also unrecognizable plants however whle | DDB0232432 | CDS | 3958340 | 7284 | - | 0.240527 |
etfa | DDB_G0290927 | electron transfer flavoprotein (ETF) serves as a specific electron acceptor for several dehydrogenases transfers the electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase ( | DDB0232432 | CDS | 4764545 | 1068 | + | 0.338951 |
etfb | DDB_G0277991 | electron transfer flavoprotein (ETF) serves as a specific electron acceptor for several dehydrogenases transfers the electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase ( | DDB0232430 | CDS | 125579 | 753 | + | 0.308101 |
etfdh | DDB_G0278849 | reduced electron-transferring flavoprotein ubiquinone electron-transferring flavoprotein ubiquinol accepts electrons from ETF and reduces ubiquinone defects in human ETFDH cause glutaric aciduria type IIc (GAIIC) | DDB0232430 | CDS | 1276262 | 1821 | - | 0.337177 |
etnkA | DDB_G0274955 | catalyzes the reaction ATP ethanolamine ADP O-phosphoethanolamine | DDB0232429 | CDS | 4656194 | 1050 | + | 0.298095 |
etnkB | DDB_G0275265 | catalyzes the reaction ATP ethanolamine ADP O-phosphoethanolamine | DDB0232429 | CDS | 5078945 | 1344 | - | 0.248512 |
exdl2A | DDB_G0278079 | very similar to mammalian exonuclease 3'-5' domain-like-containing protein 2 (EXDL2) the upstream Dictyostelium gene is very similar | DDB0232430 | CDS | 242964 | 2157 | + | 0.243394 |
exdl2B | DDB_G0278593 | very similar to mammalian exonuclease 3'-5' domain-like-containing protein 2 (EXDL2) the downstream Dictyostelium gene is very similar | DDB0232430 | CDS | 240471 | 2061 | + | 0.246482 |
exo1 | DDB_G0291570 | highly similar to S. pombe exonuclease I a 5'-3' exonuclease involved in DNA repair recombination replication and telomere integrity | DDB0232433 | CDS | 561048 | 3141 | + | 0.266794 |
exoc1 | DDB_G0285067 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232431 | CDS | 2728155 | 2640 | - | 0.285606 |
exoc2 | DDB_G0280081 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232430 | CDS | 2902757 | 3288 | + | 0.265815 |
exoc3 | DDB_G0293520 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232433 | CDS | 2981805 | 2352 | + | 0.274235 |
exoc4 | DDB_G0284833 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232431 | CDS | 2418843 | 3549 | - | 0.272753 |
exoc5 | DDB_G0287881 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232432 | CDS | 652393 | 2937 | - | 0.290092 |
exoc6 | DDB_G0293936 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232433 | CDS | 3528888 | 3078 | - | 0.273229 |
exoc7 | DDB_G0272991 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232429 | CDS | 2034015 | 2523 | - | 0.328973 |
exoc8 | DDB_G0279991 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232430 | CDS | 2824517 | 2448 | - | 0.250409 |
exosc10 | DDB_G0271572 | ortholog of mammalian EXOSC10 and yeast RRP6 exonuclease component of the nuclear exosome in human part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance | DDB0232429 | CDS | 601251 | 3588 | - | 0.298495 |
expl1 | DDB_G0267846 | similar to plant expansins which modify the cell wall to allow expansion during cell growth contains a predicted signal peptide | DDB0232428 | CDS | 962846 | 861 | + | 0.313589 |
expl2 | DDB_G0284677 | similar to plant expansins which modify the cell wall to allow expansion during cell growth contains a predicted signal peptide | DDB0232431 | CDS | 2331829 | 1224 | + | 0.363562 |
expl3 | DDB_G0276287 | similar to plant expansins which modify the cell wall to allow expansion during cell growth contains a predicted signal peptide expressed in prespore cells | DDB0232429 | CDS | 6577116 | 1008 | - | 0.281746 |
expl4_ps | DDB_G0279847 | putative pseudogene expansin-like family protein similar to plant expansins which modify the cell wall to allow expansion during cell growth | DDB0232430 | CDS | 2631222 | 534 | - | 0.299625 |
expl5 | DDB_G0276937 | similar to plant expansins which modify the cell wall to allow expansion during cell growth contains a predicted signal peptide | DDB0232429 | CDS | 7223776 | 717 | + | 0.322176 |
expl6 | DDB_G0267844 | similar to plant expansins which modify the cell wall to allow expansion during cell growth contains a predicted signal peptide | DDB0232428 | CDS | 961152 | 879 | + | 0.270762 |
expl7 | DDB_G0288331 | expressed in pstAB cells and in pstAB and stalk cells during the Mexican hat stage and culmination similar to plant expansins which modify the cell wall to allow expansion during cell growth but with a divergent carboxyl terminus contains a predicted signal peptide | DDB0232432 | CDS | 1399818 | 1662 | + | 0.377858 |
expl8 | DDB_G0293182 | similar to plant expansins which modify the cell wall to allow expansion during cell growth but with a divergent carboxyl terminus contains a predicted signal peptide | DDB0232433 | CDS | 2533687 | 1458 | + | 0.310014 |
expl9 | DDB_G0293148 | similar to plant expansins which modify the cell wall to allow expansion during cell growth but with a divergent carboxyl terminus contains a predicted signal peptide | DDB0232433 | CDS | 2538129 | 1608 | + | 0.31903 |
fadA | DDB_G0285211 | DDB0232431 | CDS | 2993554 | 1395 | - | 0.341219 | |
fadB | DDB_G0282147 | contains the histidine box motif characteristic of fatty acid desaturases expressed in pstO cells and upper cup during culmination | DDB0232430 | CDS | 5458911 | 1404 | - | 0.304843 |
fah | DDB_G0271094 | catalyzes the reaction 4-fumarylacetoacetate Hsub2subO acetoacetate fumarate | DDB0232428 | CDS | 3369734 | 1284 | - | 0.327882 |
fahd1 | DDB_G0275071 | DDB0232429 | CDS | 5119568 | 657 | + | 0.302892 | |
fahd2 | DDB_G0293650 | DDB0232433 | CDS | 3209379 | 918 | - | 0.308279 | |
fam18A | DDB_G0276319 | DDB0232429 | CDS | 6565732 | 597 | - | 0.308208 | |
fam18B | DDB_G0286703 | DDB0232431 | CDS | 4870527 | 786 | + | 0.300254 | |
fam21 | DDB_G0276221 | DDB0232429 | CDS | 6307785 | 4440 | - | 0.331532 | |
fam32 | DDB_G0283963 | DDB0232431 | CDS | 1382400 | 339 | - | 0.230089 | |
fam40 | DDB_G0288685 | DDB0232432 | CDS | 1813615 | 2742 | + | 0.243618 | |
fam45 | DDB_G0268448 | DDB0232428 | CDS | 1546946 | 1101 | - | 0.270663 | |
fam49 | DDB_G0272190 | DDB0232429 | CDS | 1409267 | 948 | - | 0.337553 | |
fam63A | DDB_G0269770 | DDB0232428 | CDS | 3523265 | 1188 | - | 0.289562 | |
fam63B | DDB_G0281445 | DDB0232430 | CDS | 4513064 | 1698 | + | 0.254417 | |
fam91 | DDB_G0274247 | DDB0232429 | CDS | 4146331 | 2793 | + | 0.253133 | |
fam96A | DDB_G0292558 | DDB0232433 | CDS | 1882209 | 453 | - | 0.233996 | |
fam96B | DDB_G0283801 | DDB0232431 | CDS | 1121919 | 492 | + | 0.264228 | |
fba | DDB_G0274375 | catalyzes the reaction fructose-16-bisphosphate dihydroxy-acetone-phosphate D-glyceraldehyde-3-phosphate expressed in pstAB cells and in upper cup during culmination | DDB0232429 | CDS | 3777877 | 1074 | - | 0.385475 |
fbl | DDB_G0269878 | utilizes the methyl donor S-adenosyl-L-methionine to catalyze the site-specific 2'-hydroxyl methylation of ribose moieties in pre-ribosomal RNA | DDB0232428 | CDS | 3783828 | 1005 | + | 0.418905 |
fbp | DDB_G0270836 | hydrolyses D-fructose 16-bisphosphate to D-fructose 6-phosphate and phosphate (EC 3.1.3.11) | DDB0232428 | CDS | 3681011 | 1041 | + | 0.354467 |
fbxA | DDB_G0276887 | F-box and WD40 domains containing protein part of a complex that targets proteins for ubiquination has the same domain composition as | DDB0232429 | CDS | 7333559 | 3744 | + | 0.311165 |
fcf1 | DDB_G0267606 | DDB0232428 | CDS | 408722 | 585 | + | 0.261538 | |
fcsA | DDB_G0269242 | catalyzes the reaction ATP a long-chain carboxylic acid CoA AMP diphosphate an acyl-CoA mediates the retrieval of fatty acids from endosomes to the cytoplasm | DDB0232428 | CDS | 2990411 | 2004 | - | 0.36477 |
fcsB | DDB_G0269474 | catalyzes the reaction ATP a long-chain carboxylic acid CoA AMP diphosphate an acyl-CoA | DDB0232428 | CDS | 2840597 | 2022 | + | 0.299703 |
fdfT | DDB_G0292072 | catalyzes the reaction farnesyl diphosphate diphosphate presqualene diphosphate | DDB0232433 | CDS | 1153510 | 1251 | + | 0.339728 |
fdxr | DDB_G0287353 | catlyzes the reaction: reduced ferredoxin NADP oxidized ferredoxin NADPH H | DDB0232432 | CDS | 169845 | 1548 | - | 0.26292 |
febA | DDB_G0291990 | DDB0232433 | CDS | 1041751 | 312 | + | 0.358974 | |
fhbA | DDB_G0292378 | DDB0232433 | CDS | 1649565 | 1194 | - | 0.333333 | |
fhbB | DDB_G0292380 | DDB0232433 | CDS | 1651520 | 1272 | - | 0.318396 | |
fhit | DDB_G0274257 | ortholog of human FHIT which is a possible tumor suppressor for specific tissues numerous tumor types are associated with aberrant forms of human FHIT protein | DDB0232429 | CDS | 4124527 | 450 | - | 0.311111 |
fhkA | DDB_G0293656 | CAMK group RAD53 family protein kinase similar to mammalian cell cycle checkpoint kinases chk2 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteinsbrbr bCommunity annotation:b The five fhk-X genes differ substantially in their response to the disruption of the retinoblastoma-like gene rblA. FhkA is substantially and highly signficantly upregulated in the ko strain while none of the other genes show major changes. Consistent with its regulation the fhkA promoter contains a putative E2F-type binding site (TTTGCGCCTTTT). Virtually all genes associated with replication fork progression are upregulated in the rblA disruptant these include cdc45 all mcm genes all gins genes all rfc genes four polA subunits three polD subunits two putatitive polE subunits PCNA the single-strand binding protein rfa1 the flap endonuclease repG as well as DNA ligase-1 and topoisomerase-2. All these genes show overexpression factors ranging from 4 to 15 | DDB0232433 | CDS | 3219230 | 1782 | - | 0.231201 |
fhkB | DDB_G0280599 | CAMK group RAD53 family protein kinase the protein kinase domain is similar to those of mammalian cell cycle checkpoint kinases chk2 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteins | DDB0232430 | CDS | 3548058 | 3429 | - | 0.26305 |
fhkC | DDB_G0281567 | CAMK group RAD53 family protein kinase similar to mammalian cell cycle checkpoint kinases chk2 and yeast RAD53 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteins | DDB0232430 | CDS | 4871788 | 1788 | + | 0.291387 |
fhkD | DDB_G0285963 | CAMK group RAD53 family protein kinase similar to mammalian cell cycle checkpoint kinases chk2 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteins | DDB0232431 | CDS | 3876403 | 2250 | - | 0.286667 |
fhkE | DDB_G0280321 | CAMK group RAD53 family protein kinase similar to mammalian cell cycle checkpoint kinases chk2 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteins | DDB0232430 | CDS | 3257414 | 2139 | + | 0.257597 |
fia | DDB_G0284389 | composed of a DUF292 domain at the amino terminus two filaminABP280 repeats and an actin domain at the carboxyl terminus | DDB0232431 | CDS | 1932445 | 2835 | - | 0.337919 |
fimA | DDB_G0277855 | calcium-regulated actin bundling protein binds F-actin enriched in gametes | DDB0232430 | CDS | 187950 | 1833 | - | 0.346427 |
fimC | DDB_G0278545 | contains 4 calponin homology (CH) domains two CH domains constitute one actin binding domain | DDB0232430 | CDS | 1046298 | 3642 | - | 0.266337 |
fimD | DDB_G0270762 | contains 4 calponin homology (CH) domains two CH domains constitute one actin binding domain | DDB0232428 | CDS | 4467278 | 5145 | + | 0.230709 |
fip-1 | DDB_G0273107 | interacts with filamin (abpC) and plays a role in development and phototaxis there is a second copy of this gene | DDB0232429 | CDS | 2554330 | 6141 | + | 0.224719 |
fip-2 | DDB_G0273839 | interacts with filamin (abpC) and plays a role in development and phototaxis there is a second copy of this gene | DDB0232429 | CDS | 3471006 | 6141 | - | 0.224719 |
fip1l1 | DDB_G0288797 | ortholog of yeast FIP1 and mmamalian FIP1L component of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs directly interacts with poly(A) polymerase | DDB0232432 | CDS | 1979163 | 1683 | + | 0.343434 |
flpA | DDB_G0286549 | DDB0232431 | CDS | 4784977 | 2148 | + | 0.268622 | |
fmoA | DDB_G0289779 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3265452 | 1578 | - | 0.255387 |
fmoB | DDB_G0271660 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232429 | CDS | 685414 | 1539 | - | 0.237167 |
fmoC | DDB_G0289605 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3016817 | 1566 | - | 0.244572 |
fmoD | DDB_G0289929 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3451742 | 1683 | + | 0.250743 |
fmoE | DDB_G0289931 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3453668 | 1614 | + | 0.245973 |
fmoF | DDB_G0289927 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3449477 | 1590 | + | 0.255346 |
fmoG | DDB_G0289925 | DDB0232432 | CDS | 3446671 | 1611 | + | 0.248293 | |
fncD2 | DDB_G0268216 | ortholog of Fanconi anaemia complementation group D2 protein involved DNA cross-link repair null mutant is sensitive to DNA damaging agents brbr mammalian ortholog is part of the Fanconi anaemia nuclear complex that includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 in human mutations in this gene cause Fanconi anaemia an autosomal recessive disorder affecting all bone marrow elements Dictyostelium has orthologs for | DDB0232428 | CDS | 1702484 | 5277 | - | 0.253932 |
fncE | DDB_G0279669 | putative ortholog of Fanconi anaemia complementation group E protein involved DNA cross-link repair null mutant is sensitive to DNA damaging agentsbrbr mammalian ortholog is part of the Fanconi anaemia nuclear complex that includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 in human mutations in this gene cause Fanconi anaemia an autosomal recessive disorder affecting all bone marrow elements Dictyostelium has orthologs for | DDB0232430 | CDS | 2411509 | 2265 | + | 0.240618 |
fncI | DDB_G0293476 | ortholog of Fanconi anaemia complementation group I protein involved DNA cross-link repair null mutant is sensitive to DNA damaging agents brbr mammalian ortholog is part of the Fanconi anaemia nuclear complex that includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 in human mutations in this gene cause Fanconi anaemia an autosomal recessive disorder affecting all bone marrow elements Dictyostelium has orthologs for | DDB0232433 | CDS | 2936457 | 5355 | + | 0.256209 |
fncJ | DDB_G0286621 | ortholog of Fanconi anaemia complementation group protein involved DNA cross-link repair also known as BRIP1 (BRCA1 Interacting Protein 1) however the Dicty gene appears to be missing the region that interacts with BRCA1 in the human protein unlike other members of the complex null mutant is not sensitive to DNA damaging agents brbr mammalian ortholog is part of the Fanconi anaemia nuclear complex that includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 in human mutations in this gene cause Fanconi anaemia an autosomal recessive disorder affecting all bone marrow elements Dictyostelium has orthologs for | DDB0232431 | CDS | 4729555 | 3237 | + | 0.296262 |
fncL | DDB_G0292744 | ortholog of Fanconi anaemia complementation group L protein involved DNA cross-link repair null mutant is sensitive to DNA damaging agents brbr mammalian ortholog is part of the Fanconi anaemia nuclear complex that includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 in human mutations in this gene cause Fanconi anaemia an autosomal recessive disorder affecting all bone marrow elements Dictyostelium has orthologs for | DDB0232433 | CDS | 2072501 | 1440 | - | 0.230556 |
fncM | DDB_G0274841 | ortholog of Fanconi anaemia complementation group M protein involved DNA cross-link repair null mutant is sensitive to DNA damaging agents brbr mammalian ortholog is part of the Fanconi anaemia nuclear complex that includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 in human mutations in this gene cause Fanconi anaemia an autosomal recessive disorder affecting all bone marrow elements Dictyostelium has orthologs for | DDB0232429 | CDS | 4112099 | 5370 | + | 0.280447 |
fnkA | DDB_G0275561 | protein kinase STE group | DDB0232429 | CDS | 5624593 | 2382 | + | 0.283375 |
fnkB | DDB_G0267934 | DDB0232428 | CDS | 1147906 | 1593 | - | 0.251726 | |
fnkC | DDB_G0276349 | contains a meprin and TRAF homology (MATH) domain and five Dictyostelium-specific FNIP repeats unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232429 | CDS | 6698814 | 3915 | + | 0.233716 |
fnkD-1 | DDB_G0273129 | contains six Dictyostelium-specific FNIP repeats unlikely to function as a kinase as it does not contain a catalytic aspartate there is a second copy of this gene | DDB0232429 | CDS | 2818823 | 2172 | - | 0.240792 |
fnkD-2 | DDB_G0273641 | contains six Dictyostelium-specific FNIP repeats unlikely to function as a kinase as it does not contain a catalytic aspartate there is a second copy of this gene | DDB0232429 | CDS | 3210585 | 2172 | + | 0.240792 |
fnkE | DDB_G0275879 | protein kinase domain similar to those of the mitogen-activated protein kinases which belong to the STE20 family contains two protein kinase domains one of which is predicted to be inactive contains several FNIP repeats | DDB0232429 | CDS | 5838829 | 3966 | + | 0.2824 |
fnkF_ps | DDB_G0275183 | putative pseudogene STEFNIP protein kinase family | DDB0232429 | CDS | 5290527 | 2628 | - | 0.270548 |
fnkG_ps-1 | DDB_G0273353 | putative pseudogene STEFNIP protein kinase family | DDB0232429 | CDS | 2671646 | 1275 | + | 0.247059 |
fnkG_ps-2 | DDB_G0273751 | putative pseudogene STEFNIP protein kinase family there is a second copy of this gene | DDB0232429 | CDS | 3358648 | 1275 | - | 0.247059 |
fntA | DDB_G0283053 | catalyzes the transfer of a farnesyl group or a geranylgeranyl group via a thioether linkage (-C-S-C-) to a cysteine at or near the carboxyl terminus of the protein forms a heterodimer with the | DDB0232431 | CDS | 15565 | 969 | - | 0.28483 |
fntB | DDB_G0270948 | catalyzes the transfer of a farnesyl group or a geranylgeranyl group via a thioether linkage (-C-S-C-) to a cysteine at or near the carboxyl terminus of the protein forms a heterodimer with the | DDB0232428 | CDS | 3561059 | 1503 | + | 0.27811 |
fol1 | DDB_G0278283 | multifunctional enzyme of the folic acid biosynthesis pathway has dihydropteroate synthetase dihydro-6-hydroxymethylpterin pyrophosphokinase and dihydroneopterin aldolase domains | DDB0232430 | CDS | 616133 | 1974 | - | 0.267477 |
folC | DDB_G0292632 | catalyzes the reaction L-glutamate H4PteGlu(n) ATP H4PteGlu(n1) phosphate ADP responsible for the addition of a polyglutamate tail to folate and folate derivatives | DDB0232433 | CDS | 1872495 | 1881 | + | 0.279638 |
forA | DDB_G0279607 | DDB0232430 | CDS | 2388583 | 3657 | + | 0.346185 | |
forB | DDB_G0282297 | DDB0232430 | CDS | 5641699 | 3381 | + | 0.313812 | |
forC | DDB_G0287295 | formin that contains an N-terminal GBD domain as well as FH2 and FH3 domains but lacks the FH1 domain | DDB0232432 | CDS | 212611 | 3477 | - | 0.297095 |
forD | DDB_G0282245 | DDB0232430 | CDS | 5565585 | 3645 | + | 0.310837 | |
forE | DDB_G0269626 | DDB0232428 | CDS | 3176439 | 4686 | + | 0.316261 | |
forF | DDB_G0289763 | diaphanous related formin that binds profilin and is a weak actin nucleator involved in development and phototaxis.br bNomenclature conflict:b Do not confuse this gene with dia1 named for the differentiation associated protein | DDB0232432 | CDS | 3237701 | 3663 | - | 0.323778 |
forG | DDB_G0277175 | DDB0232429 | CDS | 7682673 | 3225 | - | 0.310698 | |
forH | DDB_G0285589 | required for filopodia formation and maintenance through removal of capping protein and actin polymerization also important for spherical cell morphology and resulting pseudopod orientation towards a cAMP gradient | DDB0232431 | CDS | 3415704 | 3264 | + | 0.321078 |
forI | DDB_G0284519 | DDB0232431 | CDS | 2097497 | 2808 | + | 0.275641 | |
forJ | DDB_G0291378 | contains a SMADFHA domain an actin-binding FH2 (formin homology 2) domain and a RmlC-like cupin domain | DDB0232433 | CDS | 205952 | 7641 | + | 0.272085 |
fpaA | DDB_G0269230 | component of the SCF ubiquitin ligase complex the fpaA gene encodes a protein almost identical to that of fpaB differing in one amino acid only series of glycosylation reactions attaches a pentasaccharide chain to HyPro143 | DDB0232428 | CDS | 3989908 | 489 | - | 0.329243 |
fpaB-1 | DDB_G0273251 | component of the SCF ubiquitin ligase complex the fpaB gene encodes a protein almost identical to that of fpaA differing in one amino acid only series of glycosylation reactions attaches a pentasaccharide chain to HyPro143 there is a second copy of this gene | DDB0232429 | CDS | 2857157 | 489 | - | 0.331288 |
fpaB-2 | DDB_G0273615 | component of the SCF ubiquitin ligase complex the fpaB gene encodes a protein almost identical to that of fpaA differing in one amino acid only series of glycosylation reactions attaches a pentasaccharide chain to HyPro143 there is a second copy of this gene | DDB0232429 | CDS | 3173987 | 489 | + | 0.331288 |
fpgt | DDB_G0285257 | ortholog of the fucose-1-phosphate guanylyltransferase conserved among higher eukaryotes and in Dictyostelium catalyzes the reaction: GTP beta-L-fucose 1-phosphate diphosphate GDP-L-fucose | DDB0232431 | CDS | 3022479 | 1884 | + | 0.234607 |
fps | DDB_G0278735 | target for bisphosphonate drugs catalyzes the reaction geranyl diphosphate isopentenyl diphosphate diphosphate transtrans-farnesyl diphosphate | DDB0232430 | CDS | 1245549 | 1149 | - | 0.317668 |
fray1 | DDB_G0278863 | kinase domain similar to OSR1 (oxidative stress responsive 1) kinases and other STE20-like kinasesbrbr bCommunity annotation:b Fray1 and Fray2 represent the FRAY-subfamily of Ste20-like kinases in D. discoideum (see | DDB0232430 | CDS | 1298188 | 1725 | - | 0.338551 |
fray2 | DDB_G0276577 | the kinase domain is similar to mammalian stress-induced STK and OSR1 (oxidative stress responsive 1) kinases and other STE20-like kinasesbrbr bCommunity annotation:b Fray1 and Fray2 represent the FRAY-subfamily of Ste20-like kinases in D. discoideum (see | DDB0232429 | CDS | 6994954 | 3087 | - | 0.339164 |
frmA | DDB_G0291303 | involved in substrate adhesion by regulating the turnover of paxillintalin adhesion sites also involved in cell-cell adhesion and affecting tip formation during development. | DDB0232433 | CDS | 93960 | 3465 | - | 0.294372 |
frmB | DDB_G0269362 | Band 4.1 contains the FERM domain found in a number of cytoskeletal-associated proteins and involved in the linkage of cytoplasmic proteins to the membrane | DDB0232428 | CDS | 2609297 | 1437 | - | 0.320807 |
frpA | DDB_G0292068 | contains two N-terminal calponin homology (CH) domains which is similar to fimbrins and a long unrelated C-terminal tail | DDB0232433 | CDS | 1144263 | 3291 | - | 0.267396 |
fscA | DDB_G0289725 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains | DDB0232432 | CDS | 3167501 | 1650 | - | 0.2 |
fscB | DDB_G0282989 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232431 | CDS | 107175 | 1311 | + | 0.234935 |
fscC | DDB_G0292204 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232433 | CDS | 1266213 | 1536 | + | 0.276693 |
fscD | DDB_G0272240 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232429 | CDS | 1725983 | 1323 | + | 0.287226 |
fscE | DDB_G0272306 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232429 | CDS | 1727972 | 1332 | + | 0.268018 |
fscF | DDB_G0292064 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232433 | CDS | 1134651 | 1371 | + | 0.22903 |
fscG | DDB_G0292156 | has similarity to G-protein-coupled receptors frizzled and smoothened like proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232433 | CDS | 1137104 | 1362 | + | 0.236417 |
fscH | DDB_G0292100 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232433 | CDS | 1184434 | 1602 | - | 0.22784 |
fscJ | DDB_G0292102 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232433 | CDS | 1187184 | 1224 | - | 0.296569 |
fsjA | DDB_G0280483 | ortholog of the RrmJFtsJ ribosomal RNA methyltransferase a well conserved heat shock protein present in prokaryotes archaea and eukaryotes responsible for methylating 23 S rRNA | DDB0232430 | CDS | 3432872 | 813 | - | 0.264453 |
fsjB | DDB_G0271998 | RrmJFtsJ ribosomal RNA methyltransferase family member well conserved heat shock proteins present in prokaryotes archaea and eukaryotes similar to S. cerevisiae MRM2 required for methylation of U(2791) in 21S rRNA | DDB0232429 | CDS | 1135748 | 1923 | - | 0.24753 |
fsjC | DDB_G0284945 | RrmJFtsJ ribosomal RNA methyltransferase family member well conserved heat shock proteins present in prokaryotes archaea and eukaryotes this is the ortholog of H. sapiens FTSJ3 involved in rRNA processing and 60S ribosomal subunit maturation (yeast) | DDB0232431 | CDS | 2672551 | 2502 | - | 0.321343 |
fslA | DDB_G0284761 | similar to G-protein-coupled receptors contains 7 putative transmembrane domains and a potential signal sequence | DDB0232431 | CDS | 2445394 | 1785 | - | 0.270588 |
fslB | DDB_G0270730 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a potential signal sequence | DDB0232428 | CDS | 4235323 | 1929 | - | 0.258683 |
fslC | DDB_G0274287 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains | DDB0232429 | CDS | 4049951 | 1908 | + | 0.241614 |
fslD | DDB_G0269528 | similar to G-protein-coupled receptorsfrizzled proteins contains 7 putative transmembrane domains and a potential signal sequence | DDB0232428 | CDS | 2948285 | 1905 | - | 0.272441 |
fslE | DDB_G0288269 | similar to G-protein-coupled receptors weak frizzled cystein-rich domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232432 | CDS | 1290029 | 1830 | - | 0.281421 |
fslF | DDB_G0288253 | similar to G-protein-coupled receptors weak frizzled cystein-rich domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232432 | CDS | 1292298 | 1776 | - | 0.279279 |
fslG | DDB_G0288261 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a putative signal peptide | DDB0232432 | CDS | 1308843 | 1725 | + | 0.277101 |
fslH | DDB_G0274773 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a putative signal peptide | DDB0232429 | CDS | 3799719 | 1866 | + | 0.296892 |
fslJ-1 | DDB_G0272885 | identified as a suppressor of smlA null mutant cnr1 putative cell number regulator there is a second copy of this gene | DDB0232429 | CDS | 2364367 | 1824 | + | 0.284539 |
fslJ-2 | DDB_G0274011 | identified as a suppressor of smlA null mutant cnr1 putative cell number regulator there is a second copy of this gene | DDB0232429 | CDS | 3664882 | 1824 | - | 0.284539 |
fslK | DDB_G0284729 | similar to G-protein-coupled receptors predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232431 | CDS | 2327899 | 1743 | + | 0.27883 |
fslL | DDB_G0284585 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a potential signal sequence | DDB0232431 | CDS | 2184288 | 1860 | + | 0.254301 |
fslM-1 | DDB_G0273035 | has similarity to G-protein-coupled receptors predicted to have 7 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 2339145 | 1872 | - | 0.259615 |
fslM-2 | DDB_G0274033 | has similarity to G-protein-coupled receptors predicted to have 7 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 3690459 | 1872 | + | 0.259615 |
fslN | DDB_G0270672 | has similarity to G-protein-coupled receptors predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232428 | CDS | 3740758 | 1836 | - | 0.249455 |
fslO | DDB_G0278289 | has similarity to G-protein-coupled receptors predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232430 | CDS | 625261 | 2088 | + | 0.257663 |
fslP | DDB_G0286607 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins predicted to have 7 transmembrane domains | DDB0232431 | CDS | 4697072 | 1764 | - | 0.250567 |
fslQ | DDB_G0286609 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins predicted to have 7 transmembrane domains | DDB0232431 | CDS | 4699815 | 1737 | - | 0.242948 |
fspA | DDB_G0277237 | contains 9 putative transmembrane domains potential chemosensory G-protein coupled receptor which may play a role in intracellular signalling | DDB0232429 | CDS | 7761649 | 1002 | - | 0.216567 |
fszA | DDB_G0277721 | DDB0232429 | CDS | 8463906 | 1554 | + | 0.310811 | |
fszB | DDB_G0269224 | DDB0232428 | CDS | 4529920 | 1101 | + | 0.266122 | |
ftcd | DDB_G0287977 | folate-dependent enzyme displaying both transferase and deaminase activity defects of FTCD in human cause glutamate formiminotransferase deficiency also known as formiminoglutamicaciduria (FIGLU-uria) | DDB0232432 | CDS | 919913 | 1614 | - | 0.350682 |
fthS | DDB_G0290397 | catalyzes the reaction ATP formate tetrahydrofolate ADP phosphate N10-formyl-Hsub4subF in various biosynthetic pathways in plants and in Dictyostelium this is a monofunctional enzyme while in yeast and in metazoan the same enzyme has two additional activities encoded by | DDB0232432 | CDS | 4031914 | 1917 | + | 0.383933 |
fttB | DDB_G0269138 | localizes to the cell cortex binds myosin II and regulates microtubule length the cortical cytoskeleton and cytokinesis functions in the same pathway as racE to regulate these processes | DDB0232428 | CDS | 3949672 | 759 | + | 0.361001 |
fuk | DDB_G0269678 | catalyzes the reaction: ATP L-fucose ADP beta-L-fucose 1-phosphate | DDB0232428 | CDS | 3301231 | 4215 | - | 0.288493 |
fumH | DDB_G0280495 | catalyzes the reaction (S)-malate fumarate Hsub2subO hydrates fumarate into malate in the TCA | DDB0232430 | CDS | 3450744 | 2859 | + | 0.368311 |
fut1 | DDB_G0284467 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2125012 | 1170 | + | 0.249573 |
fut10 | DDB_G0286889 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 5027996 | 1998 | - | 0.287287 |
fut11 | DDB_G0268190 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232428 | CDS | 1637375 | 2457 | + | 0.282865 |
fut2 | DDB_G0284775 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2469559 | 2334 | + | 0.212939 |
fut3 | DDB_G0274297 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232429 | CDS | 4081769 | 1506 | + | 0.260292 |
fut4 | DDB_G0284551 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2055453 | 1398 | - | 0.288984 |
fut5 | DDB_G0284505 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2066316 | 1389 | + | 0.267819 |
fut6 | DDB_G0284503 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2064096 | 1392 | + | 0.295259 |
fut7 | DDB_G0283287 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 463265 | 1485 | + | 0.246465 |
fut8 | DDB_G0280571 | distant relative of CAZy family GT23 catalyzes N-linked glycosylation | DDB0232430 | CDS | 3514430 | 1812 | + | 0.175497 |
fut9 | DDB_G0293768 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232433 | CDS | 3300772 | 1668 | - | 0.311151 |
fxn | DDB_G0293246 | yeast and human orthologs regulates mitochondrial iron accumulation mutations in human homolog cause Friedrich's ataxia | DDB0232433 | CDS | 2633195 | 582 | - | 0.261168 |
g6pd-1 | DDB_G0273131 | ortholog of the human G6PD defects in G6PD cause chronic non-spherocytic hemolytic anemia (CNSHA) catalyzes the reaction D-glucose 6-phosphate NADPsupsup D-glucono-15-lactone 6-phosphate NADPH Hsupsup there is a second copy of this gene | DDB0232429 | CDS | 2821995 | 1494 | - | 0.32664 |
g6pd-2 | DDB_G0273639 | ortholog of the human G6PD defects in G6PD cause chronic non-spherocytic hemolytic anemia (CNSHA) catalyzes the reaction D-glucose 6-phosphate NADPsupsup D-glucono-15-lactone 6-phosphate NADPH Hsupsup there is a second copy of this gene | DDB0232429 | CDS | 3207904 | 1494 | + | 0.32664 |
gaa | DDB_G0269790 | ortholog of the H. sapiens lysosomal alpha-glucosidase which is essential for the degradation of glygogen to glucose in lysosomes defects in GAA are the cause of glycogen storage disease II a recessive disorder which results in a massive accumulation of glycogen in muscle heart and liver leading to a life expectancy of less than two years | DDB0232428 | CDS | 3563596 | 2604 | + | 0.329493 |
gabT | DDB_G0268104 | catalyzes the degradation of GABA :4-aminobutanoate 2-oxoglutarate succinate semialdehyde L-glutamate null mutant has a very mild developmental delay | DDB0232428 | CDS | 1461475 | 1488 | + | 0.370296 |
gacA | DDB_G0278381 | DDB0232430 | CDS | 800738 | 1017 | - | 0.292035 | |
gacB | DDB_G0278549 | DDB0232430 | CDS | 1056077 | 822 | - | 0.214112 | |
gacC | DDB_G0284571 | DDB0232431 | CDS | 2170033 | 1200 | - | 0.288333 | |
gacD | DDB_G0291021 | DDB0232432 | CDS | 4903913 | 1545 | - | 0.311327 | |
gacE | DDB_G0293654 | DDB0232433 | CDS | 3215377 | 3399 | + | 0.28832 | |
gacEE | DDB_G0291840 | DDB0232433 | CDS | 819813 | 1713 | + | 0.258611 | |
gacF | DDB_G0274243 | DDB0232429 | CDS | 4221285 | 3423 | + | 0.274613 | |
gacFF | DDB_G0275085 | DDB0232429 | CDS | 5154689 | 2658 | + | 0.265613 | |
gacG | DDB_G0283955 | DDB0232431 | CDS | 1364111 | 3939 | - | 0.25311 | |
gacGG | DDB_G0280093 | DDB0232430 | CDS | 2923710 | 3612 | - | 0.295958 | |
gacH | DDB_G0272694 | DDB0232429 | CDS | 1957484 | 1701 | + | 0.282187 | |
gacHH | DDB_G0272080 | DDB0232429 | CDS | 1238870 | 4572 | - | 0.302275 | |
gacI | DDB_G0275185 | DDB0232429 | CDS | 5262569 | 2400 | - | 0.281667 | |
gacII | DDB_G0278069 | DDB0232430 | CDS | 221612 | 2454 | + | 0.293806 | |
gacJ | DDB_G0285641 | DDB0232431 | CDS | 3519879 | 2721 | + | 0.299522 | |
gacJJ | DDB_G0290873 | DDB0232432 | CDS | 4700102 | 2622 | + | 0.300153 | |
gacK | DDB_G0285915 | DDB0232431 | CDS | 3822394 | 2913 | - | 0.296601 | |
gacL | DDB_G0290891 | DDB0232432 | CDS | 4722780 | 2205 | - | 0.28254 | |
gacM | DDB_G0287895 | DDB0232432 | CDS | 800059 | 2691 | + | 0.285396 | |
gacN | DDB_G0279315 | DDB0232430 | CDS | 1925209 | 1836 | - | 0.259804 | |
gacO | DDB_G0267568 | DDB0232428 | CDS | 355159 | 2055 | - | 0.323114 | |
gacP | DDB_G0279009 | DDB0232430 | CDS | 1510645 | 1731 | + | 0.317158 | |
gacQ | DDB_G0282395 | DDB0232430 | CDS | 5696610 | 1596 | - | 0.287594 | |
gacR | DDB_G0278755 | DDB0232430 | CDS | 1120346 | 2352 | - | 0.306122 | |
gacS | DDB_G0276833 | DDB0232429 | CDS | 7423496 | 3081 | + | 0.270042 | |
gacT | DDB_G0285163 | weakly similar to similar to RalA binding protein 1 REMI mutant forms aberrant fruiting bodies see | DDB0232431 | CDS | 2946825 | 3030 | - | 0.313531 |
gacU | DDB_G0272925 | DDB0232429 | CDS | 2028796 | 3495 | - | 0.264092 | |
gacV | DDB_G0293510 | DDB0232433 | CDS | 2976341 | 1563 | + | 0.252719 | |
gacW | DDB_G0290439 | DDB0232432 | CDS | 4129372 | 3348 | - | 0.312724 | |
gacX | DDB_G0288205 | DDB0232432 | CDS | 1235608 | 1692 | + | 0.309693 | |
gacY | DDB_G0281739 | DDB0232430 | CDS | 4898948 | 2166 | - | 0.339797 | |
gacZ | DDB_G0269496 | DDB0232428 | CDS | 2878932 | 3132 | - | 0.258301 | |
gadA | DDB_G0280199 | catalyzes the reaction L-glutamate 4-aminobutanoate COsub2sub expressed during development and enriched in prespore cells | DDB0232430 | CDS | 3097322 | 1389 | - | 0.339813 |
gadB | DDB_G0288715 | catalyzes the reaction L-glutamate 4-aminobutanoate COsub2sub expressed in vegetative cells | DDB0232432 | CDS | 1865900 | 1392 | + | 0.310345 |
gafA | DDB_G0271136 | contains a GAF domain (cGMP-specific and stimulated PDEs Anabaena adenylate cyclases and E. coli FhlA) | DDB0232429 | CDS | 83383 | 477 | + | 0.291405 |
galE | DDB_G0275295 | catalyzes the reaction UDP-glucose UDP-galactose expressed in prespore cells | DDB0232429 | CDS | 5253249 | 1035 | + | 0.343961 |
galK | DDB_G0292112 | DDB0232433 | CDS | 1203261 | 1506 | + | 0.317397 | |
gapA | DDB_G0269140 | DDB0232428 | CDS | 3059126 | 2583 | - | 0.297716 | |
gatA | DDB_G0286875 | catalyzes the reaction ATP L-glutamyl-tRNA(Gln) L-glutamine ADP phosphate L-glutaminyl-tRNA(Gln) L-glutamate | DDB0232431 | CDS | 5011319 | 1653 | + | 0.260738 |
gatB | DDB_G0268776 | catalyzes the reaction ATP L-glutamyl-tRNA(Gln) L-glutamine ADP phosphate L-glutaminyl-tRNA(Gln) L-glutamate | DDB0232428 | CDS | 2075252 | 1617 | + | 0.260359 |
gatC | DDB_G0284291 | catalyzes the reaction ATP L-glutamyl-tRNA(Gln) L-glutamine ADP phosphate L-glutaminyl-tRNA(Gln) L-glutamate | DDB0232431 | CDS | 1839037 | 300 | - | 0.276667 |
gbfA | DDB_G0288755 | DDB0232432 | CDS | 1923643 | 2127 | + | 0.316878 | |
gbpC | DDB_G0291079 | member of the TKL (tyrosine kinase-like) group and ROCO family of protein kinases belongs to the LRRK family of protein kinases contains LRR Roc COR RasGEF protein kinase DEP cyclic nucleotide-binding and GRAM domains involved in cGMP-mediated chemotaxis catalyzes GDP to GTP exchange on its own Roc domain translocates from cytoplasm to cell cortex after cAMP stimulation GRAM domain binds directly to plasma membrane | DDB0232432 | CDS | 4959991 | 7896 | + | 0.333967 |
gbpD | DDB_G0282373 | guanine nucleotide exchange factor for Rap1 involved in cell-substrate adhesion | DDB0232430 | CDS | 6118341 | 3939 | + | 0.289667 |
gbqA | DDB_G0280965 | related to guanine nucleotide-binding protein REMI mutant forms aberrant fruiting bodies see | DDB0232430 | CDS | 4042692 | 1746 | - | 0.272623 |
gcA | DDB_G0275009 | DDB0232429 | CDS | 5230828 | 4452 | + | 0.277403 | |
gcdh | DDB_G0283411 | catalyzes the reaction glutaryl-CoA acceptor crotonoyl-CoA COsub2sub reduced acceptor belongs to the acyl-CoA dehydrogenase family | DDB0232431 | CDS | 638800 | 1263 | - | 0.374505 |
gchA | DDB_G0288481 | catalyzes the reaction GTP 2 Hsub2subO formate 2-amino-4-hydroxy-6-(erythro-123-trihydroxypropyl)-dihydropteridine triphosphate the first step in the biosynthesis of tetrahydropteridines which have been shown to regulate G-protein coupled signalling the gchA gene is expressed and the enzyme is active during the onset of Dictyostelium development | DDB0232432 | CDS | 1602765 | 699 | - | 0.314735 |
gcn5 | DDB_G0283459 | DDB0232431 | CDS | 727119 | 1239 | - | 0.284907 | |
gcsA | DDB_G0284651 | catalyzes the reaction ATP L-glutamate L-cysteine ADP phosphate gamma-L-glutamyl-L-cysteine the first and limiting step in glutathione (GSH) biosynthesis | DDB0232431 | CDS | 2291954 | 1881 | + | 0.289739 |
gcvH1 | DDB_G0287773 | DDB0232432 | CDS | 678742 | 441 | + | 0.326531 | |
gcvH2 | DDB_G0290845 | DDB0232432 | CDS | 4668574 | 453 | - | 0.304636 | |
gcvH3 | DDB_G0287791 | DDB0232432 | CDS | 709302 | 450 | + | 0.26 | |
gcvH4 | DDB_G0287795 | DDB0232432 | CDS | 711021 | 630 | - | 0.177778 | |
gcvH5 | DDB_G0287861 | DDB0232432 | CDS | 711961 | 492 | - | 0.182927 | |
gcvP | DDB_G0287255 | catalyzes the reaction glycine H-protein-lipoyllysine H-protein-S-aminomethyldihydrolipoyllysine COsub2sub | DDB0232432 | CDS | 44049 | 2985 | - | 0.352094 |
gcvT | DDB_G0292326 | catalyzes the reaction protein-S-aminomethyldihydrolipoyllysine tetrahydrofolate protein-dihydrolipoyllysine 510-methylenetetrahydrofolate NHsub3sub | DDB0232433 | CDS | 1484064 | 1212 | - | 0.348185 |
gdap2 | DDB_G0284349 | ortholog of the human GDAP2 protein contains an Appr-1-p processing domain and a C-terminal cellular retinaldehyde-bindingtriple function domain | DDB0232431 | CDS | 1866926 | 1707 | - | 0.246632 |
gdcA | DDB_G0269202 | DDB0232428 | CDS | 3314988 | 1134 | - | 0.363316 | |
gdt1 | DDB_G0278723 | represses discoidin expression member of the TKL (tyrosine kinase-like) group and the GDT family unlikely to function as a kinase as it does not contain a catalytic aspartate putative transmembrane protein | DDB0232430 | CDS | 1161694 | 4986 | - | 0.239872 |
gdt10_ps | DDB_G0270548 | putative pseudogene related to the GDT (growth-development transition) family of protein kinases | DDB0232428 | CDS | 2919137 | 1644 | + | 0.275547 |
gdt2 | DDB_G0270666 | member of the TKL (tyrosine kinase-like) group and the GDT family putative transmembrane protein | DDB0232428 | CDS | 3713353 | 4914 | - | 0.252747 |
gdt3_ps | DDB_G0285891 | putative pseudogene member of the TKL (tyrosine kinase-like) group and the GDT family belongs to the MLK protein kinase family | DDB0232431 | CDS | 3781232 | 5880 | - | 0.234014 |
gdt4 | DDB_G0270550 | member of the TKL (tyrosine kinase-like) group and the GDT family putative transmembrane protein | DDB0232428 | CDS | 2926042 | 4863 | + | 0.265474 |
gdt5 | DDB_G0285895 | highly similar to other Dictyostelium GDT proteins however it does not contain a protein kinase domain | DDB0232431 | CDS | 3790076 | 3531 | - | 0.296233 |
gdt6 | DDB_G0270544 | member of the TKL (tyrosine kinase-like) group and the GDT family unlikely to function as a kinase as it does not contain a catalytic aspartate putative transmembrane protein | DDB0232428 | CDS | 2913781 | 4359 | + | 0.274145 |
gdt7 | DDB_G0292314 | highly similar to other Dictyostelium GDT proteins however it does not contain a protein kinase domain | DDB0232433 | CDS | 1457514 | 2406 | + | 0.293433 |
gdt8 | DDB_G0270668 | member of the TKL (tyrosine kinase-like) group and the GDT family putative transmembrane protein | DDB0232428 | CDS | 3723386 | 3981 | - | 0.283848 |
gdt9 | DDB_G0278879 | DDB0232430 | CDS | 1327589 | 4734 | + | 0.274398 | |
gefA | DDB_G0284329 | guanine nucleotide exchange factor for RasC promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form required for adenylyl cyclase activation | DDB0232431 | CDS | 1926792 | 1818 | + | 0.338834 |
gefAA | DDB_G0289613 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232432 | CDS | 3026939 | 4116 | - | 0.276968 |
gefB | DDB_G0269222 | DDB0232428 | CDS | 3539581 | 4590 | - | 0.252288 | |
gefBB | DDB_G0278867 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232430 | CDS | 1304620 | 6153 | - | 0.25516 |
gefC | DDB_G0282381 | DDB0232430 | CDS | 6243320 | 4374 | - | 0.299268 | |
gefD | DDB_G0289667 | DDB0232432 | CDS | 3140427 | 2007 | + | 0.256104 | |
gefE | DDB_G0269252 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232428 | CDS | 4047424 | 3114 | + | 0.279705 |
gefF | DDB_G0293006 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232433 | CDS | 2493284 | 3384 | - | 0.330378 |
gefG | DDB_G0272032 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232429 | CDS | 1107152 | 4671 | + | 0.293513 |
gefH | DDB_G0276963 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232429 | CDS | 7245854 | 1815 | + | 0.295868 |
gefI | DDB_G0277915 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232430 | CDS | 332007 | 2475 | + | 0.300606 |
gefJ | DDB_G0277913 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232430 | CDS | 202964 | 2439 | - | 0.312833 |
gefK | DDB_G0290901 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232432 | CDS | 4729019 | 4674 | + | 0.272786 |
gefL | DDB_G0276371 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232429 | CDS | 6706766 | 7071 | - | 0.28327 |
gefM | DDB_G0274607 | promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form required for adenylate cyclase activation and chemotaxis | DDB0232429 | CDS | 4024908 | 2790 | + | 0.294982 |
gefN | DDB_G0275703 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232429 | CDS | 5741117 | 3417 | + | 0.279778 |
gefO | DDB_G0290267 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232432 | CDS | 3875194 | 2835 | + | 0.274427 |
gefP | DDB_G0281573 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232430 | CDS | 4826796 | 4509 | - | 0.278998 |
gefQ | DDB_G0289665 | DDB0232432 | CDS | 3085619 | 3897 | + | 0.254298 | |
gefR | DDB_G0274605 | guanine nucleotide exchange factor required for maximal activation of RasGbr bNomenclature conflictb: gefR was originally named RasGEFA in the Insall lab as it was the second RasGEF (after aimless) to be identified there. When aimless (aleA) was renamed gefA to make the nomenclature consistent and systematic RasGEFA was renamed gefR. All published literature refers to the GEFs correctly but Kae et al. (2007) and other documents occasionally refer to the older name. | DDB0232429 | CDS | 4075525 | 5166 | + | 0.291134 |
gefS | DDB_G0271868 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232429 | CDS | 960951 | 3132 | + | 0.296296 |
gefV | DDB_G0268578 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form contains a RasGEF domain and 10 leucine-rich repeats | DDB0232428 | CDS | 1563062 | 5949 | + | 0.291478 |
gefW | DDB_G0267666 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form similar to son of sevenless | DDB0232428 | CDS | 533108 | 3519 | + | 0.276783 |
gefX | DDB_G0269298 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family contains RasGEF nucleotide exchange factor domain | DDB0232428 | CDS | 2476607 | 2883 | - | 0.312522 |
gefY | DDB_G0276019 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form similar to son of sevenless | DDB0232429 | CDS | 6203910 | 4527 | + | 0.280318 |
gemA | DDB_G0267830 | simlar to M. musculus mitochondrial Rho1 and S. cerevisiae GEM1 a conserved tail-anchored outer mitochondrial membrane GTPase contains two GTP-binding domains two EF hand domains and a C-terminal transmembrane domain | DDB0232428 | CDS | 929880 | 1977 | - | 0.265048 |
gemin1 | DDB_G0276357 | putative ortholog of Gemin 1SNM1 (Survival of motor neuron protein 1) a component of Cajal bodies (CBs) and Gems nuclear organelles responsible for spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis | DDB0232429 | CDS | 6720252 | 1113 | + | 0.250674 |
gemin2 | DDB_G0287253 | ortholog of Gemin 2SIP1 (Survival of motor neuron protein-interacting protein 1) a component of Cajal bodies (CBs) and Gems nuclear organelles responsible for spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis | DDB0232432 | CDS | 33457 | 996 | + | 0.247992 |
gemin5 | DDB_G0288425 | ortholog of Gemin 5 a component of Cajal bodies (CBs) and Gems nuclear organelles responsible for spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis | DDB0232432 | CDS | 1517710 | 3831 | + | 0.257113 |
ger | DDB_G0270184 | catalyzes the reaction GDP-L-fucose NADP GDP-4-dehydro-6-deoxy-D-mannose NADPH H | DDB0232428 | CDS | 4379266 | 963 | - | 0.284528 |
gerA | DDB_G0287293 | DDB0232432 | CDS | 191929 | 384 | + | 0.330729 | |
gerB | DDB_G0287687 | DDB0232432 | CDS | 706104 | 384 | - | 0.3125 | |
gerC | DDB_G0287583 | DDB0232432 | CDS | 460750 | 384 | + | 0.330729 | |
gerD | DDB_G0291856 | DDB0232433 | CDS | 926086 | 4338 | + | 0.297372 | |
gerE | DDB_G0286551 | contains numerous TETP repeats expressed specifically in spores | DDB0232431 | CDS | 4754201 | 1374 | - | 0.306405 |
gflB | DDB_G0286773 | similar to son of sevenless contains RhoGAP and RasGEF domains | DDB0232431 | CDS | 4946624 | 4806 | - | 0.332501 |
gflC | DDB_G0270880 | contains a plant homeodomain (PHD) finger motif no other sequence similarity exists outside this small domain | DDB0232428 | CDS | 2933712 | 5163 | - | 0.270385 |
gflC_ps | DDB_G0293458 | putative pseudogene fragment similar to D. discoideum gene | DDB0232433 | CDS | 2917476 | 264 | + | 0.359848 |
gflD | DDB_G0279569 | contains RhoGAP and RasGEF domains and a GRAM domain which is found in membrane-associated proteins | DDB0232430 | CDS | 2272081 | 5298 | - | 0.245564 |
gfm1 | DDB_G0270482 | DDB0232428 | CDS | 2561561 | 2205 | + | 0.329252 | |
gfm2 | DDB_G0267766 | DDB0232428 | CDS | 806804 | 2298 | - | 0.29765 | |
gghA | DDB_G0286535 | DDB0232431 | CDS | 4609676 | 954 | - | 0.328092 | |
gghB | DDB_G0289365 | DDB0232432 | CDS | 2708637 | 1044 | - | 0.229885 | |
ggps1 | DDB_G0293588 | ortholog of the mammalian geranylgeranyl diphosphate synthase 1 includes the enzymes dimethylallyltransferase (EC 2.5.1.1) geranyltranstransferase (EC 2.5.1.10) and farnesyltranstransferase (EC 2.5.1.29) | DDB0232433 | CDS | 3093908 | 912 | - | 0.25 |
ggtA | DDB_G0274103 | CAZy family GT24 catalyzes N-linked glucosylation REMI mutant forms aberrant fruiting bodies see | DDB0232429 | CDS | 4091903 | 5046 | - | 0.275664 |
gins1 | DDB_G0289271 | subunit 1 of the conserved replication complex GINS which is essential for initiation of DNA replication in X. laevis | DDB0232432 | CDS | 2571168 | 576 | + | 0.243056 |
gins2 | DDB_G0293564 | subunit 2 of the conserved replication complex GINS which is essential for initiation of DNA replication in X. laevis | DDB0232433 | CDS | 3050595 | 672 | - | 0.25 |
gins3 | DDB_G0291506 | subunit 3 of the conserved replication complex GINS which is essential for initiation of DNA replication in X. laevis | DDB0232433 | CDS | 450396 | 798 | - | 0.211779 |
gins4 | DDB_G0269324 | subunit 4 of the conserved replication complex GINS which is essential for initiation of DNA replication in X. laevis | DDB0232428 | CDS | 2543534 | 636 | - | 0.210692 |
glb1 | DDB_G0290217 | belongs to glycoside hydrolase family 35 hydrolyzes terminal non-reducing beta-D-galactose residues in beta-D-galactoside has a signal peptide | DDB0232432 | CDS | 3809656 | 2016 | - | 0.312996 |
glb2 | DDB_G0285637 | belongs to glycoside hydrolase family 35 hydrolyzes terminal non-reducing beta-D-galactose residues in beta-D-galactoside has a signal peptide | DDB0232431 | CDS | 3510010 | 2286 | - | 0.279528 |
glcS | DDB_G0267674 | CAZy family GT3 catalyzes the reaction UDP-glucose (14-alpha-D-glucosyl)(n) UDP (14-alpha-D-glucosyl)(n1) | DDB0232428 | CDS | 545194 | 2637 | + | 0.323853 |
glgB | DDB_G0274105 | transfers a segment of a 14-alpha-D-glucan chain to a primary hydroxyl group in a similar glucan chain | DDB0232429 | CDS | 4089271 | 2037 | + | 0.348061 |
glk | DDB_G0287631 | catalyzes the reaction ATP D-glucose ADP D-glucose 6-phosphate | DDB0232432 | CDS | 530347 | 1791 | - | 0.319933 |
glkA | DDB_G0270218 | putative protein serinethreonine kinase GSK family member of the CMGC kinase group similar to Drosophila shaggy and other glycogen synthase kinases | DDB0232428 | CDS | 4429657 | 1422 | + | 0.23699 |
glnA1 | DDB_G0276835 | catalyzes the reaction ATP L-glutamate ammonia ADP phosphate L-glutamine | DDB0232429 | CDS | 7451944 | 1500 | + | 0.260667 |
glnA2 | DDB_G0295755 | catalyzes the reaction ATP L-glutamate ammonia ADP phosphate L-glutamine | DDB0232432 | CDS | 2591112 | 1566 | - | 0.324393 |
glnA3 | DDB_G0279591 | catalyzes the reaction ATP L-glutamate ammonia ADP phosphate L-glutamine | DDB0232430 | CDS | 2109355 | 2208 | - | 0.352355 |
glnS | DDB_G0289481 | induced by cycloheximide catalyzes the reaction ATP L-glutamine tRNAGln AMP diphosphate L-glutaminyl-tRNAGln | DDB0232432 | CDS | 2857147 | 2340 | + | 0.335043 |
gloA | DDB_G0291265 | catalyzes the reaction glutathione methylglyoxal S-lactoylglutathione | DDB0232433 | CDS | 28140 | 411 | + | 0.350365 |
gloB1 | DDB_G0285717 | catalyzes the reaction S-lactoyl-glutathione H2O reduced glutathione D-lactate | DDB0232431 | CDS | 3631211 | 807 | - | 0.275093 |
gloB2 | DDB_G0291482 | catalyzes the reaction S-lactoyl-glutathione H2O reduced glutathione D-lactate | DDB0232433 | CDS | 411372 | 879 | + | 0.335609 |
glod5 | DDB_G0286857 | conserved protein ortholog of human GLOD5 | DDB0232431 | CDS | 4996053 | 390 | - | 0.269231 |
glpD | DDB_G0291123 | CAZy family GT35 5'-AMP-independent glycogen phosphorylase expressed in late development the combined activities of glpV and glpD results in constant glycogen phosphorylase activity throughout development | DDB0232432 | CDS | 5073815 | 2982 | - | 0.335345 |
glpV | DDB_G0281383 | CAZy family GT35 5'-AMP-dependent glycogen phosphorylase expressed in early development the combined activities of glpV and glpD results in constant glycogen phosphorylase activity throughout development | DDB0232430 | CDS | 4540912 | 2562 | - | 0.366511 |
gltA | DDB_G0276965 | DDB0232429 | CDS | 7216750 | 1539 | - | 0.321637 | |
gluA | DDB_G0292810 | DDB0232433 | CDS | 2240229 | 2466 | - | 0.364152 | |
gluS | DDB_G0287467 | catalyzes the reaction ATP L-glutamate tRNAGlu AMP diphosphate L-glutamyl-tRNAGlu | DDB0232432 | CDS | 295392 | 2295 | - | 0.34902 |
glud1 | DDB_G0287469 | catalyzes the reaction L-glutamate Hsub2subO NAD(P)supsup 2-oxoglutarate ammonia NAD(P)H Hsupsup acting on the CH-NHsub2sub group of donors with NADsupsup or NADPsupsup as acceptor | DDB0232432 | CDS | 298748 | 1509 | + | 0.404241 |
glud2 | DDB_G0280319 | highly similar to fungal glutamate dehydrogenases catalyzes the reaction L-glutamate Hsub2subO NAD(P)supsup 2-oxoglutarate ammonia NAD(P)H Hsupsup expressed in pstO cells and upper cup during culmination | DDB0232430 | CDS | 3249762 | 3129 | - | 0.362097 |
glyS | DDB_G0284583 | catalyzes the reaction ATP glycine tRNAGly AMP diphosphate glycyl-tRNAGly | DDB0232431 | CDS | 2181616 | 2037 | + | 0.354934 |
gmd | DDB_G0284553 | catalyzes the reaction GDP-mannose GDP-4-dehydro-6-deoxy-D-mannose Hsub2subO | DDB0232431 | CDS | 2061934 | 1071 | - | 0.327731 |
gmfA | DDB_G0282595 | glia maturation factor homolog initially identified as a growth and differentiation factor in mammals | DDB0232430 | CDS | 5984604 | 417 | - | 0.294964 |
gmkA | DDB_G0279001 | catalyzes the reaction GMP ATP GDP ADP in the de novo and salvage pathways of purine and pyrimidine nucleotides | DDB0232430 | CDS | 1502267 | 609 | + | 0.279146 |
gmppA | DDB_G0271858 | catalyzes the reaction GTP alpha-D-mannose 1-phosphate diphosphate GDP-mannose | DDB0232429 | CDS | 932853 | 1239 | - | 0.305892 |
gmppB | DDB_G0287619 | catalyzes the reaction GTP alpha-D-mannose 1-phosphate diphosphate GDP-mannose | DDB0232432 | CDS | 482074 | 1080 | + | 0.324074 |
gmsA | DDB_G0286015 | homologous to the Chlamydomonas reinhardtii a2gene enriched in gametes | DDB0232431 | CDS | 3951359 | 1347 | - | 0.368226 |
gna1 | DDB_G0279475 | gna bGblucosamibNbe-6-phosphate bAbcetyltransferase | DDB0232430 | CDS | 2113626 | 474 | - | 0.242616 |
gnb1l | DDB_G0289181 | ortholog of the mammalian GNB1L contains several WD-40 repeats | DDB0232432 | CDS | 2444140 | 1080 | + | 0.234259 |
gnd | DDB_G0277885 | catalyzes the reaction 6-phospho-D-gluconate NADPsupsup D-ribulose 5-phosphate COsub2sub NADPH | DDB0232430 | CDS | 273541 | 1482 | - | 0.398111 |
gnl1 | DDB_G0285371 | DDB0232431 | CDS | 3179167 | 2541 | - | 0.283747 | |
gnl3 | DDB_G0287147 | similar to the conserved guanine nucleotide-binding protein-like 3 also called nucleostemin in mammals a protein in the nucleolus of most stem cells and many tumor cells involved in cell-cycle progression | DDB0232431 | CDS | 5379967 | 1848 | - | 0.318182 |
gnpda1 | DDB_G0278873 | short version of the glucosamine-6-phosphate isomerase similar to fungi and metazoans catalyzes the reaction D-glucosamine 6-phosphate Hsub2subO D-fructose 6-phosphate NHsub3sub | DDB0232430 | CDS | 1321299 | 804 | - | 0.31592 |
gnrA | DDB_G0291125 | DDB0232432 | CDS | 5022395 | 3264 | - | 0.324449 | |
gnrB | DDB_G0291536 | DDB0232433 | CDS | 490155 | 5088 | - | 0.306211 | |
gnrC | DDB_G0276571 | gelsolin domain-containing protein also contains WASP-C (Wiskott-Aldrich Syndrome Protein C-terminal) domains that contain PAK-boxP21-Rho-binding domains however these domains are found near the N-terminus (upstream of the gelsolin domain) not at the C-terminus | DDB0232429 | CDS | 6967980 | 6315 | + | 0.286778 |
gnt1 | DDB_G0275699 | catalyzes the addition of GlcNAc (N-acetylglucosamine) to HyPro143-Skp1 (FpaAFpaB) in the cytosol | DDB0232429 | CDS | 5613948 | 1272 | + | 0.216981 |
gnt10 | DDB_G0269900 | distant relative of CAZy family GT14 similar to xylosyltransferase | DDB0232428 | CDS | 3823854 | 2034 | + | 0.192724 |
gnt11 | DDB_G0269558 | distant relative of CAZy family GT14 similar to xylosyltransferase | DDB0232428 | CDS | 2994626 | 1503 | - | 0.214904 |
gnt12 | DDB_G0268160 | CAZy family GT49 similar to vertebrate acetylglucosaminyltransferase-like protein | DDB0232428 | CDS | 1577150 | 1653 | - | 0.216576 |
gnt13 | DDB_G0282469 | CAZy family GT49 similar to vertebrate acetylglucosaminyltransferase-like protein | DDB0232430 | CDS | 5807533 | 1908 | - | 0.224843 |
gnt14 | DDB_G0284567 | CAZy family GT49 similar to vertebrate acetylglucosaminyltransferase-like protein | DDB0232431 | CDS | 2159197 | 1923 | + | 0.237129 |
gnt15 | DDB_G0274741 | CAZy family GT49 similar to vertebrate acetylglucosaminyltransferase-like protein (LARGE) essential for development | DDB0232429 | CDS | 3925969 | 1551 | - | 0.234043 |
gnt2 | DDB_G0291241 | DDB0232433 | CDS | 49486 | 1212 | - | 0.334158 | |
gnt3 | DDB_G0288463 | CAZy family GT13 catalyzes the reaction UDP-N-acetyl-D-glucosamine 3-(a-D-mannosyl)-b-D-mannosyl-R UDP 3-(2-[N-acetyl-b-D-glucosaminyl]-a-D-mannosyl)-b-D-mannosyl-R | DDB0232432 | CDS | 1556680 | 1497 | + | 0.204409 |
gnt4 | DDB_G0268854 | CAZy family GT13 catalyzes the reaction UDP-N-acetyl-D-glucosamine 3-(a-D-mannosyl)-b-D-mannosyl-R UDP 3-(2-[N-acetyl-b-D-glucosaminyl]-a-D-mannosyl)-b-D-mannosyl-R | DDB0232428 | CDS | 2252863 | 1887 | - | 0.301007 |
gnt5 | DDB_G0272276 | distant relative of CAZy family GT24 catalyzes N-linked glycosylation | DDB0232429 | CDS | 1522912 | 1332 | - | 0.293544 |
gnt6 | DDB_G0272172 | distant relative of CAZy family GT24 catalyzes N-linked glycosylation | DDB0232429 | CDS | 1529992 | 1464 | - | 0.322404 |
gnt7 | DDB_G0272422 | distant relative of CAZy family GT24 catalyzes N-linked glycosylation | DDB0232429 | CDS | 1528022 | 1464 | - | 0.334016 |
gnt8 | DDB_G0272170 | distant relative of CAZy family GT24 catalyzes N-linked glycosylation | DDB0232429 | CDS | 1532191 | 1320 | - | 0.300758 |
gnt9 | DDB_G0268204 | distant relative of CAZy family GT14 similar to xylosyltransferase | DDB0232428 | CDS | 1683897 | 1896 | + | 0.213608 |
gnt_ps | DDB_G0272392 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232429 | CDS | 1433985 | 201 | - | 0.348259 |
gol | DDB_G0287271 | golgi and vesicle associated protein predominantly targeted to the endosomal pathway | DDB0232432 | CDS | 91906 | 1740 | - | 0.275862 |
golt1 | DDB_G0292868 | conserved protein might be involved in fusion of ER-derived transport vesicles with the Golgi complex | DDB0232433 | CDS | 2183910 | 417 | - | 0.270983 |
gp130 | DDB_G0279921 | contains amino terminal membrane insertion signal and carboxy terminal sequences for addition of lipid anchor involved in pinocytosis | DDB0232430 | CDS | 2777162 | 2307 | - | 0.240572 |
gpaA | DDB_G0283349 | DDB0232431 | CDS | 547836 | 1071 | + | 0.323996 | |
gpaB | DDB_G0276267 | subunit of the heterotrimeric G protein that has GTPase activity involved in the chemotactic response to cAMP | DDB0232429 | CDS | 6619603 | 1074 | - | 0.309125 |
gpaC | DDB_G0287031 | subunit of the heterotrimeric G protein that has GTPase activity has N-terminal pleckstrin homology (PH) domain | DDB0232431 | CDS | 5297647 | 1713 | + | 0.27087 |
gpaD | DDB_G0285425 | subunit of the heterotrimeric G protein that has GTPase activity involved in the chemotactic response to folate | DDB0232431 | CDS | 3541732 | 1038 | + | 0.313102 |
gpaE | DDB_G0286185 | subunit of the heterotrimeric G protein that has GTPase activity involved in the chemotactic response to folate | DDB0232431 | CDS | 4227524 | 1044 | + | 0.285441 |
gpaF | DDB_G0283151 | DDB0232431 | CDS | 306164 | 1044 | - | 0.251916 | |
gpaG | DDB_G0276455 | DDB0232429 | CDS | 6800222 | 1173 | - | 0.290708 | |
gpaH | DDB_G0284469 | DDB0232431 | CDS | 2128349 | 1212 | - | 0.284653 | |
gpaI | DDB_G0283419 | DDB0232431 | CDS | 656137 | 1029 | - | 0.284742 | |
gpaJ | DDB_G0268802 | DDB0232428 | CDS | 2129299 | 1050 | + | 0.226667 | |
gpaK | DDB_G0276343 | DDB0232429 | CDS | 6669753 | 1080 | + | 0.218519 | |
gpaL | DDB_G0280351 | DDB0232430 | CDS | 3291770 | 1065 | + | 0.232864 | |
gpbA | DDB_G0277143 | DDB0232429 | CDS | 7812708 | 1044 | - | 0.3659 | |
gpbB | DDB_G0275045 | DDB0232429 | CDS | 5266629 | 990 | + | 0.419192 | |
gpdA | DDB_G0275153 | DDB0232429 | CDS | 5324765 | 1008 | + | 0.380952 | |
gpgA | DDB_G0274125 | DDB0232429 | CDS | 4285182 | 210 | + | 0.309524 | |
gphn | DDB_G0287261 | conserved microtubule-associated protein involved in membrane protein-cytoskeleton interactions implicated in molybdenum cofactor biosynthesis | DDB0232432 | CDS | 61689 | 2157 | - | 0.298563 |
gpi | DDB_G0283673 | catalyzes the reaction D-glucose 6-phosphate D-fructose 6-phosphate | DDB0232431 | CDS | 954966 | 1686 | + | 0.339265 |
gpmA | DDB_G0285311 | catalyzes the reaction 3-phosphoglycerate 2-phosphoglycerate | DDB0232431 | CDS | 3080971 | 750 | - | 0.330667 |
gpn1 | DDB_G0293220 | DDB0232433 | CDS | 2684279 | 1191 | + | 0.309824 | |
gpn2 | DDB_G0281787 | DDB0232430 | CDS | 4982225 | 948 | + | 0.256329 | |
gpn3 | DDB_G0285197 | DDB0232431 | CDS | 2952647 | 858 | + | 0.29021 | |
gppA | DDB_G0267398 | DDB0232428 | CDS | 1607815 | 1635 | - | 0.285015 | |
gpsn2 | DDB_G0270270 | very similar to human GPSN2 contains a 3-oxo-5-alpha-steroid 4-dehydrogenase C-terminal domain and 4 putative transmembrane domains | DDB0232428 | CDS | 4542640 | 903 | - | 0.306755 |
gpt1 | DDB_G0285815 | very similar to the mammalian N-acetylglucosamine-1-phosphotransferase alphabeta subunit (GNPTAB) precursor a central part of the Dictyostelium protein is not conserved in humans the precursor is cleaved and contributes to a | DDB0232431 | CDS | 3691117 | 3717 | + | 0.286252 |
gpt10 | DDB_G0281103 | DDB0232430 | CDS | 4064325 | 1098 | + | 0.320583 | |
gpt2 | DDB_G0270528 | DDB0232428 | CDS | 2803384 | 1212 | - | 0.217822 | |
gpt3 | DDB_G0277597 | DDB0232429 | CDS | 8262203 | 1452 | + | 0.217631 | |
gpt4 | DDB_G0274651 | DDB0232429 | CDS | 4496721 | 1290 | - | 0.217829 | |
gpt5 | DDB_G0274707 | DDB0232429 | CDS | 4151111 | 1293 | + | 0.222738 | |
gpt6 | DDB_G0268950 | DDB0232428 | CDS | 1984869 | 1482 | + | 0.205803 | |
gpt7 | DDB_G0274755 | DDB0232429 | CDS | 3839384 | 1443 | + | 0.2079 | |
gpt8 | DDB_G0286711 | DDB0232431 | CDS | 4880623 | 1236 | - | 0.242718 | |
gpt9 | DDB_G0286709 | DDB0232431 | CDS | 4878583 | 1131 | - | 0.236074 | |
grlA | DDB_G0271684 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature plays a role in sporulation | DDB0232429 | CDS | 779738 | 2397 | - | 0.278264 |
grlB | DDB_G0271686 | DDB0232429 | CDS | 776318 | 2268 | - | 0.283069 | |
grlC | DDB_G0282461 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232430 | CDS | 5789478 | 2403 | + | 0.27965 |
grlD | DDB_G0286895 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232431 | CDS | 5037852 | 2376 | + | 0.280724 |
grlE | DDB_G0291356 | major GABA receptor during late development GABA-B receptor with distinctive '7TM' signature also similar to metabotropic glutamate receptors also binds glutamate in a competitive manner to GABA seems to interact with two different trimeric G-proteins depending on ligand one that stimulates the PI3 kinase pathway and one acting through G | DDB0232433 | CDS | 173621 | 2451 | - | 0.337005 |
grlF | DDB_G0282175 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232430 | CDS | 5487367 | 2313 | + | 0.272806 |
grlG | DDB_G0272244 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232429 | CDS | 1741474 | 2319 | - | 0.292799 |
grlH | DDB_G0282459 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232430 | CDS | 5785479 | 2295 | + | 0.300218 |
grlJ | DDB_G0272150 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232429 | CDS | 1600728 | 2352 | + | 0.278061 |
grlK | DDB_G0269386 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232428 | CDS | 2668447 | 2115 | - | 0.327187 |
grlL | DDB_G0281211 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232430 | CDS | 4210774 | 2127 | + | 0.316408 |
grlM | DDB_G0286643 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232431 | CDS | 4778203 | 2250 | + | 0.317333 |
grlN | DDB_G0283839 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232431 | CDS | 1198222 | 2676 | - | 0.230568 |
grlO | DDB_G0271688 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232429 | CDS | 773062 | 2460 | - | 0.239837 |
grlP | DDB_G0291095 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232432 | CDS | 4986774 | 4224 | + | 0.241004 |
grlR | DDB_G0287681 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232432 | CDS | 554899 | 4815 | - | 0.244652 |
grl_ps | DDB_G0293232 | putative pseudogene fragment very similar to grl (metabotropic Glutamate Receptor-Like) genes | DDB0232433 | CDS | 2665263 | 135 | + | 0.348148 |
grn | DDB_G0283671 | very similar to H. sapiens granulins1-7 which are products of the precurser gene GRN defects in GRN cause the ubiquitin-positive frontotemporal dementia (UP-FTD) | DDB0232431 | CDS | 953712 | 393 | - | 0.279898 |
grp94 | DDB_G0280057 | DDB0232430 | CDS | 3124645 | 2304 | - | 0.320312 | |
grpA | DDB_G0293248 | involved in the unconventional secretory pathway of acbA the precurser of SDF-2 (spore differentiation factor 2) ortholog of the mammalian golgi reassembly stacking protein 2 (golgi reassembly-stacking protein of 55 kDa) | DDB0232433 | CDS | 2631684 | 984 | + | 0.311992 |
grpE | DDB_G0283763 | similar to S. cerevisiae MGE1 and H. sapiens GrpE involved in protein import into mitochondria | DDB0232431 | CDS | 1238328 | 642 | - | 0.302181 |
grwd1 | DDB_G0291566 | ortholog of the mammalian GRWD1 contains several WD-40 repeats | DDB0232433 | CDS | 556339 | 1449 | - | 0.354727 |
grxA | DDB_G0290015 | DDB0232432 | CDS | 3542247 | 303 | - | 0.290429 | |
gshB | DDB_G0291756 | catalyzes the reaction ATP gamma-L-glutamyl-L-cysteine glycine ADP phosphate glutathione in the synthesis of glutathione (GSH) | DDB0232433 | CDS | 695138 | 1431 | - | 0.29979 |
gskA | DDB_G0272110 | protein serinethreonine kinase GSK family member of the CMGC kinase group essential for cell specification activated by CAR3 through ZAK1 (prespore-) and inhibited by CAR4 (prestalk-) signalling | DDB0232429 | CDS | 1334436 | 1404 | - | 0.324786 |
gsr | DDB_G0272754 | DDB0232429 | CDS | 2099808 | 1398 | - | 0.3598 | |
gtaC | DDB_G0277589 | has 18 amino acids between the two CX2C motifs expressed in the lower and upper cups and the basal disc involved in DIF signaling leading to pstB cell sorting and basal disc formation | DDB0232429 | CDS | 8175755 | 1764 | + | 0.252268 |
gtaD | DDB_G0286855 | DDB0232431 | CDS | 4992545 | 1593 | - | 0.170747 | |
gtaE | DDB_G0267640 | DDB0232428 | CDS | 476398 | 2859 | - | 0.295208 | |
gtaF | DDB_G0268792 | DDB0232428 | CDS | 2120474 | 1872 | - | 0.261752 | |
gtaG | DDB_G0270756 | DDB0232428 | CDS | 4446395 | 3021 | - | 0.253227 | |
gtaH | DDB_G0277591 | DDB0232429 | CDS | 8180376 | 1560 | + | 0.223718 | |
gtaI | DDB_G0281661 | DDB0232430 | CDS | 4784467 | 1611 | + | 0.374302 | |
gtaJ | DDB_G0281829 | DDB0232430 | CDS | 4990977 | 2145 | + | 0.298835 | |
gtaK | DDB_G0282811 | DDB0232430 | CDS | 6187048 | 1953 | + | 0.250896 | |
gtaL | DDB_G0285139 | DDB0232431 | CDS | 2908294 | 1923 | + | 0.24909 | |
gtaM | DDB_G0286837 | DDB0232431 | CDS | 4960352 | 1527 | + | 0.207597 | |
gtaN | DDB_G0287057 | DDB0232431 | CDS | 5258336 | 2862 | - | 0.264151 | |
gtaO | DDB_G0289651 | DDB0232432 | CDS | 3001531 | 1536 | + | 0.175781 | |
gtaP | DDB_G0295707 | DDB0232433 | CDS | 624702 | 2088 | - | 0.287356 | |
gtaQ | DDB_G0286843 | DDB0232431 | CDS | 4968885 | 1071 | - | 0.340803 | |
gtaR | DDB_G0279331 | DDB0232430 | CDS | 1950418 | 714 | - | 0.253501 | |
gtaS | DDB_G0280627 | DDB0232430 | CDS | 3582758 | 945 | - | 0.245503 | |
gtaT | DDB_G0280639 | has 20 amino acids between the two CX2C motifs br brbCommunity annotation: b In a study of | DDB0232430 | CDS | 3594965 | 939 | + | 0.352503 |
gtaU | DDB_G0280853 | DDB0232430 | CDS | 3790224 | 981 | + | 0.258919 | |
gtaV | DDB_G0281087 | DDB0232430 | CDS | 4034404 | 546 | - | 0.245421 | |
gtaW | DDB_G0286839 | DDB0232431 | CDS | 4963061 | 888 | + | 0.315315 | |
gtaX | DDB_G0290665 | DDB0232432 | CDS | 4312004 | 1050 | + | 0.202857 | |
gtaY | DDB_G0279239 | contains a GATA Zinc finger but missing a cysteine residue | DDB0232430 | CDS | 1813505 | 897 | + | 0.254181 |
gtf2a1 | DDB_G0290327 | encodes the two largest subunits of TFIIA important but not essential for transcriptional activation functioning as either an antirepressor or a coactivator | DDB0232432 | CDS | 3966621 | 933 | - | 0.289389 |
gtf2a2 | DDB_G0285343 | important but not essential for transcriptional activation functioning as either an antirepressor or a coactivator | DDB0232431 | CDS | 3114831 | 348 | + | 0.284483 |
gtf2b | DDB_G0290929 | DDB0232432 | CDS | 4767056 | 978 | + | 0.373211 | |
gtf2e1-1 | DDB_G0273525 | TFIIE large subunit involved in recruitment of RNA polymerase II to the promoter activation of TFIIH and promoter opening there is a second copy of this gene | DDB0232429 | CDS | 2978253 | 1371 | + | 0.296864 |
gtf2e1-2 | DDB_G0273583 | TFIIE large subunit involved in recruitment of RNA polymerase II to the promoter activation of TFIIH and promoter opening there is a second copy of this gene | DDB0232429 | CDS | 3051445 | 1371 | - | 0.296864 |
gtf2e2 | DDB_G0287307 | DDB0232432 | CDS | 111192 | 831 | - | 0.315283 | |
gtf2f1 | DDB_G0279377 | DDB0232430 | CDS | 2008109 | 1671 | + | 0.320766 | |
gtf2f2 | DDB_G0287131 | DDB0232431 | CDS | 5353824 | 726 | - | 0.287879 | |
gtf2h1 | DDB_G0268014 | ortholog of S. cerevisiae TFB1 subunit of TFIIH and nucleotide excision repair factor 3 complexes required for nucleotide excision repair target for transcriptional activators | DDB0232428 | CDS | 1308296 | 2094 | + | 0.275549 |
gtf2h2 | DDB_G0272362 | DDB0232429 | CDS | 1296713 | 1386 | - | 0.309524 | |
gtf2h3 | DDB_G0275517 | DDB0232429 | CDS | 6059895 | 1119 | + | 0.268097 | |
gtf2h4 | DDB_G0293228 | ortholog of S. cerevisiae TFB2 subunit of TFIIH and nucleotide excision repair factor 3 complexes involved in transcription initiation required for nucleotide excision repair | DDB0232433 | CDS | 2676500 | 1452 | - | 0.303719 |
gtf2h5 | DDB_G0269906 | DDB0232428 | CDS | 3831161 | 219 | + | 0.255708 | |
gtf3C3 | DDB_G0278321 | DDB0232430 | CDS | 689224 | 2994 | + | 0.289579 | |
gtf3C5 | DDB_G0289935 | DDB0232432 | CDS | 3457434 | 2598 | - | 0.279831 | |
gtpA | DDB_G0275441 | DDB0232429 | CDS | 5822886 | 1350 | - | 0.347407 | |
gtpbp1 | DDB_G0292538 | ortholog of the mammalian GTPBP1 and very similar to GTPBP2 contains a translation elongation factor EFTuEF1A domain 2 and C-terminal domain | DDB0232433 | CDS | 1635942 | 2034 | + | 0.357915 |
gtpbp3 | DDB_G0270228 | ortholog of the mammalian GTPBP3 and S. cerevisiae MSS1 GTPases responsible for the 5-carboxymethylaminomethyl modification of the wobble uridine base in mitochondrial tRNAs | DDB0232428 | CDS | 4442110 | 1539 | + | 0.250162 |
gtpbp5 | DDB_G0277801 | similar to human GTPBP5 GTP1OBG family protein involved in the ribosome maturation process | DDB0232429 | CDS | 8429520 | 1887 | - | 0.254902 |
gtr1 | DDB_G0274373 | distant relative of CAZy family GT4 contains a central glycosyltransferase domain and a C-terminal sulfotransferase domain | DDB0232429 | CDS | 3782580 | 3942 | + | 0.277017 |
gtr2 | DDB_G0276105 | distant relative of CAZy family GT5 contains a glycosyltransferase domain and an alpha amylase catalytic domain | DDB0232429 | CDS | 6292325 | 7422 | + | 0.325115 |
gtr3 | DDB_G0286945 | distant relative of CAZy family GT8 similar to glycogenin and galactinol synthase | DDB0232431 | CDS | 5125247 | 1116 | + | 0.312724 |
guaA | DDB_G0281551 | catalyzes the reaction xanthosine-5-phosphate Hsub2subO L-glutamine ATP L-glutamate GMP pyrophosphate AMP in GMP biosynthesis | DDB0232430 | CDS | 4709076 | 2157 | + | 0.304126 |
guaB | DDB_G0283701 | catalyzes the reaction Hsub2subO NAD IMP xanthosine-5-phosphate NADH the first step of GMP biosynthesis | DDB0232431 | CDS | 1000722 | 1548 | - | 0.386305 |
guaD | DDB_G0277743 | catalyzes the reaction guanine Hsub2subO xanthine NHsub3sub | DDB0232429 | CDS | 8417392 | 1353 | + | 0.311899 |
guf1 | DDB_G0291708 | ortholog of H. sapiens and S. cerevisiae GUF1 a mitochondrial GTP binding protein believed to be involved in protein biosynthesis | DDB0232433 | CDS | 641379 | 2058 | + | 0.348397 |
gxcA | DDB_G0277987 | Rac guanyl-nucleotide exchange factor involved in chemotaxis and development there are two transcripts for this gene that seem to be differentially expressed during development with the shorter isoform expressed in vegetative cells and the longer isoform during development | DDB0232430 | CDS | 114291 | 6117 | - | 0.297695 |
gxcAA | DDB_G0282717 | DDB0232430 | CDS | 6195317 | 3210 | + | 0.270405 | |
gxcAA_ps | DDB_G0282829 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 6270236 | 366 | - | 0.243169 |
gxcB | DDB_G0269424 | DDB0232428 | CDS | 2732721 | 3597 | - | 0.263553 | |
gxcBB | DDB_G0277131 | DDB0232429 | CDS | 7605969 | 3291 | + | 0.293224 | |
gxcC | DDB_G0284845 | plays a role in the regulation of development contains N-terminal armadillo repeats a RhoGEF domain and a C-terminal pleckstrin homology (PH) domain | DDB0232431 | CDS | 2552011 | 3648 | + | 0.347039 |
gxcCC | DDB_G0279123 | contains two actin binding domains a putative calmodulin binding domain and a Dbl homology (DH) domain specific for Rho guanine nucleotide exchange factors (GEF) | DDB0232430 | CDS | 1613622 | 3438 | + | 0.3121 |
gxcD | DDB_G0267854 | DDB0232428 | CDS | 970209 | 3192 | + | 0.294486 | |
gxcDD | DDB_G0279733 | multifunctional protein containing a Rac exchange factor domain an Arf GTPase activating domain a CH domain two IQ motifs and three PH domains | DDB0232430 | CDS | 2433796 | 9348 | + | 0.295892 |
gxcE | DDB_G0291085 | DDB0232432 | CDS | 4955990 | 1641 | - | 0.252895 | |
gxcEE | DDB_G0281047 | DDB0232430 | CDS | 3973435 | 1956 | - | 0.267894 | |
gxcF | DDB_G0282475 | DDB0232430 | CDS | 5819048 | 2799 | + | 0.268667 | |
gxcFF | DDB_G0284739 | DDB0232431 | CDS | 2399480 | 2226 | - | 0.260108 | |
gxcG | DDB_G0282073 | DDB0232430 | CDS | 5205115 | 1920 | + | 0.295312 | |
gxcGG | DDB_G0268354 | DDB0232428 | CDS | 891838 | 2391 | - | 0.268507 | |
gxcH | DDB_G0288377 | DDB0232432 | CDS | 1454380 | 2787 | - | 0.268748 | |
gxcHH | DDB_G0290493 | DDB0232432 | CDS | 4148104 | 2865 | + | 0.26178 | |
gxcI | DDB_G0288383 | DDB0232432 | CDS | 1463358 | 3249 | - | 0.258541 | |
gxcII | DDB_G0278703 | DDB0232430 | CDS | 1052856 | 2625 | + | 0.258286 | |
gxcJ | DDB_G0293978 | DDB0232433 | CDS | 3500795 | 3468 | + | 0.241638 | |
gxcJJ | DDB_G0275679 | DDB0232429 | CDS | 5709701 | 3522 | - | 0.293583 | |
gxcK | DDB_G0291007 | DDB0232432 | CDS | 4881627 | 2892 | + | 0.246542 | |
gxcKK | DDB_G0293340 | DDB0232433 | CDS | 2757100 | 2004 | - | 0.25 | |
gxcL | DDB_G0290023 | DDB0232432 | CDS | 3553377 | 2418 | - | 0.296112 | |
gxcM | DDB_G0272372 | DDB0232429 | CDS | 1367731 | 3438 | - | 0.299593 | |
gxcN | DDB_G0277017 | DDB0232429 | CDS | 7226683 | 3285 | - | 0.29589 | |
gxcO | DDB_G0293396 | DDB0232433 | CDS | 2833626 | 2490 | + | 0.244177 | |
gxcP | DDB_G0285859 | DDB0232431 | CDS | 3730680 | 2916 | + | 0.281207 | |
gxcQ | DDB_G0284501 | DDB0232431 | CDS | 2058245 | 3513 | + | 0.320239 | |
gxcR | DDB_G0285303 | DDB0232431 | CDS | 3051378 | 1653 | - | 0.268603 | |
gxcS | DDB_G0280087 | DDB0232430 | CDS | 2911297 | 3414 | + | 0.298184 | |
gxcT | DDB_G0269610 | interacts with racE contains a RhoGEF domain a pleckstrin homology (PH) domain a C2H2-type zinc finger and an IQ calmodulin-binding domain | DDB0232428 | CDS | 3136522 | 4725 | + | 0.333333 |
gxcU | DDB_G0291996 | DDB0232433 | CDS | 972420 | 2961 | - | 0.311381 | |
gxcV | DDB_G0282271 | DDB0232430 | CDS | 5595367 | 1446 | + | 0.284924 | |
gxcW | DDB_G0278147 | DDB0232430 | CDS | 354814 | 3270 | + | 0.303058 | |
gxcX | DDB_G0274889 | DDB0232429 | CDS | 4349111 | 3498 | + | 0.311321 | |
gxcY | DDB_G0293266 | DDB0232433 | CDS | 2602478 | 3231 | - | 0.268957 | |
gxcY_ps | DDB_G0293338 | putative pseudogene fragment similar to D. discoideum gene | DDB0232433 | CDS | 2754113 | 579 | + | 0.246978 |
gxcZ | DDB_G0293928 | DDB0232433 | CDS | 3506582 | 3087 | - | 0.259475 | |
haao | DDB_G0282743 | catalyzes the reaction 3-hydroxyanthranilate Osub2sub 2-amino-3-carboxymuconate semialdehyde | DDB0232430 | CDS | 6232657 | 549 | + | 0.282332 |
hacl1 | DDB_G0292402 | putative 2-hydroxyacyl-CoA lyase which cleaves a 2-hydroxy-3-methylacyl-CoA into formyl-CoA and a 2-methyl-branched fatty aldehyde | DDB0232433 | CDS | 1553647 | 1743 | - | 0.324154 |
hacl1_ps | DDB_G0292762 | putative pseudogene 2-hydroxyacyl-CoA lyase (hacl) family protein | DDB0232433 | CDS | 2051654 | 138 | + | 0.355072 |
hal | DDB_G0288025 | catalyzes the reaction L-histidine urocanate NHsub3sub | DDB0232432 | CDS | 990248 | 1620 | - | 0.335185 |
hao | DDB_G0291814 | single hao ortholog in D. discoideum very similar to mammalian HAO1 an enzyme of the glycolate pathway | DDB0232433 | CDS | 804510 | 1167 | + | 0.305913 |
hapA | DDB_G0276069 | DDB0232429 | CDS | 6445628 | 2142 | - | 0.262838 | |
hapA_ps | DDB_G0272452 | putative pseudogene very similar to hapA (Hap2 protein) | DDB0232429 | CDS | 1629321 | 984 | + | 0.287602 |
hatA | DDB_G0282141 | histidine-rich pH-dependent actin binding protein N-terminal myristoylation | DDB0232430 | CDS | 5481850 | 357 | + | 0.420168 |
hatB | DDB_G0282143 | histidine-rich pH-dependent actin binding protein N-terminal myristoylation | DDB0232430 | CDS | 5482925 | 357 | + | 0.456583 |
hatC | DDB_G0292136 | almost identical to hisactophilin I and II (hatA and hatB) histidine-rich pH-dependent actin binding proteins | DDB0232433 | CDS | 1249171 | 360 | - | 0.363889 |
hat_ps | DDB_G0282003 | putative pseudogene small fragment similar to a family of D. discoideum genes including | DDB0232430 | CDS | 5234145 | 324 | - | 0.305556 |
hbs1 | DDB_G0283769 | DDB0232431 | CDS | 1138835 | 2190 | + | 0.306393 | |
hbx10 | DDB_G0284293 | DDB0232431 | CDS | 1841189 | 1917 | + | 0.27856 | |
hbx11 | DDB_G0295787 | DDB0232431 | CDS | 4544537 | 669 | - | 0.2571 | |
hbx12 | DDB_G0286733 | DDB0232431 | CDS | 4905654 | 2541 | - | 0.27194 | |
hbx13 | DDB_G0288975 | DDB0232432 | CDS | 2192060 | 4092 | + | 0.26173 | |
hbx14 | DDB_G0289677 | DDB0232432 | CDS | 3081562 | 1368 | + | 0.274854 | |
hbx2 | DDB_G0275173 | DDB0232429 | CDS | 5017002 | 2829 | - | 0.224461 | |
hbx3 | DDB_G0291197 | DDB0232432 | CDS | 5094013 | 2004 | + | 0.210579 | |
hbx4 | DDB_G0272967 | DDB0232429 | CDS | 1949614 | 2223 | - | 0.204678 | |
hbx5-1 | DDB_G0273127 | there is a second copy of this gene | DDB0232429 | CDS | 2807924 | 5172 | + | 0.265855 |
hbx5-2 | DDB_G0273645 | there is a second copy of this gene | DDB0232429 | CDS | 3218378 | 5172 | - | 0.265855 |
hbx6 | DDB_G0277505 | DDB0232429 | CDS | 7968732 | 1551 | - | 0.259832 | |
hbx7 | DDB_G0278225 | DDB0232430 | CDS | 509241 | 243 | + | 0.246914 | |
hbx8 | DDB_G0279257 | DDB0232430 | CDS | 1846173 | 984 | - | 0.234756 | |
hbx9 | DDB_G0280473 | DDB0232430 | CDS | 3412476 | 1920 | + | 0.241146 | |
hcpA | DDB_G0283023 | contains two Chromo domains locates to the centromere and plays a role in growth and mitosis forms a heterodimer with hcpB | DDB0232431 | CDS | 170065 | 678 | - | 0.297935 |
hcpB | DDB_G0282987 | contains two Chromo domains locates to the centromere and plays a role in growth forms a homodimer or a heterodimer with hcpA | DDB0232431 | CDS | 105576 | 735 | + | 0.308844 |
hcpC | DDB_G0270198 | similar to HP1 (heterochromatin protein 1) does not seem to be expressed | DDB0232428 | CDS | 4395945 | 720 | + | 0.281944 |
hdaA | DDB_G0268024 | DDB0232428 | CDS | 1320084 | 1488 | - | 0.303763 | |
hdaB | DDB_G0270338 | DDB0232428 | CDS | 4667184 | 1269 | + | 0.300236 | |
hdaC | DDB_G0280195 | DDB0232430 | CDS | 3087742 | 5115 | - | 0.307918 | |
hdaC_ps1 | DDB_G0287669 | putative pseudogene small fragment similar to | DDB0232432 | CDS | 510322 | 282 | + | 0.397163 |
hdaC_ps2 | DDB_G0285625 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3485870 | 171 | + | 0.421053 |
hdaC_ps3 | DDB_G0275193 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 5241548 | 123 | - | 0.260163 |
hdaC_ps4 | DDB_G0349111 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 4281044 | 218 | - | 0.37156 |
hdaC_ps5 | DDB_G0349153 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232430 | CDS | 3606827 | 261 | + | 0.325671 |
hdaD | DDB_G0279267 | DDB0232430 | CDS | 1861211 | 4470 | - | 0.275615 | |
hddc2 | DDB_G0290795 | conserved protein HD domains occur in a superfamily of enzymes with a predicted or known phosphohydrolase activity | DDB0232432 | CDS | 4613721 | 573 | - | 0.279232 |
helA | DDB_G0292992 | DDB0232433 | CDS | 2367392 | 3276 | + | 0.291209 | |
helB1 | DDB_G0275443 | conserved RNA helicase S. cerevisiae ortholog PRP5 is necessary for pre-spliceosome formation | DDB0232429 | CDS | 5780689 | 3456 | - | 0.335938 |
helB2 | DDB_G0277857 | conserved RNA helicase S. cerevisiae ortholog PRP28 is involved in RNA isomerization at the 5' splice site | DDB0232430 | CDS | 776296 | 2505 | + | 0.335729 |
helC | DDB_G0281553 | DDB0232430 | CDS | 4949807 | 1398 | + | 0.286838 | |
helD | DDB_G0285843 | conserved RNA helicase S. cerevisiae prp16 involved in the second catalytic step of splicing exhibits ATP-dependent RNA unwinding activity | DDB0232431 | CDS | 3861549 | 4164 | + | 0.307157 |
helE | DDB_G0281949 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232430 | CDS | 5309986 | 4623 | - | 0.237508 |
helF | DDB_G0294407 | DDB0232429 | CDS | 2123898 | 2514 | - | 0.28043 | |
hemA | DDB_G0280763 | catalyzes the reaction succinyl-CoA glycine 5-aminolevulinate CoA COsub2sub | DDB0232430 | CDS | 3708667 | 1965 | - | 0.332316 |
hemB | DDB_G0269444 | catalyzes the conversion of delta-aminolevulinic acid to porphobilinogen the second step in heme biosynthesis | DDB0232428 | CDS | 2788108 | 1002 | + | 0.329341 |
hemC | DDB_G0284697 | DDB0232431 | CDS | 2361299 | 978 | + | 0.294479 | |
hemD | DDB_G0285009 | catalyzes the reaction hydroxymethylbilane uroporphyrinogen III Hsub2subO in heme biosynthesis | DDB0232431 | CDS | 2803238 | 1152 | - | 0.171875 |
hemE | DDB_G0292294 | catalyzes the reaction uroporphyrinogen III coproporphyrinogen 4 COsub2sub in heme biosynthesis | DDB0232433 | CDS | 1412890 | 1095 | - | 0.340639 |
hemF | DDB_G0288893 | catalyzes the reaction coproporphyrinogen-III Osub2sub 2 H protoporphyrinogen-IX 2 COsub2sub 2 Hsub2subO | DDB0232432 | CDS | 2090427 | 999 | + | 0.336336 |
hemG | DDB_G0292040 | DDB0232433 | CDS | 1063213 | 1599 | + | 0.238274 | |
hemH | DDB_G0288891 | catalyzes the reaction protoporphyrin Fesup2sup protoheme 2 Hsupsup in heme biosynthesis | DDB0232432 | CDS | 2088484 | 1272 | - | 0.29717 |
hfnA | DDB_G0283983 | contains an N-terminal filaminABP280 repeat and a C-terminal HECT (Homologous to the E6-AP Carboxyl Terminus) domain the latter common in ubiquitin ligases | DDB0232431 | CDS | 1259472 | 3363 | + | 0.223313 |
hgd | DDB_G0283765 | reduction of homogentisic acid reductase results in accumulation of an intermediate in the tyrosine degradative pathway homogentisic acid which is spontaneously oxidized resulting in a brown phenotype catalyzes the reaction homogentisate Osub2sub 4-maleylacetoacetate | DDB0232431 | CDS | 1151090 | 1299 | - | 0.34719 |
hgsA | DDB_G0288461 | catalyzes the reaction acetyl-CoA H2O acetoacetyl-CoA (S)-3-hydroxy-3-methylglutaryl-CoA CoA | DDB0232432 | CDS | 1582464 | 1449 | - | 0.344375 |
hgsB | DDB_G0274871 | homolog of human HMGCS1 catalyzes the reaction acetyl-CoA H2O acetoacetyl-CoA (S)-3-hydroxy-3-methylglutaryl-CoA CoA contains a predicted peroxisomal targeting signal | DDB0232429 | CDS | 4273673 | 1407 | + | 0.282161 |
hibA | DDB_G0292566 | DDB0232433 | CDS | 1891263 | 966 | - | 0.356108 | |
hibch | DDB_G0267536 | catalyzes the reaction: 3-hydroxy-2-methylpropanoyl-CoA H2O CoA 3-hydroxy-2-methylpropanoate ortholog of the mammalian HIBCH enzyme | DDB0232428 | CDS | 289882 | 1146 | + | 0.336824 |
hipA | DDB_G0285703 | clathrin-associated protein involved in spore coat formation and regulated by epsin contains an Epsin N-terminal homology domain (ENTH) and a C-terminal ILWEQ domain that has been shown to bind to F-actin | DDB0232431 | CDS | 3610989 | 2883 | + | 0.367673 |
hira | DDB_G0276423 | ortholog of yeast HIR1 a transcriptional corepressor involved in the cell cycle-regulated transcription of histone H2A H2B H3 and H4 genes | DDB0232429 | CDS | 6881531 | 3345 | - | 0.30852 |
hisS | DDB_G0274159 | catalyzes the reaction ATP L-histidine tRNAHis AMP diphosphate L-histidyl-tRNAHis | DDB0232429 | CDS | 4879244 | 1446 | + | 0.342324 |
hlcs1 | DDB_G0288791 | functions in post-translational modification of various carboxylases by attachment of biotin similar to human HLCS which when defect causes a neonatal form of multiple carboxylase deficiency Dictytostelium contains three similar enzymes | DDB0232432 | CDS | 1968883 | 1128 | + | 0.289894 |
hlcs2 | DDB_G0288789 | functions in post-translational modification of various carboxylases by attachment of biotin similar to human HLCS which when defect causes a neonatal form of multiple carboxylase deficiency Dictytostelium contains three similar enzymes | DDB0232432 | CDS | 1967179 | 1128 | + | 0.289894 |
hlcs3 | DDB_G0289035 | functions in post-translational modification of various carboxylases by attachment of biotin similar to human HLCS which when defect causes a neonatal form of multiple carboxylase deficiency Dictytostelium contains three similar enzymes | DDB0232432 | CDS | 2283370 | 1215 | + | 0.288889 |
hmgA | DDB_G0269142 | DDB0232428 | CDS | 4072747 | 1659 | + | 0.346594 | |
hmgB | DDB_G0276615 | DDB0232429 | CDS | 7053641 | 1581 | + | 0.387097 | |
hmgL | DDB_G0283813 | catalyzes the reaction 3-hydroxy-3-methyl-glutaryl-CoA acetoacetate acetyl-CoA | DDB0232431 | CDS | 1145359 | 1221 | - | 0.354627 |
hook | DDB_G0288691 | similar to C. elegans ZYG-12 and mammalian HOOK proteins which mediates the attachment between the centrosome and the nucleus | DDB0232432 | CDS | 1822874 | 2205 | + | 0.275737 |
hop2 | DDB_G0280989 | DDB0232430 | CDS | 3917295 | 732 | - | 0.260929 | |
hpd | DDB_G0277511 | catalyzes the reaction 4-hydroxyphenylpyruvate Osub2sub homogentisate COsub2sub | DDB0232429 | CDS | 8032217 | 2214 | + | 0.342367 |
hpdl-1 | DDB_G0273429 | catalyzes the reaction 4-hydroxyphenylpyruvate Osub2sub homogentisate COsub2sub there is a second copy of this gene | DDB0232429 | CDS | 2988290 | 1485 | + | 0.227609 |
hpdl-2 | DDB_G0273513 | catalyzes the reaction 4-hydroxyphenylpyruvate Osub2sub homogentisate COsub2sub there is a second copy of this gene | DDB0232429 | CDS | 3041831 | 1485 | - | 0.227609 |
hprT | DDB_G0285193 | catalyzes the reaction PRPP hypoxanthine pyrophosphate IMP in the salvage pathways of purine nucleosides br overexpressed in dstB (STATb) null mutants | DDB0232431 | CDS | 2972049 | 543 | + | 0.281768 |
hspA | DDB_G0288181 | involved in phototaxis growth and morphogenesis and implicated in mitochondrial disease | DDB0232432 | CDS | 1238068 | 1671 | + | 0.36146 |
hspB | DDB_G0269144 | DDB0232428 | CDS | 4410084 | 1923 | - | 0.334893 | |
hspC | DDB_G0272819 | DDB0232429 | CDS | 1898278 | 846 | + | 0.341608 | |
hspD | DDB_G0267400 | DDB0232428 | CDS | 1280990 | 2103 | - | 0.336662 | |
hspE-1 | DDB_G0273249 | there is a second copy of this gene | DDB0232429 | CDS | 2848730 | 1899 | - | 0.410742 |
hspE-2 | DDB_G0273623 | there is a second copy of this gene | DDB0232429 | CDS | 3181158 | 1899 | + | 0.410742 |
hspF-1 | DDB_G0273409 | there is a second copy of this gene | DDB0232429 | CDS | 2921093 | 702 | - | 0.237892 |
hspF-2 | DDB_G0273561 | there is a second copy of this gene | DDB0232429 | CDS | 3109992 | 702 | + | 0.237892 |
hspG1 | DDB_G0275079 | DDB0232429 | CDS | 5147676 | 549 | - | 0.20765 | |
hspG10 | DDB_G0277123 | DDB0232429 | CDS | 7585241 | 225 | + | 0.24 | |
hspG11 | DDB_G0277125 | DDB0232429 | CDS | 7588267 | 333 | + | 0.252252 | |
hspG12 | DDB_G0277491 | DDB0232429 | CDS | 7996971 | 618 | - | 0.223301 | |
hspG2 | DDB_G0276003 | DDB0232429 | CDS | 6164176 | 603 | + | 0.215589 | |
hspG3 | DDB_G0276607 | DDB0232429 | CDS | 7032092 | 684 | + | 0.238304 | |
hspG4 | DDB_G0276587 | DDB0232429 | CDS | 7028602 | 600 | + | 0.218333 | |
hspG5 | DDB_G0276875 | DDB0232429 | CDS | 7572576 | 609 | + | 0.231527 | |
hspG6 | DDB_G0276949 | DDB0232429 | CDS | 7574080 | 633 | + | 0.227488 | |
hspG7 | DDB_G0276951 | DDB0232429 | CDS | 7575967 | 624 | + | 0.24359 | |
hspG8 | DDB_G0277119 | DDB0232429 | CDS | 7578926 | 636 | + | 0.243711 | |
hspG9 | DDB_G0276953 | DDB0232429 | CDS | 7581914 | 606 | + | 0.234323 | |
hspH | DDB_G0290187 | DDB0232432 | CDS | 3818443 | 2319 | + | 0.378611 | |
hspI | DDB_G0288921 | DDB0232432 | CDS | 2124478 | 672 | - | 0.258929 | |
hspJ | DDB_G0279447 | DDB0232430 | CDS | 2061353 | 486 | - | 0.17284 | |
hspK | DDB_G0275525 | DDB0232429 | CDS | 5922492 | 540 | - | 0.3 | |
hspL | DDB_G0267668 | DDB0232428 | CDS | 537016 | 399 | + | 0.263158 | |
hspM | DDB_G0280013 | DDB0232430 | CDS | 2706627 | 480 | + | 0.1875 | |
hsp_ps | DDB_G0281581 | putative pseudogene similar to a gene family in Dictyostelium including | DDB0232430 | CDS | 4662931 | 357 | + | 0.291317 |
hspc300 | DDB_G0279175 | DDB0232430 | CDS | 1727720 | 207 | - | 0.227053 | |
hssA | DDB_G0293360 | multicopy suppressor of dstA expressed in pstAO cells highly similar to other short proteins expressed in the prestalk region | DDB0232433 | CDS | 2789218 | 282 | + | 0.429078 |
hssB | DDB_G0293358 | DDB0232433 | CDS | 2787551 | 282 | - | 0.382979 | |
htt | DDB_G0272344 | ortholog of Huntington's disease protein Huntingtin (HTT not to be confused with the human serotonin transporter now named SLC6A4) in Dictyostelium regulates myosin II phosphorylation through phosphatase PP2A affecting chemotaxis and cytokinesis also involved in osmoregulation bivalent cation maintenance with effects on development including presporespore differentiation | DDB0232429 | CDS | 1346376 | 9288 | - | 0.288437 |
hus1 | DDB_G0285353 | similar to Hus1 a component of a heterotrimeric clamp (the 9-1-1 complex) that recognizes damaged DNA and initiates signal transduction for repair | DDB0232431 | CDS | 3152730 | 816 | - | 0.265931 |
hydA | DDB_G0290479 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232432 | CDS | 4230498 | 1485 | - | 0.323906 |
ibrA | DDB_G0274805 | similar to the IRSp53 and MIM families of I-BAR domains co-localizes with clathrin spots and seems to be involved in clathrin-mediated endocytosis does not localize to filopodia and is not involved in filopodium formation | DDB0232429 | CDS | 3936489 | 1074 | + | 0.296089 |
icmA-1 | DDB_G0272799 | prenylcysteine methyltransferase carries out carboyxl methylation of cleaved eukaryotic proteins that terminate in a CaaX motif such as NE81 (lmnB) there is a second copy of this gene | DDB0232429 | CDS | 2383418 | 714 | - | 0.303922 |
icmA-2 | DDB_G0273995 | carries out carboyxl methylation of cleaved eukaryotic proteins that terminate in a CaaX motif such as NE81 (lmnB) there is a second copy of this gene | DDB0232429 | CDS | 3647566 | 714 | + | 0.303922 |
icpA | DDB_G0267690 | homolog of INCENP involved in various cellular processes contains the IN-box domain known to bind Aurora B kinase null mutant has defects in cytokinesis chromosome segregation and spindle organization | DDB0232428 | CDS | 581198 | 3963 | + | 0.260661 |
idhA | DDB_G0271344 | catalyzes the reaction isocitrate NAD 2-oxoglutarate CO2 NADH | DDB0232429 | CDS | 68200 | 1065 | + | 0.34554 |
idhB | DDB_G0293872 | catalyzes the reaction isocitrate NAD 2-oxoglutarate CO2 NADH | DDB0232433 | CDS | 3407770 | 1083 | - | 0.369344 |
idhC | DDB_G0272208 | catalyzes the reaction isocitrate NADP 2-oxoglutarate CO2 NADPH | DDB0232429 | CDS | 1670009 | 1239 | + | 0.385795 |
idhM | DDB_G0272210 | catalyzes the reaction isocitrate NADP 2-oxoglutarate CO2 NADPH | DDB0232429 | CDS | 1672253 | 1287 | + | 0.346542 |
if1 | DDB_G0291988 | belongs to the wider family of mitochondrial F1F(o)-ATPase inhibitors contains a conserved ATPIF1 domain | DDB0232433 | CDS | 1251863 | 318 | - | 0.339623 |
ifdA | DDB_G0269146 | similar to eukaryotic translation initiation factor 4A isoform 2 | DDB0232428 | CDS | 2640023 | 1188 | + | 0.393939 |
ifkA | DDB_G0272837 | eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase putative protein serinethreonine kinase contains two kinase domains and a HisRS domain N-terminal kinase domain related to STE group C-terminal kinase domain related to GCN2 subfamily | DDB0232429 | CDS | 2194537 | 6777 | + | 0.273425 |
ifkB | DDB_G0276829 | putative eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase putative protein serinethreonine kinase related to the GCN2 family of protein kinases contains a kinase domain and a HisRS domain | DDB0232429 | CDS | 7412574 | 4077 | + | 0.297768 |
ifkC | DDB_G0276043 | putative eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase putative protein serinethreonine kinase contains the RWD domain found in GCN2 kinases and histidyl tRNA synthetases related to the GCN2 family of protein kinases that phosphorylate the alpha subunit of eIF2 | DDB0232429 | CDS | 6510818 | 5103 | - | 0.277288 |
iksA | DDB_G0283109 | similar to fungal kinases contains an IQ calmodulin-binding region | DDB0232431 | CDS | 257953 | 2940 | + | 0.272449 |
ileS | DDB_G0278293 | catalyzes the reaction ATP L-isoleucine tRNAIle AMP diphosphate L-isoleucyl-tRNAIle | DDB0232430 | CDS | 632971 | 3204 | - | 0.36236 |
iliA | DDB_G0285615 | contains a putative N-terminal signal sequence regulated by | DDB0232431 | CDS | 3469352 | 768 | + | 0.278646 |
iliB | DDB_G0284409 | induced by Legionella pneumophila infection | DDB0232431 | CDS | 1964242 | 597 | + | 0.278057 |
iliC | DDB_G0271068 | induced by Legionella pneumophila infection similar to D. purpureum protein | DDB0232428 | CDS | 4633487 | 663 | + | 0.346908 |
iliD | DDB_G0287717 | similar to hypothetical fungi proteins induced by Legionella pneumophila infection | DDB0232432 | CDS | 597404 | 1206 | + | 0.324212 |
iliE-1 | DDB_G0273157 | induced by Legionella pneumophila infection there is a second copy of this gene | DDB0232429 | CDS | 2479032 | 1014 | + | 0.234714 |
iliE-2 | DDB_G0273915 | induced by Legionella pneumophila infection there is a second copy of this gene | DDB0232429 | CDS | 3551741 | 1014 | - | 0.234714 |
iliE_ps | DDB_G0278287 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232430 | CDS | 623186 | 183 | - | 0.300546 |
iliF | DDB_G0280223 | induced by Legionella pneumophila infection | DDB0232430 | CDS | 3136945 | 366 | - | 0.344262 |
iliG | DDB_G0284295 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages induced by Legionella pneumophila infection | DDB0232431 | CDS | 1844275 | 1443 | + | 0.369369 |
iliH | DDB_G0271314 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages induced by Legionella pneumophila infection | DDB0232429 | CDS | 122691 | 1365 | + | 0.364103 |
iliI | DDB_G0269630 | belongs to a superfamily of metalloenzymes induced by Legionella pneumophila infection | DDB0232428 | CDS | 3187028 | 1047 | - | 0.299904 |
iliJ | DDB_G0286041 | contains a central large T4 RNA ligase RnlA-like domain a property shared by a related gene | DDB0232431 | CDS | 3987715 | 1332 | - | 0.250751 |
iliK | DDB_G0278649 | belongs to a superfamily of metalloenzymes induced by Legionella pneumophila infection | DDB0232430 | CDS | 636762 | 1002 | + | 0.336327 |
iliL | DDB_G0281853 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D contains a predicted signal peptide induced by Legionella pneumophila infection | DDB0232430 | CDS | 5017017 | 4893 | - | 0.30002 |
iliL_ps | DDB_G0276207 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 6367655 | 3561 | + | 0.286998 |
iliM | DDB_G0292328 | similar to bacterial aromatic-ring hydroxylases and fungal monooxygenases induced by Legionella pneumophila infection | DDB0232433 | CDS | 1489407 | 1272 | - | 0.259434 |
iliN | DDB_G0278481 | conserved protein induced by Legionella pneumophila infection | DDB0232430 | CDS | 950150 | 1527 | + | 0.362803 |
iliO | DDB_G0291520 | contains a DRB0094-related RNA ligase domain conserved in bacteria phages and fungi similar to D. purpureum protein induced by Legionella pneumophila infection | DDB0232433 | CDS | 473965 | 1305 | - | 0.300383 |
iliP | DDB_G0279707 | contains a predicted signal peptide induced by Legionella pneumophila infection there are two similar genes in D. discoideum | DDB0232430 | CDS | 2470281 | 654 | - | 0.324159 |
iliQ | DDB_G0292926 | contains a large ankyrin repeat region induced by Legionella pneumophila infection | DDB0232433 | CDS | 2280235 | 2490 | + | 0.214458 |
ilvB | DDB_G0278053 | catalyzes the reaction: 2 pyruvate 2-acetolactate COsub2sub | DDB0232430 | CDS | 198473 | 1935 | - | 0.331783 |
immp | DDB_G0283049 | in other organisms there are two subunits for this enzyme with relatively high sequence similarity to each other Dictyostelium appear to have a single gene | DDB0232431 | CDS | 142399 | 972 | + | 0.220165 |
imp3 | DDB_G0278983 | ortholog of the conserved eukaryotic IMP3 component of the 60-80S U3 small nucleolar ribonucleoprotein (U3 snoRNP) required for pre-18S rRNA processing forms a heterotrimeric complex containing IMP4 and MPP10 | DDB0232430 | CDS | 1474915 | 534 | + | 0.275281 |
imp4 | DDB_G0302418 | ortholog of the conserved eukaryotic IMP4 component of the 60-80S U3 small nucleolar ribonucleoprotein (U3 snoRNP) required for pre-18S rRNA processing forms a heterotrimeric complex containing IMP3 and MPP10 | DDB0232430 | CDS | 4835697 | 861 | + | 0.297329 |
impA | DDB_G0285455 | highly similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates the impA promoter is shared with and inversely regulated with dia1 during the growth-development transition | DDB0232431 | CDS | 3249271 | 585 | + | 0.324786 |
impA_ps | DDB_G0285457 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3250615 | 261 | + | 0.314176 |
impa1 | DDB_G0281239 | catalyzes the reaction myo-inositol phosphate Hsub2subO myo-inositol phosphate human IMPA1 is a pharmacological target for Li in the treatment of manic depression | DDB0232430 | CDS | 4261304 | 819 | + | 0.310134 |
ino1 | DDB_G0285505 | catalyzes the reaction D-glucose 6-phosphate 1D-myo-inositol 3-phosphate enzyme activity is reduced by valproate | DDB0232431 | CDS | 3324153 | 1536 | - | 0.363932 |
ino80 | DDB_G0292358 | similar to S. cerevisiae INO80 an ATPase that forms a large complex containing actin and several actin-related proteins that has chromatin remodeling activity and 3' to 5' DNA helicase activity in vitro chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232433 | CDS | 1406177 | 6390 | + | 0.308607 |
ints1 | DDB_G0285393 | ortholog of integrator complex subunit 1 component of a multiprotein mediator of small nuclear RNA processing | DDB0232431 | CDS | 3120198 | 7494 | - | 0.243662 |
ints11 | DDB_G0278189 | ortholog of integrator complex subunit 1 component of a multiprotein mediator of small nuclear RNA processing | DDB0232430 | CDS | 423737 | 2235 | + | 0.273825 |
ints2 | DDB_G0271040 | ortholog of integrator complex subunit 2 component of a multiprotein mediator of small nuclear RNA processing | DDB0232428 | CDS | 4285180 | 4089 | + | 0.223037 |
ints3 | DDB_G0268706 | ortholog of integrator complex subunit 3 component of a multiprotein mediator of small nuclear RNA processing | DDB0232428 | CDS | 1944951 | 4563 | + | 0.284681 |
ints4 | DDB_G0286633 | ortholog of integrator complex subunit 4 component of a multiprotein mediator of small nuclear RNA processing | DDB0232431 | CDS | 4760652 | 3702 | + | 0.23852 |
ints6 | DDB_G0277953 | ortholog of integrator complex subunit 6 component of a multiprotein mediator of small nuclear RNA processing a possible tumor suppressor | DDB0232430 | CDS | 56545 | 3324 | + | 0.301143 |
ints7 | DDB_G0284483 | ortholog of integrator complex subunit 7 component of a multiprotein mediator of small nuclear RNA processing | DDB0232431 | CDS | 2030962 | 3075 | - | 0.227967 |
ints9 | DDB_G0282473 | ortholog of integrator complex subunit 9 component of a multiprotein mediator of small nuclear RNA processing | DDB0232430 | CDS | 5815575 | 2139 | - | 0.255259 |
ionA | DDB_G0277269 | expressed in pstAB cells and in pstA cells and upper cup during culmination transports ions across membranes using ATP hydrolysis for energy contains 8 transmembrane domains | DDB0232429 | CDS | 7864423 | 3699 | + | 0.326304 |
ipi | DDB_G0290011 | DDB0232432 | CDS | 3572751 | 720 | + | 0.279167 | |
ipkA1 | DDB_G0271760 | DDB0232429 | CDS | 771015 | 948 | - | 0.283755 | |
iplA | DDB_G0292564 | required for cAMP-stimulated Ca2 uptake | DDB0232433 | CDS | 1805115 | 9534 | - | 0.266415 |
ipo13A | DDB_G0293110 | ortholog of importin 13 also known as Ran-binding protein 13 a nuclear transport receptor serves as receptor for nuclear localization signals (NLS) in cargo substrates and mediates docking of the importinsubstrate complex to the nuclear pore complex | DDB0232433 | CDS | 2522191 | 3195 | + | 0.252895 |
ipo13B | DDB_G0279441 | ortholog of importin 13 also known as Ran-binding protein 13 a nuclear transport receptor serves as receptor for nuclear localization signals (NLS) in cargo substrates and mediates docking of the importinsubstrate complex to the nuclear pore complex | DDB0232430 | CDS | 2053494 | 3360 | - | 0.263095 |
ipo4 | DDB_G0270336 | ortholog of importin 4 a nuclear transport receptor that is thought to mediate docking of the importinsubstrate complex to the nuclear pore complex | DDB0232428 | CDS | 4662405 | 3312 | - | 0.301329 |
ippA | DDB_G0275663 | converts 1D-myo-inositol 14-bisphosphate H2O to 1D-myo-inositol 4-phosphate phosphate | DDB0232429 | CDS | 5791228 | 936 | + | 0.314103 |
ippB | DDB_G0268652 | very similar to A. thaliana AHL and SAL1 phosphatases and S. pombe tol1 (halotolerance protein) all related to the S. cerevisiae HAL2 these proteins are 3'-phosphoadenosine-5'-phosphate (PAP) phosphatases that also act as inositol polyphosphate 1-phosphatases. | DDB0232428 | CDS | 1844690 | 999 | + | 0.274274 |
iptA | DDB_G0277215 | similar to plant pathogenic bacteria Ipt proteins involved in cytokinin synthesis IPP transferases modify both cytoplasmic and mitochondrial tRNAs at A(37) to give isopentenyl A(37) | DDB0232429 | CDS | 7652688 | 852 | - | 0.252347 |
iptB | DDB_G0291528 | DDB0232433 | CDS | 482754 | 1569 | + | 0.203952 | |
iptC-1 | DDB_G0273039 | IPP transferases modify both cytoplasmic and mitochondrial tRNAs at A(37) to give isopentenyl A(37) there is a second copy of this gene | DDB0232429 | CDS | 2360286 | 1242 | + | 0.223027 |
iptC-2 | DDB_G0274017 | IPP transferases modify both cytoplasmic and mitochondrial tRNAs at A(37) to give isopentenyl A(37) there is a second copy of this gene | DDB0232429 | CDS | 3669962 | 1242 | - | 0.223027 |
iqgC | DDB_G0288977 | contains a rasGAP domain similar to mammalian IQGAP proteins but lacking the calponin domain and the IQ-calmodulin binding region | DDB0232432 | CDS | 2198403 | 2454 | + | 0.347596 |
iqgD | DDB_G0275731 | similar to RasGAP proteins contains one calponin homology domain and one rasGAP domain | DDB0232429 | CDS | 5940660 | 4158 | - | 0.309524 |
ireA | DDB_G0267650 | ortholog of the yeast IRE1 serinethreonine kinaseendoribonuclease a transmembrane protein involved in the unfolded protein response contains a ribonuclease 2-5A domain and 3 pyrrolo-quinoline quinone (PQQ) domains | DDB0232428 | CDS | 495110 | 2955 | + | 0.237902 |
irlA | DDB_G0272987 | DDB0232429 | CDS | 2020830 | 4296 | + | 0.26513 | |
irlB-1 | DDB_G0273333 | putative protein serinethreonine kinase the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy there is a second copy of this gene | DDB0232429 | CDS | 2539802 | 4347 | - | 0.216931 |
irlB-2 | DDB_G0273857 | putative protein serinethreonine kinase the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy there is a second copy of this gene | DDB0232429 | CDS | 3487559 | 4347 | + | 0.216931 |
irlC | DDB_G0270894 | the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy contains a SWIM Zn-finger domain | DDB0232428 | CDS | 3195968 | 4335 | + | 0.231834 |
irlD | DDB_G0269632 | DDB0232428 | CDS | 3190841 | 4518 | + | 0.261399 | |
irlE | DDB_G0288803 | putative protein serinethreonine kinase the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy | DDB0232432 | CDS | 1985593 | 4053 | + | 0.237602 |
irlF-1 | DDB_G0273171 | putative protein serinethreonine kinase the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy there is a second copy of this gene | DDB0232429 | CDS | 2486835 | 4203 | + | 0.213657 |
irlF-2 | DDB_G0273903 | putative protein serinethreonine kinase the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy there is a second copy of this gene | DDB0232429 | CDS | 3540442 | 4203 | - | 0.213657 |
isca1 | DDB_G0280173 | DDB0232430 | CDS | 3050099 | 420 | + | 0.290476 | |
isca2 | DDB_G0284809 | DDB0232431 | CDS | 2506040 | 630 | - | 0.249206 | |
isg12 | DDB_G0272929 | DDB0232429 | CDS | 1918796 | 516 | + | 0.302326 | |
isw | DDB_G0292948 | similar to ISWI and mammalian SMARCA ATPases involved in nucleosome remodeling chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232433 | CDS | 2254360 | 3666 | + | 0.336061 |
isy1 | DDB_G0285521 | ortholog of human and yeast ISY1 which plays a role in mRNA splicing | DDB0232431 | CDS | 3341295 | 900 | + | 0.261111 |
itfg1 | DDB_G0292418 | very conserved protein the Dictyostelium protein contains 7 putative FG-GAP repeats conserved protein also known as T-cell immunomodulatory protein contains a putative N-terminal signal peptide and a C-terminal transmembrane domain. | DDB0232433 | CDS | 1576374 | 2052 | - | 0.300195 |
itpa | DDB_G0286495 | ortholog of human ITPA and S. cerevisiae HAM1 hydrolyzes ITP and dITP to their respective monophosphate derivatives defects in human ITPA cause inosine triphosphate pyrophosphohydrolase deficiency characterized by an abnormal accumulation of inosine triphosphate in erythrocytes however pathological symptoms are not known | DDB0232431 | CDS | 4555858 | 585 | - | 0.309402 |
itpk1 | DDB_G0269746 | phosphorylates 1D-myo-inositol 3456-tetrakisphosphate to 1D-myo-inositol 13456-pentakisphosphate | DDB0232428 | CDS | 3471589 | 981 | + | 0.24261 |
iunH | DDB_G0272738 | catalyzes the reaction N-D-ribosylpurine Hsub2subO purine D-ribose | DDB0232429 | CDS | 2227186 | 1023 | + | 0.311828 |
ivdA | DDB_G0279827 | catalyzes the reaction 3-methylbutanoyl-CoA acceptor 3-methylbut-2-enoyl-CoA reduced acceptor | DDB0232430 | CDS | 2597532 | 1248 | - | 0.335737 |
jcdA | DDB_G0290765 | DDB0232432 | CDS | 4576700 | 759 | + | 0.262187 | |
jcdB | DDB_G0268178 | DDB0232428 | CDS | 1602467 | 861 | + | 0.216028 | |
jcdC | DDB_G0286391 | DDB0232431 | CDS | 4401925 | 1248 | + | 0.208333 | |
jcdD | DDB_G0270906 | DDB0232428 | CDS | 3291492 | 1347 | + | 0.191537 | |
jcdE | DDB_G0292770 | DDB0232433 | CDS | 2038164 | 1062 | + | 0.249529 | |
jcdF | DDB_G0290869 | DDB0232432 | CDS | 4697072 | 1425 | - | 0.261053 | |
jcdG | DDB_G0287513 | conserved protein similar to H. sapiens C14orf169 | DDB0232432 | CDS | 349945 | 1545 | - | 0.322977 |
jcdH | DDB_G0280485 | DDB0232430 | CDS | 3434014 | 1611 | + | 0.27126 | |
jcdI | DDB_G0270006 | similar to the human JMJD6 which is required for organ differentiation during embryogenesis | DDB0232428 | CDS | 4018580 | 2952 | - | 0.281165 |
jcdJ | DDB_G0288859 | DDB0232432 | CDS | 2000009 | 2874 | + | 0.265136 | |
kcnma1 | DDB_G0269896 | ortholog of the human KCNMA1 a potassium channel activated by both membrane depolarization and increase in cytosolic Ca(2) that mediates export of K() defects in the gene cause generalized epilepsy and paroxysmal dyskinesia (GEPD) | DDB0232428 | CDS | 3812473 | 3735 | - | 0.274431 |
kctd9 | DDB_G0291330 | highly similar to vertebrate potassium channel tetramerization domain-containing proteins contains four pentapeptide repeats and a doublecourtin domain enriched in gametes | DDB0232433 | CDS | 130125 | 1467 | + | 0.324472 |
kdelr | DDB_G0272124 | endoplasmic reticulum receptor for the KDEL signal sequence of proteins resident in the endoplasmic reticulum believed to cycle between the cis side of the Golgi apparatus and the ER | DDB0232429 | CDS | 1376821 | 657 | - | 0.25723 |
keaA | DDB_G0271500 | keaA plays a role in the regulation of growth development and stress survival | DDB0232429 | CDS | 608312 | 3624 | - | 0.278422 |
kif1 | DDB_G0290963 | ortholog of C. elegans Unc104 and mammalian KIF1A involved in intracellular transport | DDB0232432 | CDS | 4896037 | 6618 | - | 0.316863 |
kif10 | DDB_G0293198 | DDB0232433 | CDS | 2654607 | 3717 | - | 0.262039 | |
kif11 | DDB_G0291039 | DDB0232432 | CDS | 4850945 | 2058 | - | 0.306122 | |
kif12 | DDB_G0268258 | MKLP1 subfamily kinesin required for cell division in suspension and for nuclei separation during karyokinesis localized in the nucleus during interphase and in the centrosome spindle and spindle midbody during cytokinesis | DDB0232428 | CDS | 1654404 | 4500 | + | 0.277333 |
kif13 | DDB_G0288361 | belongs to the BimCEg5 subfamily predicted to play a role in mitosis | DDB0232432 | CDS | 1422250 | 3798 | + | 0.28673 |
kif2 | DDB_G0267396 | belongs to the NCDKar3 subfamily predicted to play a role in mitosis | DDB0232428 | CDS | 351991 | 2379 | - | 0.286255 |
kif3 | DDB_G0280967 | kinesin-1 family protein involved in intracellular transport belongs to the kinesin KHC subfamily | DDB0232430 | CDS | 4109358 | 3582 | + | 0.303183 |
kif4 | DDB_G0285101 | belongs to the CENP-E subfamily predicted to play a role in mitosis has a putative nuclear localization signal C-terminal to its motor domain | DDB0232431 | CDS | 2856191 | 5769 | + | 0.268677 |
kif5 | DDB_G0276369 | kinesin-1 family protein belongs to the kinesin KHC subfamily binds microtubules in an ATP-dependent manner and bundles actin in vitro | DDB0232429 | CDS | 6648064 | 2973 | + | 0.282879 |
kif6 | DDB_G0267404 | belongs to the MCAKKif2 subfamily contains 1 SAM domain predicted to play a role in mitosis | DDB0232428 | CDS | 1747506 | 3093 | - | 0.282897 |
kif7 | DDB_G0281555 | DDB0232430 | CDS | 4819674 | 3768 | + | 0.286359 | |
kif8 | DDB_G0284471 | DDB0232431 | CDS | 2103969 | 5622 | - | 0.284596 | |
kif9 | DDB_G0274603 | DDB0232429 | CDS | 4280121 | 3669 | - | 0.275279 | |
kil1 | DDB_G0267630 | necessary for efficient intracellular killing of K. pneumoniae overexpression of kil1 a sulfotransferase restores the ability of | DDB0232428 | CDS | 443514 | 1416 | + | 0.246469 |
kil2 | DDB_G0279183 | DDB0232430 | CDS | 1731085 | 3477 | + | 0.33132 | |
kinX | DDB_G0283391 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family similar to LIM kinases which regulate actin dynamics | DDB0232431 | CDS | 749416 | 3285 | + | 0.312329 |
kinY | DDB_G0289661 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family similar to LIM kinases which regulate actin dynamics | DDB0232432 | CDS | 3255902 | 1740 | + | 0.251149 |
kmo | DDB_G0283173 | catalyzes the reaction L-kynurenine NADPH H Osub2sub 3-hydroxy-L-kynurenine NADP Hsub2subO during nicotinic acid biosynthesis | DDB0232431 | CDS | 359274 | 1383 | - | 0.31598 |
krsA | DDB_G0284181 | putative protein serinethreonine kinase belongs to the protein kinase MST subfamily similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase involved in signal transduction and hyperosmotic response | DDB0232431 | CDS | 1697612 | 1386 | - | 0.313853 |
krsB | DDB_G0267978 | putative protein serinethreonine kinase N-terminus similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase C-terminal half belongs to the peptidase C2 family contains 4 calpain III domains and has similarity to calpain-like cysteine protease | DDB0232428 | CDS | 1220851 | 3318 | + | 0.331826 |
ksrA-1 | DDB_G0272883 | catalyzes the reduction of sphinganine to 3-dehydrosphinganine in glycosphingolipid metabolism there is a second copy of this gene | DDB0232429 | CDS | 2361855 | 1005 | - | 0.311443 |
ksrA-2 | DDB_G0274015 | catalyzes the reduction of sphinganine to 3-dehydrosphinganine in glycosphingolipid metabolism there is a second copy of this gene | DDB0232429 | CDS | 3668724 | 1005 | + | 0.311443 |
ku70 | DDB_G0286069 | regulatory subunit of the DNA-dependent protein kinase complex DNA-PK which consists of Ku70 Ku80 and DNA-PKcs | DDB0232431 | CDS | 4023180 | 2730 | + | 0.277656 |
ku80 | DDB_G0286303 | subunit of the DNA-dependent protein kinase complex DNA-PK which consists of Ku70 Ku80 and DNA-PKcs | DDB0232431 | CDS | 4329334 | 2391 | + | 0.288164 |
kxcA | DDB_G0289859 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family contains calmodulin-binding RhoGEF and pleckstrin homology (PH) domains | DDB0232432 | CDS | 3309104 | 3936 | + | 0.256352 |
kxcA_ps | DDB_G0289983 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 3466598 | 351 | - | 0.264957 |
kxcB | DDB_G0293124 | kinase domain similar to those of stress-induced STK kinases contains a DH (Dbl homology) domain followed by a PH (pleckstrin homology) domain found in proteins shown to encode a GEF activity specific for Rho family members | DDB0232433 | CDS | 2557594 | 3378 | - | 0.301066 |
kynu | DDB_G0284203 | catalyzes the reaction L-kynurenine Hsub2subO anthranilate L-alanine during nicotinic acid biosynthesis | DDB0232431 | CDS | 1685557 | 1356 | - | 0.314897 |
l2hgdh | DDB_G0267656 | ortholog of the H. sapiens L2HGDH which when defective causes L-2-hydroxyglutaric aciduria-a rare autosomal recessive disorder | DDB0232428 | CDS | 518710 | 1341 | + | 0.282625 |
lap | DDB_G0279793 | lap bLbeucine bAbmino bPbeptidase | DDB0232430 | CDS | 2524840 | 1563 | + | 0.357646 |
ldhA | DDB_G0281101 | DDB0232430 | CDS | 4061672 | 1023 | - | 0.314761 | |
ldhd | DDB_G0270806 | catalyzes the reaction R)-lactate 2 ferricytochrome c pyruvate 2 ferrocytochrome c | DDB0232428 | CDS | 4800145 | 1665 | + | 0.306907 |
ldpA | DDB_G0291600 | DDB0232433 | CDS | 592384 | 1074 | - | 0.26257 | |
leo1 | DDB_G0286051 | component of the conserved Paf1 complex a multifunctional complex involved in histone methylation and plays a role in RNA elongation and processing | DDB0232431 | CDS | 3999753 | 1464 | - | 0.301913 |
leuS | DDB_G0285451 | catalyzes the reaction ATP L-leucine tRNALeu AMP diphosphate L-leucyl-tRNALeu | DDB0232431 | CDS | 3240792 | 3177 | + | 0.352849 |
lig1 | DDB_G0274493 | ATP-dependent DNA ligase required for the ligation of Okazaki fragments during lagging-strand DNA synthesis | DDB0232429 | CDS | 4400712 | 3579 | - | 0.299246 |
lig3 | DDB_G0283857 | ATP-dependent DNA ligase contains the BRCT domain which is also found in BRCA1 interacts with XRCC1 | DDB0232431 | CDS | 1062604 | 3528 | + | 0.289399 |
lig4 | DDB_G0292760 | ATP-dependent DNA ligase contains the BRCT domain which is also found in BRCA1 forms a complex with XRCC4 | DDB0232433 | CDS | 2052081 | 3267 | + | 0.270279 |
limA | DDB_G0283599 | DDB0232431 | CDS | 968949 | 3552 | - | 0.290259 | |
limB | DDB_G0284863 | DDB0232431 | CDS | 2691906 | 1662 | + | 0.353791 | |
limC | DDB_G0277881 | DDB0232430 | CDS | 309381 | 549 | - | 0.342441 | |
limD | DDB_G0291251 | DDB0232433 | CDS | 31751 | 2103 | - | 0.38136 | |
limD1 | DDB_G0287507 | DDB0232432 | CDS | 361279 | 597 | + | 0.335008 | |
limE | DDB_G0279415 | DDB0232430 | CDS | 2195759 | 600 | + | 0.393333 | |
limF | DDB_G0275157 | DDB0232429 | CDS | 5217220 | 594 | - | 0.254209 | |
limG | DDB_G0269548 | contains 3 zinc-binding LIM domains LIM domains are found in proteins with differing functions including gene expression and cytoskeleton organisation and development | DDB0232428 | CDS | 2974419 | 846 | - | 0.286052 |
lin54 | DDB_G0281519 | putative ortholog of human tesmin (MTL5) and C. elegans lin-54 that may play a role in chromatin remodeling or transcriptional repression has two copies of a cysteine rich motif as follows: C-X-C-X4-C-X3-YC-X-C-X6-C-X3-C-X-C-X2-Cbrbr bCommunity annotation: b Lin-54 was originally discovered in worms as a | DDB0232430 | CDS | 4464773 | 2709 | - | 0.23182 |
lin9 | DDB_G0286665 | putative ortholog of the C. elegans abnormal cell lineage protein Lin-9 the Drosophila ortholog aly is a member of a multiprotein complex containing retinoblastoma and RbAp48 (the ortholog of Dicty RbbD) which localizes to and stabilizes heterochromatin | DDB0232431 | CDS | 4807662 | 3000 | - | 0.269667 |
lip1 | DDB_G0268966 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | DDB0232428 | CDS | 2042126 | 1245 | + | 0.306827 |
lip2 | DDB_G0268740 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | DDB0232428 | CDS | 2028102 | 1248 | - | 0.250801 |
lip3 | DDB_G0268964 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | DDB0232428 | CDS | 2026277 | 1236 | - | 0.247573 |
lip4 | DDB_G0276083 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | DDB0232429 | CDS | 6415536 | 1290 | + | 0.300775 |
lip5 | DDB_G0277723 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | DDB0232429 | CDS | 8375987 | 1809 | - | 0.317302 |
lipA | DDB_G0279909 | similar to arachidonate 12-lipoxygenase which catalyzes the reaction arachidonate Osub2sub (5Z8Z10E14Z)-(12S)-12-hydroperoxyicosa-581014-tetraenoate enriched in gametes REMI mutant forms aberrant fruiting bodies see | DDB0232430 | CDS | 2734597 | 1890 | + | 0.274603 |
lis1 | DDB_G0288375 | dynein regulator associated with centrosomes and microtubules functionally interacts with dcx in cAMP signalling | DDB0232432 | CDS | 1452516 | 1260 | + | 0.35 |
litaf | DDB_G0289149 | D. dicoideum ortholog of the conserved lipopolysaccharide-induced tumor necrosis factor alpha factor (LITAF) induced in mamalian cells following treatment with lipopolysaccharide a small integral membrane protein of lysosomelate endosome contains one predicted transmembrane domain | DDB0232432 | CDS | 2419396 | 546 | + | 0.377289 |
lkb1 | DDB_G0279629 | CAMK group CAMKL family kinase protein kinase involved in regulating both development and the stress response | DDB0232430 | CDS | 2335074 | 1761 | - | 0.294719 |
lkhA | DDB_G0269148 | DDB0232428 | CDS | 4768681 | 1821 | + | 0.32235 | |
lmbd2B | DDB_G0281669 | transmembrane protein associated with endocytic cups and plays a role in cell migration | DDB0232430 | CDS | 4791599 | 2373 | + | 0.308049 |
lmcA | DDB_G0280543 | DDB0232430 | CDS | 3614124 | 483 | - | 0.372671 | |
lmcB | DDB_G0280533 | DDB0232430 | CDS | 3605551 | 483 | - | 0.374741 | |
lmnB | DDB_G0289429 | similar to mammalian lamin B1 localizes to the inner membrane of the nuclear envelope involved in chromatin and centrosome organization and stabilization | DDB0232432 | CDS | 2787284 | 2151 | + | 0.317062 |
lmpA | DDB_G0267406 | DDB0232428 | CDS | 1250161 | 2340 | - | 0.283333 | |
lmpB | DDB_G0287035 | DDB0232431 | CDS | 5254629 | 2268 | + | 0.351852 | |
lmpC | DDB_G0267440 | DDB0232428 | CDS | 1257306 | 2349 | - | 0.257556 | |
lpd | DDB_G0291648 | common component of the three 2-oxoacid dehydrogenase complexes oxidizing pyruvate 2-oxoglutarate and the branched-chain 2-oxo acids and of the glycine cleavage system complex | DDB0232433 | CDS | 70728 | 1467 | - | 0.387866 |
lrlA | DDB_G0286037 | similar to latrophilins that are a family of secretin-like G-protein-coupled receptors (GPCRs) contains 7 putative transmembrane domains | DDB0232431 | CDS | 3985122 | 921 | + | 0.243214 |
lrrA | DDB_G0294094 | putative ortholog of H. sapiens SHOC2 also known as Ras-binding protein Sur-8 | DDB0232429 | CDS | 440350 | 1533 | + | 0.332681 |
lrrB | DDB_G0287823 | DDB0232432 | CDS | 766914 | 2565 | - | 0.267057 | |
lsm1 | DDB_G0279837 | DDB0232430 | CDS | 2608266 | 390 | - | 0.282051 | |
lsm2 | DDB_G0281779 | DDB0232430 | CDS | 4953475 | 354 | + | 0.254237 | |
lsm3 | DDB_G0277107 | DDB0232429 | CDS | 7535075 | 294 | + | 0.272109 | |
lsm4 | DDB_G0287053 | DDB0232431 | CDS | 5235945 | 534 | - | 0.35206 | |
lsm5 | DDB_G0268716 | DDB0232428 | CDS | 1990918 | 294 | + | 0.265306 | |
lsm6 | DDB_G0275719 | DDB0232429 | CDS | 5998936 | 267 | + | 0.29588 | |
lsm7 | DDB_G0289499 | DDB0232432 | CDS | 2859869 | 294 | - | 0.292517 | |
lsm8 | DDB_G0288479 | DDB0232432 | CDS | 1585841 | 285 | - | 0.322807 | |
lsmd1 | DDB_G0269552 | snRNP Sm family protein similar to H. sapiens LSMD1 and to S. pombe U6 snRNP-associated protein Lsm7 | DDB0232428 | CDS | 2982129 | 345 | - | 0.281159 |
lsr1 | DDB_G0271670 | DDB0232429 | CDS | 820254 | 1125 | - | 0.395556 | |
lsrA | DDB_G0274217 | DDB0232429 | CDS | 4757826 | 2223 | - | 0.312191 | |
lst8 | DDB_G0292592 | component of the TORC2 (Tor complex 2) with Tor Rip3 and PiaA that plays a role in regulation of adenylate cyclase (ACA) and protein kinase B (PKB) activation during aggregation | DDB0232433 | CDS | 1819608 | 915 | - | 0.338798 |
ltv1 | DDB_G0275601 | similar to metazoan LVT proteins whose function is unknown | DDB0232429 | CDS | 5580042 | 1491 | + | 0.275654 |
lvsA | DDB_G0269150 | DDB0232428 | CDS | 3119127 | 10860 | - | 0.304236 | |
lvsB | DDB_G0271504 | DDB0232429 | CDS | 668886 | 12357 | + | 0.254916 | |
lvsB_ps | DDB_G0275977 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 6155469 | 189 | + | 0.312169 |
lvsC | DDB_G0280971 | DDB0232430 | CDS | 4286715 | 7476 | + | 0.290931 | |
lvsD | DDB_G0271502 | DDB0232429 | CDS | 622207 | 8904 | - | 0.260782 | |
lvsE | DDB_G0282925 | DDB0232431 | CDS | 90982 | 6579 | + | 0.286518 | |
lvsF | DDB_G0284333 | similar to mammalian FAN human LYST and mouse Beige proteins | DDB0232431 | CDS | 1946519 | 3465 | - | 0.278788 |
lvsG | DDB_G0268088 | protein with a beigeBEACH domain a weak protein kinase domain and N-terminal WD40 repeats does not contain the consensus sequences required for kinase function | DDB0232428 | CDS | 1432947 | 6540 | - | 0.272018 |
lyrm1 | DDB_G0281987 | belongs to a family of short proteins that includes ndufa6 from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | DDB0232430 | CDS | 5219597 | 354 | - | 0.271186 |
lyrm4 | DDB_G0290725 | belongs to a family of short proteins that includes proteins from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | DDB0232432 | CDS | 4502665 | 246 | - | 0.247967 |
lyrm5 | DDB_G0284341 | belongs to a family of short proteins that includes ndufa6 from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | DDB0232431 | CDS | 1857300 | 474 | + | 0.204641 |
lyrm7 | DDB_G0269218 | belongs to a family of short proteins that includes proteins from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | DDB0232428 | CDS | 3736784 | 423 | - | 0.274232 |
lysA | DDB_G0276797 | contains lysin motifLysM domain may be involved in bacterial cell wall degradation | DDB0232429 | CDS | 7337818 | 4218 | - | 0.276671 |
lysS | DDB_G0281437 | catalyzes the reaction ATP L-lysine tRNALys AMP diphosphate L-lysyl-tRNALys | DDB0232430 | CDS | 4498697 | 1656 | - | 0.384058 |
lzic | DDB_G0288823 | DDB0232432 | CDS | 2035104 | 579 | + | 0.26943 | |
macA | DDB_G0288533 | DDB0232432 | CDS | 1652258 | 6126 | - | 0.254163 | |
mad1 | DDB_G0287755 | conserved component of the spindle-assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate localized to centromeres during mitosis | DDB0232432 | CDS | 658379 | 2460 | - | 0.208537 |
maea | DDB_G0284463 | DDB0232431 | CDS | 2005913 | 1272 | - | 0.272799 | |
maf1 | DDB_G0278673 | negative regulator of RNA polymerase III homolog of H. sapiens and S. cerevisiae MAF1 | DDB0232430 | CDS | 788140 | 837 | - | 0.259259 |
magA | DDB_G0271050 | hydrolyses alkylated adenine residues on DNA releasing 3-methyladenine | DDB0232428 | CDS | 4479608 | 873 | - | 0.279496 |
magoh | DDB_G0270866 | conserved protein that is part of a post-splicing multiprotein complex involved in mRNA nuclear export the human ortholog interacts with | DDB0232428 | CDS | 2747913 | 594 | - | 0.267677 |
mai | DDB_G0278155 | catalyzes the reaction 4-maleylacetoacetate 4-fumarylacetoacetate | DDB0232430 | CDS | 376116 | 660 | + | 0.319697 |
mak16l | DDB_G0269642 | ortholog of S. cerevisiae MAK16 and mammalian RBM13 inyeast an essential nuclear protein constituent of 66S pre-ribosomal particles | DDB0232428 | CDS | 3206739 | 930 | + | 0.307527 |
malA | DDB_G0272524 | catalyzes the reaction (S)-malate NADPsupsup pyruvate COsub2sub NADPH Hsupsup transcriptionally regulated by SrfA | DDB0232429 | CDS | 1811286 | 1635 | + | 0.393272 |
malaS | DDB_G0275655 | catalyzes the reaction ATP L-alanine tRNAAla AMP diphosphate L-alanyl-tRNAAla | DDB0232429 | CDS | 5835586 | 2799 | + | 0.287245 |
manA | DDB_G0292206 | DDB0232433 | CDS | 1355092 | 3033 | - | 0.331355 | |
manA_ps | DDB_G0293896 | putative pseudogene alpha-mannosidase family protein | DDB0232433 | CDS | 3427824 | 981 | + | 0.196738 |
manB | DDB_G0278259 | DDB0232430 | CDS | 573780 | 3108 | + | 0.298584 | |
manC | DDB_G0268994 | DDB0232428 | CDS | 2093909 | 3240 | + | 0.225926 | |
manD | DDB_G0278653 | DDB0232430 | CDS | 660402 | 3669 | - | 0.24012 | |
manE | DDB_G0278651 | DDB0232430 | CDS | 655951 | 3372 | - | 0.242586 | |
manF | DDB_G0287231 | DDB0232432 | CDS | 28270 | 2985 | - | 0.271692 | |
manG | DDB_G0287577 | DDB0232432 | CDS | 413359 | 3264 | - | 0.321385 | |
maoA | DDB_G0288541 | catalyzes the reaction RCHsub2subNHsub2sub Hsub2subO Osub2sub RCHO ammonia Hsub2subOsub2sub acts on primary amines as well as on some secondary and tertiary amines | DDB0232432 | CDS | 1658897 | 1371 | - | 0.358133 |
maoB-1 | DDB_G0272582 | catalyzes the reaction RCHsub2subNHsub2sub Hsub2subO Osub2sub RCHO ammonia Hsub2subOsub2sub acts on primary amines as well as on some secondary and tertiary amines there is a second copy of this gene | DDB0232429 | CDS | 2385363 | 1416 | + | 0.28178 |
maoB-2 | DDB_G0273993 | catalyzes the reaction RCHsub2subNHsub2sub Hsub2subO Osub2sub RCHO ammonia Hsub2subOsub2sub acts on primary amines as well as on some secondary and tertiary amines there is a second copy of this gene | DDB0232429 | CDS | 3644879 | 1416 | - | 0.28178 |
maoC-1 | DDB_G0272584 | catalyzes the reaction RCHsub2subNHsub2sub Hsub2subO Osub2sub RCHO ammonia Hsub2subOsub2sub acts on primary amines as well as on some secondary and tertiary amines there is a second copy of this gene | DDB0232429 | CDS | 2388472 | 1404 | + | 0.279202 |
maoC-2 | DDB_G0273991 | catalyzes the reaction RCHsub2subNHsub2sub Hsub2subO Osub2sub RCHO ammonia Hsub2subOsub2sub acts on primary amines as well as on some secondary and tertiary amines there is a second copy of this gene | DDB0232429 | CDS | 3641808 | 1404 | - | 0.279202 |
maoD | DDB_G0282999 | catalyzes the reaction RCHsub2subNHsub2sub Hsub2subO Osub2sub RCHO ammonia Hsub2subOsub2sub acts on primary amines as well as on some secondary and tertiary amines | DDB0232431 | CDS | 133295 | 1665 | - | 0.255255 |
map1d | DDB_G0280127 | releases N-terminal amino acids preferentially methionine from peptides and arylamides ortholog of the human mitochondrial MAPD1 | DDB0232430 | CDS | 2983397 | 1215 | - | 0.283951 |
mapbpip | DDB_G0291091 | in mammalian cells involved in late endosome function mutations in the human ortholog causes an immunodeficiency syndrome | DDB0232432 | CDS | 4971500 | 372 | - | 0.276882 |
mapksp1 | DDB_G0274833 | ortholog of human MAPKSP1 which is an adaptor protein required for MAPK signaling and ERK12 activation | DDB0232429 | CDS | 4072005 | 399 | - | 0.278196 |
masA | DDB_G0275887 | catalyzes the reaction acetyl-CoA Hsub2subO glyoxylate malate coenzyme A expressed in pstAB and pstO cells and in upper cup during culmination | DDB0232429 | CDS | 5903117 | 1632 | + | 0.313113 |
masB | DDB_G0282969 | catalyzes the reaction acetyl-CoA Hsub2subO glyoxylate malate coenzyme A | DDB0232431 | CDS | 72206 | 1629 | - | 0.267649 |
maspS | DDB_G0270152 | catalyzes the reaction ATP L-aspartate tRNAAsp AMP diphosphate L-aspartyl-tRNAAsp | DDB0232428 | CDS | 4321908 | 2079 | - | 0.292929 |
matA | DDB_G0289165 | DDB0232432 | CDS | 2438822 | 324 | - | 0.317901 | |
mbtps1 | DDB_G0282397 | ortholog of H. sapiens MBTPS1 which catalyzes the first step in the proteolytic activation of sterol regulatory element-binding proteins (SREBPs) | DDB0232430 | CDS | 5699822 | 3996 | - | 0.287788 |
mbtps2 | DDB_G0275939 | ortholog of H. sapiens MBTPS2 which catalyzes the proteolytic activation of sterol regulatory element-binding proteins (SREBPs) | DDB0232429 | CDS | 6123589 | 1689 | + | 0.22913 |
mccA | DDB_G0287377 | catalyzes the reaction ATP 3-methylcrotonoyl-CoA HCOsub3subsup-sup ADP phosphate 3-methylglutaconyl-CoA | DDB0232432 | CDS | 230145 | 2100 | + | 0.369048 |
mccB | DDB_G0271960 | catalyzes the reaction ATP 3-methylcrotonoyl-CoA HCOsub3subsup-sup ADP phosphate 3-methylglutaconyl-CoA | DDB0232429 | CDS | 1078393 | 1767 | - | 0.377476 |
mcee | DDB_G0275181 | catalyzes the reaction L-methylmalonyl-CoA D-methylmalonyl-CoA | DDB0232429 | CDS | 5327661 | 501 | - | 0.291417 |
mcfA | DDB_G0291312 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane contains at least three transmembrane domainsbrbr bCommunity annotation:b Overview of the | DDB0232433 | CDS | 114038 | 984 | - | 0.28252 |
mcfB | DDB_G0285599 | similar to the H. sapiens calcium-dependent mitochondrial aspartate and glutamate carriers SLC25A24 and SLC25A25 contains two EF-handsbrbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 3430845 | 1305 | + | 0.28046 |
mcfC | DDB_G0287009 | putative orthlolog of H. sapiens SLC25A24 calcium-dependent mitochondrial ATP-MgPi carrier contains four N-terminal EF-handsbrbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 5197882 | 1419 | - | 0.284708 |
mcfD | DDB_G0269352 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | DDB0232428 | CDS | 2576335 | 1035 | - | 0.316908 |
mcfE | DDB_G0269394 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | DDB0232428 | CDS | 2699017 | 912 | + | 0.313596 |
mcfF | DDB_G0269470 | ortholog of H. sapiens SLC25A28 and D. reiro SLC25A37 involved in iron transport across the mitochondrial membranebrbr bCommunity annotation:b Overview of the | DDB0232428 | CDS | 2836764 | 927 | - | 0.340885 |
mcfG | DDB_G0293556 | ortholog of slc25a20 involved in transport of carnitineacylcarnitine across the mitochondrial membranebrbr bCommunity annotation:b Overview of the | DDB0232433 | CDS | 3039817 | 903 | - | 0.346622 |
mcfH | DDB_G0275985 | ortholog of SLC25a40 that belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membranebrbr bCommunity annotation:b Overview of the | DDB0232429 | CDS | 6144623 | 1101 | - | 0.29337 |
mcfI | DDB_G0271922 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane regulated by the MADS-box transcription factor SrfA during development brbr bCommunity annotation:b Overview of the | DDB0232429 | CDS | 1050008 | 1017 | - | 0.322517 |
mcfJ | DDB_G0280083 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membranebrbr bCommunity annotation:b Overview of the | DDB0232430 | CDS | 2907001 | 1038 | + | 0.289017 |
mcfK | DDB_G0280161 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membranebrbr bCommunity annotation:b Overview of the | DDB0232430 | CDS | 3035184 | 972 | - | 0.279835 |
mcfL | DDB_G0280021 | DDB0232430 | CDS | 2797799 | 858 | + | 0.327506 | |
mcfM | DDB_G0283751 | ortholog of SLC25A32 involved in transport of folate across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 1044239 | 921 | - | 0.261672 |
mcfN | DDB_G0293646 | ortholog of the human SLC25A3 and S. cerevisiae MIR1 which transports inorganic phosphate from the cytosol to the mitochondrion matrix brbr bCommunity annotation:b Overview of the | DDB0232433 | CDS | 3201771 | 897 | + | 0.396878 |
mcfO | DDB_G0283329 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane very similar to the calcium-dependent mitochondrial aspartate and glutamate carrier aralar1 (slc25A12) the human protein may have a function in the urea cyclebrbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 432962 | 2319 | - | 0.329021 |
mcfP | DDB_G0292034 | ortholog of Grave disease carrier protein (slc25a16) belongs to the substrate carrier proteins that are involved in transport of molecules across the mitochondrial membrane may transport coenzyme A brbr bCommunity annotation:b Overview of the | DDB0232433 | CDS | 1058459 | 894 | + | 0.318792 |
mcfQ | DDB_G0272346 | ortholog of slc25a17 a peroximal membrane protein involved in transport of solutes contains five transmembrane domains brbr bCommunity annotation:b Overview of the | DDB0232429 | CDS | 1356603 | 990 | + | 0.311111 |
mcfR | DDB_G0283811 | similar to Grave disease carrier protein (slc25a16) belongs to the substrate carrier proteins that are involved in transport of molecules across the mitochondrial membrane may transport coenzyme A brbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 1144131 | 981 | + | 0.280326 |
mcfS | DDB_G0290913 | similar to slc25a20 involved in transport of carnitineacylcarnitine across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | DDB0232432 | CDS | 4740703 | 858 | + | 0.343823 |
mcfT | DDB_G0267704 | ortholog of the yeast ODC2 and mammalian SLCA2521 which transport C5-C7 oxodicarboxylates across the mitochondrial membrane belongs to the mitochondrial substrate carrier family brbr bCommunity annotation:b Overview of the | DDB0232428 | CDS | 661668 | 903 | + | 0.345515 |
mcfU | DDB_G0282727 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membranebrbr bCommunity annotation:b Overview of the | DDB0232430 | CDS | 6213878 | 1173 | - | 0.292413 |
mcfV | DDB_G0276261 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | DDB0232429 | CDS | 6532428 | 1584 | - | 0.280303 |
mcfW | DDB_G0290669 | belongs to the substrate carrier proteins that are involved in energy transferbrbr bCommunity annotation:b Overview of the | DDB0232432 | CDS | 4316139 | 990 | - | 0.3 |
mcfX | DDB_G0276933 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane has similarity to the calcium-dependent mitochondrial aspartate and glutamate carriers aralar1 and 2 (slc25A12 and 13) but does not contain a EF-hand calcium-binding domain such as | DDB0232429 | CDS | 7219497 | 906 | + | 0.327815 |
mcfY | DDB_G0274501 | belongs to the substrate carrier proteins that are involved in energy transferbrbr bCommunity annotation:b Overview of the | DDB0232429 | CDS | 4384213 | 1311 | + | 0.22807 |
mcfZ | DDB_G0293874 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane expressed in pstAO cells and in upper and lower cups during culminationbrbr bCommunity annotation:b Overview of the | DDB0232433 | CDS | 3410167 | 906 | + | 0.36755 |
mcln | DDB_G0291275 | ortholog of mucolipin when defective causing mucolipidosis type IV putative Ca2 channel contains a potential Ca2-binding EF hand as a regulatory site and 6 putative transmembrane domains | DDB0232433 | CDS | 41617 | 2472 | + | 0.259304 |
mcm2 | DDB_G0286623 | similar to MCM2 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | DDB0232431 | CDS | 4745862 | 3027 | + | 0.320449 |
mcm3 | DDB_G0280309 | similar to MCM3 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | DDB0232430 | CDS | 3235987 | 2604 | - | 0.305684 |
mcm4 | DDB_G0275623 | similar to MCM4 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | DDB0232429 | CDS | 5936245 | 2661 | - | 0.287862 |
mcm5 | DDB_G0292958 | similar to MCM5 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | DDB0232433 | CDS | 2121500 | 2274 | - | 0.329815 |
mcm6 | DDB_G0272760 | similar to MCM6 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | DDB0232429 | CDS | 2111171 | 2604 | - | 0.300307 |
mcm7 | DDB_G0282933 | similar to MCM7 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | DDB0232431 | CDS | 12867 | 2370 | + | 0.319409 |
mcm8 | DDB_G0283009 | DDB0232431 | CDS | 149067 | 2439 | - | 0.304633 | |
mcm9 | DDB_G0286035 | DDB0232431 | CDS | 3976133 | 3828 | + | 0.299373 | |
mcysS | DDB_G0277295 | catalyzes the reaction ATP L-cysteine tRNACys AMP diphosphate L-cysteinyl-tRNACys | DDB0232429 | CDS | 7755927 | 1752 | + | 0.250571 |
mdhA | DDB_G0290207 | catalyzes the reaction malate NAD oxaloacetate NADH | DDB0232432 | CDS | 3795307 | 1176 | - | 0.330782 |
mdhB | DDB_G0292600 | catalyzes the reaction malate NAD oxaloacetate NADH contains a predicted mitochondrial transit peptide | DDB0232433 | CDS | 1826095 | 1047 | + | 0.39255 |
mdhC | DDB_G0280255 | catalyzes the reaction malate NAD oxaloacetate NADH | DDB0232430 | CDS | 3171359 | 1002 | - | 0.363273 |
mdm12 | DDB_G0278277 | similar to yeast proteins of the MDM12 family (mitochondrial distribution and morphology protein 12) S. cerevisiae MDM12 is a component of the endoplasmic reticulum-mitochondria encounter structure which is essential for maintaining the structure of mitochondria | DDB0232430 | CDS | 606213 | 609 | - | 0.27422 |
mdn1 | DDB_G0295765 | Dictyostelium ortholog of the conserved midasin a large protein containing an AAA ATPase domain and a C-terminal VWFA domain S. cerevisiae MDN1 is a rRNA processing ATPase. | DDB0232429 | CDS | 5627352 | 17703 | - | 0.282438 |
mdn1_ps1 | DDB_G0280699 | putative pseudogene fragment similar to midasin gene | DDB0232430 | CDS | 3646107 | 240 | + | 0.291667 |
mdn1_ps2 | DDB_G0271648 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 654222 | 144 | - | 0.298611 |
mdn1_ps3 | DDB_G0271582 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 642805 | 315 | + | 0.288889 |
mecr | DDB_G0278095 | ortholog of the mammalian MECR and S. cerevisiae ETR1 a mitochondrial 2-enoyl thioester reductase that belongs to the zinc-containing alcohol dehydrogenase family | DDB0232430 | CDS | 262493 | 1053 | - | 0.358025 |
med1 | DDB_G0282453 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 1 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232430 | CDS | 5777523 | 2175 | + | 0.222989 |
med10 | DDB_G0290209 | ortholog of the mediator of RNA polymerase II transcription subunit 10 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232432 | CDS | 3797080 | 660 | - | 0.234848 |
med11 | DDB_G0280109 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 11 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232430 | CDS | 2948262 | 432 | + | 0.229167 |
med12 | DDB_G0281277 | putative ortholog of the mediator of RNA polymerase II transcription subunit 12 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232430 | CDS | 4322929 | 8196 | - | 0.276232 |
med14 | DDB_G0291297 | ortholog of the mediator of RNA polymerase II transcription subunit 14 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232433 | CDS | 72961 | 4263 | + | 0.26343 |
med15 | DDB_G0293914 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 15 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232433 | CDS | 3468362 | 2556 | - | 0.267214 |
med16 | DDB_G0279157 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 16 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA | DDB0232430 | CDS | 1701022 | 4533 | + | 0.270682 |
med17 | DDB_G0279723 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 17 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232430 | CDS | 2384965 | 2571 | + | 0.296383 |
med18 | DDB_G0285713 | ortholog of the mediator of RNA polymerase II transcription subunit 18 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 3629117 | 756 | + | 0.313492 |
med19 | DDB_G0271246 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 19 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232429 | CDS | 229505 | 900 | - | 0.236667 |
med20 | DDB_G0290781 | ortholog of the mediator of RNA polymerase II transcription subunit 20 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232432 | CDS | 4593057 | 588 | - | 0.304422 |
med21 | DDB_G0289339 | ortholog of the mediator of RNA polymerase II transcription subunit 21 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232432 | CDS | 2661517 | 594 | + | 0.333333 |
med22 | DDB_G0279087 | ortholog of the mediator of RNA polymerase II transcription subunit 22 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232430 | CDS | 1601131 | 450 | - | 0.253333 |
med23 | DDB_G0270434 | ortholog of the mediator of RNA polymerase II transcription subunit 23 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232428 | CDS | 4866950 | 4989 | + | 0.258368 |
med24 | DDB_G0289971 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription 24 (metazoa) or subunit 5 (fungi) the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232432 | CDS | 3401311 | 6111 | + | 0.231222 |
med25 | DDB_G0286967 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 25 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 5053310 | 4661 | - | 0.297576 |
med26 | DDB_G0275733 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 26 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232429 | CDS | 5914994 | 6222 | + | 0.275635 |
med27 | DDB_G0271072 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 27 (metazoa) or 3 (fungi) the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232428 | CDS | 4635594 | 1353 | + | 0.274205 |
med28 | DDB_G0292324 | ortholog of the mediator of RNA polymerase II transcription subunit 28 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232433 | CDS | 1483431 | 540 | + | 0.248148 |
med29 | DDB_G0284719 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 29 (metazoa) or 2 (fungi) the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 2245895 | 1665 | + | 0.253453 |
med30 | DDB_G0274443 | putative and poorly conserved mediator of RNA polymerase II transcription subunit 30 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232429 | CDS | 4579134 | 768 | - | 0.259115 |
med31 | DDB_G0285221 | ortholog of the mediator of RNA polymerase II transcription subunit 31 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 2996613 | 531 | - | 0.265537 |
med4 | DDB_G0292608 | ortholog of the mediator of RNA polymerase II transcription subunit 4 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232433 | CDS | 1833713 | 1032 | + | 0.297481 |
med6 | DDB_G0284421 | ortholog of the mediator of RNA polymerase II transcription subunit 6 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 1975693 | 804 | - | 0.257463 |
med7 | DDB_G0269568 | ortholog of the mediator of RNA polymerase II transcription subunit 7 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232428 | CDS | 3017741 | 1038 | - | 0.231214 |
med8 | DDB_G0293824 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 8 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232433 | CDS | 3346216 | 1575 | + | 0.31873 |
med9 | DDB_G0287019 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 9 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 5209121 | 594 | + | 0.274411 |
mef2A | DDB_G0268920 | DDB0232428 | CDS | 1828316 | 3150 | - | 0.272698 | |
mekA | DDB_G0269152 | STE SerThr protein kinase family mitogen-activated protein kinase kinase involved in chemotaxis and early development phosphorylates the MAP kinase Erk1 (erkA) is sumoyalated by sumo and ubiquinated by mip1 | DDB0232428 | CDS | 4015409 | 1983 | - | 0.252143 |
melA | DDB_G0271490 | conserved protein alpha-galactosidase (melibiase) catalyses the hydrolysis of melibiose into galactose and glucose | DDB0232429 | CDS | 432789 | 1158 | - | 0.365285 |
memo1 | DDB_G0284869 | ortholog of the H. sapiens MEMO1 a mediator of ErbB2-driven cell motility | DDB0232431 | CDS | 2629450 | 873 | - | 0.293242 |
metK | DDB_G0291179 | catalyzes the reaction ATP L-methionine Hsub2subO phosphate pyrophosphate S-adenosyl-L-methionine | DDB0232432 | CDS | 5102281 | 1155 | - | 0.406926 |
metS | DDB_G0279113 | catalyzes the reaction ATP L-methionine tRNAMet AMP diphosphate L-methionyl-tRNAMet | DDB0232430 | CDS | 1648404 | 2211 | - | 0.341022 |
metap1 | DDB_G0279433 | catalyzes the release of N-terminal amino acids preferentially methionine from peptides and arylamides | DDB0232430 | CDS | 2043258 | 1104 | - | 0.320652 |
metap2 | DDB_G0270264 | catalyzes the release of N-terminal amino acids preferentially methionine from peptides and arylamides | DDB0232428 | CDS | 4531797 | 1311 | + | 0.348589 |
mettl1 | DDB_G0276491 | ortholog of the conserved methyltransferase-like 1 (METTL1) which in H. sapiens forms a complex with WDR4 catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | DDB0232429 | CDS | 6855520 | 837 | + | 0.309438 |
mf12 | DDB_G0288067 | DDB0232432 | CDS | 1125741 | 4554 | + | 0.284365 | |
mfap1 | DDB_G0282219 | ortholog of MFAP1 a component of elastin-associated microfibrils in the extracellular matrix in beef no signal peptide detected in the Dictyostelium gene | DDB0232430 | CDS | 5530765 | 1383 | - | 0.301518 |
mfeA | DDB_G0291247 | DDB0232433 | CDS | 383676 | 1326 | - | 0.390649 | |
mfeB | DDB_G0277911 | DDB0232430 | CDS | 996509 | 885 | + | 0.308475 | |
mfsd1 | DDB_G0289201 | ortholog of the human MSFD1 also knon as SMAP-4 (Smooth Muscle cell-Associated Protein 4) contains 10 putative transmembrane domains and an additional potential signal peptide | DDB0232432 | CDS | 2461603 | 1521 | - | 0.336621 |
mgluS | DDB_G0271906 | catalyzes the reaction ATP L-glutamate tRNAGlu AMP diphosphate L-glutamyl-tRNAGlu | DDB0232429 | CDS | 1062208 | 1755 | - | 0.267236 |
mgm101 | DDB_G0277451 | conserved protein in fungi and Dictyostelium in S. cerevisiae required for the repair of oxidative mtDNA damage | DDB0232429 | CDS | 8124262 | 1134 | + | 0.30776 |
mgmt | DDB_G0275095 | transfers methyl groups from DNA containing sup6supO-methylguanine to a cysteine residue | DDB0232429 | CDS | 5058865 | 618 | - | 0.237864 |
mgp1 | DDB_G0290233 | DDB0232432 | CDS | 3834823 | 2763 | + | 0.287007 | |
mgp2 | DDB_G0270024 | DDB0232428 | CDS | 4042887 | 2634 | - | 0.31549 | |
mgp3 | DDB_G0269624 | DDB0232428 | CDS | 3170314 | 4014 | + | 0.294469 | |
mgp4 | DDB_G0283899 | DDB0232431 | CDS | 1248575 | 2730 | + | 0.296337 | |
mhcA | DDB_G0286355 | myosin II heavy chain component of the actin-based molecular motor (conventional myosin) has actin-activated ATPase activity myosin II consists of two heavy chains and one essential (mlcE) and one regulatory light chain (mlcR) respectively | DDB0232431 | CDS | 4451077 | 6351 | + | 0.377893 |
mhisS | DDB_G0269822 | catalyzes the reaction ATP L-histidine tRNAHis AMP diphosphate L-histidyl-tRNAHis similar to bacterial histidine-tRNA ligase | DDB0232428 | CDS | 3669575 | 1506 | - | 0.249004 |
mhkA | DDB_G0291231 | myosin II heavy chain kinase is an atypical protein serinethreonine kinase in the Alpha kinase group phosphorylates the myosin II heavy chain and drives myosin II disassembly | DDB0232433 | CDS | 65139 | 3441 | + | 0.334496 |
mhkB | DDB_G0289115 | myosin heavy chain kinase an atypical protein serinethreonine kinase in the Alpha kinase group participates in the regulation of myosin II assembly into the cytoskeleton | DDB0232432 | CDS | 2375954 | 2199 | + | 0.289677 |
mhkC | DDB_G0290687 | myosin heavy chain kinase an atypical protein serinethreonine kinase in the Alpha kinase group drives the disassembly of myosin II filaments for efficient cytokinesis REMI mutant forms aberrant fruiting bodies see | DDB0232432 | CDS | 4426907 | 2343 | - | 0.349979 |
mhkD | DDB_G0282489 | belongs to the Atypical Alpha protein kinases highly similar to Dictyostelium mhkA contains N-terminal predicted coiled-coil domain contains C-terminal G-protein beta WD-40 repeats | DDB0232430 | CDS | 5835955 | 2826 | - | 0.279193 |
mhsp70 | DDB_G0293298 | DDB0232433 | CDS | 2761673 | 1977 | + | 0.376834 | |
midA | DDB_G0282615 | conserved protein required for mitochondrial complex I assembly both in Dictyostelium and in human interacts with the mitochondrial complex I protein | DDB0232430 | CDS | 6003476 | 1455 | + | 0.309278 |
migA | DDB_G0283263 | DDB0232431 | CDS | 453096 | 2592 | + | 0.275077 | |
mileS | DDB_G0293030 | catalyzes the reaction ATP L-isoleucine tRNAIle AMP diphosphate L-isoleucyl-tRNAIle | DDB0232433 | CDS | 2348091 | 3105 | - | 0.287601 |
miox | DDB_G0290161 | catalyzes the reaction myo-inositol Osup2sup D-glucuronate Hsup2supO | DDB0232432 | CDS | 3722127 | 879 | + | 0.269625 |
mip1-1 | DDB_G0273399 | physically interacts with and ubiquinates the MAP kinase kinase Mek1 (mekA) and controls its nuclear localizationbr there is a second copy of this gene | DDB0232429 | CDS | 2961762 | 1659 | - | 0.324895 |
mip1-2 | DDB_G0273535 | physically interacts with and ubiquinates the MAP kinase kinase Mek1 (mekA) and controls its nuclear localizationbr there is a second copy of this gene | DDB0232429 | CDS | 3068294 | 1659 | + | 0.324895 |
mipA | DDB_G0292812 | conserved hypothetical Dictyostelium protein contains a predicted signal sequence and a C-terminal transmembrane domain | DDB0232433 | CDS | 2204194 | 4182 | + | 0.24988 |
mipp1 | DDB_G0285339 | enzyme that hydrolyzes 23 bisphosphoglycerate to yield 2-phosphoglycerate | DDB0232431 | CDS | 3103340 | 1908 | + | 0.284591 |
mkcA | DDB_G0285427 | similar to MAP cascade kinases belonging to the PAK sub-family of the STE20 serinethreonine kinases partial suppressor of tagB mutation | DDB0232431 | CDS | 3440715 | 2583 | - | 0.275648 |
mkcB | DDB_G0290723 | similar to Dictyostelium mkcA and other mitogen-activated protein kinases (Ste20PAK family) REMI mutant forms aberrant fruiting bodies see | DDB0232432 | CDS | 4499748 | 2145 | + | 0.332867 |
mkcC | DDB_G0287853 | kinase domain very similar to those of Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) | DDB0232432 | CDS | 826726 | 2676 | + | 0.342302 |
mkcD | DDB_G0277413 | similar to Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) | DDB0232429 | CDS | 7960057 | 1959 | + | 0.291986 |
mkcE | DDB_G0281649 | kinase domain similar to those of Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) | DDB0232430 | CDS | 4757942 | 2148 | + | 0.271881 |
mkcF | DDB_G0270102 | similar to Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) contains one SH3 (src Homology-3) domain | DDB0232428 | CDS | 4222376 | 2034 | - | 0.319076 |
mkkA | DDB_G0283265 | developmentally regulated MEKK | DDB0232431 | CDS | 530684 | 3804 | + | 0.287066 |
mkpA | DDB_G0288249 | contains a dual specificity protein phosphatase domain and a weak gelsolin domain dual specificity protein phosphatases regulate mitogenic signal transduction and control the cell cycle REMI mutant fails to aggregate see | DDB0232432 | CDS | 1323200 | 4632 | - | 0.251727 |
mkpB-1 | DDB_G0273199 | similar to the cofilin phosphatase slingshot and to other dual-specificity phosphatasesbr there is a second copy of this gene | DDB0232429 | CDS | 2698234 | 1431 | + | 0.292802 |
mkpB-2 | DDB_G0273729 | similar to the cofilin phosphatase slingshot and to other dual-specificity phosphatasesbr there is a second copy of this gene | DDB0232429 | CDS | 3332122 | 1431 | - | 0.292802 |
mlcB | DDB_G0290077 | light chain that binds to the neck region of myoB contains two calcium-binding EF-hands | DDB0232432 | CDS | 3622051 | 222 | + | 0.315315 |
mlcC | DDB_G0289563 | light chain that binds to the neck region of myoC contains two calcium-binding EF-hand motifs but does not bind calcium | DDB0232432 | CDS | 2954406 | 225 | - | 0.311111 |
mlcD | DDB_G0277917 | DDB0232430 | CDS | 607477 | 444 | + | 0.304054 | |
mlcE | DDB_G0277859 | component of actin-based molecular motor myosin II (conventional myosin) component | DDB0232430 | CDS | 76885 | 453 | + | 0.364238 |
mlcR | DDB_G0276077 | component of actin-based molecular motor myosin II (conventional myosin) component | DDB0232429 | CDS | 6426413 | 486 | + | 0.31893 |
mleuS | DDB_G0291346 | catalyzes the reaction ATP L-leucine tRNALeu AMP diphosphate L-leucyl-tRNALeu | DDB0232433 | CDS | 154547 | 2823 | + | 0.29791 |
mlh1 | DDB_G0287393 | MLH1 ortholog required for DNA mismatch repair | DDB0232432 | CDS | 247623 | 2655 | - | 0.282109 |
mlh3 | DDB_G0283883 | MLH3 ortholog required for DNA mismatch repair | DDB0232431 | CDS | 1160700 | 4977 | + | 0.279687 |
mlkA | DDB_G0279925 | CAMK1 family protein kinase phosphorylates the myosin II regulatory light chain at S13 is not regulated by Ca2calmodulin | DDB0232430 | CDS | 2752719 | 888 | - | 0.317568 |
mlysS | DDB_G0286517 | catalyzes the reaction ATP L-lysine tRNALys AMP diphosphate L-lysyl-tRNALys | DDB0232431 | CDS | 4584316 | 1848 | + | 0.267316 |
mmetS | DDB_G0285759 | catalyzes the reaction ATP L-methionine tRNAMet AMP diphosphate L-methionyl-tRNAMet | DDB0232431 | CDS | 3423740 | 1728 | + | 0.305556 |
mmgt | DDB_G0274571 | ortholog of the magnesium transporter MMGT1 contains a putative signal sequence and one transmembrane domain | DDB0232429 | CDS | 3975881 | 318 | + | 0.257862 |
mmm1 | DDB_G0285921 | similar to S. cerevisiae MMM1 (maintenance of mitochondrial morphology protein 1) MMM1 is a component of the endoplasmic reticulum-mitochondria encounter structure which is essential for maintaining the structure of mitochondria contains one putative transmembrane domain | DDB0232431 | CDS | 3830484 | 1080 | + | 0.251852 |
mms19 | DDB_G0288217 | DDB0232432 | CDS | 1259948 | 3348 | + | 0.233572 | |
mmsdh | DDB_G0289085 | catalyzes the reaction 2-methyl-3-oxopropanoate CoA NAD propanoyl-CoA COsub2sub NADH Hsupsup | DDB0232432 | CDS | 2337171 | 1587 | + | 0.389414 |
mnat1 | DDB_G0289079 | DDB0232432 | CDS | 2330339 | 978 | + | 0.293456 | |
mnd1 | DDB_G0291750 | DDB0232433 | CDS | 686426 | 666 | - | 0.252252 | |
mobA | DDB_G0278907 | similar to the Mob1 family of proteins which are of unknown function but interact with Mps1 and NDR kinases Dictyostelium MobA has been shown to bind NdrA | DDB0232430 | CDS | 1373685 | 642 | - | 0.300623 |
mobB | DDB_G0292758 | similar to the Mob1 family of proteins which are of unknown function but interact with Mps1 and NDR kinases Dictyostelium MobB has been shown to bind NdrA | DDB0232433 | CDS | 2055578 | 651 | - | 0.285714 |
mobC | DDB_G0293706 | similar to the Mob1 family of proteins which are of unknown function but interact with Mps1 and NDR kinases | DDB0232433 | CDS | 3038260 | 651 | - | 0.264209 |
mocos | DDB_G0272935 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase defects in the human MOCOS cause xanthinuria type II (XU-II) | DDB0232429 | CDS | 1865232 | 3024 | + | 0.242725 |
mocos_ps | DDB_G0272712 | putative pseudogene similar to parts of the molybdenum cofactor sulfurase gene | DDB0232429 | CDS | 1902864 | 243 | - | 0.333333 |
mocs1 | DDB_G0285137 | DDB0232431 | CDS | 2905081 | 1893 | + | 0.24617 | |
mocs2l | DDB_G0271864 | DDB0232429 | CDS | 980070 | 477 | + | 0.251572 | |
mocs2s | DDB_G0285133 | DDB0232431 | CDS | 2902514 | 261 | - | 0.275862 | |
mocs3 | DDB_G0267980 | DDB0232428 | CDS | 1230144 | 1278 | - | 0.289515 | |
modA | DDB_G0269154 | DDB0232428 | CDS | 3274209 | 2832 | + | 0.328037 | |
mon1 | DDB_G0281773 | ortholog of MON1 homologs in animals and MON1 in yeast which functions in vacuolar fusion of autophagosomes and cvt-vesicles | DDB0232430 | CDS | 4945906 | 1437 | - | 0.280445 |
mon2 | DDB_G0271398 | ortholog of MON2 in S. cerevisiae MON2 plays a a role in endocytosis and vacuole integrity | DDB0232429 | CDS | 219294 | 5625 | + | 0.269156 |
morg1 | DDB_G0289711 | ortholog of MORG1 a molecular scaffold protein that acts as a module in the assembly of a multicomponent scaffold for the ERK (extracellular signal-regulated kinase) pathway contains 7 WD40 repeats | DDB0232432 | CDS | 3150155 | 978 | - | 0.260736 |
mpdu1 | DDB_G0295677 | contains at least three transmembrane domains ortholog of mannose-P-dolichol utilization defect 1 protein MPDU1 | DDB0232428 | CDS | 3914310 | 708 | + | 0.286723 |
mpheS | DDB_G0274371 | catalyzes the reaction ATP L-phenylalanine tRNAPhe AMP diphosphate L-phenylalanyl-tRNAPhe | DDB0232429 | CDS | 3786786 | 1365 | - | 0.276923 |
mpi | DDB_G0284685 | catalyzes the reaction D-Mannose 6-phosphate D-fructose 6-phosphate | DDB0232431 | CDS | 2341606 | 1359 | - | 0.27741 |
mpl1 | DDB_G0269918 | negatively regulates the phosphorylation state of Erk2 expressed weakly in vegetative cells and maximally at aggregation highly similar to neighboring gene | DDB0232428 | CDS | 3862624 | 2505 | + | 0.261078 |
mpl2 | DDB_G0270688 | highly similar to neighboring gene | DDB0232428 | CDS | 3859398 | 2088 | + | 0.234195 |
mpl3 | DDB_G0278445 | DDB0232430 | CDS | 890638 | 2571 | - | 0.257098 | |
mpp10 | DDB_G0279245 | ortholog of H. sapiens MPHOSPH10 and S. cerevisiae MPP10 protein component of the 60-80S U3 small nucleolar ribonucleoprotein (U3 snoRNP) required for pre-18S rRNA processing forms a heterotrimeric complex containing IMP3 IMP4 | DDB0232430 | CDS | 1824604 | 2298 | + | 0.27154 |
mppA1 | DDB_G0274809 | part of a complex that removes the transit peptide from the precursor form of proteins imported from the cytoplasm across the mitochondrial inner membrane consists of an alpha and a beta ( | DDB0232429 | CDS | 3949604 | 1965 | + | 0.279389 |
mppA2 | DDB_G0290997 | the mitochondrial processing peptidase removes the transit peptide from the precursor form of proteins imported from the cytoplasm across the mitochondrial inner membrane consists of an alpha and a beta ( | DDB0232432 | CDS | 4869039 | 1338 | - | 0.35725 |
mppB | DDB_G0288777 | removes the transit peptide from the precursor form of proteins imported from the cytoplasm across the mitochondrial inner membrane consists of an alpha ( | DDB0232432 | CDS | 1942737 | 1410 | - | 0.358156 |
mppB_ps | DDB_G0288775 | putative pseudogene fragment very similar to | DDB0232432 | CDS | 1938769 | 210 | - | 0.380952 |
mproS | DDB_G0276079 | catalyzes the reaction ATP L-proline tRNAPro AMP diphosphate L-prolyl-tRNAPro | DDB0232429 | CDS | 6422563 | 2025 | + | 0.25284 |
mps1 | DDB_G0280995 | putative protein threoninetyrosine kinase similar to yeast and zebrafish mps1 (monopolar spindle) kinase a threoninetyrosine kinase | DDB0232430 | CDS | 3923506 | 2952 | + | 0.289295 |
mrd1 | DDB_G0284663 | ortholog of yeast MRD1 and mammalian RBM19 yeast MRD1 binds to the 35S pre-rRNA and the U3 snoRNA and is involved in pre-rRNA processing contains 5 RRM domains | DDB0232431 | CDS | 2315842 | 2688 | - | 0.278646 |
mre11 | DDB_G0293546 | similar to S. cerevisiae MRE11 involved in processing double-strand DNA breaks with Rad50 in other organisms Mre11 is part of a complex with Rad50 and Nbs1 no Nbs1 ortholog has been found in Dictyostelium | DDB0232433 | CDS | 3016431 | 2070 | + | 0.304348 |
mrfA | DDB_G0284183 | regulates gene expression in pstA cells ortholog of mouse myelin-gene transcription factor | DDB0232431 | CDS | 1846274 | 2799 | - | 0.272955 |
mrhA | DDB_G0281923 | very conserved in Dictyosteliids contains a motif related to the HAP2-GCS1 domain | DDB0232430 | CDS | 5126418 | 5241 | - | 0.227247 |
mrkA | DDB_G0292304 | CAMKL family protein kinase similar to MARK kinases SNF1 kinases and AMPK kinases contains 1 kinase-associated (KA1) domain and 1 UBA domain | DDB0232433 | CDS | 1433748 | 3183 | - | 0.286836 |
mrkB | DDB_G0285643 | CAMKL family protein kinase similar to SNF1 kinases MARK kinases and AMPK kinases | DDB0232431 | CDS | 3523048 | 2148 | - | 0.284916 |
mrkC | DDB_G0281895 | CAMKL family protein kinase similar to MARK kinases SNF1 kinases and AMPK kinases contains C-terminal kinase associated domain 1 | DDB0232430 | CDS | 5083659 | 2322 | + | 0.295866 |
mrpRNA | DDB_G0295629 | RNA component of the RNase MRP ribonucleoprotein which is involved in processing of rRNA in the nucleus and replication of mitochondrial DNA | DDB0232432 | CDS | 3919905 | 366 | + | 0.363388 |
mrpl13 | DDB_G0274959 | DDB0232429 | CDS | 4669717 | 684 | + | 0.312865 | |
mrpl15 | DDB_G0284405 | DDB0232431 | CDS | 1955406 | 756 | + | 0.308201 | |
mrpl17 | DDB_G0281435 | DDB0232430 | CDS | 4497695 | 549 | + | 0.29326 | |
mrpl21 | DDB_G0288799 | DDB0232432 | CDS | 1981150 | 519 | - | 0.265896 | |
mrpl22 | DDB_G0279519 | DDB0232430 | CDS | 2194197 | 714 | - | 0.285714 | |
mrpl27 | DDB_G0278889 | DDB0232430 | CDS | 1343635 | 429 | + | 0.298368 | |
mrpl3 | DDB_G0288983 | DDB0232432 | CDS | 2204231 | 1056 | - | 0.321023 | |
mrpl33 | DDB_G0278023 | DDB0232430 | CDS | 172946 | 192 | - | 0.265625 | |
mrpl34 | DDB_G0295825 | DDB0232430 | CDS | 4856414 | 510 | - | 0.252941 | |
mrpl51 | DDB_G0283273 | homolog of S. cerevisiae MRPL51 protein component of the mitochondrial large ribosomal subunit | DDB0232431 | CDS | 441777 | 375 | - | 0.277333 |
mrpl53 | DDB_G0292420 | DDB0232433 | CDS | 1579394 | 390 | + | 0.271795 | |
mrps10 | DDB_G0279855 | DDB0232430 | CDS | 2553750 | 396 | - | 0.318182 | |
mrps17 | DDB_G0277195 | DDB0232429 | CDS | 7731826 | 384 | - | 0.273438 | |
mrrA | DDB_G0271908 | transcriptional target of MybE expressed in upper and lower cup cells contains a predicted signal peptide and a C-terminal transmembrane domain | DDB0232429 | CDS | 1024732 | 726 | - | 0.26584 |
mrt4 | DDB_G0276411 | DDB0232429 | CDS | 6846542 | 672 | - | 0.282738 | |
mscS | DDB_G0277253 | contains mechanosensitive (MS) channel domain which provides protection against hypo-osmotic shock expressed in pstO cells | DDB0232429 | CDS | 7823709 | 2613 | - | 0.295446 |
mserS | DDB_G0267604 | catalyzes the reaction ATP L-serine tRNASer AMP diphosphate L-seryl-tRNASer | DDB0232428 | CDS | 406648 | 1578 | - | 0.299113 |
msh1 | DDB_G0275999 | similar to bacterial mismatch repair protein MutS putative mitochondrial mismatch repair protein | DDB0232429 | CDS | 6158412 | 2697 | - | 0.251761 |
msh2 | DDB_G0275809 | DDB0232429 | CDS | 5513128 | 2814 | - | 0.297797 | |
msh3 | DDB_G0281683 | DDB0232430 | CDS | 4806161 | 4287 | + | 0.292279 | |
msh4 | DDB_G0283957 | DDB0232431 | CDS | 1370478 | 3126 | - | 0.240883 | |
msh5 | DDB_G0284747 | DDB0232431 | CDS | 2423376 | 2643 | - | 0.239879 | |
msh6 | DDB_G0268614 | DDB0232428 | CDS | 238722 | 3783 | + | 0.335977 | |
msp | DDB_G0277015 | contains two selenocysteine residues at positions 20 and 88 conserved in the green algae such as Chlamydomonas Ostreococcus and Volvox contains 4 transmembrane domains | DDB0232429 | CDS | 7225140 | 732 | - | 0.355191 |
msrA | DDB_G0276579 | catalyzes the reaction L-methionine thioredoxin disulfide H2O L-methionine (S)-S-oxide thioredoxin functions as a repair enzyme for proteins that have been inactivated by oxidation | DDB0232429 | CDS | 7002973 | 492 | - | 0.325203 |
msrB | DDB_G0291145 | catalyzes the reaction L-methionine oxidized thioredoxin L-methionine R-oxide reduced thioredoxin | DDB0232432 | CDS | 5047547 | 573 | + | 0.267016 |
mth | DDB_G0293766 | DDB0232433 | CDS | 3300203 | 486 | + | 0.238683 | |
mtmr15 | DDB_G0267916 | conserved eukaryotic protein contains a C-terminal VRR-NUC domain brbr bCommunity annotation:b Not a great deal seems to be known about this protein other than the fact that the myotubularin family encodes dual-specificity phosphatases. Myotubularin itself is mutated in X-linked myotubular myopathy. Dicty Mtmr15 is overexpressed sixfold in a Dicty strain lacking the retinoblastoma-like gene | DDB0232428 | CDS | 1114621 | 3264 | - | 0.25674 |
mtpn | DDB_G0268038 | Ortholog of metazoan myotrophin (MTPN) which might be involved in cerebellar morphogenesis and cardiac hypertrophy contains 2 ankyrin repeats | DDB0232428 | CDS | 1344276 | 363 | + | 0.30854 |
mtr | DDB_G0284699 | multifunctional folate synthesis enzyme catlayzes the reaction 5-methyltetrahydrofolate L-homocysteine tetrahydrofolate L-methionine. | DDB0232431 | CDS | 2362420 | 3783 | - | 0.358181 |
mtrpS | DDB_G0274567 | catalyzes the reaction ATP L-tryptophan tRNATrp AMP diphosphate L-tryptophan-tRNAThr similar to bacterial tryptophan-tRNA ligases | DDB0232429 | CDS | 3980092 | 1134 | - | 0.261023 |
mtyrS | DDB_G0279715 | catalyzes the reaction ATP L-Tyrosine tRNATyr AMP diphosphate L-tyrosyl-tRNATyr similar to bacterial tyrosine-tRNA ligases | DDB0232430 | CDS | 2475392 | 1449 | - | 0.287095 |
mus81 | DDB_G0276519 | similar to endonuclease Mus81 conserved from yeast to human involved in DNA repair and replication fork stability | DDB0232429 | CDS | 7009387 | 2763 | - | 0.239595 |
mut | DDB_G0287563 | catalyzes the reaction (R)-methylmalonyl-CoA succinyl-CoA vitamin B12 dependent based on similarity with other MUT enzymes this protein is truncated at the N-terminus and might not be catalytically active the fragment contains the B12 binding site | DDB0232432 | CDS | 422254 | 921 | - | 0.396308 |
mvd | DDB_G0278607 | catalyzes the reaction ATP (R)-5-diphosphomevalonate ADP phosphate isopentenyl diphosphate COsub2sub in steroid biosynthesis | DDB0232430 | CDS | 313759 | 1176 | + | 0.375 |
mvk | DDB_G0272018 | conserved eukaryotic kinase (human MVK yeast ERG12) that plays a role in the synthesis of isopentanyl pyrophosphate a common intermediate in pathways including cholesterol biosynthesis | DDB0232429 | CDS | 1176734 | 1173 | - | 0.300085 |
mvpA | DDB_G0269156 | DDB0232428 | CDS | 3649783 | 2532 | + | 0.387441 | |
mvpB | DDB_G0291127 | DDB0232432 | CDS | 5070813 | 2541 | + | 0.387249 | |
mybA | DDB_G0293900 | DDB0232433 | CDS | 3493719 | 3693 | - | 0.25589 | |
mybAA | DDB_G0268368 | DDB0232428 | CDS | 1003245 | 2916 | + | 0.284979 | |
mybB | DDB_G0275445 | DDB0232429 | CDS | 5702027 | 2136 | - | 0.266386 | |
mybC | DDB_G0281563 | DDB0232430 | CDS | 4766011 | 1743 | + | 0.275961 | |
mybD | DDB_G0287637 | DDB0232432 | CDS | 536098 | 1788 | + | 0.182886 | |
mybE | DDB_G0281969 | DDB0232430 | CDS | 5190182 | 2457 | + | 0.308506 | |
mybF | DDB_G0278317 | DDB0232430 | CDS | 686928 | 1695 | + | 0.231858 | |
mybG | DDB_G0288783 | DDB0232432 | CDS | 1962158 | 1272 | + | 0.284591 | |
mybH | DDB_G0277927 | DDB0232430 | CDS | 16340 | 3654 | - | 0.246305 | |
mybI | DDB_G0289151 | DDB0232432 | CDS | 2425624 | 2934 | - | 0.271643 | |
mybJ | DDB_G0274463 | DDB0232429 | CDS | 4505147 | 2205 | - | 0.297959 | |
mybK | DDB_G0276877 | DDB0232429 | CDS | 7559689 | 2685 | + | 0.32216 | |
mybL | DDB_G0285373 | DDB0232431 | CDS | 3182160 | 2568 | + | 0.264798 | |
mybM | DDB_G0267636 | DDB0232428 | CDS | 451992 | 2010 | - | 0.240796 | |
mybN | DDB_G0292782 | contains three Myb DNA-binding domains at the C-terminus of the predicted protein similar to Dictyostelium mybB and mybC | DDB0232433 | CDS | 2022556 | 1734 | - | 0.266436 |
mybO | DDB_G0290787 | bCommunity annotation:b Myb0 appears to be related to both DUO3 of plants and Gon-4 of animals. DUO3 regulates cell cycle progression in developing pollen and appear to be specifically necessary for mitosis as mutant cells accumulate in G2 or become polyploid. DUO3 is expressed in somatic plant tissues mainly in meristerms suggesting a role in cell proliferation though it is apparently has no unique function in this case. In gon-4 (gonadless) mutants of C elegans the gonadal precursors Z1 and Z4 fail to divide. The reason is not known. DUO3 Gon-4 share and MybO share two short sequence motifs called the Gc1 and Gc2 regions. Myb0 has an additional simlarity to DUO3 in the region between 876 and 1031 which is similar to the DUO3-conserved region 2. This is not present in Gon-4 proteins. Myb0 contains an extended myb-like domain at its C-terminus. In this respect MybO resembles Gon-4. Duo3 does not have a myb domain of any kind however it interacts with DUO1 which has an R2R3 class myb do | DDB0232432 | CDS | 4599542 | 3984 | + | 0.259538 |
mybP | DDB_G0270560 | contains two Myb DNA-binding domains putative ortholog of the nuclear receptor corepressor 2 (also known as NCOR2 SMRT TRAC and SMAP270 in mammalian cells) | DDB0232428 | CDS | 3042784 | 4347 | - | 0.267541 |
mybQ | DDB_G0289319 | DDB0232432 | CDS | 2641022 | 2730 | - | 0.334066 | |
mybR | DDB_G0292182 | DDB0232433 | CDS | 1172608 | 1185 | + | 0.269198 | |
mybS | DDB_G0293468 | DDB0232433 | CDS | 2922718 | 3639 | - | 0.261061 | |
mybT | DDB_G0292180 | DDB0232433 | CDS | 1164954 | 570 | + | 0.261404 | |
mybU | DDB_G0283953 | DDB0232431 | CDS | 1355165 | 7146 | - | 0.29625 | |
mybV | DDB_G0279281 | DDB0232430 | CDS | 1879453 | 2412 | - | 0.279022 | |
mybW | DDB_G0270346 | DDB0232428 | CDS | 4680332 | 2007 | - | 0.224714 | |
mybX | DDB_G0288285 | DDB0232432 | CDS | 1347341 | 4863 | - | 0.282747 | |
mybY | DDB_G0284399 | DDB0232431 | CDS | 1950553 | 1719 | + | 0.272833 | |
mybZ | DDB_G0284103 | DDB0232431 | CDS | 1573183 | 2181 | - | 0.289775 | |
myh | DDB_G0270764 | ortholog of MYH which removes misincorporated adenine residues opposite template 8-oxoguanine during DNA replication | DDB0232428 | CDS | 4483000 | 1725 | + | 0.262029 |
myoA | DDB_G0280039 | actin-based motor unconventional myosin heavy chain | DDB0232430 | CDS | 3224159 | 2985 | - | 0.305863 |
myoB | DDB_G0289117 | long tailed class-1 myosin a molecular motor protein that localizes to actin-rich structures at the leading edge of migrating cells | DDB0232432 | CDS | 2410248 | 3336 | + | 0.351619 |
myoC | DDB_G0276617 | DDB0232429 | CDS | 7046886 | 3549 | - | 0.351085 | |
myoD | DDB_G0275447 | class I (unconventiona) myosin component of actin-based molecular motor | DDB0232429 | CDS | 5600309 | 3330 | + | 0.351652 |
myoE | DDB_G0288679 | (unconventional) class I myosin fast motor molecule involved in phagocytosis | DDB0232432 | CDS | 1829072 | 3018 | - | 0.336978 |
myoF | DDB_G0289177 | DDB0232432 | CDS | 2531958 | 3216 | - | 0.28607 | |
myoG | DDB_G0276363 | required for cell polarity and chemotaxis to cAMP plays a role in mediating early chemotactic signalling contains an N-terminal motor domain two MyTH4 domains an IQ calmodulin-binding region and a SH3 domain | DDB0232429 | CDS | 6748878 | 10341 | + | 0.289237 |
myoH | DDB_G0289447 | DDB0232432 | CDS | 2840200 | 5316 | - | 0.258653 | |
myoI | DDB_G0274455 | similar to the conserved MYO7A unconventional myosin required in Dictyostelium for phagocytosis and substrate adhesion | DDB0232429 | CDS | 4534415 | 7074 | + | 0.326972 |
myoJ | DDB_G0272112 | conditional processive motor protein that can move over long distances along F-actin without disassociating processiveness depends on high physiological Mgsup2sup concentrations | DDB0232429 | CDS | 1452059 | 6738 | + | 0.309884 |
myoK | DDB_G0274575 | class 1 myosin lacking the traditional tail domains common to short-tailed myosins binds actin and is in complex with several other proteins involved in phagocytosis maintenance of cortical tension and motility | DDB0232429 | CDS | 3960245 | 2577 | + | 0.353124 |
myoM | DDB_G0292262 | unconventional myosin and guanyl-nucleotide exchange factor which acts on Rac1A Rac1B and human Rac1 but not on RacC and RacE | DDB0232433 | CDS | 1463619 | 5214 | + | 0.274262 |
naa20 | DDB_G0276345 | ortholog of the conserved catalytic subunit of the NatB N-terminal acetyltransferase (NAA20) which in yeast catalyzes the transfer of an acetyl group to the N-terminal residue of a protein that contains a Met-Glu Met-Asp Met-Asn or Met-Met N-terminus | DDB0232429 | CDS | 6679320 | 522 | + | 0.293103 |
naa50 | DDB_G0295721 | highly conserved protein ortholog of human NAA50 and yeast Mak3 | DDB0232430 | CDS | 183263 | 510 | - | 0.258824 |
nacA | DDB_G0281403 | highly similar to the alpha subunit of the nascent polypeptide-associated complex (NAC) which binds the nascent polypeptide after peptide bond formation | DDB0232430 | CDS | 4433625 | 483 | + | 0.42029 |
nacB | DDB_G0281795 | DDB0232430 | CDS | 4686750 | 429 | - | 0.41958 | |
nadsyn1 | DDB_G0285877 | catalyzes the reaction ATP deamido-NAD L-glutamine Hsub2subO AMP diphosphate NAD L-glutamate | DDB0232431 | CDS | 3760460 | 2142 | + | 0.351074 |
nae1 | DDB_G0287965 | conserved regulatory subunit of the dimeric UBA3-NEA1 E1 enzyme which activates NEDD8 necessary for cell cycle progression through the S-M checkpoint | DDB0232432 | CDS | 887341 | 1563 | + | 0.287268 |
nagA | DDB_G0287033 | DDB0232431 | CDS | 5251113 | 1599 | + | 0.333333 | |
nagB | DDB_G0282539 | DDB0232430 | CDS | 5899632 | 1626 | - | 0.311808 | |
nagB1 | DDB_G0286195 | long version of the glucosamine-6-phosphate isomerase similar to Entamoeba and ciliates catalyzes the reaction D-glucosamine 6-phosphate Hsub2subO D-fructose 6-phosphate NHsub3sub | DDB0232431 | CDS | 4161180 | 2175 | - | 0.316322 |
nagC | DDB_G0287597 | DDB0232432 | CDS | 449924 | 1683 | + | 0.24896 | |
nagD | DDB_G0287659 | DDB0232432 | CDS | 447833 | 1695 | + | 0.316814 | |
nagE | DDB_G0285647 | similar to beta-hexosaminidase but shorter on the amino terminus | DDB0232431 | CDS | 3533871 | 2088 | + | 0.221264 |
naglu | DDB_G0291998 | catalyzes the hydrolysis of terminal non-reducing N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides mutated in patients with mucopolysaccharidosis type IIIB (Sanfilippo syndrome type B) a lysosomal storage disorder | DDB0232433 | CDS | 982514 | 2397 | - | 0.358365 |
nap1 | DDB_G0269290 | NAP proteins act as histone chaperones shuttling both core and linker histones from their site of synthesis in the cytoplasm to the nucleus | DDB0232428 | CDS | 2468482 | 966 | + | 0.354037 |
napA | DDB_G0274519 | DDB0232429 | CDS | 4292502 | 3483 | + | 0.34855 | |
naprt | DDB_G0268472 | catalyzes the conversion of nicotinic acid (NA) to NA mononucleotide (NaMN) which elevates cellular NAD levels and prevent oxidative stress | DDB0232428 | CDS | 1010098 | 1770 | - | 0.337853 |
nat1 | DDB_G0288509 | DDB0232432 | CDS | 1625652 | 921 | + | 0.261672 | |
nat10 | DDB_G0268868 | highly conserved protein ortholog of human NAT10 and yeast KRE33 predicted to localize to the nucleolus | DDB0232428 | CDS | 2281503 | 3174 | - | 0.290485 |
nat2 | DDB_G0288503 | DDB0232432 | CDS | 1622564 | 978 | + | 0.230061 | |
nat3 | DDB_G0288507 | DDB0232432 | CDS | 1624317 | 900 | + | 0.243333 | |
nat4 | DDB_G0287121 | DDB0232431 | CDS | 5328050 | 837 | - | 0.222222 | |
nat5 | DDB_G0276993 | DDB0232429 | CDS | 7302630 | 870 | - | 0.227586 | |
nat6 | DDB_G0349503 | DDB0232429 | CDS | 8074596 | 903 | + | 0.180509 | |
nat7 | DDB_G0349505 | DDB0232429 | CDS | 8076554 | 900 | + | 0.176667 | |
nat9 | DDB_G0272710 | DDB0232429 | CDS | 1909663 | 639 | - | 0.256651 | |
natA | DDB_G0275449 | DDB0232429 | CDS | 5856743 | 612 | - | 0.276144 | |
nat_ps | DDB_G0276995 | putative pseudogene fragment similar to the nat family of acetyltransferases including | DDB0232429 | CDS | 7301907 | 645 | - | 0.136434 |
ncapD2 | DDB_G0293984 | component of the condensin I complex required for conversion of interphase chromatin into mitotic condensed chromosomes | DDB0232433 | CDS | 3563765 | 4212 | - | 0.243115 |
ncapD3 | DDB_G0278701 | component of the condensin II complex which is involved in physical rigidity of the chromatid axis brbr bCommunity annotation:b The involvement of ncapD3 in mitosis in Dicty is supported by its 15-fold overexpression in a Dicty strain lacking the Dicty retinoblastoma-liked gene | DDB0232430 | CDS | 1012938 | 5376 | + | 0.288132 |
ncapG2 | DDB_G0288819 | component of the condensin II complex which is involved in physical rigidity of the chromatid axis | DDB0232432 | CDS | 2028467 | 4314 | - | 0.244089 |
ncapGa | DDB_G0281419 | putative component of the condensin I complex required for conversion of interphase chromatin into mitotic condensed chromosomes There is another putative NCAPG gene in D. discoideum ( | DDB0232430 | CDS | 4452796 | 4611 | - | 0.227933 |
ncapGb | DDB_G0275129 | putative component of the condensin I complex required for conversion of interphase chromatin into mitotic condensed chromosomes There is another putative NCAPG gene in D. discoideum ( | DDB0232429 | CDS | 5012674 | 3981 | + | 0.21904 |
ncapH | DDB_G0292066 | component of the condensin I complex required for conversion of interphase chromatin into mitotic condensed chromosomes | DDB0232433 | CDS | 1141212 | 2637 | + | 0.264316 |
ncapH2 | DDB_G0291894 | component of the condensin II complex which is involved in physical rigidity of the chromatid axis | DDB0232433 | CDS | 900574 | 2769 | - | 0.27519 |
ncbp1 | DDB_G0269814 | ortholog of mammalian NCPB1 and yeast STO1 large subunit of the heterodimeric cap binding complex involved in mediating U snRNA export from the nucleus | DDB0232428 | CDS | 3661674 | 2319 | - | 0.277275 |
ncbp2 | DDB_G0287197 | ortholog of mammalian NCPB2 and yeast CBP2 small subunit of the heterodimeric cap binding complex involved in mediating U snRNA export from the nucleus | DDB0232431 | CDS | 5395993 | 705 | + | 0.299291 |
ncfA | DDB_G0288773 | homolog of the essential mammalian neutrophil cytosolic factor p67 that functions as an NADPH oxidase activator contains N-terminal TPR repeats and a C-terminal WW domain | DDB0232432 | CDS | 2003648 | 1815 | - | 0.32011 |
ncsA | DDB_G0275931 | contains four EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232429 | CDS | 6088223 | 561 | - | 0.279857 |
ncstn | DDB_G0287801 | component of the gamma-secretase complex which executes the intramembrane proteolysis of type I integral membrane proteins | DDB0232432 | CDS | 721592 | 1980 | - | 0.291414 |
ndc80 | DDB_G0284003 | ortholog of NDC80 (also known as HEC1 and TID3) a subunit of the kinetochore complex involved in microtubule binding and the spindle assembly checkpoint brbr bCommunity annotation: bndc80 is overexpressed 16-fold in a Dictyostelium | DDB0232431 | CDS | 1379527 | 2568 | + | 0.257399 |
ndkC-1 | DDB_G0273069 | catalyzes the phosphorylation of nucleoside or deoxynucleoside diphosphates into the corresponding triphosphates there is a second copy of this gene | DDB0232429 | CDS | 2603092 | 468 | - | 0.397436 |
ndkC-2 | DDB_G0273805 | catalyzes the phosphorylation of nucleoside or deoxynucleoside diphosphates into the corresponding triphosphates there is a second copy of this gene | DDB0232429 | CDS | 3427961 | 468 | + | 0.397436 |
ndkM | DDB_G0279911 | DDB0232430 | CDS | 2740248 | 663 | + | 0.380091 | |
ndm | DDB_G0272368 | contains a coiled coil C-terminal BAR-like domain | DDB0232429 | CDS | 1340572 | 5346 | - | 0.245417 |
ndrA | DDB_G0278457 | member of the AGC kinases NDR group localizes to centrosomes and to the spindle during prometaphase and is involved in phagocytosis | DDB0232430 | CDS | 907158 | 1593 | + | 0.344633 |
ndrB | DDB_G0288753 | member of the AGC kinase group similar to NDR protein kinases including yeast morphogenesis proteins ORB6 and CBK1 | DDB0232432 | CDS | 1909293 | 1629 | - | 0.324125 |
ndrC | DDB_G0284839 | member of the AGC kinase group NDR family related to mammalian LATS1 and LATS2 (LArge Tumor Suppressor homolog) kinases | DDB0232431 | CDS | 2493584 | 3939 | + | 0.307692 |
ndrD | DDB_G0289543 | member of the AGC kinase group NDR family related to mammalian LATS1 and LATS2 (LArge Tumor Suppressor homolog) kinases | DDB0232432 | CDS | 2920470 | 6339 | + | 0.255088 |
ndrJ | DDB_G0292654 | similar to class II ribonucleotide reductase a monomeric form of ribonucleotide reductase that uses ribonucletide triphosphates rather than diphosphates as substrates the only other eukaryote in which this enzyme is present is Euglena gracilis | DDB0232433 | CDS | 1906693 | 2277 | + | 0.312692 |
ndufa12 | DDB_G0285783 | DDB0232431 | CDS | 3508802 | 417 | + | 0.326139 | |
ndufa5 | DDB_G0272394 | DDB0232429 | CDS | 1434465 | 354 | + | 0.305085 | |
ndufa6 | DDB_G0291129 | accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to be not involved in catalysis | DDB0232432 | CDS | 5026489 | 375 | + | 0.290667 |
ndufa8 | DDB_G0284799 | accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to be not involved in catalysis | DDB0232431 | CDS | 2498543 | 315 | - | 0.330159 |
ndufa9 | DDB_G0272266 | DDB0232429 | CDS | 1449219 | 1071 | - | 0.323063 | |
ndufab1 | DDB_G0291866 | similar to mitochondrial matrix acyl carrier protein and the animal NADH dehydrogenase (ubiquinone) 1 alphabeta subcomplex 1 which is the carrier of the growing fatty acid chain in fatty acid biosynthesis in mitochondria | DDB0232433 | CDS | 849824 | 363 | + | 0.360882 |
ndufaf5 | DDB_G0287769 | conserved mitochondrial complex I (CI) assembly factor which when mutated in human leads to mitochondrial disease in Dictyostelium mutations in the ndufaf5 gene cause defects in growth and development and autophagy is increased. | DDB0232432 | CDS | 675763 | 1311 | - | 0.254767 |
ndufb7 | DDB_G0280595 | similar to human NDUFB7 which is an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) | DDB0232430 | CDS | 3546088 | 339 | - | 0.306785 |
ndufs4 | DDB_G0295657 | ortholog of H. sapiens NDUFS4 a component of the largest respiratory chain complex defects in NDUFS4 are a cause of complex I mitochondrial respiratory chain deficiency | DDB0232429 | CDS | 8302904 | 573 | + | 0.286213 |
ndufs7 | DDB_G0285239 | DDB0232431 | CDS | 2997614 | 537 | - | 0.374302 | |
ndufs8 | DDB_G0277231 | DDB0232429 | CDS | 7754832 | 633 | - | 0.328594 | |
ndufv1 | DDB_G0288875 | DDB0232432 | CDS | 2127210 | 1440 | + | 0.359028 | |
ndufv2 | DDB_G0291173 | DDB0232432 | CDS | 5096341 | 744 | - | 0.319892 | |
nedd8 | DDB_G0278711 | conserved ubiquitin-like protein which plays an important role in cell cycle control and in embryogenesis in animals | DDB0232430 | CDS | 1086802 | 234 | - | 0.337607 |
nedd8l1 | DDB_G0281703 | very similar to the conserved NEDD8 (neddylin) protein however the C-terminus is extended and lacks the conserved cleavage site | DDB0232430 | CDS | 4852577 | 291 | + | 0.292096 |
nedd8l2 | DDB_G0286927 | similar to the conserved NEDD8 (neddylin) protein however this is the most divergent member of the family in Dictyostelium | DDB0232431 | CDS | 5089206 | 243 | - | 0.255144 |
nek2 | DDB_G0270814 | protein serinethreonine kinase homologous to human Nek2 kinase involved in formation of microtubule-organizing centers (MTOCs) | DDB0232428 | CDS | 4847143 | 1257 | - | 0.258552 |
nek3 | DDB_G0275241 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis not a human Nek3 homolog | DDB0232429 | CDS | 4983790 | 3372 | - | 0.269276 |
nek4 | DDB_G0289277 | similar to vertebrate Nek kinases which are involved in regulation of mitosis most similar to Nek4 | DDB0232432 | CDS | 2561379 | 1494 | - | 0.222222 |
netD | DDB_G0278115 | conserved protein also known as Tmem53 contains 1 putative transmembrane domain | DDB0232430 | CDS | 296602 | 813 | + | 0.291513 |
nfaA | DDB_G0271750 | putative ortholog of human NF1 a GAP which regulates p21-ras signaling regulates chemotaxis probably though the control of RasG activity | DDB0232429 | CDS | 720888 | 2763 | + | 0.279045 |
nfu1 | DDB_G0285593 | ortholog of S. cerevisiae NFU1 involved in iron metabolism in mitochondria | DDB0232431 | CDS | 3425659 | 945 | - | 0.238095 |
nfyA | DDB_G0282697 | putative ortholog of the A subunit of the heterotrimeric transcription factor NFY composed of NfyA NfyB and NfyC | DDB0232430 | CDS | 6144529 | 1554 | + | 0.246461 |
nfyB | DDB_G0279419 | putative ortholog of the B subunit of the heterotrimeric transcription factor NFY composed of NfyA NfyB and NfyC | DDB0232430 | CDS | 2020767 | 1473 | + | 0.308893 |
nfyC-1 | DDB_G0273479 | there is a second copy of this gene | DDB0232429 | CDS | 2945279 | 2055 | - | 0.249148 |
nfyC-2 | DDB_G0273545 | there is a second copy of this gene | DDB0232429 | CDS | 3084342 | 2055 | + | 0.249148 |
ngap | DDB_G0278483 | DDB0232430 | CDS | 951936 | 2634 | - | 0.307137 | |
nhe1 | DDB_G0275711 | required for cell polarity mediates both Ksupsup facilitation of cell motility and KsupsupNasupsup requirement in chemotactic orientation the genetic interaction between aip1 and nhe1 suggest that defective chemotaxis in nhe1- mutants may be determined by loss of cofilin-dependent actin dynamics | DDB0232429 | CDS | 6042281 | 2025 | - | 0.281481 |
nhe2 | DDB_G0281877 | DDB0232430 | CDS | 5057597 | 2064 | + | 0.228682 | |
nhe3 | DDB_G0292830 | DDB0232433 | CDS | 2111344 | 2361 | - | 0.345616 | |
nhe4 | DDB_G0290253 | DDB0232432 | CDS | 3840207 | 3027 | - | 0.327387 | |
nhej1 | DDB_G0284785 | DDB0232431 | CDS | 2481017 | 1596 | - | 0.196742 | |
nhp2l1 | DDB_G0282243 | ortholog of human NHP2L1 which is believed to play a role in spliceosome assembly similar to ribosomal protein L7AE but is not likely to be a ribosomal protein | DDB0232430 | CDS | 5564223 | 390 | + | 0.348718 |
nhp6 | DDB_G0270260 | similar to S. cerevisiae nonhistone chromosomal protein 6A and B (NCP6A and NCP6B) and mammalian HMGB2 contains a single HMG12 box | DDB0232428 | CDS | 4527247 | 426 | + | 0.36385 |
nif3 | DDB_G0270854 | ortholog of human NIF3L1 belongs to the UPF0135 (NIF3) family | DDB0232428 | CDS | 2581654 | 1065 | - | 0.266667 |
nip7 | DDB_G0295477 | ortholog of the conserved NIP7 nucleolar protein that is required for 60S ribosome subunit biogenesis contains a PUA domain | DDB0232429 | CDS | 615393 | 540 | + | 0.272222 |
nipsnap | DDB_G0288989 | DDB0232432 | CDS | 2209540 | 672 | + | 0.269345 | |
nit1-1 | DDB_G0273457 | similar to mammalian NIT1 there is a second copy of this gene | DDB0232429 | CDS | 2982881 | 876 | - | 0.289954 |
nit1-2 | DDB_G0273519 | similar to mammalian NIT1 there is a second copy of this gene | DDB0232429 | CDS | 3048030 | 876 | + | 0.289954 |
nit2 | DDB_G0287939 | DDB0232432 | CDS | 872348 | 987 | - | 0.274569 | |
nle1 | DDB_G0295761 | DDB0232428 | CDS | 2884549 | 1524 | - | 0.330052 | |
nmd3 | DDB_G0271306 | conserved NMD3 protein which in S. cerevisiae is involved in the nuclear export of the large ribosomal subunit | DDB0232429 | CDS | 129822 | 1593 | - | 0.323917 |
nmd3_ps | DDB_G0288881 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 2082521 | 138 | + | 0.347826 |
nmt | DDB_G0275863 | catalyzes the reaction tetradecanoyl-CoA glycylpeptide CoA N-tetradecanoylglycylpeptide | DDB0232429 | CDS | 5768614 | 1242 | + | 0.334944 |
nog1 | DDB_G0285465 | very similar to NOG1GTPBP4 GTPases which in S. cerevisiae associates with free 60S ribosomal subunits in the nucleolus and is involved in their biogenesis | DDB0232431 | CDS | 3263032 | 2025 | - | 0.342222 |
nol1 | DDB_G0281685 | possible RNA methyltransferase ortholog of H. sapiens NOL1 and S. cerevisiae NOP2 | DDB0232430 | CDS | 4810538 | 1944 | - | 0.326646 |
nol10 | DDB_G0292466 | DDB0232433 | CDS | 1681385 | 2100 | - | 0.300476 | |
nol5a | DDB_G0285679 | ortholog of H. sapiens NOL5A and S. cerevisiae SIK1 SIK1 is a component of the box CD snoRNP complex involved in rRNA processing | DDB0232431 | CDS | 3582121 | 1623 | + | 0.325323 |
nol6 | DDB_G0291438 | putative U3 snoRNP protein ortholog of H. sapiens NOL6 and S. cerevisiae UTP22 | DDB0232433 | CDS | 304287 | 3837 | - | 0.258796 |
nol9 | DDB_G0277945 | ortholog of H. sapiens NOL9 similar to S. cerevisiae GRC3 believed to be involved in rRNA processing | DDB0232430 | CDS | 44863 | 2052 | + | 0.20614 |
nola1 | DDB_G0279013 | component of the HACA small nucleolar ribonucleoprotein (HACA snoRNP) complex required for pre-mRNA processing and pseudouridylation | DDB0232430 | CDS | 1514463 | 693 | + | 0.47619 |
nola2 | DDB_G0289699 | component of the HACA small nucleolar ribonucleoprotein (HACA snoRNP) complex required for pre-mRNA processing and pseudouridylation | DDB0232432 | CDS | 3120417 | 435 | + | 0.303448 |
nola3 | DDB_G0288347 | component of the HACA small nucleolar ribonucleoprotein (HACA snoRNP) complex required for pre-mRNA processing and pseudouridylation | DDB0232432 | CDS | 1416040 | 195 | + | 0.323077 |
nola4 | DDB_G0281933 | ortholog of human DKC1 (DysKeratosis Congenita 1) and yeast CBF5 (Centromere Binding Factor 5) component of the HACA small nucleolar ribonucleoprotein (HACA snoRNP) complex required for pre-mRNA processing and pseudouridylation | DDB0232430 | CDS | 5161271 | 1623 | - | 0.370302 |
nop14 | DDB_G0287537 | DDB0232432 | CDS | 388563 | 2955 | - | 0.264298 | |
nop58 | DDB_G0268098 | ortholog of human and S. pombe nucleolar protein 58 members of this family are involved in a variety of functions during pre-mRNA splicing | DDB0232428 | CDS | 1450677 | 1917 | - | 0.344288 |
nosA | DDB_G0292264 | DDB0232433 | CDS | 1472850 | 3270 | - | 0.284404 | |
nosip | DDB_G0270882 | DDB0232428 | CDS | 2940068 | 1002 | - | 0.238523 | |
noxA | DDB_G0289653 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation | DDB0232432 | CDS | 3117432 | 1554 | - | 0.310811 |
noxB | DDB_G0287101 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation | DDB0232431 | CDS | 5216605 | 2097 | - | 0.244158 |
noxC | DDB_G0291117 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation contains calcium-binding EF hand | DDB0232432 | CDS | 5017189 | 3429 | - | 0.222514 |
npcA | DDB_G0269158 | one of two orthologs of NPC1 (with | DDB0232428 | CDS | 4862383 | 4029 | + | 0.336808 |
npcB | DDB_G0276657 | one of two orthologs of NPC1 (with | DDB0232429 | CDS | 7081017 | 4194 | - | 0.284454 |
npl4 | DDB_G0290227 | ortholog of NPL4 together with ufd1 and cdcD involved in recognition of polyubiquitinated proteins and their presentation to the 26S proteasome for degradation | DDB0232432 | CDS | 3827990 | 1731 | - | 0.312536 |
nramp1 | DDB_G0276973 | ortholog of the mammalian SLC11a1 transports iron across the phagolysosomal membrane contains 12 transmembrane domains | DDB0232429 | CDS | 7564058 | 1602 | + | 0.314607 |
nramp2 | DDB_G0275815 | NRAMP family protein similar to bacterial manganese transport protein mntH contains 12 transmembrane domains involved in iron homeostasis and resistance to pathogenic bacteria | DDB0232429 | CDS | 5536603 | 1890 | + | 0.292593 |
nsfA | DDB_G0276153 | ATPase required for endocytosis membrane trafficking and cell motility acts as a SNAP receptor (SNARE) chaperone which binds through soluble NSF attachment proteins (SNAPs) to SNARE complexes and utilizes the energy of ATP hydrolysis to promote SNARE recycling | DDB0232429 | CDS | 6318754 | 2217 | + | 0.345963 |
nubp1 | DDB_G0277437 | ortholog of the human nucleotide binding protein NUBP1 belongs to the highly conserved MrpNBP35 ATP-binding protein family | DDB0232429 | CDS | 8068928 | 948 | - | 0.336498 |
nubp2 | DDB_G0277157 | ortholog of the human nucleotide binding protein NUBP2 belongs to the highly conserved MrpNBP35 ATP-binding protein family contains a Zinc finger C4-type domain | DDB0232429 | CDS | 7917419 | 798 | + | 0.289474 |
nubpl | DDB_G0291193 | conserved protein belongs to the MrpNBP35 ATP-binding protein family | DDB0232432 | CDS | 5087724 | 972 | - | 0.304527 |
nudE | DDB_G0272326 | DDB0232429 | CDS | 1288191 | 1197 | - | 0.265664 | |
nudc | DDB_G0286159 | DDB0232431 | CDS | 4151188 | 516 | - | 0.257752 | |
nudt19 | DDB_G0290277 | ortholog of human NUDT19 a Coenzyme A diphosphatase that mediates the hydrolysis of a wide range of CoA esters | DDB0232432 | CDS | 3853979 | 1089 | + | 0.266299 |
nuf2 | DDB_G0279553 | ortholog of NUF2 a component of the evolutionarily conserved kinetochore-associated Ndc80 complex (in S. pombe composed of: Ndc80-Nuf2-Spc24-Spc25) | DDB0232430 | CDS | 2245750 | 1410 | - | 0.289362 |
numA | DDB_G0269114 | there are three reported numA isoforms the largest 97 kDa numA2 the 66 kDa numA1 and the smallest 43 kDA numA3 all isoforms contain a nuclear localization signal a CaM binding domain and a DEED (DE repeat) domain the larger numA2 contains an additional BRCT (Breast Cancer C_Terminal) domain | DDB0232428 | CDS | 4887451 | 4803 | + | 0.290443 |
nup107 | DDB_G0285579 | component of the nuclear pore complex which plays a role in RNA export | DDB0232431 | CDS | 3398560 | 2958 | - | 0.251859 |
nup133 | DDB_G0287497 | component of the nuclear pore complex which plays a role in RNA export | DDB0232432 | CDS | 329850 | 3621 | + | 0.254073 |
nup155 | DDB_G0291163 | component of the nuclear pore complex may be involved both in binding and translocating proteins | DDB0232432 | CDS | 5077769 | 4728 | - | 0.271151 |
nup160 | DDB_G0269502 | component of the nuclear pore complex which plays a role in RNA export | DDB0232428 | CDS | 2888658 | 5376 | + | 0.232887 |
nup210 | DDB_G0288545 | similar to nuclear pore membrane glycoprotein 210 human NUP210 is essential for nuclear pore assembly contains one putative transmembrane domain and a signal sequence | DDB0232432 | CDS | 1669968 | 5751 | + | 0.311076 |
nup43 | DDB_G0277955 | component of the nuclear pore complex contains four WD40 repeats | DDB0232430 | CDS | 60115 | 1254 | - | 0.22807 |
nup54 | DDB_G0270320 | similar to mammalian Nup54 component of the nuclear pore complex | DDB0232428 | CDS | 4639723 | 1323 | - | 0.312925 |
nup62 | DDB_G0274587 | ortholog of the 62 kDa nucleoporin an essential component of the nuclear pore complex | DDB0232429 | CDS | 3866512 | 2130 | + | 0.378404 |
nup85 | DDB_G0285415 | similar to the conserved Nup85 component of the nuclear pore complex | DDB0232431 | CDS | 3200903 | 2673 | + | 0.259259 |
nup93 | DDB_G0267480 | DDB0232428 | CDS | 203419 | 2940 | - | 0.290136 | |
nup98 | DDB_G0291390 | very similar to the mammalian Nup98 precurser that is processed into two peptides Nup96 and Nup98 through autoproteolysis | DDB0232433 | CDS | 239658 | 6162 | + | 0.341448 |
nutf2 | DDB_G0276425 | involved in protein transport into the nucleus known to bind Ran in yeast and Arabidopsis | DDB0232429 | CDS | 6903295 | 384 | + | 0.322917 |
nvl | DDB_G0282181 | DDB0232430 | CDS | 5443128 | 2604 | - | 0.300307 | |
nxf | DDB_G0286455 | nxf bNbuclear RNA ebXbport bFbactor | DDB0232431 | CDS | 4446182 | 1665 | + | 0.308108 |
nxnA | DDB_G0269160 | DDB0232428 | CDS | 2864584 | 2649 | - | 0.379388 | |
nxnB | DDB_G0284261 | type I annexins inhibit phospholipase A2 following dephosphorylation by protein kinases involved in the signal transduction pathway may also associate with the cell cytoskeleton by binding to F-actin | DDB0232431 | CDS | 1793617 | 1464 | + | 0.230191 |
oatA | DDB_G0287913 | catalyzes the reaction L-ornithine a 2-oxo acid L-glutamate 5-semialdehyde an L-amino acid | DDB0232432 | CDS | 841784 | 1251 | + | 0.406875 |
odc | DDB_G0281109 | catalyzes the reaction L-ornithine putrescine COsub2sub | DDB0232430 | CDS | 4069177 | 1386 | - | 0.336219 |
odhA | DDB_G0280353 | catalyzes the reaction 2-oxoglutarate [dihydrolipoyllysine-residue succinyltransferase] lipoyllysine [dihydrolipoyllysine-residue succinyltransferase] S-succinyldihydrolipoyllysine COsub2sub E1 component of the multienzyme 2-oxoglutarate dehydrogenase complex | DDB0232430 | CDS | 3293945 | 2703 | + | 0.333333 |
odhB | DDB_G0275029 | catalyzes the reaction succinyl-CoA enzyme N6-(dihydrolipoyl)lysine CoA enzyme N6-(S-succinyldihydrolipoyl) lysine E2 component of the multienzyme 2-oxoglutarate dehydrogenase complex | DDB0232429 | CDS | 5316981 | 1320 | + | 0.364394 |
ogdh | DDB_G0288127 | component of the 2-oxoglutarate dehydrogenase complex which catalyzes the conversion of 2-oxoglutarate to succinyl-CoA and COsub2sub | DDB0232432 | CDS | 1102242 | 3042 | + | 0.36785 |
ogg1 | DDB_G0292618 | similar to E. coli MutM and OGG1 a bifunctional DNA glycosylase that contains an activity that excises 8-oxoguanine and other derivatives of guanine from DNA and a beta-lyase activity that nicks DNA 3' of the lesion | DDB0232433 | CDS | 1847428 | 1320 | - | 0.258333 |
ola1 | DDB_G0268758 | belongs to the RAS-like GTPase superfamily ortholog of human OLA1 | DDB0232428 | CDS | 2048942 | 1182 | + | 0.315567 |
omt1 | DDB_G0271590 | DDB0232429 | CDS | 696177 | 756 | + | 0.244709 | |
omt10 | DDB_G0290719 | DDB0232432 | CDS | 4487859 | 1314 | + | 0.2793 | |
omt11 | DDB_G0293886 | similar to plant and bacterial O-methyltransferases expressed in pstO cells during culmination | DDB0232433 | CDS | 3424368 | 996 | + | 0.247992 |
omt12 | DDB_G0293888 | highly similar to plant and bacterial O-methyltransferases expressed in pstA cells | DDB0232433 | CDS | 3426309 | 1110 | + | 0.243243 |
omt2 | DDB_G0274941 | DDB0232429 | CDS | 4581583 | 1011 | - | 0.20178 | |
omt3 | DDB_G0274197 | DDB0232429 | CDS | 4793181 | 1314 | - | 0.267884 | |
omt4 | DDB_G0275013 | DDB0232429 | CDS | 5190004 | 1017 | - | 0.26057 | |
omt5 | DDB_G0275499 | DDB0232429 | CDS | 6014515 | 693 | + | 0.307359 | |
omt6 | DDB_G0275501 | DDB0232429 | CDS | 6015883 | 696 | + | 0.304598 | |
omt7 | DDB_G0282591 | DDB0232430 | CDS | 5980059 | 1020 | - | 0.221569 | |
omt9 | DDB_G0289823 | DDB0232432 | CDS | 3290073 | 1074 | - | 0.286778 | |
oplah | DDB_G0284953 | catalyzes the reaction ATP 5-oxo-L-proline 2 Hsub2subO ADP phosphate L-glutamate | DDB0232431 | CDS | 2680203 | 3798 | - | 0.322012 |
orcA | DDB_G0283073 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232431 | CDS | 182130 | 1896 | - | 0.2827 |
orcB | DDB_G0269894 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232428 | CDS | 3810811 | 1176 | + | 0.256803 |
orcC | DDB_G0271078 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232428 | CDS | 4764421 | 3243 | + | 0.262103 |
orcD | DDB_G0271562 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232429 | CDS | 681736 | 1323 | + | 0.226757 |
orcE | DDB_G0293214 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232433 | CDS | 2694152 | 1716 | + | 0.238928 |
orcF | DDB_G0284771 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232431 | CDS | 2460990 | 1410 | + | 0.28156 |
orfR1062 | DDB_G0272114 | DDB0232429 | CDS | 1665521 | 2322 | - | 0.316107 | |
osbA | DDB_G0280053 | interacts with STATc enriched in pstO cells inactivation leads to a slugger phenotype | DDB0232430 | CDS | 2921032 | 1170 | - | 0.311111 |
osbB | DDB_G0269938 | DDB0232428 | CDS | 3904926 | 1176 | - | 0.244048 | |
osbC | DDB_G0269940 | similar to oxysterol binding protein however does not contain consensus binding site expressed in pstAO cells and in upper and lower cups during culmination | DDB0232428 | CDS | 3906624 | 1119 | - | 0.26899 |
osbD | DDB_G0272498 | DDB0232429 | CDS | 1803819 | 1401 | - | 0.274804 | |
osbE | DDB_G0274517 | DDB0232429 | CDS | 4297070 | 1089 | + | 0.230487 | |
osbF | DDB_G0276427 | DDB0232429 | CDS | 6936608 | 1320 | - | 0.337879 | |
osbG | DDB_G0283035 | DDB0232431 | CDS | 184491 | 1269 | - | 0.3026 | |
osbH | DDB_G0283709 | DDB0232431 | CDS | 1009391 | 1209 | + | 0.34574 | |
osbI | DDB_G0284353 | DDB0232431 | CDS | 1870805 | 1287 | - | 0.311577 | |
osbJ | DDB_G0285141 | DDB0232431 | CDS | 2910487 | 1173 | - | 0.289855 | |
osbK | DDB_G0288817 | DDB0232432 | CDS | 2025270 | 1716 | - | 0.321678 | |
osbL | DDB_G0291562 | DDB0232433 | CDS | 499055 | 1209 | - | 0.261373 | |
ost1 | DDB_G0293224 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST1 and human ribophorin I contains one C-terminal transmembrane domain and an N-terminal signal peptide | DDB0232433 | CDS | 2680686 | 1383 | + | 0.349241 |
ost2 | DDB_G0291049 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST2 and human DAD1 (Defender Against cell Death 1) contains three transmembrane domains | DDB0232432 | CDS | 4827309 | 363 | - | 0.267218 |
ost3 | DDB_G0285537 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST3 and human N33 (tumor suppressor candidate 3) contains four C-terminal transmembrane domain and an N-terminal signal peptide | DDB0232431 | CDS | 3352785 | 1056 | - | 0.287879 |
ost4 | DDB_G0280609 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST4 contains one transmembrane domain | DDB0232430 | CDS | 3565940 | 123 | - | 0.317073 |
ostc | DDB_G0306378 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of human OSTC contains three transmembrane domains | DDB0232430 | CDS | 1725633 | 432 | + | 0.284722 |
oxaA | DDB_G0284883 | similar to OXA1 a conserved inner mitochondrial membrane protein that is required for the activity and assembly of cytochrome oxidase and for the insertion of integral membrane proteins into the mitochondrial inner membrane there is a second putative oxidase assembly protein in D. discoideum | DDB0232431 | CDS | 2586982 | 1191 | + | 0.260285 |
oxaB | DDB_G0281171 | similar to OXA1 a conserved inner mitochondrial membrane protein that is required for the activity and assembly of cytochrome oxidase and for the insertion of integral membrane proteins into the mitochondrial inner membrane there is a second putative oxidase assembly protein in D. discoideum | DDB0232430 | CDS | 4148918 | 1257 | - | 0.275259 |
oxct | DDB_G0288105 | catalyzes the reaction succinyl-CoA a 3-oxo acid succinate a 3-oxoacyl-CoA defects in human OXCT1 are a cause of ketoacidosis | DDB0232432 | CDS | 1121891 | 1530 | + | 0.357516 |
p17 | DDB_G0278725 | similar to DDB_G0291255 contains a predicted signal peptide | DDB0232430 | CDS | 1316821 | 525 | - | 0.377143 |
p2xA | DDB_G0272004 | membrane ion channel activated by ATP may be involved in intracellular calcium signaling | DDB0232429 | CDS | 1165671 | 1137 | - | 0.292876 |
p2xB | DDB_G0275293 | member of the Dictyostelium P2X receptor family membrane ion channel activated by ATP may be involved in intracellular calcium signaling | DDB0232429 | CDS | 5243218 | 1110 | + | 0.263964 |
p2xC | DDB_G0275191 | DDB0232429 | CDS | 5246055 | 1107 | + | 0.262873 | |
p2xD | DDB_G0288335 | DDB0232432 | CDS | 1403868 | 1224 | + | 0.269608 | |
p2xE | DDB_G0288061 | member of the Dictyostelium P2X receptor family membrane ion channel activated by ATP may be involved in intracellular calcium signaling | DDB0232432 | CDS | 1030842 | 1167 | + | 0.291345 |
p80 | DDB_G0287297 | endosome phagosome membrane protein contains a putative signal peptide | DDB0232432 | CDS | 134806 | 1593 | - | 0.364093 |
pARTf | DDB_G0274389 | DDB0232429 | CDS | 4856309 | 1833 | - | 0.338789 | |
pARTg | DDB_G0271766 | DDB0232429 | CDS | 860066 | 4857 | - | 0.224212 | |
pARTg_ps | DDB_G0271768 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 865698 | 222 | - | 0.216216 |
pRNA | DDB_G0295593 | RNA component of ribonuclease P (RNase P) involved in generating mature 5' ends of tRNA | DDB0232431 | CDS | 2775844 | 369 | - | 0.330623 |
pXi | DDB_G0289119 | CAMK group protein serinethreonine kinase | DDB0232432 | CDS | 2420542 | 2076 | - | 0.25289 |
pabpc1A | DDB_G0293558 | similar to mammalian PABPC1 involved in cytoplasmic regulatory processes of mRNA metabolism binding the poly(A) tail of mRNA | DDB0232433 | CDS | 3041877 | 1698 | + | 0.415783 |
pabpc1B | DDB_G0290745 | similar to mammalian PABPC1 involved in cytoplasmic regulatory processes of mRNA metabolism binding the poly(A) tail of mRNA contains an additional N-terminal H-rich domain | DDB0232432 | CDS | 4494408 | 2445 | + | 0.325153 |
pabpn1 | DDB_G0277371 | similar to human PABPN1 (PAB2) which is involved in the 3'-end formation of mRNA precursors (pre-mRNA) by the addition of a poly(A) tail defects in PABPN1 may be the cause of an autosomal dominant oculopharyngeal muscular dystrophy | DDB0232429 | CDS | 7899822 | 669 | - | 0.327354 |
padA | DDB_G0286385 | involved in development and cell differentiation modulates the expression of extracellular cAMP relay genes during aggregation | DDB0232431 | CDS | 4393013 | 906 | + | 0.352097 |
paf1 | DDB_G0269412 | component of the conserved Paf1 complex a multifunctional complex involved in histone methylation and plays a role in RNA elongation and processing | DDB0232428 | CDS | 2724169 | 1500 | + | 0.306 |
pah | DDB_G0278781 | catalyzes the reaction L-phenylalanine tetrahydrobiopterin Osub2sub L-tyrosine 4a-hydroxytetrahydrobiopterin | DDB0232430 | CDS | 1172682 | 1326 | + | 0.300905 |
pakA | DDB_G0269166 | STE20PAKA protein kinase involved in the regulation of the cytoskeleton during chemotaxis and required for cytokinesis contains PAK-boxP21-Rho-binding (CRIB) domain found in the WASP C-terminal | DDB0232428 | CDS | 3436536 | 3594 | + | 0.33222 |
pakB | DDB_G0276459 | protein serinethreonine kinase that phosphorylates myoD (myosin ID) and myoK (myosin IK) heavy chains similar to p21-activated kinase belongs to the STE20 family PAKA subfamily of protein kinases | DDB0232429 | CDS | 6847900 | 2559 | - | 0.339195 |
pakC | DDB_G0267450 | STE20PAK protein kinase required for normal chemotaxis contains PAK-boxP21-Rho-binding (CRIB) domain and pleckstrin homology (PH) domain | DDB0232428 | CDS | 229145 | 1434 | - | 0.33682 |
pakD | DDB_G0269696 | similar to Dictyostelium pakA and other mitogen-activated protein kinases (Ste20PAK family) putative p21-activated kinase contains a calponin-like actin-binding domain a p21-Rho-binding domain and a PKC conserved region 1 (C1) regulates the actin cytoskeleton response during chemotaxis to cAMP | DDB0232428 | CDS | 3345400 | 5037 | + | 0.25273 |
pakE | DDB_G0293932 | putative protein serinethreonine kinase belongs to the PAKL subfamily of protein kinases the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232433 | CDS | 3512665 | 2781 | + | 0.270766 |
pakF | DDB_G0274409 | putative protein serinethreonine kinase belongs to the protein kinase PAKL subfamily the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232429 | CDS | 4648326 | 3531 | - | 0.282073 |
pakG | DDB_G0282891 | putative protein serinethreonine kinase belongs to the protein kinase PAKL subfamily the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232430 | CDS | 6346144 | 3540 | + | 0.284181 |
pakH-1 | DDB_G0273121 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases belongs to the PAKL subfamily stress-responsive kinase there is a second copy of this gene | DDB0232429 | CDS | 2532742 | 1542 | + | 0.282101 |
pakH-2 | DDB_G0273865 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases belongs to the PAKL subfamilystress-responsive kinase there is a second copy of this gene | DDB0232429 | CDS | 3497296 | 1542 | - | 0.282101 |
pan2 | DDB_G0269694 | ortholog of PAN2 a member of the Pan2p-Pan3p poly(A)-ribonuclease complex which acts to control poly(A) tail length and regulate the stoichiometry and activity of postreplication repair complexes | DDB0232428 | CDS | 3339032 | 4611 | - | 0.294079 |
panC | DDB_G0288935 | catalyzes the reaction ATP (R)-pantoate beta-alanine AMP diphosphate (R)-pantothenate | DDB0232432 | CDS | 2148704 | 903 | + | 0.27021 |
papA | DDB_G0288259 | RNA polymerase that specifically incorporates ATP at the 3' end of mRNA | DDB0232432 | CDS | 1302980 | 2430 | + | 0.327572 |
parG | DDB_G0277943 | degrades poly (ADP-ribose) polymers into monomeric subunits important for intracellular levels of poly (ADP-ribose) | DDB0232430 | CDS | 42510 | 1977 | - | 0.296915 |
patA | DDB_G0277861 | P-type ATPase that is up-regulated in calcium-adapted cells contains 10 predicted transmembrane domains | DDB0232430 | CDS | 364618 | 3348 | + | 0.373059 |
patA_ps | DDB_G0349155 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232430 | CDS | 3607110 | 161 | + | 0.329193 |
patB | DDB_G0282817 | plasma membrane P-type Hsupsup-ATPase that is necessary for survival in acidic environments | DDB0232430 | CDS | 6309404 | 3177 | + | 0.36481 |
pats1 | DDB_G0269250 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR WD40 and protein kinase domains | DDB0232428 | CDS | 2657392 | 9555 | - | 0.289901 |
paxB | DDB_G0274109 | paxillin homolog containing 4 highly conserved LIM domains and 4 paxillin LD domains involved in adhesion culmination and cell sorting slug formation and migration and endocytosis | DDB0232429 | CDS | 4174381 | 1710 | + | 0.352632 |
pcbd | DDB_G0282831 | catalyzes the dehydration of 4a-hydroxytetrahydrobiopterins might function in both as transcriptional coactivator and as pterin dehydratase similar to H. sapiens PCBD1 and PCBD2 | DDB0232430 | CDS | 6273125 | 300 | + | 0.29 |
pccA | DDB_G0275355 | catalyzes the reaction ATP HCOsub3subsup-sup propionyl-CoA ADP phosphate D-methylmalonyl-CoA | DDB0232429 | CDS | 5413401 | 2145 | + | 0.368298 |
pccB | DDB_G0276341 | catalyzes the reaction ATP HCO3sup-sup propionyl-CoA ADP phosphate D-methylmalonyl-CoA | DDB0232429 | CDS | 6663471 | 1662 | - | 0.379663 |
pcf11 | DDB_G0279559 | similar to S. cerevisiae and human PCF11 which in yeast is involved in pre-mRNA 3'-end processing | DDB0232430 | CDS | 2257247 | 2709 | - | 0.286083 |
pckA | DDB_G0271678 | DDB0232429 | CDS | 809928 | 1689 | + | 0.383659 | |
pcmA | DDB_G0280979 | similar to PIMT or PCMT (L-isoaspartylD-aspartyl protein carboxyl methyltransferase or protein-L-isoaspartate (D-aspartate) O-methyltransferase) | DDB0232430 | CDS | 4356442 | 951 | + | 0.287066 |
pcna | DDB_G0287607 | DDB0232432 | CDS | 463300 | 777 | - | 0.352638 | |
pcp | DDB_G0293196 | belongs to the paracaspase family of caspase-like cysteine proteases unlike its mammalian orthologs the Dictyostelium protein does not have an effect on apoptosis associates with the contractile vacuole membrane GFP-Pcp overexpressing cells are susceptible to osmotic stress | DDB0232433 | CDS | 2705921 | 1221 | - | 0.284193 |
pctA | DDB_G0270298 | DDB0232428 | CDS | 4600795 | 1083 | + | 0.359187 | |
pde3 | DDB_G0268634 | DDB0232428 | CDS | 2130761 | 1401 | - | 0.223412 | |
pde4 | DDB_G0289121 | DDB0232432 | CDS | 2402421 | 3120 | + | 0.233333 | |
pde7 | DDB_G0289145 | DDB0232432 | CDS | 2414259 | 1278 | - | 0.27856 | |
pdeD | DDB_G0274383 | DDB0232429 | CDS | 4904282 | 2604 | + | 0.323733 | |
pdeE | DDB_G0276027 | DDB0232429 | CDS | 6313321 | 3291 | - | 0.307809 | |
pdhA | DDB_G0292994 | catalyzes the reaction lipoamide pyruvate S-acetyldihydrolipoamide COsub2sub E1 alpha component of pyruvate dehydrogenase complex which contains multiple copies of three enzymatic components: pyruvate dehydrogenase (E1 phdA | DDB0232433 | CDS | 2563001 | 1134 | - | 0.368607 |
pdhB | DDB_G0276417 | catalyzes the reaction lipoamide pyruvate S-acetyldihydrolipoamide COsub2sub E1 beta component of pyruvate dehydrogenase complex which contains multiple copies of three enzymatic components: pyruvate dehydrogenase (E1 | DDB0232429 | CDS | 6888601 | 1071 | - | 0.344538 |
pdhC | DDB_G0277847 | catalyzes the reaction acetyl-CoA dihydrolipoamide CoA S-acetyldihydrolipoamide E2 component of pyruvate dehydrogenase complex which contains multiple copies of three enzymatic components: pyruvate dehydrogenase (E1 | DDB0232430 | CDS | 1063899 | 1908 | + | 0.34696 |
pdhX | DDB_G0271564 | putative ortholog of the pyruvate dehydrogenase complex component X (PDHX) that functions to link E2 ( | DDB0232429 | CDS | 683417 | 1242 | - | 0.302738 |
pdi1 | DDB_G0276141 | DDB0232429 | CDS | 6548168 | 1092 | + | 0.369048 | |
pdi2 | DDB_G0291434 | DDB0232433 | CDS | 299936 | 1542 | - | 0.33463 | |
pdiA | DDB_G0277863 | DDB0232430 | CDS | 246720 | 714 | + | 0.295518 | |
pdkA | DDB_G0281471 | member of the AGC kinase group similar to mammalian PDK (phosphoinositide-dependent protein kinase) known to phosphorylate AktPKB | DDB0232430 | CDS | 4550105 | 2061 | - | 0.273654 |
pdkB | DDB_G0284489 | member of the AGC kinase group similar to mammalian PDK (phosphoinositide-dependent protein kinase) known to phosphorylate AktPKB | DDB0232431 | CDS | 2038480 | 2727 | + | 0.260726 |
pds5 | DDB_G0275929 | bCommunity annotation:b similar to pds5 which interacts with the chromosomal cohesion complex and modulates the cohesion of chromosomes and kinetochores in ways that are only now being explored (a target | DDB0232429 | CDS | 6074432 | 4353 | + | 0.287847 |
pdsA | DDB_G0285995 | DDB0232431 | CDS | 3929775 | 1359 | - | 0.339956 | |
pdx1 | DDB_G0288299 | DDB0232432 | CDS | 1363519 | 918 | + | 0.37037 | |
pdx2 | DDB_G0288305 | member of the SNO glutamine amidotransferase family predicted to be involved in the pyridoxine (vitamin B6) biosynthetic pathway catalyzes the deamidation of glutamine as part of the synthesis of pyridoxal 5'-phosphate the resulting ammonia molecule is channeled to pdxS | DDB0232432 | CDS | 1361910 | 747 | - | 0.238286 |
pefA | DDB_G0291081 | similar to mammalian apoptosis component ALG-2 contains 5 EF-hand calcium binding domains | DDB0232432 | CDS | 4974992 | 594 | - | 0.340067 |
pefB | DDB_G0293530 | similar to mammalian apoptosis component ALG-2 contains 5 EF-hand calcium binding domains | DDB0232433 | CDS | 2988655 | 618 | + | 0.331715 |
pelo | DDB_G0280447 | ortholog of the conserved D. melanogaster protein pelota which is required for spindle formation and nuclear envelope breakdown during spermatogenesis and is proposed to act in protein translation. | DDB0232430 | CDS | 3368362 | 1326 | - | 0.295626 |
pemtA | DDB_G0282527 | homolog of mammalian PEMT and S. cerevisiae OPI3 which catalyzes the steps in phosphatidylcholine biosynthesis | DDB0232430 | CDS | 5888056 | 642 | + | 0.26324 |
pemtB | DDB_G0289645 | homolog of mammalian PEMT and S. cerevisiae OPI3 which catalyzes the steps in phosphatidylcholine biosynthesis | DDB0232432 | CDS | 3055772 | 603 | + | 0.263682 |
pepD | DDB_G0269382 | DDB0232428 | CDS | 2653185 | 1506 | - | 0.35591 | |
pex1 | DDB_G0289867 | ortholog of peroxin 1 AAA-family ATPase peroxin required for peroxisome biogenesis mutations in human homolog cause a variety of peroxisomal disorders | DDB0232432 | CDS | 3340420 | 3684 | + | 0.253529 |
pex10 | DDB_G0282693 | ortholog of peroxin 10 a RING finger peroxisomal membrane peroxin required for peroxisomal matrix protein import in S. cerevisiae interacts with peroxin 12 links ubiquitin-conjugating peroxin 4 to protein import machinery mutations in human homolog cause a variety of peroxisomal disorders | DDB0232430 | CDS | 6137089 | 1125 | - | 0.234667 |
pex11 | DDB_G0289623 | ortholog of peroxisomal protein peroxin 11 contains three putative transmembrane domains | DDB0232432 | CDS | 3044413 | 765 | - | 0.287582 |
pex12 | DDB_G0285523 | ortholog of peroxin 12 a RING-finger peroxisomal membrane peroxin that plays an essential role in peroxisome biogenesis and peroxisomal matrix protein import forms translocation subcomplex with peroxin 2 and peroxin 10 mutations in human homolog cause a variety of peroxisomal disorders | DDB0232431 | CDS | 3342493 | 1380 | - | 0.25 |
pex13 | DDB_G0292870 | putative peroxin 13 ortholog a component of the peroxisomal translocation machinery with peroxin 14 and peroxin 17 mutations in human homolog cause a variety of peroxisomal disorders | DDB0232433 | CDS | 2185175 | 1713 | - | 0.348511 |
pex14 | DDB_G0293264 | putative ortholog of peroxin 14 component of the peroxisomal protein import machinery mutations in human homolog cause peroxisomal disorders | DDB0232433 | CDS | 2607099 | 2247 | + | 0.282154 |
pex16 | DDB_G0277113 | ortholog of peroxin 16 involved in import of proteins into peroxisomes mutations in human homolog cause peroxisomal disorders | DDB0232429 | CDS | 7557711 | 1203 | - | 0.221114 |
pex19 | DDB_G0274873 | putative ortholog of peroxin 19 required for peroxisome biogenesis mutations in human homolog cause peroxisomal disorders | DDB0232429 | CDS | 4308167 | 1008 | - | 0.281746 |
pex2 | DDB_G0272234 | ortholog of peroxin 2 required for peroxisome biogenesis contains two putative transmembrane domains mutations in human homolog cause a variety of peroxisomal disorders | DDB0232429 | CDS | 1718471 | 1272 | + | 0.263365 |
pex3 | DDB_G0281213 | ortholog of peroxin 3 required for peroxisome biogenesis contains two transmembrane domains mutations in human homolog cause a variety of peroxisomal disorders | DDB0232430 | CDS | 4226854 | 1218 | - | 0.205255 |
pex4 | DDB_G0274313 | ortholog of peroxin 4 a peroxisomal ubiquitin conjugating enzyme required for peroxisomal matrix protein import and peroxisome biogenesis | DDB0232429 | CDS | 3939967 | 450 | - | 0.291111 |
pex5 | DDB_G0286033 | ortholog of peroxin 5 peroxisomal membrane signal receptor for C-terminal tripeptide signal sequence (PTS1) of peroxisomal matrix proteins required for peroxisomal matrix protein importmutations in human homolog cause a variety of peroxisomal disorders | DDB0232431 | CDS | 3973237 | 1926 | - | 0.336449 |
pex6 | DDB_G0292788 | ortholog of peroxin 6 required for peroxisome biogenesis mutations in human homolog cause a variety of peroxisomal disorders | DDB0232433 | CDS | 2034271 | 3606 | - | 0.22518 |
pex7 | DDB_G0279801 | ortholog of peroxin 7 binds the peroxisome targeting signal type 2 (PTS2) contains 6 WD40 repeats mutations in human homolog cause a variety of peroxisomal disorders | DDB0232430 | CDS | 2554628 | 951 | + | 0.31756 |
pfdn1 | DDB_G0287827 | DDB0232432 | CDS | 772980 | 348 | - | 0.238506 | |
pfdn2 | DDB_G0267594 | DDB0232428 | CDS | 385503 | 351 | + | 0.245014 | |
pfdn3 | DDB_G0286473 | DDB0232431 | CDS | 4502996 | 588 | - | 0.268707 | |
pfdn4 | DDB_G0281873 | DDB0232430 | CDS | 5055049 | 399 | - | 0.243108 | |
pfdn5 | DDB_G0280607 | DDB0232430 | CDS | 3564619 | 483 | + | 0.287785 | |
pfdn6 | DDB_G0286147 | DDB0232431 | CDS | 4132037 | 423 | + | 0.255319 | |
pfkA | DDB_G0274111 | catalyzes the reaction ATP D-fructose 6-phosphate ADP D-fructose 16-bisphosphate the Dictyostelium PFK has been found to be a non-allosteric enzyme that binds to tubulin and inhibits tubulin polymerization | DDB0232429 | CDS | 4510635 | 2505 | + | 0.372455 |
pfp1 | DDB_G0276405 | putative cysteine protease member of the DJ-1ThiJPfpI family which includes human PARK7 associated with Parkinson's disease | DDB0232429 | CDS | 6818286 | 585 | - | 0.317949 |
pggt1b | DDB_G0269726 | catalyzes the reaction geranylgeranyl diphosphate protein-cysteine S-geranylgeranyl-protein diphosphate | DDB0232428 | CDS | 3425762 | 1059 | - | 0.316336 |
pgkA | DDB_G0287595 | catalyzes the reaction 3-phosphoglycerate ATP 3-phospho-D-glyceroyl-phosphate ADP binds and is regulated by calmodulin | DDB0232432 | CDS | 494968 | 1263 | - | 0.364212 |
pgl | DDB_G0292898 | catalyzes the reaction 6-phospho-D-glucono-15-lactone Hsub2subO 6-phospho-D-gluconate | DDB0232433 | CDS | 2232140 | 711 | + | 0.295359 |
pgmA | DDB_G0288483 | catalyzes the reaction alpha-D-glucose 1-phosphate alpha-D-glucose 6-phosphate | DDB0232432 | CDS | 1620141 | 1719 | - | 0.34555 |
pgmB | DDB_G0280897 | ortholog of PGM2 which catalyzes the reaction alpha-D-glucose 1-phosphate alpha-D-glucose 6-phosphate | DDB0232430 | CDS | 3847722 | 1812 | + | 0.334989 |
pgpep | DDB_G0267498 | DDB0232428 | CDS | 226283 | 624 | + | 0.241987 | |
pgs1 | DDB_G0277037 | DDB0232429 | CDS | 7309123 | 1746 | + | 0.304124 | |
pgtA | DDB_G0283761 | catalyzes the beta13 addition of galactose to GlcNAc-Skp1 and the alpha12 addition of fucose to GalBeta13GlcNAc-Skp1 (FpaAFpaB) | DDB0232431 | CDS | 1235916 | 2310 | + | 0.208225 |
pgtB | DDB_G0290079 | CAZy family GT24 disruption of this gene results in abolished spore coat lectin-binding and renders spores hypersensitive to plasmolysis | DDB0232432 | CDS | 3623616 | 4017 | + | 0.300971 |
pgtC | DDB_G0284107 | CAZy family GT24 contains two glycosyltransferase domains | DDB0232431 | CDS | 1589376 | 3198 | - | 0.22733 |
pgtD | DDB_G0278731 | CAZy family GT24 expressed in prespore cells | DDB0232430 | CDS | 1197002 | 6702 | + | 0.30752 |
phaZ | DDB_G0284359 | similar to PHB depolymerase which catalyzes the reaction: H2O poly[(R)-3-hydroxybutanoate](n) poly[(R)-3-hydroxybutanoate](x) poly[(R)-3-hydroxybutanoate](n-x) where x is between 1 and 5 units polyhydroxyalkanoates (PHAs) are typical storage compounds of carbon and energy and are widely found in prokaryotes the most common PHA is poly(3-hydroxybutyrate) (PHB) | DDB0232431 | CDS | 1884053 | 1023 | - | 0.289345 |
phbA | DDB_G0290123 | ortholog of the yeast Phb1p and other prohibitins that are inner mitochondrial membrane chaperones that stabilize newly synthesized proteins also suggested to play a role in cell senescence | DDB0232432 | CDS | 3692217 | 816 | - | 0.300245 |
phbB | DDB_G0284117 | ortholog of the yeast Phb2p and other prohibitins that are inner mitochondrial membrane chaperones that stabilize newly synthesized proteins also suggested to play a role in cell senescence | DDB0232431 | CDS | 1608856 | 882 | + | 0.290249 |
phdA | DDB_G0285845 | DDB0232431 | CDS | 3755842 | 855 | - | 0.294737 | |
phdG | DDB_G0292622 | DDB0232433 | CDS | 1851269 | 1767 | + | 0.301075 | |
phdI | DDB_G0274775 | DDB0232429 | CDS | 3804521 | 1377 | + | 0.344953 | |
phesA | DDB_G0287141 | catalyzes the reaction ATP L-phenylalanine tRNAPhe AMP diphosphate L-phenylalanyl-tRNAPhe in S. cerevisiae acts as a tetramer composed of two alpha and two beta subunits | DDB0232431 | CDS | 5374001 | 1464 | + | 0.295082 |
phesB | DDB_G0277303 | catalyzes the reaction ATP L-phenylalanine tRNAPhe AMP diphosphate L-phenylalanyl-tRNAPhe in S. cerevisiae acts as a tetramer composed of two alpha and two beta subunits | DDB0232429 | CDS | 7623909 | 1854 | - | 0.302589 |
phf5a | DDB_G0284403 | DDB0232431 | CDS | 1954324 | 333 | - | 0.318318 | |
phg1A | DDB_G0267444 | involved in phagocytosis and substrate adhesion controls the levels of SibA adhesion molecules at the cell surface as well as the intracellular transport and stability of the SibA protein also involved in the intracellular killing of bacteria by determining the stability and cellular amount of the sulfotransferase Kil1br bNomenclature conflict: b Do not confuse this gene with phgA encoding drainin or with the phgA locus ( | DDB0232428 | CDS | 1310839 | 1926 | + | 0.344756 |
phg1B | DDB_G0277273 | involved in phagocytosis and substrate adhesion contains 9 transmembrane domains also involved in the intracellular killing of bacteria by determining the stability and cellular amount of the sulfotransferase Kil1 | DDB0232429 | CDS | 7806204 | 3009 | + | 0.316052 |
phg1c | DDB_G0290159 | DDB0232432 | CDS | 3751345 | 1968 | - | 0.254573 | |
phg2 | DDB_G0283699 | serinethreonine kinase regulating cell substrate adhesion phagocytosis motility and actin organization member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats | DDB0232431 | CDS | 995559 | 4164 | - | 0.304275 |
phgA | DDB_G0269130 | conserved protein involved in contractile vacuole discharge upon osmotic stressbr bNomenclature conflict: b Do not confuse this gene with phg1a encoding the putative phagocytic receptor 1a or with the phgA locus ( | DDB0232428 | CDS | 3817626 | 1317 | - | 0.347001 |
phlp1 | DDB_G0292850 | DDB0232433 | CDS | 2267210 | 951 | + | 0.283912 | |
phlp2 | DDB_G0285433 | DDB0232431 | CDS | 3253005 | 720 | + | 0.297222 | |
phlp3 | DDB_G0293848 | DDB0232433 | CDS | 3411418 | 555 | - | 0.257658 | |
pho2a | DDB_G0290263 | catalytic subunit of protein phosphatase 2A composed of a catalytic subunit (pho2A) a regulatory subunit (phr2AB) and a scaffold subunit (pppA) an additional regulatory B56 (psrA) subunit has been identified | DDB0232432 | CDS | 3933600 | 921 | - | 0.336591 |
phr2aB | DDB_G0283905 | regulatory subunit of protein phosphatase 2A composed of a catalytic subunit (pho2A) a regulatory subunit (phr2AB) and a scaffold subunit (pppA) an additional regulatory B56 (psrA) subunit has been identified | DDB0232431 | CDS | 1423354 | 1452 | - | 0.331267 |
phyA | DDB_G0277759 | catalyzes the hydroxylation of Proline 143 of the Skp1 protein (FpaAFpaB) | DDB0232429 | CDS | 8457984 | 855 | + | 0.211696 |
piaA | DDB_G0277399 | required for receptor-mediated activation of adenylyl cyclase component of the TORC2 (Tor complex 2) with Tor Lst8 and Rip3 that plays a role in regulation of adenylate cyclase (ACA) and protein kinase B (PKB) activation during aggregation | DDB0232429 | CDS | 8027686 | 3447 | + | 0.29823 |
pich | DDB_G0288873 | ortholog of human DNA excision repair protein ERCC-6-like (ERCC6L)br bCommunity annotation:b DDB_G0288873 but not ercc6 is strongly overexpressed (6x) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most cells involved in S-phase or mitosis are overexpressed in this strain. Ercc6-like is an essential component of the spindle checkpoint which localizes to the kinetochore in prometaphase it is found on thin threads that stretch between sister kinetochores. It is thought to function as part of the tension sensor the functional core of the spindle checkpoint [see Baumann et al Cell 128 101-114 (2007)]. Other spindle checkpoint components are strongly overexpressed in the rblA null. This suggests that DDB_G0288873 may actually code for the spindle tension sensor in Dicty. Harry MacWilliams May 2010br | DDB0232432 | CDS | 2065550 | 3999 | - | 0.295074 |
pif1 | DDB_G0277925 | very similar to the conserved DNA helicase PIF1 in S. cerevisiae involved in telomere formation and elongation | DDB0232430 | CDS | 12156 | 2010 | - | 0.283582 |
pigA | DDB_G0283965 | CAZy family GT4 subunit of the transferase that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-N-acetylglucosamine to phosphatidylinositol (PI) | DDB0232431 | CDS | 1382938 | 1572 | + | 0.268448 |
pigB | DDB_G0284435 | CAZy family GT22 catalyzes the addition of the third mannose to GPI (glycosylphosphatidylinositol) | DDB0232431 | CDS | 1990910 | 1644 | + | 0.230535 |
pigC | DDB_G0286221 | putative glycosyltransferase involved in GPI biosynthesis subunit of the transferase that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-N-acetylglucosamine to phosphatidylinositol (PI) | DDB0232431 | CDS | 4208827 | 1038 | - | 0.256262 |
pigF | DDB_G0284667 | involved in GPI biosynthesis functions with PigO to transfer ethanolamine phosphate to the third mannose of GPI (glycosylphosphatidylinositol) | DDB0232431 | CDS | 2319957 | 660 | + | 0.265152 |
pigH | DDB_G0277289 | putative glycosyltransferase involved in GPI biosynthesis subunit of the transferase that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-N-acetylglucosamine to phosphatidylinositol (PI) | DDB0232429 | CDS | 7844509 | 714 | - | 0.246499 |
pigK | DDB_G0285461 | DDB0232431 | CDS | 3257355 | 1341 | - | 0.266219 | |
pigL | DDB_G0293136 | DDB0232433 | CDS | 2582359 | 777 | + | 0.245817 | |
pigM | DDB_G0288899 | CAZy family GT50 catalyzes the addition of the first mannose to GPI (glycosylphosphatidylinositol) | DDB0232432 | CDS | 2094858 | 1329 | + | 0.234763 |
pigN | DDB_G0279313 | highly conserved protein involved in GPI anchor biosynthesis ortholog of yeast MCD4 | DDB0232430 | CDS | 1921668 | 3099 | + | 0.308809 |
pigO | DDB_G0278687 | putative transferase involved in GPI biosynthesis functions with PigF to transfer ethanolamine phosphate to the third mannose of GPI (glycosylphosphatidylinositol) | DDB0232430 | CDS | 887014 | 3363 | + | 0.223015 |
pigQ | DDB_G0279515 | putative glycosyltransferase involved in GPI biosynthesis subunit of the transferase that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-N-acetylglucosamine to phosphatidylinositol (PI) | DDB0232430 | CDS | 2188620 | 2979 | - | 0.25042 |
pigS | DDB_G0289515 | DDB0232432 | CDS | 2896095 | 1224 | - | 0.253268 | |
pigT | DDB_G0291490 | DDB0232433 | CDS | 421140 | 2034 | - | 0.274828 | |
pigV | DDB_G0280891 | DDB0232430 | CDS | 3836784 | 1908 | - | 0.22065 | |
pigW | DDB_G0286111 | DDB0232431 | CDS | 3995640 | 1479 | - | 0.257606 | |
pigX | DDB_G0283717 | DDB0232431 | CDS | 1018005 | 1785 | - | 0.222409 | |
pik6 | DDB_G0275635 | phosphatidylinositol phosphate kinase that binds diacylglycerol essential for normal early developmental gene expression | DDB0232429 | CDS | 6045706 | 4770 | + | 0.275681 |
pikA | DDB_G0278727 | DDB0232430 | CDS | 1154369 | 4716 | + | 0.261026 | |
pikB | DDB_G0283081 | DDB0232431 | CDS | 247398 | 5574 | - | 0.311805 | |
pikC | DDB_G0275011 | DDB0232429 | CDS | 5211773 | 5094 | + | 0.270907 | |
pikD | DDB_G0288485 | subunit of PI4K responsible for the phosphorylation of phosphatidylinositol (PI) to PI4P (ATP 1-phosphatidyl-1D-myo-inositol ADP 1-phosphatidyl-1D-myo-inositol 4-phosphate) the first committed step in the generation of phosphatidylinositol 45-bisphosphate (PIP2) a precursor of the second messenger inositol 145-trisphosphate (InsP3) | DDB0232432 | CDS | 1616073 | 3543 | + | 0.269828 |
pikE | DDB_G0289601 | ortholog of yeast VPS34 a phosphatidylinositol 3-kinase | DDB0232432 | CDS | 3005109 | 2451 | - | 0.299878 |
pikF | DDB_G0268548 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | DDB0232428 | CDS | 1099622 | 4149 | + | 0.291396 |
pikG | DDB_G0282625 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | DDB0232430 | CDS | 6013022 | 5016 | - | 0.234649 |
pikH | DDB_G0291093 | putative PI3k putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring unlike other PI3Ks does not contain a ras binding domain but a PH domain and does not localize to the cell cortex upon chemotactic stimulation | DDB0232432 | CDS | 4980832 | 5463 | - | 0.242541 |
pikI | DDB_G0267588 | DDB0232428 | CDS | 376992 | 2160 | - | 0.32963 | |
pinA | DDB_G0268618 | DDB0232428 | CDS | 1957162 | 807 | - | 0.313507 | |
pip5k3 | DDB_G0279149 | ortholog of mammlian PIP5K3 and S. cerevisiae FAB1 contains in addition to the C-terminal PIP kinase domain an N-terminal FYVE-type zinc finger domain and a central chaperonin Cpn60TCP-1 domain | DDB0232430 | CDS | 1689106 | 7971 | + | 0.275624 |
pirA | DDB_G0287855 | DDB0232432 | CDS | 727908 | 4011 | + | 0.354026 | |
pisA | DDB_G0274743 | ortholog of human PIAS1 (protein inhibitor of activated STAT) an E3 SUMO-protein ligase that acts as a transcriptional coregulation in various mammalian cellular pathways including the STAT pathway the p53 pathway and the steroid hormone signaling pathway | DDB0232429 | CDS | 3922420 | 2505 | - | 0.28503 |
pitA | DDB_G0290069 | DDB0232432 | CDS | 3651511 | 795 | + | 0.31195 | |
pitB | DDB_G0274579 | DDB0232429 | CDS | 3878722 | 780 | + | 0.291026 | |
pitC | DDB_G0280449 | belongs to the phosphatidylinositol transfer protein family similar to H. sapiens membrane-associated phosphatidylinositol transfer proteins 1 and 2 but significantly smaller protein very similar to Dictyostelium pitA and pitB | DDB0232430 | CDS | 3370546 | 864 | - | 0.291667 |
pitD | DDB_G0292426 | DDB0232433 | CDS | 1595140 | 996 | - | 0.282129 | |
pitrm1 | DDB_G0271506 | DDB0232429 | CDS | 455398 | 3201 | - | 0.282099 | |
pkaC | DDB_G0283907 | AGC group PKA family protein kinase protein serinethreonine kinase regulates spore cell differentiation | DDB0232431 | CDS | 1394958 | 1947 | + | 0.333847 |
pkaD | DDB_G0277145 | DDB0232429 | CDS | 7643321 | 2145 | - | 0.253613 | |
pkaR | DDB_G0279413 | DDB0232430 | CDS | 2222668 | 984 | - | 0.319106 | |
pkbA | DDB_G0268620 | AGC group AKT family protein serinethreonine kinase similar to other metazoan AktPKB including an N-terminal PH domain homologous kinase and C-terminal regulatory domains and phosphorylation sites required for AktPKB activation | DDB0232428 | CDS | 1977388 | 1335 | + | 0.357303 |
pkd2 | DDB_G0272999 | putative Ca2 channel similar to metazoan polycystin-2 (PKD2) defects in the human PKD2 causes polycystic kidney disease autosomal dominant type 2 (ADPKD2) characterized by progressive formation and enlargement of cysts in both kidneys contains 6 putative transmembrane domains | DDB0232429 | CDS | 2088080 | 2148 | - | 0.256052 |
pkgA | DDB_G0276157 | serinethreonine protein kinase of the MAST (Microtubule Associated SerineThreonine kinase) family | DDB0232429 | CDS | 6275918 | 4104 | - | 0.287037 |
pkgB | DDB_G0290157 | AGC group protein serinethreonine kinase cAMP-activated protein kinase involved in morphogenesis during multicellular development | DDB0232432 | CDS | 3717777 | 1440 | - | 0.324306 |
pkgC | DDB_G0286125 | serinethreonine protein kinase of the AGC group similar to mammalian ribosomal protein S6 kinase | DDB0232431 | CDS | 4067973 | 2733 | - | 0.312843 |
pkgD | DDB_G0284029 | AGC group protein serinethreonine kinase similar to cAMP-activated protein kinase catalytic subunits | DDB0232431 | CDS | 1459718 | 2979 | - | 0.28231 |
pkgE_ps | DDB_G0280981 | putative pseudogene similar to AGC protein kinases of the AKT family | DDB0232430 | CDS | 3912677 | 1095 | + | 0.343379 |
pkiA | DDB_G0289391 | DDB0232432 | CDS | 2783089 | 384 | + | 0.351562 | |
pks10 | DDB_G0271662 | DDB0232429 | CDS | 687700 | 7458 | - | 0.23639 | |
pks11_ps | DDB_G0272426 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232429 | CDS | 1535421 | 8865 | + | 0.238466 |
pks12_ps | DDB_G0272428 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232429 | CDS | 1545459 | 7749 | + | 0.243386 |
pks13 | DDB_G0272981 | DDB0232429 | CDS | 1994416 | 7656 | + | 0.251045 | |
pks14 | DDB_G0272859 | DDB0232429 | CDS | 2072143 | 8997 | - | 0.242748 | |
pks15 | DDB_G0273007 | DDB0232429 | CDS | 2126877 | 9525 | - | 0.223097 | |
pks16 | DDB_G0275069 | fatty acid synthases catalyze the formation of long-chain fatty acids from acetyl-CoA malonyl-CoA and NADPH multifunctional protein with several catalytic activities and an acyl carrier protein enriched in gametes | DDB0232429 | CDS | 5110511 | 7812 | + | 0.281234 |
pks17 | DDB_G0275077 | fatty acid synthases catalyze the formation of long-chain fatty acids from acetyl-CoA malonyl-CoA and NADPH. This multifunctional protein has several catalytic activities and an acyl carrier protein | DDB0232429 | CDS | 5134435 | 7815 | - | 0.280102 |
pks18 | DDB_G0281475 | DDB0232430 | CDS | 4556537 | 9000 | + | 0.239333 | |
pks19 | DDB_G0282027 | DDB0232430 | CDS | 5258026 | 8337 | - | 0.255967 | |
pks2 | DDB_G0270572 | DDB0232428 | CDS | 3098695 | 9033 | + | 0.275213 | |
pks20_ps | DDB_G0282079 | putative pseudogene polyketide synthase family protein | DDB0232430 | CDS | 5268803 | 8037 | - | 0.255941 |
pks21 | DDB_G0282029 | DDB0232430 | CDS | 5285533 | 8340 | - | 0.252998 | |
pks22 | DDB_G0284001 | DDB0232431 | CDS | 1312340 | 7500 | - | 0.264533 | |
pks23 | DDB_G0283931 | DDB0232431 | CDS | 1322762 | 7500 | - | 0.2616 | |
pks24 | DDB_G0287119 | DDB0232431 | CDS | 5319738 | 7416 | - | 0.237325 | |
pks25 | DDB_G0287095 | DDB0232431 | CDS | 5330551 | 7143 | + | 0.235475 | |
pks26 | DDB_G0288457 | DDB0232432 | CDS | 1543867 | 7596 | + | 0.253818 | |
pks27 | DDB_G0290467 | DDB0232432 | CDS | 4086338 | 8055 | + | 0.259963 | |
pks28 | DDB_G0290469 | DDB0232432 | CDS | 4095634 | 8073 | + | 0.25703 | |
pks29 | DDB_G0290699 | DDB0232432 | CDS | 4438040 | 9321 | - | 0.239352 | |
pks3 | DDB_G0271000 | DDB0232428 | CDS | 3963577 | 8514 | - | 0.262626 | |
pks30 | DDB_G0290701 | DDB0232432 | CDS | 4448854 | 9228 | - | 0.242306 | |
pks31 | DDB_G0290703 | DDB0232432 | CDS | 4460222 | 7872 | - | 0.244538 | |
pks32 | DDB_G0290709 | DDB0232432 | CDS | 4472163 | 9306 | - | 0.239415 | |
pks33 | DDB_G0290729 | DDB0232432 | CDS | 4507516 | 9330 | + | 0.237621 | |
pks34 | DDB_G0290737 | DDB0232432 | CDS | 4522863 | 9237 | - | 0.239472 | |
pks35 | DDB_G0295667 | DDB0232432 | CDS | 4539649 | 7545 | + | 0.249304 | |
pks36 | DDB_G0295659 | DDB0232432 | CDS | 4550115 | 8796 | + | 0.243179 | |
pks38 | DDB_G0290937 | DDB0232432 | CDS | 4772842 | 9402 | - | 0.237184 | |
pks39 | DDB_G0290943 | DDB0232432 | CDS | 4786202 | 9327 | - | 0.237483 | |
pks40 | DDB_G0291614 | DDB0232433 | CDS | 536394 | 7659 | - | 0.244288 | |
pks41 | DDB_G0291684 | DDB0232433 | CDS | 545874 | 7629 | - | 0.244593 | |
pks42 | DDB_G0292544 | DDB0232433 | CDS | 1717075 | 7968 | + | 0.244603 | |
pks43_ps | DDB_G0292488 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232433 | CDS | 1725966 | 7494 | + | 0.241793 |
pks44 | DDB_G0293902 | DDB0232433 | CDS | 3438259 | 9237 | + | 0.251922 | |
pks45 | DDB_G0293912 | DDB0232433 | CDS | 3449815 | 9279 | - | 0.250781 | |
pks4_ps | DDB_G0271222 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232429 | CDS | 266225 | 5901 | + | 0.25538 |
pks5 | DDB_G0271520 | DDB0232429 | CDS | 499181 | 7539 | + | 0.251094 | |
pks6 | DDB_G0271524 | DDB0232429 | CDS | 507457 | 8775 | + | 0.242165 | |
pks7 | DDB_G0271614 | DDB0232429 | CDS | 519478 | 7542 | + | 0.244365 | |
pks8 | DDB_G0271618 | DDB0232429 | CDS | 530981 | 7545 | + | 0.249304 | |
pks9 | DDB_G0271530 | putative type I iterative polyketide synthase expressed in upper and lower cups during culmination | DDB0232429 | CDS | 541447 | 8796 | + | 0.243179 |
pksB | DDB_G0282357 | ortholog of E. coli ydfG and S. cerevisiae TMA29 that have NADP-dependent L-serine dehydrogenase activity also acts on other amino acids such as D-threonine and L-allo-threonine homotetramer | DDB0232430 | CDS | 6131868 | 783 | + | 0.303959 |
plaA | DDB_G0278525 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232430 | CDS | 1019968 | 1161 | - | 0.289406 |
plbA | DDB_G0276767 | DDB0232429 | CDS | 7242199 | 1725 | - | 0.328696 | |
plbB | DDB_G0271126 | highly similar to | DDB0232429 | CDS | 40824 | 1719 | + | 0.272833 |
plbC | DDB_G0286095 | highly similar to | DDB0232431 | CDS | 4056446 | 1698 | + | 0.269729 |
plbD | DDB_G0284449 | highly similar to | DDB0232431 | CDS | 1876303 | 1710 | + | 0.287134 |
plbE | DDB_G0277455 | similar to | DDB0232429 | CDS | 8132946 | 1665 | - | 0.301502 |
plbF | DDB_G0275125 | similar to | DDB0232429 | CDS | 4991620 | 1692 | + | 0.304965 |
plbG | DDB_G0267392 | similar to | DDB0232428 | CDS | 1331239 | 1797 | - | 0.249304 |
plc | DDB_G0292736 | catalyzes the reaction 1-phosphatidyl-1D-myo-inositol 45-bisphosphate H2O D-myo-inositol 145-trisphosphate diacylglycero regulated by the MADS-box transcription factor SrfA during development | DDB0232433 | CDS | 2060204 | 2406 | + | 0.320864 |
pldA | DDB_G0281031 | catalyzes the reaction a phosphatidylcholine Hsub2subO choline a phosphatidate expressed throughout growth and development | DDB0232430 | CDS | 3951371 | 3810 | + | 0.29895 |
pldB | DDB_G0279483 | catalyzes the reaction a phosphatidylcholine Hsub2subO choline a phosphatidate plays a role in quorum sensing during aggregation | DDB0232430 | CDS | 2122585 | 3651 | + | 0.256368 |
pldC | DDB_G0277949 | catalyzes the reaction a phosphatidylcholine Hsub2subO choline a phosphatidate | DDB0232430 | CDS | 49404 | 4923 | - | 0.280926 |
pldG | DDB_G0276919 | similar to human PLD a GPI (glycosylphosphatidylinositol)-specific phospholipase D | DDB0232429 | CDS | 7179136 | 2847 | + | 0.293642 |
pldY | DDB_G0287649 | highly similar to mammalian PLD3 which is of unknown function | DDB0232432 | CDS | 458523 | 1317 | - | 0.290053 |
pldZ | DDB_G0282579 | highly similar to mammalian PLD3 which is of unknown function | DDB0232430 | CDS | 5966744 | 1269 | + | 0.368006 |
plip | DDB_G0272835 | phosphoinositide phosphatase with low specific activity compared to other known phosphoinositide phosphatases can dephosphorylate several phosphoinositide substrates with a preference for PI(5)P constitutively expressed putative ortholog of H. sapiens EPM2A involved in myoclonic epilepsy of Lafora | DDB0232429 | CDS | 1986849 | 699 | + | 0.273248 |
plk | DDB_G0274503 | putative protein serinethreonine kinase similar to yeast CDC5 Drosophila polo and mammalian PLK which play a role in mitosis and localize to the centrosomes | DDB0232429 | CDS | 4379150 | 2937 | - | 0.280899 |
plnA | DDB_G0279791 | DDB0232430 | CDS | 2518903 | 1146 | + | 0.287958 | |
plrg1 | DDB_G0279507 | DDB0232430 | CDS | 2174875 | 1551 | + | 0.317215 | |
pmmA | DDB_G0279289 | catalyzes the reaction alpha-D-mannose 1-phosphate D-mannose 6-phosphate | DDB0232430 | CDS | 1893937 | 750 | - | 0.262667 |
pmmB | DDB_G0272781 | catalyzes the reaction alpha-D-mannose 1-phosphate D-mannose 6-phosphate | DDB0232429 | CDS | 2170341 | 750 | - | 0.268 |
pmpA | DDB_G0269170 | DDB0232428 | CDS | 4028749 | 417 | + | 0.302158 | |
pms1 | DDB_G0283981 | ortholog of H. sapiens PMS2 and S. cerevisiae PMS1 required for DNA mismatch repair | DDB0232431 | CDS | 1418066 | 3069 | - | 0.273053 |
pncA | DDB_G0293618 | catalyzes the reaction nicotinamide Hsub2subO nicotinate NHsub3sub | DDB0232433 | CDS | 3150071 | 630 | - | 0.253968 |
png | DDB_G0268168 | involved in the degradation of misfolded glycosylated proteins required for normal multicellular development belongs to the transglutaminase-like superfamily | DDB0232428 | CDS | 1591385 | 1857 | - | 0.285407 |
pnkp | DDB_G0281229 | similar to PNKP an enzyme with dual polynucleotide kinase and 3'-phosphatase activities involved in DNA repair | DDB0232430 | CDS | 4245222 | 1635 | + | 0.338226 |
pno1 | DDB_G0287557 | conserved protein in S. cerevisiae a nucleolar protein required for pre-18S rRNA processing | DDB0232432 | CDS | 417964 | 720 | + | 0.290278 |
polA | DDB_G0267464 | contains one 5'-3' exonuclease domain and one 3'-5' exonuclease domain | DDB0232428 | CDS | 1469084 | 4110 | - | 0.29708 |
polA1 | DDB_G0282191 | ortholog of the catalytic subunit of the DNA polymerase alpha-primase complex required for the initiation of DNA replication | DDB0232430 | CDS | 5500018 | 4530 | + | 0.305519 |
polA2 | DDB_G0282731 | ortholog of the B subunit of the DNA polymerase alpha-primase complex required for the initiation of DNA replication | DDB0232430 | CDS | 6220731 | 1872 | + | 0.280983 |
polA3 | DDB_G0270442 | ortholog of the DNA primase large subunit of the DNA polymerase alpha-primase complex required for the initiation of DNA replication | DDB0232428 | CDS | 4882826 | 1413 | - | 0.279547 |
polA4 | DDB_G0285853 | ortholog of the DNA primase small subunit of the DNA polymerase alpha-primase complex required for the initiation of DNA replication | DDB0232431 | CDS | 3724070 | 1230 | - | 0.281301 |
polB | DDB_G0284713 | similar to yeast Pol4 and mammalian DNA polymerase beta involved in repair of DNA double-strand breaks by non-homologous end joining (NHEJ) | DDB0232431 | CDS | 2376164 | 1530 | - | 0.261438 |
polD1 | DDB_G0285381 | required for chromomsomal DNA replication contains a polymerase and a 3'-5' exonuclease domain | DDB0232431 | CDS | 3206066 | 3315 | - | 0.332428 |
polD2 | DDB_G0281641 | DDB0232430 | CDS | 4748825 | 1566 | - | 0.288633 | |
polD3 | DDB_G0294609 | similarity to POLD3 and cdc27 is weak but contains the PCNA-binding motif | DDB0232430 | CDS | 2461693 | 2094 | + | 0.272684 |
ponA | DDB_G0293522 | DDB0232433 | CDS | 3188338 | 432 | + | 0.326389 | |
ponB | DDB_G0286247 | protein structurally similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane expressed in bacterially grown vegetative and fusion-competent cells | DDB0232431 | CDS | 4244481 | 438 | - | 0.33105 |
ponC1 | DDB_G0286717 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to 1 downstream and 3 upstream genes | DDB0232431 | CDS | 4885049 | 444 | - | 0.34009 |
ponC2 | DDB_G0286715 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to the 4 upstream genes | DDB0232431 | CDS | 4883827 | 444 | - | 0.331081 |
ponC3 | DDB_G0286721 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to 2 downstream and 2 upstream genes | DDB0232431 | CDS | 4887442 | 444 | - | 0.335586 |
ponC4 | DDB_G0286719 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to 3 downstream and 1 upstream gene | DDB0232431 | CDS | 4886230 | 444 | - | 0.34009 |
ponC5 | DDB_G0286723 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to the 4 downstream genes | DDB0232431 | CDS | 4888589 | 444 | - | 0.333333 |
ponD | DDB_G0282423 | similar to ponticulins especially ponB ponA is a protein that anchors the actin cytoskeleton to the plasma membrane | DDB0232430 | CDS | 5750022 | 447 | - | 0.378076 |
ponE | DDB_G0293634 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane | DDB0232433 | CDS | 3189105 | 516 | + | 0.263566 |
ponF | DDB_G0286631 | structurally similar to ponticulins contains a putative signal peptide | DDB0232431 | CDS | 4759468 | 516 | - | 0.381783 |
ponH | DDB_G0286573 | structurally similar to ponticulins contains a putative signal peptide | DDB0232431 | CDS | 4646321 | 612 | + | 0.372549 |
ponJ | DDB_G0289919 | DDB0232432 | CDS | 3425059 | 705 | + | 0.296454 | |
ponK | DDB_G0268460 | DDB0232428 | CDS | 1599584 | 564 | - | 0.225177 | |
ponL | DDB_G0288649 | structurally similar to ponticulins contains a putative signal peptide | DDB0232432 | CDS | 1782283 | 435 | + | 0.271264 |
ponM | DDB_G0281989 | DDB0232430 | CDS | 5221448 | 396 | + | 0.361111 | |
pop1 | DDB_G0291320 | DDB0232433 | CDS | 120925 | 2448 | - | 0.275735 | |
pop4 | DDB_G0288543 | DDB0232432 | CDS | 1668067 | 759 | - | 0.258235 | |
pop5 | DDB_G0291662 | DDB0232433 | CDS | 281774 | 516 | - | 0.24031 | |
porA | DDB_G0271848 | porin of the outer mitochondrial membrane a wide voltage-gated channel for a variety of ions | DDB0232429 | CDS | 946406 | 828 | + | 0.380435 |
potA | DDB_G0282291 | DDB0232430 | CDS | 5660926 | 2934 | + | 0.273347 | |
poxA | DDB_G0277275 | regulated by the MADS-box transcription factor SrfA during development contains a predicted signal peptide | DDB0232429 | CDS | 7857099 | 1596 | - | 0.305138 |
ppa1 | DDB_G0284265 | inorganic pyrophosphatase 1 (PPAse) cytoplasmic enzyme in yeast IPP1 catalyzes the rapid exchange of oxygens from Pi with water | DDB0232431 | CDS | 1798190 | 840 | + | 0.333333 |
ppan | DDB_G0285515 | ortholog of the Drosophila Peter Pan gene that when mutated results in larvae that do not grow and show minimal DNA replication | DDB0232431 | CDS | 3335964 | 1281 | + | 0.299766 |
ppcdc | DDB_G0278413 | decarboxylates N-[(R)-4'-phosphopantothenoyl]-L-cysteine to pantotheine 4'-phosphate | DDB0232430 | CDS | 851201 | 594 | - | 0.249158 |
ppiA | DDB_G0282359 | DDB0232430 | CDS | 5684660 | 540 | + | 0.409259 | |
ppiD | DDB_G0283663 | ortholog of the mammalian PPID peptidyl-prolyl cis-trans isomerase (PPIase) accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232431 | CDS | 943186 | 1065 | + | 0.293897 |
ppiH | DDB_G0274281 | highly similar to human PPIH a snRNP-associated protein which interacts with PRP4 | DDB0232429 | CDS | 4043724 | 606 | + | 0.30198 |
ppil2 | DDB_G0284323 | DDB0232431 | CDS | 1783122 | 1845 | + | 0.266125 | |
ppil3 | DDB_G0291734 | DDB0232433 | CDS | 672553 | 486 | - | 0.281893 | |
ppk1 | DDB_G0293524 | similar to bacterial PPK (PPK1 family) which synthesizes poly P a polymer of up to hundreds of phosphate residues | DDB0232433 | CDS | 3029753 | 3162 | - | 0.328906 |
ppme1 | DDB_G0281651 | similar to H. sapiens PPME1 which demethylates proteins that have been reversibly carboxymethylated | DDB0232430 | CDS | 4760769 | 966 | + | 0.272257 |
ppp2r4 | DDB_G0270036 | ortholog of the human PPP2R4 (PTPA) that stimulates the phosphotyrosyl phosphatase activity of PP2A in the presence of ATP and Mg(2) in vitro | DDB0232428 | CDS | 4068160 | 978 | + | 0.287321 |
ppp4c | DDB_G0272116 | protein serinethreonine phosphatase required for chemotaxis and development suppresses the | DDB0232429 | CDS | 1426809 | 918 | - | 0.331155 |
ppp5C | DDB_G0283157 | DDB0232431 | CDS | 299093 | 1545 | - | 0.307443 | |
ppp6c | DDB_G0272118 | DDB0232429 | CDS | 1655025 | 918 | + | 0.332244 | |
pppA | DDB_G0283601 | scaffold subunit of the serinethreonine protein phosphatase 2A composed of a catalytic subunit (pho2A) a regulatory subunit (phr2AB) and a scaffold subunit (pppA) an additional regulatory B56 (psrA) subunit has been identified | DDB0232431 | CDS | 949430 | 1755 | - | 0.312251 |
pppB | DDB_G0275619 | DDB0232429 | CDS | 6106886 | 966 | - | 0.356108 | |
ppr1 | DDB_G0281483 | regulatory subunit 1 of the protein serinethreonine phosphatase 4 PPC4 ( | DDB0232430 | CDS | 4583388 | 2181 | - | 0.26685 |
ppr2 | DDB_G0272668 | regulatory subunit 2 of the protein serinethreonine phosphatase 4 PPC4 ( | DDB0232429 | CDS | 2247692 | 852 | - | 0.275822 |
pprA | DDB_G0284039 | DDB0232431 | CDS | 1595576 | 1011 | - | 0.2364 | |
ppt1 | DDB_G0285533 | ortholog of the human PPT1 an enzyme which catalyzes the reaction: palmitoyl-protein Hsub2subO palmitate protein defects in PPT1 are the cause of infantile neuronal ceroid lipofuscinosis 1 a progressive neurodegenerative disease | DDB0232431 | CDS | 3349371 | 912 | - | 0.262061 |
ppt2 | DDB_G0288807 | very similar to human PPT2 an enzyme which catalyzes the reaction: palmitoyl-protein Hsub2subO palmitate protein | DDB0232432 | CDS | 1997456 | 915 | - | 0.272131 |
ppt3 | DDB_G0292862 | similar to mammalian PPT1 an enzyme which catalyzes the reaction: palmitoyl-protein Hsub2subO palmitate protein third palmitoyl-protein thioesterase in Dictyostelium | DDB0232433 | CDS | 2173470 | 870 | - | 0.310345 |
ppwd1 | DDB_G0269054 | conserved peptidyl-prolyl isomerase and WD repeat-containing protein that might be involved in pre-mRNA processing peptidyl-prolyl cis-trans isomerase (PPIase) accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232428 | CDS | 1931476 | 1908 | + | 0.28826 |
prafA | DDB_G0278887 | belongs to a conserved family of multi-pass transmembrane proteins contains 3 predicted transmembrane domains | DDB0232430 | CDS | 1342274 | 708 | - | 0.303672 |
prafB | DDB_G0285007 | belongs to a conserved family of multi-pass transmembrane proteins contains 4 predicted transmembrane domains | DDB0232431 | CDS | 2796145 | 477 | - | 0.285115 |
prdx4 | DDB_G0274859 | expressed in prespore cells ortholog of peroxiredoxin 4 catalyzes the reaction reduced thioredoxin Hsub2subOsub2sub oxidized thioredoxin Hsub2subO | DDB0232429 | CDS | 4213176 | 1398 | + | 0.360515 |
prdx5 | DDB_G0285741 | DDB0232431 | CDS | 3255042 | 519 | + | 0.358382 | |
prfA | DDB_G0283175 | required for the termination of protein biosynthesis class I release factors bind to ribosomes that have encountered a stop codon at their decoding site and induce release of the nascent polypeptide mediates UAA and UAG-dependent termination in prokaryotes | DDB0232431 | CDS | 360952 | 1293 | + | 0.329466 |
prfB | DDB_G0288835 | required for the termination of protein biosynthesis class I release factors bind to ribosomes that have encountered a stop codon at their decoding site and induce release of the nascent polypeptide mediates UAA and UGA-dependent termination in prokaryotes | DDB0232432 | CDS | 2047432 | 1275 | + | 0.28549 |
prkab | DDB_G0281089 | DDB0232430 | CDS | 4037372 | 1044 | - | 0.316092 | |
prkag | DDB_G0272542 | non-catalytic subunit of the AMP-activated protein kinase (AMPK) complex contains two CBS domains | DDB0232429 | CDS | 1788557 | 1734 | - | 0.277393 |
prlA | DDB_G0282361 | DDB0232430 | CDS | 5825075 | 1158 | + | 0.358377 | |
prmt1 | DDB_G0291556 | DDB0232433 | CDS | 504463 | 1026 | - | 0.287524 | |
prmt2 | DDB_G0289445 | DDB0232432 | CDS | 2803733 | 1539 | - | 0.275504 | |
prmt5 | DDB_G0287327 | Skb1 (Shk1 kinase-binding protein 1) family protein ortholog of S. cerevisiae HSL7 and H. sapiens PRMT5 involved in methylation of small nuclear ribonucleoproteins | DDB0232432 | CDS | 141257 | 1929 | - | 0.287714 |
proA | DDB_G0287125 | G-actin binding protein very similar to proB involved in F-actin regulation cytokinesis and development | DDB0232431 | CDS | 5417279 | 381 | - | 0.377953 |
proB | DDB_G0286187 | G-actin binding protein very similar to proA involved in F-actin regulation cytokinesis and development | DDB0232431 | CDS | 4278216 | 375 | - | 0.429333 |
proC | DDB_G0271142 | G-actin binding protein that is located to filopodia binds to VASP and is involved in chemotaxis | DDB0232429 | CDS | 57583 | 381 | + | 0.341207 |
proS | DDB_G0284197 | catalyzes the reaction ATP L-proline tRNAPro AMP diphosphate L-prolyl-tRNAPro | DDB0232431 | CDS | 1680128 | 1647 | + | 0.375228 |
prosc | DDB_G0278713 | highly similar to mammalian PROSC a homolog of a bacterial gene co-transcribed with proline synthetase | DDB0232430 | CDS | 1087624 | 768 | - | 0.24349 |
prp18 | DDB_G0274555 | DDB0232429 | CDS | 4164827 | 1170 | + | 0.286325 | |
prp19 | DDB_G0276803 | ortholog of the Prp19 protein in mammals a nuclear matrix protein protein that plays a role in DNA double-strand break repair in S. cerevisiae and in S. pombe a RNA splicing factor and a ubiquitin-protein ligase contains 6 WD-40 repeats and an N-terminal U-box motif | DDB0232429 | CDS | 7360384 | 1545 | - | 0.337864 |
prp40 | DDB_G0283543 | ortholog of prp40 which in yeast is a U1 snRNP protein involved in splicing | DDB0232431 | CDS | 792074 | 2046 | - | 0.280547 |
prpD | DDB_G0288681 | DDB0232432 | CDS | 1873609 | 1479 | + | 0.354293 | |
prpD_ps | DDB_G0288721 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232432 | CDS | 1876627 | 147 | + | 0.197279 |
prpf3 | DDB_G0274213 | component of the U4U6-U5 snRNP complex human PRP3 interacts with PRP4 | DDB0232429 | CDS | 4766016 | 1716 | - | 0.29021 |
prpf31 | DDB_G0289595 | component of the U4U6-U5 snRNP complex defects in human PRPF31 are the cause of retinitis pigmentosa 11 (RP11) | DDB0232432 | CDS | 2984110 | 1383 | - | 0.295734 |
prpf38a | DDB_G0274361 | DDB0232429 | CDS | 3801963 | 1548 | - | 0.284238 | |
prpf38b | DDB_G0288401 | DDB0232432 | CDS | 1492016 | 1257 | - | 0.287192 | |
prpf39 | DDB_G0283307 | contains a putative HAT (Half A TPR) repeat PRP39 in yeast is involved in mRNA splicing | DDB0232431 | CDS | 508620 | 2100 | - | 0.25 |
prpf4 | DDB_G0287635 | ortholog of the prp4 splicing factor component of the U4U6-U5 snRNP complex contains 7 WD repeats and a splicing factor motif | DDB0232432 | CDS | 533367 | 1803 | - | 0.297837 |
prpf4B | DDB_G0279703 | protein serinethreonine kinase DYRK family member of the CMGC kinase group similar to mammalian pre-mRNA processing factor PRP4 kinase and DYRK kinases | DDB0232430 | CDS | 2466144 | 2436 | + | 0.296388 |
prpf6 | DDB_G0272374 | component of the U5 sRNP complex may act in the tri-snRNP complex as a bridging factor between U5 and U4U6 snRNPs | DDB0232429 | CDS | 1378065 | 3045 | + | 0.324138 |
prpf8 | DDB_G0274229 | central component of the U4U6-U5 snRNP complex contains the PRO8NT PROCN PRO C-terminal and Mov34MPNPAD-1 domains found in pre-mRNA splicing factors of the PRO8 family | DDB0232429 | CDS | 4703192 | 6984 | - | 0.33362 |
prsA | DDB_G0284669 | ortholog of PRS involved in nucleotide histidine and tryptophan biosynthesis | DDB0232431 | CDS | 2322296 | 954 | + | 0.318658 |
prsB | DDB_G0272246 | highly similar to PRS involved in nucleotide histidine and tryptophan biosynthesis | DDB0232429 | CDS | 1758981 | 990 | - | 0.29596 |
prsC | DDB_G0283627 | highly similar to PRS involved in nucleotide histidine and tryptophan biosynthesis | DDB0232431 | CDS | 883884 | 966 | - | 0.284679 |
prtA | DDB_G0271696 | DDB0232429 | CDS | 741000 | 1536 | - | 0.288411 | |
prtB | DDB_G0271666 | DDB0232429 | CDS | 738043 | 1542 | - | 0.29572 | |
psaA | DDB_G0270994 | highly similar to mammalian puromycin-sensitive aminopeptidase belonging to the peptidase M1 family (metallopeptidases) contains a peptidase M1 domain including a zinc-binding site | DDB0232428 | CDS | 3842009 | 2586 | + | 0.319412 |
psaB | DDB_G0270670 | highly similar to mammalian puromycin-sensitive aminopeptidase belonging to the peptidase M1 family (metallopeptidases) contains a peptidase M1 domain including a zinc-binding site | DDB0232428 | CDS | 3731263 | 2571 | + | 0.325165 |
psaB_ps | DDB_G0269852 | putative pseudogene fragment similar to the puromycin-sensitive aminopeptidase-like protein | DDB0232428 | CDS | 3728354 | 648 | - | 0.319444 |
pscA | DDB_G0271902 | ortholog of prokaryotic penicillin-binding protein 4 (PBP4) inhibited by penicillin G | DDB0232429 | CDS | 1056759 | 1569 | - | 0.280433 |
psenA | DDB_G0291352 | putative catalytic subunit of the gamma-secretase complex similar to presenilin 2 a gene that has been associated with early-onset familial Alzheimer's disease | DDB0232433 | CDS | 166985 | 1869 | + | 0.240235 |
psenB | DDB_G0292310 | putative catalytic component of the gamma-secretase complex similar to presenilin 2 a gene that has been associated with early-onset familial Alzheimer's disease | DDB0232433 | CDS | 1442668 | 1422 | - | 0.287623 |
psenen | DDB_G0293484 | component of the gamma-secretase complex which executes the intramembrane proteolysis of type I integral membrane proteins such as Notch | DDB0232433 | CDS | 2946443 | 210 | - | 0.266667 |
psiA | DDB_G0291982 | DDB0232433 | CDS | 1023224 | 1674 | - | 0.310633 | |
psiB | DDB_G0268000 | contains a signal peptide a PA14 (anthrax protection antigen) domain and 5 Dictyostelium (CTDC) repeats | DDB0232428 | CDS | 1276791 | 1659 | + | 0.29777 |
psiC | DDB_G0290245 | similar to dicA1 contains a signal peptide a PA14 (anthrax protection antigen) domain 3 Dictyostelium (CTDC) repeats expressed in prespore cells | DDB0232432 | CDS | 3769697 | 1551 | + | 0.322373 |
psiD | DDB_G0290925 | similar to dicA1 contains a signal peptide expressed in prespore cells | DDB0232432 | CDS | 4761330 | 1515 | - | 0.342574 |
psiE | DDB_G0268556 | DDB0232428 | CDS | 1271527 | 1503 | + | 0.284764 | |
psiF | DDB_G0278581 | forms a discoidin-inducing complex (DIC) with dicB pdsA and an unknown protein contains a signal peptide a PA14 (anthrax protection antigen) domain 8 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | DDB0232430 | CDS | 109696 | 2127 | + | 0.345557 |
psiG-1 | DDB_G0273389 | contains a PA14 (anthrax protection antigen) domain and 6 Dictyostelium (CTDC) repeats there is a second copy of this gene | DDB0232429 | CDS | 2866812 | 2121 | - | 0.310231 |
psiG-2 | DDB_G0273605 | contains a signal peptide a PA14 (anthrax protection antigen) domain 6 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain there is a second copy of this gene | DDB0232429 | CDS | 3162717 | 2121 | + | 0.310231 |
psiH | DDB_G0289393 | contains a signal peptide a PA14 (anthrax protection antigen) domain 4 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | DDB0232432 | CDS | 2790892 | 2148 | + | 0.341248 |
psiI | DDB_G0288919 | contains a signal peptide a PA14 (anthrax protection antigen) domain 6 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | DDB0232432 | CDS | 2120577 | 2160 | - | 0.316667 |
psiJ | DDB_G0290317 | DDB0232432 | CDS | 3947753 | 2160 | - | 0.319444 | |
psiK | DDB_G0292014 | DDB0232433 | CDS | 1018381 | 2187 | - | 0.328304 | |
psiL | DDB_G0274441 | contains a signal peptide a PA14 (anthrax protection antigen) domain 4 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | DDB0232429 | CDS | 4588497 | 2193 | + | 0.331053 |
psiM | DDB_G0284759 | contains a signal peptide a PA14 domain and 4 Dictyostelium (slime mold) repeats enriched in gametes | DDB0232431 | CDS | 2442205 | 2202 | + | 0.336512 |
psiN | DDB_G0292912 | contains a PA14 (anthrax protection antigen) domain and 7 Dictyostelium (CTDC) repeats expressed in pstAO cells and in upper cup during culmination | DDB0232433 | CDS | 2264405 | 2241 | + | 0.33378 |
psiO | DDB_G0280167 | contains a signal peptide a PA14 (anthrax protection antigen) domain 7 Dictyostelium (CTDC) repeats and a carboxyl terminal transmembrane domain | DDB0232430 | CDS | 3041998 | 2253 | + | 0.324456 |
psiP | DDB_G0280171 | contains a signal peptide a PA14 (anthrax protection antigen) domain 4 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | DDB0232430 | CDS | 3046316 | 2271 | + | 0.3417 |
psiQ | DDB_G0293288 | similar to dicA1 an extracellular signaling molecule and ecmB an extracellular matrix protein contains a signal peptide a PA14 (anthrax protection antigen) domain and 14 Dictyostelium (CTDC) repeats significantly longer than other family members | DDB0232433 | CDS | 2665567 | 2958 | - | 0.320825 |
psiR | DDB_G0293286 | similar to dicA1 an extracellular signaling molecule and ecmB an extracellular matrix protein expressed in prespore cells | DDB0232433 | CDS | 2670579 | 2991 | - | 0.337011 |
psiS | DDB_G0267998 | contains a signal peptide similar to PsiA and related proteins but missing the carboxyl terminus compared to similar proteins | DDB0232428 | CDS | 1274009 | 804 | + | 0.274876 |
pslA | DDB_G0267410 | nuclear protein possible transcription factor contains a possible ankyrin repeat region | DDB0232428 | CDS | 1603473 | 3819 | - | 0.229118 |
psmA1 | DDB_G0282363 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) suppressor of tagB-stb10 | DDB0232430 | CDS | 5739737 | 747 | - | 0.309237 |
psmA2 | DDB_G0292122 | subunit of an endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232433 | CDS | 1227398 | 699 | + | 0.317597 |
psmA3 | DDB_G0267408 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232428 | CDS | 277655 | 747 | - | 0.323963 |
psmA4 | DDB_G0280969 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232430 | CDS | 4147505 | 753 | - | 0.335989 |
psmA5 | DDB_G0268538 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232428 | CDS | 1022895 | 726 | + | 0.331956 |
psmA6 | DDB_G0278847 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232430 | CDS | 1274786 | 753 | + | 0.330677 |
psmA7 | DDB_G0272831 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232429 | CDS | 2102038 | 753 | - | 0.321381 |
psmB1 | DDB_G0272969 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232429 | CDS | 1952612 | 711 | - | 0.322082 |
psmB2 | DDB_G0269472 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232428 | CDS | 2839118 | 597 | + | 0.304858 |
psmB3 | DDB_G0269772 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232428 | CDS | 3525818 | 618 | + | 0.317152 |
psmB4-1 | DDB_G0273163 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) there is a second copy of this gene | DDB0232429 | CDS | 2482779 | 780 | + | 0.303846 |
psmB4-2 | DDB_G0273909 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) there is a second copy of this gene | DDB0232429 | CDS | 3547766 | 780 | - | 0.303846 |
psmB5 | DDB_G0293784 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232433 | CDS | 3275662 | 819 | - | 0.328449 |
psmB6 | DDB_G0267390 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) shift of Dictyostelium cells from the proliferative to differentiated state highly expressed during the early stage of differentiation | DDB0232428 | CDS | 487456 | 645 | - | 0.339535 |
psmB7 | DDB_G0283679 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232431 | CDS | 967091 | 801 | - | 0.340824 |
psmC1 | DDB_G0270784 | ATPase subunit and regulatory subcomplex of the 26S proteasome TAT binding protein homolog involved in growth and morphogenesis | DDB0232428 | CDS | 4684536 | 1320 | - | 0.37197 |
psmC2 | DDB_G0276917 | DDB0232429 | CDS | 7234040 | 1287 | - | 0.367521 | |
psmC3 | DDB_G0284415 | DDB0232431 | CDS | 1968066 | 1266 | + | 0.347551 | |
psmC4 | DDB_G0289003 | ATPase subunit and regulatory subcomplex of the 26S proteasome developmentally regulated TAT binding protein homolog | DDB0232432 | CDS | 2227887 | 1212 | + | 0.326733 |
psmC5 | DDB_G0292382 | ATPase subunit and regulatory subcomplex of the 26S proteasome developmentally regulated TAT binding protein homolog | DDB0232433 | CDS | 1673522 | 1212 | - | 0.334158 |
psmC6 | DDB_G0284517 | DDB0232431 | CDS | 2090141 | 1182 | + | 0.335871 | |
psmD1 | DDB_G0287953 | DDB0232432 | CDS | 881632 | 2928 | - | 0.35929 | |
psmD10 | DDB_G0289189 | DDB0232432 | CDS | 2453090 | 699 | - | 0.304721 | |
psmD11 | DDB_G0281315 | DDB0232430 | CDS | 4153223 | 1242 | + | 0.274557 | |
psmD12 | DDB_G0281051 | DDB0232430 | CDS | 3979792 | 1344 | + | 0.284226 | |
psmD13 | DDB_G0285105 | DDB0232431 | CDS | 2852779 | 1158 | + | 0.273748 | |
psmD14 | DDB_G0272566 | DDB0232429 | CDS | 1896679 | 921 | + | 0.313789 | |
psmD2 | DDB_G0293752 | DDB0232433 | CDS | 3279468 | 2682 | + | 0.346383 | |
psmD3 | DDB_G0288621 | DDB0232432 | CDS | 1750413 | 1515 | + | 0.287129 | |
psmD4 | DDB_G0275775 | contains one von Willebrand factor type A (VWFA) domain and two ubiquitin interacting motifs | DDB0232429 | CDS | 5689186 | 1050 | + | 0.32381 |
psmD6 | DDB_G0270188 | DDB0232428 | CDS | 4382128 | 1149 | + | 0.278503 | |
psmD7 | DDB_G0279633 | DDB0232430 | CDS | 2343459 | 978 | - | 0.304703 | |
psmD8-1 | DDB_G0272564 | there is a second copy of this gene | DDB0232429 | CDS | 2397564 | 792 | + | 0.243687 |
psmD8-2 | DDB_G0273979 | there is a second copy of this gene | DDB0232429 | CDS | 3633103 | 792 | - | 0.243687 |
psmD9 | DDB_G0275753 | DDB0232429 | CDS | 5851635 | 789 | - | 0.281369 | |
psmE3 | DDB_G0285099 | PA28 activator subunit of the 20S proteasome animals contain 3 different subunits: alpha beta and gamma the alpha and beta subunits are only present in animals possessing an adaptive immune system Dictyostelium has the gamma ortholog only PsmE3 is localized to the nucleus similar to the gamma class of REG proteasome activator in metazoans | DDB0232431 | CDS | 2880074 | 678 | + | 0.261062 |
psmE4 | DDB_G0292398 | activator subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232433 | CDS | 1544203 | 5718 | - | 0.26128 |
psmF1 | DDB_G0282617 | inhibitor subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232430 | CDS | 6005174 | 981 | - | 0.333333 |
psmG1 | DDB_G0279769 | conserved chaperone protein which promotes assembly of the 20S proteasome may form a dimer with psmG2 and act in concert with psmG3psmG4 | DDB0232430 | CDS | 2535702 | 819 | - | 0.242979 |
psmG2 | DDB_G0274447 | conserved chaperone protein which promotes assembly of the 20S proteasome may form a dimer with psmG1 and act in concert with psmG3psmG4 | DDB0232429 | CDS | 4577027 | 810 | - | 0.246914 |
psmG3 | DDB_G0268522 | conserved chaperone protein which promotes assembly of the 20S proteasome may form a dimer with psmG4 and act in concert with psmG1psmG2 | DDB0232428 | CDS | 816236 | 438 | + | 0.232877 |
psmG4 | DDB_G0304543 | conserved chaperone protein which promotes assembly of the 20S proteasome may form a dimer with psmG3 and act in concert with psmG1psmG2 | DDB0232432 | CDS | 1134744 | 402 | - | 0.246269 |
pspA | DDB_G0267412 | expressed in prespore cells structurally similar to ponticulins | DDB0232428 | CDS | 1093913 | 507 | - | 0.366864 |
pspB | DDB_G0276939 | prespore gene expressed in prespore cells | DDB0232429 | CDS | 7418011 | 1599 | - | 0.387117 |
pspC | DDB_G0269172 | DDB0232428 | CDS | 3354771 | 4053 | - | 0.246484 | |
pspD | DDB_G0277379 | DDB0232429 | CDS | 7932696 | 2034 | - | 0.369715 | |
pspD_ps | DDB_G0288063 | putative pseudogene simlar to prespore-specific protein pspD | DDB0232432 | CDS | 1037957 | 1068 | - | 0.345506 |
pspE | DDB_G0286905 | DDB0232431 | CDS | 5076581 | 468 | - | 0.348291 | |
pspG | DDB_G0286499 | DDB0232431 | CDS | 4569135 | 741 | - | 0.330634 | |
psrA | DDB_G0280469 | DDB0232430 | CDS | 3399574 | 1887 | - | 0.311076 | |
pssA | DDB_G0278159 | catalyzes a base-exchange reaction in which the polar head group of phosphatidylethanolamine is replaced by L-serine mammals have two similar phosphatidylserine synthases PTDSS1 and PTDSS2 while Dictyostelium contains one which is an ortholog of PTDSS2 contains 9 putative transmembrane domains | DDB0232430 | CDS | 378150 | 1464 | - | 0.27459 |
psvA | DDB_G0276869 | DDB0232429 | CDS | 7537012 | 1545 | + | 0.405825 | |
ptcA | DDB_G0293882 | DDB0232433 | CDS | 3419922 | 1518 | + | 0.216733 | |
ptcB | DDB_G0288027 | antisense inhibition of ptcB expression leads to slower growth localizes to the mitochondria | DDB0232432 | CDS | 992896 | 1587 | - | 0.236925 |
ptcC | DDB_G0287775 | DDB0232432 | CDS | 679687 | 1836 | - | 0.267429 | |
ptcD | DDB_G0287997 | DDB0232432 | CDS | 944155 | 4218 | + | 0.221669 | |
ptcE | DDB_G0268718 | DDB0232428 | CDS | 1991527 | 2241 | - | 0.285141 | |
ptcF | DDB_G0278273 | DDB0232430 | CDS | 601284 | 1596 | - | 0.22619 | |
ptcG | DDB_G0277013 | DDB0232429 | CDS | 7205190 | 1272 | + | 0.246069 | |
ptcH | DDB_G0278855 | DDB0232430 | CDS | 1285622 | 3174 | - | 0.18305 | |
ptcI | DDB_G0275823 | DDB0232429 | CDS | 5546562 | 3492 | - | 0.269759 | |
ptcJ-1 | DDB_G0273037 | there is a second copy of this gene | DDB0232429 | CDS | 2346179 | 3777 | + | 0.230342 |
ptcJ-2 | DDB_G0274029 | there is a second copy of this gene | DDB0232429 | CDS | 3681740 | 3777 | - | 0.230342 |
ptcK | DDB_G0277611 | DDB0232429 | CDS | 8306699 | 3447 | + | 0.235567 | |
ptcL | DDB_G0291794 | DDB0232433 | CDS | 753746 | 3351 | + | 0.223217 | |
pten | DDB_G0286557 | DDB0232431 | CDS | 4733890 | 1602 | - | 0.315855 | |
pter | DDB_G0293394 | DDB0232433 | CDS | 2831683 | 1113 | - | 0.277628 | |
ptpA1-1 | DDB_G0273097 | there is a second copy of this gene | DDB0232429 | CDS | 2586710 | 1569 | - | 0.289994 |
ptpA1-2 | DDB_G0273817 | there is a second copy of this gene | DDB0232429 | CDS | 3443306 | 1569 | + | 0.289994 |
ptpB | DDB_G0277865 | DDB0232430 | CDS | 381607 | 1134 | + | 0.277778 | |
ptpC | DDB_G0282145 | DDB0232430 | CDS | 5439955 | 2973 | + | 0.28927 | |
ptsA | DDB_G0279095 | catalyzes the reaction 6-(L-erythro-12-dihydroxypropyl 3-triphosphate)-78-dihydropterin 6-(12-dioxopropyl)-5678-tetrahydropterin triphosphate | DDB0232430 | CDS | 1624152 | 408 | + | 0.254902 |
purA | DDB_G0285429 | catalyzes the reaction L-aspartate IMP GTP adenylo-succinate phosphate GDP in de novo DNA synthesis | DDB0232431 | CDS | 3358729 | 1284 | + | 0.348131 |
purB | DDB_G0288333 | catalyzes two reactions in de novo DNA synthesis: 5'-phosphoribosyl-4-(N-succinocarboxamide)-5-aminoimidazole fumarate AICAR and adenylo-succinate fumarate AMP | DDB0232432 | CDS | 1402047 | 1401 | + | 0.33262 |
purC%2FE | DDB_G0283987 | bifunctional enzyme composed of SAICAR synthase and AIR carboxylase that catalyze steps in de novo DNA synthesis | DDB0232431 | CDS | 1280148 | 2994 | + | 0.325985 |
purD | DDB_G0290121 | bifunctional enzyme of the de novo DNA synthesis pathway contains aminoimidazole ribotide synthetase and glycinamide ribotide synthetase activities | DDB0232432 | CDS | 3683216 | 2448 | + | 0.318219 |
purF | DDB_G0274321 | catalyzes the reaction L-glutamine PRPP Hsub2subO 5-phospho-beta-D-ribosyl-amine pyrophosphate L-glutamate the first step in de novo DNA synthesis | DDB0232429 | CDS | 3954678 | 1566 | + | 0.393997 |
purH | DDB_G0277087 | bifunctional enzyme that catalyzes the reactions Nsup10sup-formyl-Hsub4subF AICAR tetrahydrofolate phosphoribosyl-formamido-carboxamide and phosphoribosyl-formamido-carboxamide IMP Hsub2subO expressed in prespore cells | DDB0232429 | CDS | 7485197 | 1629 | - | 0.349908 |
purL | DDB_G0288145 | catayzes the reaction ATP 5'-phosphoribosyl-N-formylglycineamide L-glutamine Hsub2subO ADP phosphate 5-phosphoribosyl-n-formylglycineamidine L-glutamate in de novo DNA synthesis | DDB0232432 | CDS | 1141268 | 4068 | + | 0.342429 |
purN | DDB_G0288985 | catalyzes the reaction N10-formyl-Hsub4subF 5-phospho-ribosyl-glycineamide tetrahydrofolate 5'-phosphoribosyl-N-formylglycineamide in de novo DNA synthesis | DDB0232432 | CDS | 2206145 | 621 | + | 0.275362 |
pus1 | DDB_G0290987 | ortholog of S. cerevisiae PUS1a tRNA:pseudouridine synthase that introduces pseudouridines at positions 26-28 34-36 65 and 67 of tRNA nuclear protein that appears to be involved in tRNA export also acts on U2 snRNA | DDB0232432 | CDS | 4857087 | 1791 | - | 0.289224 |
pus3 | DDB_G0288909 | similar to S. cerevisiae pus3 which introduces pseudouridines at position 38 or 39 in tRNA | DDB0232432 | CDS | 2110038 | 1476 | + | 0.25271 |
pus7 | DDB_G0271632 | ortholog of S. cerevisiae PUS7 which catalyzes pseudouridylation at position 35 in U2 snRNA position 50 in 5S rRNA position 13 in cytoplasmic tRNAs and position 35 in pre-tRNA(Tyr) conserved in archaea vertebrates and some bacteria | DDB0232429 | CDS | 580601 | 2190 | + | 0.296347 |
pwp1 | DDB_G0275073 | DDB0232429 | CDS | 5128411 | 1710 | + | 0.334503 | |
pwp2 | DDB_G0284621 | DDB0232431 | CDS | 2240813 | 2769 | - | 0.298664 | |
pyd1 | DDB_G0267966 | ortholog of S. cerevisiae URA1 and human DPYD defects in DPYD cause dihydropyrimidine dehydrogenase deficiency catalyzes the reaction 56-dihydrouracil NADP uracil NADPH H | DDB0232428 | CDS | 1202711 | 3030 | + | 0.367327 |
pyd2 | DDB_G0269246 | ortholog of the human DPYS defects in DPYS cause cause of DHP (dihydropyrimidinase) deficiency second enzyme in the reductive pyrimidine degradation pathway (EC 3.5.2.2) catalyzes the reaction: 56-dihydrouracil Hsub2subO 3-ureidopropanoate | DDB0232428 | CDS | 3157203 | 1512 | - | 0.355159 |
pyd3 | DDB_G0274123 | DDB0232429 | CDS | 4571492 | 1176 | + | 0.333333 | |
pyk | DDB_G0283247 | catalyzes the reaction ATP pyruvate ADP phosphoenolpyruvate | DDB0232431 | CDS | 344914 | 1524 | - | 0.358268 |
pyk3 | DDB_G0289001 | member of the TKL (tyrosine kinase-like) group and the DPYK (Dictyostelium protein tyrosine kinase) family of protein kinases contains two kinase domains one of which is predicted to be inactive the C-terminal kinase domain has tyrosine kinase activitybr bCommunity annotation:b Pyk3 appears to be involved in differentiation pathway choice as the KO shows reduced pstO differentiation and compensatory expansion of the prespore region. Pyk3 has been proposed to act in a pathway involving ptpC and statC effectively potentiating the action of DIF-1. One of the factors that influences pathway choice is cell cycle position classic experiments show that cold-synchronized cells which enter development shortly after warming prefer the stalk pathway. This is due to an increased DIF sensitivity. New results (Strasser Tsang and MacWilliams in preparation) now show that the pyk3 transcript is upregulated roughly fivefold after cold synchronization at a time when cells show strong stalk preference (p | DDB0232432 | CDS | 2269413 | 4017 | - | 0.283047 |
pykA | DDB_G0268628 | phosphorylates pyridoxal to pyridoxal 5'-phosphate member of the TKL (tyrosine kinase-like) group of protein kinases belongs to the MLK protein kinase family | DDB0232428 | CDS | 2219371 | 909 | + | 0.254125 |
pyr1-3 | DDB_G0276335 | multifunctional enzyme that carries out the three first enzymatic activities of the de novo pyrimidine biosynthetic pathway very similar to the tri-functional human CAD enzyme | DDB0232429 | CDS | 6728694 | 6678 | + | 0.351003 |
pyr4 | DDB_G0276331 | catalyzes the reaction Osub2sub dihydroorotate Hsub2subOsub2sub orotate in de novo biosynthesis of pyrimidine ribonucleotides | DDB0232429 | CDS | 6726246 | 1113 | - | 0.34142 |
pyr56 | DDB_G0280041 | bifunctional enzyme that catalyzes the reactions PRPP orotate orotidine-5'-phosphate pyrophosphate and orotidine-5'-phosphate COsub2sub UMP in de novo biosynthesis of pyrimidine ribonucleotides | DDB0232430 | CDS | 3010631 | 1437 | + | 0.338205 |
pyrK | DDB_G0287495 | phosphorylates dCMP and dUMP to dCDP and dUDP respectively | DDB0232432 | CDS | 334067 | 588 | + | 0.289116 |
pyroxd1 | DDB_G0289727 | DDB0232432 | CDS | 3170582 | 1641 | + | 0.233394 | |
qdpr | DDB_G0272684 | ortholog of QDPR which catalyzes the NADH-mediated reduction of quinonoid dihydrobiopterin (a 5678-tetrahydropteridine NAD(P) a 67-dihydropteridine NAD(P)H H) the last step of tetrahydrobiopterin (BH4) recycling in higher eukaryotes an essential cofactor | DDB0232429 | CDS | 1985270 | 696 | - | 0.329023 |
qkgA-1 | DDB_G0273259 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains there is a second copy of this gene | DDB0232429 | CDS | 2831844 | 4662 | + | 0.27885 |
qkgA-2 | DDB_G0273635 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains there is a second copy of this gene | DDB0232429 | CDS | 3195191 | 4662 | - | 0.27885 |
qpct | DDB_G0293986 | catalyzes the reaction L-glutaminyl-peptide 5-oxoprolyl-peptide NHsub3sub during the biosynthesis of pyroglutamyl peptides | DDB0232433 | CDS | 3571398 | 1083 | + | 0.228994 |
qpct_ps | DDB_G0293952 | putative pseudogene similar to glutaminyl-peptide cyclotransferase qpct | DDB0232433 | CDS | 3568849 | 603 | + | 0.223881 |
qprt | DDB_G0272462 | catalyzes the reaction nicotinate D-ribonucleotide diphosphate COsub2sub pyridine-23-dicarboxylate 5-phospho-alpha-D-ribose 1-diphosphate | DDB0232429 | CDS | 1703083 | 903 | - | 0.317829 |
qtrt1 | DDB_G0291802 | catalyzes the reaction [tRNA]-guanine queuine [tRNA]-queuine guanine | DDB0232433 | CDS | 770747 | 1344 | - | 0.385417 |
r21 | DDB_G0294415 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 956823 | 55 | - | 0.4 |
r22 | DDB_G0295571 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 960281 | 58 | - | 0.344828 |
r23A | DDB_G0295585 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1668807 | 57 | - | 0.368421 |
r23B | DDB_G0295579 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1666945 | 57 | - | 0.368421 |
r23C | DDB_G0295575 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1662690 | 57 | - | 0.368421 |
r24A | DDB_G0295577 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1663884 | 58 | + | 0.413793 |
r24B | DDB_G0295587 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1675652 | 58 | - | 0.413793 |
r25 | DDB_G0295539 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232430 | CDS | 1101057 | 57 | - | 0.403509 |
r26 | DDB_G0295583 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1668202 | 58 | + | 0.396552 |
r28 | DDB_G0295487 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232428 | CDS | 1449845 | 65 | + | 0.338462 |
r29 | DDB_G0295535 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232429 | CDS | 8304316 | 54 | - | 0.388889 |
r30 | DDB_G0295503 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232428 | CDS | 4375331 | 58 | - | 0.37931 |
r31 | DDB_G0295607 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232432 | CDS | 1473461 | 61 | + | 0.344262 |
r32 | DDB_G0295599 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 2793917 | 55 | + | 0.327273 |
r33 | DDB_G0295553 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232430 | CDS | 4352682 | 60 | - | 0.366667 |
r34 | DDB_G0295601 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 3575039 | 50 | + | 0.4 |
r35 | DDB_G0295495 | small non-coding RNA (59-60 nt) containing 5' and 3' ends predicted to form a stem structure localizes to the cytoplasm | DDB0232428 | CDS | 3001192 | 59 | + | 0.38983 |
r36 | DDB_G0295547 | small non-coding RNA (59-60 nt) containing 5' and 3' ends predicted to form a stem structure localizes to the cytoplasm | DDB0232430 | CDS | 2300516 | 62 | - | 0.403226 |
r41 | DDB_G0295513 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232429 | CDS | 5946993 | 58 | + | 0.362069 |
r42 | DDB_G0295507 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232429 | CDS | 4084607 | 46 | - | 0.369565 |
r43 | DDB_G0295509 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232429 | CDS | 4084929 | 44 | - | 0.340909 |
r44 | DDB_G0295515 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232429 | CDS | 5966046 | 44 | - | 0.454545 |
r45 | DDB_G0295533 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232429 | CDS | 8303967 | 43 | - | 0.465116 |
r46 | DDB_G0295537 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232430 | CDS | 1100393 | 53 | - | 0.358491 |
r47 | DDB_G0295541 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232430 | CDS | 1101587 | 61 | - | 0.393443 |
r48 | DDB_G0295563 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 77659 | 43 | - | 0.395349 |
r49 | DDB_G0295565 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 958244 | 58 | - | 0.37931 |
r50 | DDB_G0295567 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 959090 | 57 | - | 0.333333 |
r51 | DDB_G0295569 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 959587 | 58 | - | 0.413793 |
r52 | DDB_G0295573 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 961592 | 58 | + | 0.431034 |
r53 | DDB_G0295581 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 1667874 | 32 | + | 0.40625 |
r54 | DDB_G0295589 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 1675966 | 56 | + | 0.339286 |
r55 | DDB_G0295591 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 2757052 | 94 | + | 0.255319 |
r56 | DDB_G0295595 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 2792181 | 58 | - | 0.344828 |
r57 | DDB_G0295597 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 2793529 | 49 | + | 0.367347 |
r58 | DDB_G0295609 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232432 | CDS | 1517413 | 54 | - | 0.314815 |
r59 | DDB_G0295633 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232433 | CDS | 2295180 | 62 | + | 0.290323 |
r60 | DDB_G0295635 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232433 | CDS | 2298172 | 59 | + | 0.288136 |
r61 | DDB_G0295637 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232433 | CDS | 2298272 | 66 | + | 0.318182 |
r62 | DDB_G0295639 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232433 | CDS | 3354232 | 43 | + | 0.395349 |
rab11A | DDB_G0269238 | DDB0232428 | CDS | 4269122 | 645 | - | 0.344186 | |
rab11B | DDB_G0287211 | DDB0232432 | CDS | 41773 | 663 | + | 0.235294 | |
rab11C | DDB_G0277101 | DDB0232429 | CDS | 7509311 | 675 | - | 0.317037 | |
rab14 | DDB_G0281337 | DDB0232430 | CDS | 4383385 | 621 | - | 0.339775 | |
rab18 | DDB_G0289827 | DDB0232432 | CDS | 3292859 | 609 | - | 0.287356 | |
rab1A | DDB_G0283757 | DDB0232431 | CDS | 1241175 | 609 | - | 0.326765 | |
rab1B | DDB_G0277867 | DDB0232430 | CDS | 743092 | 621 | - | 0.330113 | |
rab1C | DDB_G0269174 | DDB0232428 | CDS | 2911005 | 606 | - | 0.310231 | |
rab1D | DDB_G0284985 | DDB0232431 | CDS | 2756032 | 615 | - | 0.304065 | |
rab1E | DDB_G0275969 | DDB0232429 | CDS | 6179943 | 651 | + | 0.274962 | |
rab21 | DDB_G0286553 | DDB0232431 | CDS | 4804109 | 639 | + | 0.309859 | |
rab24 | DDB_G0268402 | DDB0232428 | CDS | 1157427 | 609 | - | 0.325123 | |
rab2A | DDB_G0292268 | DDB0232433 | CDS | 1422661 | 624 | + | 0.310897 | |
rab2B | DDB_G0272138 | DDB0232429 | CDS | 1483407 | 609 | + | 0.297209 | |
rab32A | DDB_G0283603 | DDB0232431 | CDS | 965063 | 660 | - | 0.309091 | |
rab32B | DDB_G0269416 | DDB0232428 | CDS | 2727197 | 783 | + | 0.265645 | |
rab32C | DDB_G0275675 | DDB0232429 | CDS | 5696031 | 675 | + | 0.302222 | |
rab32D | DDB_G0285051 | DDB0232431 | CDS | 2597422 | 687 | + | 0.263464 | |
rab4 | DDB_G0292406 | DDB0232433 | CDS | 1558648 | 618 | + | 0.302589 | |
rab5A | DDB_G0271984 | DDB0232429 | CDS | 1113320 | 606 | + | 0.328383 | |
rab5B | DDB_G0282847 | similar to rab5 but has a long amino extension and is missing two conserved cysteine residues at the carboxyl terminus | DDB0232430 | CDS | 6292039 | 645 | + | 0.311628 |
rab6 | DDB_G0268068 | DDB0232428 | CDS | 1398472 | 627 | + | 0.287081 | |
rab7A | DDB_G0269236 | rab family small GTPase involved in vesicle fusion during endocytosis there is another rab7 homolog rab7B | DDB0232428 | CDS | 2627248 | 612 | + | 0.348039 |
rab7B | DDB_G0287553 | there is another rab7 homolog rab7A | DDB0232432 | CDS | 408133 | 594 | - | 0.294613 |
rab8A | DDB_G0280043 | regulates contractile vacuole discharging in response to osmotic stress regulated by | DDB0232430 | CDS | 3266503 | 627 | + | 0.317384 |
rab8B | DDB_G0276399 | DDB0232429 | CDS | 6878753 | 612 | - | 0.328431 | |
rabA | DDB_G0291233 | DDB0232433 | CDS | 312209 | 606 | - | 0.268977 | |
rabC | DDB_G0271736 | DDB0232429 | CDS | 718547 | 591 | + | 0.291032 | |
rabF1-1 | DDB_G0272905 | there is a second copy of this gene | DDB0232429 | CDS | 2459564 | 573 | - | 0.277487 |
rabF1-2 | DDB_G0273935 | there is a second copy of this gene | DDB0232429 | CDS | 3571468 | 585 | + | 0.273504 |
rabF2_ps | DDB_G0276053 | putative pseudogene Rab family protein | DDB0232429 | CDS | 6482785 | 291 | - | 0.33677 |
rabG1 | DDB_G0291738 | DDB0232433 | CDS | 677353 | 591 | + | 0.323181 | |
rabG2 | DDB_G0290783 | DDB0232432 | CDS | 4595466 | 483 | + | 0.335404 | |
rabH | DDB_G0275955 | DDB0232429 | CDS | 6208676 | 597 | - | 0.211055 | |
rabJ | DDB_G0277441 | DDB0232429 | CDS | 8110957 | 771 | + | 0.273671 | |
rabK1 | DDB_G0290833 | DDB0232432 | CDS | 4609179 | 642 | - | 0.239875 | |
rabK2 | DDB_G0290791 | DDB0232432 | CDS | 4611869 | 444 | - | 0.236486 | |
rabK3 | DDB_G0290831 | DDB0232432 | CDS | 4607175 | 447 | - | 0.272931 | |
rabL | DDB_G0290779 | DDB0232432 | CDS | 4606115 | 615 | - | 0.297561 | |
rabM | DDB_G0290829 | DDB0232432 | CDS | 4605000 | 609 | - | 0.284072 | |
rabN1 | DDB_G0290789 | DDB0232432 | CDS | 4608094 | 651 | - | 0.254992 | |
rabN2 | DDB_G0290793 | DDB0232432 | CDS | 4612672 | 555 | - | 0.27027 | |
rabO | DDB_G0290407 | DDB0232432 | CDS | 4047054 | 657 | + | 0.232877 | |
rabP | DDB_G0290875 | DDB0232432 | CDS | 4703255 | 699 | + | 0.250358 | |
rabQ | DDB_G0268760 | DDB0232428 | CDS | 2054001 | 615 | + | 0.282927 | |
rabR | DDB_G0271980 | DDB0232429 | CDS | 1097988 | 924 | - | 0.27381 | |
rabS | DDB_G0282537 | DDB0232430 | CDS | 5897353 | 666 | - | 0.234234 | |
rabT1 | DDB_G0268910 | DDB0232428 | CDS | 2365532 | 669 | + | 0.22571 | |
rabT2 | DDB_G0269262 | DDB0232428 | CDS | 2416810 | 657 | + | 0.235921 | |
rabU | DDB_G0291293 | DDB0232433 | CDS | 69908 | 585 | + | 0.268376 | |
rabV | DDB_G0282899 | DDB0232430 | CDS | 6281058 | 702 | + | 0.176638 | |
rabW | DDB_G0276295 | DDB0232429 | CDS | 6558113 | 657 | + | 0.226788 | |
rabX | DDB_G0275327 | DDB0232429 | CDS | 5352310 | 1335 | + | 0.147566 | |
rabY | DDB_G0282203 | DDB0232430 | CDS | 5519409 | 711 | - | 0.255977 | |
rabZ | DDB_G0286169 | DDB0232431 | CDS | 4062977 | 690 | - | 0.298551 | |
rab_ps1 | DDB_G0294579 | putative pseudogene similar to Rab GTPase family proteins | DDB0232429 | CDS | 6212260 | 874 | - | 0.188787 |
rab_ps2 | DDB_G0275101 | putative pseudogene Rab family protein | DDB0232429 | CDS | 5064677 | 321 | - | 0.286604 |
rabggta | DDB_G0269570 | catalyzes the transfer of a geranyl-geranyl moiety from geranyl-geranyl pyrophosphate to both cysteines in Rab proteins with an -XXCC -XCXC and -CCXX C-terminal forms a hetero-dimer with the | DDB0232428 | CDS | 3019090 | 936 | + | 0.244658 |
rabggtb | DDB_G0290671 | catalyzes the transfer of a geranyl-geranyl moiety from geranyl-geranyl pyrophosphate to both cysteines in Rab proteins with an -XXCC -XCXC and -CCXX C-terminal forms a hetero-dimer with the | DDB0232432 | CDS | 4317912 | 1020 | + | 0.281373 |
rabif | DDB_G0295697 | DDB0232430 | CDS | 79952 | 492 | + | 0.288618 | |
rac1A | DDB_G0277869 | DDB0232430 | CDS | 441220 | 585 | - | 0.358974 | |
rac1B | DDB_G0268622 | DDB0232428 | CDS | 2364212 | 585 | - | 0.317949 | |
rac1C | DDB_G0282365 | DDB0232430 | CDS | 6045140 | 582 | - | 0.324742 | |
racA | DDB_G0286555 | RhoBTB subfamily protein which have a unique domain architecture composed of a N-terminal GTPase domain two bric a brac domains (BTB and a conserved C-terminal domain there are orthoolgs in several eukaryotes including mammals but are absent from fungi and plants in Dictyostelium appears to be involved in the regulation of the actin cytoskeleton | DDB0232431 | CDS | 4692759 | 1797 | - | 0.327212 |
racB | DDB_G0279605 | DDB0232430 | CDS | 2370154 | 588 | - | 0.323129 | |
racC | DDB_G0293526 | DDB0232433 | CDS | 3000314 | 579 | + | 0.322971 | |
racD | DDB_G0291976 | DDB0232433 | CDS | 1210911 | 765 | + | 0.32549 | |
racE | DDB_G0280975 | interacts with gxcT rgaA and darA acts together with fttB (14-3-3) to regulate the cortical cytoskeleton and cleavage furrow progression during cytokinesis | DDB0232430 | CDS | 4354163 | 672 | - | 0.360119 |
racF1 | DDB_G0269176 | DDB0232428 | CDS | 3007465 | 582 | + | 0.271478 | |
racF2 | DDB_G0276967 | DDB0232429 | CDS | 7215630 | 582 | - | 0.274914 | |
racG | DDB_G0269178 | DDB0232428 | CDS | 3735334 | 606 | - | 0.250825 | |
racH | DDB_G0269240 | DDB0232428 | CDS | 3360340 | 603 | + | 0.325041 | |
racI | DDB_G0277897 | DDB0232430 | CDS | 93233 | 618 | - | 0.273463 | |
racJ | DDB_G0292560 | DDB0232433 | CDS | 1884330 | 618 | + | 0.263754 | |
racK_ps | DDB_G0268908 | putative pseudogene rac family gene | DDB0232428 | CDS | 2363310 | 435 | - | 0.252874 |
racL | DDB_G0292816 | DDB0232433 | CDS | 2181555 | 591 | + | 0.279188 | |
racM | DDB_G0289103 | DDB0232432 | CDS | 2368291 | 570 | - | 0.27193 | |
racN | DDB_G0278009 | DDB0232430 | CDS | 154173 | 660 | + | 0.259091 | |
racO | DDB_G0277791 | DDB0232429 | CDS | 8401462 | 831 | + | 0.202166 | |
racP | DDB_G0285453 | DDB0232431 | CDS | 3245052 | 1131 | + | 0.312113 | |
racQ | DDB_G0278011 | DDB0232430 | CDS | 155490 | 558 | + | 0.256272 | |
rad1 | DDB_G0269378 | similar to Rad1 a component of a heterotrimeric clamp (the 9-1-1 complex) that recognizes damaged DNA and initiates signal transduction for repair | DDB0232428 | CDS | 2644089 | 1350 | + | 0.303704 |
rad17 | DDB_G0292504 | similar to S. pombe and H. sapiens RAD17 and S. cerevisiae RAD24 component of Rad17-RFC complex which loads the 9-1-1 (Rad9-Rad1-Hus1) complex onto damaged DNA | DDB0232433 | CDS | 1748396 | 3576 | + | 0.245526 |
rad18 | DDB_G0278935 | RAD18 ortholog a E3 ubiquitin ligase required for postreplicational DNA repair forms a heterodimer with RAD6 | DDB0232430 | CDS | 1193824 | 2007 | + | 0.223717 |
rad21 | DDB_G0276977 | ortholog of RAD21SCC1 component of the cohesin complex involved in chromosome cohesion during cell cycle in DNA repair and in apoptosis brbr bCommunity annotation:b The role of rad21 in Dictyostelium cell cycle control is supported by its 13-fold overexpression in a Dicty strain lacking the Dicty retinoblastoma-like protein | DDB0232429 | CDS | 7505297 | 2424 | - | 0.320545 |
rad50 | DDB_G0292786 | similar to S. cerevisiae RAD50 involved in processing double-strand DNA breaks with Mre11 in other organisms Rad50 is part of a complex with Mre11 and Nbs1 no Nbs1 ortholog has been found in Dictyostelium | DDB0232433 | CDS | 2029933 | 4056 | + | 0.272189 |
rad51-1 | DDB_G0273139 | ortholog of Rad51 which is involved in activation of homologous recombination and double-strand break repair and interacts with XRCC3 there is a second copy of this gene | DDB0232429 | CDS | 2861364 | 1056 | - | 0.344697 |
rad51-2 | DDB_G0273611 | ortholog of Rad51 which is involved in activation of homologous recombination and double-strand break repair and interacts with XRCC3 there is a second copy of this gene | DDB0232429 | CDS | 3169189 | 1056 | + | 0.344697 |
rad52 | DDB_G0269406 | DDB0232428 | CDS | 2715190 | 906 | - | 0.364238 | |
rad54 | DDB_G0282997 | similar to RAD54 DNA repair protein chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232431 | CDS | 118731 | 2796 | + | 0.33226 |
rad54_ps | DDB_G0267628 | putative pseudogene fragment similar to | DDB0232428 | CDS | 441679 | 123 | - | 0.325203 |
rad54b | DDB_G0285117 | similar to RAD54b DNA repair protein chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232431 | CDS | 2873116 | 2970 | - | 0.278788 |
rad6 | DDB_G0275787 | RAD6 homolog an E2 ubiquitin-conjugating enzyme involved in postreplication repair forms a heterodimer with RAD18 | DDB0232429 | CDS | 5646909 | 456 | + | 0.350877 |
rad9 | DDB_G0274525 | similar to S. pombe Rad9 a component of a heterotrimeric clamp (the 9-1-1 complex) that recognizes damaged DNA and initiates signal transduction for repair | DDB0232429 | CDS | 4278392 | 1443 | + | 0.293832 |
rae1 | DDB_G0283835 | DDB0232431 | CDS | 1191439 | 1029 | + | 0.308066 | |
ragA | DDB_G0288701 | ortholog of S. cerevisiae GTR1 and H. sapiens RagA and RagB a cytoplasmic GTP binding protein | DDB0232432 | CDS | 1844809 | 906 | + | 0.296909 |
ragC | DDB_G0284495 | ortholog of S. cerevisiae GTR2 and H. sapiens RagC a cytoplasmic GTP binding protein | DDB0232431 | CDS | 2047442 | 1083 | - | 0.277008 |
ranA | DDB_G0291235 | DDB0232433 | CDS | 78789 | 639 | + | 0.363067 | |
ranB | DDB_G0274943 | DDB0232429 | CDS | 4583590 | 2265 | - | 0.316998 | |
ranbp1 | DDB_G0287391 | DDB0232432 | CDS | 246455 | 585 | + | 0.353846 | |
rapA | DDB_G0291237 | DDB0232433 | CDS | 98914 | 561 | + | 0.354724 | |
rapB | DDB_G0272857 | DDB0232429 | CDS | 2094380 | 618 | - | 0.305825 | |
rapC | DDB_G0270340 | DDB0232428 | CDS | 4670322 | 837 | + | 0.296296 | |
rapgap1 | DDB_G0271734 | stimulates the RapA (Rap1) GTPase activity during chemotaxis which results in the downregulation of actin polymerization at the leading edge | DDB0232429 | CDS | 882440 | 3168 | + | 0.29798 |
rapgap3 | DDB_G0271806 | DDB0232429 | CDS | 787444 | 3504 | + | 0.30508 | |
rapgap9 | DDB_G0284065 | similar to H. sapiens Rap1GAP involved in morphogenesis development and cell adhesion | DDB0232431 | CDS | 1493285 | 1101 | - | 0.348774 |
rapgapB | DDB_G0282247 | DDB0232430 | CDS | 5570015 | 1257 | - | 0.280827 | |
raptor | DDB_G0270398 | putative Raptor protein ortholog a component of the TORC1 complex in yeasts with Lst8 and Tor does not co-immunoprecipitate with the TORC2 complex | DDB0232428 | CDS | 4758927 | 4530 | - | 0.330905 |
rasB | DDB_G0292998 | nuclear Ras that may have a role in cell division andor nuclear division expressed throughout growth and development | DDB0232433 | CDS | 2415988 | 594 | - | 0.3367 |
rasC | DDB_G0281385 | Ras protein required for aggregation activated by rasGEF GefA enriched in prestalk cellsbr bCommunity annotation:b Gene expression is greatly perturbed in vegetative rasC-rasG- double null mutants and in early development a subset of important signalling genes are not induced adequately. Notable among these early genes are acaA dagA erkA erkB gpaB and csbA. The discoidin I genes are also underexpresed. The expression of most of these genes (not the discoidins) is rescued when carA is overexpressed in the double null line. Most remarkably the overall profile of gene expression changes in vegetative double null mutants compared to the parent strain is highly similar to that of wild-type cells six hours after infection with Legionella pneumophila compared to uninfected cells (in terms of gene expression changes correlation coefficient 0.61) (Li et al 2009) making this strain phenocopy the Legionella-resistant dupA mutant to some extent (correlation coefficient 0.49). Of 55 genes overe | DDB0232430 | CDS | 4519070 | 570 | + | 0.333333 |
rasD | DDB_G0292996 | DDB0232433 | CDS | 2530991 | 564 | - | 0.294326 | |
rasG | DDB_G0293434 | maximally expressed during growth activated by rasGEF GefRbr bCommunity annotation:b Gene expression is greatly perturbed in vegetative rasC-rasG- double null mutants and in early development a subset of important signalling genes are not induced adequately. Notable among these early genes are acaA dagA erkA erkB gpaB and csbA. The discoidin I genes are also underexpresed. The expression of most of these genes (not the discoidins) is rescued when carA is overexpressed in the double null line. Most remarkably the overall profile of gene expression changes in vegetative double null mutants compared to the parent strain is highly similar to that of wild-type cells six hours after infection with Legionella pneumophila compared to uninfected cells (correlation coefficient 0.61) (Li et al 2009) making this strain partially phenocopy the Legionella-resistant dupA mutant (in terms of gene expression changes correlation coefficient 0.49). Of 55 genes overexpressed at least 4-fold in the veget | DDB0232433 | CDS | 2877682 | 570 | - | 0.368421 |
rasS | DDB_G0283537 | DDB0232431 | CDS | 849934 | 585 | - | 0.305983 | |
rasU | DDB_G0270138 | DDB0232428 | CDS | 4299011 | 642 | + | 0.253894 | |
rasV | DDB_G0270736 | DDB0232428 | CDS | 4279831 | 690 | - | 0.234783 | |
rasW | DDB_G0270122 | DDB0232428 | CDS | 4277085 | 651 | - | 0.282642 | |
rasX | DDB_G0270124 | DDB0232428 | CDS | 4281896 | 642 | - | 0.267913 | |
rasY | DDB_G0270126 | DDB0232428 | CDS | 4283626 | 651 | - | 0.282642 | |
rasZ | DDB_G0270140 | DDB0232428 | CDS | 4300316 | 645 | + | 0.272868 | |
rbbB | DDB_G0268778 | DDB0232428 | CDS | 2082803 | 3597 | + | 0.272727 | |
rbbD | DDB_G0282529 | similar to H. sapiens Retinoblastoma binding proteins RBBP4 and RBBP7 and S. cerevisiae HAT2 a subunit of the HAT1HAT2 histone acetyltransferase complex | DDB0232430 | CDS | 5888997 | 1272 | - | 0.331761 |
rbbE | DDB_G0285847 | DDB0232431 | CDS | 3858078 | 1578 | + | 0.292142 | |
rbg3 | DDB_G0281891 | DDB0232430 | CDS | 5076786 | 3051 | - | 0.270403 | |
rblA | DDB_G0290551 | putative ortholog of Retinoblastoma protein (Rb) which inhibits progression from G1 to S phase of the cell cycle through interactions with the E2F family of transcription factors expressed in prespore zone seems to work with Btg in cell fate commitment during development | DDB0232432 | CDS | 4252151 | 3939 | - | 0.236101 |
rbm8A | DDB_G0286007 | conserved protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance the human ortholog has been shown to interact with | DDB0232431 | CDS | 3939784 | 564 | - | 0.281915 |
rbrA | DDB_G0286961 | required for cell type proportioning contains two IBR (In Between Ring fingers) domains | DDB0232431 | CDS | 5132945 | 1563 | - | 0.31286 |
rbsk | DDB_G0280893 | catalyzes the reaction D-ribose ATP D-ribose-5-phosphate ADP | DDB0232430 | CDS | 3840063 | 957 | + | 0.239289 |
rbx1 | DDB_G0287629 | DDB0232432 | CDS | 496993 | 315 | + | 0.342857 | |
rcaA | DDB_G0272120 | DDB0232429 | CDS | 1622396 | 2535 | - | 0.341617 | |
rcbA | DDB_G0286357 | DDB0232431 | CDS | 4412389 | 1029 | + | 0.371234 | |
rccA | DDB_G0271758 | DDB0232429 | CDS | 766288 | 1986 | - | 0.193353 | |
rcdBB | DDB_G0274551 | DDB0232429 | CDS | 4193351 | 609 | - | 0.415435 | |
rcdII | DDB_G0284041 | DDB0232431 | CDS | 1500251 | 1395 | - | 0.26595 | |
rcdJJ | DDB_G0287213 | DDB0232432 | CDS | 34540 | 861 | - | 0.213705 | |
rcdP | DDB_G0269180 | DDB0232428 | CDS | 3226604 | 2457 | - | 0.301994 | |
rchy | DDB_G0281595 | DDB0232430 | CDS | 4685430 | 1029 | + | 0.278912 | |
rckA | DDB_G0278737 | member of the TKL (tyrosine kinase-like) group contains an RGS (Regulator of G protein Signaling) domain | DDB0232430 | CDS | 1218919 | 3378 | + | 0.261693 |
rcl1 | DDB_G0282803 | DDB0232430 | CDS | 6124057 | 1116 | - | 0.305556 | |
rcnA | DDB_G0271536 | DDB0232429 | CDS | 555496 | 1218 | + | 0.286535 | |
rdeA | DDB_G0282923 | DDB0232431 | CDS | 67134 | 765 | + | 0.299346 | |
rdiA | DDB_G0291077 | DDB0232432 | CDS | 4973539 | 594 | + | 0.380471 | |
rdiB | DDB_G0280049 | DDB0232430 | CDS | 3280488 | 459 | + | 0.298475 | |
recA | DDB_G0276073 | similar to recombinase A proteins found in bacteria and in A. thaliana plays a role in DNA repair | DDB0232429 | CDS | 6430683 | 1359 | - | 0.288447 |
redA | DDB_G0293904 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein involved in the metabolism of compounds that control Dictyostelium cell differentiation | DDB0232433 | CDS | 3580985 | 1896 | - | 0.339135 |
redB | DDB_G0269912 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein similar to the H. sapiens POR protein that is defect in adrenal hyperplasia variant type (AHV) a syndrome with disordered steroidogenesis | DDB0232428 | CDS | 3848909 | 2004 | - | 0.335329 |
redC | DDB_G0287983 | similar to the H. sapiens NDOR1 an oxidoreductase that catalyzes the NADP-dependent reduction of cytochrome c and one-electron acceptors | DDB0232432 | CDS | 927535 | 1902 | + | 0.244479 |
regA | DDB_G0284331 | contains a 3'5'-cyclic nucleotide phosphodiesterase and an RR domain found in two-component signal transduction systems | DDB0232431 | CDS | 1956975 | 2382 | - | 0.290932 |
repB | DDB_G0278729 | ortholog of H. sapiens xeroderma pigmentosum group B (XPB) M. musculus ERCC3 and S. cerevisiae RAD25 upregulated in the presence of DNA damaging agents | DDB0232430 | CDS | 1389108 | 2403 | + | 0.33042 |
repD | DDB_G0267414 | ortholog of H. sapiens xeroderma pigmentosum group D (XPD) M. musculus ERCC2 and S. cerevisiae RAD3 | DDB0232428 | CDS | 833130 | 2331 | - | 0.33891 |
repE | DDB_G0286013 | ortholog of H. sapiens | DDB0232431 | CDS | 3955941 | 3546 | - | 0.278624 |
repG | DDB_G0284987 | similar to H. sapiens xeroderma pigmentosum group G (XPG) M. musculus ERCC5 and S. pombe RAD2 cleaves 5' overhang flap structure generated when DNA polymerase encounters the 5'end of a downstream Okazaki fragment | DDB0232431 | CDS | 2762877 | 1155 | - | 0.309091 |
rer1 | DDB_G0292588 | conserved protein involved in the retrieval of some endoplasmic reticulum membrane proteins from the early golgi compartment contains 3 predicted transmembrane domains | DDB0232433 | CDS | 1815723 | 567 | - | 0.292769 |
rev3 | DDB_G0271608 | ortholog of DNA polymerase zeta catalytic subunit involed in DNA repair | DDB0232429 | CDS | 480277 | 8106 | + | 0.253886 |
rexo1 | DDB_G0291590 | similar to S. cerevisiae REX1 or RNH70 a 3'-5' RNA exonuclease | DDB0232433 | CDS | 580025 | 2085 | + | 0.251799 |
rexo2-1 | DDB_G0273355 | similar to H. sapiens REXO2 and S. cerevisiae REX2 a mitochondrial 3'-5' RNA exonuclease there is a second copy of this gene | DDB0232429 | CDS | 2683400 | 573 | + | 0.30541 |
rexo2-2 | DDB_G0273741 | similar to H. sapiens REXO2 and S. cerevisiae REX2 a mitochondrial 3'-5' RNA exonuclease there is a second copy of this gene | DDB0232429 | CDS | 3347298 | 573 | - | 0.30541 |
rexo4 | DDB_G0281327 | DDB0232430 | CDS | 4193116 | 897 | + | 0.235229 | |
rfa1 | DDB_G0289513 | DDB0232432 | CDS | 2891660 | 2040 | + | 0.320098 | |
rfc1 | DDB_G0285961 | ortholog of H. sapiens RFC 140 kDa subunit | DDB0232431 | CDS | 3845828 | 4206 | + | 0.3136 |
rfc2 | DDB_G0291868 | ortholog of H. sapiens RFC2 (40 kDa subunit) and S. cerevisiae RFC2 | DDB0232433 | CDS | 850606 | 1017 | + | 0.328417 |
rfc3 | DDB_G0293702 | ortholog of H. sapiens RFC3 (38 kDa subunit) and S. cerevisiae RFC5 | DDB0232433 | CDS | 3014705 | 1044 | - | 0.331418 |
rfc4 | DDB_G0286027 | ortholog of H. sapiens RFC4 (37 kDa subunit) and S. cerevisiae RFC2 | DDB0232431 | CDS | 3966261 | 1044 | + | 0.314176 |
rfc5 | DDB_G0282235 | ortholog of H. sapiens RFC5 (36 kDa subunit) and S. cerevisiae RFC3 | DDB0232430 | CDS | 5553806 | 1044 | + | 0.267241 |
rfk | DDB_G0305357 | DDB0232429 | CDS | 5767351 | 489 | - | 0.286299 | |
rft1 | DDB_G0288491 | ortholog of yeast RFT1 an essential integral membrane protein that is required for translocation of Man5GlcNac2-PP-Dol from the cytoplasmic side to the lumenal side of the ER membrane but is not the flippase | DDB0232432 | CDS | 1600467 | 1623 | - | 0.190388 |
rgaA | DDB_G0287585 | DDB0232432 | CDS | 498740 | 2469 | + | 0.357635 | |
rgfA | DDB_G0272038 | DDB0232429 | CDS | 1119945 | 2148 | + | 0.223464 | |
rgn | DDB_G0277535 | similar to regucalcin a calcium binding protein that controls many cellular functions | DDB0232429 | CDS | 7984797 | 897 | + | 0.334448 |
rheb | DDB_G0277041 | DDB0232429 | CDS | 7321470 | 558 | + | 0.28853 | |
rhgA | DDB_G0283389 | similar to human Rh50 protein a glycoprotein present on the surface of red blood cells contains 10 transmembrane domains | DDB0232431 | CDS | 634252 | 1584 | - | 0.33649 |
rhgB | DDB_G0280059 | DDB0232430 | CDS | 3188254 | 1803 | + | 0.345535 | |
ric8 | DDB_G0292036 | similar to human RIC8A (synembryn-A) non-receptor guanine nucleotide exchange factor for G | DDB0232433 | CDS | 1059972 | 1314 | - | 0.307458 |
rif1 | DDB_G0287899 | ortholog of RIF1 associated with the telomeres and in human required for checkpoint mediated arrest of cell cycle progression in response to DNA damage during S-phase brbr bCommunity annotation:b In budding yeast RIF1 is a telomere-associated protein which has been shown to suppress the recruitment of the ATM DNA-damage signalling complex to the telomere ends and play a role in telomere length regulation (see | DDB0232432 | CDS | 816399 | 3942 | + | 0.236428 |
rimA | DDB_G0277891 | ortholog of S. cerevisiae RIM2 and mammalian SLC25a36 a mitochondrion carrier protein that imports pyrimidine nucleoside triphosphates and exports pyrimidine nucleoside monophosphates | DDB0232430 | CDS | 96863 | 1098 | - | 0.317851 |
rio1 | DDB_G0280431 | atypical RIO family protein kinase yeast serinethreonine kinase RIO1 plays a role in cell cycle progression | DDB0232430 | CDS | 3344181 | 1725 | - | 0.302609 |
rio2 | DDB_G0282099 | atypical RIO family protein kinase contains winged helix DNA-binding domain in addition to RIO domain yeast serinethreonine kinase RIO1 plays a role in cell cycle progression | DDB0232430 | CDS | 5366397 | 1569 | + | 0.291906 |
ripA | DDB_G0284611 | component of the TORC2 (Tor complex 2) with Tor Lst8 and PiaA that plays a role in regulation of adenylate cyclase (ACA) and protein kinase B (PKB) activation during aggregation | DDB0232431 | CDS | 2346926 | 5055 | + | 0.321464 |
rliA | DDB_G0272783 | twelve transmembrane domain protein that may act as a transporter repressed after Legionella pneumophila infection | DDB0232429 | CDS | 2172067 | 1416 | + | 0.267655 |
rliB | DDB_G0278243 | repressed after Legionella pneumophila infection contains a signal peptide similar to | DDB0232430 | CDS | 541492 | 3354 | - | 0.328265 |
rliC | DDB_G0276149 | repressed after Legionella pneumophila infection | DDB0232429 | CDS | 6400232 | 987 | + | 0.214792 |
rliD | DDB_G0280603 | repressed after Legionella pneumophila infection | DDB0232430 | CDS | 3559151 | 2913 | - | 0.25884 |
rliF | DDB_G0288289 | very similar to bacterial beta-xylosidases and also but less similar to mammalian alpha-L-iduronidase repressed after Legionella pneumophila infection | DDB0232432 | CDS | 1354074 | 1473 | + | 0.32315 |
rlp24 | DDB_G0272789 | ortholog of the mammalian C15orf15 gene and the S. cerevisiae RLP24 protein which is involved in the biogenesis of the 60S ribosomal subunit and at the end of biogenesis is likely to be exchanged for its ribosomal homologue rpl24 | DDB0232429 | CDS | 2178487 | 495 | - | 0.290909 |
rmd5 | DDB_G0274829 | ortholog of the conserved RMD5 which in yeast has has an E3-like ubiquitin ligase activity | DDB0232429 | CDS | 4057449 | 1335 | - | 0.262921 |
rmp | DDB_G0289477 | DDB0232432 | CDS | 2835235 | 1470 | + | 0.258503 | |
rnaseh2A | DDB_G0292584 | catalytic subunit of RNase HII an endonuclease that specifically degrades the RNA of RNA:DNA hybrids defects in H. sapiens RNASEH2A cause Aicardi-Goutieres syndrome type 4 a genetically heterogeneous autosomal recessive encephalopathy | DDB0232433 | CDS | 1802425 | 870 | - | 0.287356 |
rnf10 | DDB_G0269996 | DDB0232428 | CDS | 3992422 | 2478 | + | 0.233253 | |
rnf113 | DDB_G0267870 | DDB0232428 | CDS | 995736 | 1068 | + | 0.251873 | |
rnf160 | DDB_G0274875 | DDB0232429 | CDS | 4311743 | 5595 | - | 0.235746 | |
rngB | DDB_G0268860 | DDB0232428 | CDS | 2266964 | 2832 | + | 0.278249 | |
rnpA | DDB_G0282293 | DDB0232430 | CDS | 5604394 | 1656 | - | 0.226449 | |
rnrA | DDB_G0284071 | catalyzes the reaction 2'-deoxyribonucleoside diphosphate thioredoxin disulfide Hsub2subO ribonucleoside diphosphate reduced thioredoxin | DDB0232431 | CDS | 1503516 | 2613 | + | 0.381554 |
rnrB-1 | DDB_G0272616 | catalyzes the reaction 2'-deoxyribonucleoside diphosphate thioredoxin disulfide Hsub2subO ribonucleoside diphosphate reduced thioredoxin there is a second copy of this gene | DDB0232429 | CDS | 2355911 | 1017 | + | 0.301868 |
rnrB-2 | DDB_G0274021 | catalyzes the reaction 2'-deoxyribonucleoside diphosphate thioredoxin disulfide Hsub2subO ribonucleoside diphosphate reduced thioredoxin there is a second copy of this gene | DDB0232429 | CDS | 3674573 | 1017 | - | 0.301868 |
rnu1a | DDB_G0294411 | DDB0232430 | CDS | 2763788 | 161 | + | 0.378882 | |
rnu1b | DDB_G0295549 | DDB0232430 | CDS | 2739612 | 161 | - | 0.378882 | |
rnu1c | DDB_G0295611 | DDB0232432 | CDS | 1846430 | 163 | + | 0.361963 | |
rnu1d | DDB_G0295613 | DDB0232432 | CDS | 1870152 | 163 | - | 0.368098 | |
rnu1e_ps | DDB_G0295519 | putative pseudogene similar to U1 snRNA a component of the spliceosome involved in pre-mRNA splicing | DDB0232429 | CDS | 6485825 | 162 | + | 0.333333 |
rnu2a | DDB_G0295491 | DDB0232428 | CDS | 1479198 | 206 | + | 0.42233 | |
rnu2b | DDB_G0295497 | DDB0232428 | CDS | 3189743 | 206 | - | 0.42233 | |
rnu2c | DDB_G0295489 | DDB0232428 | CDS | 1478649 | 206 | - | 0.417476 | |
rnu2d | DDB_G0295623 | DDB0232432 | CDS | 2747783 | 244 | - | 0.311475 | |
rnu2e | DDB_G0295521 | DDB0232429 | CDS | 7277171 | 261 | + | 0.295019 | |
rnu2f | DDB_G0295523 | DDB0232429 | CDS | 7281154 | 262 | + | 0.29771 | |
rnu2g | DDB_G0295501 | DDB0232428 | CDS | 4038698 | 262 | - | 0.30916 | |
rnu4a | DDB_G0295559 | DDB0232430 | CDS | 4929751 | 123 | - | 0.430894 | |
rnu4b | DDB_G0295557 | DDB0232430 | CDS | 4929179 | 122 | + | 0.434426 | |
rnu4c | DDB_G0295529 | DDB0232429 | CDS | 7584569 | 122 | - | 0.459016 | |
rnu5a | DDB_G0295625 | DDB0232432 | CDS | 3164865 | 118 | - | 0.372881 | |
rnu5b | DDB_G0295627 | DDB0232432 | CDS | 3165224 | 118 | + | 0.364407 | |
rnu6 | DDB_G0295505 | DDB0232429 | CDS | 23987 | 110 | + | 0.454545 | |
roco10 | DDB_G0291710 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains RhoGAP LRR Roc COR RGS (regulator of G-protein signaling) Kelch repeats and protein kinase domains | DDB0232433 | CDS | 648952 | 7941 | - | 0.290769 |
roco11 | DDB_G0268636 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains | DDB0232428 | CDS | 2199646 | 4464 | + | 0.267473 |
roco4 | DDB_G0288251 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains | DDB0232432 | CDS | 1284583 | 5181 | + | 0.332947 |
roco5 | DDB_G0294533 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains RhoGEF PH LRR Roc COR and protein kinase domains | DDB0232432 | CDS | 1439427 | 8403 | - | 0.309413 |
roco6 | DDB_G0279417 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR WD40 PH and protein kinase domains | DDB0232430 | CDS | 2094570 | 6444 | + | 0.293451 |
roco7 | DDB_G0267472 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains Roc COR WD40 and protein kinase domains related to LRR-containing kinases but does not contain an LRR domain | DDB0232428 | CDS | 628403 | 7848 | - | 0.293833 |
roco8 | DDB_G0286127 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains DEP LRR Roc COR and protein kinase domains | DDB0232431 | CDS | 4112361 | 5604 | - | 0.267131 |
roco9 | DDB_G0288183 | member of the TKL (tyrosine kinase-like) group and ROCO family of protein kinases contains RhoGAP LRR Roc Cor and protein kinase domains | DDB0232432 | CDS | 1219231 | 10098 | - | 0.264706 |
romo1 | DDB_G0286181 | conserved mitochondrial protein ROMO1 in H. sapiens and MGR2 (Mitochondrial Genome Required) in S. cerevisiae involved in reactive oxygen species production contains 2 predicted transmembrane domains | DDB0232431 | CDS | 4077065 | 387 | + | 0.27907 |
rpa1 | DDB_G0275759 | component of the RNA polymerase I complex ortholog of S. cerevisiae RPA190 | DDB0232429 | CDS | 5808489 | 4848 | + | 0.323432 |
rpa12 | DDB_G0278263 | component of the RNA polymerase I complex ortholog of S. cerevisiae RPA12 | DDB0232430 | CDS | 579706 | 975 | - | 0.254359 |
rpa2 | DDB_G0293560 | component of the RNA polymerase I complex ortholog of S. cerevisiae RPA135 | DDB0232433 | CDS | 3044865 | 3393 | - | 0.328912 |
rpa43 | DDB_G0268198 | component of the RNA polymerase I complex ortholog of S. cerevisiae RPA43 | DDB0232428 | CDS | 1645550 | 1071 | + | 0.250233 |
rpa49 | DDB_G0290909 | component of the RNA polymerase I complex weakly similar to S. cerevisiae RPA49 and M. musculus RNA polymerase I associated factor 53 | DDB0232432 | CDS | 4737794 | 1128 | + | 0.265957 |
rpa5 | DDB_G0282339 | subunit common to RNA polymerases I and III ortholog of H. sapiens RPA5 S. cerevisiae RPC40 | DDB0232430 | CDS | 5656917 | 1038 | + | 0.293834 |
rpb1 | DDB_G0279193 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPO21 | DDB0232430 | CDS | 1783778 | 5184 | + | 0.368248 |
rpb10 | DDB_G0272036 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPB10 | DDB0232429 | CDS | 1094076 | 213 | + | 0.300469 |
rpb11 | DDB_G0277677 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB11 | DDB0232429 | CDS | 8346240 | 363 | - | 0.294766 |
rpb12 | DDB_G0283365 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPC10 | DDB0232431 | CDS | 585874 | 141 | + | 0.347518 |
rpb2 | DDB_G0288257 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB2 | DDB0232432 | CDS | 1296275 | 3513 | - | 0.366354 |
rpb3 | DDB_G0292244 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB3 | DDB0232433 | CDS | 1368967 | 909 | + | 0.29703 |
rpb4 | DDB_G0282739 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB4 | DDB0232430 | CDS | 6226742 | 468 | - | 0.25 |
rpb5 | DDB_G0291636 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPB5 | DDB0232433 | CDS | 457932 | 546 | - | 0.302198 |
rpb6 | DDB_G0291037 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPO26 | DDB0232432 | CDS | 4838044 | 402 | - | 0.348259 |
rpb7 | DDB_G0284891 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB7 | DDB0232431 | CDS | 2602996 | 519 | + | 0.306358 |
rpb8 | DDB_G0278039 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPB8 | DDB0232430 | CDS | 186227 | 429 | + | 0.27972 |
rpb9 | DDB_G0268306 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB9 | DDB0232428 | CDS | 558538 | 339 | - | 0.330383 |
rpc1 | DDB_G0277199 | component of the RNA polymerase III complex ortholog of S. cerevisiae RPO31 | DDB0232429 | CDS | 7733653 | 4353 | + | 0.336779 |
rpc11 | DDB_G0287707 | component of the RNA polymerase III complex ortholog of H. sapiens RPC10 and S. cerevisiae RPC11 | DDB0232432 | CDS | 584047 | 336 | + | 0.285714 |
rpc19 | DDB_G0291362 | subunit common to RNA polymerases I and III ortholog of S. cerevisiae RPC19 | DDB0232433 | CDS | 182518 | 351 | + | 0.290598 |
rpc2 | DDB_G0288449 | component of the RNA polymerase III complex ortholog of S. cerevisiae RPC2 | DDB0232432 | CDS | 1494028 | 4827 | + | 0.310131 |
rpc25-1 | DDB_G0273425 | component of the RNA polymerase III complex ortholog of S. cerevisiae RPC25 and H. sapiens RPC8 there is a second copy of this gene | DDB0232429 | CDS | 2980579 | 759 | - | 0.31357 |
rpc25-2 | DDB_G0273523 | component of the RNA polymerase III complex ortholog of S. cerevisiae RPC25 and H. sapiens RPC8 there is a second copy of this gene | DDB0232429 | CDS | 3050335 | 759 | + | 0.31357 |
rpc3 | DDB_G0268080 | component of the RNA polymerase III complex has similarity to H. sapiens RPC3RPC62 and S. cerevisiae RPC82 | DDB0232428 | CDS | 1420168 | 2001 | + | 0.310345 |
rpc34 | DDB_G0272022 | component of the RNA polymerase III complex has similarity to H. sapiens RPC6RPC39 and S. cerevisiae RPC34 | DDB0232429 | CDS | 1182004 | 882 | - | 0.302721 |
rpc4 | DDB_G0277671 | component of the RNA polymerase III complex weakly similar to H. sapiens RPC4 and S. cerevisiae RPC53 | DDB0232429 | CDS | 8301218 | 1293 | + | 0.313225 |
rpc5 | DDB_G0271514 | component of the RNA polymerase III complex has similarity to H. sapiens RPC5 and S. cerevisiae RPC37 | DDB0232429 | CDS | 469596 | 1974 | - | 0.291793 |
rpc9 | DDB_G0286521 | DDB0232431 | CDS | 4587626 | 393 | - | 0.239186 | |
rpe | DDB_G0278275 | catalyzes the reaction D-ribulose 5-phosphate D-xylulose 5-phosphate | DDB0232430 | CDS | 603034 | 678 | - | 0.325959 |
rpiA | DDB_G0276711 | catalyzes the reaction D-ribose 5-phosphate D-ribulose 5-phosphate | DDB0232429 | CDS | 7091221 | 699 | - | 0.311874 |
rpkA | DDB_G0283615 | DDB0232431 | CDS | 1020192 | 2487 | - | 0.291516 | |
rpl10 | DDB_G0288273 | DDB0232432 | CDS | 1312496 | 654 | - | 0.408257 | |
rpl10a | DDB_G0276871 | DDB0232429 | CDS | 7540396 | 654 | + | 0.382263 | |
rpl11 | DDB_G0279189 | DDB0232430 | CDS | 1766422 | 609 | - | 0.403941 | |
rpl12 | DDB_G0288295 | DDB0232432 | CDS | 1359447 | 501 | + | 0.411178 | |
rpl13 | DDB_G0291870 | DDB0232433 | CDS | 852689 | 630 | + | 0.420635 | |
rpl13a | DDB_G0275881 | DDB0232429 | CDS | 5876511 | 564 | + | 0.423759 | |
rpl14 | DDB_G0277975 | DDB0232430 | CDS | 87206 | 474 | + | 0.413502 | |
rpl15-1 | DDB_G0272893 | protein component of the large (60S) ribosomal subunit there is a second copy of this gene | DDB0232429 | CDS | 2395262 | 618 | - | 0.435275 |
rpl15-2 | DDB_G0273983 | protein component of the large (60S) ribosomal subunitthere is a second copy of this gene | DDB0232429 | CDS | 3635653 | 618 | + | 0.435275 |
rpl17 | DDB_G0285277 | DDB0232431 | CDS | 3049805 | 543 | + | 0.412523 | |
rpl18 | DDB_G0279997 | DDB0232430 | CDS | 2837555 | 546 | + | 0.380952 | |
rpl18a | DDB_G0285881 | DDB0232431 | CDS | 3775456 | 516 | + | 0.395349 | |
rpl19 | DDB_G0281565 | DDB0232430 | CDS | 4825161 | 561 | + | 0.4082 | |
rpl21 | DDB_G0279387 | DDB0232430 | CDS | 1751733 | 483 | - | 0.434783 | |
rpl22 | DDB_G0288101 | DDB0232432 | CDS | 1106395 | 351 | - | 0.367521 | |
rpl22a | DDB_G0290091 | DDB0232432 | CDS | 3652594 | 351 | - | 0.347578 | |
rpl23 | DDB_G0290315 | DDB0232432 | CDS | 3946402 | 411 | - | 0.420925 | |
rpl23a | DDB_G0293502 | DDB0232433 | CDS | 2967908 | 510 | + | 0.4 | |
rpl24 | DDB_G0280229 | DDB0232430 | CDS | 3141943 | 384 | + | 0.393229 | |
rpl26 | DDB_G0283741 | DDB0232431 | CDS | 1048980 | 420 | + | 0.390476 | |
rpl27 | DDB_G0271298 | DDB0232429 | CDS | 140424 | 435 | - | 0.425287 | |
rpl27a | DDB_G0292388 | DDB0232433 | CDS | 1592145 | 447 | - | 0.411633 | |
rpl28 | DDB_G0282379 | DDB0232430 | CDS | 6061184 | 399 | - | 0.413534 | |
rpl29 | DDB_G0281469 | DDB0232430 | CDS | 4548958 | 282 | - | 0.414894 | |
rpl3 | DDB_G0291862 | protein component of the large (60S) ribosomal subunit ribosomal protein L3 homolog | DDB0232433 | CDS | 954736 | 1197 | - | 0.404344 |
rpl30 | DDB_G0270380 | DDB0232428 | CDS | 4730345 | 339 | - | 0.362832 | |
rpl31 | DDB_G0279061 | DDB0232430 | CDS | 1578225 | 336 | - | 0.407738 | |
rpl32 | DDB_G0271976 | DDB0232429 | CDS | 1095789 | 402 | + | 0.405473 | |
rpl34 | DDB_G0286389 | DDB0232431 | CDS | 4400738 | 369 | - | 0.365854 | |
rpl35 | DDB_G0288349 | DDB0232432 | CDS | 1418812 | 381 | - | 0.39895 | |
rpl35a | DDB_G0270424 | DDB0232428 | CDS | 4849685 | 318 | + | 0.389937 | |
rpl36 | DDB_G0271668 | DDB0232429 | CDS | 733224 | 318 | - | 0.399371 | |
rpl36a | DDB_G0270984 | DDB0232428 | CDS | 3772004 | 312 | + | 0.394231 | |
rpl37 | DDB_G0285971 | DDB0232431 | CDS | 3886590 | 276 | + | 0.42029 | |
rpl37A | DDB_G0281093 | DDB0232430 | CDS | 4045953 | 276 | + | 0.431159 | |
rpl38 | DDB_G0268302 | DDB0232428 | CDS | 485945 | 228 | - | 0.364035 | |
rpl39 | DDB_G0302511 | DDB0232432 | CDS | 657459 | 156 | - | 0.333333 | |
rpl4 | DDB_G0277803 | protein component of the large (60S) ribosomal subunit ribosomal protein L4 homolog | DDB0232429 | CDS | 8431684 | 1110 | + | 0.443243 |
rpl5 | DDB_G0278539 | protein component of the large (60S) ribosomal subunit ribosomal protein L5 homolog | DDB0232430 | CDS | 1039561 | 879 | - | 0.416382 |
rpl6 | DDB_G0292460 | protein component of the large (60S) ribosomal subunit ribosomal protein L6 homolog | DDB0232433 | CDS | 1676096 | 711 | + | 0.410689 |
rpl7 | DDB_G0276441 | DDB0232429 | CDS | 6956284 | 741 | - | 0.395412 | |
rpl7a | DDB_G0277629 | protein component of the large (60S) ribosomal subunit ribosomal protein L7a homolog | DDB0232429 | CDS | 8280728 | 858 | - | 0.405594 |
rpl8 | DDB_G0274113 | protein component of the large (60S) ribosomal subunit ribosomal protein L8 homolog | DDB0232429 | CDS | 4593609 | 768 | - | 0.440104 |
rpl9 | DDB_G0278959 | protein component of the large (60S) ribosomal subunit ribosomal protein L9 homolog | DDB0232430 | CDS | 1387306 | 567 | - | 0.368607 |
rplP0 | DDB_G0286501 | DDB0232431 | CDS | 4590677 | 918 | - | 0.418301 | |
rplP1 | DDB_G0277907 | DDB0232430 | CDS | 1026839 | 342 | + | 0.453216 | |
rplP2 | DDB_G0283393 | DDB0232431 | CDS | 661727 | 321 | - | 0.485981 | |
rplp1B | DDB_G0287995 | DDB0232432 | CDS | 942400 | 303 | + | 0.475248 | |
rpmA | DDB_G0267416 | DDB0232428 | CDS | 950030 | 2853 | - | 0.343148 | |
rps10 | DDB_G0286117 | protein component of the small (40S) ribosomal subunit highly expressed in vegetative cells and in early development | DDB0232431 | CDS | 4072416 | 465 | - | 0.415054 |
rps11 | DDB_G0282601 | protein component of the small (40S) ribosomal subunit ribosomal protein S11 homolog | DDB0232430 | CDS | 5991308 | 468 | + | 0.40812 |
rps12 | DDB_G0284237 | protein component of the small (40S) ribosomal subunit ribosomal protein S12 homolog | DDB0232431 | CDS | 1729814 | 411 | - | 0.413625 |
rps13 | DDB_G0284533 | protein component of the small (40S) ribosomal subunit ribosomal protein S13 homolog | DDB0232431 | CDS | 2127182 | 456 | - | 0.388158 |
rps14 | DDB_G0291526 | protein component of the small (40S) ribosomal subunit ribosomal protein S14 homolog | DDB0232433 | CDS | 481211 | 459 | - | 0.444444 |
rps15 | DDB_G0285561 | protein component of the small (40S) ribosomal subunit ribosomal protein S15 homolog | DDB0232431 | CDS | 3385002 | 435 | + | 0.402299 |
rps15a | DDB_G0276457 | protein component of the small (40S) ribosomal subunit ribosomal protein S15a homolog | DDB0232429 | CDS | 6809160 | 393 | + | 0.391858 |
rps16 | DDB_G0284093 | protein component of the small (40S) ribosomal subunit ribosomal protein S16 homolog | DDB0232431 | CDS | 1558362 | 444 | + | 0.387387 |
rps17 | DDB_G0290141 | protein component of the small (40S) ribosomal subunit ribosomal protein S17 homolog | DDB0232432 | CDS | 3706333 | 408 | + | 0.377451 |
rps18 | DDB_G0276415 | protein component of the small (40S) ribosomal subunit ribosomal protein S18 homolog | DDB0232429 | CDS | 6891141 | 465 | + | 0.382796 |
rps19 | DDB_G0279207 | protein component of the small (40S) ribosomal subunit ribosomal protein S19 homolog | DDB0232430 | CDS | 1760514 | 447 | + | 0.434004 |
rps2 | DDB_G0293742 | protein component of the small (40S) ribosomal subunit expressed in vegetative cells and in prestalk cells during culmination | DDB0232433 | CDS | 3277669 | 798 | + | 0.45614 |
rps20 | DDB_G0278429 | protein component of the small (40S) ribosomal subunit ribosomal protein S20 homolog | DDB0232430 | CDS | 871775 | 375 | - | 0.405333 |
rps21 | DDB_G0293700 | protein component of the small (40S) ribosomal subunit ribosomal protein S21 homolog | DDB0232433 | CDS | 3013335 | 237 | - | 0.443038 |
rps23 | DDB_G0272250 | protein component of the small (40S) ribosomal subunit ribosomal protein S23 homolog | DDB0232429 | CDS | 1373618 | 432 | + | 0.416667 |
rps24 | DDB_G0275473 | protein component of the small (40S) ribosomal subunit ribosomal protein S24 homolog | DDB0232429 | CDS | 6089719 | 381 | - | 0.406824 |
rps25 | DDB_G0271148 | protein component of the small (40S) ribosomal subunit ribosomal protein S25 homolog | DDB0232429 | CDS | 133239 | 333 | - | 0.399399 |
rps26 | DDB_G0281677 | protein component of the small (40S) ribosomal subunit ribosomal protein S26 homolog | DDB0232430 | CDS | 4801949 | 339 | - | 0.430678 |
rps27 | DDB_G0277635 | protein component of the small (40S) ribosomal subunit ribosomal protein S27 homolog | DDB0232429 | CDS | 8305176 | 258 | + | 0.406977 |
rps28 | DDB_G0285597 | protein component of the small (40S) ribosomal subunit ribosomal protein S28 homolog | DDB0232431 | CDS | 3428530 | 219 | - | 0.429224 |
rps28_ps | DDB_G0275657 | putative pseudogene short fragment similar to D. discoideum gene | DDB0232429 | CDS | 5820628 | 165 | - | 0.30303 |
rps29 | DDB_G0272308 | protein component of the small (40S) ribosomal subunit ribosomal protein S29 homolog | DDB0232429 | CDS | 1258878 | 168 | + | 0.446429 |
rps3 | DDB_G0293000 | DDB0232433 | CDS | 2556040 | 657 | - | 0.418569 | |
rps30-1 | DDB_G0273191 | protein component of the small (40S) ribosomal subunit there is a second copy of this gene | DDB0232429 | CDS | 2681849 | 201 | - | 0.427861 |
rps30-2 | DDB_G0273743 | protein component of the small (40S) ribosomal subunit there is a second copy of this gene | DDB0232429 | CDS | 3349136 | 201 | + | 0.427861 |
rps3a | DDB_G0277345 | DDB0232429 | CDS | 7795600 | 822 | + | 0.417275 | |
rps4 | DDB_G0272825 | protein component of the small (40S) ribosomal subunit highly expressed in vegetative cells and in early development | DDB0232429 | CDS | 2019070 | 804 | - | 0.422886 |
rps5 | DDB_G0286075 | DDB0232431 | CDS | 4031568 | 573 | + | 0.418848 | |
rps6 | DDB_G0280823 | DDB0232430 | CDS | 1442353 | 711 | + | 0.419128 | |
rps7 | DDB_G0289025 | DDB0232432 | CDS | 2252902 | 582 | - | 0.364261 | |
rps8 | DDB_G0291864 | DDB0232433 | CDS | 844628 | 636 | + | 0.418239 | |
rps9 | DDB_G0289877 | DDB0232432 | CDS | 3486480 | 558 | + | 0.40681 | |
rpsA | DDB_G0270316 | 40S ribosomal protein SA (p40) homolog belongs to the ribosomal protein S2P family contains ribosomal protein S2 domain | DDB0232428 | CDS | 4628419 | 738 | - | 0.415989 |
rrpA | DDB_G0289659 | DDB0232432 | CDS | 3196021 | 7254 | + | 0.263441 | |
rrpB | DDB_G0291249 | one of the three D. discoideum RNA-directed RNA polymerases for which a distinct function has not yet been identified | DDB0232433 | CDS | 442657 | 7212 | - | 0.266916 |
rrpB_ps | DDB_G0272010 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232429 | CDS | 1127658 | 516 | - | 0.242248 |
rrpC | DDB_G0280963 | RNA-directed RNA polymerase involved in RNA interference and the production of siRNA also involved in the metabolism of other miRNAs | DDB0232430 | CDS | 3986737 | 6858 | + | 0.247302 |
rrs1 | DDB_G0274521 | ortholog of S. cerevisiae RRS1 an essential protein that binds ribosomal protein L11 and is required for nuclear export of the 60S pre-ribosomal subunit during ribosome biogenesis mouse homolog shows altered expression in Huntington's disease model mice | DDB0232429 | CDS | 4289980 | 954 | - | 0.303983 |
rsc11-1 | DDB_G0272791 | conserved protein of unknown function there is a second copy of this gene | DDB0232429 | CDS | 2268088 | 1731 | + | 0.306759 |
rsc11-2 | DDB_G0295699 | conserved protein of unknown function there is a second copy of this gene | DDB0232429 | CDS | 3761741 | 1731 | - | 0.306759 |
rsc12 | DDB_G0277871 | DDB0232430 | CDS | 845743 | 3189 | - | 0.40577 | |
rsc43 | DDB_G0285251 | DDB0232431 | CDS | 3035959 | 771 | - | 0.293126 | |
rsc5 | DDB_G0269182 | DDB0232428 | CDS | 3809035 | 1095 | + | 0.283105 | |
rsmA | DDB_G0283547 | DDB0232431 | CDS | 800136 | 660 | + | 0.260606 | |
rsmB | DDB_G0281253 | DDB0232430 | CDS | 4295825 | 783 | + | 0.219668 | |
rsmC | DDB_G0278449 | DDB0232430 | CDS | 896854 | 723 | + | 0.236515 | |
rsmD | DDB_G0292318 | DDB0232433 | CDS | 1471614 | 684 | + | 0.19152 | |
rsmE-1 | DDB_G0273099 | there is a second copy of this gene | DDB0232429 | CDS | 2580465 | 663 | + | 0.205128 |
rsmE-2 | DDB_G0273825 | there is a second copy of this gene | DDB0232429 | CDS | 3450554 | 663 | - | 0.205128 |
rsmF | DDB_G0278389 | DDB0232430 | CDS | 814663 | 627 | + | 0.239234 | |
rsmG | DDB_G0278717 | DDB0232430 | CDS | 501817 | 609 | - | 0.192118 | |
rsmH | DDB_G0278403 | DDB0232430 | CDS | 825274 | 819 | + | 0.229548 | |
rsmJ | DDB_G0279305 | DDB0232430 | CDS | 1907472 | 579 | + | 0.219344 | |
rsmK | DDB_G0278217 | DDB0232430 | CDS | 491519 | 588 | + | 0.19898 | |
rsmM | DDB_G0292300 | DDB0232433 | CDS | 1426160 | 645 | + | 0.308527 | |
rsmN | DDB_G0282651 | DDB0232430 | CDS | 6058470 | 651 | + | 0.248848 | |
rtaA | DDB_G0271852 | the rtaA expression pattern in a subset of anterior-like cells has led to the identification of a prestalk cell type: the pstU cells which preferentially populate the upper cup region at culmination contains 7 predicted transmembrane domains | DDB0232429 | CDS | 965144 | 870 | - | 0.297701 |
rtc1 | DDB_G0276159 | ortholog of RTC1 which catalyzes the conversion of 3'-phosphate to a 2'3'-cyclic phosphodiester at the end of RNA | DDB0232429 | CDS | 6274208 | 1302 | - | 0.320276 |
rtnlc | DDB_G0293088 | DDB0232433 | CDS | 2461261 | 951 | - | 0.335436 | |
rtoA | DDB_G0271916 | contains several repeats of a serine-rich motif which catalyzes the fusion of phospholipid vesicles | DDB0232429 | CDS | 1014827 | 1104 | + | 0.377717 |
rvb1 | DDB_G0293226 | similar to S. cerevisiae RVB1 a component of chromatin remodeling complexes | DDB0232433 | CDS | 2678243 | 1572 | - | 0.357506 |
rvb2 | DDB_G0280775 | similar to S. cerevisiae RVB2 a component of chromatin remodeling complexes | DDB0232430 | CDS | 3727138 | 1410 | - | 0.355319 |
rzpA | DDB_G0269184 | DDB0232428 | CDS | 4793277 | 816 | - | 0.316176 | |
sac1 | DDB_G0271630 | conserved protein from yeast to human in yeast involved in protein trafficking and secretion | DDB0232429 | CDS | 575486 | 1746 | + | 0.344788 |
sadA | DDB_G0288511 | DDB0232432 | CDS | 1638800 | 2859 | - | 0.349423 | |
sae1 | DDB_G0279641 | conserved protein forms a heterodimer with sae2 (uba2) acts as a E1 ligase for sumo | DDB0232430 | CDS | 2354365 | 993 | + | 0.254783 |
sahA | DDB_G0267418 | highly similar to mammalian SAHH (catalyzes the hydrolysis of S-adenosyl-L-homocysteine into adenosine and homocysteine) localizes to actin rods found in spores | DDB0232428 | CDS | 1662307 | 1296 | + | 0.415895 |
sahA_ps | DDB_G0278037 | putative pseudogene similar to S-adenosyl-L-homocysteine hydrolase sahA | DDB0232430 | CDS | 184302 | 1518 | + | 0.242424 |
samkA | DDB_G0269876 | DDB0232428 | CDS | 3775693 | 1923 | + | 0.228289 | |
samkB | DDB_G0284859 | putative protein kinase containing a SAM (sterile alpha motif) homology domain a putative protein interaction module | DDB0232431 | CDS | 2549067 | 1782 | + | 0.251403 |
samkB_ps1 | DDB_G0270988 | putative pseudogene SAMK (SAM domain-containing kinase) family | DDB0232428 | CDS | 3791042 | 1593 | - | 0.264909 |
samkB_ps2 | DDB_G0284851 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 2551418 | 183 | + | 0.295082 |
samkC | DDB_G0270678 | putative protein kinase containing a SAM (sterile alpha motif) homology domain a putative protein interaction module | DDB0232428 | CDS | 3778203 | 2628 | + | 0.251903 |
samkD | DDB_G0270680 | similar to SNF1-like kinases unlikely to function as a kinase as it lacks the catalytic aspartate | DDB0232428 | CDS | 3781297 | 1662 | + | 0.197954 |
samkE_ps1 | DDB_G0283165 | putative pseudogene SAMK (SAM domain-containing kinase) family | DDB0232431 | CDS | 352482 | 1272 | - | 0.26022 |
samkE_ps2 | DDB_G0283257 | putative pseudogene SAMK (SAM domain-containing kinase) family does not contain the consensus sequences required for kinase function | DDB0232431 | CDS | 404751 | 624 | + | 0.280449 |
samm50 | DDB_G0269550 | similar to the mammalian SAMM50 proteins homologs of yeast SAM50 a component of the mitochondrial outer membrane sorting assembly complex | DDB0232428 | CDS | 2975759 | 1191 | + | 0.261965 |
sarA | DDB_G0272296 | similar to budding yeast Sar1 a 21 kDa GTP- binding protein involved in vesicular transport between the endoplasmic reticulum and the Golgi | DDB0232429 | CDS | 1644732 | 567 | - | 0.33157 |
sarB | DDB_G0278477 | weakly similar to budding yeast Sar1 a 21 kDa GTP- binding protein involved in vesicular transport between the endoplasmic reticulum and the Golgi | DDB0232430 | CDS | 934441 | 585 | - | 0.268376 |
sas10 | DDB_G0269972 | DDB0232428 | CDS | 3952196 | 2064 | - | 0.285368 | |
sbds | DDB_G0272324 | orthlog of the human SBDS protein which is mutated in a majority of patients with Shwachman-Bodian-Diamond syndrome localizes to the pseudopodia in cAMP gradient | DDB0232429 | CDS | 1287157 | 825 | + | 0.299394 |
scdA | DDB_G0283375 | DDB0232431 | CDS | 574408 | 2586 | + | 0.287703 | |
scfd1 | DDB_G0288719 | DDB0232432 | CDS | 1870694 | 2022 | - | 0.271019 | |
scfd2 | DDB_G0277343 | involved in vesicle-mediated transport weakly similar to H. sapiens SCFD2 | DDB0232429 | CDS | 7784936 | 2715 | + | 0.236464 |
scrA | DDB_G0285253 | adaptor protein that couples Rho GTPases and the Arp23 complex to stimulate actin polymerization | DDB0232431 | CDS | 3055336 | 1332 | + | 0.388889 |
scsA | DDB_G0289325 | catalyzes the reaction GTP succinate CoA GDP phosphate succinyl-CoA | DDB0232432 | CDS | 2650999 | 948 | - | 0.381857 |
scsB | DDB_G0274449 | catalyzes the reaction GTP succinate CoA GDP phosphate succinyl-CoA | DDB0232429 | CDS | 4574977 | 1263 | - | 0.364212 |
scsC | DDB_G0271842 | catalyzes the reaction ATP succinate CoA ADP phosphate succinyl-CoA | DDB0232429 | CDS | 912630 | 1338 | + | 0.355007 |
scy1 | DDB_G0267540 | N-terminal kinase-like (NTKL) protein does not contain the consensus sequences required for kinase function however the SCY1 family encodes highly conserved non-canonical kinases that are believed to function | DDB0232428 | CDS | 300608 | 2442 | - | 0.283374 |
scy2 | DDB_G0270808 | highly similar to SCY1 family kinases does not contain the consensus sequences required for kinase function however the SCY1 family encodes highly conserved non-canonical kinases that are believed to function | DDB0232428 | CDS | 4802064 | 3378 | - | 0.268206 |
sdad1 | DDB_G0269688 | conserved protein in S.cerevisiae required for 60S pre-ribosomal subunits export to the cytoplasm | DDB0232428 | CDS | 3323737 | 2271 | - | 0.294144 |
sdh | DDB_G0285267 | catalyzes the reaction saccharopine NADsupsup Hsub2subO L-glutamate 2-aminoadipate 6-semialdehyde NADH Hsupsup there is also a bifunctional enzyme ( | DDB0232431 | CDS | 3034209 | 1443 | + | 0.348579 |
sdhA | DDB_G0280535 | catalyzes the reaction succinate ubiquinone fumarate ubiquinol | DDB0232430 | CDS | 3543819 | 1881 | + | 0.405635 |
sdhB | DDB_G0270120 | catalyzes the reaction succinate ubiquinone fumarate ubiquinol | DDB0232428 | CDS | 4273481 | 864 | + | 0.327546 |
sdhC | DDB_G0275115 | catalyzes the reaction succinate ubiquinone fumarate ubiquinol cytochrome b560 subunit contains 2 transmembrane domains | DDB0232429 | CDS | 5046259 | 579 | + | 0.345423 |
sdhD | DDB_G0278157 | catalyzes the reaction succinate ubiquinone fumarate ubiquinol cytochrome b small subunit contains 3 transmembrane domains | DDB0232430 | CDS | 377175 | 540 | + | 0.316667 |
sdhaf1A | DDB_G0289475 | DDB0232432 | CDS | 2834711 | 276 | - | 0.264493 | |
sdhaf1B | DDB_G0270818 | DDB0232428 | CDS | 4894629 | 336 | - | 0.241071 | |
sdrA | DDB_G0290659 | DDB0232432 | CDS | 4286973 | 873 | + | 0.290951 | |
sds | DDB_G0272787 | catalyzes the reaction L-serine pyruvate NHsub3sub | DDB0232429 | CDS | 2176582 | 1053 | - | 0.306743 |
sec1 | DDB_G0283937 | highly similar to mammalian Sec1 (also known as syntaxin binding protein 1) which plays a role in vesicle transport by binding to t-SNAREs expressed in prespore cells involved in osmoregulation and hence cell motility | DDB0232431 | CDS | 1335851 | 1797 | + | 0.329994 |
sec11 | DDB_G0276359 | ortholog of the conserved SEC11 the signal peptidase complex is a membrane-bound endoproteinase that removes signal peptides from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum contains two putative transmembrane domains | DDB0232429 | CDS | 6742578 | 540 | - | 0.303704 |
sec13 | DDB_G0292052 | DDB0232433 | CDS | 1099513 | 906 | + | 0.34106 | |
sec20 | DDB_G0267646 | DDB0232428 | CDS | 490625 | 732 | + | 0.210383 | |
sec23 | DDB_G0281985 | DDB0232430 | CDS | 5216752 | 2253 | + | 0.376831 | |
sec24 | DDB_G0281255 | DDB0232430 | CDS | 4298212 | 3042 | + | 0.359303 | |
sec24l | DDB_G0277797 | component of COPII (coat protein complex II) involved in ER to Golgi transport similar to SEC24C and SEC24D | DDB0232429 | CDS | 8422539 | 3402 | + | 0.357731 |
sec31 | DDB_G0270992 | DDB0232428 | CDS | 3837509 | 4068 | + | 0.346853 | |
sec61a | DDB_G0278885 | alpha subunit of the SEC61 complex (composed of | DDB0232430 | CDS | 1338636 | 1428 | - | 0.366947 |
sec61b | DDB_G0278117 | beta subunit of the SEC61 complex (composed of | DDB0232430 | CDS | 306850 | 186 | + | 0.344086 |
sec61g | DDB_G0287777 | gamma subunit of the SEC61 complex (composed of | DDB0232432 | CDS | 682723 | 210 | + | 0.328571 |
sec63 | DDB_G0286131 | similar to the widely conserved SEC63 which seems to be required for integral membrane and secreted preprotein translocation across the endoplasmic reticulum membrane | DDB0232431 | CDS | 4064803 | 2445 | - | 0.350102 |
sec7 | DDB_G0272486 | belongs to the Sec7 superfamily involved in phagocytosis and cell motility | DDB0232429 | CDS | 1791640 | 2796 | - | 0.299714 |
secG | DDB_G0287459 | Arf-guanyl-nucleotide exchange factor of the cytohesin family involved in chemotaxis to cAMP during development and substrate adhesion | DDB0232432 | CDS | 318028 | 2961 | - | 0.372847 |
selD | DDB_G0282367 | contains a selenocysteine residue (U) at position 25 catalyzes the reaction ATP selenide Hsub2subO AMP selenophosphate phosphate | DDB0232430 | CDS | 5741356 | 1095 | + | 0.336073 |
selk | DDB_G0268720 | DDB0232428 | CDS | 1994316 | 348 | + | 0.37069 | |
senp8 | DDB_G0278795 | ortholog of SENP8 a conserved protease that catalyzes two essential functions in the NEDD8 pathway: processing of full-length NEDD8 to its mature form and deconjugation of NEDD8 from targeted proteins such as cullins | DDB0232430 | CDS | 1191521 | 732 | + | 0.214481 |
sep15 | DDB_G0268396 | contains a selenocysteine residue (U) at position 100 conserved protein which may be involved in protein folding in the endoplasmic reticulum | DDB0232428 | CDS | 1139853 | 501 | - | 0.293413 |
sepA | DDB_G0276465 | plays a role in the regulation of cleavage furrow formation similar to S. pombe cdc7 | DDB0232429 | CDS | 6942806 | 3504 | + | 0.32363 |
sepsecs | DDB_G0280197 | DDB0232430 | CDS | 3095673 | 1440 | + | 0.254861 | |
serA | DDB_G0281071 | catalyzes the reaction 3-phosphoglycerate NAD 3-phospho-hydroxypyruvate NADH | DDB0232430 | CDS | 4007757 | 1224 | + | 0.330882 |
serB | DDB_G0291368 | catalyzes the reaction 3-phospho-serine Hsub2subO L-serine phosphate | DDB0232433 | CDS | 185417 | 1098 | + | 0.26776 |
serC | DDB_G0269950 | catalyzes the reaction 3-phospho-hydroxypyruvate L-glutamate 2-oxoglutarate 3-phospho-serine | DDB0232428 | CDS | 3920593 | 1125 | + | 0.266667 |
serS | DDB_G0272660 | catalyzes the reaction ATP L-serine tRNASer AMP diphosphate L-seryl-tRNASer | DDB0232429 | CDS | 2243539 | 1356 | + | 0.343658 |
set1 | DDB_G0289257 | DDB0232432 | CDS | 2551579 | 4461 | + | 0.297467 | |
sevA | DDB_G0289327 | Ca2-dependent F-actin fragmenting protein | DDB0232432 | CDS | 2683596 | 1089 | - | 0.325987 |
sf1 | DDB_G0293554 | ortholog of the conserved splicing factor 1 binds to the intron branch point sequence (BPS) of the pre-mRNA necessary for the ATP-dependent first step of spliceosome assembly | DDB0232433 | CDS | 3035802 | 1506 | + | 0.308101 |
sf3a1 | DDB_G0272676 | DDB0232429 | CDS | 2037250 | 2283 | + | 0.344284 | |
sf3a2 | DDB_G0293876 | DDB0232433 | CDS | 3412404 | 648 | + | 0.274691 | |
sf3a3 | DDB_G0270020 | subunit of the splicing factor SF3A required for spliceosome assembly contains PRP9 domain characteristic of splicing factor 3A subunit 3 expressed in pstO cells | DDB0232428 | CDS | 4032294 | 1635 | + | 0.223242 |
sf3b1 | DDB_G0275957 | DDB0232429 | CDS | 6197621 | 3156 | - | 0.359949 | |
sf3b2 | DDB_G0284555 | DDB0232431 | CDS | 2068357 | 1878 | + | 0.305112 | |
sf3b3 | DDB_G0282569 | DDB0232430 | CDS | 5947254 | 3771 | - | 0.334394 | |
sf3b4 | DDB_G0267714 | DDB0232428 | CDS | 676187 | 1080 | - | 0.333333 | |
sf3b5 | DDB_G0271312 | subunit of the splicing factor SF3B required for spliceosome assembly belongs to the SF3b10 (splicing factor 3B 10 kDa subunit) family | DDB0232429 | CDS | 124590 | 285 | - | 0.315789 |
sfbA | DDB_G0274107 | DDB0232429 | CDS | 4320828 | 1878 | - | 0.358892 | |
sfxn | DDB_G0285029 | very similar to mammalian sideroflexins especially SFXN 5 and SFXN3 and to S. cerevisieae FSF1 contains five putative transmembrane domains | DDB0232431 | CDS | 2834988 | 990 | - | 0.279798 |
sgcA | DDB_G0276269 | DDB0232429 | CDS | 6582943 | 8532 | - | 0.290319 | |
sgkA | DDB_G0272522 | homolog of human Sphk1 phosphorylates sphinganine to sphinganine 1-phosphate | DDB0232429 | CDS | 1846158 | 1875 | + | 0.3088 |
sgkB | DDB_G0284545 | homolog of human Sphk2 phosphorylates sphinganine to sphinganine 1-phosphate | DDB0232431 | CDS | 2087340 | 2283 | + | 0.251862 |
sgkC | DDB_G0272350 | DDB0232429 | CDS | 1700447 | 2178 | + | 0.344812 | |
sgkD | DDB_G0289343 | DDB0232432 | CDS | 2664172 | 2052 | + | 0.203704 | |
sglA | DDB_G0282819 | null mutant is 25-fold more resistant to cisplatin compared to parent catalyzes the reaction sphinganine 1-phosphate phosphoethanolamine palmitaldehyde | DDB0232430 | CDS | 6335773 | 1587 | + | 0.344045 |
sglB | DDB_G0280183 | catalyzes the reaction sphinganine 1-phosphate phosphoethanolamine palmitaldehyde | DDB0232430 | CDS | 3069484 | 1596 | + | 0.304511 |
sgmA | DDB_G0270834 | DDB0232428 | CDS | 4562741 | 1752 | - | 0.324201 | |
sgmB | DDB_G0293210 | DDB0232433 | CDS | 2708230 | 1914 | + | 0.306165 | |
sgmC | DDB_G0282265 | DDB0232430 | CDS | 5590476 | 1341 | + | 0.266965 | |
sgmD | DDB_G0268330 | similar to acid sphingomyelinase which hydrolyze the phosphodiester bond in sphingomyelin to form ceramide | DDB0232428 | CDS | 704053 | 1317 | - | 0.292331 |
sgtA | DDB_G0280345 | DDB0232430 | CDS | 3286144 | 1005 | - | 0.311443 | |
shkA | DDB_G0283267 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain negative regulator of phosphoinositol signaling | DDB0232431 | CDS | 438511 | 1584 | + | 0.318182 |
shkB | DDB_G0288617 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232432 | CDS | 1745652 | 1962 | - | 0.331295 |
shkC | DDB_G0278409 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232430 | CDS | 836437 | 1521 | - | 0.332676 |
shkD | DDB_G0281343 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232430 | CDS | 4376038 | 2235 | + | 0.314541 |
shkE | DDB_G0290451 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232432 | CDS | 4058161 | 2133 | + | 0.284107 |
shmt1 | DDB_G0277947 | cytoplasmic serine hydroxymethyltransferase catalyzes the reaction L-serine tetrahydrofolate L-glycine 510-methylene-tetrahydrofolate Hsub2subO | DDB0232430 | CDS | 47291 | 1374 | - | 0.351528 |
shmt2 | DDB_G0291652 | mitochondrial serine hydroxymethyltransferase catalyzes the reaction L-serine tetrahydrofolate L-glycine 510-methylene-tetrahydrofolate Hsub2subO | DDB0232433 | CDS | 91358 | 1446 | - | 0.350622 |
sibA | DDB_G0287363 | similar to the integrin beta family cytosolic domain binds talin involved in substrate adhesion and phagocytosisbr bnoteb the sequence in dictyBase has mismatches and does not contain a clear signal sequence whereas the published sequence available from the | DDB0232432 | CDS | 192610 | 5784 | - | 0.331604 |
sibB | DDB_G0288103 | integrin beta family protein cytosolic domain binds talin | DDB0232432 | CDS | 1110992 | 5826 | + | 0.331102 |
sibC | DDB_G0288195 | integrin beta family protein cytosolic domain binds talin expression increases when cells are under conditions that promote adhesiveness | DDB0232432 | CDS | 1194946 | 5865 | - | 0.350725 |
sibD | DDB_G0288197 | integrin beta family protein cytosolic domain binds talin | DDB0232432 | CDS | 1202242 | 5874 | - | 0.312223 |
sibE | DDB_G0288239 | integrin beta family protein cytosolic domain binds talin | DDB0232432 | CDS | 1209765 | 5841 | - | 0.34857 |
sid1 | DDB_G0290761 | ortholog of C. elegans sid1 that enables passive cellular uptake of dsRNA contains 10 transmembrane domains | DDB0232432 | CDS | 4572699 | 1299 | - | 0.265589 |
sigB | DDB_G0293364 | DDB0232433 | CDS | 2822106 | 2049 | + | 0.307467 | |
sigD | DDB_G0267474 | DDB0232428 | CDS | 1199961 | 1338 | + | 0.348281 | |
sigD_ps | DDB_G0284317 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 1740402 | 387 | + | 0.361757 |
sigE | DDB_G0277921 | regulated by the MADS-box transcription factor SrfA during development contains one transmembrane domain | DDB0232430 | CDS | 302308 | 894 | - | 0.214765 |
sigF | DDB_G0289885 | DDB0232432 | CDS | 3500701 | 696 | - | 0.24569 | |
sigG | DDB_G0290071 | DDB0232432 | CDS | 3632186 | 1278 | - | 0.293427 | |
sigH | DDB_G0276757 | expressed in prespore cells contains two predicted transmembrane domains | DDB0232429 | CDS | 7176768 | 177 | - | 0.355932 |
sigI | DDB_G0275177 | DDB0232429 | CDS | 5054068 | 915 | - | 0.27541 | |
sigJ | DDB_G0269254 | weakly related to blackjack a protein associated with microtubules but without similarity to MAPs regulated by the MADS-box transcription factor SrfA during development expressed in prespore cells | DDB0232428 | CDS | 3751652 | 1074 | + | 0.335196 |
sigK | DDB_G0267476 | regulated by the MADS-box transcription factor SrfA during development expressed in stalk cells contains two EGF domains | DDB0232428 | CDS | 1084166 | 1281 | + | 0.338017 |
sigL-1 | DDB_G0273261 | regulated by the MADS-box transcription factor SrfA during development expressed in stalk cells contains one EGF domain and a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 2871173 | 1239 | - | 0.298628 |
sigL-2 | DDB_G0273601 | regulated by the MADS-box transcription factor SrfA during development expressed in stalk cells contains one EGF domain and a predicted signal peptide there is a second copy of this gene | DDB0232429 | CDS | 3159375 | 1239 | + | 0.298628 |
sigM | DDB_G0286563 | regulated by the MADS-box transcription factor SrfA during development contains two EGF domains | DDB0232431 | CDS | 4725803 | 1491 | + | 0.298457 |
sir2A | DDB_G0283917 | NAD-dependent deacetylase Sirutin 2 family protein that regulates various biological processes by deacetylating histones and other target proteins expressed more highly during vegetative growth | DDB0232431 | CDS | 1272110 | 1539 | + | 0.293047 |
sir2B | DDB_G0286671 | N-terminus has several ankyrin repeats C-terminus has a Sirutin (Sir2) domain a NAD-dependent deacetylase that regulates various biological processes by deacetylating histones and other target proteins expressed more highly during development localized to prestalk and rearguard region of the slug and to the apical disc and upper and lower cups in the culminant (similar expression pattern as sir2E) | DDB0232431 | CDS | 4818681 | 2337 | + | 0.267009 |
sir2C | DDB_G0284795 | NAD-dependent deacetylase Sirutin 2 family protein that regulates various biological processes by deacetylating histones and other target proteins expressed more highly during vegetative growth | DDB0232431 | CDS | 2489743 | 1371 | - | 0.231947 |
sir2D | DDB_G0289967 | NAD-dependent deacetylase Sirutin 2 family protein that regulates various biological processes by deacetylating histones and other target proteins expressed more highly during vegetative growth | DDB0232432 | CDS | 3383269 | 1629 | - | 0.281768 |
sir2E | DDB_G0270928 | NAD-dependent deacetylase Sirutin 2 family protein that regulate various biological processes by deacetylating histones and other target proteins nuclear protein expressed in pstA and pstO cells in the slug and to the apical disc upper and lower cups in the culminant (similar expression pattern as sir2B) | DDB0232428 | CDS | 3398987 | 1032 | + | 0.281008 |
sky1 | DDB_G0275627 | similar to SRPKs (Serinearginine-Rich Protein specific Kinases) serinethreonine kinases that specifically phosphoryate arginine-serine rich domains found in the SR family of splicing factors | DDB0232429 | CDS | 5951942 | 1971 | - | 0.318113 |
slbp | DDB_G0288225 | binds the stem-loop structure of replication-dependent histone pre-mRNAs and contributes to histone mRNA 3' end processing | DDB0232432 | CDS | 1277134 | 1086 | + | 0.207182 |
slc35b2 | DDB_G0269602 | belongs to the drugmetabolite transporter (DMT) superfamily similar to D. melanogaster sll human SLC35B2 contains 8 predicted transmembrane domains | DDB0232428 | CDS | 3110201 | 1080 | - | 0.297222 |
slc35b4 | DDB_G0275061 | homolog of human SLC35B4 S. cerevisiae YEA4 contains 9 putative transmembrane domains | DDB0232429 | CDS | 5092894 | 1056 | + | 0.243371 |
slc4 | DDB_G0270422 | DDB0232428 | CDS | 4842234 | 2307 | - | 0.229736 | |
slc44a2 | DDB_G0289013 | DDB0232432 | CDS | 2230553 | 1887 | + | 0.325384 | |
slmo | DDB_G0290499 | conserved protein in D. melanogaster lack of SLMO leads to defects in locomotor behavior and die during larval development contains a PRELIMSF1 domain | DDB0232432 | CDS | 4156073 | 687 | + | 0.310044 |
slob1 | DDB_G0281863 | similar to D. melanogaster Slob (Slowpoke binding protein) and mammalian Pxk (PX domain-containing kinase) does not contain the consensus sequences required for kinase function however the Slob family encodes highly conserved non-canonical kinases that are believed to function | DDB0232430 | CDS | 5040353 | 1758 | - | 0.279863 |
slob2 | DDB_G0279303 | similar to D. melanogaster Slob (Slowpoke binding protein) and mammalian Pxk (PX domain-containing kinase) does not contain the consensus sequences required for kinase function however the Slob family encodes highly conserved non-canonical kinases that are believed to function | DDB0232430 | CDS | 1904584 | 1725 | + | 0.305507 |
slrA | DDB_G0282069 | enriched expression in Sentinel cells in the slug contains plant-specific leucine-rich repeats | DDB0232430 | CDS | 5176361 | 4137 | + | 0.237854 |
slu7 | DDB_G0281901 | DDB0232430 | CDS | 5091808 | 1677 | - | 0.317829 | |
sma | DDB_G0281803 | DDB0232430 | CDS | 4733270 | 3651 | + | 0.213366 | |
smc1 | DDB_G0291752 | functions in chromosome dynamics heterodimerizes with smc3 | DDB0232433 | CDS | 688164 | 4122 | + | 0.312712 |
smc2 | DDB_G0284499 | functions in chromosome dynamics heterodimerizes with smc4 | DDB0232431 | CDS | 2051268 | 3555 | - | 0.320394 |
smc3 | DDB_G0276101 | functions in chromosome dynamics heterodimerizes with smc1 | DDB0232429 | CDS | 6321257 | 4314 | - | 0.309458 |
smc4 | DDB_G0286403 | functions in chromosome dynamics heterodimerizes with smc2 | DDB0232431 | CDS | 4414331 | 4248 | - | 0.318974 |
smc5 | DDB_G0290919 | functions in chromosome dynamics heterodimerizes with smc6 | DDB0232432 | CDS | 4745027 | 3396 | - | 0.328033 |
smc6 | DDB_G0288993 | functions in chromosome dynamics heterodimerizes with smc5 | DDB0232432 | CDS | 2211609 | 3558 | - | 0.324902 |
smdA | DDB_G0288495 | DDB0232432 | CDS | 1605485 | 1599 | + | 0.229518 | |
smg1 | DDB_G0275845 | atypical PIKK family protein kinase similar to the PI-3-kinase-related kinase SMG1 which functions in nonsense-mediated mRNA decay belongs to the PIKK family of protein kinases | DDB0232429 | CDS | 5665840 | 7035 | + | 0.267235 |
smkA | DDB_G0289067 | suppressor of | DDB0232432 | CDS | 2315722 | 3141 | - | 0.24801 |
smlA | DDB_G0287587 | DDB0232432 | CDS | 461888 | 852 | + | 0.279343 | |
smlA_ps | DDB_G0281717 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232430 | CDS | 4870585 | 255 | + | 0.294118 |
smlA_ps1 | DDB_G0281715 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232430 | CDS | 4870020 | 243 | - | 0.300412 |
smp3 | DDB_G0291660 | CAZy family GT76 catalyzes the addition of the fourth mannose to GPI (glycosylphosphatidylinositol) | DDB0232433 | CDS | 189530 | 2004 | + | 0.211577 |
smtA | DDB_G0288907 | DDB0232432 | CDS | 2108749 | 1065 | + | 0.421596 | |
smu1 | DDB_G0278353 | DDB0232430 | CDS | 737677 | 1593 | - | 0.266164 | |
snd1 | DDB_G0279659 | DDB0232430 | CDS | 2397433 | 2766 | + | 0.339841 | |
snf12-1 | DDB_G0273203 | nuclear protein and ortholog of yeast SNF12 and human SMARCD1 that are involved in chromatin remodeling there is a second copy of this gene | DDB0232429 | CDS | 2700893 | 1371 | - | 0.277899 |
snf12-2 | DDB_G0273725 | nuclear protein and ortholog of yeast SNF12 and human SMARCD1 that are involved in chromatin remodeling there is a second copy of this gene | DDB0232429 | CDS | 3329319 | 1371 | + | 0.277899 |
snf2a | DDB_G0285205 | SNF2 family protein similar to human SMARCA4 putative regulator of chromatin | DDB0232431 | CDS | 2921996 | 4815 | + | 0.304673 |
snf2b | DDB_G0271052 | SNF2 family protein similar to human SMARCA4 putative regulator of chromatin | DDB0232428 | CDS | 4502537 | 9744 | - | 0.313218 |
snf5 | DDB_G0279373 | SNF5 homolog putative chromatin remodeling complex subunit | DDB0232430 | CDS | 2004876 | 1491 | + | 0.344064 |
snfA | DDB_G0277905 | CAMKL family protein kinase catalytic subunit of the AMP-activated protein kinase (AMPK) complex similar to SNF1 kinases and AMPK experiments in Dictyostelium show that AMPK signaling plays an important role in mitochondrial disease. | DDB0232430 | CDS | 589784 | 2184 | + | 0.250458 |
sno1 | DDB_G0294409 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232430 | CDS | 4409414 | 64 | + | 0.359375 |
sno10 | DDB_G0295511 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232429 | CDS | 5045624 | 80 | + | 0.25 |
sno11a | DDB_G0295527 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232429 | CDS | 7539525 | 67 | - | 0.373134 |
sno11b | DDB_G0295525 | similar to sno11a CD box snoRNAs are involved in rRNA processing and methylation | DDB0232429 | CDS | 7539245 | 67 | - | 0.358209 |
sno12 | DDB_G0295605 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 1152280 | 75 | - | 0.293333 |
sno13 | DDB_G0295621 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2600252 | 80 | - | 0.4375 |
sno14 | DDB_G0295551 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232430 | CDS | 3885498 | 65 | - | 0.307692 |
sno15 | DDB_G0295561 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232431 | CDS | 59280 | 113 | + | 0.362832 |
sno16 | DDB_G0295631 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2586031 | 78 | - | 0.333333 |
sno17 | DDB_G0295517 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232429 | CDS | 6122802 | 70 | + | 0.228571 |
sno18 | DDB_G0295543 | expressed non-coding RNA HACA box snoRNAs are involved in rRNA processing | DDB0232430 | CDS | 1341335 | 146 | + | 0.349315 |
sno2 | DDB_G0295619 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2599917 | 83 | - | 0.337349 |
sno3 | DDB_G0295499 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232428 | CDS | 3858015 | 85 | - | 0.341176 |
sno4 | DDB_G0295545 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232430 | CDS | 1341617 | 105 | + | 0.333333 |
sno5 | DDB_G0295617 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2585363 | 81 | - | 0.320988 |
sno6 | DDB_G0295531 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232429 | CDS | 7681951 | 86 | - | 0.348837 |
sno7 | DDB_G0295615 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2249624 | 98 | - | 0.438776 |
sno8 | DDB_G0295603 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232431 | CDS | 4444849 | 88 | - | 0.397727 |
sno9 | DDB_G0295555 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232430 | CDS | 4409131 | 80 | + | 0.4125 |
snpA | DDB_G0285111 | DDB0232431 | CDS | 2863727 | 876 | - | 0.3379 | |
snpC | DDB_G0269186 | DDB0232428 | CDS | 4853471 | 975 | + | 0.286154 | |
snrp70 | DDB_G0268004 | ortholog of human SNRP70 a component of the U1 snRNP involved in mRNA splicing | DDB0232428 | CDS | 1286207 | 1380 | + | 0.334783 |
snrpA1 | DDB_G0284101 | ortholog of human SNRPA1 a component of the U2 snRNP involved in mRNA splicing | DDB0232431 | CDS | 1571395 | 735 | + | 0.240816 |
snrpB2 | DDB_G0288391 | ortholog of human SNRPB2 a component of the U2 snRNP involved in mRNA splicing also similar to human SNRPA | DDB0232432 | CDS | 1486880 | 726 | - | 0.296143 |
snrpC | DDB_G0278335 | DDB0232430 | CDS | 716610 | 525 | - | 0.342857 | |
snrpD1 | DDB_G0278027 | DDB0232430 | CDS | 175913 | 396 | + | 0.335859 | |
snrpD2 | DDB_G0285395 | DDB0232431 | CDS | 3142648 | 339 | - | 0.294985 | |
snrpD3 | DDB_G0273003 | DDB0232429 | CDS | 2118091 | 441 | + | 0.378685 | |
snrpE | DDB_G0302414 | conserved SMLSM core protein also known as SME1 associates with U1 U2 U4U6 and U5 snRNP | DDB0232432 | CDS | 1315343 | 279 | - | 0.25448 |
snrpF | DDB_G0278821 | DDB0232430 | CDS | 1243062 | 276 | + | 0.315217 | |
snrpG | DDB_G0282863 | DDB0232430 | CDS | 6319736 | 258 | - | 0.282946 | |
snrpb | DDB_G0272320 | DDB0232429 | CDS | 1283864 | 825 | - | 0.453333 | |
snwA | DDB_G0269188 | SKIP ortholog binds cyclophilin E (cypE) in a cyclosporin-independent manner | DDB0232428 | CDS | 2978336 | 2058 | - | 0.325559 |
sod2 | DDB_G0271106 | ortholog of the human SOD2 the mitochondrial superoxide dismutase belongs to the ironmanganese superoxide dismutase family | DDB0232429 | CDS | 35093 | 681 | + | 0.325991 |
sodA | DDB_G0267420 | superoxide dismutase of the SOD1 family expressed at constant levels throughout the life cycle and upregulated upon oxidative stress enriched in prespore cells | DDB0232428 | CDS | 338107 | 462 | + | 0.391775 |
sodB | DDB_G0283021 | DDB0232431 | CDS | 167774 | 1284 | - | 0.351246 | |
sodC | DDB_G0282993 | GPI-anchored plasma membrane superoxide dismutase upregulated upon oxidative stress mutants have defects in cytokinesis chemotaxis and localization of several protein during aggregation | DDB0232431 | CDS | 110200 | 1224 | - | 0.332516 |
sodD | DDB_G0281493 | DDB0232430 | CDS | 4612258 | 456 | - | 0.361842 | |
sodE | DDB_G0290343 | very similar to human SOD1 defects in which cause familial amyotrophic lateral sclerosis (ALS) belongs to the Cu-Zn superoxide dismutase family | DDB0232432 | CDS | 3992463 | 459 | + | 0.294118 |
sodF | DDB_G0281461 | DDB0232430 | CDS | 4537876 | 456 | + | 0.346491 | |
sonA | DDB_G0267452 | DDB0232428 | CDS | 1168646 | 1572 | - | 0.371501 | |
sort1 | DDB_G0290081 | ortholog of S. cerevisiae PEP1 and mammalian sortilin a sorting receptor of the Golgi apparatus | DDB0232432 | CDS | 3627939 | 2316 | - | 0.335924 |
spc1 | DDB_G0278371 | ortholog of the conserved microsomal signal peptidase 12 kDa subunit the signal peptidase complex is a membrane-bound endoproteinase that removes signal peptides from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum contains a putative signal peptide and one transmembrane domain | DDB0232430 | CDS | 770499 | 243 | - | 0.26749 |
spc2 | DDB_G0270510 | ortholog of the conserved microsomal signal peptidase 25 kDa subunit the signal peptidase complex is a membrane-bound endoproteinase that removes signal peptides from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum contains two putative transmembrane domains | DDB0232428 | CDS | 2718039 | 552 | + | 0.246377 |
spc25 | DDB_G0284013 | ortholog of Spc25 which interacts with Ndc80 in the attachment of microtubules to kinetochores brbr bCommunity annotation: b spc25 is overexpressed 16-fold in a | DDB0232431 | CDS | 1432537 | 975 | + | 0.220513 |
spc3 | DDB_G0290851 | ortholog of the conserved microsomal signal peptidase 23 kDa subunit the signal peptidase complex is a membrane-bound endoproteinase that removes signal peptides from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum contains a putative signal peptide | DDB0232432 | CDS | 4675467 | 513 | + | 0.288499 |
spc97 | DDB_G0285849 | DDB0232431 | CDS | 3719511 | 4008 | + | 0.262974 | |
spc98 | DDB_G0283909 | DDB0232431 | CDS | 1376667 | 2442 | - | 0.269042 | |
spf27 | DDB_G0282763 | ortholog of the mammalian BCAS2 (breast carcinoma amplified sequence 2) protein a spliceosome-associated protein | DDB0232430 | CDS | 5822824 | 681 | - | 0.245228 |
spg1 | DDB_G0291269 | DDB0232433 | CDS | 37774 | 612 | + | 0.338235 | |
spiA | DDB_G0289075 | regulated by the MADS-box transcription factor SrfA during development expressed in prespore cells | DDB0232432 | CDS | 2352021 | 810 | - | 0.351852 |
spkA-1 | DDB_G0273445 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family kinase activity stimulated by hyperosmolarity and heat shock there is a second copy of this gene | DDB0232429 | CDS | 2969377 | 1917 | - | 0.310381 |
spkA-2 | DDB_G0273531 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family kinase activity stimulated by hyperosmolarity and heat shock there is a second copy of this gene | DDB0232429 | CDS | 3060166 | 1917 | + | 0.310381 |
splA | DDB_G0283385 | dual-specificity protein kinase involved in spore coat formation and morphogenesis member of the TKL (tyrosine kinase-like) group and the CZAK (C-terminal domain of ZakA) family | DDB0232431 | CDS | 623097 | 7233 | + | 0.323655 |
splB | DDB_G0285321 | member of the TKL (tyrosine kinase-like) group activates the transcriptional regulator STATc | DDB0232431 | CDS | 3131349 | 3468 | + | 0.27797 |
spnA | DDB_G0276155 | gene essential for Dictyostelium development with an N-terminal Galpha regulatory domain and a C-terminal PP2C serinethreonine phosphatase domain | DDB0232429 | CDS | 6284187 | 2928 | - | 0.311134 |
spoT | DDB_G0287233 | DDB0232432 | CDS | 32102 | 627 | - | 0.271132 | |
sppA | DDB_G0272260 | DDB0232429 | CDS | 1421226 | 1221 | + | 0.283374 | |
spsA | DDB_G0268630 | DDB0232428 | CDS | 2217041 | 855 | - | 0.367251 | |
spt16 | DDB_G0282677 | similar to SPT16 of the FACT complex a heterodimer of ssrp1 and spt16 the FACT complex is a general chromatin factor that acts to reorganize nucleosomes involved in multiple processes that require DNA as a template such as mRNA elongation DNA replication and DNA repair | DDB0232430 | CDS | 6105920 | 3219 | - | 0.339546 |
spt16_ps | DDB_G0282775 | putative pseudogene similar to D. discoideum gene | DDB0232430 | CDS | 5907328 | 582 | + | 0.359107 |
spt4 | DDB_G0285293 | ortholog of the human SUPT4H1 and S. cerevisiae SPT4 (suppressor of Ty 4) a transcription-elongation factor that is tightly associated in a complex with SPT5 | DDB0232431 | CDS | 3068070 | 276 | + | 0.344203 |
spt5 | DDB_G0287661 | ortholog of the human SUPT5H and S. cerevisiae SPT5 (suppressor of Ty 5) a transcription-elongation factor that is tightly associated in a complex with SPT4 | DDB0232432 | CDS | 473577 | 3396 | - | 0.325383 |
spt6 | DDB_G0272354 | DDB0232429 | CDS | 1271354 | 5265 | - | 0.350807 | |
sptA | DDB_G0268056 | similar to S. cerevisiae LCB1 dimerizes with SptB to catalyze the conversion of palmitoyl-CoA L-serine into CoA 3-dehydro-D-sphinganine COsub2sub | DDB0232428 | CDS | 1366267 | 1440 | - | 0.277083 |
sptB | DDB_G0291283 | similar to S. cerevisiae LCB2 dimerizes with SptA to catalyze the conversion of palmitoyl-CoA L-serine into CoA 3-dehydro-D-sphinganine COsub2sub | DDB0232433 | CDS | 51803 | 1473 | + | 0.35981 |
spyA | DDB_G0285263 | CAZy family GT41 contains 7 TPRs (Tetratrico Peptide Repeats) | DDB0232431 | CDS | 3029506 | 2595 | - | 0.246243 |
sqle | DDB_G0293584 | catalyzes the reaction squalene AH2 O2 (S)-squalene-23-epoxide A H2O catalyzes the first oxygenation step in sterol biosynthesis | DDB0232433 | CDS | 3076225 | 1509 | + | 0.307488 |
sqpA | DDB_G0277873 | DDB0232430 | CDS | 467909 | 2169 | + | 0.244813 | |
sqrdl | DDB_G0292250 | ortholog of the conserved sulfide quinone reductase-like protein in S. pombe this oxidoreductase is involved in mitochondrial sulfide oxidation | DDB0232433 | CDS | 1300465 | 1359 | - | 0.341428 |
sqstm1 | DDB_G0270098 | similar to the conserved ubiquitin-binding protein p62SQSTM1 in Dictyostelium found in large ubiquitinated protein aggregates present in vmp1- and atg1- autophagy mutants | DDB0232428 | CDS | 4208288 | 1941 | - | 0.289541 |
sr | DDB_G0290009 | catalyzes the reaction 78-dihydrobiopterin NADPsupsup sepiapterin NADPH Hsupsup the final step in L-erythro-tetrahydrobiopterin (BH4) biosynthesis a cofactor for aromatic amino acid oxidationbr | DDB0232432 | CDS | 3552302 | 804 | + | 0.238806 |
srfA | DDB_G0281387 | transcription factor expressed in prespore cells required for expression of several genes involved terminal spore differentiation | DDB0232430 | CDS | 4494019 | 1257 | + | 0.292761 |
srfB | DDB_G0282835 | DDB0232430 | CDS | 6278818 | 1404 | + | 0.267094 | |
srfD | DDB_G0283483 | DDB0232431 | CDS | 775937 | 1341 | - | 0.246831 | |
srp14-1 | DDB_G0272590 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum there is a second copy of this gene | DDB0232429 | CDS | 2398894 | 372 | - | 0.282258 |
srp14-2 | DDB_G0273977 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum there is a second copy of this gene | DDB0232429 | CDS | 3632343 | 372 | + | 0.282258 |
srp19 | DDB_G0275211 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232429 | CDS | 5011473 | 537 | + | 0.312849 |
srp54 | DDB_G0275455 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232429 | CDS | 6110111 | 1629 | - | 0.361572 |
srp68 | DDB_G0285821 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232431 | CDS | 3701203 | 1845 | + | 0.280217 |
srp72 | DDB_G0291412 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232433 | CDS | 275731 | 2019 | - | 0.270926 |
srp9 | DDB_G0267622 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232428 | CDS | 438237 | 228 | - | 0.25 |
srpA | DDB_G0294413 | signal recognition particle (SRP) RNA forms the SRP complex with the SRP 72 68 54 19 14 and 9 proteins | DDB0232431 | CDS | 2767691 | 278 | + | 0.471223 |
srpB | DDB_G0295493 | signal recognition particle (SRP) RNA forms the SRP complex with the SRP 72 68 54 19 14 and 9 proteins | DDB0232428 | CDS | 1758352 | 283 | - | 0.44523 |
srpR | DDB_G0277377 | DDB0232429 | CDS | 7920699 | 1848 | - | 0.308983 | |
srpRB | DDB_G0278543 | DDB0232430 | CDS | 1043259 | 873 | + | 0.269187 | |
srr | DDB_G0289463 | converts L-serine into D-serine activated in vitro by Mg as well as Na pyridoxal 5'-phosphate (PLP)-dependent enzyme that catalyzes racemization and dehydration of both isomers of serine | DDB0232432 | CDS | 2816488 | 975 | + | 0.308718 |
srrm1 | DDB_G0286425 | very similar to the mammalian serinearginine repetitive matrix protein 1 (SRRM1) which is part of pre- and post-splicing multiprotein mRNP complexes involved in numerous pre-mRNA processing events | DDB0232431 | CDS | 4471381 | 1812 | + | 0.291943 |
srsA | DDB_G0289521 | immidiate-early gene expressed immidiately after nutrition removal involved in starvation response development and spore differentiation there are two transcripts of this gene both contain a putative transmembrane domain | DDB0232432 | CDS | 2911167 | 495 | + | 0.252525 |
ssbA | DDB_G0277875 | DDB0232430 | CDS | 113091 | 861 | - | 0.307782 | |
sslA1 | DDB_G0284335 | mutation in the sslA1 gene increases the fruiting body size of smlA mutants positively regulates group size there is an identical gene on chromosome 3 | DDB0232431 | CDS | 1885441 | 1737 | - | 0.270581 |
sslA2 | DDB_G0278309 | there is an identical gene on chromosome 4 | DDB0232430 | CDS | 665995 | 1737 | + | 0.270581 |
sslA_ps1 | DDB_G0282869 | putative pseudogene almost identical to sslA | DDB0232430 | CDS | 6323600 | 1596 | - | 0.272556 |
sslA_ps2 | DDB_G0272526 | putative pseudogene very similar to sslA | DDB0232429 | CDS | 1785431 | 561 | + | 0.299465 |
ssr1 | DDB_G0283497 | DDB0232431 | CDS | 648667 | 711 | - | 0.331927 | |
ssr2 | DDB_G0280313 | DDB0232430 | CDS | 3245211 | 555 | - | 0.322523 | |
ssr3 | DDB_G0267524 | DDB0232428 | CDS | 271374 | 513 | - | 0.325536 | |
ssrp1 | DDB_G0290331 | ortholog of the SSRP1 component of the FACT complex a heterodimer of ssrp1 and spt16 the FACT complex is a general chromatin factor that acts to reorganize nucleosomes involved in multiple processes that require DNA as a template such as mRNA elongation DNA replication and DNA repair | DDB0232432 | CDS | 3969916 | 1584 | - | 0.342172 |
ssu72 | DDB_G0272871 | ortholog of human and S. cerevisiae SSU72 (suppressor of SUA7 protein 2) S. cerevisiae SSU72 is involved in several roles including 3' end formation of pre-mRNA and snoRNAs and dephosphorylation of RNA polymerase II the D. discoideum homolog of yeast SUA7 is | DDB0232429 | CDS | 2056744 | 645 | + | 0.297674 |
st15 | DDB_G0292218 | similar to beta-14-endoglucanase expressed in pstO cells expression is decreased in | DDB0232433 | CDS | 1328404 | 369 | + | 0.333333 |
staA | DDB_G0294473 | DIF-inducible highly similar to staB | DDB0232430 | CDS | 3196112 | 474 | + | 0.297468 |
staB | DDB_G0294499 | expressed in prestalk cells and in the basal disc during culmination highly similar to staA | DDB0232430 | CDS | 3194120 | 474 | + | 0.299578 |
sti1 | DDB_G0292404 | DDB0232433 | CDS | 1556012 | 1695 | - | 0.362242 | |
stip-1 | DDB_G0272608 | conserved protein ortholog of the D. melanogaster sip1 gene (septin interaction protein) and to the H. sapiens tuftelin-interacting protein 11 (TFIP11) there is a second copy of this gene | DDB0232429 | CDS | 2335396 | 2685 | - | 0.243948 |
stip-2 | DDB_G0274035 | conserved protein ortholog of the D. melanogaster sip1 gene (septin interaction protein) and to the H. sapiens tuftelin-interacting protein 11 (TFIP11) there is a second copy of this gene | DDB0232429 | CDS | 3693611 | 2685 | + | 0.243948 |
stkA | DDB_G0277147 | transcription factor required for sporulation expressed in prespore cells has 18 amino acids between the two CX2C motifs | DDB0232429 | CDS | 7615234 | 2619 | + | 0.244368 |
stlA | DDB_G0269364 | belongs to the beta-ketoacyl synthase family type III polyketide synthase catalyzes iterative polyketide extension from hexanoyl-CoA can catalyze three polyketide chain extensions followed by aldol cyclization to synthesize demethyl-4-methyl-5-pentylbenzene-13-diol (MPBD) starter unit can vary from acyl CoA substrates ranging from 3-20 carbons br bNomenclature conflict:b Do not confuse the stlA gene encoding a polyketide synthase with the stlA locus associated with deficient stalk formation ( | DDB0232428 | CDS | 2612482 | 9444 | - | 0.285155 |
stlB | DDB_G0290853 | belongs to the beta-ketoacyl synthase family type III polyketide synthase responsible for phlorocaprophenone (PCP) production the first step in DIF-1 biosynthesis required for the formation of the outer basal disc and the lower cup | DDB0232432 | CDS | 4652248 | 8907 | + | 0.270461 |
strM | DDB_G0288323 | conserved in other Dictyosteliabr bNomenclature note:b named by colleagues of M. Satre as the protein sequence starts with MSATRE | DDB0232432 | CDS | 1389621 | 894 | + | 0.316555 |
strap | DDB_G0286457 | ortholog of the serine-threonine kinase receptor-associated protein STRAP an inhibitor of TGF-beta signaling contains 7 WD40 repeats | DDB0232431 | CDS | 4462466 | 882 | - | 0.349206 |
strn | DDB_G0288327 | homolog of mammalians striatins calmodulin-binding proteins expressed in the central nervous system and Drosophila Cka involved in the Jun kinase pathway | DDB0232432 | CDS | 1395012 | 2484 | + | 0.288647 |
stt3 | DDB_G0285159 | CAZy family GT66 subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST1 contains 13 transmembrane domains | DDB0232431 | CDS | 2899851 | 2145 | + | 0.359441 |
sugt1 | DDB_G0269292 | ortholog of S. cerevisiae SGT1 and mammalian SUGT1 associated with the SCF (Skp1pCdc53pF box protein) ubiquitin ligase complex | DDB0232428 | CDS | 2470067 | 1164 | + | 0.293814 |
sumo | DDB_G0286189 | sumoylates the MAP kinase kinase Mek1 (mekA) sumoylation is involved in cellular translocation after cAMP stimulation and activation of the kinase | DDB0232431 | CDS | 4217038 | 297 | + | 0.356902 |
sun1 | DDB_G0272869 | localizes to the inner and outer nuclear membrane mediates the attachment between centrosome and nucleus associates the centromere cluster with the centrosome and stabilizes the genome during mitosis contains one transmembrane domain | DDB0232429 | CDS | 2057584 | 2718 | - | 0.270419 |
sunB | DDB_G0285925 | SUN-like protein with a centrally located domain contains a predicted N-terminal signal sequence | DDB0232431 | CDS | 3835569 | 3837 | + | 0.250195 |
suox | DDB_G0278893 | catalyzes the reaction sulfite Osub2sub Hsub2subO sulfate Hsub2subOsub2subbr ortholog of H. sapiens SUOX of which defects cause isolated sulfite oxidase deficiency (ISOD) characterized by neurological abnormalities requires molybdopterin cofactor | DDB0232430 | CDS | 1346298 | 1197 | - | 0.324144 |
surf1-1 | DDB_G0272889 | ortholog of SURF1 encoding a factor involved in the biogenesis of cytochrome c oxidase mutated in Leigh syndrome there is a second copy of this gene | DDB0232429 | CDS | 2379312 | 813 | - | 0.280443 |
surf1-2 | DDB_G0274001 | ortholog of SURF1 encoding a factor involved in the biogenesis of cytochrome c oxidase mutated in Leigh syndrome there is a second copy of this gene | DDB0232429 | CDS | 3651662 | 813 | + | 0.280443 |
suvA | DDB_G0269554 | the D. melanogaster ortholog su(var)3-9 has a central role in heterochromatin-induced gene silencing | DDB0232428 | CDS | 2983180 | 4605 | + | 0.283388 |
svkA | DDB_G0286359 | very similar to mammalian ST25 kinase (SOK1) and other STE20-like kinases stress-responsive kinase phosphorylates severin essential for cell separation during cytokinesis | DDB0232431 | CDS | 4476218 | 1437 | + | 0.343076 |
swi3 | DDB_G0277033 | similar to H. sapiens SWISNF subunit SMARCC1 and the yeast subunit SWI3 of the chromatin remodeling complex | DDB0232429 | CDS | 7295274 | 3672 | - | 0.301471 |
swip | DDB_G0283355 | DDB0232431 | CDS | 559359 | 3408 | - | 0.314847 | |
swp1 | DDB_G0289479 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae SWP1 and human ribophorin II contains three putative C-terminal transmembrane domains and an N-terminal signal peptide | DDB0232432 | CDS | 2823825 | 2058 | - | 0.336249 |
sybA | DDB_G0280061 | DDB0232430 | CDS | 2954586 | 288 | + | 0.284722 | |
sybB | DDB_G0290363 | very similar to sybA a gene that is regulated by the MADS-box transcription factor SrfA during development | DDB0232432 | CDS | 3879007 | 306 | + | 0.251634 |
syf2 | DDB_G0284573 | D. discoideum SYF2 homolog SYF2 proteins are involved in cell cycle progression and pre-mRNA splicing | DDB0232431 | CDS | 2172315 | 882 | + | 0.250567 |
symA | DDB_G0292814 | DDB0232433 | CDS | 2158906 | 1371 | - | 0.33698 | |
sympk | DDB_G0284319 | in mammals symplekin is a component of the tight junction plaque but has also been detected in a wide range of cell types that do not form tight junctions may be required for pre-mRNA polyadenylation | DDB0232431 | CDS | 1741477 | 4482 | + | 0.280455 |
syn10 | DDB_G0284385 | similar to syntaxin a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232431 | CDS | 1923544 | 774 | - | 0.31137 |
syn16A | DDB_G0276575 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232429 | CDS | 6993306 | 945 | + | 0.256085 |
syn16B | DDB_G0276469 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232429 | CDS | 6988936 | 1008 | + | 0.249008 |
syn1A | DDB_G0289379 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232432 | CDS | 2678322 | 1002 | - | 0.297405 |
syn1B | DDB_G0270556 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232428 | CDS | 2999912 | 1005 | + | 0.250746 |
syn5 | DDB_G0277565 | similar to syntaxin 5 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232429 | CDS | 8154194 | 909 | - | 0.265127 |
syn6 | DDB_G0284185 | similar to syntaxin a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232431 | CDS | 1791019 | 696 | + | 0.178161 |
syn7A | DDB_G0287733 | member of the SNARE family (Soluble NSF Attachment Protein REceptor) plays a role in endosomal fusion | DDB0232432 | CDS | 617723 | 1071 | + | 0.289449 |
syn7B | DDB_G0279133 | DDB0232430 | CDS | 1672697 | 861 | + | 0.271777 | |
syn8A | DDB_G0275429 | member of the SNARE family (Soluble NSF Attachment Protein REceptor) localizes to endosome and interacts with syn7A | DDB0232429 | CDS | 5478950 | 459 | + | 0.259259 |
syn8B | DDB_G0288439 | DDB0232432 | CDS | 1539443 | 753 | - | 0.26162 | |
tRNA-Ala-AGC-1 | DDB_G0294775 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3431190 | 73 | - | 0.534247 |
tRNA-Ala-AGC-10 | DDB_G0295297 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 254727 | 73 | - | 0.534247 |
tRNA-Ala-AGC-11 | DDB_G0295361 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3132339 | 73 | + | 0.534247 |
tRNA-Ala-AGC-12 | DDB_G0295415 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2625762 | 73 | - | 0.534247 |
tRNA-Ala-AGC-13 | DDB_G0295419 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2624351 | 73 | - | 0.534247 |
tRNA-Ala-AGC-14 | DDB_G0295425 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2479676 | 73 | - | 0.534247 |
tRNA-Ala-AGC-15 | DDB_G0295449 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1529428 | 73 | - | 0.534247 |
tRNA-Ala-AGC-2 | DDB_G0294881 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7122699 | 73 | + | 0.534247 |
tRNA-Ala-AGC-3 | DDB_G0294899 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 8141487 | 73 | + | 0.534247 |
tRNA-Ala-AGC-4 | DDB_G0294903 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 8364904 | 73 | + | 0.534247 |
tRNA-Ala-AGC-5 | DDB_G0295043 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4014778 | 73 | + | 0.534247 |
tRNA-Ala-AGC-6 | DDB_G0295045 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4067961 | 73 | + | 0.534247 |
tRNA-Ala-AGC-7 | DDB_G0295139 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 3993886 | 73 | - | 0.534247 |
tRNA-Ala-AGC-8 | DDB_G0295209 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3947721 | 73 | - | 0.534247 |
tRNA-Ala-AGC-9 | DDB_G0295239 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2265374 | 73 | + | 0.534247 |
tRNA-Ala-UGC-1 | DDB_G0294763 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4185581 | 96 | - | 0.427083 |
tRNA-Ala-UGC-2 | DDB_G0294885 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7430263 | 96 | + | 0.4375 |
tRNA-Ala-UGC-3 | DDB_G0294919 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7434539 | 96 | - | 0.4375 |
tRNA-Ala-UGC-4 | DDB_G0295047 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4194528 | 96 | + | 0.4375 |
tRNA-Ala-UGC-5 | DDB_G0295129 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4297271 | 96 | - | 0.4375 |
tRNA-Ala-UGC-6 | DDB_G0295137 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4090199 | 96 | - | 0.447917 |
tRNA-Ala-UGC-7 | DDB_G0295207 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 4682789 | 96 | - | 0.427083 |
tRNA-Ala-UGC-8 | DDB_G0295267 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3987062 | 96 | - | 0.427083 |
tRNA-Arg-ACG-1 | DDB_G0294703 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2023312 | 74 | + | 0.527027 |
tRNA-Arg-ACG-2 | DDB_G0294815 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1760348 | 74 | - | 0.527027 |
tRNA-Arg-ACG-3 | DDB_G0294869 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6386977 | 74 | + | 0.527027 |
tRNA-Arg-ACG-4 | DDB_G0294889 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7473728 | 74 | + | 0.527027 |
tRNA-Arg-ACG-5 | DDB_G0294911 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7837550 | 74 | - | 0.527027 |
tRNA-Arg-ACG-6 | DDB_G0294933 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6724130 | 74 | - | 0.527027 |
tRNA-Arg-ACG-7 | DDB_G0295145 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2876124 | 74 | - | 0.527027 |
tRNA-Arg-CCU-1 | DDB_G0295385 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3587001 | 74 | - | 0.486486 |
tRNA-Arg-UCG-1 | DDB_G0295159 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 1773594 | 74 | - | 0.486486 |
tRNA-Arg-UCU-10 | DDB_G0295143 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 3102884 | 73 | - | 0.561644 |
tRNA-Arg-UCU-11 | DDB_G0295257 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3693576 | 73 | + | 0.561644 |
tRNA-Arg-UCU-12 | DDB_G0295281 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2593624 | 73 | - | 0.561644 |
tRNA-Arg-UCU-2 | DDB_G0294829 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 618267 | 73 | + | 0.561644 |
tRNA-Arg-UCU-3 | DDB_G0294865 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6187314 | 73 | + | 0.561644 |
tRNA-Arg-UCU-4 | DDB_G0294875 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6640387 | 73 | + | 0.561644 |
tRNA-Arg-UCU-5 | DDB_G0294939 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6647152 | 73 | - | 0.561644 |
tRNA-Arg-UCU-6 | DDB_G0294947 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6227029 | 73 | - | 0.561644 |
tRNA-Arg-UCU-7 | DDB_G0295101 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5654004 | 73 | - | 0.561644 |
tRNA-Arg-UCU-8 | DDB_G0295113 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5126146 | 73 | - | 0.561644 |
tRNA-Arg-UCU-9 | DDB_G0295119 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4567934 | 73 | - | 0.561644 |
tRNA-Asn-GUU-10 | DDB_G0295015 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 1045240 | 73 | + | 0.60274 |
tRNA-Asn-GUU-11 | DDB_G0295021 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2443914 | 73 | + | 0.60274 |
tRNA-Asn-GUU-12 | DDB_G0295031 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 3060646 | 73 | + | 0.60274 |
tRNA-Asn-GUU-13 | DDB_G0295217 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3320206 | 73 | - | 0.60274 |
tRNA-Asn-GUU-14 | DDB_G0295241 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2321011 | 73 | + | 0.60274 |
tRNA-Asn-GUU-15 | DDB_G0295285 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 1592074 | 73 | - | 0.60274 |
tRNA-Asn-GUU-16 | DDB_G0295317 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1833377 | 73 | + | 0.60274 |
tRNA-Asn-GUU-17 | DDB_G0295369 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3182148 | 73 | + | 0.60274 |
tRNA-Asn-GUU-18 | DDB_G0295371 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3235027 | 73 | + | 0.60274 |
tRNA-Asn-GUU-19 | DDB_G0295441 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1801506 | 73 | - | 0.60274 |
tRNA-Asn-GUU-2 | DDB_G0294685 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1632774 | 73 | + | 0.60274 |
tRNA-Asn-GUU-3 | DDB_G0294695 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1956750 | 73 | + | 0.60274 |
tRNA-Asn-GUU-4 | DDB_G0294697 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1970455 | 73 | + | 0.60274 |
tRNA-Asn-GUU-5 | DDB_G0294737 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3579771 | 73 | + | 0.60274 |
tRNA-Asn-GUU-6 | DDB_G0294777 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3431040 | 73 | - | 0.60274 |
tRNA-Asn-GUU-7 | DDB_G0294797 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2390365 | 73 | - | 0.60274 |
tRNA-Asn-GUU-8 | DDB_G0294827 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 750033 | 73 | - | 0.60274 |
tRNA-Asn-GUU-9 | DDB_G0294953 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5934172 | 73 | - | 0.60274 |
tRNA-Asp-GUC-1 | DDB_G0294707 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2278096 | 72 | + | 0.569444 |
tRNA-Asp-GUC-10 | DDB_G0294917 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7675988 | 72 | - | 0.569444 |
tRNA-Asp-GUC-11 | DDB_G0294973 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5197716 | 72 | - | 0.569444 |
tRNA-Asp-GUC-12 | DDB_G0295175 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2841024 | 72 | + | 0.569444 |
tRNA-Asp-GUC-13 | DDB_G0295177 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3073029 | 72 | + | 0.569444 |
tRNA-Asp-GUC-14 | DDB_G0295185 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3942404 | 72 | + | 0.569444 |
tRNA-Asp-GUC-15 | DDB_G0295213 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3919822 | 72 | - | 0.569444 |
tRNA-Asp-GUC-16 | DDB_G0295221 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3057091 | 72 | - | 0.569444 |
tRNA-Asp-GUC-17 | DDB_G0295223 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3029253 | 72 | - | 0.569444 |
tRNA-Asp-GUC-18 | DDB_G0295225 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2845703 | 72 | - | 0.569444 |
tRNA-Asp-GUC-19 | DDB_G0295263 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 4005478 | 72 | + | 0.569444 |
tRNA-Asp-GUC-2 | DDB_G0294739 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3865846 | 72 | + | 0.569444 |
tRNA-Asp-GUC-20 | DDB_G0295279 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2728188 | 72 | - | 0.569444 |
tRNA-Asp-GUC-21 | DDB_G0295345 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2777486 | 72 | + | 0.569444 |
tRNA-Asp-GUC-22 | DDB_G0295401 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3008610 | 72 | - | 0.569444 |
tRNA-Asp-GUC-3 | DDB_G0294743 | DDB0232428 | CDS | 4201373 | 72 | + | 0.569444 | |
tRNA-Asp-GUC-4 | DDB_G0294759 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4250554 | 72 | - | 0.569444 |
tRNA-Asp-GUC-5 | DDB_G0294761 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4249798 | 72 | - | 0.569444 |
tRNA-Asp-GUC-6 | DDB_G0294803 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2265532 | 72 | - | 0.569444 |
tRNA-Asp-GUC-7 | DDB_G0294809 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2099322 | 72 | - | 0.569444 |
tRNA-Asp-GUC-8 | DDB_G0294863 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6132328 | 72 | + | 0.569444 |
tRNA-Asp-GUC-9 | DDB_G0294915 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7715120 | 72 | - | 0.569444 |
tRNA-Cys-GCA-1 | DDB_G0294677 | transfers a cysteine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 818921 | 72 | + | 0.5 |
tRNA-Cys-GCA-2 | DDB_G0295019 | transfers a cysteine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2330677 | 72 | + | 0.5 |
tRNA-Cys-GCA-3 | DDB_G0295023 | transfers a cysteine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2450297 | 72 | + | 0.5 |
tRNA-Cys-GCA-4 | DDB_G0295025 | transfers a cysteine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2632482 | 72 | + | 0.5 |
tRNA-Cys-GCA-5 | DDB_G0295161 | transfers a cysteine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 1671338 | 72 | - | 0.5 |
tRNA-Cys-GCA-6 | DDB_G0295163 | transfers a cysteine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 1574082 | 72 | - | 0.5 |
tRNA-Cys-GCA-7 | DDB_G0295333 | transfers a cysteine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2258615 | 72 | + | 0.5 |
tRNA-Cys-GCA-8 | DDB_G0295447 | transfers a cysteine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1664089 | 72 | - | 0.5 |
tRNA-Gln-CUG-1 | DDB_G0294975 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5171836 | 89 | - | 0.438202 |
tRNA-Gln-UUG-10 | DDB_G0294985 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 3853359 | 73 | - | 0.410959 |
tRNA-Gln-UUG-11 | DDB_G0295035 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 3366146 | 73 | + | 0.410959 |
tRNA-Gln-UUG-12 | DDB_G0295237 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 1989890 | 73 | + | 0.410959 |
tRNA-Gln-UUG-13 | DDB_G0295309 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1453608 | 73 | + | 0.410959 |
tRNA-Gln-UUG-14 | DDB_G0295335 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2286132 | 73 | + | 0.410959 |
tRNA-Gln-UUG-2 | DDB_G0294711 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2371018 | 73 | + | 0.410959 |
tRNA-Gln-UUG-3 | DDB_G0294729 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2850044 | 73 | + | 0.410959 |
tRNA-Gln-UUG-4 | DDB_G0294787 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2855252 | 73 | - | 0.410959 |
tRNA-Gln-UUG-5 | DDB_G0294799 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2370125 | 73 | - | 0.410959 |
tRNA-Gln-UUG-6 | DDB_G0294833 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 1825599 | 73 | + | 0.410959 |
tRNA-Gln-UUG-7 | DDB_G0294935 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6705104 | 73 | - | 0.410959 |
tRNA-Gln-UUG-8 | DDB_G0294945 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6364519 | 73 | - | 0.410959 |
tRNA-Gln-UUG-9 | DDB_G0294955 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5907958 | 73 | - | 0.410959 |
tRNA-Glu-CUC-1 | DDB_G0295063 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5321663 | 72 | + | 0.555556 |
tRNA-Glu-CUC-2 | DDB_G0295339 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2365116 | 72 | + | 0.555556 |
tRNA-Glu-CUC-3 | DDB_G0295427 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2478517 | 72 | - | 0.555556 |
tRNA-Glu-UUC-10 | DDB_G0294989 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 3533566 | 72 | - | 0.513889 |
tRNA-Glu-UUC-11 | DDB_G0295041 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 3889342 | 72 | + | 0.513889 |
tRNA-Glu-UUC-12 | DDB_G0295149 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2675536 | 72 | - | 0.513889 |
tRNA-Glu-UUC-13 | DDB_G0295155 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2156654 | 72 | - | 0.513889 |
tRNA-Glu-UUC-14 | DDB_G0295271 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3245733 | 72 | - | 0.513889 |
tRNA-Glu-UUC-15 | DDB_G0295299 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 323423 | 72 | + | 0.513889 |
tRNA-Glu-UUC-16 | DDB_G0295329 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2120506 | 72 | + | 0.513889 |
tRNA-Glu-UUC-17 | DDB_G0295357 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3053148 | 72 | + | 0.513889 |
tRNA-Glu-UUC-18 | DDB_G0295395 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3291634 | 72 | - | 0.513889 |
tRNA-Glu-UUC-19 | DDB_G0295399 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3069439 | 72 | - | 0.513889 |
tRNA-Glu-UUC-2 | DDB_G0294709 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2366931 | 72 | + | 0.513889 |
tRNA-Glu-UUC-20 | DDB_G0295413 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2730062 | 72 | - | 0.513889 |
tRNA-Glu-UUC-3 | DDB_G0294723 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2687279 | 72 | + | 0.513889 |
tRNA-Glu-UUC-4 | DDB_G0294783 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3008412 | 72 | - | 0.513889 |
tRNA-Glu-UUC-5 | DDB_G0294789 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2698672 | 72 | - | 0.513889 |
tRNA-Glu-UUC-6 | DDB_G0294801 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2368298 | 72 | - | 0.513889 |
tRNA-Glu-UUC-7 | DDB_G0294837 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 2498149 | 72 | + | 0.513889 |
tRNA-Glu-UUC-8 | DDB_G0294961 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5454647 | 72 | - | 0.513889 |
tRNA-Glu-UUC-9 | DDB_G0294963 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5452266 | 72 | - | 0.513889 |
tRNA-Gly-GCC-1 | DDB_G0294981 | DDB0232429 | CDS | 4356024 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-10 | DDB_G0295157 | DDB0232430 | CDS | 2103501 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-11 | DDB_G0295219 | DDB0232431 | CDS | 3320060 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-12 | DDB_G0295235 | DDB0232432 | CDS | 284121 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-13 | DDB_G0295291 | DDB0232432 | CDS | 409584 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-14 | DDB_G0295303 | DDB0232433 | CDS | 859158 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-15 | DDB_G0295319 | DDB0232433 | CDS | 1836361 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-16 | DDB_G0295323 | DDB0232433 | CDS | 1912886 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-17 | DDB_G0295433 | DDB0232433 | CDS | 1927240 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-18 | DDB_G0295439 | DDB0232433 | CDS | 1837565 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-2 | DDB_G0294983 | DDB0232429 | CDS | 4109270 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-3 | DDB_G0295005 | DDB0232429 | CDS | 996180 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-4 | DDB_G0295029 | DDB0232430 | CDS | 2940647 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-5 | DDB_G0295037 | DDB0232430 | CDS | 3875955 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-6 | DDB_G0295039 | DDB0232430 | CDS | 3876679 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-7 | DDB_G0295053 | DDB0232430 | CDS | 4413344 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-8 | DDB_G0295121 | DDB0232430 | CDS | 4565971 | 71 | - | 0.549296 | |
tRNA-Gly-GCC-9 | DDB_G0295125 | DDB0232430 | CDS | 4400356 | 71 | - | 0.549296 | |
tRNA-Gly-UCC-1 | DDB_G0295049 | DDB0232430 | CDS | 4240788 | 71 | + | 0.535211 | |
tRNA-Gly-UCC-2 | DDB_G0295095 | DDB0232430 | CDS | 5706954 | 71 | - | 0.535211 | |
tRNA-Gly-UCC-3 | DDB_G0295097 | DDB0232430 | CDS | 5706517 | 71 | - | 0.535211 | |
tRNA-Gly-UCC-4 | DDB_G0295111 | DDB0232430 | CDS | 5325920 | 71 | - | 0.535211 | |
tRNA-Gly-UCC-5 | DDB_G0295135 | DDB0232430 | CDS | 4247160 | 71 | - | 0.535211 | |
tRNA-His-GUG-10 | DDB_G0295437 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1837996 | 71 | - | 0.521127 |
tRNA-His-GUG-2 | DDB_G0294901 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 8290826 | 71 | + | 0.521127 |
tRNA-His-GUG-3 | DDB_G0294905 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 8084436 | 71 | - | 0.521127 |
tRNA-His-GUG-4 | DDB_G0294951 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5947196 | 71 | - | 0.521127 |
tRNA-His-GUG-5 | DDB_G0294971 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5290018 | 71 | - | 0.521127 |
tRNA-His-GUG-6 | DDB_G0295013 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 549066 | 71 | + | 0.521127 |
tRNA-His-GUG-7 | DDB_G0295151 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2623274 | 71 | - | 0.521127 |
tRNA-His-GUG-8 | DDB_G0295353 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2840392 | 71 | + | 0.521127 |
tRNA-His-GUG-9 | DDB_G0295367 | transfers a histidine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3173627 | 71 | + | 0.521127 |
tRNA-Ile-AAU-1 | DDB_G0294741 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4125226 | 73 | + | 0.589041 |
tRNA-Ile-AAU-10 | DDB_G0295169 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 1879566 | 73 | + | 0.589041 |
tRNA-Ile-AAU-11 | DDB_G0295293 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 278611 | 73 | - | 0.589041 |
tRNA-Ile-AAU-12 | DDB_G0295307 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1374085 | 73 | + | 0.589041 |
tRNA-Ile-AAU-13 | DDB_G0295347 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2784596 | 73 | + | 0.589041 |
tRNA-Ile-AAU-14 | DDB_G0295363 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3133759 | 73 | + | 0.589041 |
tRNA-Ile-AAU-15 | DDB_G0295381 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3534943 | 73 | + | 0.589041 |
tRNA-Ile-AAU-16 | DDB_G0295407 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2936034 | 73 | - | 0.589041 |
tRNA-Ile-AAU-17 | DDB_G0295465 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1013913 | 73 | - | 0.589041 |
tRNA-Ile-AAU-2 | DDB_G0294751 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4562415 | 73 | - | 0.589041 |
tRNA-Ile-AAU-3 | DDB_G0294753 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4551714 | 73 | - | 0.589041 |
tRNA-Ile-AAU-4 | DDB_G0294765 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4163571 | 73 | - | 0.589041 |
tRNA-Ile-AAU-5 | DDB_G0294781 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3256805 | 73 | - | 0.589041 |
tRNA-Ile-AAU-6 | DDB_G0294831 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 1492518 | 73 | + | 0.589041 |
tRNA-Ile-AAU-7 | DDB_G0294893 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7651928 | 73 | + | 0.589041 |
tRNA-Ile-AAU-8 | DDB_G0295085 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 6072152 | 73 | + | 0.589041 |
tRNA-Ile-AAU-9 | DDB_G0295147 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2700535 | 73 | - | 0.589041 |
tRNA-Ile-UAU-1 | DDB_G0295373 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3312699 | 91 | + | 0.428571 |
tRNA-Ile-UAU-2 | DDB_G0295393 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3299859 | 91 | - | 0.428571 |
tRNA-Ile-UAU-3 | DDB_G0295409 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2771961 | 91 | - | 0.43956 |
tRNA-Ile-UAU-4 | DDB_G0295411 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2770337 | 91 | - | 0.43956 |
tRNA-Leu-AAG-1 | DDB_G0294913 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7738676 | 82 | - | 0.463415 |
tRNA-Leu-AAG-10 | DDB_G0295349 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2836863 | 82 | + | 0.463415 |
tRNA-Leu-AAG-11 | DDB_G0295391 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3407225 | 82 | - | 0.463415 |
tRNA-Leu-AAG-2 | DDB_G0295057 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4523794 | 82 | + | 0.463415 |
tRNA-Leu-AAG-3 | DDB_G0295091 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5937248 | 82 | - | 0.463415 |
tRNA-Leu-AAG-4 | DDB_G0295199 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5435309 | 82 | + | 0.463415 |
tRNA-Leu-AAG-5 | DDB_G0295201 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5435936 | 82 | + | 0.463415 |
tRNA-Leu-AAG-6 | DDB_G0295283 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2550132 | 82 | - | 0.463415 |
tRNA-Leu-AAG-7 | DDB_G0295289 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 432078 | 82 | - | 0.463415 |
tRNA-Leu-AAG-8 | DDB_G0295325 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2082530 | 82 | + | 0.451219 |
tRNA-Leu-AAG-9 | DDB_G0295341 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2728442 | 82 | + | 0.463415 |
tRNA-Leu-CAA-1 | DDB_G0294859 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5492551 | 81 | + | 0.45679 |
tRNA-Leu-CAA-2 | DDB_G0294943 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6482159 | 81 | - | 0.45679 |
tRNA-Leu-CAA-3 | DDB_G0294959 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5489684 | 81 | - | 0.518519 |
tRNA-Leu-CAA-4 | DDB_G0295471 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 310825 | 81 | - | 0.45679 |
tRNA-Leu-CAG-1 | DDB_G0294923 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7144841 | 84 | - | 0.511905 |
tRNA-Leu-UAA-1 | DDB_G0294841 | transfers a leucine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 2661584 | 83 | + | 0.481928 |
tRNA-Leu-UAA-10 | DDB_G0295123 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4511889 | 83 | - | 0.481928 |
tRNA-Leu-UAA-11 | DDB_G0295195 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5168273 | 83 | + | 0.481928 |
tRNA-Leu-UAA-12 | DDB_G0295203 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5226859 | 83 | - | 0.481928 |
tRNA-Leu-UAA-13 | DDB_G0295313 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1776201 | 83 | + | 0.481928 |
tRNA-Leu-UAA-14 | DDB_G0295387 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3448553 | 83 | - | 0.481928 |
tRNA-Leu-UAA-15 | DDB_G0295389 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3431954 | 83 | - | 0.481928 |
tRNA-Leu-UAA-16 | DDB_G0295417 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2624493 | 83 | - | 0.481928 |
tRNA-Leu-UAA-17 | DDB_G0295435 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1870453 | 83 | - | 0.481928 |
tRNA-Leu-UAA-18 | DDB_G0295463 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1044809 | 83 | - | 0.481928 |
tRNA-Leu-UAA-2 | DDB_G0294849 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 4103357 | 83 | + | 0.481928 |
tRNA-Leu-UAA-3 | DDB_G0294909 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7871755 | 83 | - | 0.481928 |
tRNA-Leu-UAA-4 | DDB_G0294925 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6948162 | 83 | - | 0.481928 |
tRNA-Leu-UAA-5 | DDB_G0294941 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6646491 | 83 | - | 0.481928 |
tRNA-Leu-UAA-6 | DDB_G0294993 | transfers a leucine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 3370120 | 83 | - | 0.481928 |
tRNA-Leu-UAA-7 | DDB_G0295055 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4458032 | 83 | + | 0.481928 |
tRNA-Leu-UAA-8 | DDB_G0295059 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4606291 | 83 | + | 0.481928 |
tRNA-Leu-UAA-9 | DDB_G0295117 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4613433 | 83 | - | 0.481928 |
tRNA-Leu-UAG-1 | DDB_G0294847 | transfers a leucine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 3524835 | 79 | + | 0.544304 |
tRNA-Leu-UAG-2 | DDB_G0294999 | transfers a leucine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 2506873 | 79 | - | 0.544304 |
tRNA-Leu-UAG-3 | DDB_G0295469 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 604764 | 80 | - | 0.5 |
tRNA-Lys-CUU-1 | DDB_G0294691 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1759767 | 73 | + | 0.671233 |
tRNA-Lys-CUU-10 | DDB_G0295405 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2954533 | 73 | - | 0.671233 |
tRNA-Lys-CUU-2 | DDB_G0294725 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2697090 | 73 | + | 0.671233 |
tRNA-Lys-CUU-3 | DDB_G0294791 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2560506 | 73 | - | 0.671233 |
tRNA-Lys-CUU-4 | DDB_G0294967 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5400772 | 73 | - | 0.671233 |
tRNA-Lys-CUU-5 | DDB_G0295051 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4266691 | 73 | + | 0.671233 |
tRNA-Lys-CUU-6 | DDB_G0295067 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5652919 | 73 | + | 0.671233 |
tRNA-Lys-CUU-7 | DDB_G0295265 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 4947710 | 73 | - | 0.671233 |
tRNA-Lys-CUU-8 | DDB_G0295355 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2985396 | 73 | + | 0.671233 |
tRNA-Lys-CUU-9 | DDB_G0295403 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2956996 | 73 | - | 0.671233 |
tRNA-Lys-UUU-10 | DDB_G0295133 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4268093 | 73 | - | 0.616438 |
tRNA-Lys-UUU-11 | DDB_G0295141 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 3574246 | 73 | - | 0.616438 |
tRNA-Lys-UUU-12 | DDB_G0295165 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 1431187 | 73 | - | 0.616438 |
tRNA-Lys-UUU-13 | DDB_G0295167 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 1112773 | 73 | - | 0.616438 |
tRNA-Lys-UUU-14 | DDB_G0295187 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3970863 | 73 | + | 0.616438 |
tRNA-Lys-UUU-15 | DDB_G0295229 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 1802373 | 73 | - | 0.616438 |
tRNA-Lys-UUU-16 | DDB_G0295233 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 40886 | 73 | + | 0.616438 |
tRNA-Lys-UUU-17 | DDB_G0295243 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2727390 | 73 | + | 0.616438 |
tRNA-Lys-UUU-18 | DDB_G0295245 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2768640 | 73 | + | 0.616438 |
tRNA-Lys-UUU-19 | DDB_G0295275 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3113136 | 73 | - | 0.616438 |
tRNA-Lys-UUU-2 | DDB_G0294671 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 448541 | 71 | + | 0.56338 |
tRNA-Lys-UUU-20 | DDB_G0295315 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1794634 | 73 | + | 0.616438 |
tRNA-Lys-UUU-21 | DDB_G0295365 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3141444 | 73 | + | 0.616438 |
tRNA-Lys-UUU-22 | DDB_G0295397 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3137397 | 73 | - | 0.616438 |
tRNA-Lys-UUU-23 | DDB_G0295445 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1703275 | 73 | - | 0.616438 |
tRNA-Lys-UUU-3 | DDB_G0294713 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2398344 | 73 | + | 0.616438 |
tRNA-Lys-UUU-4 | DDB_G0294719 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2503577 | 73 | + | 0.616438 |
tRNA-Lys-UUU-5 | DDB_G0294731 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2877753 | 73 | + | 0.616438 |
tRNA-Lys-UUU-6 | DDB_G0294767 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4158870 | 73 | - | 0.616438 |
tRNA-Lys-UUU-7 | DDB_G0294927 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6863248 | 73 | - | 0.616438 |
tRNA-Lys-UUU-8 | DDB_G0294977 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 4989791 | 73 | - | 0.616438 |
tRNA-Lys-UUU-9 | DDB_G0295131 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4270315 | 73 | - | 0.616438 |
tRNA-Met-CAU-10 | DDB_G0294991 | transfers a methionine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 3515101 | 72 | - | 0.513889 |
tRNA-Met-CAU-11 | DDB_G0294997 | transfers a methionine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 2513207 | 72 | - | 0.513889 |
tRNA-Met-CAU-12 | DDB_G0295115 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4660155 | 72 | - | 0.513889 |
tRNA-Met-CAU-13 | DDB_G0295251 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3259687 | 73 | + | 0.493151 |
tRNA-Met-CAU-14 | DDB_G0295261 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3845621 | 73 | + | 0.520548 |
tRNA-Met-CAU-15 | DDB_G0295295 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 268971 | 73 | - | 0.493151 |
tRNA-Met-CAU-16 | DDB_G0295351 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2840202 | 73 | + | 0.493151 |
tRNA-Met-CAU-17 | DDB_G0295431 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1948217 | 72 | - | 0.513889 |
tRNA-Met-CAU-3 | DDB_G0294705 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2166447 | 72 | + | 0.513889 |
tRNA-Met-CAU-4 | DDB_G0294805 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2164854 | 72 | - | 0.513889 |
tRNA-Met-CAU-5 | DDB_G0294839 | transfers a methionine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 2516614 | 72 | + | 0.513889 |
tRNA-Met-CAU-6 | DDB_G0294845 | transfers a methionine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 3518508 | 72 | + | 0.513889 |
tRNA-Met-CAU-7 | DDB_G0294965 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5416778 | 73 | - | 0.493151 |
tRNA-Met-CAU-8 | DDB_G0294969 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5314110 | 73 | - | 0.493151 |
tRNA-Met-CAU-9 | DDB_G0294979 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 4972878 | 73 | - | 0.493151 |
tRNA-Phe-GAA-10 | DDB_G0295127 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 4353450 | 74 | - | 0.554054 |
tRNA-Phe-GAA-11 | DDB_G0295173 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2563537 | 74 | + | 0.554054 |
tRNA-Phe-GAA-12 | DDB_G0295189 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 4598294 | 74 | + | 0.554054 |
tRNA-Phe-GAA-13 | DDB_G0295193 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 4999193 | 74 | + | 0.554054 |
tRNA-Phe-GAA-14 | DDB_G0295377 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3387585 | 74 | + | 0.554054 |
tRNA-Phe-GAA-15 | DDB_G0295383 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3574106 | 74 | + | 0.540541 |
tRNA-Phe-GAA-16 | DDB_G0295467 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 898266 | 74 | - | 0.554054 |
tRNA-Phe-GAA-3 | DDB_G0294835 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 2492015 | 74 | + | 0.554054 |
tRNA-Phe-GAA-4 | DDB_G0294853 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 4981255 | 74 | + | 0.554054 |
tRNA-Phe-GAA-5 | DDB_G0294877 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6766972 | 74 | + | 0.554054 |
tRNA-Phe-GAA-6 | DDB_G0294883 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7187981 | 74 | + | 0.554054 |
tRNA-Phe-GAA-7 | DDB_G0294929 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6771686 | 74 | - | 0.554054 |
tRNA-Phe-GAA-8 | DDB_G0294987 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 3539698 | 74 | - | 0.554054 |
tRNA-Phe-GAA-9 | DDB_G0295001 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 1465351 | 74 | - | 0.554054 |
tRNA-Pro-AGG-1 | DDB_G0295321 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1869424 | 71 | + | 0.422535 |
tRNA-Pro-UGG-10 | DDB_G0295003 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 1365573 | 71 | - | 0.492958 |
tRNA-Pro-UGG-11 | DDB_G0295065 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5518229 | 71 | + | 0.492958 |
tRNA-Pro-UGG-12 | DDB_G0295103 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5519054 | 71 | - | 0.492958 |
tRNA-Pro-UGG-13 | DDB_G0295247 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2956680 | 71 | + | 0.492958 |
tRNA-Pro-UGG-14 | DDB_G0295277 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2970447 | 71 | - | 0.492958 |
tRNA-Pro-UGG-15 | DDB_G0295453 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1299996 | 71 | - | 0.492958 |
tRNA-Pro-UGG-16 | DDB_G0295455 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1250562 | 71 | - | 0.492958 |
tRNA-Pro-UGG-2 | DDB_G0294679 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 835755 | 71 | + | 0.492958 |
tRNA-Pro-UGG-3 | DDB_G0294681 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 843216 | 71 | + | 0.492958 |
tRNA-Pro-UGG-4 | DDB_G0294779 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3314085 | 71 | - | 0.492958 |
tRNA-Pro-UGG-5 | DDB_G0294817 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1618454 | 71 | - | 0.492958 |
tRNA-Pro-UGG-6 | DDB_G0294819 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1615509 | 71 | - | 0.492958 |
tRNA-Pro-UGG-7 | DDB_G0294879 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7004296 | 71 | + | 0.492958 |
tRNA-Pro-UGG-8 | DDB_G0294891 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7524451 | 71 | + | 0.492958 |
tRNA-Pro-UGG-9 | DDB_G0294931 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6771543 | 71 | - | 0.492958 |
tRNA-Sec-UGA | DDB_G0302695 | transfers an selenocysteine residue to a growing polypeptide chain during protein synthesis opposite some TGA codons there are several selenoproteins in Dictyostelium | DDB0232431 | CDS | 2475153 | 81 | + | 0.506173 |
tRNA-Ser-AGA-1 | DDB_G0294721 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2558667 | 82 | + | 0.548781 |
tRNA-Ser-AGA-2 | DDB_G0294851 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 4399881 | 82 | + | 0.548781 |
tRNA-Ser-AGA-3 | DDB_G0294867 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6379305 | 82 | + | 0.548781 |
tRNA-Ser-AGA-4 | DDB_G0294873 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6571351 | 82 | + | 0.548781 |
tRNA-Ser-AGA-5 | DDB_G0294907 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7878701 | 82 | - | 0.548781 |
tRNA-Ser-AGA-6 | DDB_G0294921 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7237204 | 82 | - | 0.548781 |
tRNA-Ser-AGA-7 | DDB_G0295033 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 3143611 | 82 | + | 0.548781 |
tRNA-Ser-AGA-8 | DDB_G0295153 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2539790 | 82 | - | 0.548781 |
tRNA-Ser-AGA-9 | DDB_G0295337 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2340655 | 82 | + | 0.548781 |
tRNA-Ser-CGA-1 | DDB_G0295099 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5679957 | 96 | - | 0.479167 |
tRNA-Ser-GCU-1 | DDB_G0294717 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2414216 | 81 | + | 0.592593 |
tRNA-Ser-GCU-10 | DDB_G0295171 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2227631 | 81 | + | 0.592593 |
tRNA-Ser-GCU-11 | DDB_G0295227 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2220197 | 81 | - | 0.592593 |
tRNA-Ser-GCU-12 | DDB_G0295429 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2347717 | 81 | - | 0.592593 |
tRNA-Ser-GCU-2 | DDB_G0294793 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2424793 | 81 | - | 0.592593 |
tRNA-Ser-GCU-3 | DDB_G0295075 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5898457 | 81 | + | 0.592593 |
tRNA-Ser-GCU-4 | DDB_G0295077 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5902871 | 81 | + | 0.592593 |
tRNA-Ser-GCU-5 | DDB_G0295079 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5906903 | 81 | + | 0.592593 |
tRNA-Ser-GCU-6 | DDB_G0295093 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5781580 | 81 | - | 0.592593 |
tRNA-Ser-GCU-7 | DDB_G0295105 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5339366 | 81 | - | 0.592593 |
tRNA-Ser-GCU-8 | DDB_G0295107 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5335122 | 81 | - | 0.592593 |
tRNA-Ser-GCU-9 | DDB_G0295109 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5333581 | 81 | - | 0.592593 |
tRNA-Ser-UGA-1 | DDB_G0294675 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 818727 | 82 | + | 0.52439 |
tRNA-Ser-UGA-10 | DDB_G0295311 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1758891 | 82 | + | 0.52439 |
tRNA-Ser-UGA-11 | DDB_G0295375 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3325552 | 82 | + | 0.52439 |
tRNA-Ser-UGA-12 | DDB_G0295443 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1761326 | 82 | - | 0.52439 |
tRNA-Ser-UGA-13 | DDB_G0295457 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1133095 | 82 | - | 0.52439 |
tRNA-Ser-UGA-14 | DDB_G0295459 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1129630 | 82 | - | 0.52439 |
tRNA-Ser-UGA-15 | DDB_G0295461 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1097223 | 82 | - | 0.52439 |
tRNA-Ser-UGA-2 | DDB_G0294683 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 946092 | 82 | + | 0.52439 |
tRNA-Ser-UGA-3 | DDB_G0294785 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2967080 | 82 | - | 0.52439 |
tRNA-Ser-UGA-4 | DDB_G0294825 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 822333 | 82 | - | 0.52439 |
tRNA-Ser-UGA-5 | DDB_G0294871 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6473009 | 78 | + | 0.487179 |
tRNA-Ser-UGA-6 | DDB_G0295069 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5751386 | 82 | + | 0.52439 |
tRNA-Ser-UGA-7 | DDB_G0295211 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3945723 | 82 | - | 0.52439 |
tRNA-Ser-UGA-8 | DDB_G0295231 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 1589109 | 82 | - | 0.52439 |
tRNA-Ser-UGA-9 | DDB_G0295305 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1124940 | 82 | + | 0.52439 |
tRNA-Thr-AGU-10 | DDB_G0294745 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4214694 | 72 | + | 0.5 |
tRNA-Thr-AGU-11 | DDB_G0294749 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4709052 | 72 | - | 0.5 |
tRNA-Thr-AGU-12 | DDB_G0294773 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3644185 | 72 | - | 0.5 |
tRNA-Thr-AGU-13 | DDB_G0294843 | transfers a threonine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 2662753 | 72 | + | 0.5 |
tRNA-Thr-AGU-14 | DDB_G0294897 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7936345 | 72 | + | 0.5 |
tRNA-Thr-AGU-15 | DDB_G0294995 | transfers a threonine residue to a growing polypeptide chain during protein synthesis there is a second copy of this gene | DDB0232429 | CDS | 3368962 | 72 | - | 0.5 |
tRNA-Thr-AGU-16 | DDB_G0295081 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5918532 | 72 | + | 0.5 |
tRNA-Thr-AGU-17 | DDB_G0295083 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5981778 | 72 | + | 0.5 |
tRNA-Thr-AGU-18 | DDB_G0295421 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2598517 | 72 | - | 0.5 |
tRNA-Thr-AGU-3 | DDB_G0294673 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 735884 | 72 | + | 0.5 |
tRNA-Thr-AGU-4 | DDB_G0294689 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1688222 | 72 | + | 0.5 |
tRNA-Thr-AGU-5 | DDB_G0294693 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1863435 | 72 | + | 0.5 |
tRNA-Thr-AGU-6 | DDB_G0294699 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1995560 | 72 | + | 0.5 |
tRNA-Thr-AGU-7 | DDB_G0294701 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1997247 | 72 | + | 0.5 |
tRNA-Thr-AGU-8 | DDB_G0294715 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2404737 | 72 | + | 0.5 |
tRNA-Thr-AGU-9 | DDB_G0294735 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3222819 | 72 | + | 0.5 |
tRNA-Thr-CGU-1 | DDB_G0295061 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5070744 | 86 | + | 0.430233 |
tRNA-Thr-UGU-1 | DDB_G0294857 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5288579 | 90 | + | 0.455556 |
tRNA-Thr-UGU-2 | DDB_G0294937 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6680526 | 90 | - | 0.466667 |
tRNA-Thr-UGU-3 | DDB_G0295183 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3710357 | 90 | + | 0.466667 |
tRNA-Thr-UGU-4 | DDB_G0295215 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3717164 | 90 | - | 0.455556 |
tRNA-Thr-UGU-5 | DDB_G0295269 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3336512 | 90 | - | 0.455556 |
tRNA-Thr-UGU-6 | DDB_G0295287 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 712716 | 90 | - | 0.455556 |
tRNA-Trp-CCA-1 | DDB_G0294727 | transfers a tryptophan residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2817548 | 87 | + | 0.448276 |
tRNA-Trp-CCA-2 | DDB_G0294733 | transfers a tryptophan residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2913067 | 87 | + | 0.448276 |
tRNA-Trp-CCA-3 | DDB_G0294795 | transfers a tryptophan residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2411874 | 87 | - | 0.448276 |
tRNA-Trp-CCA-4 | DDB_G0294821 | transfers a tryptophan residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1511351 | 87 | - | 0.448276 |
tRNA-Trp-CCA-5 | DDB_G0294823 | transfers a tryptophan residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1508042 | 87 | - | 0.448276 |
tRNA-Trp-CCA-6 | DDB_G0294855 | transfers a tryptophan residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 4995095 | 87 | + | 0.448276 |
tRNA-Trp-CCA-7 | DDB_G0294957 | transfers a tryptophan residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 5820963 | 87 | - | 0.448276 |
tRNA-Tyr-GUA-10 | DDB_G0295331 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2176055 | 83 | + | 0.493976 |
tRNA-Tyr-GUA-11 | DDB_G0295359 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3068583 | 83 | + | 0.506024 |
tRNA-Tyr-GUA-12 | DDB_G0295379 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3430565 | 82 | + | 0.5 |
tRNA-Tyr-GUA-13 | DDB_G0295423 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2597197 | 83 | - | 0.493976 |
tRNA-Tyr-GUA-2 | DDB_G0294687 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 1686235 | 83 | + | 0.506024 |
tRNA-Tyr-GUA-3 | DDB_G0294769 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4009415 | 83 | - | 0.506024 |
tRNA-Tyr-GUA-4 | DDB_G0295011 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 506383 | 83 | + | 0.493976 |
tRNA-Tyr-GUA-5 | DDB_G0295179 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3366227 | 83 | + | 0.493976 |
tRNA-Tyr-GUA-6 | DDB_G0295181 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3658459 | 83 | + | 0.493976 |
tRNA-Tyr-GUA-7 | DDB_G0295191 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 4844157 | 84 | + | 0.488095 |
tRNA-Tyr-GUA-8 | DDB_G0295197 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5312947 | 83 | + | 0.518072 |
tRNA-Tyr-GUA-9 | DDB_G0295327 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2088994 | 83 | + | 0.493976 |
tRNA-Val-AAC-10 | DDB_G0294949 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6162014 | 74 | - | 0.486486 |
tRNA-Val-AAC-11 | DDB_G0295007 | DDB0232429 | CDS | 386413 | 74 | - | 0.486486 | |
tRNA-Val-AAC-12 | DDB_G0295009 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 347022 | 74 | - | 0.486486 |
tRNA-Val-AAC-13 | DDB_G0295027 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 2745400 | 74 | + | 0.486486 |
tRNA-Val-AAC-14 | DDB_G0295071 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5868008 | 74 | + | 0.486486 |
tRNA-Val-AAC-15 | DDB_G0295073 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5870128 | 74 | + | 0.486486 |
tRNA-Val-AAC-16 | DDB_G0295087 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 6078780 | 74 | + | 0.486486 |
tRNA-Val-AAC-17 | DDB_G0295089 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 5940507 | 74 | - | 0.486486 |
tRNA-Val-AAC-18 | DDB_G0295205 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5047177 | 74 | - | 0.486486 |
tRNA-Val-AAC-19 | DDB_G0295273 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3208187 | 74 | - | 0.486486 |
tRNA-Val-AAC-2 | DDB_G0294747 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4338908 | 74 | + | 0.486486 |
tRNA-Val-AAC-20 | DDB_G0295301 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 586137 | 74 | + | 0.486486 |
tRNA-Val-AAC-21 | DDB_G0295451 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1321993 | 74 | - | 0.486486 |
tRNA-Val-AAC-3 | DDB_G0294755 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4301392 | 74 | - | 0.486486 |
tRNA-Val-AAC-4 | DDB_G0294757 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 4298314 | 74 | - | 0.486486 |
tRNA-Val-AAC-5 | DDB_G0294807 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2099470 | 74 | - | 0.486486 |
tRNA-Val-AAC-6 | DDB_G0294813 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2064611 | 74 | - | 0.486486 |
tRNA-Val-AAC-7 | DDB_G0294861 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 6127229 | 74 | + | 0.486486 |
tRNA-Val-AAC-8 | DDB_G0294887 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7435671 | 74 | + | 0.486486 |
tRNA-Val-AAC-9 | DDB_G0294895 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232429 | CDS | 7845634 | 74 | + | 0.486486 |
tRNA-Val-CAC-1 | DDB_G0294771 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 3928023 | 73 | - | 0.520548 |
tRNA-Val-UAC-1 | DDB_G0294811 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232428 | CDS | 2073265 | 74 | - | 0.540541 |
tRNA-Val-UAC-2 | DDB_G0295017 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232430 | CDS | 1807996 | 74 | + | 0.5 |
tRNA-Val-UAC-3 | DDB_G0295249 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3061365 | 74 | + | 0.513514 |
tRNA-Val-UAC-4 | DDB_G0295253 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3658887 | 74 | + | 0.540541 |
tRNA-Val-UAC-5 | DDB_G0295255 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3660287 | 74 | + | 0.540541 |
tRNA-Val-UAC-6 | DDB_G0295259 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3761819 | 74 | + | 0.540541 |
tRNA-Val-UAC-7 | DDB_G0295343 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2768404 | 74 | + | 0.540541 |
tacA | DDB_G0291342 | transcription factor regulated by calcineurin to localize from the cytosol to the nucleus where it might be phosphorylated by GskA involved in stalk cell differentiation and the stress response to lithium | DDB0232433 | CDS | 140829 | 2433 | + | 0.286478 |
tacc | DDB_G0275391 | promotes microtubule growth localizes to the centromer and has been shown to physically interact with | DDB0232429 | CDS | 5495060 | 4437 | - | 0.320036 |
taf1 | DDB_G0292242 | ortholog of H. sapiens and S. cerevisiae TAF1 an atypical TAF1 family protein kinase and contains a bromodomain putative HAF group protein (histone acetyltransferase) | DDB0232433 | CDS | 1360709 | 6933 | - | 0.301457 |
taf11 | DDB_G0278843 | DDB0232430 | CDS | 1267448 | 1353 | - | 0.321508 | |
taf12 | DDB_G0274697 | subunit of TFIID and SAGA complexes involved in RNA polymerase II transcription initiation and in chromatin modification | DDB0232429 | CDS | 4205325 | 1884 | + | 0.321125 |
taf13 | DDB_G0292838 | DDB0232433 | CDS | 2136060 | 321 | - | 0.267913 | |
taf2 | DDB_G0292724 | TFIID subunit involved in RNA polymerase II transcription initiation ortholog of H. sapiens and S. cerevisiae TAF2 | DDB0232433 | CDS | 1853349 | 6135 | - | 0.292258 |
taf5 | DDB_G0287337 | subunit of TFIID and SAGA complexes involved in RNA polymerase II transcription initiation and in chromatin modification | DDB0232432 | CDS | 150447 | 2847 | + | 0.316473 |
taf6 | DDB_G0288471 | similar to S. cerevisiae TAF6 subunit of TFIID and SAGA complexes involved in transcription initiation of RNA polymerase II and in chromatin modification | DDB0232432 | CDS | 1566143 | 1629 | - | 0.279926 |
taf7 | DDB_G0271338 | TFIID subunit involved in RNA polymerase II transcription initiation | DDB0232429 | CDS | 80918 | 2097 | - | 0.288507 |
taf9 | DDB_G0272360 | subunit of TFIID and SAGA complexes involved in RNA polymerase II transcription initiation and in chromatin modification | DDB0232429 | CDS | 1294745 | 1860 | + | 0.306452 |
tagA | DDB_G0293002 | amino terminus has a serine protease domain carboxyl terminus consists of a half-transporter of the ABCB family | DDB0232433 | CDS | 2501320 | 5259 | + | 0.296254 |
tagB | DDB_G0286119 | amino terminus has a serine protease domain carboxyl terminus consists of a half-transporter of the ABCB family | DDB0232431 | CDS | 4091463 | 5721 | + | 0.301695 |
tagC | DDB_G0286121 | amino terminus has a serine protease domain carboxy terminus consists of a half-transporter of the ABCB family | DDB0232431 | CDS | 4085057 | 5226 | + | 0.293724 |
tagD | DDB_G0286123 | amino terminus has a serine protease domain carboxy terminus consists of a half-transporter of the ABCB family | DDB0232431 | CDS | 4078435 | 5478 | + | 0.288244 |
tal | DDB_G0280909 | catalyzes the reaction sedoheptulose 7-phosphate D-glyceraldehyde 3-phosphate D-erythrose 4-phosphate D-fructose 6-phosphate | DDB0232430 | CDS | 3865707 | 966 | - | 0.331263 |
talA | DDB_G0290481 | The bAX4b talin gene has a confirmed stop codon (R. Kay private communication) that terminates the protein after residue 1279 immunohistochemistry shows the presence of a very faint truncated talin (A. Mueller-Taubenberger private communication)br bAX2b talin is the full length homolog of mammalian talin and other proteins of the band 4.1 superfamily all functional data is derived from AX2 involved in cell-substrate adhesion and cytokinesis the AX2 protein sequence is available from the | DDB0232432 | CDS | 4257563 | 3840 | + | 0.33724 |
talB | DDB_G0287505 | talin with an unusual villin headpiece-like domain involved in multicellular development and in autophagic cell death | DDB0232432 | CDS | 376738 | 7845 | + | 0.391714 |
tat | DDB_G0287515 | catalyzes the reaction L-tyrosine 2-oxoglutarate 4-hydroxyphenylpyruvate L-glutamate | DDB0232432 | CDS | 352517 | 1254 | + | 0.297448 |
taz | DDB_G0291922 | ortholog of S. cerevisiae TAZ1 and H. sapiens tafazzin implicated in Barth syndrome | DDB0232433 | CDS | 950884 | 858 | + | 0.270396 |
tbcA | DDB_G0271706 | DDB0232429 | CDS | 829537 | 342 | - | 0.22807 | |
tbcB | DDB_G0277983 | DDB0232430 | CDS | 98599 | 813 | - | 0.276753 | |
tbcC | DDB_G0284313 | DDB0232431 | CDS | 1725990 | 1263 | - | 0.200317 | |
tbcD | DDB_G0268516 | DDB0232428 | CDS | 802089 | 4443 | + | 0.238352 | |
tbcE | DDB_G0269990 | DDB0232428 | CDS | 3986134 | 1578 | + | 0.209759 | |
tbccd | DDB_G0281221 | DDB0232430 | CDS | 4236950 | 1329 | + | 0.212942 | |
tbck | DDB_G0267760 | similar to TBCK in human fly and worm TBC domain-containing proteins in yeast are GTPase activator proteins unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232428 | CDS | 792299 | 3102 | + | 0.275306 |
tbpA | DDB_G0275617 | general transcription factor that binds to the TATA-box promoter element component of the transcription factor TFIIIB shown to bind to subunits brf1 and weakly to bdp1 interacts with the non LTR retrotransposons TRE5-A and TRE5-B | DDB0232429 | CDS | 6092208 | 618 | - | 0.326861 |
tcea1 | DDB_G0278241 | general transcription elongation factor TFIIS enables RNA polymerase II to read through blocks to elongation by stimulating cleavage of nascent transcripts stalled at transcription arrest sites | DDB0232430 | CDS | 539874 | 960 | + | 0.301042 |
tcp1 | DDB_G0269190 | DDB0232428 | CDS | 4885046 | 1647 | + | 0.364299 | |
tdo | DDB_G0269714 | catalyzes the reactoin L-tryptophan Osub2sub L-formylkynurenine | DDB0232428 | CDS | 3391649 | 1203 | - | 0.308396 |
tert | DDB_G0293918 | DDB0232433 | CDS | 3475961 | 3813 | - | 0.190401 | |
tfb1m | DDB_G0286199 | DDB0232431 | CDS | 4166229 | 1458 | - | 0.268176 | |
tfdp2 | DDB_G0276799 | similar to Homo sapiens transcription factor Dp-2 (E2F dimerization partner 2) which binds to E2F to activate the expression of cell cycle-regulated genes (SwissProt Q14188) | DDB0232429 | CDS | 7346120 | 1974 | + | 0.223911 |
tfiiiA | DDB_G0281085 | DDB0232430 | CDS | 4032257 | 1731 | - | 0.277296 | |
tgds | DDB_G0279465 | similar to dTDP-D-glucose 46-dehydratase which catalyzes the reaction dTDP-glucose dTDP-4-dehydro-6-deoxy-D-glucose Hsub2subO | DDB0232430 | CDS | 2090462 | 1305 | - | 0.185441 |
tgrA1 | DDB_G0291622 | contains a putative signal peptide and a C-terminal transmembrane domain in a cluster of recently duplicated genes and almost identical to | DDB0232433 | CDS | 344609 | 2541 | + | 0.243998 |
tgrA2 | DDB_G0291666 | in a cluster of recently duplicated genes and almost identical to | DDB0232433 | CDS | 352396 | 2535 | + | 0.242209 |
tgrA3 | DDB_G0291668 | contains a predicted signal peptide and an additional transmembrane domain in a cluster of recently duplicated genes and very similar to | DDB0232433 | CDS | 359944 | 3264 | + | 0.254289 |
tgrA4 | DDB_G0291514 | contains a putative signal peptide and one additional transmembrane domain almost identical to | DDB0232433 | CDS | 462725 | 3117 | - | 0.256015 |
tgrA5 | DDB_G0274225 | DDB0232429 | CDS | 4714057 | 2805 | - | 0.237077 | |
tgrA_ps1 | DDB_G0291624 | putative pseudogene immunoglobulin E-set family gene | DDB0232433 | CDS | 356398 | 2589 | + | 0.248358 |
tgrA_ps10 | DDB_G0349532 | putative pseudogene fragment of immunoglobulin E-set family genes including | DDB0232431 | CDS | 1602101 | 832 | - | 0.253606 |
tgrA_ps2 | DDB_G0291460 | putative pseudogene immunoglobulin E-set family gene | DDB0232433 | CDS | 348356 | 2541 | + | 0.241244 |
tgrA_ps3 | DDB_G0291500 | putative pseudogene immunoglobulin E-set family gene | DDB0232433 | CDS | 440410 | 1200 | + | 0.253333 |
tgrA_ps4 | DDB_G0272817 | putative pseudogene immunoglobulin E-set family gene | DDB0232429 | CDS | 1878915 | 1833 | + | 0.253137 |
tgrA_ps5 | DDB_G0278109 | putative pseudogene immunoglobulin E-set family gene | DDB0232430 | CDS | 288911 | 2148 | - | 0.286313 |
tgrA_ps6 | DDB_G0289747 | putative pseudogene fragment of immunoglobulin E-set family gene | DDB0232432 | CDS | 3203632 | 611 | - | 0.227496 |
tgrA_ps7 | DDB_G0291458 | putative pseudogene fragment of immunoglobulin E-set family genes including | DDB0232433 | CDS | 342766 | 417 | + | 0.213429 |
tgrA_ps8 | DDB_G0349267 | putative pseudogene fragment of immunoglobulin E-set family genes including | DDB0232430 | CDS | 389147 | 482 | - | 0.23444 |
tgrA_ps9 | DDB_G0349268 | putative pseudogene fragment of immunoglobulin E-set family genes including | DDB0232430 | CDS | 389635 | 303 | + | 0.224422 |
tgrB1 | DDB_G0280689 | contains a predicted signal peptide IPTTIG domain found in cell surface receptors and a C-terminal transmembrane domain plays a role in kin discrimination and is highly polymorphic between different isolates of D. discoideum | DDB0232430 | CDS | 3633930 | 2709 | + | 0.324474 |
tgrB2 | DDB_G0280693 | similar to tgr family proteins contains a predicted signal peptide | DDB0232430 | CDS | 3640963 | 1020 | + | 0.304902 |
tgrB_ps | DDB_G0280651 | putative pseudogene immunoglobulin E-set family gene | DDB0232430 | CDS | 3611170 | 246 | + | 0.349593 |
tgrC1 | DDB_G0280531 | contains a predicted signal peptide IPTTIG domain found in cell surface receptors and a C-terminal transmembrane domain plays a role in aggregation during development in kin discrimination and is highly polymorphic between different isolates of D. discoideum | DDB0232430 | CDS | 3630672 | 2670 | - | 0.291386 |
tgrC2 | DDB_G0280635 | DDB0232430 | CDS | 3587080 | 2658 | - | 0.282543 | |
tgrC3 | DDB_G0280623 | DDB0232430 | CDS | 3578410 | 2598 | - | 0.2806 | |
tgrC4 | DDB_G0291454 | DDB0232433 | CDS | 333292 | 2685 | - | 0.279702 | |
tgrC5 | DDB_G0281407 | DDB0232430 | CDS | 4435413 | 2658 | + | 0.29082 | |
tgrC_ps1 | DDB_G0280743 | putative pseudogene immunoglobulin E-set family gene | DDB0232430 | CDS | 3608634 | 1734 | - | 0.28143 |
tgrC_ps2 | DDB_G0280745 | putative pseudogene immunoglobulin E-set family gene | DDB0232430 | CDS | 3644331 | 798 | - | 0.280702 |
tgrC_ps3 | DDB_G0293238 | putative pseudogene immunoglobulin E-set family gene | DDB0232433 | CDS | 2646511 | 258 | + | 0.267442 |
tgrD1 | DDB_G0286825 | contains three immunolubulin-like folds (IPTTIG domains) | DDB0232431 | CDS | 4985657 | 2688 | + | 0.289062 |
tgrE1 | DDB_G0286851 | conserved hypothetical protein contains an IPTTIG domain found in cell surface receptors | DDB0232431 | CDS | 4982216 | 2739 | - | 0.319825 |
tgrE_ps | DDB_G0285217 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 2989226 | 216 | - | 0.291667 |
tgrF1 | DDB_G0292732 | DDB0232433 | CDS | 2005101 | 2754 | - | 0.245461 | |
tgrG1 | DDB_G0292772 | DDB0232433 | CDS | 2009912 | 2928 | + | 0.239413 | |
tgrH1 | DDB_G0283323 | DDB0232431 | CDS | 482981 | 3369 | - | 0.240427 | |
tgrH_ps1 | DDB_G0283341 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 518010 | 1107 | - | 0.257453 |
tgrH_ps2 | DDB_G0283183 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 373477 | 999 | + | 0.248248 |
tgrI1 | DDB_G0283335 | DDB0232431 | CDS | 487136 | 2568 | + | 0.222741 | |
tgrI2 | DDB_G0283317 | DDB0232431 | CDS | 522108 | 2553 | + | 0.221308 | |
tgrI3 | DDB_G0283249 | DDB0232431 | CDS | 370291 | 2559 | - | 0.221962 | |
tgrI_ps1 | DDB_G0283873 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 1129091 | 492 | - | 0.21748 |
tgrI_ps2 | DDB_G0282981 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 98815 | 459 | - | 0.230937 |
tgrI_ps3 | DDB_G0283299 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 477747 | 285 | - | 0.238596 |
tgrJ1 | DDB_G0271556 | conserved hypothetical protein contains an IPTTIG domain found in cell surface receptors | DDB0232429 | CDS | 644311 | 2658 | - | 0.31076 |
tgrJ_ps1 | DDB_G0271650 | putative pseudogene immunoglobulin E-set family gene | DDB0232429 | CDS | 657094 | 477 | - | 0.314465 |
tgrJ_ps2 | DDB_G0271652 | putative pseudogene immunoglobulin E-set family gene | DDB0232429 | CDS | 659629 | 1395 | + | 0.281004 |
tgrK1 | DDB_G0271586 | DDB0232429 | CDS | 647755 | 2733 | + | 0.267472 | |
tgrK2 | DDB_G0271646 | DDB0232429 | CDS | 651346 | 2490 | + | 0.263855 | |
tgrK3 | DDB_G0271654 | DDB0232429 | CDS | 661610 | 858 | + | 0.304196 | |
tgrL1 | DDB_G0284659 | DDB0232431 | CDS | 2306298 | 2214 | - | 0.266486 | |
tgrM1 | DDB_G0288711 | DDB0232432 | CDS | 1859437 | 2562 | - | 0.323575 | |
tgrM2 | DDB_G0288709 | DDB0232432 | CDS | 1856022 | 2664 | - | 0.298048 | |
tgrN1 | DDB_G0272736 | DDB0232429 | CDS | 2222634 | 2838 | - | 0.269556 | |
tgrO1 | DDB_G0268490 | DDB0232428 | CDS | 507666 | 2664 | + | 0.231607 | |
tgrO2 | DDB_G0267654 | DDB0232428 | CDS | 511341 | 2673 | + | 0.237561 | |
tgrO3 | DDB_G0268304 | DDB0232428 | CDS | 515177 | 3117 | + | 0.247674 | |
tgrO4 | DDB_G0268284 | DDB0232428 | CDS | 348371 | 3117 | + | 0.253128 | |
tgrO_ps1 | DDB_G0268488 | putative pseudogene immunoglobulin E-set family gene | DDB0232428 | CDS | 504172 | 2370 | + | 0.229536 |
tgrO_ps2 | DDB_G0267678 | putative pseudogene small fragment similar to genes of the tgrO family | DDB0232428 | CDS | 556660 | 333 | + | 0.249249 |
tgrP1 | DDB_G0287605 | DDB0232432 | CDS | 454900 | 1620 | - | 0.169753 | |
tgrQ1 | DDB_G0292562 | DDB0232433 | CDS | 1885258 | 2016 | - | 0.244048 | |
tgrR1 | DDB_G0275745 | DDB0232429 | CDS | 5877842 | 2616 | - | 0.299312 | |
tgrR2 | DDB_G0277627 | DDB0232429 | CDS | 8277760 | 2556 | + | 0.266823 | |
tgrS1 | DDB_G0271598 | DDB0232429 | CDS | 451802 | 2952 | - | 0.237127 | |
tgrT_ps1 | DDB_G0283029 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 175761 | 552 | - | 0.320652 |
tgrT_ps2 | DDB_G0283027 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 174707 | 234 | - | 0.282051 |
thfA | DDB_G0277725 | catalyzes the reaction 510-methylenetetrahydrofolate NADsupsup 510-methenyl-tetrahydrofolate NADH Hsupsup enriched in prespore cells | DDB0232429 | CDS | 8379878 | 942 | - | 0.316348 |
thg1 | DDB_G0291830 | conserved eukaryotic protein that has been shown in S. cerevisiae to be an essential tRNAHis guanylyltransferase that adds a guanosine residue to the 5' end of tRNAHis after transcription and RNase P cleavage conserved domain also known as DUF549 domain | DDB0232433 | CDS | 833386 | 771 | + | 0.265888 |
thoc1 | DDB_G0275717 | ortholog of human THOC1 and yeast THO1 which exist in the THO complex required for transcriptional elongation | DDB0232429 | CDS | 6009402 | 2181 | + | 0.274645 |
thoc2 | DDB_G0291063 | ortholog of human THOC2 and yeast RLR1 which exist in the THO complex required for transcriptional elongation | DDB0232432 | CDS | 4908746 | 6333 | + | 0.291963 |
thoc6 | DDB_G0287653 | ortholog of THOC6 which exists in the THO complex required for transcriptional elongation | DDB0232432 | CDS | 441079 | 1440 | + | 0.271528 |
thoc7 | DDB_G0275979 | ortholog of THOC7 which exists in the THO complex required for transcriptional elongation | DDB0232429 | CDS | 6151550 | 648 | + | 0.225309 |
thrS1 | DDB_G0288267 | catalyzes the reaction ATP L-threonine tRNAThr AMP diphosphate L-threonyl-tRNAThr | DDB0232432 | CDS | 1320046 | 2133 | - | 0.33849 |
thrS2 | DDB_G0274545 | catalyzes the reaction ATP L-threonine tRNAThr AMP diphosphate L-threonyl-tRNAThr | DDB0232429 | CDS | 4202893 | 2097 | - | 0.251311 |
thyA | DDB_G0280045 | catalyzes the reaction 510-methylenetetrahydrofolate dUMP FADHsub2sub dTMP tetrahydrofolate FAD in de novo biosynthesis of pyrimidine deoxyribonucleotides | DDB0232430 | CDS | 3175236 | 912 | + | 0.337719 |
thyB | DDB_G0289179 | calmodulin-binding thymidine kinase 1 that is very similar to human TK1 catalyzes the reaction ATP thymidine ADP thymidine 5'-phosphate | DDB0232432 | CDS | 2508266 | 684 | - | 0.330409 |
tifA | DDB_G0269192 | similar to eukaryotic initiation factor 4A isoform 3 | DDB0232428 | CDS | 3537960 | 1218 | + | 0.316092 |
timm10 | DDB_G0284911 | conserved component of the mitochondrial intermembrane space forms a complex with Timm9 which mediates insertion of hydrophobic proteins at the inner membrane. | DDB0232431 | CDS | 2631200 | 267 | - | 0.348315 |
timm16 | DDB_G0282195 | DDB0232430 | CDS | 5506037 | 342 | - | 0.304094 | |
timm17 | DDB_G0287627 | DDB0232432 | CDS | 494298 | 552 | + | 0.344203 | |
timm22 | DDB_G0283865 | DDB0232431 | CDS | 1077530 | 537 | - | 0.340782 | |
timm23 | DDB_G0286541 | DDB0232431 | CDS | 4635713 | 495 | - | 0.339394 | |
timm9 | DDB_G0272931 | conserved component of the mitochondrial intermembrane space forms a complex with Timm10 which mediates insertion of hydrophobic proteins at the inner membrane. | DDB0232429 | CDS | 1862767 | 255 | - | 0.258824 |
tipA | DDB_G0281561 | involved in early development and tip formation the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232430 | CDS | 4845968 | 2280 | - | 0.339474 |
tipB | DDB_G0276333 | DDB0232429 | CDS | 6717804 | 1137 | - | 0.308707 | |
tipC | DDB_G0267422 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention in D. discoideum involved in early development and tip formation | DDB0232428 | CDS | 1494431 | 11547 | + | 0.250108 |
tipD | DDB_G0275323 | ortholog of the mammalian ATG16l1 which is involved in autophagy defects in human cause inflammatory bowel disease type 10 in D. discoideum involved in early development and tip formation | DDB0232429 | CDS | 5406103 | 1839 | + | 0.334965 |
tirA | DDB_G0289237 | DDB0232432 | CDS | 2526970 | 4011 | - | 0.222638 | |
tkrA | DDB_G0292104 | catalyzes the reaction D-gluconate NADPsupsup 2-dehydro-D-gluconate NADPH Hsupsup | DDB0232433 | CDS | 1190069 | 1005 | + | 0.300498 |
tkt-1 | DDB_G0272618 | catalyzes the reaction D-ribose-5-phosphate D-xylulose-5-phosphate D-sedoheptulose-7-phosphate D-glyceraldehyde-3-phosphate there is a second copy of this gene | DDB0232429 | CDS | 2357975 | 1986 | + | 0.39577 |
tkt-2 | DDB_G0274019 | catalyzes the reaction D-ribose-5-phosphate D-xylulose-5-phosphate D-sedoheptulose-7-phosphate D-glyceraldehyde-3-phosphate there is a second copy of this gene | DDB0232429 | CDS | 3671700 | 1986 | - | 0.39577 |
tmcB | DDB_G0289207 | contains two HAT (half a TPR) repeats and 13 predicted transmembrane domains involved in macrocyst formation | DDB0232432 | CDS | 2473231 | 4251 | + | 0.307457 |
tmcC | DDB_G0289253 | contains two HAT (half a TPR) repeats and 13 predicted transmembrane domains null mutant has an increased number of peripheral cells in macrocyst formation | DDB0232432 | CDS | 2544506 | 4167 | - | 0.287257 |
tmc_ps1 | DDB_G0282503 | putative pseudogene similar to a gene family in Dictyostelium including | DDB0232430 | CDS | 5863004 | 543 | + | 0.292818 |
tmc_ps2 | DDB_G0288839 | putative pseudogene similar to a gene family in Dictyostelium including | DDB0232432 | CDS | 2049688 | 2436 | + | 0.267652 |
tmc_ps3 | DDB_G0288843 | putative pseudogene similar to a gene family in Dictyostelium including | DDB0232432 | CDS | 2054056 | 1116 | + | 0.266129 |
tmem104 | DDB_G0282723 | integral membrane protein that is involved in the transport of amino acids into the cell contains 10 putative transmembrane domains and an additional signal sequence | DDB0232430 | CDS | 6203669 | 1500 | + | 0.274 |
tmem111 | DDB_G0278153 | DDB0232430 | CDS | 374402 | 945 | - | 0.267725 | |
tmem115 | DDB_G0278061 | DDB0232430 | CDS | 209901 | 867 | - | 0.262976 | |
tmem120 | DDB_G0288699 | conserved transmembrane protein contains 4 putative transmembrane domains | DDB0232432 | CDS | 1842289 | 1107 | - | 0.311653 |
tmem128 | DDB_G0277893 | DDB0232430 | CDS | 95820 | 627 | + | 0.23764 | |
tmem144A | DDB_G0280505 | similar to human TMEM144 contains 10 predicted transmembrane domains | DDB0232430 | CDS | 3457915 | 1077 | + | 0.329619 |
tmem144B | DDB_G0267928 | similar to human TMEM144 contains 10 predicted transmembrane domains | DDB0232428 | CDS | 1141518 | 1110 | + | 0.285586 |
tmem14A | DDB_G0288759 | one of two Dictyostelium proteins in the eukaryotic transmembrane protein 14 (TMEM14) family contains four putative transmembrane domains | DDB0232432 | CDS | 1930552 | 309 | - | 0.304207 |
tmem14B | DDB_G0271790 | one of two Dictyostelium proteins in the eukaryotic transmembrane protein 14 (TMEM14) family contains four putative transmembrane domains | DDB0232429 | CDS | 728723 | 339 | - | 0.309735 |
tmem164 | DDB_G0287401 | conserved transmembrane protein contains 7 putative transmembrane domains | DDB0232432 | CDS | 257909 | 828 | - | 0.242754 |
tmem167 | DDB_G0289451 | DDB0232432 | CDS | 2806080 | 219 | + | 0.296804 | |
tmem170 | DDB_G0290053 | DDB0232432 | CDS | 3567000 | 387 | - | 0.302326 | |
tmem184A | DDB_G0284525 | similar to H. sapiens TMEM184A and B contains 7 predicted transmembrane domains | DDB0232431 | CDS | 2111778 | 1482 | - | 0.2861 |
tmem184B | DDB_G0276041 | TMEM184 family protein similar to H. sapiens TMEM184A B C contains 6 predicted transmembrane domains | DDB0232429 | CDS | 6519312 | 1524 | + | 0.230315 |
tmem184C | DDB_G0279555 | putative ortholog of the human transmembrane protein 184C contains 6 predicted transmembrane domains | DDB0232430 | CDS | 2248374 | 1056 | + | 0.268939 |
tmem184D | DDB_G0291287 | TMEM184 family protein contains 7 predicted transmembrane domains | DDB0232433 | CDS | 57345 | 1494 | + | 0.261714 |
tmem184E | DDB_G0304961 | TMEM184 family protein contains 7 predicted transmembrane domains | DDB0232432 | CDS | 2986116 | 1689 | - | 0.212552 |
tmem184F | DDB_G0284327 | TMEM184 family protein the long splice variant contains 6 putative transmembrane domains and an additional signal sequence the short splice variant contains 4 putative transmembrane domains | DDB0232431 | CDS | 1812405 | 1863 | + | 0.263017 |
tmem20 | DDB_G0292606 | putative drugmetabolite transporter containing 10 predicted transmembrane domains | DDB0232433 | CDS | 1830985 | 2097 | + | 0.311874 |
tmem208 | DDB_G0281177 | DDB0232430 | CDS | 4165613 | 522 | - | 0.266284 | |
tmem33 | DDB_G0286009 | DDB0232431 | CDS | 3940845 | 873 | + | 0.293242 | |
tmem50 | DDB_G0281983 | conserved hypothetical protein contains a signal peptide and three transmembrane domains | DDB0232430 | CDS | 5214975 | 471 | - | 0.299363 |
tmem56A | DDB_G0277027 | homolog of mammalian TMEM56 there are three genes in Dictyostelium: tmem56A tmem56B and tmem56C contains 7 putative transmembrane domains | DDB0232429 | CDS | 7271007 | 777 | - | 0.199485 |
tmem56B | DDB_G0277029 | homolog of mammalian TMEM56 there are three genes in Dictyostelium: tmem56A tmem56B and tmem56C contains 7 putative transmembrane domains | DDB0232429 | CDS | 7272592 | 774 | - | 0.211886 |
tmem56C | DDB_G0270414 | homolog of mammalian TMEM56 there are three genes in Dictyostelium: tmem56A tmem56B and tmem56C contains 7 putative transmembrane domains | DDB0232428 | CDS | 4822178 | 819 | + | 0.23199 |
tmem93 | DDB_G0280399 | DDB0232430 | CDS | 3149782 | 372 | + | 0.258065 | |
tnpo | DDB_G0269948 | homolog of H. sapiens TNPO12 and S. cervisiae KAP104 (karyopherin 104) involved in nuclear protein import | DDB0232428 | CDS | 3916816 | 2796 | + | 0.327253 |
tom1 | DDB_G0290163 | contains a VHS domain and a GAT domain amino terminus is similar to mammalian TOM1 protein which is involved in intracellular protein transport | DDB0232432 | CDS | 3723872 | 1992 | + | 0.316767 |
tom40 | DDB_G0277155 | homologous to mitochondrial import protein 40 kDa subunit contains a putative transmembrane beta-barrel | DDB0232429 | CDS | 7918767 | 945 | + | 0.293122 |
tom7 | DDB_G0282897 | homologous to mitochondrial import protein 7 kDa subunit associates with TOM40 in yeast | DDB0232430 | CDS | 6256774 | 168 | + | 0.267857 |
top1 | DDB_G0283205 | ortholog of TOP1 a nuclear topoisomerase responsible for relaxing single-stranded supercoiled DNA | DDB0232431 | CDS | 416900 | 2682 | + | 0.35123 |
top2 | DDB_G0270418 | controls the topological state of DNA by transient double-strand breakage and subsequent rejoining of DNA strands this is predicted to be a nuclear topoisomerase II | DDB0232428 | CDS | 4831688 | 4566 | - | 0.329172 |
top2mt | DDB_G0279737 | controls the topological state of DNA by transient double-strand breakage and subsequent rejoining of DNA strands Top2mt has been shown to be localized to the mitochondria | DDB0232430 | CDS | 2512313 | 3855 | - | 0.284566 |
top3 | DDB_G0275257 | ortholog of TOP3 a nuclear topoisomerase responsible for relaxing single-stranded negatively-supercoiled DNA | DDB0232429 | CDS | 5038466 | 2487 | - | 0.300362 |
topbp1 | DDB_G0279167 | contains 7 BRCT domainsbr bCommunity annotation:b Cut genes were originally identified in fission yeast as mutants that lead to cytokinesis in the absense of nuclear division the name is derived from | DDB0232430 | CDS | 1718126 | 3954 | - | 0.263531 |
tor | DDB_G0281569 | atypical PIKK family FRAP subfamily protein kinase ortholog of tor a protein kinase that plays a central role in response to nutrients stress and intracellular energy state called mTOR in mammals in dTOR in Drosophila | DDB0232430 | CDS | 4934791 | 7143 | - | 0.347893 |
torA | DDB_G0276353 | required for chemotaxis largely alpha-helical protein with a predicted C-terminal coiled-coil domainbr bNomenclature conflict:b Do not confuse this gene with tor the ortholog of target of rapamycin gene | DDB0232429 | CDS | 6655928 | 2427 | - | 0.223321 |
tpc2 | DDB_G0289105 | similar to human TPC2 a two-pore calcium channel contains Ca2-binding EF-hands and 2 x 5 (10 total) putative transmembrane domains | DDB0232432 | CDS | 2361958 | 6183 | + | 0.253275 |
tpiA | DDB_G0274471 | catalyzes the reaction D-glyceraldehyde 3-phosphate glycerone phosphate defects in human TPI1 are the cause of triosephosphate isomerase deficiency severe clinical disorder of glycolysis | DDB0232429 | CDS | 4481626 | 774 | + | 0.330749 |
tpp1 | DDB_G0269914 | ortholog of CLN2TPP1 contains a predicted signal peptide enriched in prespore cells | DDB0232428 | CDS | 3852049 | 1803 | - | 0.32335 |
tpsA | DDB_G0287657 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain enriched in prestalk cells | DDB0232432 | CDS | 444388 | 2202 | - | 0.321072 |
tpsB | DDB_G0284975 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain | DDB0232431 | CDS | 2735507 | 2373 | - | 0.307206 |
tpsC | DDB_G0290405 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain | DDB0232432 | CDS | 4043666 | 2700 | + | 0.303333 |
tra1 | DDB_G0281947 | atypical protein kinase belongs to the PIKK family of protein kinases similar to transformationtranscription domain-associated protein (TRRAP) | DDB0232430 | CDS | 5137846 | 13749 | + | 0.291294 |
tra2 | DDB_G0278349 | similar to the conserved Tra2 proteins (including human TRA2A TRA2B and SFRS10) that have splicing regulatory function involved in sex-determination in Drosophila | DDB0232430 | CDS | 731119 | 981 | + | 0.415902 |
trap1 | DDB_G0276947 | similar to metazoan TRAP1 member of the HSP90 family translocates to mitochondria during the prestarvation response | DDB0232429 | CDS | 7541980 | 2136 | + | 0.309457 |
trappc10-1 | DDB_G0273209 | ortholog of the trafficking protein particle complex subunit 10 part of the multisubunit TRAPP (transport protein particle) complex there is a second copy of this gene | DDB0232429 | CDS | 2711050 | 4329 | + | 0.280896 |
trappc10-2 | DDB_G0273719 | ortholog of the trafficking protein particle complex subunit 10 part of the multisubunit TRAPP (transport protein particle) complex there is a second copy of this gene | DDB0232429 | CDS | 3316025 | 4329 | - | 0.280896 |
trappc2 | DDB_G0282887 | DDB0232430 | CDS | 6341041 | 402 | - | 0.238806 | |
trappc2l | DDB_G0292690 | DDB0232433 | CDS | 1953634 | 423 | - | 0.238771 | |
trappc3 | DDB_G0277135 | ortholog of the conserved trafficking protein particle complex subunit 3 part of the multisubunit TRAPP (transport protein particle) complex (BET3 in yeast) | DDB0232429 | CDS | 7604054 | 561 | - | 0.26738 |
trappc4 | DDB_G0280827 | ortholog of the trafficking protein particle complex subunit 4 part of the multisubunit TRAPP (transport protein particle) complex | DDB0232430 | CDS | 1440057 | 408 | - | 0.272059 |
trappc5 | DDB_G0278643 | homolog of human TRAPPC5 a component of the multisubunit TRAPP (transport protein particle) complex which may play a role in vesicular transport from endoplasmic reticulum to Golgi | DDB0232430 | CDS | 551038 | 561 | + | 0.286988 |
treh | DDB_G0283473 | homolog of human TREH catalyzes the reaction alphaalpha-trehalose H2O 2 D-glucose contains a predicted signal peptide | DDB0232431 | CDS | 746464 | 1785 | + | 0.341737 |
trfA | DDB_G0269194 | DDB0232428 | CDS | 3020703 | 4173 | - | 0.309609 | |
triA | DDB_G0292436 | prespore-specific gene that regulates cell sorting and morphogenesis in mutants the spore mass is suspended halfway up the stalkbr bNomenclature note:b trishanku is the king in Hindu mythology who is suspended halfway between heaven and earth | DDB0232433 | CDS | 1620628 | 2094 | - | 0.309933 |
trmt11 | DDB_G0283969 | DDB0232431 | CDS | 1400103 | 1524 | + | 0.270341 | |
trmt5 | DDB_G0279739 | ortholog of the mammalian TRMT5 and the S. cerevisiae TRM5 tRNAmethyltransferase that methylates guanosine-37 in various tRNAs | DDB0232430 | CDS | 2486411 | 1383 | - | 0.253796 |
trmt6 | DDB_G0281175 | ortholog of the human TRM6 and yeast GCD10 which catalyzes the formation of N(1)-methyladenine at position 58 (m1A58) in initiator methionyl-tRNA as a heterodimer with | DDB0232430 | CDS | 4163655 | 1566 | + | 0.268199 |
trmt61 | DDB_G0271512 | ortholog of the human TRM61 and yeast GCD14 which catalyzes the formation of N(1)-methyladenine at position 58 (m1A58) in initiator methionyl-tRNA as a heterodimer with | DDB0232429 | CDS | 468500 | 939 | + | 0.286475 |
trmu | DDB_G0288979 | catalyzes the reaction: S-adenosyl-L-methionine tRNA S-adenosyl-L-homocysteine tRNA containing 5-methylaminomethyl-2-thiouridylate | DDB0232432 | CDS | 2201638 | 1356 | + | 0.266962 |
trpS | DDB_G0269454 | catalyzes the reaction ATP L-tryptophan tRNATrp AMP diphosphate L-tryptophan-tRNAThr | DDB0232428 | CDS | 2807320 | 1203 | - | 0.296758 |
trrA | DDB_G0280815 | catalyzes the reaction thioredoxin NADP thioredoxin disulfide NADPH H | DDB0232430 | CDS | 3775563 | 960 | - | 0.377083 |
trxC | DDB_G0294489 | small disulphide-containing redox protein that serves as a general protein disulphide oxidoreductase up-regulated at 6 hr developmental stage | DDB0232433 | CDS | 2335005 | 315 | - | 0.32381 |
trxD | DDB_G0287849 | DDB0232432 | CDS | 820586 | 315 | - | 0.260317 | |
trxE | DDB_G0287227 | DDB0232432 | CDS | 23737 | 318 | + | 0.393082 | |
trx_ps | DDB_G0270780 | putative pseudogene similar to D. discoideum thioredoxin genes including | DDB0232428 | CDS | 4661712 | 420 | - | 0.188095 |
tsfm | DDB_G0286399 | DDB0232431 | CDS | 4409316 | 1068 | + | 0.305243 | |
tsg101 | DDB_G0286797 | DDB0232431 | CDS | 4717096 | 1437 | - | 0.314544 | |
tsn | DDB_G0270384 | ortholog of human TSN DNA-binding protein that specifically recognizes consensus sequences at the breakpoint junctions in chromosomal translocations interacts with translin-associated protein X (TSNAX) | DDB0232428 | CDS | 4733677 | 645 | - | 0.232558 |
tsnax | DDB_G0284837 | ortholog of human TSNAX interacts with translin (TSN) may be involved in RNA metabolism | DDB0232431 | CDS | 2473632 | 855 | - | 0.247953 |
tspA | DDB_G0269110 | similar to the mammalian CD9 antigen contains a tetraspanin and 4 putative transmembrane domains | DDB0232428 | CDS | 3795204 | 708 | + | 0.323446 |
tspB | DDB_G0269872 | similar to the mammalian CD9 antigen contains a tetraspanin and 4 putative transmembrane domains | DDB0232428 | CDS | 3769162 | 708 | - | 0.299435 |
tspC | DDB_G0270986 | similar to the mammalian CD9 antigen contains a tetraspanin and 4 putative transmembrane domains | DDB0232428 | CDS | 3789005 | 717 | + | 0.297071 |
tspD | DDB_G0270682 | similar to the mammalian CD9 antigen contains a tetraspanin and 4 putative transmembrane domains | DDB0232428 | CDS | 3796607 | 693 | + | 0.277056 |
tspE | DDB_G0291177 | has similarity to the mammalian CD9 antigen contains a tetraspanin and 4 putative transmembrane domains | DDB0232432 | CDS | 5101333 | 696 | + | 0.244253 |
tssc1 | DDB_G0274279 | DDB0232429 | CDS | 4037996 | 1203 | + | 0.267664 | |
tsuA | DDB_G0267962 | putative protein serinethreonine kinase similar to mammalian STK36 and fly fused kinase (fu) a ST kinase involved in the hedgehog signal transduction pathway belongs to the ULK (Unc-51-like kinase) family of kinases | DDB0232428 | CDS | 1191800 | 6744 | + | 0.248517 |
ttc27 | DDB_G0293372 | DDB0232433 | CDS | 2801637 | 2562 | - | 0.296253 | |
ttc4 | DDB_G0286253 | DDB0232431 | CDS | 4254280 | 1194 | - | 0.278057 | |
tubA | DDB_G0287689 | monomeric subunit of microtubules as most other species Dicty has two alpha-tubulin genes and only one of each beta- and gamma-tubulin the other alpha tubulin gene is | DDB0232432 | CDS | 707217 | 1374 | - | 0.381368 |
tubA2 | DDB_G0281889 | bCommunity annotationb: As most other species Dicty has two alpha-tubulin genes and only one of each beta- and gamma-tubulin. Dicty's two alpha tubulin genes are both moderately upregulated in the Dicty rblA disruptant but tubA2 is substantially more so. In development tubA2 shows an expression trajectory approximating that of mitotic genes while tubA does not. The promoter of tubA2 contains a likely E2F binding sequence (ATTGGCGCT). It is possible but perhaps not compelling that tubA2 has specific mitotic functions. Harry MacWilliams July 2010br | DDB0232430 | CDS | 5074777 | 1359 | + | 0.293598 |
tubB | DDB_G0269196 | DDB0232428 | CDS | 3261649 | 1368 | - | 0.388889 | |
tubC | DDB_G0271738 | DDB0232429 | CDS | 727031 | 1389 | + | 0.332613 | |
tufM | DDB_G0289593 | mitochondrial translation elongation factor Tu highly similar to bacterial elongation factor Tu | DDB0232432 | CDS | 2977521 | 1275 | - | 0.418039 |
tupA | DDB_G0282189 | DDB0232430 | CDS | 5574241 | 1740 | + | 0.331034 | |
twfA | DDB_G0274437 | A6 family protein kinase very similar to human and mouse twinfilin (A6 protein) which is a tyrosine kinase and an actin monomer binding protein contains two ADF domains (actin depolymerization factorcofilin-like domains) | DDB0232429 | CDS | 4596611 | 1008 | - | 0.31746 |
txnl4a | DDB_G0275407 | DDB0232429 | CDS | 5420626 | 426 | - | 0.300469 | |
tyrS | DDB_G0276721 | catalyzes the reaction ATP L-Tyrosine tRNATyr AMP diphosphate L-tyrosyl-tRNATyr | DDB0232429 | CDS | 7137404 | 1152 | - | 0.326389 |
u2af1 | DDB_G0285077 | small subunit of the U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) which is a splicing factor that forms a heterodimer with | DDB0232431 | CDS | 2799520 | 1416 | + | 0.366525 |
u2af2 | DDB_G0286395 | large subunit of the U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) which is a splicing factor that forms a heterodimer with | DDB0232431 | CDS | 4405482 | 2016 | + | 0.361607 |
uae1 | DDB_G0270272 | DDB0232428 | CDS | 4544769 | 3054 | + | 0.341519 | |
uap1 | DDB_G0290055 | catalyzes the reaction UTP N-acetyl-alpha-D-glucosamine 1-phosphate diphosphate UDP-N-acetyl-D-glucosamine | DDB0232432 | CDS | 3567893 | 1464 | - | 0.304645 |
uap56 | DDB_G0269932 | conserved splice factor that is required for the first ATP-dependent step in spliceosome assembly and for the interaction of U2 snRNP with the branchpoint the human ortholog (BAT1) forms a homodimer and interacts directly with | DDB0232428 | CDS | 3893359 | 1287 | - | 0.359751 |
uba2 | DDB_G0286919 | conserved protein forms a heterodimer with sae1 acts as a E1 ligase for sumo | DDB0232431 | CDS | 5077667 | 1986 | - | 0.302618 |
uba5 | DDB_G0293306 | DDB0232433 | CDS | 2741328 | 1146 | + | 0.287086 | |
ubc9 | DDB_G0287693 | DDB0232432 | CDS | 688286 | 480 | - | 0.33125 | |
ubcB | DDB_G0284865 | high similarity to E2ubiquitin-conjugating enzymes from yeast metazoans and plants ubiquitin-conjugating enzymes (EC: 6.3.2.19) (UBC or E2 enzymes) catalyze the covalent attachment of ubiquitin to target proteins | DDB0232431 | CDS | 2571519 | 447 | - | 0.340045 |
ubcC | DDB_G0284009 | DDB0232431 | CDS | 1428069 | 708 | + | 0.310734 | |
ube1c | DDB_G0283891 | conserved catalytic subunit of the dimeric UBE1C-APPBP1 E1 enzyme which activates NEDD8 necessary for cell cycle progression through the S-M checkpoint | DDB0232431 | CDS | 1193106 | 1329 | - | 0.311512 |
ube2c | DDB_G0278775 | putative ortholog of S. pombe ubc11 and H. sapiens UBE2C involved in the destruction of cyclins during mitosisbrbr bCommunity annotation:b A role of this gene in cell cycle progression is supported by its sevenfold overexpression in a Dicty strain lacking the Dicty retinoblastoma like gene | DDB0232430 | CDS | 1152307 | 462 | + | 0.30303 |
ube2m | DDB_G0281725 | DDB0232430 | CDS | 4883727 | 693 | + | 0.314574 | |
ube2n | DDB_G0277267 | DDB0232429 | CDS | 7854255 | 465 | + | 0.344086 | |
ube2s | DDB_G0289021 | DDB0232432 | CDS | 2250572 | 648 | + | 0.290123 | |
ube2t | DDB_G0291199 | interacts with the Fanconi anaemia complex involved DNA cross-link repair null mutant is sensitive to DNA damaging agents brbr the mammalian Fanconi anaemia nuclear complex includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 Dictyostelium has orthologs for | DDB0232432 | CDS | 5123925 | 879 | - | 0.246871 |
ube2v | DDB_G0292596 | DDB0232433 | CDS | 1823383 | 417 | - | 0.290168 | |
ube2w | DDB_G0268938 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | DDB0232428 | CDS | 1961102 | 450 | + | 0.317778 |
ube3a | DDB_G0290179 | DDB0232432 | CDS | 3742663 | 2163 | - | 0.273694 | |
ubl5 | DDB_G0284205 | ortholog of human UBL5 and yeast HUB1 human UBL5 interacts with cyclin-dependent kinase CLK4 | DDB0232431 | CDS | 1687407 | 204 | - | 0.289216 |
ublcp1-1 | DDB_G0273117 | ortholog of the H. sapiens UBLCP1 a conserved protein that contains a ubiquitin and a NLI interacting factor domain there is a second copy of this gene | DDB0232429 | CDS | 2537016 | 1200 | + | 0.263333 |
ublcp1-2 | DDB_G0273861 | ortholog of the H. sapiens UBLCP1 a conserved protein that contains a ubiquitin and a NLI interacting factor domain there is a second copy of this gene | DDB0232429 | CDS | 3493474 | 1200 | - | 0.263333 |
ubpA | DDB_G0291239 | DDB0232433 | CDS | 283328 | 2514 | + | 0.333731 | |
ubpB | DDB_G0275021 | ubiquitin carboxyl-terminal hydrolase shown to deubiquinate mkkA putative ortholog of H. sapiens USP10 | DDB0232429 | CDS | 5178139 | 1356 | + | 0.286136 |
ubqA | DDB_G0282295 | DDB0232430 | CDS | 5639999 | 1146 | + | 0.362129 | |
ubqB | DDB_G0280755 | DDB0232430 | CDS | 3722395 | 387 | - | 0.372093 | |
ubqC | DDB_G0276765 | DDB0232429 | CDS | 7198772 | 465 | - | 0.372043 | |
ubqD | DDB_G0286907 | DDB0232431 | CDS | 5083931 | 690 | - | 0.327536 | |
ubqF | DDB_G0289449 | DDB0232432 | CDS | 2811202 | 1602 | + | 0.359551 | |
ubqG | DDB_G0282369 | DDB0232430 | CDS | 5878544 | 1146 | - | 0.331588 | |
ubqH | DDB_G0279721 | DDB0232430 | CDS | 2331609 | 1146 | + | 0.319372 | |
ubqI | DDB_G0291928 | DDB0232433 | CDS | 961035 | 918 | + | 0.308279 | |
ubqJ | DDB_G0269458 | DDB0232428 | CDS | 2811310 | 918 | + | 0.310458 | |
ubqK | DDB_G0280585 | DDB0232430 | CDS | 3532604 | 945 | + | 0.291005 | |
ubqK_ps1 | DDB_G0280589 | putative pseudogene ubiquitin family very similar to the upstream | DDB0232430 | CDS | 3534995 | 828 | + | 0.278986 |
ubqK_ps2 | DDB_G0280587 | DDB0232430 | CDS | 3534055 | 447 | + | 0.279642 | |
ubqK_ps3 | DDB_G0280739 | putative pseudogene ubiquitin family very similar to the upstream | DDB0232430 | CDS | 3536455 | 681 | + | 0.306902 |
ubqN | DDB_G0292984 | DDB0232433 | CDS | 2259430 | 222 | - | 0.247748 | |
ubqO | DDB_G0292908 | DDB0232433 | CDS | 2261064 | 234 | - | 0.311966 | |
ubqP | DDB_G0286031 | DDB0232431 | CDS | 3971817 | 939 | - | 0.28754 | |
ubq_ps | DDB_G0292910 | putative pseudogene fragment similar to D. discoideum ubiquitin genes including | DDB0232433 | CDS | 2262456 | 144 | - | 0.326389 |
ubr7 | DDB_G0292022 | DDB0232433 | CDS | 1035856 | 1398 | - | 0.253934 | |
uch1 | DDB_G0282007 | catalyzes the thiol-dependent hydrolysis of ester thiolester amide peptide and isopeptide bonds formed by the C-terminal Gly of ubiquitin most closely related to human UCHL1 aned UCHL3 | DDB0232430 | CDS | 5236311 | 768 | + | 0.285156 |
uch2 | DDB_G0285527 | catalyzes the thiol-dependent hydrolysis of ester thiolester amide peptide and isopeptide bonds formed by the C-terminal Gly of ubiquitin most closely related to human BAP1 and UCHL5 genes | DDB0232431 | CDS | 3345269 | 1032 | + | 0.26938 |
ucpA | DDB_G0271310 | ortholog of S. cerevisiae OAC1 involved in transport of oxaloacetate sulfate and thiosulfate across the mitochondrial membrane contains two transmembrane domains | DDB0232429 | CDS | 125735 | 921 | - | 0.299674 |
ucpB | DDB_G0283333 | ortholog of slc25a30 that belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane | DDB0232431 | CDS | 469001 | 885 | - | 0.309605 |
ucpC | DDB_G0284225 | ortholog of slc25a11 catalyzes the transport of 2-oxoglutarate across the inner mitochondrial membrane in an electroneutral exchange for malate or other dicarboxylic acids plays a role in several metabolic processes such as the malate-aspartate shuttle the oxoglutaratesocitrate shuttle in gluconeogenesis from lactate and in nitrogen metabolism | DDB0232431 | CDS | 1714783 | 957 | + | 0.315569 |
ucr | DDB_G0284947 | conserved ubiquinol-cytochrome c oxidoreductase subunit a component of the mitochondrial inner membrane electron transport chain | DDB0232431 | CDS | 2675998 | 645 | + | 0.384496 |
udkA | DDB_G0269034 | catalyzes the reaction ATP uridine ADP UMP | DDB0232428 | CDS | 2213969 | 1500 | - | 0.292 |
udkB | DDB_G0274559 | catalyzes the reaction ATP uridine ADP UMP | DDB0232429 | CDS | 4144032 | 732 | - | 0.325137 |
udkC | DDB_G0283371 | contains a N-terminal uridine kinase domaine domain and a C-terminal adenylate cyclase domain like the UdkD protein and other plant proteins | DDB0232431 | CDS | 600577 | 1350 | - | 0.297778 |
udkD | DDB_G0271146 | contains a N-terminal uridine kinase domaine domain and a C-terminal adenylate cyclase domain like the UdkC protein and other plant proteins | DDB0232429 | CDS | 69676 | 1479 | - | 0.294118 |
udpA | DDB_G0284431 | catalyzes the reaction phosphate uridine ribose-1-phosphate uracil in salvage pathways of pyrimidine ribonucleotides and deoxyribose phosphate degradation | DDB0232431 | CDS | 1983105 | 750 | - | 0.4 |
udpB | DDB_G0280985 | catalyzes the reaction phosphate uridine ribose-1-phosphate uracil in salvage pathways of pyrimidine ribonucleotides and deoxyribose phosphate degradation | DDB0232430 | CDS | 3914149 | 870 | - | 0.310345 |
uduA1 | DDB_G0268332 | upregulated in the uninfected | DDB0232428 | CDS | 708045 | 525 | + | 0.350476 |
uduA2 | DDB_G0267726 | upregulated in the uninfected | DDB0232428 | CDS | 711088 | 525 | + | 0.348571 |
uduA3 | DDB_G0267728 | upregulated in the uninfected | DDB0232428 | CDS | 713027 | 528 | + | 0.350379 |
uduB | DDB_G0268600 | upregulated in the uninfected | DDB0232428 | CDS | 1700922 | 492 | - | 0.345528 |
uduC | DDB_G0270726 | underexpressed in | DDB0232428 | CDS | 4216280 | 2280 | + | 0.334211 |
uduD1 | DDB_G0277083 | upregulated in the uninfected | DDB0232429 | CDS | 7474022 | 1455 | - | 0.2811 |
uduD2 | DDB_G0283125 | upregulated in the uninfected | DDB0232431 | CDS | 281753 | 1455 | + | 0.285911 |
uduE | DDB_G0277099 | upregulated in the uninfected | DDB0232429 | CDS | 7502309 | 294 | - | 0.227891 |
uduF | DDB_G0277097 | upregulated in the uninfected | DDB0232429 | CDS | 7498825 | 1452 | - | 0.284435 |
uduG | DDB_G0286953 | upregulated in the uninfected | DDB0232431 | CDS | 5140537 | 957 | + | 0.406479 |
uduH | DDB_G0276851 | upregulated in the uninfected | DDB0232429 | CDS | 7482048 | 2469 | - | 0.255974 |
ufc1 | DDB_G0289037 | DDB0232432 | CDS | 2284637 | 495 | - | 0.30101 | |
ufd1 | DDB_G0271122 | similar to S. cerevisiae UDF1 together with npl4 and cdcD involved in recognition of polyubiquitinated proteins and their presentation to the 26S proteasome for degradation | DDB0232429 | CDS | 33552 | 993 | - | 0.288016 |
ufm1 | DDB_G0295709 | DDB0232433 | CDS | 620919 | 258 | + | 0.302326 | |
uglA | DDB_G0277877 | DDB0232430 | CDS | 330250 | 1041 | + | 0.332373 | |
uglB | DDB_G0273013 | DDB0232429 | CDS | 2160250 | 1794 | - | 0.230769 | |
ugpB | DDB_G0277879 | DDB0232430 | CDS | 140895 | 1509 | - | 0.313453 | |
ugt1 | DDB_G0290339 | CAZy family GT28 contains a glycosyltransferase 28 domain and a partial MurG acetylglucosaminetransferase domain | DDB0232432 | CDS | 3987458 | 1197 | + | 0.233918 |
ugt2 | DDB_G0268540 | CAZy family GT28 highly similar to ugt3 | DDB0232428 | CDS | 1089190 | 1314 | - | 0.227549 |
ugt3 | DDB_G0268544 | CAZy family GT28 highly similar to ugt2 | DDB0232428 | CDS | 1091709 | 1314 | - | 0.225266 |
ugt52 | DDB_G0288655 | CAZy family GT1 catalyzes the reaction UDP-glucose a sterol UDP a glucosylsterol | DDB0232432 | CDS | 1802347 | 5094 | - | 0.291323 |
uox | DDB_G0286427 | catalyzes the reaction urate Osub2sub Hsub2subO 5-hydroxyisourate Hsub2subOsub2sub | DDB0232431 | CDS | 4473628 | 864 | - | 0.366898 |
upf1 | DDB_G0288923 | ortholog of yeast NAM7 and the mammalian UPF1 (up-frameshift suppressor 1) or RENT1 protein part of a post-splicing multiprotein complex and involved in nonsense-mediated decay (NMD) of mRNAs containing premature stop codons | DDB0232432 | CDS | 2130048 | 3996 | + | 0.318068 |
upf2 | DDB_G0281623 | DDB0232430 | CDS | 4719332 | 4188 | - | 0.294651 | |
uppA | DDB_G0289875 | catalyzes the reaction UTP alpha-D-glucose 1-phosphate diphosphate UDP-glucose | DDB0232432 | CDS | 3439159 | 1536 | - | 0.287109 |
uprt | DDB_G0267560 | catalyzes the reaction UMP diphosphate uracil 5-phospho-alpha-D-ribose 1-diphosphate | DDB0232428 | CDS | 336383 | 651 | + | 0.294931 |
uqcrb | DDB_G0286171 | ortholog of mammalian UQCRB a component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex) which is part of the mitochondrial respiratory chain | DDB0232431 | CDS | 4097397 | 330 | - | 0.30303 |
uqcrh | DDB_G0271774 | similar to the hinge protein of the ubiquinol-cytochrome C reductase complex involved in respiration | DDB0232429 | CDS | 890518 | 210 | + | 0.366667 |
uqcrq | DDB_G0280569 | ortholog of mammalian UQCRQ a component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex) which is part of the mitochondrial respiratory chain | DDB0232430 | CDS | 3513680 | 222 | + | 0.346847 |
urm1 | DDB_G0283737 | homolog of human and S. cerevisiae URM1 yeast URM1 is involved in tRNA modification and is alsoindirectly involved in oxidative stress response and regulation of budding and haploid invasive growth | DDB0232431 | CDS | 1046828 | 291 | - | 0.261168 |
uroc1 | DDB_G0277727 | catalyzes the reaction 3-(5-oxo-45-dihydro-3H-imidazol-4-yl)propanoate urocanate Hsub2subO the second step in the degradation of histidine | DDB0232429 | CDS | 8385798 | 2019 | - | 0.343735 |
usp12 | DDB_G0290453 | DDB0232432 | CDS | 4071585 | 1428 | - | 0.226891 | |
usp14 | DDB_G0271264 | DDB0232429 | CDS | 183660 | 1539 | + | 0.302794 | |
usp39 | DDB_G0278929 | similar to Arabidopsis thaliana ubiquitin carboxyl-terminal hydrolase family protein ortholog of yeast SAD1 which plays a role in pre-mRNA splicing | DDB0232430 | CDS | 1417023 | 2157 | + | 0.236439 |
usp40 | DDB_G0289611 | DDB0232432 | CDS | 3021100 | 5034 | - | 0.283472 | |
usp7 | DDB_G0276443 | DDB0232429 | CDS | 6959828 | 3921 | - | 0.263453 | |
utp11 | DDB_G0270230 | DDB0232428 | CDS | 4445249 | 753 | + | 0.260292 | |
utp13 | DDB_G0276283 | component of the small subunit (SSU) processome containing the U3 snoRNA involved in processing of pre-18S rRNA highly similar to H. sapiens transducin beta-like 3 (TBL3) | DDB0232429 | CDS | 6600384 | 2709 | + | 0.277593 |
utp14 | DDB_G0279371 | DDB0232430 | CDS | 2000722 | 2964 | - | 0.263833 | |
utp15 | DDB_G0283581 | DDB0232431 | CDS | 863530 | 1590 | - | 0.3 | |
utp18 | DDB_G0271240 | putative U3 snoRNP protein ortholog of H. sapiens and S. cerevisiae UTP18 | DDB0232429 | CDS | 234746 | 1563 | + | 0.25144 |
utp20 | DDB_G0279083 | component of the small subunit (SSU) processome containing the U3 snoRNA involved in processing of pre-18S rRNA contains a DRIM domain (Down-Regulated In Metastasis) | DDB0232430 | CDS | 1583286 | 9312 | + | 0.251396 |
utp23 | DDB_G0283685 | putative U3 snoRNP protein ortholog of H. sapiens C8orf53 and S. cerevisiae UTP23 | DDB0232431 | CDS | 980287 | 1320 | + | 0.266667 |
utp5 | DDB_G0275141 | putative ortholog of H. sapiens WDR43 and S. cerevisiae UTP4 component of the small subunit (SSU) processome containing the U3 snoRNA involved in processing of pre-18S rRNA | DDB0232429 | CDS | 4955753 | 1710 | - | 0.256725 |
utp6 | DDB_G0279601 | DDB0232430 | CDS | 2214566 | 1830 | + | 0.227322 | |
v4-7 | DDB_G0281823 | DDB0232430 | CDS | 5023432 | 2109 | - | 0.373637 | |
vacA | DDB_G0289485 | DDB0232432 | CDS | 2888908 | 1797 | + | 0.341681 | |
vacB | DDB_G0279191 | marker of the post-lysosomal vacuole plays a role late in the endocytic pathway may target the vacuole for exocytosis | DDB0232430 | CDS | 1911215 | 1779 | + | 0.323215 |
vacC | DDB_G0279307 | very similar to Dictyostelium vacuolin A and B | DDB0232430 | CDS | 1908644 | 1761 | + | 0.319137 |
valS1 | DDB_G0277733 | catalyzes the reaction ATP L-valine tRNAVal AMP diphosphate L-valyl-tRNAVal | DDB0232429 | CDS | 8402743 | 3219 | + | 0.352594 |
valS2 | DDB_G0288939 | catalyzes the reaction ATP L-valine tRNAVal AMP diphosphate L-valyl-tRNAVal | DDB0232432 | CDS | 2152189 | 3156 | + | 0.270279 |
vamp7A | DDB_G0284951 | member of the SNARE family (Soluble NSF Attachment Protein REceptor) localizes to endosome and interacts with syn7A | DDB0232431 | CDS | 2678890 | 651 | + | 0.288786 |
vamp7B | DDB_G0277173 | SNARE protein interacts with AP180 (clmA) which retrieves Vamp7B from the contractile vacuole | DDB0232429 | CDS | 7680323 | 783 | + | 0.297573 |
vasP | DDB_G0289541 | DDB0232432 | CDS | 2893954 | 1143 | - | 0.43657 | |
vatA | DDB_G0287127 | ortholog of the A subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the A subunit is part of the V1 subunit | DDB0232431 | CDS | 5370324 | 1857 | - | 0.367798 |
vatA_ps | DDB_G0287137 | putative pseudogene small fragment almost identical with parts of | DDB0232431 | CDS | 5367030 | 285 | - | 0.322807 |
vatB | DDB_G0277401 | ortholog of the B subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the B subunit is part of the V1 subunit | DDB0232429 | CDS | 8008207 | 1482 | + | 0.365722 |
vatC | DDB_G0284473 | ortholog of the C subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the C subunit is part of the V1 subunit | DDB0232431 | CDS | 2149008 | 1107 | - | 0.31346 |
vatD-1 | DDB_G0273071 | ortholog of the D subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the D subunit is part of the V1 subunit there is a second copy of this gene | DDB0232429 | CDS | 2787988 | 1071 | + | 0.323996 |
vatD-2 | DDB_G0273657 | ortholog of the D subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the D subunit is part of the V1 subunit there is a second copy of this gene | DDB0232429 | CDS | 3242326 | 1071 | - | 0.323996 |
vatE | DDB_G0275701 | ortholog of the E subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the E subunit is part of the V1 subunit | DDB0232429 | CDS | 5679309 | 702 | - | 0.324786 |
vatF | DDB_G0271882 | ortholog of the F subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the F subunit is part of the V1 subunit | DDB0232429 | CDS | 942083 | 363 | - | 0.316804 |
vatG | DDB_G0277971 | ortholog of the G subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the G subunit is part of the V1 subunit | DDB0232430 | CDS | 80768 | 324 | - | 0.333333 |
vatH | DDB_G0274553 | ortholog of the H subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the H subunit is part of the V1 subunit | DDB0232429 | CDS | 4167400 | 1338 | + | 0.29148 |
vatM | DDB_G0291858 | ortholog of the mammalian V-type proton ATPase 116 kDa subunit a the transmembrane subunit of the vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes this protein is part of the V0 complex | DDB0232433 | CDS | 889796 | 2454 | + | 0.368786 |
vatP | DDB_G0274381 | ortholog of the mammalian V-type proton ATPase 16 kDa proteolipid subunit the proton-conducting pore forming subunit of the vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes this protein is part of the V0 complex | DDB0232429 | CDS | 4920282 | 591 | + | 0.373942 |
veg111 | DDB_G0282371 | DDB0232430 | CDS | 6080613 | 1077 | + | 0.321263 | |
vilA | DDB_G0288557 | DDB0232432 | CDS | 1709022 | 5115 | - | 0.324536 | |
vilB | DDB_G0276453 | belongs to the villingelsolin family contains 6 gelsolin-like repeats and a villin headpiece domain | DDB0232429 | CDS | 6792443 | 2880 | - | 0.304167 |
vilC | DDB_G0271058 | belongs to the villingelsolin family contains 5 gelsolin-like repeats and one villin headpiece domain | DDB0232428 | CDS | 4570908 | 4587 | - | 0.297362 |
vilD | DDB_G0282725 | belongs to the villingelsolin family contains 7 gelsolin-like repeats and one villin headpiece domain | DDB0232430 | CDS | 6207123 | 5328 | - | 0.306869 |
vinB | DDB_G0281499 | DDB0232430 | CDS | 4621318 | 5355 | + | 0.320635 | |
vmp1 | DDB_G0285175 | conserved protein required for biogenesis of the contractile vacuole in response to osmotic stress contains 8 predicted transmembrane domains | DDB0232431 | CDS | 2937306 | 1212 | + | 0.291254 |
vps11 | DDB_G0278141 | DDB0232430 | CDS | 343671 | 2859 | - | 0.33893 | |
vps13A | DDB_G0286725 | putative ortholog of S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 4889609 | 10122 | - | 0.30488 |
vps13B | DDB_G0274917 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232429 | CDS | 4457216 | 18186 | - | 0.252777 |
vps13D | DDB_G0286545 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 4616198 | 13779 | - | 0.252994 |
vps13D_ps1 | DDB_G0270804 | putative pseudogene fragment similar to D. discoideum gene | DDB0232428 | CDS | 4775472 | 243 | - | 0.205761 |
vps13D_ps2 | DDB_G0274983 | putative pseudogene fragmnent similar to D. discoideum gene | DDB0232429 | CDS | 4789311 | 486 | - | 0.283951 |
vps13E | DDB_G0268886 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232428 | CDS | 2311232 | 12726 | + | 0.274399 |
vps13F | DDB_G0287055 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 5237174 | 12741 | - | 0.271172 |
vps13l | DDB_G0277219 | DDB0232429 | CDS | 7662227 | 1962 | - | 0.285933 | |
vps15 | DDB_G0282627 | putative protein serinethreonine kinase similar to human PIK3R4 and yeast VPS15 which regulate the phosphatidylinositol 3 kinase VPS34 (hVps34) yeast VPS15VPS34 complex known to be involved in vacuolar protein sorting | DDB0232430 | CDS | 6019111 | 5901 | + | 0.306219 |
vps16 | DDB_G0270754 | DDB0232428 | CDS | 4423807 | 2499 | + | 0.322929 | |
vps18 | DDB_G0269924 | DDB0232428 | CDS | 3875953 | 3234 | + | 0.302412 | |
vps20 | DDB_G0287021 | component of the ESCRT-III complex (endosomal sorting complex required for transport) putative ortholog of human CHMP6 (Chromatin Modifying Protein 6) and yeast VPS20 | DDB0232431 | CDS | 5201277 | 657 | - | 0.284627 |
vps22 | DDB_G0283203 | component of the ELL complex an RNA polymerase II transcription factor and of the ESCRT-II complex (endosomal sorting complex required for transport) | DDB0232431 | CDS | 415279 | 741 | + | 0.25641 |
vps24 | DDB_G0284769 | DDB0232431 | CDS | 2459478 | 624 | - | 0.304487 | |
vps25 | DDB_G0267708 | component of the ELL complex an RNA polymerase II transcription factor and of the ESCRT-II complex (endosomal sorting complex required for transport) | DDB0232428 | CDS | 670930 | 585 | - | 0.246154 |
vps26 | DDB_G0269168 | ortholog of VSP26 a vacuolar sortingtargeting protein | DDB0232428 | CDS | 4319399 | 1050 | - | 0.300952 |
vps26l | DDB_G0292212 | ortholog of H. sapiens DSCR3 the Down syndrome critical region gene 3 | DDB0232433 | CDS | 1334023 | 915 | + | 0.288525 |
vps28 | DDB_G0285295 | DDB0232431 | CDS | 3068985 | 867 | - | 0.229527 | |
vps29 | DDB_G0288787 | ortholog of VPS29 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | DDB0232432 | CDS | 1965193 | 552 | - | 0.311594 |
vps2A | DDB_G0290087 | putative ortholog of human CHMP2A (Chromatin Modifying Protein 2A) and yeast DID4 (Doa4-Independent Degradation) component of the ESCRT-III complex (endosomal sorting complex required for transport) | DDB0232432 | CDS | 3647628 | 621 | - | 0.299517 |
vps2B | DDB_G0292400 | putative ortholog of human CHMP2A (Chromatin Modifying Protein 2A) and yeast DID4 (Doa4-Independent Degradation) component of the ESCRT-III complex (endosomal sorting complex required for transport) | DDB0232433 | CDS | 1551408 | 597 | - | 0.296482 |
vps32 | DDB_G0275573 | involved in vesicle trafficking in yeast and mammals expressed in endosome | DDB0232429 | CDS | 5525678 | 648 | + | 0.291667 |
vps33 | DDB_G0291097 | DDB0232432 | CDS | 4992025 | 1935 | - | 0.328165 | |
vps35 | DDB_G0293218 | ortholog of VPS35 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | DDB0232433 | CDS | 2686279 | 2346 | + | 0.323529 |
vps36 | DDB_G0282045 | component of the ELL complex an RNA polymerase II transcription factor and of the ESCRT-II complex (endosomal sorting complex required for transport) | DDB0232430 | CDS | 5326311 | 1836 | - | 0.276144 |
vps37 | DDB_G0269510 | DDB0232428 | CDS | 2905172 | 1002 | - | 0.272455 | |
vps39 | DDB_G0279169 | DDB0232430 | CDS | 1722504 | 2556 | - | 0.321205 | |
vps4 | DDB_G0284347 | DDB0232431 | CDS | 1865073 | 1335 | + | 0.326592 | |
vps41 | DDB_G0286803 | DDB0232431 | CDS | 4738365 | 3264 | - | 0.33701 | |
vps45 | DDB_G0290213 | putative ortholog of VPS45 involved in vacuolar protein sorting | DDB0232432 | CDS | 3802462 | 1692 | - | 0.278369 |
vps46 | DDB_G0267394 | DDB0232428 | CDS | 1659361 | 579 | - | 0.305699 | |
vps5 | DDB_G0272989 | putative ortholog of mammalian sorting nexin and S. cerevisiae VPS5 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | DDB0232429 | CDS | 2025586 | 1638 | - | 0.339438 |
vps52A | DDB_G0293772 | putative ortholog of S. cerevisiae VPS52 component of the GARP (Golgi-associated retrograde protein) complex | DDB0232433 | CDS | 3307775 | 2517 | + | 0.222487 |
vps52B | DDB_G0293496 | similar to S. cerevisiae VPS52 component of the GARP (Golgi-associated retrograde protein) complex | DDB0232433 | CDS | 2961150 | 2631 | - | 0.247815 |
vps52C | DDB_G0271856 | similar to S. cerevisiae VPS52 component of the GARP (Golgi-associated retrograde protein) complex | DDB0232429 | CDS | 970613 | 2397 | - | 0.261994 |
vps54 | DDB_G0272985 | putative ortholog of S. cerevisiae VPS54 component of the GARP (Golgi-associated retrograde protein) complex | DDB0232429 | CDS | 2012543 | 2955 | + | 0.244332 |
vps55 | DDB_G0280219 | DDB0232430 | CDS | 3127670 | 378 | - | 0.304233 | |
vps60 | DDB_G0287993 | ortholog of yeast VPS60 and human CHMP5 (CHromatin Modifying Protein 5) which associates with the ESCRT-III complex (endosomal sorting complex required for transport) | DDB0232432 | CDS | 940480 | 648 | - | 0.333333 |
vps8 | DDB_G0291606 | putative ortholog of VPS8 involved in vacuolar protein localization | DDB0232433 | CDS | 397697 | 5256 | + | 0.296233 |
vta1 | DDB_G0271488 | DDB0232429 | CDS | 430599 | 1653 | - | 0.318209 | |
vti1A | DDB_G0292974 | DDB0232433 | CDS | 2202494 | 654 | - | 0.281346 | |
vti1B | DDB_G0283363 | DDB0232431 | CDS | 584359 | 810 | + | 0.308642 | |
vwkA | DDB_G0268144 | belongs to the Atypical Alpha protein kinases and contains a von Willebrand factor type A (VWFA) domain does not phosphorylate myosin heavy chain | DDB0232428 | CDS | 1533586 | 1878 | - | 0.291267 |
wacA | DDB_G0280537 | member of the major intrinsic protein (MIP) family of membrane transporters expressed starting at culmination stage in prespore cells | DDB0232430 | CDS | 3567052 | 825 | + | 0.368485 |
warA | DDB_G0291075 | DDB0232432 | CDS | 5009348 | 2412 | - | 0.283167 | |
wasA | DDB_G0293834 | colocalizes with clathrin spots suggesting involvement in endocytosis does not localize to pseudopods in wild type in SCAR depleted mutants WASP replaces the functions of SCAR and localizes to pseudopods | DDB0232433 | CDS | 3376698 | 1200 | + | 0.4025 |
wasB | DDB_G0272811 | contains a WASP-C domain and a WH2 actin-binding motif plays a role in the regulation of F-actin polymerization and pseudopod formation | DDB0232429 | CDS | 2232918 | 1752 | - | 0.365297 |
wbp1 | DDB_G0291780 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae WBP1 and human OST48 contains one C-terminal transmembrane domain and an N-terminal signal peptide | DDB0232433 | CDS | 737175 | 1281 | + | 0.297424 |
wdr12 | DDB_G0279903 | DDB0232430 | CDS | 2678219 | 1392 | + | 0.30819 | |
wdr13 | DDB_G0291596 | DDB0232433 | CDS | 588031 | 1464 | + | 0.268443 | |
wdr18 | DDB_G0288659 | DDB0232432 | CDS | 1790292 | 1683 | + | 0.273321 | |
wdr23 | DDB_G0291832 | DDB0232433 | CDS | 834929 | 1986 | - | 0.291541 | |
wdr24 | DDB_G0287817 | DDB0232432 | CDS | 760582 | 3072 | - | 0.277995 | |
wdr3 | DDB_G0282623 | DDB0232430 | CDS | 6010118 | 2829 | + | 0.308236 | |
wdr36 | DDB_G0277019 | putative U3 snoRNP protein ortholog of H. sapiens WDR36 and S. cerevisiae UTP21 WDR36 has been implicated in open angle glaucoma 1 type G (GLC1G) | DDB0232429 | CDS | 7238641 | 3081 | + | 0.278156 |
wdr4 | DDB_G0281061 | similar to H. sapiens WDR4 which is required for 7-methylguanosine modification of tRNA and forms a complex with METTL1 | DDB0232430 | CDS | 3999282 | 1404 | - | 0.254274 |
wdr45l | DDB_G0282581 | ortholog of the conserved WDR45 like protein that is up-regulated in a variety of human cancers contains 3 WD-40 repeats | DDB0232430 | CDS | 5969861 | 1053 | + | 0.304843 |
wdr46 | DDB_G0280489 | DDB0232430 | CDS | 3437042 | 1869 | + | 0.308186 | |
wdr5 | DDB_G0287273 | highly similar to WDR5 protein involved in histone H3 K4 methylation | DDB0232432 | CDS | 72820 | 1008 | + | 0.298611 |
wdr53 | DDB_G0293608 | DDB0232433 | CDS | 3130386 | 1107 | + | 0.226739 | |
wdr57 | DDB_G0271788 | ortholog of human WDR57 which binds PRP8 contains 7 WD40 repeats | DDB0232429 | CDS | 716526 | 1068 | + | 0.32397 |
wdr61 | DDB_G0282793 | DDB0232430 | CDS | 6064156 | 900 | + | 0.306667 | |
wdr68 | DDB_G0275925 | DDB0232429 | CDS | 6064231 | 978 | + | 0.312883 | |
wdr7 | DDB_G0272771 | putative ortholog of H. sapiens WDR7 also known as TGF-beta resistance-associated protein (TRAG) and rabconnectin-3 beta | DDB0232429 | CDS | 2154360 | 4029 | - | 0.327128 |
wdr75 | DDB_G0268898 | DDB0232428 | CDS | 2341344 | 3048 | - | 0.262139 | |
wdr85 | DDB_G0270178 | DDB0232428 | CDS | 4375992 | 1104 | - | 0.246377 | |
wdr89 | DDB_G0283635 | DDB0232431 | CDS | 891645 | 1080 | + | 0.285185 | |
wdr91 | DDB_G0268084 | DDB0232428 | CDS | 1428913 | 2301 | - | 0.263798 | |
wdr92 | DDB_G0291822 | DDB0232433 | CDS | 825936 | 1074 | + | 0.255121 | |
wfdc | DDB_G0274699 | contains a putative N-terminal signal sequence secreted protein | DDB0232429 | CDS | 4201191 | 438 | - | 0.267123 |
wimA | DDB_G0269198 | DDB0232428 | CDS | 4776808 | 5979 | - | 0.329152 | |
wimA_ps1 | DDB_G0288117 | putative pseudogene similar to the wimA gene contains also a short region of similarity with the forC gene | DDB0232432 | CDS | 1065579 | 1581 | - | 0.285895 |
wipA | DDB_G0270430 | interacts with WASP ( | DDB0232428 | CDS | 4856092 | 594 | - | 0.493266 |
wrky1 | DDB_G0275267 | DDB0232429 | CDS | 5120434 | 3816 | - | 0.224843 | |
wrn | DDB_G0268512 | E. coli ATP-dependent DNA helicase RecQ is involved in genome maintenance this is the ortholog of the H. sapiens Werner syndrome protein defects in WRN cause the premature onset of multiple age-related disorders | DDB0232428 | CDS | 769229 | 3411 | - | 0.230431 |
wrnip1 | DDB_G0272158 | ortholog of Werner helicase-interacting protein 1 a modulator for initiation or reinitiation events during DNA polymerase delta-mediated DNA synthesis | DDB0232429 | CDS | 1585133 | 2631 | + | 0.302547 |
wshA | DDB_G0292878 | contains a C-terminal actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domain | DDB0232433 | CDS | 2194668 | 1419 | + | 0.349542 |
xab2 | DDB_G0277977 | DDB0232430 | CDS | 88368 | 2553 | + | 0.278104 | |
xacA | DDB_G0291978 | contains a RhoGAP domain an SH3 domain and two RhoGEF domains separated by a PH domain | DDB0232433 | CDS | 988440 | 4053 | + | 0.304713 |
xacB | DDB_G0278417 | DDB0232430 | CDS | 859128 | 3828 | + | 0.268548 | |
xacC | DDB_G0285391 | DDB0232431 | CDS | 3109098 | 4134 | - | 0.341558 | |
xdh | DDB_G0291047 | catalyzes the reactions xanthine NAD Hsub2subO urate NADH H and xanthine Hsub2subO Osub2sub urate Hsub2subOsub2sub | DDB0232432 | CDS | 4822800 | 4077 | + | 0.347559 |
xpc | DDB_G0292296 | DDB0232433 | CDS | 1414792 | 2904 | + | 0.266529 | |
xpf | DDB_G0284419 | DDB0232431 | CDS | 1971161 | 2895 | + | 0.245596 | |
xpnpep1 | DDB_G0290501 | probable Xaa-Pro aminopeptidase 1 that releases any N-terminal amino acid including proline that is linked to proline even from a dipeptide or tripeptide | DDB0232432 | CDS | 4157355 | 1884 | + | 0.300955 |
xpnpep3 | DDB_G0282075 | probable Xaa-Pro aminopeptidase 3 that releases any N-terminal amino acid including proline that is linked to proline even from a dipeptide or tripeptide | DDB0232430 | CDS | 5239385 | 1557 | - | 0.287091 |
xpo1 | DDB_G0291306 | DDB0232433 | CDS | 102439 | 3174 | - | 0.3431 | |
xpo2 | DDB_G0291838 | bCommunity annotation:b DDB_G0291838 is highly similar to cse1 of budding yeast and CAS of metazoans. In yeast this protein has been shown to be essential for the re-export of importin alpha (see Schroeder et al Mol Gen Genet 261 788-795 (1999). CSE stands for | DDB0232433 | CDS | 815672 | 2856 | - | 0.308473 |
xpo4 | DDB_G0280907 | DDB0232430 | CDS | 3862138 | 3402 | + | 0.276896 | |
xpo5 | DDB_G0284379 | DDB0232431 | CDS | 1912156 | 3408 | - | 0.289319 | |
xpo6 | DDB_G0293076 | DDB0232433 | CDS | 2441945 | 3144 | + | 0.265585 | |
xpo7 | DDB_G0291986 | DDB0232433 | CDS | 1213027 | 3024 | + | 0.263228 | |
xpot | DDB_G0283119 | DDB0232431 | CDS | 269911 | 3267 | - | 0.277319 | |
xpr1 | DDB_G0285957 | ortholog of XPR1 which in mammals confers susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | DDB0232431 | CDS | 3794131 | 2760 | - | 0.294203 |
xrcc1 | DDB_G0275653 | putative ortholog of XRCC1 which is involved in single-strand break repair interacts with DNA ligase III | DDB0232429 | CDS | 5843218 | 2844 | - | 0.268987 |
xrcc2 | DDB_G0290297 | putative ortholog of XRCC2 which is involved in double-strand break repair interacts with RAD51 | DDB0232432 | CDS | 3921390 | 1167 | + | 0.251928 |
xrcc3 | DDB_G0283637 | putative ortholog of XRCC3 which is involved in double-strand break repair interacts with RAD51 | DDB0232431 | CDS | 893273 | 1695 | + | 0.220059 |
xrcc4 | DDB_G0278203 | putative ortholog of XRCC4 which is involved in double-strand break repair including V(D)J recombination in T-cell receptor genes forms a complex with DNA ligase IV | DDB0232430 | CDS | 471533 | 1365 | + | 0.21685 |
xrn1 | DDB_G0276137 | DDB0232429 | CDS | 6232603 | 5250 | - | 0.333333 | |
xrn2 | DDB_G0269922 | DDB0232428 | CDS | 3871046 | 3573 | - | 0.285195 | |
yakA | DDB_G0283605 | belongs to the CMGC group of protein kinases putative protein serinethreonine kinase | DDB0232431 | CDS | 868454 | 4377 | + | 0.303404 |
ybl1 | DDB_G0272222 | member of the histone H2A-H2B sub-family related to the NF-YB subunit of the CCAAT-binding activator NF-Y | DDB0232429 | CDS | 1710917 | 417 | - | 0.297362 |
yelA | DDB_G0280047 | DDB0232430 | CDS | 2965418 | 2730 | - | 0.274725 | |
yipf1 | DDB_G0281587 | very similar to Yip1 domain family member 1 (YIPF1) in S. cerevisiae YIPF1 localizes to the Golgi and interacts with GTPases contains five putative transmembrane domains | DDB0232430 | CDS | 4674842 | 1896 | + | 0.269515 |
yipf5 | DDB_G0283541 | very similar to Yip1 domain family member 5 (YIPF5) in yeast YIP1 localizes to the Golgi and interacts with GTPases contains four putative transmembrane domains | DDB0232431 | CDS | 791068 | 639 | + | 0.273865 |
yipf6 | DDB_G0282825 | very similar to Yip1 domain family member 6 (YIPF6) in yeast YIP1 localizes to the Golgi and interacts with GTPases contains five putative transmembrane domains | DDB0232430 | CDS | 6266209 | 549 | - | 0.300546 |
ykt6 | DDB_G0291656 | DDB0232433 | CDS | 180176 | 609 | + | 0.320197 | |
yod1 | DDB_G0271346 | DDB0232429 | CDS | 66274 | 978 | + | 0.284254 | |
ypel | DDB_G0267990 | single D. discoideum ortholog of the highly conserved yippee protein family | DDB0232428 | CDS | 1242726 | 390 | - | 0.302564 |
zak2 | DDB_G0276187 | contains two kinase domains N-terminal kinase domain related to STE group C-terminal domain similar to TKL group highly similar to zakA and has overlapping function with zakA shown to be a tyrosine kinase and regulator of GSK3 also regulates pattern formation during development via dstC (STATc) signaling | DDB0232429 | CDS | 6396810 | 1908 | - | 0.253145 |
zakA | DDB_G0276025 | contains two kinase domains N-terminal kinase domain related to STE group C-terminal domain similar to TKL group | DDB0232429 | CDS | 6393550 | 2346 | - | 0.239983 |
zfaA | DDB_G0290961 | DDB0232432 | CDS | 4810278 | 1383 | - | 0.263919 | |
zfaA_ps | DDB_G0290935 | putative pseudogene similar to a family of D. discoideum zinc finger containing genes including | DDB0232432 | CDS | 4771025 | 543 | - | 0.244936 |
zfand | DDB_G0270362 | DDB0232428 | CDS | 4713592 | 498 | + | 0.289157 | |
zipA | DDB_G0286985 | DDB0232431 | CDS | 5171363 | 3075 | - | 0.294959 | |
zizA | DDB_G0275035 | DDB0232429 | CDS | 5293775 | 6855 | - | 0.288257 | |
zizB | DDB_G0293084 | DDB0232433 | CDS | 2452128 | 6444 | - | 0.301055 | |
zizC | DDB_G0275239 | DDB0232429 | CDS | 4945321 | 7866 | + | 0.291126 | |
zizD | DDB_G0268888 | DDB0232428 | CDS | 2324197 | 6489 | - | 0.300663 | |
zmpste24 | DDB_G0290849 | proteolytically removes the C-terminal three residues of farnesylated proteins contains 6 putative transmembrane domains and an additional signal peptide | DDB0232432 | CDS | 4673270 | 1281 | - | 0.251366 |
zntA | DDB_G0268426 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | DDB0232428 | CDS | 1375259 | 1524 | + | 0.256562 |
zntB | DDB_G0286345 | ZIP family zinc transporter LZT subfamily member contains 7 transmembrane domains expressed in pstAB cells | DDB0232431 | CDS | 4327628 | 1119 | + | 0.314567 |
zntC | DDB_G0286049 | ZIP family zinc transporter LZT subfamily member contains 7 transmembrane domains expressed in pstAB cells | DDB0232431 | CDS | 3998261 | 1206 | + | 0.333333 |
zntD | DDB_G0269326 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | DDB0232428 | CDS | 2544681 | 2052 | - | 0.273879 |
zpr1 | DDB_G0269438 | ortholog of ZPR1 a eukaryotic zinc finger protein | DDB0232428 | CDS | 2767401 | 1434 | - | 0.288703 |