Gene list
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Genomic element: DDB0232433
Number of genes found: 1442
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 |
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_G0294555 | DDB_G0294555 | DDB0232433 | CDS | 100153 | 1659 | + | 0.246534 | |
DDB_G0294573 | DDB_G0294573 | similar to | DDB0232433 | CDS | 3288367 | 360 | - | 0.261111 |
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_G0295475 | DDB_G0295475 | DDB0232433 | CDS | 418715 | 1710 | - | 0.283626 | |
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_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_G0295683 | DDB_G0295683 | DDB0232433 | CDS | 1769740 | 4770 | + | 0.291614 | |
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_G0295705 | DDB_G0295705 | DDB0232433 | CDS | 621820 | 2340 | - | 0.191026 | |
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_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_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_G0304683 | DDB_G0304683 | DDB0232433 | CDS | 1860016 | 2583 | - | 0.258227 | |
DDB_G0349136 | DDB_G0349136 | DDB0232433 | CDS | 1350474 | 3105 | + | 0.260225 | |
DDB_G0349138 | DDB_G0349138 | DDB0232433 | CDS | 1354305 | 492 | + | 0.243902 | |
DDB_G0349347 | DDB_G0349347 | DDB0232433 | CDS | 3330793 | 354 | - | 0.282486 | |
DG1098 | DDB_G0293192 | DDB0232433 | CDS | 2617515 | 6132 | + | 0.21396 | |
Dd5P3 | DDB_G0292392 | DDB0232433 | CDS | 1583730 | 4140 | - | 0.320773 | |
H2Bv1 | DDB_G0293758 | DDB0232433 | CDS | 3289579 | 681 | - | 0.330396 | |
X69101 | DDB_G0294501 | DDB0232433 | CDS | 3385382 | 116 | + | 0.362069 | |
abcA1 | DDB_G0291994 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 1093282 | 2634 | + | 0.319286 |
abcA3 | DDB_G0293436 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 2880255 | 5109 | + | 0.267371 |
abcA6 | DDB_G0291245 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 313947 | 4896 | - | 0.278595 |
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 |
abcB5 | DDB_G0292554 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 1786504 | 2094 | - | 0.294651 |
abcC7 | DDB_G0291243 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 391713 | 3987 | - | 0.251818 |
abcD2 | DDB_G0293194 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 2712310 | 2226 | + | 0.32929 |
abcG10 | DDB_G0292986 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 2306939 | 4401 | + | 0.310384 |
abcG9 | DDB_G0293450 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232433 | CDS | 2911255 | 4347 | + | 0.326202 |
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 | |
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 |
act24_ps | DDB_G0293368 | putative pseudogene contains an incomplete actin domain similar to | DDB0232433 | CDS | 2797121 | 126 | - | 0.31746 |
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 |
adi1 | DDB_G0291376 | DDB0232433 | CDS | 203637 | 444 | - | 0.259009 | |
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 |
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 |
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 |
alg11 | DDB_G0292118 | CAZy family GT4 catalyzes N-linked mannosylation | DDB0232433 | CDS | 1220852 | 1518 | + | 0.28722 |
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 |
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 |
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 |
ap1s2 | DDB_G0295711 | DDB0232433 | CDS | 619891 | 465 | - | 0.260215 | |
apeh | DDB_G0292456 | DDB0232433 | CDS | 1668118 | 2295 | - | 0.290632 | |
aplD | DDB_G0293010 | DDB0232433 | CDS | 2590611 | 432 | + | 0.252315 | |
aplP | DDB_G0292508 | DDB0232433 | CDS | 1757953 | 486 | - | 0.279835 | |
arcC | DDB_G0292804 | component of the Dictyostelium Arp2Arp3 complex | DDB0232433 | CDS | 2116342 | 525 | + | 0.361905 |
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 |
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 |
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 |
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 |
atp12 | DDB_G0292678 | DDB0232433 | CDS | 1937753 | 993 | - | 0.257805 | |
atp5C1 | DDB_G0292306 | DDB0232433 | CDS | 1438508 | 921 | + | 0.373507 | |
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 |
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 |
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 |
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 |
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 |
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 |
carmil | DDB_G0292386 | DDB0232433 | CDS | 1735919 | 3153 | - | 0.326673 | |
cbfB | DDB_G0293470 | similar to Dictyostelium cbfA contains a jmjC domain | DDB0232433 | CDS | 2928133 | 4425 | - | 0.250847 |
cct2 | DDB_G0291358 | DDB0232433 | CDS | 177191 | 1599 | - | 0.358349 | |
cct4 | DDB_G0292872 | DDB0232433 | CDS | 2188382 | 1602 | - | 0.373908 | |
cct7 | DDB_G0291225 | DDB0232433 | CDS | 201367 | 1668 | + | 0.41307 | |
cdc26 | DDB_G0293230 | cdc26 ortholog missing about half of the carboxyl terminus | DDB0232433 | CDS | 2676069 | 210 | + | 0.304762 |
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 |
cepA | DDB_G0292142 | DDB0232433 | CDS | 1258240 | 1041 | + | 0.232469 | |
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 |
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 |
cirh1a | DDB_G0293462 | DDB0232433 | CDS | 2920900 | 1389 | + | 0.24982 | |
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 |
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 |
cnrK | DDB_G0292120 | DDB0232433 | CDS | 1222744 | 3645 | - | 0.266941 | |
coaA | DDB_G0293898 | DDB0232433 | CDS | 3517422 | 441 | + | 0.387755 | |
cofB | DDB_G0291970 | coding region identical to cofA the 15 kDa actin severing protein | DDB0232433 | CDS | 1044327 | 414 | - | 0.391304 |
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 |
colA | DDB_G0292696 | collagen-binding surface protein Cna-like B-type domain-containing large protein | DDB0232433 | CDS | 1959495 | 33312 | - | 0.32826 |
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 |
comG | DDB_G0292270 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232433 | CDS | 1403334 | 1413 | + | 0.339703 |
commd1 | DDB_G0292074 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232433 | CDS | 1155156 | 564 | - | 0.210993 |
commd8 | DDB_G0292688 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232433 | CDS | 1952596 | 618 | + | 0.205502 |
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 |
coq4 | DDB_G0292620 | similar to S. cerevisiae COQ4 a protein of unknown function required for ubiquinone biosynthesis | DDB0232433 | CDS | 1849018 | 861 | + | 0.269454 |
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 |
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 |
cpnA | DDB_G0293008 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232433 | CDS | 2395700 | 1803 | + | 0.321131 |
cpnF | DDB_G0291498 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232433 | CDS | 437512 | 1653 | - | 0.255898 |
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 |
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 |
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 |
cspB | DDB_G0292808 | DDB0232433 | CDS | 2157251 | 177 | - | 0.38983 | |
ctaA | DDB_G0293004 | DDB0232433 | CDS | 2385585 | 3897 | - | 0.308442 | |
ctnnbl1 | DDB_G0292778 | DDB0232433 | CDS | 2017543 | 1578 | + | 0.225602 | |
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 |
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 |
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 |
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 |
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 |
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 | |
cyp516A1 | DDB_G0292168 | DDB0232433 | CDS | 1087783 | 1464 | + | 0.267076 | |
cyp519D1 | DDB_G0291448 | DDB0232433 | CDS | 323966 | 1701 | - | 0.240447 | |
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 | |
cysK | DDB_G0292840 | catalyzes the reaction O-acetyl-L-serine Hsub2subS L-cysteine acetate | DDB0232433 | CDS | 2136817 | 1137 | + | 0.333333 |
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 |
dduC | DDB_G0292604 | downregulated in the uninfected | DDB0232433 | CDS | 1828931 | 372 | + | 0.276882 |
ddx17 | DDB_G0293168 | conserved RNA helicase very similar to mammalian DDX17 (p72) and DDX5 (p68) and yeast DBP2 | DDB0232433 | CDS | 2360817 | 2358 | - | 0.370229 |
ddx5 | DDB_G0293036 | DDB0232433 | CDS | 2373448 | 2094 | + | 0.258835 | |
ddx51 | DDB_G0293740 | DDB0232433 | CDS | 3249527 | 1692 | - | 0.229905 | |
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 |
ddx6 | DDB_G0291804 | ortholog of H. sapiens DDX6 and S. cerevisiae DHH1 (DExDH-box Helicase) | DDB0232433 | CDS | 773358 | 1272 | + | 0.367925 |
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 |
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 |
dnaja1 | DDB_G0291568 | conserved molecular chaperone DnaJ homolog subfamily A member 1 | DDB0232433 | CDS | 558877 | 1380 | + | 0.365942 |
docA | DDB_G0291974 | DDB0232433 | CDS | 1105862 | 6666 | + | 0.30348 | |
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 |
dph4 | DDB_G0292980 | DDB0232433 | CDS | 2253222 | 513 | + | 0.224172 | |
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 |
dscE | DDB_G0292552 | DDB0232433 | CDS | 1899844 | 774 | - | 0.320413 | |
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 |
dstC | DDB_G0293532 | DDB0232433 | CDS | 3253627 | 2796 | - | 0.331545 | |
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 |
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 |
dync1li1 | DDB_G0292904 | DDB0232433 | CDS | 2245112 | 1515 | - | 0.280528 | |
dyrk2 | DDB_G0293750 | DDB0232433 | CDS | 3272270 | 2748 | + | 0.306405 | |
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 |
eif2b2 | DDB_G0291271 | DDB0232433 | CDS | 38541 | 1167 | - | 0.288775 | |
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 |
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 |
eloA | DDB_G0292896 | fatty acid elongase with substrate specificity for monounsaturated fatty acids in particular elongates 16:1 | DDB0232433 | CDS | 2229613 | 816 | - | 0.261029 |
empB | DDB_G0293540 | DDB0232433 | CDS | 3021203 | 630 | + | 0.314286 | |
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 |
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 |
esf2 | DDB_G0293576 | DDB0232433 | CDS | 3063826 | 891 | - | 0.258137 | |
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 |
exoc3 | DDB_G0293520 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232433 | CDS | 2981805 | 2352 | + | 0.274235 |
exoc6 | DDB_G0293936 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232433 | CDS | 3528888 | 3078 | - | 0.273229 |
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 |
fahd2 | DDB_G0293650 | DDB0232433 | CDS | 3209379 | 918 | - | 0.308279 | |
fam96A | DDB_G0292558 | DDB0232433 | CDS | 1882209 | 453 | - | 0.233996 | |
fdfT | DDB_G0292072 | catalyzes the reaction farnesyl diphosphate diphosphate presqualene diphosphate | DDB0232433 | CDS | 1153510 | 1251 | + | 0.339728 |
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 | |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
gacE | DDB_G0293654 | DDB0232433 | CDS | 3215377 | 3399 | + | 0.28832 | |
gacEE | DDB_G0291840 | DDB0232433 | CDS | 819813 | 1713 | + | 0.258611 | |
gacV | DDB_G0293510 | DDB0232433 | CDS | 2976341 | 1563 | + | 0.252719 | |
galK | DDB_G0292112 | DDB0232433 | CDS | 1203261 | 1506 | + | 0.317397 | |
gcvT | DDB_G0292326 | catalyzes the reaction protein-S-aminomethyldihydrolipoyllysine tetrahydrofolate protein-dihydrolipoyllysine 510-methylenetetrahydrofolate NHsub3sub | DDB0232433 | CDS | 1484064 | 1212 | - | 0.348185 |
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 |
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 |
gerD | DDB_G0291856 | DDB0232433 | CDS | 926086 | 4338 | + | 0.297372 | |
gflC_ps | DDB_G0293458 | putative pseudogene fragment similar to D. discoideum gene | DDB0232433 | CDS | 2917476 | 264 | + | 0.359848 |
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 |
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 |
gloA | DDB_G0291265 | catalyzes the reaction glutathione methylglyoxal S-lactoylglutathione | DDB0232433 | CDS | 28140 | 411 | + | 0.350365 |
gloB2 | DDB_G0291482 | catalyzes the reaction S-lactoyl-glutathione H2O reduced glutathione D-lactate | DDB0232433 | CDS | 411372 | 879 | + | 0.335609 |
gluA | DDB_G0292810 | DDB0232433 | CDS | 2240229 | 2466 | - | 0.364152 | |
gnrB | DDB_G0291536 | DDB0232433 | CDS | 490155 | 5088 | - | 0.306211 | |
gnt2 | DDB_G0291241 | DDB0232433 | CDS | 49486 | 1212 | - | 0.334158 | |
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 |
gpn1 | DDB_G0293220 | DDB0232433 | CDS | 2684279 | 1191 | + | 0.309824 | |
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 |
grl_ps | DDB_G0293232 | putative pseudogene fragment very similar to grl (metabotropic Glutamate Receptor-Like) genes | DDB0232433 | CDS | 2665263 | 135 | + | 0.348148 |
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 |
grwd1 | DDB_G0291566 | ortholog of the mammalian GRWD1 contains several WD-40 repeats | DDB0232433 | CDS | 556339 | 1449 | - | 0.354727 |
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 |
gtaP | DDB_G0295707 | DDB0232433 | CDS | 624702 | 2088 | - | 0.287356 | |
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 |
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 |
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 |
gxcJ | DDB_G0293978 | DDB0232433 | CDS | 3500795 | 3468 | + | 0.241638 | |
gxcKK | DDB_G0293340 | DDB0232433 | CDS | 2757100 | 2004 | - | 0.25 | |
gxcO | DDB_G0293396 | DDB0232433 | CDS | 2833626 | 2490 | + | 0.244177 | |
gxcU | DDB_G0291996 | DDB0232433 | CDS | 972420 | 2961 | - | 0.311381 | |
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 | |
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 |
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 |
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 |
helA | DDB_G0292992 | DDB0232433 | CDS | 2367392 | 3276 | + | 0.291209 | |
hemE | DDB_G0292294 | catalyzes the reaction uroporphyrinogen III coproporphyrinogen 4 COsub2sub in heme biosynthesis | DDB0232433 | CDS | 1412890 | 1095 | - | 0.340639 |
hemG | DDB_G0292040 | DDB0232433 | CDS | 1063213 | 1599 | + | 0.238274 | |
hibA | DDB_G0292566 | DDB0232433 | CDS | 1891263 | 966 | - | 0.356108 | |
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 | |
idhB | DDB_G0293872 | catalyzes the reaction isocitrate NAD 2-oxoglutarate CO2 NADH | DDB0232433 | CDS | 3407770 | 1083 | - | 0.369344 |
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 |
iliM | DDB_G0292328 | similar to bacterial aromatic-ring hydroxylases and fungal monooxygenases induced by Legionella pneumophila infection | DDB0232433 | CDS | 1489407 | 1272 | - | 0.259434 |
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 |
iliQ | DDB_G0292926 | contains a large ankyrin repeat region induced by Legionella pneumophila infection | DDB0232433 | CDS | 2280235 | 2490 | + | 0.214458 |
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 |
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 |
iptB | DDB_G0291528 | DDB0232433 | CDS | 482754 | 1569 | + | 0.203952 | |
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 |
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 |
jcdE | DDB_G0292770 | DDB0232433 | CDS | 2038164 | 1062 | + | 0.249529 | |
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 |
kif10 | DDB_G0293198 | DDB0232433 | CDS | 2654607 | 3717 | - | 0.262039 | |
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 |
ldpA | DDB_G0291600 | DDB0232433 | CDS | 592384 | 1074 | - | 0.26257 | |
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 |
limD | DDB_G0291251 | DDB0232433 | CDS | 31751 | 2103 | - | 0.38136 | |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
mdhB | DDB_G0292600 | catalyzes the reaction malate NAD oxaloacetate NADH contains a predicted mitochondrial transit peptide | DDB0232433 | CDS | 1826095 | 1047 | + | 0.39255 |
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 |
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 |
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 |
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 |
mfeA | DDB_G0291247 | DDB0232433 | CDS | 383676 | 1326 | - | 0.390649 | |
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 |
mhsp70 | DDB_G0293298 | DDB0232433 | CDS | 2761673 | 1977 | + | 0.376834 | |
mileS | DDB_G0293030 | catalyzes the reaction ATP L-isoleucine tRNAIle AMP diphosphate L-isoleucyl-tRNAIle | DDB0232433 | CDS | 2348091 | 3105 | - | 0.287601 |
mipA | DDB_G0292812 | conserved hypothetical Dictyostelium protein contains a predicted signal sequence and a C-terminal transmembrane domain | DDB0232433 | CDS | 2204194 | 4182 | + | 0.24988 |
mleuS | DDB_G0291346 | catalyzes the reaction ATP L-leucine tRNALeu AMP diphosphate L-leucyl-tRNALeu | DDB0232433 | CDS | 154547 | 2823 | + | 0.29791 |
mnd1 | DDB_G0291750 | DDB0232433 | CDS | 686426 | 666 | - | 0.252252 | |
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 |
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 |
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 |
mrpl53 | DDB_G0292420 | DDB0232433 | CDS | 1579394 | 390 | + | 0.271795 | |
mth | DDB_G0293766 | DDB0232433 | CDS | 3300203 | 486 | + | 0.238683 | |
mybA | DDB_G0293900 | DDB0232433 | CDS | 3493719 | 3693 | - | 0.25589 | |
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 |
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 | |
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 |
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 |
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 |
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 |
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 |
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 |
nhe3 | DDB_G0292830 | DDB0232433 | CDS | 2111344 | 2361 | - | 0.345616 | |
nol10 | DDB_G0292466 | DDB0232433 | CDS | 1681385 | 2100 | - | 0.300476 | |
nol6 | DDB_G0291438 | putative U3 snoRNP protein ortholog of H. sapiens NOL6 and S. cerevisiae UTP22 | DDB0232433 | CDS | 304287 | 3837 | - | 0.258796 |
nosA | DDB_G0292264 | DDB0232433 | CDS | 1472850 | 3270 | - | 0.284404 | |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
pdi2 | DDB_G0291434 | DDB0232433 | CDS | 299936 | 1542 | - | 0.33463 | |
pefB | DDB_G0293530 | similar to mammalian apoptosis component ALG-2 contains 5 EF-hand calcium binding domains | DDB0232433 | CDS | 2988655 | 618 | + | 0.331715 |
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 |
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 |
pgl | DDB_G0292898 | catalyzes the reaction 6-phospho-D-glucono-15-lactone Hsub2subO 6-phospho-D-gluconate | DDB0232433 | CDS | 2232140 | 711 | + | 0.295359 |
phdG | DDB_G0292622 | DDB0232433 | CDS | 1851269 | 1767 | + | 0.301075 | |
phlp1 | DDB_G0292850 | DDB0232433 | CDS | 2267210 | 951 | + | 0.283912 | |
phlp3 | DDB_G0293848 | DDB0232433 | CDS | 3411418 | 555 | - | 0.257658 | |
pigL | DDB_G0293136 | DDB0232433 | CDS | 2582359 | 777 | + | 0.245817 | |
pigT | DDB_G0291490 | DDB0232433 | CDS | 421140 | 2034 | - | 0.274828 | |
pitD | DDB_G0292426 | DDB0232433 | CDS | 1595140 | 996 | - | 0.282129 | |
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 | |
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 |
pncA | DDB_G0293618 | catalyzes the reaction nicotinamide Hsub2subO nicotinate NHsub3sub | DDB0232433 | CDS | 3150071 | 630 | - | 0.253968 |
ponA | DDB_G0293522 | DDB0232433 | CDS | 3188338 | 432 | + | 0.326389 | |
ponE | DDB_G0293634 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane | DDB0232433 | CDS | 3189105 | 516 | + | 0.263566 |
pop1 | DDB_G0291320 | DDB0232433 | CDS | 120925 | 2448 | - | 0.275735 | |
pop5 | DDB_G0291662 | DDB0232433 | CDS | 281774 | 516 | - | 0.24031 | |
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 |
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 |
prmt1 | DDB_G0291556 | DDB0232433 | CDS | 504463 | 1026 | - | 0.287524 | |
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 | |
psiK | DDB_G0292014 | DDB0232433 | CDS | 1018381 | 2187 | - | 0.328304 | |
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 |
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 |
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 |
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 |
psmC5 | DDB_G0292382 | ATPase subunit and regulatory subcomplex of the 26S proteasome developmentally regulated TAT binding protein homolog | DDB0232433 | CDS | 1673522 | 1212 | - | 0.334158 |
psmD2 | DDB_G0293752 | DDB0232433 | CDS | 3279468 | 2682 | + | 0.346383 | |
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 |
ptcA | DDB_G0293882 | DDB0232433 | CDS | 3419922 | 1518 | + | 0.216733 | |
ptcL | DDB_G0291794 | DDB0232433 | CDS | 753746 | 3351 | + | 0.223217 | |
pter | DDB_G0293394 | DDB0232433 | CDS | 2831683 | 1113 | - | 0.277628 | |
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 |
qtrt1 | DDB_G0291802 | catalyzes the reaction [tRNA]-guanine queuine [tRNA]-queuine guanine | DDB0232433 | CDS | 770747 | 1344 | - | 0.385417 |
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 |
rab2A | DDB_G0292268 | DDB0232433 | CDS | 1422661 | 624 | + | 0.310897 | |
rab4 | DDB_G0292406 | DDB0232433 | CDS | 1558648 | 618 | + | 0.302589 | |
rabA | DDB_G0291233 | DDB0232433 | CDS | 312209 | 606 | - | 0.268977 | |
rabG1 | DDB_G0291738 | DDB0232433 | CDS | 677353 | 591 | + | 0.323181 | |
rabU | DDB_G0291293 | DDB0232433 | CDS | 69908 | 585 | + | 0.268376 | |
racC | DDB_G0293526 | DDB0232433 | CDS | 3000314 | 579 | + | 0.322971 | |
racD | DDB_G0291976 | DDB0232433 | CDS | 1210911 | 765 | + | 0.32549 | |
racJ | DDB_G0292560 | DDB0232433 | CDS | 1884330 | 618 | + | 0.263754 | |
racL | DDB_G0292816 | DDB0232433 | CDS | 2181555 | 591 | + | 0.279188 | |
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 |
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 |
ranA | DDB_G0291235 | DDB0232433 | CDS | 78789 | 639 | + | 0.363067 | |
rapA | DDB_G0291237 | DDB0232433 | CDS | 98914 | 561 | + | 0.354724 | |
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 |
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 |
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 |
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 |
rexo1 | DDB_G0291590 | similar to S. cerevisiae REX1 or RNH70 a 3'-5' RNA exonuclease | DDB0232433 | CDS | 580025 | 2085 | + | 0.251799 |
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 |
ric8 | DDB_G0292036 | similar to human RIC8A (synembryn-A) non-receptor guanine nucleotide exchange factor for G | DDB0232433 | CDS | 1059972 | 1314 | - | 0.307458 |
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 |
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 |
rpa2 | DDB_G0293560 | component of the RNA polymerase I complex ortholog of S. cerevisiae RPA135 | DDB0232433 | CDS | 3044865 | 3393 | - | 0.328912 |
rpb3 | DDB_G0292244 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB3 | DDB0232433 | CDS | 1368967 | 909 | + | 0.29703 |
rpb5 | DDB_G0291636 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPB5 | DDB0232433 | CDS | 457932 | 546 | - | 0.302198 |
rpc19 | DDB_G0291362 | subunit common to RNA polymerases I and III ortholog of S. cerevisiae RPC19 | DDB0232433 | CDS | 182518 | 351 | + | 0.290598 |
rpl13 | DDB_G0291870 | DDB0232433 | CDS | 852689 | 630 | + | 0.420635 | |
rpl23a | DDB_G0293502 | DDB0232433 | CDS | 2967908 | 510 | + | 0.4 | |
rpl27a | DDB_G0292388 | DDB0232433 | CDS | 1592145 | 447 | - | 0.411633 | |
rpl3 | DDB_G0291862 | protein component of the large (60S) ribosomal subunit ribosomal protein L3 homolog | DDB0232433 | CDS | 954736 | 1197 | - | 0.404344 |
rpl6 | DDB_G0292460 | protein component of the large (60S) ribosomal subunit ribosomal protein L6 homolog | DDB0232433 | CDS | 1676096 | 711 | + | 0.410689 |
rps14 | DDB_G0291526 | protein component of the small (40S) ribosomal subunit ribosomal protein S14 homolog | DDB0232433 | CDS | 481211 | 459 | - | 0.444444 |
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 |
rps21 | DDB_G0293700 | protein component of the small (40S) ribosomal subunit ribosomal protein S21 homolog | DDB0232433 | CDS | 3013335 | 237 | - | 0.443038 |
rps3 | DDB_G0293000 | DDB0232433 | CDS | 2556040 | 657 | - | 0.418569 | |
rps8 | DDB_G0291864 | DDB0232433 | CDS | 844628 | 636 | + | 0.418239 | |
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 |
rsmD | DDB_G0292318 | DDB0232433 | CDS | 1471614 | 684 | + | 0.19152 | |
rsmM | DDB_G0292300 | DDB0232433 | CDS | 1426160 | 645 | + | 0.308527 | |
rtnlc | DDB_G0293088 | DDB0232433 | CDS | 2461261 | 951 | - | 0.335436 | |
rvb1 | DDB_G0293226 | similar to S. cerevisiae RVB1 a component of chromatin remodeling complexes | DDB0232433 | CDS | 2678243 | 1572 | - | 0.357506 |
sec13 | DDB_G0292052 | DDB0232433 | CDS | 1099513 | 906 | + | 0.34106 | |
serB | DDB_G0291368 | catalyzes the reaction 3-phospho-serine Hsub2subO L-serine phosphate | DDB0232433 | CDS | 185417 | 1098 | + | 0.26776 |
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 |
sf3a2 | DDB_G0293876 | DDB0232433 | CDS | 3412404 | 648 | + | 0.274691 | |
sgmB | DDB_G0293210 | DDB0232433 | CDS | 2708230 | 1914 | + | 0.306165 | |
shmt2 | DDB_G0291652 | mitochondrial serine hydroxymethyltransferase catalyzes the reaction L-serine tetrahydrofolate L-glycine 510-methylene-tetrahydrofolate Hsub2subO | DDB0232433 | CDS | 91358 | 1446 | - | 0.350622 |
sigB | DDB_G0293364 | DDB0232433 | CDS | 2822106 | 2049 | + | 0.307467 | |
smc1 | DDB_G0291752 | functions in chromosome dynamics heterodimerizes with smc3 | DDB0232433 | CDS | 688164 | 4122 | + | 0.312712 |
smp3 | DDB_G0291660 | CAZy family GT76 catalyzes the addition of the fourth mannose to GPI (glycosylphosphatidylinositol) | DDB0232433 | CDS | 189530 | 2004 | + | 0.211577 |
spg1 | DDB_G0291269 | DDB0232433 | CDS | 37774 | 612 | + | 0.338235 | |
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 |
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 |
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 |
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 |
st15 | DDB_G0292218 | similar to beta-14-endoglucanase expressed in pstO cells expression is decreased in | DDB0232433 | CDS | 1328404 | 369 | + | 0.333333 |
sti1 | DDB_G0292404 | DDB0232433 | CDS | 1556012 | 1695 | - | 0.362242 | |
symA | DDB_G0292814 | DDB0232433 | CDS | 2158906 | 1371 | - | 0.33698 | |
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-Arg-CCU-1 | DDB_G0295385 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 3587001 | 74 | - | 0.486486 |
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-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-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-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-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-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-20 | DDB_G0295413 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2730062 | 72 | - | 0.513889 |
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-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-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-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-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-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-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-4 | DDB_G0295471 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 310825 | 81 | - | 0.45679 |
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-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-10 | DDB_G0295405 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2954533 | 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-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-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-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-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-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-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-GCU-12 | DDB_G0295429 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2347717 | 81 | - | 0.592593 |
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-9 | DDB_G0295305 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 1124940 | 82 | + | 0.52439 |
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-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-9 | DDB_G0295327 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232433 | CDS | 2088994 | 83 | + | 0.493976 |
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-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 |
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 |
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 |
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 |
taz | DDB_G0291922 | ortholog of S. cerevisiae TAZ1 and H. sapiens tafazzin implicated in Barth syndrome | DDB0232433 | CDS | 950884 | 858 | + | 0.270396 |
tert | DDB_G0293918 | DDB0232433 | CDS | 3475961 | 3813 | - | 0.190401 | |
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 |
tgrA_ps1 | DDB_G0291624 | putative pseudogene immunoglobulin E-set family gene | DDB0232433 | CDS | 356398 | 2589 | + | 0.248358 |
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_ps7 | DDB_G0291458 | putative pseudogene fragment of immunoglobulin E-set family genes including | DDB0232433 | CDS | 342766 | 417 | + | 0.213429 |
tgrC4 | DDB_G0291454 | DDB0232433 | CDS | 333292 | 2685 | - | 0.279702 | |
tgrC_ps3 | DDB_G0293238 | putative pseudogene immunoglobulin E-set family gene | DDB0232433 | CDS | 2646511 | 258 | + | 0.267442 |
tgrF1 | DDB_G0292732 | DDB0232433 | CDS | 2005101 | 2754 | - | 0.245461 | |
tgrG1 | DDB_G0292772 | DDB0232433 | CDS | 2009912 | 2928 | + | 0.239413 | |
tgrQ1 | DDB_G0292562 | DDB0232433 | CDS | 1885258 | 2016 | - | 0.244048 | |
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 |
tkrA | DDB_G0292104 | catalyzes the reaction D-gluconate NADPsupsup 2-dehydro-D-gluconate NADPH Hsupsup | DDB0232433 | CDS | 1190069 | 1005 | + | 0.300498 |
tmem184D | DDB_G0291287 | TMEM184 family protein contains 7 predicted transmembrane domains | DDB0232433 | CDS | 57345 | 1494 | + | 0.261714 |
tmem20 | DDB_G0292606 | putative drugmetabolite transporter containing 10 predicted transmembrane domains | DDB0232433 | CDS | 1830985 | 2097 | + | 0.311874 |
trappc2l | DDB_G0292690 | DDB0232433 | CDS | 1953634 | 423 | - | 0.238771 | |
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 |
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 |
ttc27 | DDB_G0293372 | DDB0232433 | CDS | 2801637 | 2562 | - | 0.296253 | |
uba5 | DDB_G0293306 | DDB0232433 | CDS | 2741328 | 1146 | + | 0.287086 | |
ube2v | DDB_G0292596 | DDB0232433 | CDS | 1823383 | 417 | - | 0.290168 | |
ubpA | DDB_G0291239 | DDB0232433 | CDS | 283328 | 2514 | + | 0.333731 | |
ubqI | DDB_G0291928 | DDB0232433 | CDS | 961035 | 918 | + | 0.308279 | |
ubqN | DDB_G0292984 | DDB0232433 | CDS | 2259430 | 222 | - | 0.247748 | |
ubqO | DDB_G0292908 | DDB0232433 | CDS | 2261064 | 234 | - | 0.311966 | |
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 | |
ufm1 | DDB_G0295709 | DDB0232433 | CDS | 620919 | 258 | + | 0.302326 | |
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 |
vps26l | DDB_G0292212 | ortholog of H. sapiens DSCR3 the Down syndrome critical region gene 3 | DDB0232433 | CDS | 1334023 | 915 | + | 0.288525 |
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 |
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 |
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 |
vps8 | DDB_G0291606 | putative ortholog of VPS8 involved in vacuolar protein localization | DDB0232433 | CDS | 397697 | 5256 | + | 0.296233 |
vti1A | DDB_G0292974 | DDB0232433 | CDS | 2202494 | 654 | - | 0.281346 | |
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 |
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 |
wdr13 | DDB_G0291596 | DDB0232433 | CDS | 588031 | 1464 | + | 0.268443 | |
wdr23 | DDB_G0291832 | DDB0232433 | CDS | 834929 | 1986 | - | 0.291541 | |
wdr53 | DDB_G0293608 | DDB0232433 | CDS | 3130386 | 1107 | + | 0.226739 | |
wdr92 | DDB_G0291822 | DDB0232433 | CDS | 825936 | 1074 | + | 0.255121 | |
wshA | DDB_G0292878 | contains a C-terminal actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domain | DDB0232433 | CDS | 2194668 | 1419 | + | 0.349542 |
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 |
xpc | DDB_G0292296 | DDB0232433 | CDS | 1414792 | 2904 | + | 0.266529 | |
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 |
xpo6 | DDB_G0293076 | DDB0232433 | CDS | 2441945 | 3144 | + | 0.265585 | |
xpo7 | DDB_G0291986 | DDB0232433 | CDS | 1213027 | 3024 | + | 0.263228 | |
ykt6 | DDB_G0291656 | DDB0232433 | CDS | 180176 | 609 | + | 0.320197 | |
zizB | DDB_G0293084 | DDB0232433 | CDS | 2452128 | 6444 | - | 0.301055 |