Gene list
Applied filters:
Genomic element: DDB0232432
Number of genes found: 1946
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 |
DD8-14 | DDB_G0289467 | DDB0232432 | CDS | 2821081 | 1992 | - | 0.317269 | |
DDB_G0267212_RTE | DDB_G0267212 | Fused fragments of the DIRS1 retrotransposon refer to Genbank M11339 for full-length element | DDB0232432 | CDS | 4280779 | 2064 | + | 0.212209 |
DDB_G0287215 | DDB_G0287215 | DDB0232432 | CDS | 3070 | 1113 | - | 0.28841 | |
DDB_G0287217 | DDB_G0287217 | DDB0232432 | CDS | 5282 | 3435 | + | 0.2131 | |
DDB_G0287219 | DDB_G0287219 | conserved Dictyostelium protein similar to bacterial proteins contains a predicted signal peptide | DDB0232432 | CDS | 8994 | 408 | - | 0.291667 |
DDB_G0287221 | DDB_G0287221 | similar to TRIP12 (thyroid hormone receptor interactor 12) a component of PA700 an ATP-dependent multisubunit protein that activates the proteolytic activities of the 20S proteasome | DDB0232432 | CDS | 10149 | 6294 | - | 0.317445 |
DDB_G0287225 | DDB_G0287225 | DDB0232432 | CDS | 21182 | 2106 | + | 0.195632 | |
DDB_G0287235_ps | DDB_G0287235 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 35600 | 2313 | - | 0.242542 |
DDB_G0287237_ps | DDB_G0287237 | putative pseudogene contains a kinase domain that lacks a RD signature | DDB0232432 | CDS | 42818 | 972 | - | 0.255144 |
DDB_G0287239 | DDB_G0287239 | DDB0232432 | CDS | 52532 | 921 | - | 0.230185 | |
DDB_G0287241 | DDB_G0287241 | DDB0232432 | CDS | 58745 | 939 | + | 0.217252 | |
DDB_G0287243 | DDB_G0287243 | DDB0232432 | CDS | 60363 | 1077 | + | 0.275766 | |
DDB_G0287249_TE | DDB_G0287249 | ORF1 encoding a protein of unknown function of the putative DNA transposon DDT-A refer to AF298201 for full-length consensus element | DDB0232432 | CDS | 101 | 1535 | - | 0.225407 |
DDB_G0287251 | DDB_G0287251 | DDB0232432 | CDS | 19093 | 744 | - | 0.215054 | |
DDB_G0287257 | DDB_G0287257 | DDB0232432 | CDS | 49910 | 1513 | - | 0.356907 | |
DDB_G0287263 | DDB_G0287263 | DDB0232432 | CDS | 64505 | 213 | + | 0.267606 | |
DDB_G0287265 | DDB_G0287265 | DDB0232432 | CDS | 65084 | 1470 | - | 0.238776 | |
DDB_G0287267 | DDB_G0287267 | DDB0232432 | CDS | 67613 | 2187 | - | 0.306813 | |
DDB_G0287275 | DDB_G0287275 | DDB0232432 | CDS | 77605 | 4059 | + | 0.272974 | |
DDB_G0287277 | DDB_G0287277 | members of the NAD-dependent epimerasedehydratase family use nucleotide-sugar substrates for a variety of chemical reactions | DDB0232432 | CDS | 82214 | 1014 | - | 0.300789 |
DDB_G0287279 | DDB_G0287279 | belongs to the UPF0203 family similar to human TRIAP1 (TP53-regulated inhibitor of apoptosis 1) | DDB0232432 | CDS | 83567 | 243 | - | 0.255144 |
DDB_G0287281 | DDB_G0287281 | DDB0232432 | CDS | 84160 | 1254 | - | 0.261563 | |
DDB_G0287283 | DDB_G0287283 | DDB0232432 | CDS | 91412 | 153 | - | 0.24183 | |
DDB_G0287287 | DDB_G0287287 | DDB0232432 | CDS | 74321 | 2298 | - | 0.239774 | |
DDB_G0287289 | DDB_G0287289 | DDB0232432 | CDS | 86247 | 4419 | + | 0.283548 | |
DDB_G0287299 | DDB_G0287299 | DDB0232432 | CDS | 94597 | 1266 | + | 0.2109 | |
DDB_G0287303 | DDB_G0287303 | amino acid permeases are integral membrane proteins involved in the transport of amino acids into the cell contains 12 putative transmembrane domains | DDB0232432 | CDS | 104846 | 1998 | - | 0.278278 |
DDB_G0287305 | DDB_G0287305 | DDB0232432 | CDS | 110292 | 543 | - | 0.246777 | |
DDB_G0287309 | DDB_G0287309 | DDB0232432 | CDS | 112586 | 600 | + | 0.26 | |
DDB_G0287311_ps | DDB_G0287311 | putative pseudogene similar to D. discoideum genes | DDB0232432 | CDS | 113384 | 336 | - | 0.27381 |
DDB_G0287313 | DDB_G0287313 | DDB0232432 | CDS | 114376 | 2025 | + | 0.185185 | |
DDB_G0287315 | DDB_G0287315 | DDB0232432 | CDS | 120470 | 4677 | + | 0.297199 | |
DDB_G0287317 | DDB_G0287317 | DDB0232432 | CDS | 125370 | 1839 | - | 0.290375 | |
DDB_G0287319 | DDB_G0287319 | similar to human SLC35E2 (solute carrier family 35 member E2) contains 10 putative transmembrane domains | DDB0232432 | CDS | 129877 | 1047 | + | 0.30468 |
DDB_G0287321 | DDB_G0287321 | DDB0232432 | CDS | 131270 | 399 | - | 0.205514 | |
DDB_G0287323 | DDB_G0287323 | contains an N-terminal oxidoreductase domain and a partial C-terminal oxidoreductase domain the GfoIdhMocA family proteins utilize NADP or NAD | DDB0232432 | CDS | 133013 | 1293 | + | 0.28925 |
DDB_G0287325 | DDB_G0287325 | similar to mammalian EPS15 a clathrin adaptor that binds to the AP2 alpha subunit in mammalian cells | DDB0232432 | CDS | 137312 | 3591 | + | 0.310498 |
DDB_G0287329 | DDB_G0287329 | DDB0232432 | CDS | 143681 | 219 | - | 0.342466 | |
DDB_G0287331 | DDB_G0287331 | DDB0232432 | CDS | 144715 | 2136 | + | 0.267322 | |
DDB_G0287335 | DDB_G0287335 | has similarity to human cold inducible RNA binding protein (CIRBP) however it is considreably shorter | DDB0232432 | CDS | 148219 | 276 | + | 0.344203 |
DDB_G0287339 | DDB_G0287339 | DDB0232432 | CDS | 154225 | 2106 | + | 0.188509 | |
DDB_G0287341 | DDB_G0287341 | DDB0232432 | CDS | 157067 | 738 | + | 0.216802 | |
DDB_G0287343 | DDB_G0287343 | DDB0232432 | CDS | 158259 | 837 | - | 0.215054 | |
DDB_G0287347 | DDB_G0287347 | DDB0232432 | CDS | 162247 | 2343 | - | 0.216389 | |
DDB_G0287355 | DDB_G0287355 | DDB0232432 | CDS | 172169 | 126 | - | 0.412698 | |
DDB_G0287357 | DDB_G0287357 | DDB0232432 | CDS | 172540 | 2127 | - | 0.29149 | |
DDB_G0287359 | DDB_G0287359 | DDB0232432 | CDS | 175065 | 1446 | - | 0.280083 | |
DDB_G0287365 | DDB_G0287365 | DDB0232432 | CDS | 199757 | 3300 | - | 0.267576 | |
DDB_G0287367 | DDB_G0287367 | DDB0232432 | CDS | 204023 | 981 | + | 0.24261 | |
DDB_G0287369 | DDB_G0287369 | DDB0232432 | CDS | 205200 | 858 | - | 0.19697 | |
DDB_G0287373 | DDB_G0287373 | DDB0232432 | CDS | 217435 | 933 | - | 0.230439 | |
DDB_G0287375 | DDB_G0287375 | DDB0232432 | CDS | 219071 | 2973 | + | 0.215607 | |
DDB_G0287379 | DDB_G0287379 | DDB0232432 | CDS | 233763 | 3231 | + | 0.320644 | |
DDB_G0287381 | DDB_G0287381 | DDB0232432 | CDS | 237838 | 843 | + | 0.200475 | |
DDB_G0287383 | DDB_G0287383 | DDB0232432 | CDS | 239046 | 510 | + | 0.294118 | |
DDB_G0287385 | DDB_G0287385 | DDB0232432 | CDS | 239982 | 1125 | + | 0.249778 | |
DDB_G0287387 | DDB_G0287387 | DDB0232432 | CDS | 241597 | 879 | - | 0.196815 | |
DDB_G0287389 | DDB_G0287389 | DDB0232432 | CDS | 243540 | 2307 | + | 0.202427 | |
DDB_G0287395 | DDB_G0287395 | DDB0232432 | CDS | 250770 | 843 | + | 0.238434 | |
DDB_G0287397 | DDB_G0287397 | DDB0232432 | CDS | 251848 | 2013 | - | 0.273224 | |
DDB_G0287399 | DDB_G0287399 | DDB0232432 | CDS | 255717 | 1461 | - | 0.370979 | |
DDB_G0287403 | DDB_G0287403 | similar to | DDB0232432 | CDS | 259377 | 459 | - | 0.254902 |
DDB_G0287405 | DDB_G0287405 | conserved protein of unknown function contains 9 putative transmembrane domains | DDB0232432 | CDS | 260619 | 1533 | - | 0.307893 |
DDB_G0287407 | DDB_G0287407 | similar to nephrocystin 3 Grp94 neighboring nucleotidase and other TPR repeat-containing proteins | DDB0232432 | CDS | 263392 | 4992 | + | 0.313902 |
DDB_G0287409_RTE | DDB_G0287409 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232432 | CDS | 269267 | 1335 | + | 0.307865 |
DDB_G0287411 | DDB_G0287411 | DDB0232432 | CDS | 271707 | 2298 | - | 0.219756 | |
DDB_G0287413 | DDB_G0287413 | DDB0232432 | CDS | 274270 | 666 | + | 0.202703 | |
DDB_G0287415 | DDB_G0287415 | DDB0232432 | CDS | 275303 | 3039 | + | 0.303389 | |
DDB_G0287417 | DDB_G0287417 | DDB0232432 | CDS | 181547 | 1680 | + | 0.232738 | |
DDB_G0287421_RTE | DDB_G0287421 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232432 | CDS | 278825 | 561 | + | 0.342246 |
DDB_G0287423 | DDB_G0287423 | DDB0232432 | CDS | 96074 | 1515 | - | 0.264026 | |
DDB_G0287425 | DDB_G0287425 | DDB0232432 | CDS | 98175 | 1521 | - | 0.286654 | |
DDB_G0287427 | DDB_G0287427 | DDB0232432 | CDS | 107640 | 1023 | + | 0.256109 | |
DDB_G0287429 | DDB_G0287429 | DDB0232432 | CDS | 109242 | 810 | + | 0.216049 | |
DDB_G0287431_ps | DDB_G0287431 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 117395 | 1494 | - | 0.271754 |
DDB_G0287433 | DDB_G0287433 | DDB0232432 | CDS | 118782 | 222 | - | 0.220721 | |
DDB_G0287437 | DDB_G0287437 | DDB0232432 | CDS | 131874 | 663 | - | 0.227753 | |
DDB_G0287439 | DDB_G0287439 | DDB0232432 | CDS | 148729 | 888 | - | 0.269144 | |
DDB_G0287441 | DDB_G0287441 | contains six predicted transmembrane domains similar to a D. purpureum protein | DDB0232432 | CDS | 160889 | 969 | + | 0.275542 |
DDB_G0287445 | DDB_G0287445 | conserved protein ortholog of the human C11orf2 (Chromosome 11 Open Reading Frame 2) protein contains a putative Dor1 domain which in yeast is involved in vesicle targeting to the Golgi apparatus and complexes with a number of other trafficking proteins | DDB0232432 | CDS | 177577 | 2754 | + | 0.289397 |
DDB_G0287447 | DDB_G0287447 | ortholog of the bacterial epsilon subunit of DNA polymerase III a multisubunit enzyme responsible for most of the replicative synthesis in bacteria the contain the editing function and is a proofreading 3'-5' exonuclease the Dictyostelium gene is missing approximately 100 amino acids at the carboxyl terminus | DDB0232432 | CDS | 185922 | 1452 | + | 0.232782 |
DDB_G0287449 | DDB_G0287449 | DDB0232432 | CDS | 189973 | 903 | + | 0.272425 | |
DDB_G0287451_ps | DDB_G0287451 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232432 | CDS | 229012 | 624 | - | 0.232372 |
DDB_G0287453_ps | DDB_G0287453 | putative pseudogene fragment similar to EGF repeat-containing proteins | DDB0232432 | CDS | 280003 | 714 | - | 0.285714 |
DDB_G0287455_RTE | DDB_G0287455 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232432 | CDS | 282346 | 1666 | - | 0.264106 |
DDB_G0287457 | DDB_G0287457 | DDB0232432 | CDS | 209576 | 2334 | - | 0.191088 | |
DDB_G0287463 | DDB_G0287463 | DDB0232432 | CDS | 290618 | 1269 | - | 0.19937 | |
DDB_G0287465 | DDB_G0287465 | DDB0232432 | CDS | 292797 | 1356 | + | 0.272861 | |
DDB_G0287471 | DDB_G0287471 | contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232432 | CDS | 300793 | 1047 | - | 0.282713 |
DDB_G0287473_ps | DDB_G0287473 | putative pseudogene paramecium surface antigen repeat-containing protein family gene | DDB0232432 | CDS | 302500 | 1475 | - | 0.231186 |
DDB_G0287475 | DDB_G0287475 | DDB0232432 | CDS | 312971 | 810 | - | 0.233333 | |
DDB_G0287477 | DDB_G0287477 | conserved Dictyostelium protein contains one putative transmembrane domain and an additional putative signal sequence | DDB0232432 | CDS | 314532 | 1944 | - | 0.277263 |
DDB_G0287479 | DDB_G0287479 | DDB0232432 | CDS | 323189 | 1881 | - | 0.150984 | |
DDB_G0287489 | DDB_G0287489 | DDB0232432 | CDS | 294648 | 264 | - | 0.19697 | |
DDB_G0287491 | DDB_G0287491 | contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232432 | CDS | 308656 | 1077 | - | 0.299907 |
DDB_G0287493_ps | DDB_G0287493 | putative pseudogene paramecium surface antigen repeat-containing family protein | DDB0232432 | CDS | 310846 | 426 | - | 0.293427 |
DDB_G0287499 | DDB_G0287499 | DDB0232432 | CDS | 334918 | 1125 | - | 0.200889 | |
DDB_G0287501 | DDB_G0287501 | similar to polyketide synthases but missing more than half of the amino terminus | DDB0232432 | CDS | 336533 | 3795 | - | 0.253228 |
DDB_G0287503 | DDB_G0287503 | DDB0232432 | CDS | 327483 | 2048 | + | 0.132324 | |
DDB_G0287509 | DDB_G0287509 | similar to bacterial 14-dihydroxy-2-naphthoate octaprenyltransferase which catalyzes the reaction 14-dihydroxy-2-naphthoate polyprenylpyrophosphate demethylmenaquinone-8 pyrophosphate COsub2sub and similar to mammalian transitional epithelia response protein of unknown function | DDB0232432 | CDS | 341417 | 993 | - | 0.266868 |
DDB_G0287511 | DDB_G0287511 | DDB0232432 | CDS | 343078 | 3939 | - | 0.262503 | |
DDB_G0287517 | DDB_G0287517 | DDB0232432 | CDS | 360366 | 351 | - | 0.264957 | |
DDB_G0287519 | DDB_G0287519 | catalyzes the reaction acetoacetyl-CoA Hsub2subO CoA acetoacetate | DDB0232432 | CDS | 362168 | 1599 | - | 0.3596 |
DDB_G0287521 | DDB_G0287521 | ortholog of the conserved signal peptide peptidase-like 3 (SPPL3) contains 8 predicted transmembrane domains and an additional N-terminal signal sequence | DDB0232432 | CDS | 364712 | 1116 | - | 0.236559 |
DDB_G0287525 | DDB_G0287525 | DDB0232432 | CDS | 366594 | 255 | - | 0.215686 | |
DDB_G0287527 | DDB_G0287527 | DDB0232432 | CDS | 367089 | 357 | + | 0.235294 | |
DDB_G0287529 | DDB_G0287529 | DDB0232432 | CDS | 369718 | 1296 | - | 0.329475 | |
DDB_G0287533 | DDB_G0287533 | DDB0232432 | CDS | 373625 | 1149 | + | 0.260226 | |
DDB_G0287535 | DDB_G0287535 | DDB0232432 | CDS | 385388 | 1848 | + | 0.209957 | |
DDB_G0287541 | DDB_G0287541 | DDB0232432 | CDS | 397759 | 2010 | + | 0.21592 | |
DDB_G0287543 | DDB_G0287543 | very similar to H. sapiens B-cell receptor-associated protein 29 and 31 (BCAP2931) and S. cerevisiae endoplasmic reticulum transmembrane protein 1 and 3 (YET13) contains a putative signal peptide and two transmembrane domains | DDB0232432 | CDS | 400560 | 588 | + | 0.270408 |
DDB_G0287545 | DDB_G0287545 | DDB0232432 | CDS | 401763 | 1128 | + | 0.286348 | |
DDB_G0287547 | DDB_G0287547 | DDB0232432 | CDS | 403298 | 1140 | - | 0.219298 | |
DDB_G0287549 | DDB_G0287549 | DDB0232432 | CDS | 405148 | 387 | - | 0.322997 | |
DDB_G0287551 | DDB_G0287551 | DDB0232432 | CDS | 406658 | 1368 | + | 0.284357 | |
DDB_G0287555 | DDB_G0287555 | catalyzes the reaction L-cysteine Osub2sub 3-sulfinoalanine | DDB0232432 | CDS | 412142 | 798 | + | 0.275689 |
DDB_G0287559 | DDB_G0287559 | DDB0232432 | CDS | 419276 | 579 | - | 0.262522 | |
DDB_G0287561 | DDB_G0287561 | DDB0232432 | CDS | 420291 | 1248 | - | 0.321314 | |
DDB_G0287565_ps | DDB_G0287565 | putative pseudogene similar to a family of Zinc finger N-recognin domain-containing Dictyostelium proteins | DDB0232432 | CDS | 347764 | 930 | + | 0.267742 |
DDB_G0287571 | DDB_G0287571 | DDB0232432 | CDS | 367808 | 1500 | + | 0.222667 | |
DDB_G0287573 | DDB_G0287573 | DDB0232432 | CDS | 391871 | 1398 | - | 0.205293 | |
DDB_G0287575 | DDB_G0287575 | DDB0232432 | CDS | 393959 | 1830 | + | 0.248087 | |
DDB_G0287579_TE | DDB_G0287579 | DDB0232432 | CDS | 424020 | 381 | - | 0.32021 | |
DDB_G0287581 | DDB_G0287581 | putative extracellular protein contains a predicted N-terminal signal sequence | DDB0232432 | CDS | 433923 | 804 | + | 0.287313 |
DDB_G0287591 | DDB_G0287591 | DDB0232432 | CDS | 517253 | 2562 | - | 0.215847 | |
DDB_G0287599 | DDB_G0287599 | DDB0232432 | CDS | 452628 | 354 | + | 0.175141 | |
DDB_G0287601 | DDB_G0287601 | DDB0232432 | CDS | 453256 | 399 | - | 0.273183 | |
DDB_G0287603 | DDB_G0287603 | DDB0232432 | CDS | 453942 | 324 | - | 0.243827 | |
DDB_G0287609 | DDB_G0287609 | highly similar to cinB (94 | DDB0232432 | CDS | 464998 | 1014 | + | 0.272189 |
DDB_G0287611 | DDB_G0287611 | DDB0232432 | CDS | 466151 | 720 | - | 0.297222 | |
DDB_G0287613 | DDB_G0287613 | DDB0232432 | CDS | 467594 | 1011 | - | 0.237389 | |
DDB_G0287615 | DDB_G0287615 | DDB0232432 | CDS | 470940 | 2349 | + | 0.304811 | |
DDB_G0287617 | DDB_G0287617 | similar to Bax inhibitor 1 that may have a role in inhibition of apoptosis contains 7 transmembrane domains | DDB0232432 | CDS | 479630 | 765 | + | 0.284967 |
DDB_G0287621 | DDB_G0287621 | DDB0232432 | CDS | 483890 | 2637 | + | 0.293515 | |
DDB_G0287623 | DDB_G0287623 | DDB0232432 | CDS | 486671 | 1677 | - | 0.189028 | |
DDB_G0287625 | DDB_G0287625 | DDB0232432 | CDS | 489912 | 2937 | - | 0.244127 | |
DDB_G0287633 | DDB_G0287633 | weakly similar to S. cerevisiae SEM1 a short acidic protein which regulates exocyst function and pseudohyphal differentiation | DDB0232432 | CDS | 532724 | 231 | + | 0.324675 |
DDB_G0287639 | DDB_G0287639 | DDB0232432 | CDS | 538405 | 2037 | + | 0.258714 | |
DDB_G0287641 | DDB_G0287641 | DDB0232432 | CDS | 540812 | 609 | - | 0.298851 | |
DDB_G0287643 | DDB_G0287643 | DDB0232432 | CDS | 543713 | 897 | - | 0.326644 | |
DDB_G0287645 | DDB_G0287645 | similar to the human transmembrane protein 112 contains 5 putative transmembrane domains | DDB0232432 | CDS | 550085 | 2316 | + | 0.250432 |
DDB_G0287647 | DDB_G0287647 | DDB0232432 | CDS | 552795 | 1266 | - | 0.333333 | |
DDB_G0287651 | DDB_G0287651 | belongs to a large D. discoideum protein family of unknown function this protein is a putative guanylate cyclase family protein | DDB0232432 | CDS | 436285 | 4053 | + | 0.23168 |
DDB_G0287655 | DDB_G0287655 | DDB0232432 | CDS | 443153 | 1020 | + | 0.276471 | |
DDB_G0287663 | DDB_G0287663 | DDB0232432 | CDS | 477935 | 522 | - | 0.300766 | |
DDB_G0287665 | DDB_G0287665 | DDB0232432 | CDS | 501928 | 3654 | + | 0.288725 | |
DDB_G0287667 | DDB_G0287667 | DDB0232432 | CDS | 506343 | 2208 | + | 0.294837 | |
DDB_G0287671 | DDB_G0287671 | DDB0232432 | CDS | 512195 | 633 | + | 0.28278 | |
DDB_G0287673 | DDB_G0287673 | DDB0232432 | CDS | 513198 | 324 | + | 0.175926 | |
DDB_G0287675 | DDB_G0287675 | DDB0232432 | CDS | 515703 | 1314 | + | 0.177321 | |
DDB_G0287677 | DDB_G0287677 | similar to NAD-dependent epimerasedehydratase family proteins that use nucleotide-sugar substrates for a variety of chemical reactions contains a partial NmrA-like domain near the N-terminus | DDB0232432 | CDS | 541940 | 1005 | - | 0.313433 |
DDB_G0287679 | DDB_G0287679 | DDB0232432 | CDS | 545368 | 3369 | - | 0.290591 | |
DDB_G0287695 | DDB_G0287695 | DDB0232432 | CDS | 566252 | 2037 | + | 0.26215 | |
DDB_G0287697 | DDB_G0287697 | DDB0232432 | CDS | 569375 | 2262 | + | 0.259063 | |
DDB_G0287699 | DDB_G0287699 | DDB0232432 | CDS | 573108 | 2229 | + | 0.212651 | |
DDB_G0287701 | DDB_G0287701 | DDB0232432 | CDS | 575637 | 897 | + | 0.264214 | |
DDB_G0287703 | DDB_G0287703 | DDB0232432 | CDS | 576895 | 4362 | - | 0.251719 | |
DDB_G0287705 | DDB_G0287705 | DDB0232432 | CDS | 582459 | 1122 | - | 0.272727 | |
DDB_G0287709 | DDB_G0287709 | DDB0232432 | CDS | 584610 | 2652 | - | 0.245098 | |
DDB_G0287711 | DDB_G0287711 | belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family homolog of human AADAT (kynureninealpha-aminoadipate aminotransferase) and S. cerevisiae ARO8 (aromatic amino acid aminotransferase) | DDB0232432 | CDS | 588099 | 1323 | - | 0.281179 |
DDB_G0287713 | DDB_G0287713 | DDB0232432 | CDS | 594468 | 1425 | + | 0.226667 | |
DDB_G0287715 | DDB_G0287715 | DDB0232432 | CDS | 596372 | 147 | - | 0.244898 | |
DDB_G0287719 | DDB_G0287719 | DDB0232432 | CDS | 598885 | 180 | - | 0.222222 | |
DDB_G0287721 | DDB_G0287721 | DDB0232432 | CDS | 600318 | 1041 | + | 0.304515 | |
DDB_G0287723 | DDB_G0287723 | DDB0232432 | CDS | 601565 | 2796 | - | 0.341559 | |
DDB_G0287725 | DDB_G0287725 | DDB0232432 | CDS | 605033 | 1716 | + | 0.262238 | |
DDB_G0287727 | DDB_G0287727 | DDB0232432 | CDS | 609137 | 3261 | + | 0.272002 | |
DDB_G0287729 | DDB_G0287729 | DDB0232432 | CDS | 613467 | 2121 | + | 0.296558 | |
DDB_G0287731 | DDB_G0287731 | belongs to the PLAC8 family (placenta-specific gene 8 protein) a family of cysteine-rich proteins with highly divergent low complexity amino terminal regions | DDB0232432 | CDS | 616064 | 426 | - | 0.328638 |
DDB_G0287735 | DDB_G0287735 | catalyzes the reaction a 5'-ribonucleotide Hsub2subO a ribonucleoside phosphate | DDB0232432 | CDS | 620499 | 1380 | + | 0.266667 |
DDB_G0287737 | DDB_G0287737 | DDB0232432 | CDS | 635143 | 564 | - | 0.242908 | |
DDB_G0287741 | DDB_G0287741 | DDB0232432 | CDS | 638654 | 1284 | - | 0.288941 | |
DDB_G0287743 | DDB_G0287743 | DDB0232432 | CDS | 640479 | 600 | + | 0.14 | |
DDB_G0287745 | DDB_G0287745 | putative ortholog of human cdk5rap3LZAP an ARF binding protein involved in cell cycle regulation | DDB0232432 | CDS | 644291 | 1800 | - | 0.225556 |
DDB_G0287749 | DDB_G0287749 | DDB0232432 | CDS | 647248 | 387 | - | 0.307494 | |
DDB_G0287751 | DDB_G0287751 | DDB0232432 | CDS | 648202 | 1707 | + | 0.207967 | |
DDB_G0287753 | DDB_G0287753 | DDB0232432 | CDS | 656012 | 891 | + | 0.251403 | |
DDB_G0287757 | DDB_G0287757 | ortholog of the conserved IMPACT (Imprinted and ancient) protein a translational regulator that ensures constant high levels of translation under amino acid starvation | DDB0232432 | CDS | 661336 | 1038 | + | 0.233141 |
DDB_G0287759 | DDB_G0287759 | DDB0232432 | CDS | 662849 | 1140 | - | 0.261404 | |
DDB_G0287761 | DDB_G0287761 | DDB0232432 | CDS | 664647 | 1455 | - | 0.262543 | |
DDB_G0287763 | DDB_G0287763 | similar to D. melanogaster slv (saliva) and human RAG1AP1 RAG1AP1 facilitates gene activation of recombination activating gene 1 contains 2 MtN3_slv domains contains 7 putative transmembrane domains | DDB0232432 | CDS | 669499 | 663 | + | 0.239819 |
DDB_G0287765 | DDB_G0287765 | overexpressed in | DDB0232432 | CDS | 671692 | 1317 | - | 0.297646 |
DDB_G0287767_ps | DDB_G0287767 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 675515 | 135 | + | 0.222222 |
DDB_G0287771 | DDB_G0287771 | DDB0232432 | CDS | 677716 | 399 | + | 0.270677 | |
DDB_G0287783 | DDB_G0287783 | DDB0232432 | CDS | 687490 | 498 | + | 0.307229 | |
DDB_G0287787_ps | DDB_G0287787 | putative pseudogene similar to many different classes of protein kinases | DDB0232432 | CDS | 701445 | 2061 | - | 0.289665 |
DDB_G0287789_ps | DDB_G0287789 | putative pseudogene similar to | DDB0232432 | CDS | 703769 | 282 | - | 0.195035 |
DDB_G0287793 | DDB_G0287793 | similar to human GSTT2 (glutathione S-transferase theta-2) glutathione transferases participate in the detoxification of reactive electrophilic compounds by catalysing their conjugation to glutathione contains a predicted peroxisomal targeting signal | DDB0232432 | CDS | 710171 | 669 | + | 0.246637 |
DDB_G0287797 | DDB_G0287797 | DDB0232432 | CDS | 713390 | 2088 | - | 0.244732 | |
DDB_G0287799 | DDB_G0287799 | contains a putative N-end rule-based degradation signal which targets a protein for ubiquitin-dependent proteolysis | DDB0232432 | CDS | 715755 | 5445 | + | 0.279339 |
DDB_G0287805 | DDB_G0287805 | DDB0232432 | CDS | 739515 | 4788 | - | 0.266708 | |
DDB_G0287807 | DDB_G0287807 | DDB0232432 | CDS | 744839 | 1485 | - | 0.256566 | |
DDB_G0287809 | DDB_G0287809 | DDB0232432 | CDS | 746961 | 852 | - | 0.223005 | |
DDB_G0287811 | DDB_G0287811 | DDB0232432 | CDS | 748966 | 309 | + | 0.326861 | |
DDB_G0287813 | DDB_G0287813 | DDB0232432 | CDS | 756116 | 1182 | + | 0.319797 | |
DDB_G0287815 | DDB_G0287815 | weak ortholog of the conserved chromatin assembly factor 1 (CAF1) subunit Abr bNote:b Do not confuse this gene with | DDB0232432 | CDS | 758176 | 2199 | + | 0.295589 |
DDB_G0287821 | DDB_G0287821 | DDB0232432 | CDS | 765881 | 498 | - | 0.309237 | |
DDB_G0287825 | DDB_G0287825 | DDB0232432 | CDS | 771339 | 1386 | + | 0.277778 | |
DDB_G0287831 | DDB_G0287831 | DDB0232432 | CDS | 776635 | 1629 | + | 0.228361 | |
DDB_G0287833 | DDB_G0287833 | DDB0232432 | CDS | 779158 | 4344 | + | 0.267726 | |
DDB_G0287835 | DDB_G0287835 | DDB0232432 | CDS | 783822 | 402 | - | 0.149254 | |
DDB_G0287837 | DDB_G0287837 | DDB0232432 | CDS | 787959 | 738 | + | 0.188347 | |
DDB_G0287839 | DDB_G0287839 | DDB0232432 | CDS | 789237 | 1452 | + | 0.309917 | |
DDB_G0287841 | DDB_G0287841 | DDB0232432 | CDS | 797545 | 1236 | - | 0.267799 | |
DDB_G0287843 | DDB_G0287843 | DDB0232432 | CDS | 806278 | 1923 | - | 0.333853 | |
DDB_G0287845 | DDB_G0287845 | DDB0232432 | CDS | 809663 | 2763 | - | 0.175896 | |
DDB_G0287847 | DDB_G0287847 | DDB0232432 | CDS | 813389 | 2040 | + | 0.260294 | |
DDB_G0287851 | DDB_G0287851 | DDB0232432 | CDS | 822730 | 2889 | + | 0.317411 | |
DDB_G0287857 | DDB_G0287857 | DDB0232432 | CDS | 667105 | 1599 | - | 0.243277 | |
DDB_G0287859 | DDB_G0287859 | contains a putative N-end rule-based degradation signal which targets a protein for ubiquitin-dependent proteolysis | DDB0232432 | CDS | 694189 | 4743 | + | 0.292009 |
DDB_G0287863 | DDB_G0287863 | developmental expression pattern altered in GBF null cells highly repetitive protein serine and glycine rich contains a predicted signal peptide | DDB0232432 | CDS | 733543 | 5790 | + | 0.383765 |
DDB_G0287865 | DDB_G0287865 | DDB0232432 | CDS | 829648 | 189 | - | 0.21164 | |
DDB_G0287869 | DDB_G0287869 | DDB0232432 | CDS | 591245 | 948 | - | 0.300633 | |
DDB_G0287871 | DDB_G0287871 | DDB0232432 | CDS | 607163 | 171 | - | 0.169591 | |
DDB_G0287873 | DDB_G0287873 | DDB0232432 | CDS | 622124 | 6861 | - | 0.288005 | |
DDB_G0287875 | DDB_G0287875 | contains a calponin-like actin binding domain and a pleckstrin homology domain and two ras association domains | DDB0232432 | CDS | 630862 | 3636 | + | 0.300055 |
DDB_G0287877 | DDB_G0287877 | DDB0232432 | CDS | 641447 | 2784 | + | 0.195402 | |
DDB_G0287879 | DDB_G0287879 | DDB0232432 | CDS | 650440 | 1206 | + | 0.276949 | |
DDB_G0287885 | DDB_G0287885 | DDB0232432 | CDS | 670518 | 783 | + | 0.297573 | |
DDB_G0287889 | DDB_G0287889 | DDB0232432 | CDS | 749668 | 948 | - | 0.341772 | |
DDB_G0287893 | DDB_G0287893 | DDB0232432 | CDS | 784589 | 534 | - | 0.226592 | |
DDB_G0287897 | DDB_G0287897 | DDB0232432 | CDS | 803720 | 1821 | - | 0.267435 | |
DDB_G0287903 | DDB_G0287903 | DDB0232432 | CDS | 830599 | 210 | - | 0.285714 | |
DDB_G0287907 | DDB_G0287907 | DDB0232432 | CDS | 833038 | 753 | + | 0.229748 | |
DDB_G0287909 | DDB_G0287909 | DDB0232432 | CDS | 833953 | 3585 | - | 0.271409 | |
DDB_G0287911 | DDB_G0287911 | DDB0232432 | CDS | 838039 | 1467 | - | 0.250852 | |
DDB_G0287927 | DDB_G0287927 | DDB0232432 | CDS | 859603 | 1485 | + | 0.256566 | |
DDB_G0287929 | DDB_G0287929 | DDB0232432 | CDS | 861720 | 1377 | + | 0.302832 | |
DDB_G0287931 | DDB_G0287931 | DDB0232432 | CDS | 863622 | 507 | + | 0.220907 | |
DDB_G0287933 | DDB_G0287933 | DDB0232432 | CDS | 864291 | 1515 | - | 0.279208 | |
DDB_G0287935 | DDB_G0287935 | DDB0232432 | CDS | 867361 | 2139 | - | 0.295465 | |
DDB_G0287943 | DDB_G0287943 | DDB0232432 | CDS | 852371 | 1944 | - | 0.261317 | |
DDB_G0287947 | DDB_G0287947 | DDB0232432 | CDS | 874209 | 633 | - | 0.268562 | |
DDB_G0287949 | DDB_G0287949 | DDB0232432 | CDS | 875204 | 1155 | + | 0.27013 | |
DDB_G0287951 | DDB_G0287951 | carboxyl terminus is highly similar to Ataxin-7-like protein 3 the rest of the protein is extremely repetitive | DDB0232432 | CDS | 876413 | 4344 | - | 0.315838 |
DDB_G0287955 | DDB_G0287955 | DDB0232432 | CDS | 885768 | 1221 | + | 0.242424 | |
DDB_G0287957 | DDB_G0287957 | DDB0232432 | CDS | 889459 | 1623 | - | 0.162662 | |
DDB_G0287959 | DDB_G0287959 | putative copper transporter contains 3 predicted transmembrane domains | DDB0232432 | CDS | 893285 | 633 | + | 0.271722 |
DDB_G0287961 | DDB_G0287961 | DDB0232432 | CDS | 894476 | 5595 | - | 0.27328 | |
DDB_G0287963 | DDB_G0287963 | DDB0232432 | CDS | 892450 | 144 | - | 0.270833 | |
DDB_G0287967 | DDB_G0287967 | DDB0232432 | CDS | 902212 | 333 | + | 0.279279 | |
DDB_G0287971 | DDB_G0287971 | DDB0232432 | CDS | 914990 | 1539 | - | 0.246914 | |
DDB_G0287973 | DDB_G0287973 | DDB0232432 | CDS | 917728 | 1032 | + | 0.306202 | |
DDB_G0287975 | DDB_G0287975 | DDB0232432 | CDS | 919012 | 501 | - | 0.243513 | |
DDB_G0287979 | DDB_G0287979 | DDB0232432 | CDS | 922041 | 3255 | - | 0.242704 | |
DDB_G0287985 | DDB_G0287985 | DDB0232432 | CDS | 933669 | 912 | + | 0.3125 | |
DDB_G0287989 | DDB_G0287989 | DDB0232432 | CDS | 937712 | 1149 | - | 0.255004 | |
DDB_G0287991 | DDB_G0287991 | DDB0232432 | CDS | 939192 | 831 | - | 0.322503 | |
DDB_G0287999 | DDB_G0287999 | DDB0232432 | CDS | 948929 | 3615 | + | 0.237344 | |
DDB_G0288001 | DDB_G0288001 | related to fatty acyl-CoA synthetase catalyzes the reaction ATP a long-chain carboxylic acid CoA AMP diphosphate an acyl-CoA mediates the retrieval of fatty acids from endosomes to the cytoplasm | DDB0232432 | CDS | 953191 | 3816 | + | 0.280136 |
DDB_G0288003 | DDB_G0288003 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 957063 | 4110 | - | 0.251825 |
DDB_G0288005 | DDB_G0288005 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232432 | CDS | 962125 | 960 | - | 0.314583 |
DDB_G0288007 | DDB_G0288007 | DDB0232432 | CDS | 963824 | 5637 | - | 0.284016 | |
DDB_G0288009 | DDB_G0288009 | putative ortholog of human UPF0663 downregulated in multiple cancers | DDB0232432 | CDS | 970396 | 2718 | + | 0.292127 |
DDB_G0288011 | DDB_G0288011 | DDB0232432 | CDS | 974125 | 780 | + | 0.305128 | |
DDB_G0288013 | DDB_G0288013 | DDB0232432 | CDS | 975395 | 756 | - | 0.244709 | |
DDB_G0288017 | DDB_G0288017 | DDB0232432 | CDS | 978356 | 1377 | - | 0.315904 | |
DDB_G0288019 | DDB_G0288019 | DDB0232432 | CDS | 981451 | 720 | - | 0.306944 | |
DDB_G0288023 | DDB_G0288023 | DDB0232432 | CDS | 988438 | 1356 | - | 0.235251 | |
DDB_G0288029 | DDB_G0288029 | member of the aspartateglutamateuridylate kinase family similar to glutamate 5-kinase | DDB0232432 | CDS | 994876 | 891 | - | 0.243547 |
DDB_G0288031 | DDB_G0288031 | large protein with cysteine-containing leucine-rich repeats and a C-terminal villin headpiece contains an unknown domain (residues 300-620) found in different species and in several Dictyostelium proteins represented in Pfam-B domains PB008617 and PB046085 | DDB0232432 | CDS | 996657 | 6630 | + | 0.265309 |
DDB_G0288033 | DDB_G0288033 | DDB0232432 | CDS | 1003620 | 735 | - | 0.22585 | |
DDB_G0288035 | DDB_G0288035 | DDB0232432 | CDS | 1006610 | 204 | + | 0.303922 | |
DDB_G0288037 | DDB_G0288037 | DDB0232432 | CDS | 1008144 | 447 | - | 0.149888 | |
DDB_G0288039 | DDB_G0288039 | DDB0232432 | CDS | 1009340 | 771 | + | 0.268482 | |
DDB_G0288041 | DDB_G0288041 | DDB0232432 | CDS | 1011026 | 8853 | + | 0.276403 | |
DDB_G0288043 | DDB_G0288043 | DDB0232432 | CDS | 1021151 | 1041 | - | 0.283381 | |
DDB_G0288045 | DDB_G0288045 | DDB0232432 | CDS | 1024941 | 1809 | + | 0.254284 | |
DDB_G0288049_ps | DDB_G0288049 | putative pseudogene fragment of group of large D. discoideum proteins including | DDB0232432 | CDS | 1032772 | 351 | + | 0.17094 |
DDB_G0288051 | DDB_G0288051 | DDB0232432 | CDS | 1034769 | 1014 | - | 0.288955 | |
DDB_G0288055 | DDB_G0288055 | belongs to a family of conserved potassium transporters in bacteria yeast and plants overexpressed in | DDB0232432 | CDS | 929613 | 2151 | - | 0.317992 |
DDB_G0288057 | DDB_G0288057 | DDB0232432 | CDS | 983015 | 852 | - | 0.187793 | |
DDB_G0288059 | DDB_G0288059 | DDB0232432 | CDS | 1029614 | 630 | + | 0.284127 | |
DDB_G0288069 | DDB_G0288069 | DDB0232432 | CDS | 1045172 | 3249 | + | 0.271776 | |
DDB_G0288073 | DDB_G0288073 | DDB0232432 | CDS | 1051212 | 6114 | - | 0.292607 | |
DDB_G0288075 | DDB_G0288075 | DDB0232432 | CDS | 1059598 | 1896 | - | 0.262658 | |
DDB_G0288077_ps | DDB_G0288077 | almost identical to a small portion of scy1 a protein kinase | DDB0232432 | CDS | 1063204 | 171 | - | 0.292398 |
DDB_G0288079_ps | DDB_G0288079 | similar to DDB_G0277993 a protein of the importin family | DDB0232432 | CDS | 1063770 | 1194 | - | 0.326633 |
DDB_G0288081 | DDB_G0288081 | DDB0232432 | CDS | 1079984 | 399 | + | 0.305764 | |
DDB_G0288087 | DDB_G0288087 | DDB0232432 | CDS | 1082632 | 633 | - | 0.271722 | |
DDB_G0288089 | DDB_G0288089 | possible homolog of human GCFC (C21orf66) a putative transcription factor | DDB0232432 | CDS | 1084262 | 2832 | + | 0.234463 |
DDB_G0288091 | DDB_G0288091 | DDB0232432 | CDS | 1087651 | 834 | + | 0.323741 | |
DDB_G0288093 | DDB_G0288093 | contains a putative N-end rule-based degradation signal which targets a protein for ubiquitin-dependent proteolysis | DDB0232432 | CDS | 1089133 | 5268 | + | 0.278094 |
DDB_G0288095 | DDB_G0288095 | conserved in Dictyostelium and Polysphondylium contains a predicted signal peptide | DDB0232432 | CDS | 1094749 | 1521 | + | 0.322814 |
DDB_G0288097 | DDB_G0288097 | DDB0232432 | CDS | 1097291 | 1554 | + | 0.311454 | |
DDB_G0288099 | DDB_G0288099 | DDB0232432 | CDS | 1100340 | 765 | - | 0.256209 | |
DDB_G0288107 | DDB_G0288107 | the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232432 | CDS | 1124020 | 1182 | + | 0.267343 |
DDB_G0288109 | DDB_G0288109 | DDB0232432 | CDS | 1042048 | 2142 | + | 0.288049 | |
DDB_G0288111 | DDB_G0288111 | DDB0232432 | CDS | 1058090 | 717 | + | 0.217573 | |
DDB_G0288113_ps | DDB_G0288113 | similar to a large family of D. discoideum genes | DDB0232432 | CDS | 1061950 | 120 | + | 0.308333 |
DDB_G0288121 | DDB_G0288121 | DDB0232432 | CDS | 1069064 | 4308 | + | 0.246054 | |
DDB_G0288123 | DDB_G0288123 | DDB0232432 | CDS | 1076323 | 2790 | + | 0.25448 | |
DDB_G0288125 | DDB_G0288125 | DDB0232432 | CDS | 1099194 | 795 | - | 0.262893 | |
DDB_G0288129 | DDB_G0288129 | DDB0232432 | CDS | 1107652 | 2739 | + | 0.280029 | |
DDB_G0288133 | DDB_G0288133 | DDB0232432 | CDS | 1130852 | 798 | - | 0.421053 | |
DDB_G0288135 | DDB_G0288135 | DDB0232432 | CDS | 1132899 | 1545 | - | 0.206472 | |
DDB_G0288137 | DDB_G0288137 | DDB0232432 | CDS | 1135535 | 966 | + | 0.34265 | |
DDB_G0288139 | DDB_G0288139 | DDB0232432 | CDS | 1136855 | 753 | + | 0.247012 | |
DDB_G0288141 | DDB_G0288141 | DDB0232432 | CDS | 1137934 | 261 | - | 0.325671 | |
DDB_G0288143 | DDB_G0288143 | similar to lysozyme C proteins from insects contains an additional serine-rich C-terminal region | DDB0232432 | CDS | 1139463 | 564 | - | 0.320922 |
DDB_G0288147 | DDB_G0288147 | member of the tyrosine kinase-like (TKL) group similar to plant serinethreonine kinases contains a phorbol esterdiacylglycerol-binding domain | DDB0232432 | CDS | 1147360 | 4044 | + | 0.271513 |
DDB_G0288149 | DDB_G0288149 | DDB0232432 | CDS | 1152736 | 723 | + | 0.260028 | |
DDB_G0288151 | DDB_G0288151 | DDB0232432 | CDS | 1156915 | 1704 | - | 0.200117 | |
DDB_G0288153 | DDB_G0288153 | belongs to the thioredoxin family lacks redox-active cysteines compared with many homologs so may be catalytically inactive | DDB0232432 | CDS | 1158956 | 327 | - | 0.235474 |
DDB_G0288155 | DDB_G0288155 | DDB0232432 | CDS | 1159975 | 741 | - | 0.333333 | |
DDB_G0288157 | DDB_G0288157 | DDB0232432 | CDS | 1161244 | 732 | - | 0.266393 | |
DDB_G0288159 | DDB_G0288159 | DDB0232432 | CDS | 1166139 | 147 | + | 0.346939 | |
DDB_G0288161 | DDB_G0288161 | DDB0232432 | CDS | 1166708 | 2844 | - | 0.307665 | |
DDB_G0288165 | DDB_G0288165 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232432 | CDS | 1172053 | 1116 | - | 0.292115 |
DDB_G0288167 | DDB_G0288167 | DDB0232432 | CDS | 1174416 | 219 | + | 0.406393 | |
DDB_G0288175 | DDB_G0288175 | DDB0232432 | CDS | 1154137 | 2475 | + | 0.245253 | |
DDB_G0288185 | DDB_G0288185 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232432 | CDS | 1178682 | 276 | - | 0.362319 |
DDB_G0288189 | DDB_G0288189 | DDB0232432 | CDS | 1182370 | 1299 | + | 0.193995 | |
DDB_G0288191 | DDB_G0288191 | DDB0232432 | CDS | 1183802 | 2115 | - | 0.249645 | |
DDB_G0288193 | DDB_G0288193 | DDB0232432 | CDS | 1186484 | 1440 | + | 0.241667 | |
DDB_G0288199_ps | DDB_G0288199 | putative pseudogene xpr1 family gene | DDB0232432 | CDS | 1217412 | 1167 | + | 0.172237 |
DDB_G0288201 | DDB_G0288201 | DDB0232432 | CDS | 1230521 | 942 | - | 0.266454 | |
DDB_G0288203 | DDB_G0288203 | amino terminal region is similar to the interferon-related developmental regulator family contains one HEAT repeat similar to D. purpureum protein | DDB0232432 | CDS | 1233063 | 1383 | + | 0.292842 |
DDB_G0288207 | DDB_G0288207 | DDB0232432 | CDS | 1245352 | 492 | - | 0.223577 | |
DDB_G0288209 | DDB_G0288209 | ortholog of mitochondrial twinkle protein involved in mitochondrial DNA (mtDNA) metabolism defects in this gene cause progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal dominant type 3 | DDB0232432 | CDS | 1246731 | 2319 | + | 0.269082 |
DDB_G0288211 | DDB_G0288211 | DDB0232432 | CDS | 1249148 | 1485 | - | 0.238384 | |
DDB_G0288213 | DDB_G0288213 | DDB0232432 | CDS | 1254786 | 288 | - | 0.229167 | |
DDB_G0288215 | DDB_G0288215 | DDB0232432 | CDS | 1256711 | 2808 | - | 0.226496 | |
DDB_G0288219 | DDB_G0288219 | DDB0232432 | CDS | 1267913 | 1779 | - | 0.32715 | |
DDB_G0288221 | DDB_G0288221 | DDB0232432 | CDS | 1272181 | 1188 | + | 0.313131 | |
DDB_G0288227 | DDB_G0288227 | similar to the mammalian SET domain-containing protein 7 (SETD7) a histone methyltransferase that specifically monomethylates Lys-4 of histone H3 | DDB0232432 | CDS | 1280700 | 1194 | + | 0.303183 |
DDB_G0288231 | DDB_G0288231 | DDB0232432 | CDS | 1264761 | 3036 | + | 0.301713 | |
DDB_G0288233 | DDB_G0288233 | DDB0232432 | CDS | 1270786 | 633 | - | 0.238547 | |
DDB_G0288235 | DDB_G0288235 | DDB0232432 | CDS | 1177513 | 1008 | + | 0.172619 | |
DDB_G0288237 | DDB_G0288237 | DDB0232432 | CDS | 1188181 | 4467 | - | 0.283412 | |
DDB_G0288241 | DDB_G0288241 | DDB0232432 | CDS | 1240397 | 4431 | + | 0.296547 | |
DDB_G0288243 | DDB_G0288243 | DDB0232432 | CDS | 1278382 | 1209 | - | 0.263854 | |
DDB_G0288255 | DDB_G0288255 | very similar to bacterial ribosomal RNA large subunit methyltransferase Nalso known as radical SAM protein or Cfr family protein | DDB0232432 | CDS | 1294679 | 1224 | - | 0.287582 |
DDB_G0288263 | DDB_G0288263 | DDB0232432 | CDS | 1310716 | 1266 | - | 0.226698 | |
DDB_G0288265 | DDB_G0288265 | very similar to S. cerevisiae HSP10 A. thaliana CPN10 and human HSPE1 (HSP10)mitochondrial chaperonins | DDB0232432 | CDS | 1314543 | 309 | + | 0.291262 |
DDB_G0288271 | DDB_G0288271 | DDB0232432 | CDS | 1300715 | 1119 | - | 0.242181 | |
DDB_G0288277 | DDB_G0288277 | DDB0232432 | CDS | 1329697 | 2394 | - | 0.281537 | |
DDB_G0288279 | DDB_G0288279 | DDB0232432 | CDS | 1332303 | 747 | + | 0.253012 | |
DDB_G0288281 | DDB_G0288281 | DDB0232432 | CDS | 1341246 | 156 | + | 0.403846 | |
DDB_G0288283 | DDB_G0288283 | DDB0232432 | CDS | 1345783 | 783 | + | 0.305236 | |
DDB_G0288291 | DDB_G0288291 | contains 1 RRM (RNA recognition motif) domain similar to the RRM domain of eukaryotic peptidyl-prolyl cis-trans isomerase E | DDB0232432 | CDS | 1356313 | 372 | + | 0.266129 |
DDB_G0288293 | DDB_G0288293 | conserved protein contains 5 predicted transmembrane domains | DDB0232432 | CDS | 1357343 | 846 | + | 0.301418 |
DDB_G0288297 | DDB_G0288297 | DDB0232432 | CDS | 1360320 | 1422 | - | 0.174402 | |
DDB_G0288301 | DDB_G0288301 | DDB0232432 | CDS | 1364968 | 4233 | + | 0.282542 | |
DDB_G0288303 | DDB_G0288303 | DDB0232432 | CDS | 1375029 | 627 | - | 0.274322 | |
DDB_G0288309 | DDB_G0288309 | DDB0232432 | CDS | 1333499 | 540 | - | 0.222222 | |
DDB_G0288311 | DDB_G0288311 | DDB0232432 | CDS | 1334323 | 2226 | + | 0.1469 | |
DDB_G0288315 | DDB_G0288315 | conserved protein contains 8 predicted transmembrane domains and is similar to transmembrane proteins of unknown function in other species | DDB0232432 | CDS | 1343263 | 1746 | + | 0.299542 |
DDB_G0288317 | DDB_G0288317 | DDB0232432 | CDS | 1370056 | 4095 | + | 0.275214 | |
DDB_G0288325 | DDB_G0288325 | conserved uncharacterized transmembrane protein contains 2 predicted transmembrane domains | DDB0232432 | CDS | 1394062 | 231 | - | 0.320346 |
DDB_G0288329 | DDB_G0288329 | DDB0232432 | CDS | 1397987 | 654 | + | 0.292049 | |
DDB_G0288339 | DDB_G0288339 | DDB0232432 | CDS | 1405893 | 2724 | - | 0.179148 | |
DDB_G0288341 | DDB_G0288341 | DDB0232432 | CDS | 1409331 | 1149 | + | 0.261967 | |
DDB_G0288343 | DDB_G0288343 | DDB0232432 | CDS | 1412629 | 126 | + | 0.261905 | |
DDB_G0288345 | DDB_G0288345 | DDB0232432 | CDS | 1413915 | 1554 | + | 0.261261 | |
DDB_G0288351 | DDB_G0288351 | DDB0232432 | CDS | 1420134 | 1560 | + | 0.207051 | |
DDB_G0288353 | DDB_G0288353 | DDB0232432 | CDS | 1428760 | 507 | - | 0.220907 | |
DDB_G0288355 | DDB_G0288355 | possible ortholog of THOC5 which exists in the THO complex required for transcriptional elongation | DDB0232432 | CDS | 1430508 | 2505 | + | 0.266667 |
DDB_G0288357 | DDB_G0288357 | DDB0232432 | CDS | 1434151 | 312 | + | 0.221154 | |
DDB_G0288363 | DDB_G0288363 | belongs to the peptidase S8 family contains a predicted signal peptide contains one EGF-like domain | DDB0232432 | CDS | 1391586 | 2037 | + | 0.311733 |
DDB_G0288367 | DDB_G0288367 | DDB0232432 | CDS | 1434816 | 3597 | - | 0.2263 | |
DDB_G0288369 | DDB_G0288369 | DDB0232432 | CDS | 1416573 | 1035 | - | 0.269565 | |
DDB_G0288371 | DDB_G0288371 | weakly similar to S. cerevisiae VPS74 a protein of unknown function involved in vacuolar protein sorting | DDB0232432 | CDS | 1426752 | 789 | - | 0.244613 |
DDB_G0288379 | DDB_G0288379 | small cortactin protein a putative actin binding protein conserved in Dictyostelids | DDB0232432 | CDS | 1459573 | 291 | - | 0.32646 |
DDB_G0288381 | DDB_G0288381 | DDB0232432 | CDS | 1460823 | 1650 | - | 0.270303 | |
DDB_G0288385 | DDB_G0288385 | DDB0232432 | CDS | 1467682 | 1113 | - | 0.233603 | |
DDB_G0288389 | DDB_G0288389 | DDB0232432 | CDS | 1486099 | 450 | + | 0.224444 | |
DDB_G0288393 | DDB_G0288393 | DDB0232432 | CDS | 1488951 | 639 | + | 0.211268 | |
DDB_G0288395 | DDB_G0288395 | DDB0232432 | CDS | 1489692 | 339 | - | 0.247788 | |
DDB_G0288397 | DDB_G0288397 | DDB0232432 | CDS | 1490397 | 267 | - | 0.348315 | |
DDB_G0288399 | DDB_G0288399 | DDB0232432 | CDS | 1491224 | 222 | - | 0.301802 | |
DDB_G0288403 | DDB_G0288403 | DDB0232432 | CDS | 1499232 | 1455 | - | 0.243299 | |
DDB_G0288405 | DDB_G0288405 | DDB0232432 | CDS | 1502693 | 2202 | + | 0.265668 | |
DDB_G0288407 | DDB_G0288407 | DDB0232432 | CDS | 1505496 | 687 | - | 0.269287 | |
DDB_G0288411_ps | DDB_G0288411 | putative pseudogene similar to | DDB0232432 | CDS | 1506576 | 1704 | + | 0.231808 |
DDB_G0288417 | DDB_G0288417 | DDB0232432 | CDS | 1511045 | 384 | - | 0.335938 | |
DDB_G0288419 | DDB_G0288419 | DDB0232432 | CDS | 1511818 | 1455 | + | 0.383505 | |
DDB_G0288429 | DDB_G0288429 | belongs to the short-chain dehydrogenasesreductases (SDR) family | DDB0232432 | CDS | 1527197 | 993 | + | 0.281974 |
DDB_G0288433 | DDB_G0288433 | DDB0232432 | CDS | 1528754 | 825 | + | 0.232727 | |
DDB_G0288435 | DDB_G0288435 | DDB0232432 | CDS | 1530778 | 1554 | + | 0.328829 | |
DDB_G0288437 | DDB_G0288437 | DDB0232432 | CDS | 1535366 | 3909 | + | 0.300588 | |
DDB_G0288441 | DDB_G0288441 | DDB0232432 | CDS | 1540991 | 804 | + | 0.263682 | |
DDB_G0288443 | DDB_G0288443 | DDB0232432 | CDS | 1542340 | 975 | + | 0.260513 | |
DDB_G0288447 | DDB_G0288447 | DDB0232432 | CDS | 1482942 | 2028 | - | 0.236686 | |
DDB_G0288451_ps | DDB_G0288451 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 1513586 | 846 | + | 0.20331 |
DDB_G0288453 | DDB_G0288453 | DDB0232432 | CDS | 1521809 | 2913 | - | 0.270855 | |
DDB_G0288455_ps | DDB_G0288455 | putative pseudogene similar to | DDB0232432 | CDS | 1532524 | 1620 | + | 0.295679 |
DDB_G0288459 | DDB_G0288459 | DDB0232432 | CDS | 1551650 | 3717 | - | 0.304009 | |
DDB_G0288465 | DDB_G0288465 | converts pantetheine 4'-phosphate to 3'-dephospho-CoA in other organisms this activity is part of a bifunctional enzyme that also has dephospho-CoA kinase activity in Dictyostelium the latter activity is encoded by | DDB0232432 | CDS | 1558211 | 1230 | - | 0.233333 |
DDB_G0288467 | DDB_G0288467 | DDB0232432 | CDS | 1559882 | 531 | - | 0.293785 | |
DDB_G0288469 | DDB_G0288469 | DDB0232432 | CDS | 1563184 | 2883 | + | 0.226153 | |
DDB_G0288473 | DDB_G0288473 | DDB0232432 | CDS | 1569035 | 6093 | + | 0.278516 | |
DDB_G0288475 | DDB_G0288475 | DDB0232432 | CDS | 1575886 | 3360 | + | 0.34256 | |
DDB_G0288477 | DDB_G0288477 | DDB0232432 | CDS | 1580012 | 1914 | - | 0.3093 | |
DDB_G0288489 | DDB_G0288489 | DDB0232432 | CDS | 1599423 | 843 | + | 0.313167 | |
DDB_G0288493 | DDB_G0288493 | DDB0232432 | CDS | 1604662 | 480 | - | 0.30625 | |
DDB_G0288497 | DDB_G0288497 | DDB0232432 | CDS | 1611473 | 3741 | - | 0.190323 | |
DDB_G0288499 | DDB_G0288499 | DDB0232432 | CDS | 1594285 | 2853 | + | 0.222222 | |
DDB_G0288505_RTE | DDB_G0288505 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232432 | CDS | 1590688 | 908 | - | 0.409692 |
DDB_G0288513 | DDB_G0288513 | DDB0232432 | CDS | 1631607 | 1245 | + | 0.204819 | |
DDB_G0288515 | DDB_G0288515 | DDB0232432 | CDS | 1633091 | 786 | + | 0.198473 | |
DDB_G0288517 | DDB_G0288517 | DDB0232432 | CDS | 1633993 | 831 | + | 0.223827 | |
DDB_G0288519 | DDB_G0288519 | DDB0232432 | CDS | 1635029 | 1323 | - | 0.247166 | |
DDB_G0288521 | DDB_G0288521 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232432 | CDS | 1636790 | 1512 | + | 0.315476 |
DDB_G0288525 | DDB_G0288525 | DDB0232432 | CDS | 1644947 | 1674 | - | 0.247909 | |
DDB_G0288529 | DDB_G0288529 | DDB0232432 | CDS | 1628807 | 1587 | + | 0.267171 | |
DDB_G0288531 | DDB_G0288531 | DDB0232432 | CDS | 1649759 | 2196 | + | 0.255009 | |
DDB_G0288535 | DDB_G0288535 | DDB0232432 | CDS | 1660756 | 1395 | - | 0.235842 | |
DDB_G0288537 | DDB_G0288537 | DDB0232432 | CDS | 1662584 | 2541 | - | 0.277056 | |
DDB_G0288539 | DDB_G0288539 | DDB0232432 | CDS | 1648133 | 798 | - | 0.177945 | |
DDB_G0288547 | DDB_G0288547 | DDB0232432 | CDS | 1676407 | 1038 | - | 0.259152 | |
DDB_G0288549 | DDB_G0288549 | DDB0232432 | CDS | 1677926 | 822 | - | 0.244526 | |
DDB_G0288551 | DDB_G0288551 | conserved protein contains 5 PUF domains D. melanogaster pumilio binds through a PUF domain to the 3' UTR of target mRNAs | DDB0232432 | CDS | 1679413 | 2040 | + | 0.283333 |
DDB_G0288555 | DDB_G0288555 | DDB0232432 | CDS | 1681661 | 2182 | - | 0.192026 | |
DDB_G0288559 | DDB_G0288559 | DDB0232432 | CDS | 1685010 | 1650 | + | 0.303636 | |
DDB_G0288561_ps | DDB_G0288561 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 1686921 | 834 | - | 0.257794 |
DDB_G0288563 | DDB_G0288563 | DDB0232432 | CDS | 1689437 | 945 | - | 0.368254 | |
DDB_G0288567 | DDB_G0288567 | DDB0232432 | CDS | 1693029 | 522 | + | 0.16092 | |
DDB_G0288569 | DDB_G0288569 | DDB0232432 | CDS | 1693802 | 3495 | - | 0.303577 | |
DDB_G0288571 | DDB_G0288571 | DDB0232432 | CDS | 1698545 | 1134 | + | 0.251323 | |
DDB_G0288573 | DDB_G0288573 | DDB0232432 | CDS | 1700402 | 684 | + | 0.276316 | |
DDB_G0288575 | DDB_G0288575 | DDB0232432 | CDS | 1706213 | 369 | + | 0.306233 | |
DDB_G0288577 | DDB_G0288577 | DDB0232432 | CDS | 1717040 | 159 | + | 0.402516 | |
DDB_G0288579 | DDB_G0288579 | DDB0232432 | CDS | 1717737 | 369 | + | 0.325203 | |
DDB_G0288581 | DDB_G0288581 | DDB0232432 | CDS | 1718254 | 972 | - | 0.256173 | |
DDB_G0288583 | DDB_G0288583 | DDB0232432 | CDS | 1719547 | 708 | - | 0.258475 | |
DDB_G0288585 | DDB_G0288585 | DDB0232432 | CDS | 1720817 | 759 | + | 0.200264 | |
DDB_G0288587 | DDB_G0288587 | DDB0232432 | CDS | 1721620 | 714 | - | 0.22549 | |
DDB_G0288589 | DDB_G0288589 | DDB0232432 | CDS | 1722609 | 1338 | - | 0.272048 | |
DDB_G0288591 | DDB_G0288591 | DDB0232432 | CDS | 1726934 | 861 | + | 0.293844 | |
DDB_G0288593 | DDB_G0288593 | DDB0232432 | CDS | 1728286 | 2085 | - | 0.313669 | |
DDB_G0288595 | DDB_G0288595 | DDB0232432 | CDS | 1730911 | 1224 | + | 0.227124 | |
DDB_G0288597 | DDB_G0288597 | DDB0232432 | CDS | 1732418 | 1926 | - | 0.226895 | |
DDB_G0288599 | DDB_G0288599 | MBOAT family protein membrane proteins that contains a variety of acyltransferase enzymes most similar to S. cerevisiae glycerol uptake protein 1 (GUP1) contains 11 predicted transmembrane domains | DDB0232432 | CDS | 1734624 | 1695 | + | 0.315634 |
DDB_G0288601_ps | DDB_G0288601 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 1725951 | 189 | + | 0.227513 |
DDB_G0288615 | DDB_G0288615 | DDB0232432 | CDS | 1744822 | 285 | + | 0.287719 | |
DDB_G0288619 | DDB_G0288619 | DDB0232432 | CDS | 1748711 | 828 | - | 0.286232 | |
DDB_G0288625 | DDB_G0288625 | DDB0232432 | CDS | 1759888 | 2316 | - | 0.295337 | |
DDB_G0288627 | DDB_G0288627 | DDB0232432 | CDS | 1763068 | 1212 | + | 0.229373 | |
DDB_G0288629 | DDB_G0288629 | DDB0232432 | CDS | 1764970 | 792 | + | 0.285354 | |
DDB_G0288631 | DDB_G0288631 | DDB0232432 | CDS | 1767936 | 2103 | - | 0.262958 | |
DDB_G0288635 | DDB_G0288635 | DDB0232432 | CDS | 1774014 | 663 | - | 0.315234 | |
DDB_G0288637_ps | DDB_G0288637 | putative pseudogene similar to | DDB0232432 | CDS | 1772020 | 1164 | + | 0.268041 |
DDB_G0288639 | DDB_G0288639 | conserved protein DnaJ homolog subfamily C member 7 (DNAJC7) | DDB0232432 | CDS | 1756684 | 1620 | + | 0.334568 |
DDB_G0288641 | DDB_G0288641 | DDB0232432 | CDS | 1759110 | 639 | + | 0.242567 | |
DDB_G0288643 | DDB_G0288643 | DDB0232432 | CDS | 1766588 | 1185 | + | 0.24135 | |
DDB_G0288645 | DDB_G0288645 | DDB0232432 | CDS | 1776536 | 1650 | - | 0.277576 | |
DDB_G0288651 | DDB_G0288651 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232432 | CDS | 1782938 | 1353 | - | 0.317812 |
DDB_G0288653 | DDB_G0288653 | DDB0232432 | CDS | 1786499 | 453 | - | 0.181015 | |
DDB_G0288657 | DDB_G0288657 | DDB0232432 | CDS | 1789768 | 249 | - | 0.281125 | |
DDB_G0288661 | DDB_G0288661 | DDB0232432 | CDS | 1792404 | 924 | + | 0.208874 | |
DDB_G0288663 | DDB_G0288663 | DDB0232432 | CDS | 1793780 | 591 | + | 0.28934 | |
DDB_G0288665 | DDB_G0288665 | DDB0232432 | CDS | 1795019 | 594 | + | 0.311448 | |
DDB_G0288667 | DDB_G0288667 | DDB0232432 | CDS | 1796243 | 441 | - | 0.265306 | |
DDB_G0288669 | DDB_G0288669 | DDB0232432 | CDS | 1797088 | 930 | - | 0.230108 | |
DDB_G0288671 | DDB_G0288671 | catalyzes the reaction L-proline NAD(P)supsup 1-pyrroline-5-carboxylate NAD(P)H Hsupsup | DDB0232432 | CDS | 1798454 | 1656 | - | 0.341184 |
DDB_G0288673 | DDB_G0288673 | DDB0232432 | CDS | 1800597 | 972 | - | 0.236626 | |
DDB_G0288675 | DDB_G0288675 | DDB0232432 | CDS | 1808800 | 396 | - | 0.217172 | |
DDB_G0288683 | DDB_G0288683 | DDB0232432 | CDS | 1810485 | 2562 | + | 0.26815 | |
DDB_G0288687 | DDB_G0288687 | DDB0232432 | CDS | 1817419 | 1746 | + | 0.182131 | |
DDB_G0288689 | DDB_G0288689 | DDB0232432 | CDS | 1819614 | 1800 | - | 0.215556 | |
DDB_G0288693 | DDB_G0288693 | DDB0232432 | CDS | 1834141 | 1806 | + | 0.296788 | |
DDB_G0288695 | DDB_G0288695 | DDB0232432 | CDS | 1836785 | 2718 | - | 0.181015 | |
DDB_G0288697 | DDB_G0288697 | DDB0232432 | CDS | 1839851 | 1758 | - | 0.303185 | |
DDB_G0288707 | DDB_G0288707 | DDB0232432 | CDS | 1852460 | 2958 | - | 0.281947 | |
DDB_G0288713 | DDB_G0288713 | DDB0232432 | CDS | 1863605 | 609 | + | 0.208539 | |
DDB_G0288717 | DDB_G0288717 | DDB0232432 | CDS | 1867636 | 1647 | - | 0.333333 | |
DDB_G0288723 | DDB_G0288723 | DDB0232432 | CDS | 1876927 | 966 | - | 0.279503 | |
DDB_G0288725 | DDB_G0288725 | DDB0232432 | CDS | 1879264 | 3498 | - | 0.193253 | |
DDB_G0288727 | DDB_G0288727 | DDB0232432 | CDS | 1883551 | 435 | + | 0.25977 | |
DDB_G0288729 | DDB_G0288729 | ortholog of the mammalian reticulon-4-interacting protein 1 a zinc-containing alcohol dehydrogenase | DDB0232432 | CDS | 1887042 | 1059 | - | 0.249292 |
DDB_G0288731 | DDB_G0288731 | highly similar to mammalian myotubularin-related protein 2 in sequence and in domain architecture a dual-specific lipid phosphatase that dephosphorylates phosphatidylinositol 3-phosphate and phosphatidylinositol (35)-bi-phosphate | DDB0232432 | CDS | 1888714 | 3684 | + | 0.266015 |
DDB_G0288733_ps | DDB_G0288733 | putative pseudogene similar to a family of genes including | DDB0232432 | CDS | 1894171 | 375 | + | 0.352 |
DDB_G0288735 | DDB_G0288735 | very similar to acyl-coenzyme A oxidases but lacks the full domain | DDB0232432 | CDS | 1895573 | 1959 | + | 0.338948 |
DDB_G0288737 | DDB_G0288737 | DDB0232432 | CDS | 1864937 | 612 | + | 0.228758 | |
DDB_G0288739 | DDB_G0288739 | DDB0232432 | CDS | 1826054 | 1398 | - | 0.261087 | |
DDB_G0288745 | DDB_G0288745 | DDB0232432 | CDS | 1892916 | 642 | + | 0.291277 | |
DDB_G0288747 | DDB_G0288747 | contains one Myb DNA-binding domain similar to D. rerio DNA methyltransferase 1 associated protein 1 | DDB0232432 | CDS | 1912921 | 3129 | + | 0.282838 |
DDB_G0288751 | DDB_G0288751 | DDB0232432 | CDS | 1903969 | 3690 | + | 0.250677 | |
DDB_G0288757 | DDB_G0288757 | catalyzes the reaction ATP nicotinamide ribonucleotide diphosphate NAD | DDB0232432 | CDS | 1926304 | 579 | - | 0.229706 |
DDB_G0288761 | DDB_G0288761 | DDB0232432 | CDS | 1927278 | 129 | - | 0.24031 | |
DDB_G0288763 | DDB_G0288763 | DDB0232432 | CDS | 1933766 | 1119 | + | 0.304736 | |
DDB_G0288765 | DDB_G0288765 | DDB0232432 | CDS | 1935972 | 255 | + | 0.215686 | |
DDB_G0288767 | DDB_G0288767 | DDB0232432 | CDS | 1936647 | 609 | + | 0.275862 | |
DDB_G0288779 | DDB_G0288779 | DDB0232432 | CDS | 1950277 | 1482 | + | 0.212551 | |
DDB_G0288781 | DDB_G0288781 | DDB0232432 | CDS | 1951922 | 1371 | - | 0.340627 | |
DDB_G0288793 | DDB_G0288793 | DDB0232432 | CDS | 1973649 | 1521 | - | 0.26167 | |
DDB_G0288795 | DDB_G0288795 | putative protein serinethreonine kinase AGC group similar to the kinase domains of mammalian AKTPKB similar to yeast protein kinases GAD8 and SCH9 | DDB0232432 | CDS | 1975761 | 1926 | - | 0.317757 |
DDB_G0288801 | DDB_G0288801 | DDB0232432 | CDS | 1982434 | 2106 | - | 0.349003 | |
DDB_G0288805 | DDB_G0288805 | DDB0232432 | CDS | 1990254 | 2601 | + | 0.235679 | |
DDB_G0288811 | DDB_G0288811 | very similar to TBC1 domain family member 15 proteins and yeast GYP7 TBC domain-containing proteins in yeast are GTPase activator proteins | DDB0232432 | CDS | 2006806 | 2490 | + | 0.284739 |
DDB_G0288813 | DDB_G0288813 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 2010767 | 4197 | + | 0.245413 |
DDB_G0288815 | DDB_G0288815 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 2016292 | 4173 | + | 0.259286 |
DDB_G0288821 | DDB_G0288821 | DDB0232432 | CDS | 2033361 | 951 | - | 0.33123 | |
DDB_G0288825 | DDB_G0288825 | DDB0232432 | CDS | 2036092 | 2901 | - | 0.247156 | |
DDB_G0288827 | DDB_G0288827 | DDB0232432 | CDS | 2040745 | 2988 | + | 0.218541 | |
DDB_G0288829 | DDB_G0288829 | DDB0232432 | CDS | 2043960 | 252 | - | 0.297619 | |
DDB_G0288841 | DDB_G0288841 | DDB0232432 | CDS | 2053563 | 216 | + | 0.412037 | |
DDB_G0288847 | DDB_G0288847 | DDB0232432 | CDS | 2055893 | 450 | - | 0.295556 | |
DDB_G0288849 | DDB_G0288849 | contains a predicted signal peptide and a putative C-terminal transmembrane domain similar to S. cerevisiae ERO1 (endoplasmic oxidoreductin-1) which is required for the formation of disulfide bonds in the proteins in the endoplasmic reticulum | DDB0232432 | CDS | 2057527 | 1662 | - | 0.253309 |
DDB_G0288851 | DDB_G0288851 | DDB0232432 | CDS | 2060041 | 432 | + | 0.24537 | |
DDB_G0288853 | DDB_G0288853 | DDB0232432 | CDS | 2063858 | 1374 | + | 0.201601 | |
DDB_G0288861 | DDB_G0288861 | DDB0232432 | CDS | 1954614 | 2169 | + | 0.319963 | |
DDB_G0288865 | DDB_G0288865 | DDB0232432 | CDS | 1959111 | 486 | - | 0.257202 | |
DDB_G0288867 | DDB_G0288867 | DDB0232432 | CDS | 1970396 | 2844 | - | 0.182841 | |
DDB_G0288869 | DDB_G0288869 | contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one extracellular EGF-2 domain | DDB0232432 | CDS | 2021392 | 3024 | + | 0.257275 |
DDB_G0288871 | DDB_G0288871 | DDB0232432 | CDS | 2060725 | 240 | - | 0.320833 | |
DDB_G0288883 | DDB_G0288883 | DDB0232432 | CDS | 2083221 | 450 | - | 0.246667 | |
DDB_G0288885 | DDB_G0288885 | DDB0232432 | CDS | 2083996 | 918 | + | 0.308279 | |
DDB_G0288887 | DDB_G0288887 | DDB0232432 | CDS | 2086198 | 135 | - | 0.303704 | |
DDB_G0288889 | DDB_G0288889 | DDB0232432 | CDS | 2086808 | 1437 | - | 0.177453 | |
DDB_G0288895 | DDB_G0288895 | contains one BAR (BINAmphiphysinRvs) domain and SH3 domain | DDB0232432 | CDS | 2091691 | 1395 | - | 0.324014 |
DDB_G0288897 | DDB_G0288897 | DDB0232432 | CDS | 2093655 | 1050 | - | 0.202857 | |
DDB_G0288901 | DDB_G0288901 | DDB0232432 | CDS | 2103495 | 1563 | + | 0.221369 | |
DDB_G0288905 | DDB_G0288905 | DDB0232432 | CDS | 2106066 | 1797 | - | 0.188091 | |
DDB_G0288911 | DDB_G0288911 | contains a predicted signal sequence similar to a D. purpureum protein | DDB0232432 | CDS | 2112807 | 420 | + | 0.307143 |
DDB_G0288913 | DDB_G0288913 | DDB0232432 | CDS | 2113860 | 432 | + | 0.217593 | |
DDB_G0288915 | DDB_G0288915 | DDB0232432 | CDS | 2114788 | 3561 | - | 0.329683 | |
DDB_G0288917 | DDB_G0288917 | similar to retinol dehydrogenase and eukaryotic proteins of the short chain dehydrogenasesreductases family | DDB0232432 | CDS | 2119308 | 954 | + | 0.240042 |
DDB_G0288925 | DDB_G0288925 | DDB0232432 | CDS | 2134650 | 399 | - | 0.243108 | |
DDB_G0288929 | DDB_G0288929 | DDB0232432 | CDS | 2135701 | 1179 | + | 0.245123 | |
DDB_G0288931 | DDB_G0288931 | DDB0232432 | CDS | 2137477 | 564 | + | 0.281915 | |
DDB_G0288941 | DDB_G0288941 | DDB0232432 | CDS | 2158460 | 303 | + | 0.280528 | |
DDB_G0288943 | DDB_G0288943 | DDB0232432 | CDS | 2159616 | 1023 | + | 0.298143 | |
DDB_G0288945 | DDB_G0288945 | DDB0232432 | CDS | 2161054 | 186 | - | 0.258065 | |
DDB_G0288947 | DDB_G0288947 | DDB0232432 | CDS | 2162285 | 4416 | + | 0.279212 | |
DDB_G0288949 | DDB_G0288949 | DDB0232432 | CDS | 2101452 | 1392 | - | 0.236351 | |
DDB_G0288951 | DDB_G0288951 | DDB0232432 | CDS | 2077569 | 2955 | + | 0.226058 | |
DDB_G0288953 | DDB_G0288953 | DDB0232432 | CDS | 2080789 | 1446 | - | 0.276625 | |
DDB_G0288955 | DDB_G0288955 | contains multiple EGF-like domains contains contains a predicted signal sequece and a putative transmembrane domain | DDB0232432 | CDS | 2096747 | 3462 | - | 0.234258 |
DDB_G0288957 | DDB_G0288957 | DDB0232432 | CDS | 2140408 | 2229 | + | 0.236429 | |
DDB_G0288959 | DDB_G0288959 | DDB0232432 | CDS | 2143283 | 1257 | - | 0.247414 | |
DDB_G0288963 | DDB_G0288963 | similar to the conserved metallocarboxypeptidase D (CPD) a membrane bound protein the Dictyostelium protein is shorter and has only one M14 peptidase domain versus three such domains in the animal proteins and also does not seem to contain a transmembrane domain | DDB0232432 | CDS | 2155528 | 1500 | - | 0.266 |
DDB_G0288965 | DDB_G0288965 | DDB0232432 | CDS | 2174329 | 1749 | - | 0.256146 | |
DDB_G0288967 | DDB_G0288967 | DDB0232432 | CDS | 2179762 | 2721 | + | 0.246968 | |
DDB_G0288969 | DDB_G0288969 | DDB0232432 | CDS | 2182982 | 3108 | + | 0.223616 | |
DDB_G0288971 | DDB_G0288971 | DDB0232432 | CDS | 2186215 | 354 | - | 0.271186 | |
DDB_G0288973 | DDB_G0288973 | DDB0232432 | CDS | 2186905 | 1386 | + | 0.155844 | |
DDB_G0288981 | DDB_G0288981 | DDB0232432 | CDS | 2203346 | 441 | - | 0.206349 | |
DDB_G0288987 | DDB_G0288987 | DDB0232432 | CDS | 2206848 | 2130 | - | 0.239906 | |
DDB_G0288991 | DDB_G0288991 | DDB0232432 | CDS | 2210519 | 273 | - | 0.300366 | |
DDB_G0288997 | DDB_G0288997 | DDB0232432 | CDS | 2215599 | 609 | + | 0.229885 | |
DDB_G0288999_ps | DDB_G0288999 | putative pseudogene highly conserved family containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232432 | CDS | 2216611 | 453 | - | 0.267108 |
DDB_G0289007 | DDB_G0289007 | DDB0232432 | CDS | 2223594 | 1284 | + | 0.246106 | |
DDB_G0289009 | DDB_G0289009 | DDB0232432 | CDS | 2225715 | 708 | - | 0.185028 | |
DDB_G0289011 | DDB_G0289011 | similar to human C20orf24 (Rab5-interacting protein) contains 2 putative transmembrane domains | DDB0232432 | CDS | 2226660 | 342 | - | 0.263158 |
DDB_G0289015 | DDB_G0289015 | DDB0232432 | CDS | 2232832 | 1026 | - | 0.344055 | |
DDB_G0289017 | DDB_G0289017 | DDB0232432 | CDS | 2236776 | 4179 | - | 0.228045 | |
DDB_G0289019 | DDB_G0289019 | DDB0232432 | CDS | 2243747 | 2748 | - | 0.290393 | |
DDB_G0289023 | DDB_G0289023 | DDB0232432 | CDS | 2251614 | 1221 | + | 0.207207 | |
DDB_G0289027 | DDB_G0289027 | DDB0232432 | CDS | 2254543 | 513 | - | 0.302144 | |
DDB_G0289029 | DDB_G0289029 | conserved protein similar to S. cerevisiae IST1 (Increased Sodium Tolerance) that plays a role in the endosome to vacuole transport via the multivesicular body sorting pathway contains an N-terminal DUF292 domain | DDB0232432 | CDS | 2256321 | 1110 | - | 0.288288 |
DDB_G0289031 | DDB_G0289031 | ortholog of the conserved spastic paraplegia 21 (SPG21) also known as Maspardin defects in human SPG21 are the cause of the neurodegenerative disorder spastic paraplegia also known as Mast syndrome | DDB0232432 | CDS | 2258354 | 1155 | - | 0.256277 |
DDB_G0289033 | DDB_G0289033 | DDB0232432 | CDS | 2277325 | 4770 | - | 0.292243 | |
DDB_G0289039 | DDB_G0289039 | DDB0232432 | CDS | 2286110 | 1287 | + | 0.262626 | |
DDB_G0289041 | DDB_G0289041 | DDB0232432 | CDS | 2287957 | 2334 | + | 0.24036 | |
DDB_G0289043 | DDB_G0289043 | DDB0232432 | CDS | 2291494 | 5457 | + | 0.226315 | |
DDB_G0289045 | DDB_G0289045 | DDB0232432 | CDS | 2297386 | 654 | - | 0.266055 | |
DDB_G0289047 | DDB_G0289047 | highly similar to bacterial ClpB expressed in prespore cells | DDB0232432 | CDS | 2299492 | 2388 | - | 0.348827 |
DDB_G0289049_RTE | DDB_G0289049 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232432 | CDS | 2260286 | 3960 | + | 0.194697 |
DDB_G0289051 | DDB_G0289051 | DDB0232432 | CDS | 2275554 | 1257 | + | 0.290374 | |
DDB_G0289053 | DDB_G0289053 | similar to mammalian RNPS1 (RNA-binding protein with serine-rich domain 1) part of pre- and post-splicing multiprotein mRNP complexes | DDB0232432 | CDS | 2302813 | 1539 | - | 0.322287 |
DDB_G0289057 | DDB_G0289057 | DDB0232432 | CDS | 2307545 | 936 | + | 0.238248 | |
DDB_G0289059 | DDB_G0289059 | DDB0232432 | CDS | 2308883 | 996 | + | 0.252008 | |
DDB_G0289061 | DDB_G0289061 | DDB0232432 | CDS | 2310384 | 1002 | + | 0.257485 | |
DDB_G0289063 | DDB_G0289063 | DDB0232432 | CDS | 2312279 | 816 | + | 0.281863 | |
DDB_G0289065 | DDB_G0289065 | similar to yeast ERG28 an endoplasmic reticulum protein involved in ergosterol biosynthesis contains 4 putative transmembrane domains | DDB0232432 | CDS | 2314833 | 372 | + | 0.252688 |
DDB_G0289071_RTE | DDB_G0289071 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232432 | CDS | 2321624 | 458 | + | 0.395196 |
DDB_G0289077 | DDB_G0289077 | DDB0232432 | CDS | 2326670 | 3246 | - | 0.254775 | |
DDB_G0289081 | DDB_G0289081 | contains a NAD(P)-binding domain contains a predicted peroxisomal targeting signal | DDB0232432 | CDS | 2331738 | 3840 | - | 0.336198 |
DDB_G0289089 | DDB_G0289089 | DDB0232432 | CDS | 2339443 | 222 | - | 0.220721 | |
DDB_G0289091 | DDB_G0289091 | DDB0232432 | CDS | 2340065 | 2028 | - | 0.233235 | |
DDB_G0289093 | DDB_G0289093 | DDB0232432 | CDS | 2345850 | 1074 | + | 0.264432 | |
DDB_G0289095 | DDB_G0289095 | DDB0232432 | CDS | 2348039 | 1677 | + | 0.214669 | |
DDB_G0289097 | DDB_G0289097 | DDB0232432 | CDS | 2349881 | 1350 | - | 0.298519 | |
DDB_G0289099 | DDB_G0289099 | DDB0232432 | CDS | 2356325 | 2355 | + | 0.290021 | |
DDB_G0289101 | DDB_G0289101 | DDB0232432 | CDS | 2361177 | 261 | + | 0.291188 | |
DDB_G0289107_RTE | DDB_G0289107 | DDB0232432 | CDS | 2322480 | 1791 | + | 0.349525 | |
DDB_G0289109 | DDB_G0289109 | DDB0232432 | CDS | 2325208 | 735 | - | 0.382313 | |
DDB_G0289111 | DDB_G0289111 | DDB0232432 | CDS | 2353928 | 942 | + | 0.335456 | |
DDB_G0289113 | DDB_G0289113 | DDB0232432 | CDS | 2369676 | 3660 | + | 0.269126 | |
DDB_G0289123 | DDB_G0289123 | DDB0232432 | CDS | 2378873 | 5022 | - | 0.263839 | |
DDB_G0289125 | DDB_G0289125 | DDB0232432 | CDS | 2384391 | 768 | + | 0.22526 | |
DDB_G0289127 | DDB_G0289127 | DDB0232432 | CDS | 2385358 | 861 | - | 0.304297 | |
DDB_G0289129 | DDB_G0289129 | DDB0232432 | CDS | 2386701 | 885 | - | 0.310734 | |
DDB_G0289131 | DDB_G0289131 | DDB0232432 | CDS | 2388498 | 1101 | + | 0.167121 | |
DDB_G0289133 | DDB_G0289133 | DDB0232432 | CDS | 2389784 | 1341 | - | 0.221477 | |
DDB_G0289137 | DDB_G0289137 | DDB0232432 | CDS | 2392822 | 273 | - | 0.296703 | |
DDB_G0289141 | DDB_G0289141 | DDB0232432 | CDS | 2395095 | 5412 | + | 0.320584 | |
DDB_G0289143 | DDB_G0289143 | contains 11 putative transmembrane domains similar to D. purpureum protein | DDB0232432 | CDS | 2407681 | 1719 | + | 0.285049 |
DDB_G0289147 | DDB_G0289147 | DDB0232432 | CDS | 2417343 | 804 | - | 0.253731 | |
DDB_G0289159 | DDB_G0289159 | DDB0232432 | CDS | 2435887 | 333 | + | 0.225225 | |
DDB_G0289161 | DDB_G0289161 | DDB0232432 | CDS | 2436601 | 477 | - | 0.287212 | |
DDB_G0289163 | DDB_G0289163 | DDB0232432 | CDS | 2437452 | 297 | - | 0.191919 | |
DDB_G0289167 | DDB_G0289167 | similar to bacterial short-chain dehydrogenasereductase family proteins and human RDH8 (retinol dehydrogenase 8) | DDB0232432 | CDS | 2441551 | 972 | - | 0.244856 |
DDB_G0289171 | DDB_G0289171 | DDB0232432 | CDS | 2439587 | 1059 | - | 0.260623 | |
DDB_G0289183 | DDB_G0289183 | DDB0232432 | CDS | 2445521 | 2337 | - | 0.307231 | |
DDB_G0289185 | DDB_G0289185 | DDB0232432 | CDS | 2448283 | 3081 | + | 0.212918 | |
DDB_G0289191 | DDB_G0289191 | DDB0232432 | CDS | 2454071 | 837 | + | 0.216249 | |
DDB_G0289195 | DDB_G0289195 | DDB0232432 | CDS | 2456763 | 891 | + | 0.260382 | |
DDB_G0289199 | DDB_G0289199 | DDB0232432 | CDS | 2458510 | 1899 | - | 0.282254 | |
DDB_G0289203 | DDB_G0289203 | DDB0232432 | CDS | 2464468 | 444 | + | 0.286036 | |
DDB_G0289205 | DDB_G0289205 | DDB0232432 | CDS | 2467250 | 4203 | + | 0.305972 | |
DDB_G0289209 | DDB_G0289209 | DDB0232432 | CDS | 2478124 | 927 | - | 0.242718 | |
DDB_G0289211 | DDB_G0289211 | contains a central large T4 RNA ligase RnlA-like domain a property shared by a related gene | DDB0232432 | CDS | 2485943 | 1392 | + | 0.26796 |
DDB_G0289213 | DDB_G0289213 | DDB0232432 | CDS | 2487904 | 1593 | + | 0.209667 | |
DDB_G0289215 | DDB_G0289215 | DDB0232432 | CDS | 2489574 | 1527 | - | 0.206287 | |
DDB_G0289217 | DDB_G0289217 | DDB0232432 | CDS | 2491401 | 1482 | + | 0.274629 | |
DDB_G0289219_ps | DDB_G0289219 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 2493243 | 234 | - | 0.226496 |
DDB_G0289221 | DDB_G0289221 | DDB0232432 | CDS | 2494619 | 2382 | + | 0.274139 | |
DDB_G0289225_ps | DDB_G0289225 | putative pseudogene partial similar to IPTTIG domain-containing proteins e.g | DDB0232432 | CDS | 2497743 | 1587 | - | 0.271582 |
DDB_G0289227 | DDB_G0289227 | DDB0232432 | CDS | 2500724 | 2433 | - | 0.21866 | |
DDB_G0289231 | DDB_G0289231 | member of the peptidase S28 family of serine proteases a group containing lysosomal Pro-X carboxypeptidase dipeptidyl-peptidase II and thymus-specific serine peptidase | DDB0232432 | CDS | 2519340 | 1542 | + | 0.275616 |
DDB_G0289233 | DDB_G0289233 | similar to human and S. cerevisiae VAC14 (vacuole morphology and inheritance protein 14) contains 3 HEAT repeats | DDB0232432 | CDS | 2521042 | 2343 | - | 0.24968 |
DDB_G0289235 | DDB_G0289235 | DDB0232432 | CDS | 2524160 | 2523 | + | 0.266746 | |
DDB_G0289243 | DDB_G0289243 | bCommunity annotation:b The computer has already noticed that this gene is similar to the widely-conserved folliculin interacting protein FNIP. Dicty in fact has a homolog of folliculin (DDB_G0281111) which the computer has also identified. In mammals folliculin is a tumor suppressor protein mutation of which in the Birt-Hogg-Dube syndrome leads to renal and pulmonary cysts renal cancer and noncancerous tumors of the hair follicles. Folliculin participates in a complex with FNIP1 and FNIP2 which | DDB0232432 | CDS | 2504135 | 2916 | - | 0.258573 |
DDB_G0289245 | DDB_G0289245 | DDB0232432 | CDS | 2518176 | 165 | - | 0.387879 | |
DDB_G0289249 | DDB_G0289249 | DDB0232432 | CDS | 2541277 | 1887 | + | 0.294648 | |
DDB_G0289251 | DDB_G0289251 | belongs to the PLAC8 family (placenta-specific gene 8 protein) a family of cysteine-rich proteins with highly divergent low complexity amino terminal regions similar to D. purpureum protein | DDB0232432 | CDS | 2543934 | 417 | + | 0.280576 |
DDB_G0289255 | DDB_G0289255 | DDB0232432 | CDS | 2550795 | 132 | + | 0.265152 | |
DDB_G0289259 | DDB_G0289259 | similar to bacterial fungal and plant proteins from the short-chain dehydrogenasereductase family | DDB0232432 | CDS | 2556391 | 879 | - | 0.265074 |
DDB_G0289261_ps | DDB_G0289261 | putative pseudogene similar to family of Endotoxin_N-terminal domain-containing proteins including | DDB0232432 | CDS | 2538517 | 1782 | - | 0.274972 |
DDB_G0289263 | DDB_G0289263 | DDB0232432 | CDS | 2557966 | 2799 | - | 0.246874 | |
DDB_G0289265 | DDB_G0289265 | has similarity to flavin containing monoamine oxidases contains one amino oxidase domain | DDB0232432 | CDS | 2564981 | 1395 | - | 0.341935 |
DDB_G0289267 | DDB_G0289267 | DDB0232432 | CDS | 2568808 | 219 | + | 0.30137 | |
DDB_G0289269 | DDB_G0289269 | DDB0232432 | CDS | 2569964 | 483 | + | 0.329193 | |
DDB_G0289273 | DDB_G0289273 | DDB0232432 | CDS | 2572028 | 3111 | - | 0.270653 | |
DDB_G0289275 | DDB_G0289275 | DDB0232432 | CDS | 2576362 | 1002 | - | 0.281437 | |
DDB_G0289279_RTE | DDB_G0289279 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 2578513 | 934 | + | 0.334047 |
DDB_G0289285 | DDB_G0289285 | putative secreted protein contains a predicted signal sequence similar to D. purpureum protein | DDB0232432 | CDS | 2598434 | 1101 | + | 0.300636 |
DDB_G0289287 | DDB_G0289287 | DDB0232432 | CDS | 2600762 | 3828 | + | 0.161181 | |
DDB_G0289293 | DDB_G0289293 | DDB0232432 | CDS | 2607143 | 399 | + | 0.305764 | |
DDB_G0289295 | DDB_G0289295 | DDB0232432 | CDS | 2607639 | 186 | + | 0.397849 | |
DDB_G0289303 | DDB_G0289303 | DDB0232432 | CDS | 2604715 | 1350 | - | 0.295556 | |
DDB_G0289307_ps | DDB_G0289307 | putative pseudogene highly similar to | DDB0232432 | CDS | 2609390 | 933 | - | 0.424437 |
DDB_G0289309 | DDB_G0289309 | carboxyl terminus is highly similar to that of cup (calcium up-regulated) genes but the rest of the protein shares little similarity | DDB0232432 | CDS | 2616286 | 3024 | - | 0.18287 |
DDB_G0289311 | DDB_G0289311 | DDB0232432 | CDS | 2622270 | 2025 | - | 0.222222 | |
DDB_G0289315 | DDB_G0289315 | DDB0232432 | CDS | 2619812 | 861 | - | 0.163763 | |
DDB_G0289321 | DDB_G0289321 | DDB0232432 | CDS | 2637678 | 2571 | + | 0.28238 | |
DDB_G0289333 | DDB_G0289333 | DDB0232432 | CDS | 2646115 | 1866 | - | 0.343516 | |
DDB_G0289335 | DDB_G0289335 | DDB0232432 | CDS | 2652694 | 2064 | - | 0.28876 | |
DDB_G0289337 | DDB_G0289337 | DDB0232432 | CDS | 2656525 | 4587 | + | 0.240026 | |
DDB_G0289341 | DDB_G0289341 | C-terminal half has similarity to yeast E3 SUMO-protein ligase MMS21 (NSE2) which acts in a DNA repair pathway for removal of UV-induced DNA damagebrbr bCommunity annotation:b DDB_G0289341 is similar (best Blast hit both ways) to nse2 an E3 sumo protein ligase which acts in a complex with SMC5 and SMC6 in homologous recombination and telomere maintenance (see Murray and Carr Nature Reviews Molecular Cell Biology 9 177-182 (2008)). Both of these processes are associated with chromosomal replication. DDB_G0289341 is overexpressed threefold in a Dicty strain in which the retinoblastoma-like gene rblA is disrupted ( | DDB0232432 | CDS | 2662531 | 756 | + | 0.292328 |
DDB_G0289345 | DDB_G0289345 | DDB0232432 | CDS | 2666970 | 1257 | + | 0.284805 | |
DDB_G0289347 | DDB_G0289347 | DDB0232432 | CDS | 2668661 | 738 | - | 0.227642 | |
DDB_G0289349 | DDB_G0289349 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity also contains an N-terminal transmembrane domain | DDB0232432 | CDS | 2670443 | 1479 | + | 0.279919 |
DDB_G0289351 | DDB_G0289351 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and 4 extracellular EGF domains | DDB0232432 | CDS | 2672362 | 3669 | + | 0.292178 |
DDB_G0289355 | DDB_G0289355 | DDB0232432 | CDS | 2681578 | 1893 | + | 0.216587 | |
DDB_G0289357 | DDB_G0289357 | DDB0232432 | CDS | 2685876 | 1671 | + | 0.285458 | |
DDB_G0289359 | DDB_G0289359 | DDB0232432 | CDS | 2687826 | 165 | - | 0.278788 | |
DDB_G0289363 | DDB_G0289363 | DDB0232432 | CDS | 2707148 | 372 | - | 0.287634 | |
DDB_G0289369 | DDB_G0289369 | contains an AN1-type at the amino terminus and a UBX domain found in ubiquitin-regulatory proteins at the carboxyl terminus | DDB0232432 | CDS | 2722171 | 1263 | + | 0.243864 |
DDB_G0289377 | DDB_G0289377 | DDB0232432 | CDS | 2645520 | 189 | - | 0.333333 | |
DDB_G0289381 | DDB_G0289381 | DDB0232432 | CDS | 2697784 | 2541 | + | 0.237308 | |
DDB_G0289385 | DDB_G0289385 | DDB0232432 | CDS | 2714901 | 6525 | + | 0.235709 | |
DDB_G0289387_RTE | DDB_G0289387 | ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232432 | CDS | 2728693 | 1094 | + | 0.297075 |
DDB_G0289397 | DDB_G0289397 | DDB0232432 | CDS | 2739034 | 1200 | - | 0.3925 | |
DDB_G0289399 | DDB_G0289399 | contains 3 laminin-type EGF-like domains contains one IPTTIG domain that has an immunoglobulin-like fold contains one predicted C-terminal transmembrane domain | DDB0232432 | CDS | 2743899 | 2010 | + | 0.289055 |
DDB_G0289401 | DDB_G0289401 | DDB0232432 | CDS | 2748299 | 780 | - | 0.255128 | |
DDB_G0289403 | DDB_G0289403 | DDB0232432 | CDS | 2749137 | 966 | - | 0.315735 | |
DDB_G0289405_ps | DDB_G0289405 | putative pseudogene very similar to parts of DDB_G0289409 | DDB0232432 | CDS | 2751258 | 471 | + | 0.301486 |
DDB_G0289407 | DDB_G0289407 | almost identical to | DDB0232432 | CDS | 2752168 | 2412 | - | 0.274461 |
DDB_G0289409 | DDB_G0289409 | DDB0232432 | CDS | 2755696 | 11793 | + | 0.287628 | |
DDB_G0289411 | DDB_G0289411 | DDB0232432 | CDS | 2771756 | 444 | - | 0.335586 | |
DDB_G0289413 | DDB_G0289413 | DDB0232432 | CDS | 2773421 | 1524 | + | 0.17126 | |
DDB_G0289415 | DDB_G0289415 | DDB0232432 | CDS | 2775105 | 2037 | - | 0.307806 | |
DDB_G0289419_ps | DDB_G0289419 | putative pseudogene fragment very similar to | DDB0232432 | CDS | 2780778 | 594 | - | 0.239057 |
DDB_G0289421 | DDB_G0289421 | has limited similarity to mammalian Mis18-alpha and beta (MIS18A MIS18B) that are required for normal chromosome segregation during mitosisbrbr bCommunity annotation:b DDB G0289421 is weakly similar (first Blast hit both ways) to Mis18-alpha and Mis18-beta. In mammals these two closely related proteins are necessary for loading histone H3 variant CENP-A onto centromeric chromatin at the telophaseG1 boundary (see Fujita et al Developmental Cell 12 17-30 (2007). Knockdown of Mis18-alpha Mis18-beta or the third component of this complex (M18BP1) leads to misalignment of mitotic chromosomes presumably at the following mitosis and apparently without activation of the spindle checkpoint.br In Dicty there appears to be only one Mis18 and neither M18BP1 nor CENP-A itself is identifiable. DDB_G0289421 nonetheless appears to be a cell cycle gene: it is overexpressed threefold (p5e-11) in a strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes with known functions in S- | DDB0232432 | CDS | 2784742 | 1599 | - | 0.285178 |
DDB_G0289423 | DDB_G0289423 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | DDB0232432 | CDS | 2794822 | 3246 | + | 0.279421 |
DDB_G0289427 | DDB_G0289427 | DDB0232432 | CDS | 2779634 | 270 | - | 0.244444 | |
DDB_G0289433_ps | DDB_G0289433 | putative pseudogene almost identical to | DDB0232432 | CDS | 2741182 | 1998 | + | 0.29029 |
DDB_G0289437 | DDB_G0289437 | DDB0232432 | CDS | 2750374 | 420 | - | 0.209524 | |
DDB_G0289439 | DDB_G0289439 | DDB0232432 | CDS | 2778983 | 405 | + | 0.367901 | |
DDB_G0289441_RTE | DDB_G0289441 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232432 | CDS | 2730874 | 211 | + | 0.393365 |
DDB_G0289443 | DDB_G0289443 | small Dictyostelium protein family expressed in pstO cells and in upper cup during culmination | DDB0232432 | CDS | 2802474 | 240 | - | 0.320833 |
DDB_G0289453 | DDB_G0289453 | possible homolog of human LSM11 a U7 snRNA-associated Sm-like protein | DDB0232432 | CDS | 2807299 | 774 | - | 0.277778 |
DDB_G0289455 | DDB_G0289455 | DDB0232432 | CDS | 2808377 | 1071 | + | 0.278245 | |
DDB_G0289457 | DDB_G0289457 | DDB0232432 | CDS | 2809612 | 750 | - | 0.217333 | |
DDB_G0289459 | DDB_G0289459 | DDB0232432 | CDS | 2812938 | 582 | - | 0.223368 | |
DDB_G0289461 | DDB_G0289461 | putative ortholog of H. sapiens CNOT6 and S. cerevisiae CCR4 component of the CCR4-NOT transcription complex | DDB0232432 | CDS | 2814027 | 1722 | - | 0.260163 |
DDB_G0289465 | DDB_G0289465 | DDB0232432 | CDS | 2818342 | 2496 | + | 0.23758 | |
DDB_G0289469 | DDB_G0289469 | similar to D. purpureum and P. pallidum protein C-terminal region similar to ribosomal protein S15P family | DDB0232432 | CDS | 2826905 | 1824 | + | 0.307018 |
DDB_G0289473 | DDB_G0289473 | ortholog of the conserved plasma membrane calcium ATPases (PMCA) such as Dictyostelium PAT1 contains at least 8 predicted transmembrane domains | DDB0232432 | CDS | 2830601 | 3234 | - | 0.310761 |
DDB_G0289491 | DDB_G0289491 | DDB0232432 | CDS | 2849682 | 174 | - | 0.229885 | |
DDB_G0289493 | DDB_G0289493 | DDB0232432 | CDS | 2850667 | 378 | - | 0.293651 | |
DDB_G0289495 | DDB_G0289495 | DDB0232432 | CDS | 2851858 | 3594 | + | 0.258486 | |
DDB_G0289497 | DDB_G0289497 | bCommunity annotation:b DDB_G0289497 has been alleged to be a member of the dickkopf family (Guder et al 2006 Development 133 901-911 ). Mammals have four dickkopf genes (Dkk1 Dkk2 Dkk3 and Dkk4) of which Dkk1 2 and 4 have been shown to be secreted antagonists of wingless signalling. Heterologous expression of any of these in vertebrate embryos leads to a reduction of posterior structures with accompanying enhancement of the head hence the name dickkopf which literally means fathead in German (Glinka et al 1998 Nature 391 357-362). The Dictyostelium gene is most similar to Dkk3 which is somewhat divergent from the others (see Niehrs 2006 Oncogene 25 7469-7481). Members of the Dkk3 subfamily have signal peptides (as does DDB_G0289497) and are probably secreted proteins. | DDB0232432 | CDS | 2856146 | 246 | + | 0.378049 |
DDB_G0289503_ps | DDB_G0289503 | putative pseudogene almost identical to neighboring gene | DDB0232432 | CDS | 2868325 | 5166 | - | 0.258227 |
DDB_G0289517 | DDB_G0289517 | DDB0232432 | CDS | 2901066 | 2139 | - | 0.266947 | |
DDB_G0289519 | DDB_G0289519 | DDB0232432 | CDS | 2904697 | 1626 | - | 0.278598 | |
DDB_G0289527 | DDB_G0289527 | DDB0232432 | CDS | 2912060 | 231 | + | 0.264069 | |
DDB_G0289529 | DDB_G0289529 | DDB0232432 | CDS | 2862639 | 5034 | - | 0.265395 | |
DDB_G0289537 | DDB_G0289537 | DDB0232432 | CDS | 2908181 | 1749 | + | 0.227559 | |
DDB_G0289539 | DDB_G0289539 | DDB0232432 | CDS | 2914742 | 1590 | + | 0.296226 | |
DDB_G0289545 | DDB_G0289545 | DDB0232432 | CDS | 2926893 | 3675 | - | 0.163265 | |
DDB_G0289547 | DDB_G0289547 | DDB0232432 | CDS | 2930859 | 1164 | + | 0.28866 | |
DDB_G0289549 | DDB_G0289549 | DDB0232432 | CDS | 2932427 | 270 | + | 0.285185 | |
DDB_G0289551 | DDB_G0289551 | DDB0232432 | CDS | 2933097 | 2163 | - | 0.306981 | |
DDB_G0289557 | DDB_G0289557 | DDB0232432 | CDS | 2946489 | 2328 | - | 0.226804 | |
DDB_G0289561 | DDB_G0289561 | DDB0232432 | CDS | 2951390 | 2777 | + | 0.218581 | |
DDB_G0289567_ps | DDB_G0289567 | putative pseudogene fragment similar to FNIP repeat containing proteins | DDB0232432 | CDS | 2957193 | 498 | + | 0.259036 |
DDB_G0289571 | DDB_G0289571 | DDB0232432 | CDS | 2958707 | 2739 | + | 0.262505 | |
DDB_G0289573 | DDB_G0289573 | DDB0232432 | CDS | 2973076 | 372 | - | 0.266129 | |
DDB_G0289575 | DDB_G0289575 | DDB0232432 | CDS | 2971496 | 1149 | + | 0.288077 | |
DDB_G0289577 | DDB_G0289577 | DDB0232432 | CDS | 2964470 | 2190 | + | 0.257078 | |
DDB_G0289579 | DDB_G0289579 | DDB0232432 | CDS | 2967354 | 456 | + | 0.300439 | |
DDB_G0289581 | DDB_G0289581 | DDB0232432 | CDS | 2997750 | 741 | - | 0.237517 | |
DDB_G0289583 | DDB_G0289583 | ortholog of human SDCCAG1 (serologically defined colon cancer antigen 1) a conserved eukaryotic protein of unknown function | DDB0232432 | CDS | 2992157 | 3807 | - | 0.276333 |
DDB_G0289585 | DDB_G0289585 | leucine-rich repeat protein with filaminABP280 at the carboxyl terminus | DDB0232432 | CDS | 2989530 | 1497 | - | 0.297261 |
DDB_G0289587 | DDB_G0289587 | belongs to the RRN3 family similar to human and S. cerevisiae RRN3 (RNA polymerase I-specific transcription initiation factor RRN3) | DDB0232432 | CDS | 2981034 | 2121 | + | 0.290429 |
DDB_G0289591 | DDB_G0289591 | DDB0232432 | CDS | 2974797 | 2421 | + | 0.173895 | |
DDB_G0289603 | DDB_G0289603 | DDB0232432 | CDS | 3013032 | 3603 | - | 0.189564 | |
DDB_G0289607 | DDB_G0289607 | DDB0232432 | CDS | 3018845 | 504 | - | 0.238095 | |
DDB_G0289609 | DDB_G0289609 | contains two CBS domains expressed in pstAO cells and in upper cup during culmination | DDB0232432 | CDS | 3019826 | 438 | - | 0.296804 |
DDB_G0289615 | DDB_G0289615 | DDB0232432 | CDS | 3032158 | 2073 | + | 0.242161 | |
DDB_G0289617 | DDB_G0289617 | DDB0232432 | CDS | 3034658 | 774 | + | 0.158915 | |
DDB_G0289619_ps | DDB_G0289619 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3042065 | 771 | + | 0.267185 |
DDB_G0289621 | DDB_G0289621 | DDB0232432 | CDS | 3043521 | 714 | + | 0.317927 | |
DDB_G0289625 | DDB_G0289625 | DDB0232432 | CDS | 3045458 | 615 | + | 0.252033 | |
DDB_G0289627 | DDB_G0289627 | DDB0232432 | CDS | 3046500 | 2223 | - | 0.304094 | |
DDB_G0289629 | DDB_G0289629 | DDB0232432 | CDS | 3049902 | 2181 | - | 0.279688 | |
DDB_G0289631_ps | DDB_G0289631 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 3054610 | 615 | + | 0.265041 |
DDB_G0289635 | DDB_G0289635 | DDB0232432 | CDS | 3008595 | 3279 | - | 0.174748 | |
DDB_G0289637 | DDB_G0289637 | DDB0232432 | CDS | 3035690 | 3093 | + | 0.259295 | |
DDB_G0289641 | DDB_G0289641 | DDB0232432 | CDS | 3039503 | 1542 | + | 0.219844 | |
DDB_G0289643 | DDB_G0289643 | DDB0232432 | CDS | 3052862 | 849 | - | 0.254417 | |
DDB_G0289647_ps | DDB_G0289647 | putative pseudogene fragment similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3056743 | 1062 | - | 0.193032 |
DDB_G0289649 | DDB_G0289649 | DDB0232432 | CDS | 3058125 | 168 | - | 0.25 | |
DDB_G0289669 | DDB_G0289669 | DDB0232432 | CDS | 3069414 | 1626 | - | 0.264453 | |
DDB_G0289671 | DDB_G0289671 | similar to human ABHD13 (Abhydrolase domain-containing protein 13) and S. pombe bem46 contains one putative transmembrane domain | DDB0232432 | CDS | 3072697 | 864 | + | 0.280093 |
DDB_G0289673 | DDB_G0289673 | DDB0232432 | CDS | 3074556 | 2979 | + | 0.249413 | |
DDB_G0289679 | DDB_G0289679 | DDB0232432 | CDS | 3090972 | 288 | - | 0.354167 | |
DDB_G0289681 | DDB_G0289681 | DDB0232432 | CDS | 3092553 | 864 | - | 0.212963 | |
DDB_G0289683 | DDB_G0289683 | DDB0232432 | CDS | 3093903 | 2787 | + | 0.175099 | |
DDB_G0289685 | DDB_G0289685 | DDB0232432 | CDS | 3096922 | 2607 | + | 0.169544 | |
DDB_G0289687 | DDB_G0289687 | DDB0232432 | CDS | 3103046 | 2694 | + | 0.199332 | |
DDB_G0289689 | DDB_G0289689 | DDB0232432 | CDS | 3108150 | 2832 | - | 0.248588 | |
DDB_G0289691 | DDB_G0289691 | DDB0232432 | CDS | 3111862 | 672 | - | 0.206845 | |
DDB_G0289693 | DDB_G0289693 | DDB0232432 | CDS | 3113883 | 360 | - | 0.305556 | |
DDB_G0289695 | DDB_G0289695 | DDB0232432 | CDS | 3114892 | 501 | - | 0.265469 | |
DDB_G0289697 | DDB_G0289697 | DDB0232432 | CDS | 3115871 | 1359 | + | 0.314202 | |
DDB_G0289701 | DDB_G0289701 | has similarity to nuclear pore protein 214 contains a Wd40-like region and a moesin C-terminal domain | DDB0232432 | CDS | 3121180 | 5115 | - | 0.324145 |
DDB_G0289703 | DDB_G0289703 | DDB0232432 | CDS | 3127157 | 2931 | + | 0.247015 | |
DDB_G0289705 | DDB_G0289705 | DDB0232432 | CDS | 3136742 | 6009 | + | 0.305542 | |
DDB_G0289707 | DDB_G0289707 | DDB0232432 | CDS | 3143077 | 1071 | + | 0.267974 | |
DDB_G0289713 | DDB_G0289713 | DDB0232432 | CDS | 3151658 | 1668 | + | 0.251199 | |
DDB_G0289715 | DDB_G0289715 | DDB0232432 | CDS | 3153407 | 846 | - | 0.326241 | |
DDB_G0289717 | DDB_G0289717 | contains one B-box zinc-finger domain and 7 FNIP repeats contains one coiled-coil domain | DDB0232432 | CDS | 3156042 | 1977 | - | 0.231158 |
DDB_G0289719 | DDB_G0289719 | DDB0232432 | CDS | 3159163 | 4260 | + | 0.28662 | |
DDB_G0289729 | DDB_G0289729 | DDB0232432 | CDS | 3173059 | 534 | - | 0.237828 | |
DDB_G0289731 | DDB_G0289731 | DDB0232432 | CDS | 3175755 | 1404 | - | 0.294872 | |
DDB_G0289733 | DDB_G0289733 | similar to fungal and plant proteins contains 4 putative transmembrane domains | DDB0232432 | CDS | 3177932 | 561 | - | 0.28877 |
DDB_G0289735 | DDB_G0289735 | DDB0232432 | CDS | 3179530 | 1626 | + | 0.245387 | |
DDB_G0289737 | DDB_G0289737 | DDB0232432 | CDS | 3181881 | 4692 | + | 0.249787 | |
DDB_G0289739 | DDB_G0289739 | DDB0232432 | CDS | 3188713 | 414 | - | 0.272947 | |
DDB_G0289741 | DDB_G0289741 | DDB0232432 | CDS | 3189387 | 3300 | - | 0.213333 | |
DDB_G0289743 | DDB_G0289743 | DDB0232432 | CDS | 3193439 | 1002 | + | 0.215569 | |
DDB_G0289745_ps | DDB_G0289745 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 3194481 | 285 | - | 0.221053 |
DDB_G0289749 | DDB_G0289749 | member of the peptidase S28 family of serine proteases a group containing lysosomal Pro-X carboxypeptidase dipeptidyl-peptidase II and thymus-specific serine peptidase | DDB0232432 | CDS | 3208495 | 1542 | - | 0.346952 |
DDB_G0289751 | DDB_G0289751 | DDB0232432 | CDS | 3211024 | 1194 | + | 0.259631 | |
DDB_G0289753 | DDB_G0289753 | DDB0232432 | CDS | 3213101 | 2283 | + | 0.242225 | |
DDB_G0289755 | DDB_G0289755 | DDB0232432 | CDS | 3219108 | 3510 | + | 0.27037 | |
DDB_G0289757 | DDB_G0289757 | DDB0232432 | CDS | 3223411 | 1173 | + | 0.238704 | |
DDB_G0289759 | DDB_G0289759 | DDB0232432 | CDS | 3225323 | 1719 | + | 0.270506 | |
DDB_G0289761 | DDB_G0289761 | DDB0232432 | CDS | 3227434 | 5901 | - | 0.239451 | |
DDB_G0289765 | DDB_G0289765 | DDB0232432 | CDS | 3243093 | 297 | - | 0.262626 | |
DDB_G0289767 | DDB_G0289767 | DDB0232432 | CDS | 3244131 | 192 | - | 0.291667 | |
DDB_G0289769 | DDB_G0289769 | DDB0232432 | CDS | 3246114 | 1446 | + | 0.239281 | |
DDB_G0289771 | DDB_G0289771 | belongs to the major facilitator superfamily similar to human SLC43A3 (solute carrier family 43 member 3) contains 12 putative transmembrane domains | DDB0232432 | CDS | 3247669 | 1539 | - | 0.250162 |
DDB_G0289773 | DDB_G0289773 | DDB0232432 | CDS | 3250091 | 1101 | - | 0.260672 | |
DDB_G0289777_ps | DDB_G0289777 | putative pseudogene fragment similar to FNIP repeat containing proteins | DDB0232432 | CDS | 3258199 | 996 | - | 0.210843 |
DDB_G0289781 | DDB_G0289781 | DDB0232432 | CDS | 3268015 | 1821 | - | 0.213619 | |
DDB_G0289783_ps | DDB_G0289783 | putative pseudogene similar to a family of small D. discoideum genes including | DDB0232432 | CDS | 3079913 | 180 | - | 0.277778 |
DDB_G0289787 | DDB_G0289787 | DDB0232432 | CDS | 3105859 | 1590 | - | 0.284906 | |
DDB_G0289789 | DDB_G0289789 | DDB0232432 | CDS | 3131180 | 3711 | + | 0.162759 | |
DDB_G0289793_RTE | DDB_G0289793 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232432 | CDS | 3060165 | 1020 | - | 0.385294 |
DDB_G0289795 | DDB_G0289795 | DDB0232432 | CDS | 3100083 | 1872 | + | 0.223291 | |
DDB_G0289797_ps | DDB_G0289797 | putative pseudogene small fragment of D. discoideum gene | DDB0232432 | CDS | 3215546 | 522 | + | 0.258621 |
DDB_G0289799_ps | DDB_G0289799 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3216855 | 756 | + | 0.251323 |
DDB_G0289801_ps | DDB_G0289801 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3234217 | 1794 | + | 0.238016 |
DDB_G0289805_RTE | DDB_G0289805 | partial ORF1 and ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 3259385 | 4881 | + | 0.314075 |
DDB_G0289807 | DDB_G0289807 | DDB0232432 | CDS | 3270257 | 2403 | - | 0.265501 | |
DDB_G0289809_ps | DDB_G0289809 | putative pseudogene similar to | DDB0232432 | CDS | 3273269 | 303 | - | 0.290429 |
DDB_G0289817_ps | DDB_G0289817 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3280631 | 1827 | - | 0.231527 |
DDB_G0289819 | DDB_G0289819 | DDB0232432 | CDS | 3283950 | 3210 | - | 0.250156 | |
DDB_G0289825 | DDB_G0289825 | DDB0232432 | CDS | 3292116 | 450 | + | 0.217778 | |
DDB_G0289829 | DDB_G0289829 | DDB0232432 | CDS | 3294597 | 13773 | + | 0.253467 | |
DDB_G0289831 | DDB_G0289831 | contains a HDc domain (metal-dependent phosphohydrolases with conserved | DDB0232432 | CDS | 3320745 | 657 | + | 0.210046 |
DDB_G0289833 | DDB_G0289833 | DDB0232432 | CDS | 3325551 | 561 | + | 0.279857 | |
DDB_G0289835 | DDB_G0289835 | DDB0232432 | CDS | 3326670 | 708 | + | 0.276836 | |
DDB_G0289837 | DDB_G0289837 | DDB0232432 | CDS | 3338795 | 1320 | + | 0.234091 | |
DDB_G0289839 | DDB_G0289839 | DDB0232432 | CDS | 3349145 | 2481 | - | 0.232568 | |
DDB_G0289841_ps | DDB_G0289841 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 3351960 | 360 | - | 0.294444 |
DDB_G0289843_ps | DDB_G0289843 | putative pseudogene very similar to | DDB0232432 | CDS | 3352483 | 303 | + | 0.316832 |
DDB_G0289845_ps | DDB_G0289845 | putative pseudogene similar to Dictyostelium genes | DDB0232432 | CDS | 3355012 | 3663 | - | 0.205296 |
DDB_G0289849 | DDB_G0289849 | DDB0232432 | CDS | 3275554 | 1533 | - | 0.21983 | |
DDB_G0289851_ps | DDB_G0289851 | putative pseudogene similar to a larger gene family including | DDB0232432 | CDS | 3287942 | 780 | - | 0.219231 |
DDB_G0289853 | DDB_G0289853 | DDB0232432 | CDS | 3274098 | 861 | - | 0.259001 | |
DDB_G0289855_ps | DDB_G0289855 | putative pseudogene fragment similar to FNIP repeat containing proteins | DDB0232432 | CDS | 3277922 | 621 | - | 0.249597 |
DDB_G0289857 | DDB_G0289857 | DDB0232432 | CDS | 3279027 | 861 | - | 0.259001 | |
DDB_G0289861 | DDB_G0289861 | DDB0232432 | CDS | 3321520 | 2409 | - | 0.268991 | |
DDB_G0289863 | DDB_G0289863 | DDB0232432 | CDS | 3327630 | 4173 | - | 0.288521 | |
DDB_G0289865 | DDB_G0289865 | DDB0232432 | CDS | 3333090 | 2580 | - | 0.156589 | |
DDB_G0289869 | DDB_G0289869 | DDB0232432 | CDS | 3345167 | 3852 | + | 0.22352 | |
DDB_G0289871 | DDB_G0289871 | DDB0232432 | CDS | 3353422 | 999 | - | 0.298298 | |
DDB_G0289887 | DDB_G0289887 | DDB0232432 | CDS | 3364902 | 927 | - | 0.20712 | |
DDB_G0289889 | DDB_G0289889 | DDB0232432 | CDS | 3366559 | 663 | - | 0.236802 | |
DDB_G0289891 | DDB_G0289891 | DDB0232432 | CDS | 3367899 | 873 | - | 0.254296 | |
DDB_G0289895 | DDB_G0289895 | DDB0232432 | CDS | 3370229 | 3180 | - | 0.199686 | |
DDB_G0289897 | DDB_G0289897 | DDB0232432 | CDS | 3373542 | 2934 | - | 0.190866 | |
DDB_G0289899 | DDB_G0289899 | DDB0232432 | CDS | 3376818 | 432 | - | 0.275463 | |
DDB_G0289901 | DDB_G0289901 | highly repetitive protein serine and glycine rich contains a predicted signal peptide | DDB0232432 | CDS | 3379595 | 3432 | + | 0.456002 |
DDB_G0289903 | DDB_G0289903 | DDB0232432 | CDS | 3385552 | 3060 | - | 0.186601 | |
DDB_G0289905 | DDB_G0289905 | DDB0232432 | CDS | 3389153 | 870 | + | 0.265517 | |
DDB_G0289907 | DDB_G0289907 | DDB0232432 | CDS | 3390166 | 4527 | - | 0.279435 | |
DDB_G0289909 | DDB_G0289909 | DDB0232432 | CDS | 3396878 | 3282 | - | 0.240402 | |
DDB_G0289911_ps | DDB_G0289911 | putative pseudogene fragment similar to | DDB0232432 | CDS | 3408321 | 330 | - | 0.30303 |
DDB_G0289913 | DDB_G0289913 | DDB0232432 | CDS | 3412058 | 894 | + | 0.229306 | |
DDB_G0289915 | DDB_G0289915 | DDB0232432 | CDS | 3412976 | 951 | - | 0.218717 | |
DDB_G0289917 | DDB_G0289917 | similar to neighboring gene | DDB0232432 | CDS | 3415174 | 2907 | + | 0.318885 |
DDB_G0289921 | DDB_G0289921 | DDB0232432 | CDS | 3426110 | 3708 | + | 0.263484 | |
DDB_G0289933 | DDB_G0289933 | DDB0232432 | CDS | 3455388 | 1629 | - | 0.274401 | |
DDB_G0289937 | DDB_G0289937 | DDB0232432 | CDS | 3460667 | 2694 | + | 0.224944 | |
DDB_G0289939 | DDB_G0289939 | DDB0232432 | CDS | 3468286 | 2919 | + | 0.224049 | |
DDB_G0289941 | DDB_G0289941 | DDB0232432 | CDS | 3478416 | 1446 | + | 0.296681 | |
DDB_G0289943 | DDB_G0289943 | DDB0232432 | CDS | 3479964 | 4653 | - | 0.27939 | |
DDB_G0289945 | DDB_G0289945 | DDB0232432 | CDS | 3488380 | 741 | + | 0.219973 | |
DDB_G0289947 | DDB_G0289947 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 3490340 | 4692 | + | 0.27728 |
DDB_G0289949 | DDB_G0289949 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 3495799 | 4452 | + | 0.287511 |
DDB_G0289951 | DDB_G0289951 | DDB0232432 | CDS | 3502780 | 297 | - | 0.212121 | |
DDB_G0289953 | DDB_G0289953 | DDB0232432 | CDS | 3505573 | 2313 | - | 0.26243 | |
DDB_G0289955 | DDB_G0289955 | DDB0232432 | CDS | 3508916 | 594 | - | 0.311448 | |
DDB_G0289957 | DDB_G0289957 | DDB0232432 | CDS | 3510343 | 225 | - | 0.244444 | |
DDB_G0289961 | DDB_G0289961 | ortholog of mammalian lunapark (LNP) that may be involved in limb and central nervous system development contains two transmembrane domains | DDB0232432 | CDS | 3444195 | 1359 | + | 0.256806 |
DDB_G0289963 | DDB_G0289963 | DDB0232432 | CDS | 3511088 | 1584 | + | 0.243687 | |
DDB_G0289965 | DDB_G0289965 | DDB0232432 | CDS | 3377583 | 876 | - | 0.200913 | |
DDB_G0289969 | DDB_G0289969 | DDB0232432 | CDS | 3396462 | 216 | + | 0.333333 | |
DDB_G0289973 | DDB_G0289973 | DDB0232432 | CDS | 3409130 | 1653 | - | 0.199637 | |
DDB_G0289975 | DDB_G0289975 | similar to neighboring gene | DDB0232432 | CDS | 3419568 | 3099 | + | 0.247822 |
DDB_G0289977_ps | DDB_G0289977 | putative pseudogene similar to D. discoideum gene | DDB0232432 | CDS | 3430004 | 1452 | - | 0.174242 |
DDB_G0289979 | DDB_G0289979 | has similarity to mammalian tensin a cytoplasmic phosphoprotein | DDB0232432 | CDS | 3435700 | 2715 | - | 0.299079 |
DDB_G0289985 | DDB_G0289985 | similar to human protein KIAA0195 a transmembrane protein contains 8 putative transmembrane domains | DDB0232432 | CDS | 3471284 | 5832 | - | 0.290123 |
DDB_G0289987 | DDB_G0289987 | DDB0232432 | CDS | 3515224 | 3111 | + | 0.309547 | |
DDB_G0289989 | DDB_G0289989 | DDB0232432 | CDS | 3520850 | 168 | + | 0.166667 | |
DDB_G0289991 | DDB_G0289991 | DDB0232432 | CDS | 3521273 | 1203 | - | 0.284289 | |
DDB_G0289993 | DDB_G0289993 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub | DDB0232432 | CDS | 3523290 | 2103 | - | 0.269615 |
DDB_G0289995 | DDB_G0289995 | DDB0232432 | CDS | 3525827 | 1377 | - | 0.276688 | |
DDB_G0289997 | DDB_G0289997 | DDB0232432 | CDS | 3527673 | 456 | - | 0.203947 | |
DDB_G0289999 | DDB_G0289999 | DDB0232432 | CDS | 3529568 | 879 | - | 0.25711 | |
DDB_G0290001 | DDB_G0290001 | DDB0232432 | CDS | 3530853 | 855 | - | 0.260819 | |
DDB_G0290003 | DDB_G0290003 | DDB0232432 | CDS | 3519269 | 174 | + | 0.178161 | |
DDB_G0290005 | DDB_G0290005 | similar to myotubularin a dual-specific lipid phosphatase that dephosphorylates phosphatidylinositol 3-phosphate and phosphatidylinositol (35)-bi-phosphate | DDB0232432 | CDS | 3532204 | 3975 | - | 0.27195 |
DDB_G0290007 | DDB_G0290007 | DDB0232432 | CDS | 3538386 | 591 | - | 0.233503 | |
DDB_G0290013 | DDB_G0290013 | DDB0232432 | CDS | 3541529 | 168 | + | 0.196429 | |
DDB_G0290017 | DDB_G0290017 | DDB0232432 | CDS | 3543307 | 531 | - | 0.271186 | |
DDB_G0290019 | DDB_G0290019 | DDB0232432 | CDS | 3544279 | 3753 | + | 0.229683 | |
DDB_G0290021 | DDB_G0290021 | DDB0232432 | CDS | 3549059 | 2955 | + | 0.171912 | |
DDB_G0290025 | DDB_G0290025 | contains one UBA-like domain and one DCUN1 domain homolog of human DCUN1D1 and S. cerevisiae DCN1 (defective in cullin neddylation protein 1) defects in DCUN1D1 may be a cause of squamous cell carcinomas | DDB0232432 | CDS | 3556440 | 750 | + | 0.261333 |
DDB_G0290027 | DDB_G0290027 | DDB0232432 | CDS | 3557818 | 264 | + | 0.265152 | |
DDB_G0290029 | DDB_G0290029 | DDB0232432 | CDS | 3560404 | 1209 | - | 0.292804 | |
DDB_G0290031 | DDB_G0290031 | belongs to the ribosomal protein S8e family ortholog of human TINP1 (TGF-beta-inducible nuclear protein 1) and S. cerevisiae NSA2 NSA2 (NOP seven associated 2) is involved in the biogenesis of the 60S ribosomal subunit | DDB0232432 | CDS | 3562515 | 783 | + | 0.342273 |
DDB_G0290035 | DDB_G0290035 | DDB0232432 | CDS | 3574815 | 3498 | + | 0.242996 | |
DDB_G0290037 | DDB_G0290037 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232432 | CDS | 3583640 | 4218 | - | 0.252015 |
DDB_G0290039 | DDB_G0290039 | DDB0232432 | CDS | 3601688 | 3279 | - | 0.191217 | |
DDB_G0290041 | DDB_G0290041 | DDB0232432 | CDS | 3605172 | 234 | - | 0.311966 | |
DDB_G0290043 | DDB_G0290043 | DDB0232432 | CDS | 3605816 | 1656 | - | 0.209541 | |
DDB_G0290045_ps | DDB_G0290045 | putative pseudogene fragment similar to UNC93-like protein MFSD11 family members | DDB0232432 | CDS | 3608057 | 288 | + | 0.322917 |
DDB_G0290047_ps | DDB_G0290047 | putative pseudogene fragment similar to | DDB0232432 | CDS | 3609197 | 285 | - | 0.140351 |
DDB_G0290051 | DDB_G0290051 | putative pseudogene similar to a large gene family encoding FNIP repeat-containing proteins including | DDB0232432 | CDS | 3563896 | 1875 | - | 0.245867 |
DDB_G0290057 | DDB_G0290057 | DDB0232432 | CDS | 3570445 | 1620 | - | 0.223457 | |
DDB_G0290059_ps | DDB_G0290059 | putative pseudogene similar to Dictyostelium genes | DDB0232432 | CDS | 3578349 | 4047 | - | 0.255004 |
DDB_G0290061 | DDB_G0290061 | DDB0232432 | CDS | 3588988 | 4158 | - | 0.263107 | |
DDB_G0290063 | DDB_G0290063 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain enriched in gametes | DDB0232432 | CDS | 3595858 | 4200 | - | 0.267381 |
DDB_G0290065 | DDB_G0290065 | DDB0232432 | CDS | 3610142 | 226 | - | 0.252212 | |
DDB_G0290073 | DDB_G0290073 | DDB0232432 | CDS | 3614348 | 2481 | - | 0.261588 | |
DDB_G0290075 | DDB_G0290075 | protein phosphatase 2C is a serinethreonine specific protein phosphatase with broad substrate specificity and dependent on divalent cations (mainly manganese and magnesium) for its activity | DDB0232432 | CDS | 3618710 | 1620 | - | 0.297531 |
DDB_G0290083 | DDB_G0290083 | DDB0232432 | CDS | 3631373 | 612 | - | 0.269608 | |
DDB_G0290085 | DDB_G0290085 | DDB0232432 | CDS | 3636614 | 4683 | + | 0.26009 | |
DDB_G0290089 | DDB_G0290089 | involved in fatty acid biosynthesis catalyzes the conversion of malonyl-CoA to acetyl-CoA | DDB0232432 | CDS | 3648784 | 1350 | - | 0.221481 |
DDB_G0290093 | DDB_G0290093 | DDB0232432 | CDS | 3653634 | 651 | - | 0.25192 | |
DDB_G0290095 | DDB_G0290095 | DDB0232432 | CDS | 3611605 | 2532 | + | 0.189573 | |
DDB_G0290097 | DDB_G0290097 | DDB0232432 | CDS | 3634285 | 1608 | + | 0.174129 | |
DDB_G0290101 | DDB_G0290101 | putative pseudogene similar to a large gene family encoding FNIP repeat-containing proteins including | DDB0232432 | CDS | 3664675 | 1980 | + | 0.239899 |
DDB_G0290105 | DDB_G0290105 | DDB0232432 | CDS | 3654997 | 674 | - | 0.327893 | |
DDB_G0290107 | DDB_G0290107 | contains 9 putative transmembrane domains conserved in Polysphondylium pallidum and D. purpureum | DDB0232432 | CDS | 3660841 | 1782 | - | 0.255331 |
DDB_G0290109 | DDB_G0290109 | DDB0232432 | CDS | 3667946 | 2235 | + | 0.22774 | |
DDB_G0290113 | DDB_G0290113 | DDB0232432 | CDS | 3675019 | 2826 | + | 0.225407 | |
DDB_G0290119_ps | DDB_G0290119 | putative pseudogene FNIP repeat family protein | DDB0232432 | CDS | 3679131 | 1260 | + | 0.216667 |
DDB_G0290125 | DDB_G0290125 | DDB0232432 | CDS | 3685883 | 2517 | - | 0.196663 | |
DDB_G0290127 | DDB_G0290127 | DDB0232432 | CDS | 3689897 | 1950 | + | 0.212308 | |
DDB_G0290129_RTE | DDB_G0290129 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232432 | CDS | 3694123 | 518 | + | 0.401544 |
DDB_G0290133 | DDB_G0290133 | DDB0232432 | CDS | 3697750 | 267 | + | 0.254682 | |
DDB_G0290135 | DDB_G0290135 | DDB0232432 | CDS | 3699370 | 129 | - | 0.186047 | |
DDB_G0290137 | DDB_G0290137 | DDB0232432 | CDS | 3700826 | 785 | + | 0.17707 | |
DDB_G0290139 | DDB_G0290139 | DDB0232432 | CDS | 3695903 | 1431 | + | 0.331936 | |
DDB_G0290143 | DDB_G0290143 | DDB0232432 | CDS | 3704919 | 651 | - | 0.302611 | |
DDB_G0290145 | DDB_G0290145 | DDB0232432 | CDS | 3707194 | 3378 | - | 0.204263 | |
DDB_G0290147 | DDB_G0290147 | DDB0232432 | CDS | 3711190 | 345 | + | 0.292754 | |
DDB_G0290151 | DDB_G0290151 | DDB0232432 | CDS | 3703699 | 840 | + | 0.22619 | |
DDB_G0290153 | DDB_G0290153 | DDB0232432 | CDS | 3712218 | 1545 | - | 0.318447 | |
DDB_G0290155 | DDB_G0290155 | DDB0232432 | CDS | 3702246 | 877 | + | 0.163056 | |
DDB_G0290167 | DDB_G0290167 | DDB0232432 | CDS | 3729972 | 159 | - | 0.245283 | |
DDB_G0290175 | DDB_G0290175 | contains a predicted signal peptide and a C-teminal transmembrane domain small gene family in D. discoideum and D. purpureum | DDB0232432 | CDS | 3738710 | 1260 | - | 0.251587 |
DDB_G0290177 | DDB_G0290177 | contains an N-terminal signal sequence and a C-terminal transmembrane domain underexpressed in | DDB0232432 | CDS | 3740464 | 1170 | - | 0.346154 |
DDB_G0290181 | DDB_G0290181 | similar to S.cerevisiae RRP5 and animal PDCD11 (Programmed cell death protein 11) | DDB0232432 | CDS | 3746723 | 2730 | - | 0.25641 |
DDB_G0290183 | DDB_G0290183 | DDB0232432 | CDS | 3749810 | 1344 | + | 0.238095 | |
DDB_G0290189 | DDB_G0290189 | DDB0232432 | CDS | 3766463 | 930 | + | 0.263441 | |
DDB_G0290191 | DDB_G0290191 | DDB0232432 | CDS | 3774102 | 471 | + | 0.248408 | |
DDB_G0290193 | DDB_G0290193 | DDB0232432 | CDS | 3774767 | 3828 | - | 0.269854 | |
DDB_G0290195 | DDB_G0290195 | DDB0232432 | CDS | 3779790 | 333 | - | 0.237237 | |
DDB_G0290197 | DDB_G0290197 | similar to plant and fungi NADH dehydrogenases such as S. cerevisiae NDE1 and NDE2 the external mitochondrial NADH dehydrogenases that catalyze the oxidation of cytosolic NADH | DDB0232432 | CDS | 3781653 | 1965 | + | 0.293639 |
DDB_G0290199 | DDB_G0290199 | DDB0232432 | CDS | 3783788 | 651 | - | 0.241167 | |
DDB_G0290201 | DDB_G0290201 | DDB0232432 | CDS | 3784827 | 1467 | + | 0.236537 | |
DDB_G0290203 | DDB_G0290203 | DDB0232432 | CDS | 3792983 | 801 | + | 0.252185 | |
DDB_G0290205 | DDB_G0290205 | DDB0232432 | CDS | 3794310 | 738 | + | 0.258808 | |
DDB_G0290211 | DDB_G0290211 | DDB0232432 | CDS | 3798435 | 3669 | + | 0.271191 | |
DDB_G0290215 | DDB_G0290215 | DDB0232432 | CDS | 3805894 | 3354 | + | 0.233751 | |
DDB_G0290219 | DDB_G0290219 | DDB0232432 | CDS | 3812159 | 1095 | - | 0.251142 | |
DDB_G0290223 | DDB_G0290223 | DDB0232432 | CDS | 3816109 | 555 | + | 0.32973 | |
DDB_G0290225 | DDB_G0290225 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity enriched in gametes | DDB0232432 | CDS | 3824091 | 1212 | - | 0.287954 |
DDB_G0290229 | DDB_G0290229 | catalyzes the reaction CTP choline phosphate diphosphate CDPcholine | DDB0232432 | CDS | 3830807 | 1251 | + | 0.295763 |
DDB_G0290231 | DDB_G0290231 | DDB0232432 | CDS | 3832338 | 1356 | - | 0.233038 | |
DDB_G0290235 | DDB_G0290235 | DDB0232432 | CDS | 3838039 | 123 | - | 0.284553 | |
DDB_G0290239 | DDB_G0290239 | DDB0232432 | CDS | 3786795 | 930 | + | 0.203226 | |
DDB_G0290241_RTE | DDB_G0290241 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 3764090 | 1506 | + | 0.294821 |
DDB_G0290247 | DDB_G0290247 | DDB0232432 | CDS | 3789362 | 2946 | + | 0.191785 | |
DDB_G0290249 | DDB_G0290249 | DDB0232432 | CDS | 3821076 | 2871 | - | 0.223267 | |
DDB_G0290251_ps | DDB_G0290251 | putative pseudogene related to the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232432 | CDS | 3826055 | 1125 | - | 0.286222 |
DDB_G0290255 | DDB_G0290255 | DDB0232432 | CDS | 3846563 | 391 | + | 0.140665 | |
DDB_G0290273 | DDB_G0290273 | DDB0232432 | CDS | 3847142 | 1959 | + | 0.135784 | |
DDB_G0290275 | DDB_G0290275 | DDB0232432 | CDS | 3849199 | 951 | - | 0.209253 | |
DDB_G0290283 | DDB_G0290283 | DDB0232432 | CDS | 3859451 | 3438 | - | 0.232984 | |
DDB_G0290285 | DDB_G0290285 | DDB0232432 | CDS | 3865328 | 2463 | + | 0.279334 | |
DDB_G0290289 | DDB_G0290289 | DDB0232432 | CDS | 3884030 | 5952 | + | 0.243112 | |
DDB_G0290291 | DDB_G0290291 | similar to MAPEG (membrane associated proteins in eicosanoid and glutathione metabolism) family which includes microsomal glutathione S-transferase II and 5-lipoxygenase activating protein expressed in prespore cells | DDB0232432 | CDS | 3893526 | 450 | - | 0.337778 |
DDB_G0290295 | DDB_G0290295 | DDB0232432 | CDS | 3920410 | 636 | - | 0.286164 | |
DDB_G0290299 | DDB_G0290299 | DDB0232432 | CDS | 3922756 | 363 | - | 0.289256 | |
DDB_G0290301 | DDB_G0290301 | DDB0232432 | CDS | 3923457 | 3717 | - | 0.29244 | |
DDB_G0290305 | DDB_G0290305 | DDB0232432 | CDS | 3936242 | 1716 | + | 0.287296 | |
DDB_G0290307 | DDB_G0290307 | contains three RRM domains homolog of ELAVL1 (embryonic lethal abnormal vision-like 1) | DDB0232432 | CDS | 3938585 | 1380 | + | 0.300725 |
DDB_G0290309 | DDB_G0290309 | DDB0232432 | CDS | 3940357 | 486 | - | 0.228395 | |
DDB_G0290311 | DDB_G0290311 | DDB0232432 | CDS | 3942085 | 1086 | - | 0.300184 | |
DDB_G0290313 | DDB_G0290313 | DDB0232432 | CDS | 3944329 | 1656 | + | 0.221014 | |
DDB_G0290319 | DDB_G0290319 | DDB0232432 | CDS | 3952440 | 456 | + | 0.27193 | |
DDB_G0290321 | DDB_G0290321 | DDB0232432 | CDS | 3953111 | 2394 | - | 0.190894 | |
DDB_G0290323 | DDB_G0290323 | DDB0232432 | CDS | 3955755 | 2274 | - | 0.174142 | |
DDB_G0290329 | DDB_G0290329 | DDB0232432 | CDS | 3968559 | 906 | - | 0.335541 | |
DDB_G0290333 | DDB_G0290333 | belongs to the peptidase S53 family similar to P. polycephalum physarolisin contains a predicted signal peptide | DDB0232432 | CDS | 3973178 | 1797 | + | 0.413467 |
DDB_G0290335 | DDB_G0290335 | DDB0232432 | CDS | 3975307 | 1080 | + | 0.203704 | |
DDB_G0290337 | DDB_G0290337 | DDB0232432 | CDS | 3983670 | 2439 | + | 0.275933 | |
DDB_G0290341 | DDB_G0290341 | similar to S. cerevisiae SFT2 contains 4 putative transmembrane domains similar to D. purpureum protein | DDB0232432 | CDS | 3989030 | 621 | - | 0.259259 |
DDB_G0290347 | DDB_G0290347 | DDB0232432 | CDS | 4001426 | 1203 | - | 0.23857 | |
DDB_G0290349 | DDB_G0290349 | DDB0232432 | CDS | 3868716 | 2133 | + | 0.263479 | |
DDB_G0290351 | DDB_G0290351 | DDB0232432 | CDS | 3890601 | 2304 | + | 0.249132 | |
DDB_G0290359 | DDB_G0290359 | the N-terminal half of the protein is very similar to human EFR3A (Protein EFR3 homolog A) similar to D. purpureum protein | DDB0232432 | CDS | 3850328 | 2790 | - | 0.260215 |
DDB_G0290361_ps | DDB_G0290361 | putative pseudogene similar to a D. discoideum gene family including the just upstream | DDB0232432 | CDS | 3871677 | 1176 | + | 0.27551 |
DDB_G0290369 | DDB_G0290369 | DDB0232432 | CDS | 3976953 | 5661 | + | 0.242183 | |
DDB_G0290371 | DDB_G0290371 | DDB0232432 | CDS | 3991148 | 930 | + | 0.272043 | |
DDB_G0290373 | DDB_G0290373 | DDB0232432 | CDS | 3993062 | 4971 | - | 0.206196 | |
DDB_G0290375_RTE | DDB_G0290375 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232432 | CDS | 4004269 | 1032 | + | 0.325581 |
DDB_G0290379 | DDB_G0290379 | DDB0232432 | CDS | 4011706 | 1023 | - | 0.252199 | |
DDB_G0290381 | DDB_G0290381 | DDB0232432 | CDS | 4013215 | 2118 | + | 0.259207 | |
DDB_G0290383 | DDB_G0290383 | DDB0232432 | CDS | 4017007 | 330 | + | 0.221212 | |
DDB_G0290387 | DDB_G0290387 | similar to D. purpureum proteins small gene family in both species | DDB0232432 | CDS | 4019200 | 927 | + | 0.307443 |
DDB_G0290391 | DDB_G0290391 | DDB0232432 | CDS | 4027524 | 927 | - | 0.289105 | |
DDB_G0290393 | DDB_G0290393 | similar to yeast ERG28 an endoplasmic reticulum protein involved in ergosterol biosynthesis contains 3 putative transmembrane domains | DDB0232432 | CDS | 4028814 | 372 | - | 0.290323 |
DDB_G0290395 | DDB_G0290395 | DDB0232432 | CDS | 4029574 | 1143 | - | 0.343832 | |
DDB_G0290399 | DDB_G0290399 | DDB0232432 | CDS | 4034032 | 3270 | - | 0.195107 | |
DDB_G0290401 | DDB_G0290401 | phosphorylates (R)-pantothenate to (R)-4'-phosphopantothenate | DDB0232432 | CDS | 4038671 | 2058 | + | 0.270651 |
DDB_G0290403 | DDB_G0290403 | DDB0232432 | CDS | 4041398 | 495 | + | 0.282828 | |
DDB_G0290409 | DDB_G0290409 | DDB0232432 | CDS | 4048204 | 1410 | + | 0.284397 | |
DDB_G0290411 | DDB_G0290411 | DDB0232432 | CDS | 4050217 | 726 | - | 0.30303 | |
DDB_G0290415 | DDB_G0290415 | DDB0232432 | CDS | 4053731 | 3303 | + | 0.277929 | |
DDB_G0290419 | DDB_G0290419 | DDB0232432 | CDS | 4062441 | 315 | - | 0.273016 | |
DDB_G0290421 | DDB_G0290421 | DDB0232432 | CDS | 4063431 | 2082 | - | 0.246878 | |
DDB_G0290423 | DDB_G0290423 | DDB0232432 | CDS | 4067949 | 1743 | + | 0.242111 | |
DDB_G0290425 | DDB_G0290425 | DDB0232432 | CDS | 4070123 | 1191 | + | 0.279597 | |
DDB_G0290427 | DDB_G0290427 | DDB0232432 | CDS | 4113138 | 963 | - | 0.311526 | |
DDB_G0290429 | DDB_G0290429 | DDB0232432 | CDS | 4115465 | 396 | + | 0.275253 | |
DDB_G0290431 | DDB_G0290431 | DDB0232432 | CDS | 4116429 | 1458 | + | 0.222222 | |
DDB_G0290433 | DDB_G0290433 | DDB0232432 | CDS | 4118281 | 4869 | - | 0.326556 | |
DDB_G0290435 | DDB_G0290435 | DDB0232432 | CDS | 4124662 | 2559 | + | 0.19109 | |
DDB_G0290437 | DDB_G0290437 | DDB0232432 | CDS | 4128169 | 327 | + | 0.287462 | |
DDB_G0290441 | DDB_G0290441 | DDB0232432 | CDS | 4134020 | 1353 | + | 0.195861 | |
DDB_G0290443 | DDB_G0290443 | DDB0232432 | CDS | 4111634 | 975 | - | 0.215385 | |
DDB_G0290447_RTE | DDB_G0290447 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 4006163 | 406 | + | 0.283251 |
DDB_G0290449 | DDB_G0290449 | DDB0232432 | CDS | 4015567 | 924 | - | 0.238095 | |
DDB_G0290457 | DDB_G0290457 | DDB0232432 | CDS | 4077605 | 1323 | - | 0.244142 | |
DDB_G0290459 | DDB_G0290459 | DDB0232432 | CDS | 4079741 | 1215 | + | 0.185185 | |
DDB_G0290461 | DDB_G0290461 | DDB0232432 | CDS | 4081599 | 636 | + | 0.232704 | |
DDB_G0290463 | DDB_G0290463 | DDB0232432 | CDS | 4082312 | 318 | - | 0.163522 | |
DDB_G0290465 | DDB_G0290465 | conserved hypothetical 695 aa Dictyostelium protein centrosomal component | DDB0232432 | CDS | 4083295 | 2088 | + | 0.28592 |
DDB_G0290471 | DDB_G0290471 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats does not contain the consensus sequences required for kinase function | DDB0232432 | CDS | 4105828 | 1059 | - | 0.234183 |
DDB_G0290473 | DDB_G0290473 | DDB0232432 | CDS | 4107607 | 1965 | - | 0.205089 | |
DDB_G0290475 | DDB_G0290475 | DDB0232432 | CDS | 4110262 | 339 | + | 0.271386 | |
DDB_G0290487 | DDB_G0290487 | DDB0232432 | CDS | 4140984 | 2082 | + | 0.161383 | |
DDB_G0290489 | DDB_G0290489 | DDB0232432 | CDS | 4143852 | 1467 | + | 0.179959 | |
DDB_G0290491 | DDB_G0290491 | DDB0232432 | CDS | 4146073 | 381 | - | 0.272966 | |
DDB_G0290495 | DDB_G0290495 | DDB0232432 | CDS | 4151099 | 702 | - | 0.230769 | |
DDB_G0290497 | DDB_G0290497 | DDB0232432 | CDS | 4152368 | 1875 | - | 0.231467 | |
DDB_G0290503 | DDB_G0290503 | DDB0232432 | CDS | 4159418 | 4479 | - | 0.20384 | |
DDB_G0290505 | DDB_G0290505 | DDB0232432 | CDS | 4164699 | 1908 | - | 0.226415 | |
DDB_G0290507 | DDB_G0290507 | DDB0232432 | CDS | 4167405 | 2142 | - | 0.203081 | |
DDB_G0290513 | DDB_G0290513 | DDB0232432 | CDS | 4175909 | 3162 | + | 0.183744 | |
DDB_G0290519 | DDB_G0290519 | DDB0232432 | CDS | 4199032 | 144 | + | 0.263889 | |
DDB_G0290521 | DDB_G0290521 | DDB0232432 | CDS | 4200324 | 1293 | - | 0.354988 | |
DDB_G0290523 | DDB_G0290523 | DDB0232432 | CDS | 4204192 | 1035 | - | 0.261836 | |
DDB_G0290525 | DDB_G0290525 | DDB0232432 | CDS | 4212337 | 1275 | - | 0.20549 | |
DDB_G0290527 | DDB_G0290527 | DDB0232432 | CDS | 4214740 | 2307 | - | 0.21023 | |
DDB_G0290531 | DDB_G0290531 | DDB0232432 | CDS | 4228089 | 297 | + | 0.309764 | |
DDB_G0290533 | DDB_G0290533 | DDB0232432 | CDS | 4229551 | 885 | + | 0.273446 | |
DDB_G0290535 | DDB_G0290535 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232432 | CDS | 4232732 | 1488 | - | 0.346102 |
DDB_G0290537 | DDB_G0290537 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232432 | CDS | 4235159 | 1485 | + | 0.333333 |
DDB_G0290539 | DDB_G0290539 | DDB0232432 | CDS | 4236850 | 714 | - | 0.219888 | |
DDB_G0290541 | DDB_G0290541 | DDB0232432 | CDS | 4238133 | 1398 | - | 0.316881 | |
DDB_G0290543 | DDB_G0290543 | DDB0232432 | CDS | 4242895 | 837 | - | 0.25687 | |
DDB_G0290545 | DDB_G0290545 | DDB0232432 | CDS | 4245577 | 2238 | + | 0.224754 | |
DDB_G0290547 | DDB_G0290547 | DDB0232432 | CDS | 4248317 | 444 | - | 0.34009 | |
DDB_G0290549 | DDB_G0290549 | DDB0232432 | CDS | 4250883 | 1152 | + | 0.197917 | |
DDB_G0290553 | DDB_G0290553 | DDB0232432 | CDS | 4265295 | 1506 | - | 0.233732 | |
DDB_G0290555 | DDB_G0290555 | DDB0232432 | CDS | 4267110 | 1527 | + | 0.264571 | |
DDB_G0290557 | DDB_G0290557 | DDB0232432 | CDS | 4269452 | 2061 | + | 0.280932 | |
DDB_G0290559 | DDB_G0290559 | DDB0232432 | CDS | 4272924 | 2013 | - | 0.232489 | |
DDB_G0290561_ps | DDB_G0290561 | putative pseudogene similar to a family of genes including | DDB0232432 | CDS | 4275359 | 1089 | - | 0.199265 |
DDB_G0290565_ps | DDB_G0290565 | DDB0232432 | CDS | 4282644 | 1452 | - | 0.220386 | |
DDB_G0290567_ps | DDB_G0290567 | putative pseudogene similar to Dictyostelium genes | DDB0232432 | CDS | 4284701 | 1191 | - | 0.248531 |
DDB_G0290569_ps | DDB_G0290569 | putative pseudogene very similar to FNIP-domain containing protein coding genes | DDB0232432 | CDS | 4288392 | 1953 | - | 0.229903 |
DDB_G0290571 | DDB_G0290571 | contains 7 FNIP domains conserved in Dictyostelium similar to D. purpureum protein | DDB0232432 | CDS | 4292030 | 2154 | - | 0.221913 |
DDB_G0290573 | DDB_G0290573 | DDB0232432 | CDS | 4295576 | 1344 | - | 0.25744 | |
DDB_G0290575 | DDB_G0290575 | DDB0232432 | CDS | 4299544 | 1419 | + | 0.34179 | |
DDB_G0290579 | DDB_G0290579 | DDB0232432 | CDS | 4310280 | 336 | + | 0.244048 | |
DDB_G0290583 | DDB_G0290583 | DDB0232432 | CDS | 4319294 | 168 | - | 0.333333 | |
DDB_G0290585 | DDB_G0290585 | DDB0232432 | CDS | 4319962 | 171 | - | 0.25731 | |
DDB_G0290587 | DDB_G0290587 | DDB0232432 | CDS | 4322112 | 2199 | - | 0.331514 | |
DDB_G0290589 | DDB_G0290589 | DDB0232432 | CDS | 4325235 | 192 | - | 0.25 | |
DDB_G0290591 | DDB_G0290591 | DDB0232432 | CDS | 4327797 | 6255 | - | 0.264748 | |
DDB_G0290593 | DDB_G0290593 | DDB0232432 | CDS | 4335292 | 435 | + | 0.344828 | |
DDB_G0290595 | DDB_G0290595 | DDB0232432 | CDS | 4337348 | 687 | + | 0.257642 | |
DDB_G0290597 | DDB_G0290597 | DDB0232432 | CDS | 4338558 | 1113 | + | 0.286613 | |
DDB_G0290599 | DDB_G0290599 | DDB0232432 | CDS | 4343609 | 192 | - | 0.260417 | |
DDB_G0290603 | DDB_G0290603 | DDB0232432 | CDS | 4352727 | 1866 | - | 0.339228 | |
DDB_G0290605 | DDB_G0290605 | DDB0232432 | CDS | 4356438 | 1155 | + | 0.27619 | |
DDB_G0290607_ps | DDB_G0290607 | putative pseudogene similar to FNIP domain-containing proteins | DDB0232432 | CDS | 4360447 | 726 | + | 0.241047 |
DDB_G0290613 | DDB_G0290613 | DDB0232432 | CDS | 4370850 | 2274 | + | 0.207124 | |
DDB_G0290619 | DDB_G0290619 | DDB0232432 | CDS | 4380155 | 2163 | - | 0.283403 | |
DDB_G0290621 | DDB_G0290621 | DDB0232432 | CDS | 4383355 | 2904 | - | 0.22865 | |
DDB_G0290623 | DDB_G0290623 | DDB0232432 | CDS | 4387215 | 2436 | + | 0.2578 | |
DDB_G0290625 | DDB_G0290625 | DDB0232432 | CDS | 4389816 | 1641 | - | 0.193784 | |
DDB_G0290627 | DDB_G0290627 | DDB0232432 | CDS | 4392045 | 1833 | - | 0.233497 | |
DDB_G0290629 | DDB_G0290629 | DDB0232432 | CDS | 4394537 | 2913 | - | 0.252317 | |
DDB_G0290631 | DDB_G0290631 | DDB0232432 | CDS | 4398765 | 558 | - | 0.297491 | |
DDB_G0290633 | DDB_G0290633 | DDB0232432 | CDS | 4403175 | 1824 | + | 0.22807 | |
DDB_G0290635 | DDB_G0290635 | DDB0232432 | CDS | 4405679 | 3762 | + | 0.249867 | |
DDB_G0290637 | DDB_G0290637 | similar to | DDB0232432 | CDS | 4321079 | 366 | - | 0.308743 |
DDB_G0290639 | DDB_G0290639 | DDB0232432 | CDS | 4378104 | 1851 | + | 0.219341 | |
DDB_G0290641 | DDB_G0290641 | DDB0232432 | CDS | 4179788 | 17406 | + | 0.258704 | |
DDB_G0290645 | DDB_G0290645 | DDB0232432 | CDS | 4303636 | 1074 | + | 0.199255 | |
DDB_G0290647 | DDB_G0290647 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | DDB0232432 | CDS | 4170905 | 2784 | + | 0.30819 |
DDB_G0290649 | DDB_G0290649 | conserved RNA binding motif protein ortholog of mammalian RBM22 and similar to yeast ECM2 a pre-mRNA splicing factor | DDB0232432 | CDS | 4202596 | 1224 | + | 0.258987 |
DDB_G0290651 | DDB_G0290651 | DDB0232432 | CDS | 4206508 | 2913 | + | 0.283556 | |
DDB_G0290653 | DDB_G0290653 | DDB0232432 | CDS | 4220163 | 5154 | - | 0.28832 | |
DDB_G0290655 | DDB_G0290655 | DDB0232432 | CDS | 4241124 | 126 | + | 0.301587 | |
DDB_G0290657 | DDB_G0290657 | DDB0232432 | CDS | 4241742 | 225 | + | 0.328889 | |
DDB_G0290663 | DDB_G0290663 | DDB0232432 | CDS | 4305581 | 2754 | + | 0.172476 | |
DDB_G0290667 | DDB_G0290667 | DDB0232432 | CDS | 4313752 | 1107 | - | 0.226739 | |
DDB_G0290673 | DDB_G0290673 | DDB0232432 | CDS | 4340691 | 1059 | + | 0.17186 | |
DDB_G0290675 | DDB_G0290675 | DDB0232432 | CDS | 4342512 | 756 | + | 0.268519 | |
DDB_G0290677 | DDB_G0290677 | DDB0232432 | CDS | 4347032 | 5175 | + | 0.182222 | |
DDB_G0290679 | DDB_G0290679 | DDB0232432 | CDS | 4358106 | 1911 | + | 0.239142 | |
DDB_G0290681_ps | DDB_G0290681 | putative pseudogene similar to FNIP domain-containing proteins | DDB0232432 | CDS | 4365656 | 1485 | + | 0.250505 |
DDB_G0290683_ps | DDB_G0290683 | putative pseudogene similar to FNIP domain-containing proteins | DDB0232432 | CDS | 4368520 | 1164 | + | 0.239691 |
DDB_G0290689 | DDB_G0290689 | homolog of E. coli rppH very similar to | DDB0232432 | CDS | 4419333 | 552 | - | 0.278986 |
DDB_G0290691 | DDB_G0290691 | DDB0232432 | CDS | 4421497 | 1581 | - | 0.25933 | |
DDB_G0290695 | DDB_G0290695 | DDB0232432 | CDS | 4432334 | 1095 | - | 0.273973 | |
DDB_G0290697 | DDB_G0290697 | DDB0232432 | CDS | 4431661 | 276 | + | 0.318841 | |
DDB_G0290711_ps | DDB_G0290711 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232432 | CDS | 4483031 | 1929 | - | 0.270607 |
DDB_G0290713_RTE | DDB_G0290713 | partial ORF1 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 4485678 | 594 | + | 0.321549 |
DDB_G0290715 | DDB_G0290715 | DDB0232432 | CDS | 4435379 | 2469 | + | 0.203321 | |
DDB_G0290721 | DDB_G0290721 | similar to bacterial aminotransferase class-III proteins which are pyridoxal-phosphate-dependent enzymes | DDB0232432 | CDS | 4489219 | 1485 | - | 0.346128 |
DDB_G0290727 | DDB_G0290727 | DDB0232432 | CDS | 4504173 | 2274 | + | 0.223395 | |
DDB_G0290739_ps | DDB_G0290739 | putative pseudogene fragment very similar to several other genes e.g. | DDB0232432 | CDS | 4533356 | 348 | + | 0.117816 |
DDB_G0290747_ps | DDB_G0290747 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232432 | CDS | 4517745 | 3564 | + | 0.250281 |
DDB_G0290749_RTE | DDB_G0290749 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 4537600 | 1174 | - | 0.291312 |
DDB_G0290753 | DDB_G0290753 | contains a C2 calciumlipid-binding region (CaLB) | DDB0232432 | CDS | 4566125 | 588 | + | 0.289116 |
DDB_G0290755 | DDB_G0290755 | contains a C2 calciumlipid-binding region (CaLB) | DDB0232432 | CDS | 4567289 | 546 | + | 0.291209 |
DDB_G0290763 | DDB_G0290763 | DDB0232432 | CDS | 4563065 | 2667 | + | 0.170229 | |
DDB_G0290767 | DDB_G0290767 | DDB0232432 | CDS | 4586394 | 837 | + | 0.210275 | |
DDB_G0290771 | DDB_G0290771 | DDB0232432 | CDS | 4578736 | 5247 | - | 0.27673 | |
DDB_G0290773 | DDB_G0290773 | DDB0232432 | CDS | 4584906 | 414 | - | 0.251208 | |
DDB_G0290777 | DDB_G0290777 | DDB0232432 | CDS | 4587507 | 3095 | - | 0.187399 | |
DDB_G0290785 | DDB_G0290785 | DDB0232432 | CDS | 4596636 | 1551 | - | 0.294004 | |
DDB_G0290797 | DDB_G0290797 | DDB0232432 | CDS | 4615081 | 393 | + | 0.236641 | |
DDB_G0290799 | DDB_G0290799 | conserved protein brbr bCommunity annotation:b DDB_G0290799 is highly conserved throughout the eukaryotes. It contains a YjeF domain which in other systems has been implicated in the regulation of RNA stability specifically of genes involved in eukaryotic cell cycle regulation [see Anantharaman and Aravind BMC Genomics 5:45 (2004)]. A budding yeast homolog YKL151C is expressed at MG1 after temperature-sensitive cdc28 synchronization (see a target | DDB0232432 | CDS | 4616309 | 921 | + | 0.299674 |
DDB_G0290801 | DDB_G0290801 | DDB0232432 | CDS | 4618085 | 756 | + | 0.260582 | |
DDB_G0290803 | DDB_G0290803 | DDB0232432 | CDS | 4619234 | 1104 | - | 0.247283 | |
DDB_G0290805 | DDB_G0290805 | DDB0232432 | CDS | 4624322 | 1275 | - | 0.238431 | |
DDB_G0290807_ps | DDB_G0290807 | putative pseudogenes fragment similar to a family of D. discoideum genes including | DDB0232432 | CDS | 4626001 | 579 | - | 0.264249 |
DDB_G0290811 | DDB_G0290811 | DDB0232432 | CDS | 4626993 | 387 | - | 0.387597 | |
DDB_G0290815 | DDB_G0290815 | DDB0232432 | CDS | 4628184 | 7365 | - | 0.281874 | |
DDB_G0290817_ps | DDB_G0290817 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232432 | CDS | 4642551 | 1287 | + | 0.212898 |
DDB_G0290819 | DDB_G0290819 | DDB0232432 | CDS | 4644346 | 126 | + | 0.253968 | |
DDB_G0290821 | DDB_G0290821 | DDB0232432 | CDS | 4644529 | 1194 | - | 0.252931 | |
DDB_G0290823 | DDB_G0290823 | DDB0232432 | CDS | 4646192 | 1224 | - | 0.251634 | |
DDB_G0290827 | DDB_G0290827 | DDB0232432 | CDS | 4603659 | 753 | - | 0.200531 | |
DDB_G0290835 | DDB_G0290835 | DDB0232432 | CDS | 4620639 | 3231 | - | 0.244197 | |
DDB_G0290837 | DDB_G0290837 | DDB0232432 | CDS | 4637184 | 2280 | + | 0.307456 | |
DDB_G0290839 | DDB_G0290839 | DDB0232432 | CDS | 4590906 | 1278 | - | 0.21518 | |
DDB_G0290841 | DDB_G0290841 | DDB0232432 | CDS | 4662421 | 4242 | + | 0.269448 | |
DDB_G0290843 | DDB_G0290843 | DDB0232432 | CDS | 4667305 | 168 | - | 0.196429 | |
DDB_G0290847 | DDB_G0290847 | DDB0232432 | CDS | 4672145 | 957 | + | 0.236155 | |
DDB_G0290855 | DDB_G0290855 | DDB0232432 | CDS | 4670841 | 357 | + | 0.280112 | |
DDB_G0290857 | DDB_G0290857 | DDB0232432 | CDS | 4682925 | 1560 | + | 0.286538 | |
DDB_G0290859 | DDB_G0290859 | member of the AGC kinase group similar to NDR (nuclear Dbf2-related) and RSK (ribosomal S6 kinase) family members | DDB0232432 | CDS | 4688665 | 1260 | + | 0.307143 |
DDB_G0290863 | DDB_G0290863 | DDB0232432 | CDS | 4694739 | 1020 | - | 0.22549 | |
DDB_G0290865_ps | DDB_G0290865 | putative pseudogene fragment similar to | DDB0232432 | CDS | 4696122 | 519 | - | 0.267823 |
DDB_G0290871 | DDB_G0290871 | DDB0232432 | CDS | 4698932 | 210 | + | 0.204762 | |
DDB_G0290877 | DDB_G0290877 | DDB0232432 | CDS | 4704549 | 2475 | - | 0.288081 | |
DDB_G0290879 | DDB_G0290879 | DDB0232432 | CDS | 4708116 | 531 | + | 0.220339 | |
DDB_G0290881 | DDB_G0290881 | DDB0232432 | CDS | 4709313 | 492 | + | 0.243902 | |
DDB_G0290883 | DDB_G0290883 | highly similar (93 | DDB0232432 | CDS | 4710716 | 1383 | + | 0.261027 |
DDB_G0290885 | DDB_G0290885 | conserved Dictyostelium protein contains a putative signal sequence underexpressed in | DDB0232432 | CDS | 4714181 | 543 | - | 0.303867 |
DDB_G0290887 | DDB_G0290887 | conserved Dictyostelium protein contains a putative signal sequence | DDB0232432 | CDS | 4716370 | 543 | - | 0.311234 |
DDB_G0290893 | DDB_G0290893 | DDB0232432 | CDS | 4676692 | 5457 | + | 0.230346 | |
DDB_G0290895_ps | DDB_G0290895 | putative pseudogene similar to the family of FNIP repeat-containing genes such as | DDB0232432 | CDS | 4690806 | 1434 | + | 0.226639 |
DDB_G0290897_ps | DDB_G0290897 | putative pseudogene similar to | DDB0232432 | CDS | 4712501 | 1170 | + | 0.286325 |
DDB_G0290903 | DDB_G0290903 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232432 | CDS | 4735255 | 228 | - | 0.337719 |
DDB_G0290905 | DDB_G0290905 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232432 | CDS | 4735853 | 228 | + | 0.324561 |
DDB_G0290907 | DDB_G0290907 | DDB0232432 | CDS | 4736810 | 192 | - | 0.296875 | |
DDB_G0290911 | DDB_G0290911 | DDB0232432 | CDS | 4739761 | 150 | - | 0.253333 | |
DDB_G0290915 | DDB_G0290915 | DDB0232432 | CDS | 4742302 | 1170 | + | 0.22906 | |
DDB_G0290923 | DDB_G0290923 | DDB0232432 | CDS | 4757036 | 4101 | + | 0.18971 | |
DDB_G0290931 | DDB_G0290931 | DDB0232432 | CDS | 4768327 | 1536 | - | 0.251302 | |
DDB_G0290933_ps | DDB_G0290933 | putative pseudogene fragment similar to TRAF-type zinc finger-containing proteins including | DDB0232432 | CDS | 4770388 | 339 | - | 0.20944 |
DDB_G0290941_ps | DDB_G0290941 | putative pseudogene N-terminal fragment of RING zinc finger- and TRAF-type zinc finger-containing proteins including | DDB0232432 | CDS | 4785018 | 567 | - | 0.231041 |
DDB_G0290945 | DDB_G0290945 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | DDB0232432 | CDS | 4734513 | 258 | + | 0.333333 |
DDB_G0290947 | DDB_G0290947 | DDB0232432 | CDS | 4749424 | 4317 | - | 0.28214 | |
DDB_G0290953_TE | DDB_G0290953 | DDB0232432 | CDS | 4796402 | 432 | + | 0.314815 | |
DDB_G0290955_TE | DDB_G0290955 | ORF1 encoding a protein of unknown function of the putative DNA transposon Tdd-5 refer to AF298206 for full-length consensus element | DDB0232432 | CDS | 4798680 | 889 | - | 0.31946 |
DDB_G0290965 | DDB_G0290965 | DDB0232432 | CDS | 4802105 | 1728 | - | 0.23669 | |
DDB_G0290967 | DDB_G0290967 | DDB0232432 | CDS | 4806120 | 1563 | - | 0.272553 | |
DDB_G0290969 | DDB_G0290969 | DDB0232432 | CDS | 4808227 | 1179 | - | 0.189992 | |
DDB_G0290971 | DDB_G0290971 | DDB0232432 | CDS | 4814825 | 1338 | - | 0.27429 | |
DDB_G0290973 | DDB_G0290973 | similar to Polysphondylium pallidum protein contains at least two predicted coiled-coil domains | DDB0232432 | CDS | 4816558 | 5334 | - | 0.250469 |
DDB_G0290975 | DDB_G0290975 | highly similar to cinB (99 | DDB0232432 | CDS | 4829775 | 1014 | + | 0.270217 |
DDB_G0290977 | DDB_G0290977 | DDB0232432 | CDS | 4841153 | 1599 | + | 0.245779 | |
DDB_G0290983 | DDB_G0290983 | DDB0232432 | CDS | 4844885 | 4008 | - | 0.221307 | |
DDB_G0290985 | DDB_G0290985 | DDB0232432 | CDS | 4854167 | 2370 | + | 0.28481 | |
DDB_G0290989 | DDB_G0290989 | DDB0232432 | CDS | 4859470 | 3462 | - | 0.253611 | |
DDB_G0290991 | DDB_G0290991 | DDB0232432 | CDS | 4863621 | 1368 | - | 0.233918 | |
DDB_G0290993 | DDB_G0290993 | DDB0232432 | CDS | 4865936 | 603 | - | 0.303483 | |
DDB_G0290995 | DDB_G0290995 | DDB0232432 | CDS | 4867138 | 909 | - | 0.246425 | |
DDB_G0290999 | DDB_G0290999 | DDB0232432 | CDS | 4872338 | 2757 | - | 0.219804 | |
DDB_G0291001 | DDB_G0291001 | DDB0232432 | CDS | 4875486 | 219 | - | 0.324201 | |
DDB_G0291003 | DDB_G0291003 | DDB0232432 | CDS | 4876763 | 2598 | - | 0.299461 | |
DDB_G0291005 | DDB_G0291005 | DDB0232432 | CDS | 4879944 | 909 | + | 0.214521 | |
DDB_G0291011 | DDB_G0291011 | DDB0232432 | CDS | 4886164 | 2919 | - | 0.258993 | |
DDB_G0291013 | DDB_G0291013 | DDB0232432 | CDS | 4889905 | 1149 | + | 0.302872 | |
DDB_G0291015 | DDB_G0291015 | possible homolog of human LSM10 a U7 snRNA-associated Sm-like protein | DDB0232432 | CDS | 4891178 | 414 | - | 0.23913 |
DDB_G0291017_ps | DDB_G0291017 | putative pseudogene fragment similar to | DDB0232432 | CDS | 4893398 | 495 | - | 0.284848 |
DDB_G0291019 | DDB_G0291019 | DDB0232432 | CDS | 4894200 | 1023 | - | 0.234604 | |
DDB_G0291023 | DDB_G0291023 | DDB0232432 | CDS | 4906011 | 1734 | - | 0.27797 | |
DDB_G0291025 | DDB_G0291025 | DDB0232432 | CDS | 4915458 | 2445 | + | 0.251534 | |
DDB_G0291027 | DDB_G0291027 | DDB0232432 | CDS | 4918030 | 4254 | - | 0.271979 | |
DDB_G0291029 | DDB_G0291029 | catalyzes the reaction SOsub4subsup2-sup ATP APS pyrophosphate | DDB0232432 | CDS | 4928744 | 1767 | - | 0.367289 |
DDB_G0291033 | DDB_G0291033 | DDB0232432 | CDS | 4933146 | 2238 | - | 0.298481 | |
DDB_G0291035_ps | DDB_G0291035 | putative pseudogene similar to genes of the RING zinc finger family such as the | DDB0232432 | CDS | 4832043 | 339 | - | 0.218289 |
DDB_G0291041_ps | DDB_G0291041 | putative pseudogene fragment similar to a D. discoideum gene family including | DDB0232432 | CDS | 4805100 | 306 | - | 0.238562 |
DDB_G0291045 | DDB_G0291045 | DDB0232432 | CDS | 4923512 | 4269 | - | 0.271024 | |
DDB_G0291051_ps | DDB_G0291051 | putative pseudogene fragment similar to | DDB0232432 | CDS | 4829057 | 204 | + | 0.245098 |
DDB_G0291053_ps | DDB_G0291053 | putative pseudogene similar gene the | DDB0232432 | CDS | 4830916 | 492 | - | 0.315041 |
DDB_G0291055 | DDB_G0291055 | homolog of human SFT2D1 (SFT2 domain-containing protein 1) contains 4 putative transmembrane domains | DDB0232432 | CDS | 4835830 | 477 | + | 0.295597 |
DDB_G0291057 | DDB_G0291057 | DDB0232432 | CDS | 4836534 | 1035 | - | 0.211594 | |
DDB_G0291059 | DDB_G0291059 | contains two ankyrin repeats and two K homology (KH) domains similar to high density lipoprotein-binding protein (vigilin) | DDB0232432 | CDS | 4839561 | 1155 | + | 0.303896 |
DDB_G0291061 | DDB_G0291061 | DDB0232432 | CDS | 4868366 | 234 | + | 0.294872 | |
DDB_G0291065 | DDB_G0291065 | DDB0232432 | CDS | 4936261 | 7389 | + | 0.280282 | |
DDB_G0291067_RTE | DDB_G0291067 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232432 | CDS | 4945727 | 1063 | - | 0.292568 |
DDB_G0291069_RTE | DDB_G0291069 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | DDB0232432 | CDS | 4946964 | 645 | - | 0.294574 |
DDB_G0291071 | DDB_G0291071 | DDB0232432 | CDS | 4948671 | 1275 | - | 0.278431 | |
DDB_G0291073 | DDB_G0291073 | DDB0232432 | CDS | 4950352 | 963 | - | 0.187954 | |
DDB_G0291083 | DDB_G0291083 | DDB0232432 | CDS | 4954952 | 606 | - | 0.20132 | |
DDB_G0291087_ps | DDB_G0291087 | putative pseudogene very similar to | DDB0232432 | CDS | 4958200 | 177 | + | 0.338983 |
DDB_G0291089 | DDB_G0291089 | DDB0232432 | CDS | 4970973 | 249 | + | 0.297189 | |
DDB_G0291099 | DDB_G0291099 | DDB0232432 | CDS | 4996259 | 1752 | + | 0.260274 | |
DDB_G0291101 | DDB_G0291101 | DDB0232432 | CDS | 4998499 | 426 | + | 0.241784 | |
DDB_G0291103 | DDB_G0291103 | DDB0232432 | CDS | 4999483 | 327 | + | 0.275229 | |
DDB_G0291107 | DDB_G0291107 | DDB0232432 | CDS | 4952079 | 1350 | - | 0.295556 | |
DDB_G0291109 | DDB_G0291109 | DDB0232432 | CDS | 4968619 | 1329 | - | 0.239278 | |
DDB_G0291111 | DDB_G0291111 | DDB0232432 | CDS | 4977011 | 3294 | - | 0.245598 | |
DDB_G0291115 | DDB_G0291115 | DDB0232432 | CDS | 5000155 | 5757 | - | 0.265763 | |
DDB_G0291119 | DDB_G0291119 | DDB0232432 | CDS | 5015686 | 1308 | + | 0.248471 | |
DDB_G0291131 | DDB_G0291131 | DDB0232432 | CDS | 5027479 | 2148 | + | 0.363128 | |
DDB_G0291133 | DDB_G0291133 | putative protein tyrosine kinase similar to S. pombe wee1 inhibitor of mitosis through phosphorylation of cdc2 | DDB0232432 | CDS | 5030354 | 2337 | + | 0.26059 |
DDB_G0291135 | DDB_G0291135 | DDB0232432 | CDS | 5033227 | 1185 | + | 0.263291 | |
DDB_G0291137 | DDB_G0291137 | DDB0232432 | CDS | 5040435 | 558 | + | 0.344086 | |
DDB_G0291139 | DDB_G0291139 | DDB0232432 | CDS | 5041464 | 906 | - | 0.236203 | |
DDB_G0291141 | DDB_G0291141 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 15 putative transmembrane domains | DDB0232432 | CDS | 5043001 | 2313 | + | 0.278859 |
DDB_G0291143 | DDB_G0291143 | DDB0232432 | CDS | 5045979 | 810 | - | 0.21358 | |
DDB_G0291147 | DDB_G0291147 | DDB0232432 | CDS | 5049086 | 2817 | + | 0.242457 | |
DDB_G0291149 | DDB_G0291149 | DDB0232432 | CDS | 5052148 | 1569 | - | 0.251115 | |
DDB_G0291151 | DDB_G0291151 | DDB0232432 | CDS | 5054416 | 1134 | + | 0.250441 | |
DDB_G0291153_ps | DDB_G0291153 | putative pseudogene similar gene the | DDB0232432 | CDS | 5057151 | 522 | - | 0.310345 |
DDB_G0291155 | DDB_G0291155 | DDB0232432 | CDS | 5058540 | 936 | - | 0.317308 | |
DDB_G0291159 | DDB_G0291159 | DDB0232432 | CDS | 5062119 | 855 | + | 0.263158 | |
DDB_G0291161 | DDB_G0291161 | DDB0232432 | CDS | 5063347 | 4944 | - | 0.303803 | |
DDB_G0291165 | DDB_G0291165 | DDB0232432 | CDS | 5083069 | 228 | + | 0.201754 | |
DDB_G0291167 | DDB_G0291167 | DDB0232432 | CDS | 5083393 | 681 | - | 0.251101 | |
DDB_G0291169 | DDB_G0291169 | DDB0232432 | CDS | 5089340 | 894 | + | 0.279642 | |
DDB_G0291171 | DDB_G0291171 | DDB0232432 | CDS | 5090921 | 882 | + | 0.297052 | |
DDB_G0291175 | DDB_G0291175 | DDB0232432 | CDS | 5097563 | 3102 | + | 0.297872 | |
DDB_G0291181 | DDB_G0291181 | DDB0232432 | CDS | 5105448 | 1080 | + | 0.327778 | |
DDB_G0291187 | DDB_G0291187 | similar to A. thaliana PCS1 (phytochelatin synthase 1) catalyzes the reaction glutathione (Glu(-Cys))(n)-Gly Gly (Glu(-Cys))(n1)-Gly | DDB0232432 | CDS | 5037394 | 1881 | - | 0.290803 |
DDB_G0291189 | DDB_G0291189 | DDB0232432 | CDS | 5084851 | 696 | + | 0.238506 | |
DDB_G0291191 | DDB_G0291191 | DDB0232432 | CDS | 5086072 | 1059 | - | 0.367328 | |
DDB_G0291195 | DDB_G0291195 | DDB0232432 | CDS | 5092325 | 792 | + | 0.294192 | |
DDB_G0291203 | DDB_G0291203 | similar to D. purpureum protein contains a region conserved with eukaryotic transmembrane receptors (lung_7-TM_R: PF06814) contains 7 putative transmembrane domains | DDB0232432 | CDS | 5116417 | 1593 | + | 0.254237 |
DDB_G0291205 | DDB_G0291205 | DDB0232432 | CDS | 5120775 | 2727 | + | 0.268794 | |
DDB_G0294571 | DDB_G0294571 | DDB0232432 | CDS | 4610784 | 612 | - | 0.28268 | |
DDB_G0294591 | DDB_G0294591 | contains three putative transmembrane domains not similar to any other protein | DDB0232432 | CDS | 1587124 | 1209 | + | 0.257237 |
DDB_G0294603 | DDB_G0294603 | DDB0232432 | CDS | 4577727 | 525 | - | 0.259048 | |
DDB_G0294611 | DDB_G0294611 | DDB0232432 | CDS | 2837078 | 1836 | - | 0.314815 | |
DDB_G0295479 | DDB_G0295479 | similar to polyketide synthases but only 179 amino acids long other polyketide synthase genes encode proteins of about 3000 amino acids | DDB0232432 | CDS | 4104623 | 537 | + | 0.232775 |
DDB_G0295661 | DDB_G0295661 | there is an identical copy of this gene on chromosome 2 | DDB0232432 | CDS | 4559095 | 1755 | - | 0.317949 |
DDB_G0295665 | DDB_G0295665 | DDB0232432 | CDS | 4561968 | 564 | + | 0.271277 | |
DDB_G0295675 | DDB_G0295675 | DDB0232432 | CDS | 2700736 | 2478 | + | 0.282486 | |
DDB_G0295689 | DDB_G0295689 | contains a predicted signal peptide and two transmembrane domains has no known homologs | DDB0232432 | CDS | 188514 | 405 | + | 0.301235 |
DDB_G0295693 | DDB_G0295693 | similar to | DDB0232432 | CDS | 4571270 | 969 | - | 0.177503 |
DDB_G0295701 | DDB_G0295701 | contains a predicted signal peptide contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232432 | CDS | 304647 | 1002 | - | 0.287425 |
DDB_G0295735 | DDB_G0295735 | DDB0232432 | CDS | 1928245 | 1809 | + | 0.210061 | |
DDB_G0295737 | DDB_G0295737 | DDB0232432 | CDS | 3359151 | 2817 | - | 0.29535 | |
DDB_G0295739 | DDB_G0295739 | DDB0232432 | CDS | 3772467 | 999 | - | 0.309309 | |
DDB_G0295743 | DDB_G0295743 | DDB0232432 | CDS | 2586654 | 2175 | - | 0.262989 | |
DDB_G0295745 | DDB_G0295745 | DDB0232432 | CDS | 2584317 | 192 | - | 0.223958 | |
DDB_G0295747 | DDB_G0295747 | DDB0232432 | CDS | 2582433 | 1590 | - | 0.215094 | |
DDB_G0295749 | DDB_G0295749 | highly similar to | DDB0232432 | CDS | 2579548 | 1714 | - | 0.280047 |
DDB_G0295753 | DDB_G0295753 | very similar to Dictyostelium mcfN and to human SLC25A3 and S. cerevisiae MIR1 which transports inorganic phosphate from the cytosol to the mitochondrion matrix | DDB0232432 | CDS | 2590095 | 900 | + | 0.342222 |
DDB_G0295759 | DDB_G0295759 | DDB0232432 | CDS | 2606597 | 267 | - | 0.303371 | |
DDB_G0295777 | DDB_G0295777 | DDB0232432 | CDS | 428287 | 927 | - | 0.186624 | |
DDB_G0295779 | DDB_G0295779 | DDB0232432 | CDS | 1450193 | 528 | - | 0.327652 | |
DDB_G0295813 | DDB_G0295813 | DDB0232432 | CDS | 2607950 | 396 | - | 0.29798 | |
DDB_G0295815_ps | DDB_G0295815 | putative pseudogene very similar to | DDB0232432 | CDS | 2608554 | 204 | - | 0.348039 |
DDB_G0346536 | DDB_G0346536 | DDB0232432 | CDS | 3206289 | 1596 | - | 0.231203 | |
DDB_G0346538 | DDB_G0346538 | DDB0232432 | CDS | 3204528 | 1599 | - | 0.232645 | |
DDB_G0346922 | DDB_G0346922 | DDB0232432 | CDS | 102942 | 1521 | - | 0.277449 | |
DDB_G0346924 | DDB_G0346924 | DDB0232432 | CDS | 100675 | 1521 | - | 0.275477 | |
DDB_G0347550 | DDB_G0347550 | DDB0232432 | CDS | 4718494 | 1497 | + | 0.279893 | |
DDB_G0347551 | DDB_G0347551 | DDB0232432 | CDS | 4720437 | 1845 | + | 0.211382 | |
DDB_G0347657 | DDB_G0347657 | DDB0232432 | CDS | 3251908 | 1257 | + | 0.215593 | |
DDB_G0347658 | DDB_G0347658 | DDB0232432 | CDS | 3253562 | 1257 | + | 0.351631 | |
DDB_G0348143 | DDB_G0348143 | DDB0232432 | CDS | 514890 | 93 | + | 0.408602 | |
DDB_G0348183 | DDB_G0348183 | DDB0232432 | CDS | 4073745 | 2241 | + | 0.279786 | |
DDB_G0348184 | DDB_G0348184 | DDB0232432 | CDS | 4076581 | 900 | + | 0.26 | |
DDB_G0348868 | DDB_G0348868 | DDB0232432 | CDS | 2648590 | 117 | - | 0.418803 | |
DDB_G0349042 | DDB_G0349042 | DDB0232432 | CDS | 1339549 | 1050 | - | 0.287619 | |
DDB_G0349043 | DDB_G0349043 | DDB0232432 | CDS | 1336627 | 1767 | - | 0.271647 | |
DDB_G0349319 | DDB_G0349319 | DDB0232432 | CDS | 4344171 | 903 | + | 0.219269 | |
DDB_G0349321 | DDB_G0349321 | DDB0232432 | CDS | 4345695 | 702 | + | 0.274929 | |
DDB_G0349444 | DDB_G0349444 | putative pseudogene similar to a large gene family encoding FNIP repeat-containing proteins including | DDB0232432 | CDS | 3645353 | 1455 | - | 0.195876 |
DG1037 | DDB_G0287925 | DDB0232432 | CDS | 857146 | 1815 | + | 0.251791 | |
DG1091 | DDB_G0289175 | DDB0232432 | CDS | 2479410 | 5478 | - | 0.220701 | |
H2Av1 | DDB_G0289187 | DDB0232432 | CDS | 2451919 | 783 | + | 0.246488 | |
H2Av2 | DDB_G0289193 | DDB0232432 | CDS | 2455467 | 861 | + | 0.339141 | |
H2Av3 | DDB_G0289197 | DDB0232432 | CDS | 2457890 | 378 | + | 0.195767 | |
H3v1 | DDB_G0291185 | DDB0232432 | CDS | 5034573 | 1860 | - | 0.374731 | |
aarA | DDB_G0288877 | component of actin-associated intercellular junctions and involved in cell-cell adhesion signal transduction and stalk formation during development binds to Ctnna the Dictyostelium alpha-catenin related protein | DDB0232432 | CDS | 2168858 | 2274 | - | 0.255937 |
abcC14 | DDB_G0287589 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 520445 | 3954 | - | 0.250379 |
abcC3 | DDB_G0287691 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 792495 | 4239 | + | 0.338759 |
abcC6 | DDB_G0287593 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 525231 | 4056 | - | 0.256657 |
abcE1 | DDB_G0290483 | DDB0232432 | CDS | 4209815 | 1812 | - | 0.34989 | |
abcG16 | DDB_G0289331 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 2688872 | 4587 | + | 0.276651 |
abcG3 | DDB_G0287461 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232432 | CDS | 284599 | 4182 | - | 0.308943 |
abcG4 | DDB_G0289657 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232432 | CDS | 3066245 | 2397 | - | 0.254068 |
abcG7 | DDB_G0289655 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232432 | CDS | 3062303 | 2448 | - | 0.226307 |
abcG_ps1 | DDB_G0287785 | putative pseudogene similar to abcG family proteins | DDB0232432 | CDS | 699242 | 207 | - | 0.309179 |
abhd | DDB_G0289723 | DDB0232432 | CDS | 3165541 | 1188 | - | 0.289562 | |
abkA | DDB_G0288749 | atypical protein serinethreonine kinase contains ABC1 kinase (protein kinase-like) domain yeast ABC1 essential for the electron transfer in the BC(1) complex E.coli homolog required for ubiquinone biosynthesis | DDB0232432 | CDS | 1916080 | 1698 | - | 0.246761 |
abpD | DDB_G0287291 | actin binding protein that is developmentally and cAMP-regulated associates with intracellular membranes | DDB0232432 | CDS | 222824 | 5217 | + | 0.242285 |
acad8 | DDB_G0288647 | ortholog of the H. sapiens ACAD8 that has very high activity toward isobutyryl-CoA and might be an isobutyryl-CoA dehydrogenase that functions in valine catabolism | DDB0232432 | CDS | 1779747 | 1251 | - | 0.384492 |
acbd6 | DDB_G0290237 | DDB0232432 | CDS | 3838664 | 867 | + | 0.260669 | |
accA | DDB_G0288387 | catalizes the reactions BCCP-biotin-COsub2sub acetyl-CoA ATP malonyl-CoA BCCP-biotin phosphate ADP bandb BCCP-biotin COsub2sub ATP phosphate ADP BCCP-biotin-COsub2sub | DDB0232432 | CDS | 1474122 | 6849 | - | 0.327201 |
act1 | DDB_G0289553 | has 94 | DDB0232432 | CDS | 2938326 | 1131 | - | 0.365164 |
act10 | DDB_G0289811 | has 94 | DDB0232432 | CDS | 3337403 | 1131 | + | 0.415561 |
act11 | DDB_G0288879 | has 94 | DDB0232432 | CDS | 2167534 | 1131 | + | 0.421751 |
act18 | DDB_G0289489 | has 83 | DDB0232432 | CDS | 2886806 | 1143 | + | 0.343832 |
act24 | DDB_G0289505 | has 80 | DDB0232432 | CDS | 2876728 | 1134 | + | 0.347443 |
act25 | DDB_G0289507 | has 74 | DDB0232432 | CDS | 2878511 | 1158 | + | 0.337651 |
act27 | DDB_G0289533 | has 61 | DDB0232432 | CDS | 2880348 | 1119 | + | 0.328865 |
act28 | DDB_G0289511 | contributes to DdPPK2 activity also described as member of the polyphosphate kinase PPK3 family | DDB0232432 | CDS | 2883081 | 1062 | + | 0.335217 |
act3 | DDB_G0289487 | has 92 | DDB0232432 | CDS | 2884652 | 1131 | + | 0.358974 |
act30_ps | DDB_G0289525 | putative pseudogene contains an actin domain | DDB0232432 | CDS | 2874594 | 1098 | + | 0.343352 |
act33 | DDB_G0287981 | similar to macronuclear actin 1 of ciliates also similar to A. thaliana ACT11 | DDB0232432 | CDS | 925837 | 1245 | - | 0.236948 |
act36_ps | DDB_G0289509 | putative pseudogene contains a partial actin domain | DDB0232432 | CDS | 2881811 | 408 | + | 0.338235 |
act39_ps | DDB_G0290243 | putative pseudogene contains a partial actin domain | DDB0232432 | CDS | 3768414 | 369 | - | 0.319783 |
act4 | DDB_G0289005 | has 94 | DDB0232432 | CDS | 2234318 | 1131 | - | 0.419982 |
act5 | DDB_G0289663 | has 94 | DDB0232432 | CDS | 3186992 | 1131 | - | 0.419098 |
ada | DDB_G0287371 | catalyzes the reaction Hsub2subO adenosine NHsub3sub inosine in salvage pathways of nucleosides contains two tandem repeats of the adenosine deaminase domain | DDB0232432 | CDS | 206705 | 2319 | + | 0.287193 |
adcF | DDB_G0289229 | DDB0232432 | CDS | 2510064 | 3093 | - | 0.201423 | |
adhfe1 | DDB_G0290111 | DDB0232432 | CDS | 3671708 | 1644 | + | 0.317518 | |
adprh | DDB_G0289675 | conserved enzyme catalyzes the reaction: N(omega)-(ADP-D-ribosyl)-L-arginine H(2)O ADP-ribose L-arginine reverses the reaction of mono-ADP-ribosylation | DDB0232432 | CDS | 3077727 | 1179 | - | 0.31637 |
agl | DDB_G0287569 | DDB0232432 | CDS | 354336 | 4827 | - | 0.311995 | |
agnB | DDB_G0290377 | DDB0232432 | CDS | 4008116 | 2703 | - | 0.290788 | |
agnE | DDB_G0289367 | DDB0232432 | CDS | 2710003 | 3603 | - | 0.251457 | |
agpB | DDB_G0288523 | DDB0232432 | CDS | 1643762 | 1038 | + | 0.310212 | |
agpC | DDB_G0288863 | DDB0232432 | CDS | 1956943 | 1299 | - | 0.294842 | |
agxt | DDB_G0289923 | ortholog of the conserved AGXT defects in the human AGXT cause primary hyperoxaluria type I | DDB0232432 | CDS | 3442183 | 1224 | + | 0.356209 |
aif | DDB_G0288247 | involved in caspase-independent mitochondrial cell death similar to H. sapiens AIFM1 the mitochondrial Apoptosis-Inducing Factor 1 | DDB0232432 | CDS | 1306170 | 1599 | - | 0.317699 |
anapc3 | DDB_G0288223 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232432 | CDS | 1273822 | 2913 | - | 0.278064 |
ankrd39 | DDB_G0287345 | DDB0232432 | CDS | 159445 | 525 | - | 0.266667 | |
ap2s1 | DDB_G0289721 | DDB0232432 | CDS | 3163717 | 429 | - | 0.261072 | |
aplM | DDB_G0291113 | DDB0232432 | CDS | 4994396 | 1251 | - | 0.242206 | |
apl_ps | DDB_G0288605 | putative pseudogene fragment similar to the family of saposin domain-containing amoebapore-like proteins | DDB0232432 | CDS | 1708038 | 288 | + | 0.25 |
apm1 | DDB_G0289247 | shares 69 | DDB0232432 | CDS | 2536641 | 1287 | + | 0.317793 |
arcE | DDB_G0288319 | component of the Dictyostelium Arp2Arp3 complex | DDB0232432 | CDS | 1410951 | 417 | - | 0.366906 |
arfA | DDB_G0289173 | DDB0232432 | CDS | 2516577 | 549 | + | 0.35337 | |
argS2 | DDB_G0287803 | catalyzes the reaction ATP L-arginine tRNAArg AMP diphosphate L-arginyl-tRNAArg | DDB0232432 | CDS | 724797 | 2217 | + | 0.280108 |
arkA | DDB_G0289555 | suppressor of spalten (spnA) mutant member of the TKL (tyrosine kinase-like) group and ARK (ankyrin repeat-containing kinase) family | DDB0232432 | CDS | 2941850 | 4383 | + | 0.300707 |
arl1 | DDB_G0288163 | DDB0232432 | CDS | 1170444 | 552 | - | 0.304348 | |
arpA | DDB_G0288937 | centrosome-associated actin homolog contributes to the dynactin complex contributes to DdPPK2 activity also described as member of the polyphosphate kinase PPK3 family | DDB0232432 | CDS | 2149735 | 1152 | - | 0.329861 |
arpG | DDB_G0287779 | similar to the actin related protein ARP8 in mammalian called ACTR8 a putative component of a chromatin-remodeling complex | DDB0232432 | CDS | 683410 | 2622 | - | 0.272311 |
arpH | DDB_G0287739 | similar to mammalian and yeast actin related protein 10 part of the dynactin complex | DDB0232432 | CDS | 636584 | 1428 | - | 0.238095 |
arpin | DDB_G0291009 | DDB0232432 | CDS | 4884944 | 675 | - | 0.278519 | |
arrD | DDB_G0289069 | DDB0232432 | CDS | 2306273 | 651 | + | 0.265745 | |
arrF | DDB_G0289435 | DDB0232432 | CDS | 2746763 | 573 | + | 0.273997 | |
arrH | DDB_G0288015 | bCommunity annotations: b The arrH arrJ and arrK genes and no others of the arrX group are strongly (6 to 30-fold) overexpressed in a Dictyostelium strain in which the retinoblastoma-like gene rblA has been disrupted. Most of the genes overexpressed in this strain are associated with cell cycle progression and this suggests that the main role of the corresponding proteins is in S-phase or mitosis. Human Arf1 has been reported to be essential for Golgi complex fragmentation during mitosis (Tang et al JBC 283 6085-94 (2008) Xiang et al JBC 282 21829-37 (2007). It thus seems possible that ArrH ArrJ and ArrK are involved in this process in Dicty. Harry MacWilliams September 2009brbr We have found very similar results including human C. elegans and D. melanogaster sequences in the set of proteins used for the tree. See Weeks G Gaudet P and Insall RH. (2005) The small GTPase superfamily. in Dictyostelium Genomics. Horizon Bioscience. Pascale Gaudet October 2009br | DDB0232432 | CDS | 977719 | 570 | + | 0.282456 |
arsB | DDB_G0289879 | has two putative transmembrane domains bacterial homolog associates with ArsA to transport arsenate selenate and other anionic compounds outside the cell | DDB0232432 | CDS | 3431951 | 1692 | + | 0.253546 |
arv1 | DDB_G0290221 | ortholog of in S. cerevisiae ARV1 that transports glycosylphosphatidylinositol intermediates into the ER lumen required for normal intracellular sterol distribution and for sphingolipid metabolism and required for viability in the absence of ARE2 (ACAT-related enzyme 2) | DDB0232432 | CDS | 3814762 | 741 | + | 0.264507 |
ascc3 | DDB_G0290389 | ortholog of human ASCC3 part of the TRIP4 complex that enhances activation of NF-kappa-B SRF and AP1 | DDB0232432 | CDS | 4020336 | 6588 | - | 0.307377 |
atg101 | DDB_G0288287 | DDB0232432 | CDS | 1352566 | 561 | - | 0.263815 | |
atg5 | DDB_G0289881 | Dictyostelium homolog of yeast atg5 conjugated to atg12 | DDB0232432 | CDS | 3433996 | 1197 | + | 0.230576 |
atg6B | DDB_G0288021 | homolog of S. cerevisiae ATG6 and H. sapiens beclin (BECN1) involved in autophagy and apoptosis | DDB0232432 | CDS | 985635 | 2568 | + | 0.308022 |
auh | DDB_G0289471 | catalyzes the reaction: (S)-3-hydroxy-3-methylglutaryl-CoA trans-3-methylglutaconyl-CoA H2O ortholog of the human AUH protein that was identified as an RNA-binding protein that binds to clustered 5'-AUUUA-3' motifs (EC 4.2.1.18) | DDB0232432 | CDS | 2829282 | 912 | - | 0.309211 |
bcs1lA | DDB_G0289135 | conserved mitochondrial chaperone necessary for the assembly of mitochondrial respiratory chain complex III Dictyostelium has a second BCS1-like protein | DDB0232432 | CDS | 2391473 | 1266 | + | 0.304897 |
bloc1s6 | DDB_G0290921 | ortholog of human BLOC1S6 a component of the BLOC-1 complex mutations in human BLOC1S6 have been linked to Hermansky-Pudlak syndrome 9 | DDB0232432 | CDS | 4755734 | 624 | - | 0.213141 |
bms1l | DDB_G0287891 | DDB0232432 | CDS | 751626 | 3618 | + | 0.298784 | |
bud13 | DDB_G0288703 | ortholog of BUD13 which is involved in mRNA splicing in yeast | DDB0232432 | CDS | 1846726 | 1428 | - | 0.270308 |
bxdc2 | DDB_G0287937 | ortholog of the H. sapiens BXDC2 and S. cerevisiae BRX1 a nucleolar protein involved in the assembly of the large ribosomal subunit | DDB0232432 | CDS | 871082 | 981 | - | 0.313965 |
bysl | DDB_G0288565 | conserved protein in H. sapiens required for processing of 20S pre-rRNA precursor and biogenesis of 40S ribosomal subunits and possibly for trophinin-dependent regulation of cell adhesion | DDB0232432 | CDS | 1691217 | 1428 | - | 0.308123 |
bzpI | DDB_G0290173 | DDB0232432 | CDS | 3736207 | 2226 | - | 0.298293 | |
bzpO | DDB_G0290169 | DDB0232432 | CDS | 3730693 | 2151 | - | 0.251511 | |
bzpP | DDB_G0290303 | DDB0232432 | CDS | 3929845 | 2496 | + | 0.314503 | |
bzpQ | DDB_G0288705 | DDB0232432 | CDS | 1849253 | 2931 | + | 0.282497 | |
bzpR | DDB_G0290165 | DDB0232432 | CDS | 3726519 | 2694 | - | 0.250557 | |
bzpS | DDB_G0290171 | DDB0232432 | CDS | 3733307 | 2532 | - | 0.232622 | |
cap | DDB_G0288769 | component of the endo-lysosomal system links with actin cytoskeleton br bNomenclature conflict:b Do not confuse this gene with capA the cAMP-binding protein | DDB0232432 | CDS | 1946096 | 1395 | + | 0.354839 |
carB | DDB_G0288179 | low affinity cAMP receptor belongs to the serpentineG-protein coupled receptor family | DDB0232432 | CDS | 1252723 | 1128 | + | 0.289007 |
cbpH | DDB_G0288623 | DDB0232432 | CDS | 1770590 | 498 | - | 0.238956 | |
cbpL | DDB_G0288785 | putative Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232432 | CDS | 1964055 | 576 | + | 0.258681 |
ccbl | DDB_G0287269 | catalyzes the reaction L-kynurenine 2-oxoglutarate 4-(2-aminophenyl)-24-dioxobutanoate L-glutamate | DDB0232432 | CDS | 47854 | 1308 | - | 0.33104 |
ccdc124 | DDB_G0289893 | DDB0232432 | CDS | 3369167 | 744 | + | 0.310484 | |
ccs | DDB_G0291031 | copper chaperone that specifically delivers Cu to sod1 copperzinc superoxide dismutase | DDB0232432 | CDS | 4931620 | 951 | - | 0.270242 |
cda | DDB_G0288933 | catalyzes the reactions cytidine Hsub2subO uridine NHsub3sub and Hsub2subO deoxycytidine NHsub3sub deoxyuridine | DDB0232432 | CDS | 2144804 | 444 | - | 0.351351 |
cdc40 | DDB_G0289501 | conserved splicing factor S. cerevisiae cdc40 is important for catalytic step II of pre-mRNA splicing and plays a role in cell cycle progression | DDB0232432 | CDS | 2860682 | 1788 | + | 0.319351 |
cdcD | DDB_G0288065 | highly conserved protein CDC48 in yeasts | DDB0232432 | CDS | 1118593 | 2382 | + | 0.398825 |
cdh1 | DDB_G0287259 | ortholog of FZR1CDH1 that regulates the ubiquitin ligase activity of the anaphase promoting complexcyclosome (APCC) which directs ubiquitination of cyclins resulting in mitotic exit related to cdc20 | DDB0232432 | CDS | 54882 | 2265 | - | 0.284768 |
cdk5 | DDB_G0288677 | CMGC group protein kinase highly similar to mammalian cdk5 localizes to the nucleus and shuttles to the cytoplasm during late mitosis binds calmodulin PsaA | DDB0232432 | CDS | 1885785 | 879 | + | 0.302617 |
cenA | DDB_G0288427 | similar to human Centrin 2 EF-hand protein localizes to the centromer from which it dissociates during mitosis | DDB0232432 | CDS | 1525659 | 456 | + | 0.245614 |
cepC | DDB_G0290509 | DDB0232432 | CDS | 4173965 | 1413 | - | 0.219391 | |
cfrA | DDB_G0290257 | DDB0232432 | CDS | 3901077 | 2193 | + | 0.279982 | |
cfrB | DDB_G0290259 | DDB0232432 | CDS | 3906804 | 2205 | + | 0.277551 | |
cfrC | DDB_G0290261 | DDB0232432 | CDS | 3911024 | 2241 | + | 0.277108 | |
cfrD | DDB_G0290265 | DDB0232432 | CDS | 3914845 | 2259 | + | 0.27977 | |
cfr_ps1 | DDB_G0290271 | putative pseudogene highly similar to cfr (Cell Fusion Related) genes (cell surface glycoprotein GP138) | DDB0232432 | CDS | 3898353 | 2238 | + | 0.262735 |
cfr_ps2 | DDB_G0290269 | putative pseudogene highly similar to cfr (Cell Fusion Related) genes (cell surface glycoprotein GP138) | DDB0232432 | CDS | 3918589 | 543 | + | 0.290976 |
chdh | DDB_G0287229 | catalyzes the reaction: choline acceptor betaine aldehyde reduced acceptor ortholog of the mammalian CHDH contains a putative signal sequence | DDB0232432 | CDS | 24322 | 1770 | - | 0.327684 |
chid1 | DDB_G0290417 | DDB0232432 | CDS | 4060970 | 1158 | - | 0.244387 | |
chlA | DDB_G0290825 | catalyzes the chlorination step in DIF-1 biosynthesis belongs to the FAD-dependent oxidoreductase family belongs to the tryptophan halogenase family | DDB0232432 | CDS | 4647665 | 1812 | - | 0.313466 |
chtB | DDB_G0290617 | DDB0232432 | CDS | 4375423 | 2166 | + | 0.211911 | |
chtC | DDB_G0290959 | similar to heat shock protein Hsp20 domain-containing protein but does not contain a Hsp20 domain | DDB0232432 | CDS | 4833259 | 1956 | + | 0.249489 |
cigA | DDB_G0288245 | DDB0232432 | CDS | 1317088 | 2445 | + | 0.274847 | |
cigB | DDB_G0290067 | DDB0232432 | CDS | 3642812 | 2235 | - | 0.229978 | |
cinB | DDB_G0291121 | DDB0232432 | CDS | 5056007 | 1014 | + | 0.269231 | |
cinC | DDB_G0287685 | translocates peptidyl-tRNA from the aminoacyl site to the peptidyl site on the ribosome during protein synthesis induced by cycloheximide knockdown has significantly reduced ability for protein synthesis | DDB0232432 | CDS | 689907 | 2562 | + | 0.358314 |
cln3 | DDB_G0291157 | ortholog of Cln3 responsible for Batten's disease a juvenile neurological disorder | DDB0232432 | CDS | 5060161 | 1266 | - | 0.313586 |
cmbB | DDB_G0288131 | calmodulin-binding protein comprised of tandem repeats of newly identified IP22 motifs which occur in mimivirus and Dictyostelium IP22 motifs may play a role in cell motility and chemotaxis | DDB0232432 | CDS | 1162843 | 1242 | - | 0.309984 |
cmfB | DDB_G0289157 | DDB0232432 | CDS | 2432359 | 1533 | + | 0.395303 | |
cnrG | DDB_G0287483 | identified as a suppressor of smlA null mutant cnr6 contains a predicted signal peptide similar to Polysphondylium pallidum 64 kDa cell surface glycoprotein | DDB0232432 | CDS | 306749 | 984 | - | 0.273374 |
cnrM | DDB_G0288307 | DDB0232432 | CDS | 1376942 | 4920 | - | 0.293089 | |
cnrN | DDB_G0287969 | identified as a suppressor of smlA null mutant cnr14 phosphatase involved in late-aggregation events including the regulation of fruiting body size as well as cAMP and PI3K signaling | DDB0232432 | CDS | 912043 | 1920 | + | 0.25625 |
cog5 | DDB_G0289535 | highly similar to COG5 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | DDB0232432 | CDS | 2897974 | 2697 | + | 0.229885 |
colA_ps1 | DDB_G0290367 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232432 | CDS | 3904303 | 330 | - | 0.336364 |
colA_ps2 | DDB_G0290293 | putative pseudogene small fragment similar to the large colossin A gene | DDB0232432 | CDS | 3899689 | 312 | - | 0.355769 |
comA | DDB_G0289599 | connects the actin cytoskeleton to the Golgi apparatus bundles actin filaments which is inhibited by mannose | DDB0232432 | CDS | 3003747 | 558 | - | 0.370968 |
copG | DDB_G0289371 | DDB0232432 | CDS | 2724036 | 2697 | + | 0.309974 | |
copZa | DDB_G0289523 | zeta subunit of the coatomer complex essential for the secretory pathway there is another gene encoding a zeta subunit | DDB0232432 | CDS | 2913451 | 528 | - | 0.242424 |
cox10 | DDB_G0288169 | ortholog of COX10 which catalyzes the first step in the conversion of protoheme to the heme A prosthetic group required for cytochrome c oxidase activity contains seven transmembrane domains | DDB0232432 | CDS | 1175200 | 1350 | - | 0.302222 |
cox11 | DDB_G0289353 | ortholog of COX11 the mitochondrial inner membrane protein required for delivering copper to subunit 1 of cytochrome c oxidase. | DDB0232432 | CDS | 2677137 | 939 | + | 0.27263 |
cox17 | DDB_G0288831 | DDB0232432 | CDS | 2045007 | 183 | - | 0.338798 | |
cox19 | DDB_G0288903 | DDB0232432 | CDS | 2105412 | 321 | + | 0.292835 | |
cpnE | DDB_G0290529 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232432 | CDS | 4217898 | 1740 | - | 0.275862 |
cprA | DDB_G0290957 | DDB0232432 | CDS | 4812963 | 1032 | + | 0.312984 | |
crlB | DDB_G0289395 | belongs to the serpentineG-protein coupled receptor family | DDB0232432 | CDS | 2737271 | 1329 | + | 0.243792 |
crlF | DDB_G0290185 | similar to serpentineG-protein coupled receptors contains 7 putative transmembrane domains | DDB0232432 | CDS | 3754060 | 957 | - | 0.267503 |
csaA | DDB_G0289073 | DDB0232432 | CDS | 2342795 | 1545 | - | 0.350809 | |
csn2 | DDB_G0289361 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232432 | CDS | 2705143 | 1350 | + | 0.28 |
ctdspl2 | DDB_G0290365 | DDB0232432 | CDS | 3881786 | 1704 | + | 0.297535 | |
ctrC | DDB_G0291201 | similar to mammalian SLC7A1-4 (solute carrier family 7 members 1 to 4) multi-pass membrane protein contains 15 predicted transmembrane domains | DDB0232432 | CDS | 5112561 | 1641 | - | 0.343693 |
ctxA | DDB_G0289483 | member of the alpha-actininspectrin superfamily dimerizes with cortexillin II involved in cytokinesis and development and associates with the actin cytoskeleton | DDB0232432 | CDS | 2847194 | 1335 | - | 0.347566 |
cupB | DDB_G0289815 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells cells overexpressing antisense mRNA fail to aggregate | DDB0232432 | CDS | 3313764 | 2310 | + | 0.3 |
cupC | DDB_G0289283 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells | DDB0232432 | CDS | 2612450 | 2310 | - | 0.305195 |
cupF | DDB_G0289813 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells | DDB0232432 | CDS | 3317807 | 2310 | + | 0.303463 |
cupG | DDB_G0289883 | highly conserved protein family up-regulated by Ca2 expressed throughout vegetative cells and in the cortex of aggregating cells | DDB0232432 | CDS | 3463581 | 2307 | - | 0.302557 |
cupH | DDB_G0290563 | DDB0232432 | CDS | 4277976 | 2307 | + | 0.303424 | |
cutc | DDB_G0287539 | DDB0232432 | CDS | 396188 | 843 | - | 0.269276 | |
cyp513A2_ps | DDB_G0290981 | putative pseudogene related to the cytochrome P450 family | DDB0232432 | CDS | 4843316 | 924 | + | 0.239177 |
cyp513C1 | DDB_G0291105 | DDB0232432 | CDS | 5007182 | 1488 | - | 0.280914 | |
cyp514A1 | DDB_G0290743 | DDB0232432 | CDS | 4534228 | 1728 | - | 0.24537 | |
cyp514A1_ps | DDB_G0288119 | similar to parts of CYP514A1 a cytochrome P450 family protein | DDB0232432 | CDS | 1068215 | 423 | - | 0.236407 |
cyp514A2 | DDB_G0294561 | DDB0232432 | CDS | 3895673 | 1503 | + | 0.245509 | |
cyp514A4 | DDB_G0290707 | DDB0232432 | CDS | 4469976 | 1509 | + | 0.241219 | |
darA | DDB_G0288771 | putative ortholog of the mammalian guanine nucleotide exchange factor smgGDS a GEF that acts on a broad spectrum of small GTPases (rap1 rac1 cdc42) in Dictyostelium darlin contains 11 armadillo-like repeats it binds to racE and racC but the GEF activity could not be detected using racE as a substrate the darA null mutant is aggregation defective when developed in buffer but the development is normal in the presence of bacteria | DDB0232432 | CDS | 1994269 | 2301 | - | 0.269013 |
dcd3A | DDB_G0288359 | catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine regulated by the MADS-box transcription factor SrfA during developmentbr bNomenclature conflictb: Do not confuse dcd3A (alkaline dihydroceramidase adcA) with adcA (arrestin domain-containing protein) | DDB0232432 | CDS | 1387850 | 867 | + | 0.310265 |
ddi1 | DDB_G0288187 | conserved protein that in S. cerevisiae is a DNA damage-inducible v-SNARE binding protein | DDB0232432 | CDS | 1180046 | 1353 | - | 0.318551 |
ddx41 | DDB_G0287361 | conserved RNA helicase ortholog of D. melanogaster DEAD box protein abstrakt which is required during post-transcriptional gene expression | DDB0232432 | CDS | 183547 | 2016 | - | 0.315476 |
ddx42 | DDB_G0288501 | conserved putative RNA helicase very similar to mammalian DDX42 | DDB0232432 | CDS | 1607944 | 2961 | + | 0.274232 |
derl1 | DDB_G0288833 | component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins contains 5 putative transmembrane domains | DDB0232432 | CDS | 2045678 | 729 | - | 0.292181 |
dgat2 | DDB_G0290279 | conserved diglyceride acyltransferase most similar to U. ramanniana DGAT2B and H. sapiens DGAT2 catalyzing the reaction: acyl-CoA 12-diacylglycerol CoA triacylglycerol | DDB0232432 | CDS | 3856720 | 993 | - | 0.300101 |
dgtA | DDB_G0288321 | CAZy family GT2 catalyzes the reaction UDP-glucose dolichyl phosphate UDP dolichyl beta-D-glucosyl phosphate | DDB0232432 | CDS | 1385100 | 984 | + | 0.272358 |
dhx37 | DDB_G0287351 | ortholog of H. sapiens DHX37 and S. cerevisiae ECM16 an RNA helicase involved in ribosomal biosynthesis | DDB0232432 | CDS | 165026 | 4386 | - | 0.287278 |
dhx8 | DDB_G0291183 | conserved RNA helicase S. cerevisiae ortholog PRP22 mediates ATP-dependent mRNA release from the spliceosome and unwinds RNA duplexes | DDB0232432 | CDS | 5107365 | 3483 | - | 0.335343 |
dlrA | DDB_G0290485 | DDB0232432 | CDS | 4410371 | 2457 | - | 0.299959 | |
dmtA | DDB_G0289329 | DDB0232432 | CDS | 2694067 | 1092 | - | 0.271978 | |
dnase2 | DDB_G0290577 | mammals have two lysosomal DNase II enzymes while Dictyosyelium has just one DNase II catalyzes endonucleolytic cleavage of preferably double-stranded DNA to nucleoside 3'-phosphates and 3'-phosphooligonucleotide end-products. | DDB0232432 | CDS | 4301494 | 1128 | - | 0.29344 |
dnmA | DDB_G0288047 | methylates cytosines in DNA belongs to the dnmt2 subfamily which has weak methylase activity | DDB0232432 | CDS | 1026957 | 1140 | - | 0.240351 |
drg1 | DDB_G0289317 | ortholog of human DRG1 which may be involved in cell proliferation differentiation and death highly conserved in eukaryotes belongs to the GTP1OBG family | DDB0232432 | CDS | 2634493 | 1113 | - | 0.337826 |
drkA | DDB_G0289791 | DDB0232432 | CDS | 3144874 | 1929 | + | 0.276827 | |
drkB | DDB_G0289709 | DDB0232432 | CDS | 3147575 | 2073 | + | 0.2904 | |
drpp20 | DDB_G0289139 | DDB0232432 | CDS | 2393417 | 687 | + | 0.254731 | |
drpp20_ps | DDB_G0289083 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 2336464 | 339 | - | 0.221239 |
drpp21 | DDB_G0290281 | ortholog of RPR2 a subunit of nuclear RNase P which cleaves tRNA precursors to generate mature 5' ends | DDB0232432 | CDS | 3858234 | 675 | - | 0.185185 |
dst4 | DDB_G0288071 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232432 | CDS | 1048762 | 1458 | - | 0.325789 |
dtfA | DDB_G0289389 | DDB0232432 | CDS | 2732174 | 4209 | - | 0.248278 | |
dtymk | DDB_G0290033 | catalyzes the reaction dTMP ATP dTDP ADP in de novo biosynthesis of pyrimidine deoxyribonucleotides | DDB0232432 | CDS | 3573621 | 669 | - | 0.258595 |
dynF | DDB_G0290757 | DDB0232432 | CDS | 4567986 | 570 | - | 0.27193 | |
ecd | DDB_G0287829 | ortholog of the eukaryotic SGT1 or ECD a putative transcription coactivator | DDB0232432 | CDS | 773675 | 2460 | - | 0.222764 |
ecmK | DDB_G0287819 | DDB0232432 | CDS | 764642 | 498 | - | 0.307229 | |
efbA | DDB_G0288373 | translocates peptidyl-tRNA from the aminoacyl site to the peptidyl site on the ribosome during protein synthesis null mutants still synthesis protein suggesting that EF-2b (cinC) is the real translation elongation gector | DDB0232432 | CDS | 1470619 | 2520 | + | 0.418651 |
eif2b1 | DDB_G0288961 | DDB0232432 | CDS | 2146739 | 966 | + | 0.295031 | |
eif2b3 | DDB_G0290693 | EIF2B3 ortholog the eukaryotic initiation factor 2B gamma subunit guanyl nucleotide exchange factor for eIF2 defects are linked to leukoencephalopathy with vanishing white matter | DDB0232432 | CDS | 4424632 | 1323 | + | 0.265306 |
eif2b4 | DDB_G0290759 | ortholog of human EIF2B4 delta subunit of the translation initiation factor eIF2B the guanine-nucleotide exchange factor for eIF2 | DDB0232432 | CDS | 4569158 | 1860 | + | 0.317204 |
eif3J | DDB_G0287333 | EIF3J ortholog the eukaryotic initiation factor alpha subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232432 | CDS | 147100 | 660 | - | 0.263636 |
elp | DDB_G0287987 | similar to elongation factor 2 (EF-2) but lacks the EF-Tu binding domain 2 and EF-G domain EF-2 translocates peptidyl-tRNA from the aminoacyl site to the peptidyl site on the ribosome during protein synthesis | DDB0232432 | CDS | 934832 | 2520 | + | 0.271429 |
elp3 | DDB_G0290103 | similar to ELP3 the histone acetyltransferase subunit of the subunit of the RNA polymerase II elongator complex | DDB0232432 | CDS | 3656306 | 1680 | + | 0.335119 |
empA | DDB_G0288053 | DDB0232432 | CDS | 1036458 | 618 | - | 0.289644 | |
eral1 | DDB_G0288609 | DDB0232432 | CDS | 1740020 | 1197 | - | 0.3066 | |
erf1 | DDB_G0288613 | class I release factor of the translation termination machinery in eukaryotes with the universal genetic code predicted to recognizes all stop codons (UAA UAG and UGA) | DDB0232432 | CDS | 1753244 | 1326 | - | 0.361991 |
espl1 | DDB_G0290325 | caspase-like protease also called separin (ESP1) which plays a central role in sister chromosome segregation in yeastbrbr bCommunity annotation:b espl1 is highly similar to separase (aka separin) a widely-conserved peptidase which cleaves the rad21ssc1 non-SMC subunit of cohesin rings remaining at the centromere at metaphase allowing the sister chromatids to separate. Consistent with this homology espl1 is overexpressed fourfold (p6e-14) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes with roles in S-phase or mitosis are overexpressed in this strain and most of the overexpressed genes have identifiable cell cycle functions. espl1 also shows the developmental time course most typical of cell cycle genes.br The separase inhibitor securin conserved between yeast and humans which is broken down at the metaphaseanaphase junction under control of the spindle checkpoint is not recognizable in Dicty. Securin is also unrecognizable plants however whle | DDB0232432 | CDS | 3958340 | 7284 | - | 0.240527 |
etfa | DDB_G0290927 | electron transfer flavoprotein (ETF) serves as a specific electron acceptor for several dehydrogenases transfers the electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase ( | DDB0232432 | CDS | 4764545 | 1068 | + | 0.338951 |
exoc5 | DDB_G0287881 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232432 | CDS | 652393 | 2937 | - | 0.290092 |
expl7 | DDB_G0288331 | expressed in pstAB cells and in pstAB and stalk cells during the Mexican hat stage and culmination similar to plant expansins which modify the cell wall to allow expansion during cell growth but with a divergent carboxyl terminus contains a predicted signal peptide | DDB0232432 | CDS | 1399818 | 1662 | + | 0.377858 |
fam40 | DDB_G0288685 | DDB0232432 | CDS | 1813615 | 2742 | + | 0.243618 | |
fdxr | DDB_G0287353 | catlyzes the reaction: reduced ferredoxin NADP oxidized ferredoxin NADPH H | DDB0232432 | CDS | 169845 | 1548 | - | 0.26292 |
fip1l1 | DDB_G0288797 | ortholog of yeast FIP1 and mmamalian FIP1L component of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs directly interacts with poly(A) polymerase | DDB0232432 | CDS | 1979163 | 1683 | + | 0.343434 |
fmoA | DDB_G0289779 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3265452 | 1578 | - | 0.255387 |
fmoC | DDB_G0289605 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3016817 | 1566 | - | 0.244572 |
fmoD | DDB_G0289929 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3451742 | 1683 | + | 0.250743 |
fmoE | DDB_G0289931 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3453668 | 1614 | + | 0.245973 |
fmoF | DDB_G0289927 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3449477 | 1590 | + | 0.255346 |
fmoG | DDB_G0289925 | DDB0232432 | CDS | 3446671 | 1611 | + | 0.248293 | |
forC | DDB_G0287295 | formin that contains an N-terminal GBD domain as well as FH2 and FH3 domains but lacks the FH1 domain | DDB0232432 | CDS | 212611 | 3477 | - | 0.297095 |
forF | DDB_G0289763 | diaphanous related formin that binds profilin and is a weak actin nucleator involved in development and phototaxis.br bNomenclature conflict:b Do not confuse this gene with dia1 named for the differentiation associated protein | DDB0232432 | CDS | 3237701 | 3663 | - | 0.323778 |
fscA | DDB_G0289725 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains | DDB0232432 | CDS | 3167501 | 1650 | - | 0.2 |
fslE | DDB_G0288269 | similar to G-protein-coupled receptors weak frizzled cystein-rich domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232432 | CDS | 1290029 | 1830 | - | 0.281421 |
fslF | DDB_G0288253 | similar to G-protein-coupled receptors weak frizzled cystein-rich domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232432 | CDS | 1292298 | 1776 | - | 0.279279 |
fslG | DDB_G0288261 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a putative signal peptide | DDB0232432 | CDS | 1308843 | 1725 | + | 0.277101 |
ftcd | DDB_G0287977 | folate-dependent enzyme displaying both transferase and deaminase activity defects of FTCD in human cause glutamate formiminotransferase deficiency also known as formiminoglutamicaciduria (FIGLU-uria) | DDB0232432 | CDS | 919913 | 1614 | - | 0.350682 |
fthS | DDB_G0290397 | catalyzes the reaction ATP formate tetrahydrofolate ADP phosphate N10-formyl-Hsub4subF in various biosynthetic pathways in plants and in Dictyostelium this is a monofunctional enzyme while in yeast and in metazoan the same enzyme has two additional activities encoded by | DDB0232432 | CDS | 4031914 | 1917 | + | 0.383933 |
gacD | DDB_G0291021 | DDB0232432 | CDS | 4903913 | 1545 | - | 0.311327 | |
gacJJ | DDB_G0290873 | DDB0232432 | CDS | 4700102 | 2622 | + | 0.300153 | |
gacL | DDB_G0290891 | DDB0232432 | CDS | 4722780 | 2205 | - | 0.28254 | |
gacM | DDB_G0287895 | DDB0232432 | CDS | 800059 | 2691 | + | 0.285396 | |
gacW | DDB_G0290439 | DDB0232432 | CDS | 4129372 | 3348 | - | 0.312724 | |
gacX | DDB_G0288205 | DDB0232432 | CDS | 1235608 | 1692 | + | 0.309693 | |
gadB | DDB_G0288715 | catalyzes the reaction L-glutamate 4-aminobutanoate COsub2sub expressed in vegetative cells | DDB0232432 | CDS | 1865900 | 1392 | + | 0.310345 |
gbfA | DDB_G0288755 | DDB0232432 | CDS | 1923643 | 2127 | + | 0.316878 | |
gbpC | DDB_G0291079 | member of the TKL (tyrosine kinase-like) group and ROCO family of protein kinases belongs to the LRRK family of protein kinases contains LRR Roc COR RasGEF protein kinase DEP cyclic nucleotide-binding and GRAM domains involved in cGMP-mediated chemotaxis catalyzes GDP to GTP exchange on its own Roc domain translocates from cytoplasm to cell cortex after cAMP stimulation GRAM domain binds directly to plasma membrane | DDB0232432 | CDS | 4959991 | 7896 | + | 0.333967 |
gchA | DDB_G0288481 | catalyzes the reaction GTP 2 Hsub2subO formate 2-amino-4-hydroxy-6-(erythro-123-trihydroxypropyl)-dihydropteridine triphosphate the first step in the biosynthesis of tetrahydropteridines which have been shown to regulate G-protein coupled signalling the gchA gene is expressed and the enzyme is active during the onset of Dictyostelium development | DDB0232432 | CDS | 1602765 | 699 | - | 0.314735 |
gcvH1 | DDB_G0287773 | DDB0232432 | CDS | 678742 | 441 | + | 0.326531 | |
gcvH2 | DDB_G0290845 | DDB0232432 | CDS | 4668574 | 453 | - | 0.304636 | |
gcvH3 | DDB_G0287791 | DDB0232432 | CDS | 709302 | 450 | + | 0.26 | |
gcvH4 | DDB_G0287795 | DDB0232432 | CDS | 711021 | 630 | - | 0.177778 | |
gcvH5 | DDB_G0287861 | DDB0232432 | CDS | 711961 | 492 | - | 0.182927 | |
gcvP | DDB_G0287255 | catalyzes the reaction glycine H-protein-lipoyllysine H-protein-S-aminomethyldihydrolipoyllysine COsub2sub | DDB0232432 | CDS | 44049 | 2985 | - | 0.352094 |
gefAA | DDB_G0289613 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232432 | CDS | 3026939 | 4116 | - | 0.276968 |
gefD | DDB_G0289667 | DDB0232432 | CDS | 3140427 | 2007 | + | 0.256104 | |
gefK | DDB_G0290901 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232432 | CDS | 4729019 | 4674 | + | 0.272786 |
gefO | DDB_G0290267 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | DDB0232432 | CDS | 3875194 | 2835 | + | 0.274427 |
gefQ | DDB_G0289665 | DDB0232432 | CDS | 3085619 | 3897 | + | 0.254298 | |
gemin2 | DDB_G0287253 | ortholog of Gemin 2SIP1 (Survival of motor neuron protein-interacting protein 1) a component of Cajal bodies (CBs) and Gems nuclear organelles responsible for spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis | DDB0232432 | CDS | 33457 | 996 | + | 0.247992 |
gemin5 | DDB_G0288425 | ortholog of Gemin 5 a component of Cajal bodies (CBs) and Gems nuclear organelles responsible for spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis | DDB0232432 | CDS | 1517710 | 3831 | + | 0.257113 |
gerA | DDB_G0287293 | DDB0232432 | CDS | 191929 | 384 | + | 0.330729 | |
gerB | DDB_G0287687 | DDB0232432 | CDS | 706104 | 384 | - | 0.3125 | |
gerC | DDB_G0287583 | DDB0232432 | CDS | 460750 | 384 | + | 0.330729 | |
gghB | DDB_G0289365 | DDB0232432 | CDS | 2708637 | 1044 | - | 0.229885 | |
gins1 | DDB_G0289271 | subunit 1 of the conserved replication complex GINS which is essential for initiation of DNA replication in X. laevis | DDB0232432 | CDS | 2571168 | 576 | + | 0.243056 |
glb1 | DDB_G0290217 | belongs to glycoside hydrolase family 35 hydrolyzes terminal non-reducing beta-D-galactose residues in beta-D-galactoside has a signal peptide | DDB0232432 | CDS | 3809656 | 2016 | - | 0.312996 |
glk | DDB_G0287631 | catalyzes the reaction ATP D-glucose ADP D-glucose 6-phosphate | DDB0232432 | CDS | 530347 | 1791 | - | 0.319933 |
glnA2 | DDB_G0295755 | catalyzes the reaction ATP L-glutamate ammonia ADP phosphate L-glutamine | DDB0232432 | CDS | 2591112 | 1566 | - | 0.324393 |
glnS | DDB_G0289481 | induced by cycloheximide catalyzes the reaction ATP L-glutamine tRNAGln AMP diphosphate L-glutaminyl-tRNAGln | DDB0232432 | CDS | 2857147 | 2340 | + | 0.335043 |
glpD | DDB_G0291123 | CAZy family GT35 5'-AMP-independent glycogen phosphorylase expressed in late development the combined activities of glpV and glpD results in constant glycogen phosphorylase activity throughout development | DDB0232432 | CDS | 5073815 | 2982 | - | 0.335345 |
gluS | DDB_G0287467 | catalyzes the reaction ATP L-glutamate tRNAGlu AMP diphosphate L-glutamyl-tRNAGlu | DDB0232432 | CDS | 295392 | 2295 | - | 0.34902 |
glud1 | DDB_G0287469 | catalyzes the reaction L-glutamate Hsub2subO NAD(P)supsup 2-oxoglutarate ammonia NAD(P)H Hsupsup acting on the CH-NHsub2sub group of donors with NADsupsup or NADPsupsup as acceptor | DDB0232432 | CDS | 298748 | 1509 | + | 0.404241 |
gmppB | DDB_G0287619 | catalyzes the reaction GTP alpha-D-mannose 1-phosphate diphosphate GDP-mannose | DDB0232432 | CDS | 482074 | 1080 | + | 0.324074 |
gnb1l | DDB_G0289181 | ortholog of the mammalian GNB1L contains several WD-40 repeats | DDB0232432 | CDS | 2444140 | 1080 | + | 0.234259 |
gnrA | DDB_G0291125 | DDB0232432 | CDS | 5022395 | 3264 | - | 0.324449 | |
gnt3 | DDB_G0288463 | CAZy family GT13 catalyzes the reaction UDP-N-acetyl-D-glucosamine 3-(a-D-mannosyl)-b-D-mannosyl-R UDP 3-(2-[N-acetyl-b-D-glucosaminyl]-a-D-mannosyl)-b-D-mannosyl-R | DDB0232432 | CDS | 1556680 | 1497 | + | 0.204409 |
gol | DDB_G0287271 | golgi and vesicle associated protein predominantly targeted to the endosomal pathway | DDB0232432 | CDS | 91906 | 1740 | - | 0.275862 |
gphn | DDB_G0287261 | conserved microtubule-associated protein involved in membrane protein-cytoskeleton interactions implicated in molybdenum cofactor biosynthesis | DDB0232432 | CDS | 61689 | 2157 | - | 0.298563 |
grlP | DDB_G0291095 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232432 | CDS | 4986774 | 4224 | + | 0.241004 |
grlR | DDB_G0287681 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232432 | CDS | 554899 | 4815 | - | 0.244652 |
grxA | DDB_G0290015 | DDB0232432 | CDS | 3542247 | 303 | - | 0.290429 | |
gtaO | DDB_G0289651 | DDB0232432 | CDS | 3001531 | 1536 | + | 0.175781 | |
gtaX | DDB_G0290665 | DDB0232432 | CDS | 4312004 | 1050 | + | 0.202857 | |
gtf2a1 | DDB_G0290327 | encodes the two largest subunits of TFIIA important but not essential for transcriptional activation functioning as either an antirepressor or a coactivator | DDB0232432 | CDS | 3966621 | 933 | - | 0.289389 |
gtf2b | DDB_G0290929 | DDB0232432 | CDS | 4767056 | 978 | + | 0.373211 | |
gtf2e2 | DDB_G0287307 | DDB0232432 | CDS | 111192 | 831 | - | 0.315283 | |
gtf3C5 | DDB_G0289935 | DDB0232432 | CDS | 3457434 | 2598 | - | 0.279831 | |
gxcE | DDB_G0291085 | DDB0232432 | CDS | 4955990 | 1641 | - | 0.252895 | |
gxcH | DDB_G0288377 | DDB0232432 | CDS | 1454380 | 2787 | - | 0.268748 | |
gxcHH | DDB_G0290493 | DDB0232432 | CDS | 4148104 | 2865 | + | 0.26178 | |
gxcI | DDB_G0288383 | DDB0232432 | CDS | 1463358 | 3249 | - | 0.258541 | |
gxcK | DDB_G0291007 | DDB0232432 | CDS | 4881627 | 2892 | + | 0.246542 | |
gxcL | DDB_G0290023 | DDB0232432 | CDS | 3553377 | 2418 | - | 0.296112 | |
hal | DDB_G0288025 | catalyzes the reaction L-histidine urocanate NHsub3sub | DDB0232432 | CDS | 990248 | 1620 | - | 0.335185 |
hbx13 | DDB_G0288975 | DDB0232432 | CDS | 2192060 | 4092 | + | 0.26173 | |
hbx14 | DDB_G0289677 | DDB0232432 | CDS | 3081562 | 1368 | + | 0.274854 | |
hbx3 | DDB_G0291197 | DDB0232432 | CDS | 5094013 | 2004 | + | 0.210579 | |
hdaC_ps1 | DDB_G0287669 | putative pseudogene small fragment similar to | DDB0232432 | CDS | 510322 | 282 | + | 0.397163 |
hdaC_ps4 | DDB_G0349111 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 4281044 | 218 | - | 0.37156 |
hddc2 | DDB_G0290795 | conserved protein HD domains occur in a superfamily of enzymes with a predicted or known phosphohydrolase activity | DDB0232432 | CDS | 4613721 | 573 | - | 0.279232 |
hemF | DDB_G0288893 | catalyzes the reaction coproporphyrinogen-III Osub2sub 2 H protoporphyrinogen-IX 2 COsub2sub 2 Hsub2subO | DDB0232432 | CDS | 2090427 | 999 | + | 0.336336 |
hemH | DDB_G0288891 | catalyzes the reaction protoporphyrin Fesup2sup protoheme 2 Hsupsup in heme biosynthesis | DDB0232432 | CDS | 2088484 | 1272 | - | 0.29717 |
hgsA | DDB_G0288461 | catalyzes the reaction acetyl-CoA H2O acetoacetyl-CoA (S)-3-hydroxy-3-methylglutaryl-CoA CoA | DDB0232432 | CDS | 1582464 | 1449 | - | 0.344375 |
hlcs1 | DDB_G0288791 | functions in post-translational modification of various carboxylases by attachment of biotin similar to human HLCS which when defect causes a neonatal form of multiple carboxylase deficiency Dictytostelium contains three similar enzymes | DDB0232432 | CDS | 1968883 | 1128 | + | 0.289894 |
hlcs2 | DDB_G0288789 | functions in post-translational modification of various carboxylases by attachment of biotin similar to human HLCS which when defect causes a neonatal form of multiple carboxylase deficiency Dictytostelium contains three similar enzymes | DDB0232432 | CDS | 1967179 | 1128 | + | 0.289894 |
hlcs3 | DDB_G0289035 | functions in post-translational modification of various carboxylases by attachment of biotin similar to human HLCS which when defect causes a neonatal form of multiple carboxylase deficiency Dictytostelium contains three similar enzymes | DDB0232432 | CDS | 2283370 | 1215 | + | 0.288889 |
hook | DDB_G0288691 | similar to C. elegans ZYG-12 and mammalian HOOK proteins which mediates the attachment between the centrosome and the nucleus | DDB0232432 | CDS | 1822874 | 2205 | + | 0.275737 |
hspA | DDB_G0288181 | involved in phototaxis growth and morphogenesis and implicated in mitochondrial disease | DDB0232432 | CDS | 1238068 | 1671 | + | 0.36146 |
hspH | DDB_G0290187 | DDB0232432 | CDS | 3818443 | 2319 | + | 0.378611 | |
hspI | DDB_G0288921 | DDB0232432 | CDS | 2124478 | 672 | - | 0.258929 | |
hydA | DDB_G0290479 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | DDB0232432 | CDS | 4230498 | 1485 | - | 0.323906 |
iliD | DDB_G0287717 | similar to hypothetical fungi proteins induced by Legionella pneumophila infection | DDB0232432 | CDS | 597404 | 1206 | + | 0.324212 |
ipi | DDB_G0290011 | DDB0232432 | CDS | 3572751 | 720 | + | 0.279167 | |
iqgC | DDB_G0288977 | contains a rasGAP domain similar to mammalian IQGAP proteins but lacking the calponin domain and the IQ-calmodulin binding region | DDB0232432 | CDS | 2198403 | 2454 | + | 0.347596 |
irlE | DDB_G0288803 | putative protein serinethreonine kinase the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy | DDB0232432 | CDS | 1985593 | 4053 | + | 0.237602 |
jcdA | DDB_G0290765 | DDB0232432 | CDS | 4576700 | 759 | + | 0.262187 | |
jcdF | DDB_G0290869 | DDB0232432 | CDS | 4697072 | 1425 | - | 0.261053 | |
jcdG | DDB_G0287513 | conserved protein similar to H. sapiens C14orf169 | DDB0232432 | CDS | 349945 | 1545 | - | 0.322977 |
jcdJ | DDB_G0288859 | DDB0232432 | CDS | 2000009 | 2874 | + | 0.265136 | |
kif1 | DDB_G0290963 | ortholog of C. elegans Unc104 and mammalian KIF1A involved in intracellular transport | DDB0232432 | CDS | 4896037 | 6618 | - | 0.316863 |
kif11 | DDB_G0291039 | DDB0232432 | CDS | 4850945 | 2058 | - | 0.306122 | |
kif13 | DDB_G0288361 | belongs to the BimCEg5 subfamily predicted to play a role in mitosis | DDB0232432 | CDS | 1422250 | 3798 | + | 0.28673 |
kinY | DDB_G0289661 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family similar to LIM kinases which regulate actin dynamics | DDB0232432 | CDS | 3255902 | 1740 | + | 0.251149 |
kxcA | DDB_G0289859 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family contains calmodulin-binding RhoGEF and pleckstrin homology (PH) domains | DDB0232432 | CDS | 3309104 | 3936 | + | 0.256352 |
kxcA_ps | DDB_G0289983 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 3466598 | 351 | - | 0.264957 |
limD1 | DDB_G0287507 | DDB0232432 | CDS | 361279 | 597 | + | 0.335008 | |
lis1 | DDB_G0288375 | dynein regulator associated with centrosomes and microtubules functionally interacts with dcx in cAMP signalling | DDB0232432 | CDS | 1452516 | 1260 | + | 0.35 |
litaf | DDB_G0289149 | D. dicoideum ortholog of the conserved lipopolysaccharide-induced tumor necrosis factor alpha factor (LITAF) induced in mamalian cells following treatment with lipopolysaccharide a small integral membrane protein of lysosomelate endosome contains one predicted transmembrane domain | DDB0232432 | CDS | 2419396 | 546 | + | 0.377289 |
lmnB | DDB_G0289429 | similar to mammalian lamin B1 localizes to the inner membrane of the nuclear envelope involved in chromatin and centrosome organization and stabilization | DDB0232432 | CDS | 2787284 | 2151 | + | 0.317062 |
lrrB | DDB_G0287823 | DDB0232432 | CDS | 766914 | 2565 | - | 0.267057 | |
lsm7 | DDB_G0289499 | DDB0232432 | CDS | 2859869 | 294 | - | 0.292517 | |
lsm8 | DDB_G0288479 | DDB0232432 | CDS | 1585841 | 285 | - | 0.322807 | |
lyrm4 | DDB_G0290725 | belongs to a family of short proteins that includes proteins from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | DDB0232432 | CDS | 4502665 | 246 | - | 0.247967 |
lzic | DDB_G0288823 | DDB0232432 | CDS | 2035104 | 579 | + | 0.26943 | |
macA | DDB_G0288533 | DDB0232432 | CDS | 1652258 | 6126 | - | 0.254163 | |
mad1 | DDB_G0287755 | conserved component of the spindle-assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate localized to centromeres during mitosis | DDB0232432 | CDS | 658379 | 2460 | - | 0.208537 |
manF | DDB_G0287231 | DDB0232432 | CDS | 28270 | 2985 | - | 0.271692 | |
manG | DDB_G0287577 | DDB0232432 | CDS | 413359 | 3264 | - | 0.321385 | |
maoA | DDB_G0288541 | catalyzes the reaction RCHsub2subNHsub2sub Hsub2subO Osub2sub RCHO ammonia Hsub2subOsub2sub acts on primary amines as well as on some secondary and tertiary amines | DDB0232432 | CDS | 1658897 | 1371 | - | 0.358133 |
mapbpip | DDB_G0291091 | in mammalian cells involved in late endosome function mutations in the human ortholog causes an immunodeficiency syndrome | DDB0232432 | CDS | 4971500 | 372 | - | 0.276882 |
matA | DDB_G0289165 | DDB0232432 | CDS | 2438822 | 324 | - | 0.317901 | |
mccA | DDB_G0287377 | catalyzes the reaction ATP 3-methylcrotonoyl-CoA HCOsub3subsup-sup ADP phosphate 3-methylglutaconyl-CoA | DDB0232432 | CDS | 230145 | 2100 | + | 0.369048 |
mcfS | DDB_G0290913 | similar to slc25a20 involved in transport of carnitineacylcarnitine across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | DDB0232432 | CDS | 4740703 | 858 | + | 0.343823 |
mcfW | DDB_G0290669 | belongs to the substrate carrier proteins that are involved in energy transferbrbr bCommunity annotation:b Overview of the | DDB0232432 | CDS | 4316139 | 990 | - | 0.3 |
mdhA | DDB_G0290207 | catalyzes the reaction malate NAD oxaloacetate NADH | DDB0232432 | CDS | 3795307 | 1176 | - | 0.330782 |
med10 | DDB_G0290209 | ortholog of the mediator of RNA polymerase II transcription subunit 10 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232432 | CDS | 3797080 | 660 | - | 0.234848 |
med20 | DDB_G0290781 | ortholog of the mediator of RNA polymerase II transcription subunit 20 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232432 | CDS | 4593057 | 588 | - | 0.304422 |
med21 | DDB_G0289339 | ortholog of the mediator of RNA polymerase II transcription subunit 21 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232432 | CDS | 2661517 | 594 | + | 0.333333 |
med24 | DDB_G0289971 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription 24 (metazoa) or subunit 5 (fungi) the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232432 | CDS | 3401311 | 6111 | + | 0.231222 |
metK | DDB_G0291179 | catalyzes the reaction ATP L-methionine Hsub2subO phosphate pyrophosphate S-adenosyl-L-methionine | DDB0232432 | CDS | 5102281 | 1155 | - | 0.406926 |
mf12 | DDB_G0288067 | DDB0232432 | CDS | 1125741 | 4554 | + | 0.284365 | |
mfsd1 | DDB_G0289201 | ortholog of the human MSFD1 also knon as SMAP-4 (Smooth Muscle cell-Associated Protein 4) contains 10 putative transmembrane domains and an additional potential signal peptide | DDB0232432 | CDS | 2461603 | 1521 | - | 0.336621 |
mgp1 | DDB_G0290233 | DDB0232432 | CDS | 3834823 | 2763 | + | 0.287007 | |
mhkB | DDB_G0289115 | myosin heavy chain kinase an atypical protein serinethreonine kinase in the Alpha kinase group participates in the regulation of myosin II assembly into the cytoskeleton | DDB0232432 | CDS | 2375954 | 2199 | + | 0.289677 |
mhkC | DDB_G0290687 | myosin heavy chain kinase an atypical protein serinethreonine kinase in the Alpha kinase group drives the disassembly of myosin II filaments for efficient cytokinesis REMI mutant forms aberrant fruiting bodies see | DDB0232432 | CDS | 4426907 | 2343 | - | 0.349979 |
miox | DDB_G0290161 | catalyzes the reaction myo-inositol Osup2sup D-glucuronate Hsup2supO | DDB0232432 | CDS | 3722127 | 879 | + | 0.269625 |
mkcB | DDB_G0290723 | similar to Dictyostelium mkcA and other mitogen-activated protein kinases (Ste20PAK family) REMI mutant forms aberrant fruiting bodies see | DDB0232432 | CDS | 4499748 | 2145 | + | 0.332867 |
mkcC | DDB_G0287853 | kinase domain very similar to those of Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) | DDB0232432 | CDS | 826726 | 2676 | + | 0.342302 |
mkpA | DDB_G0288249 | contains a dual specificity protein phosphatase domain and a weak gelsolin domain dual specificity protein phosphatases regulate mitogenic signal transduction and control the cell cycle REMI mutant fails to aggregate see | DDB0232432 | CDS | 1323200 | 4632 | - | 0.251727 |
mlcB | DDB_G0290077 | light chain that binds to the neck region of myoB contains two calcium-binding EF-hands | DDB0232432 | CDS | 3622051 | 222 | + | 0.315315 |
mlcC | DDB_G0289563 | light chain that binds to the neck region of myoC contains two calcium-binding EF-hand motifs but does not bind calcium | DDB0232432 | CDS | 2954406 | 225 | - | 0.311111 |
mlh1 | DDB_G0287393 | MLH1 ortholog required for DNA mismatch repair | DDB0232432 | CDS | 247623 | 2655 | - | 0.282109 |
mms19 | DDB_G0288217 | DDB0232432 | CDS | 1259948 | 3348 | + | 0.233572 | |
mmsdh | DDB_G0289085 | catalyzes the reaction 2-methyl-3-oxopropanoate CoA NAD propanoyl-CoA COsub2sub NADH Hsupsup | DDB0232432 | CDS | 2337171 | 1587 | + | 0.389414 |
mnat1 | DDB_G0289079 | DDB0232432 | CDS | 2330339 | 978 | + | 0.293456 | |
morg1 | DDB_G0289711 | ortholog of MORG1 a molecular scaffold protein that acts as a module in the assembly of a multicomponent scaffold for the ERK (extracellular signal-regulated kinase) pathway contains 7 WD40 repeats | DDB0232432 | CDS | 3150155 | 978 | - | 0.260736 |
mppA2 | DDB_G0290997 | the mitochondrial processing peptidase removes the transit peptide from the precursor form of proteins imported from the cytoplasm across the mitochondrial inner membrane consists of an alpha and a beta ( | DDB0232432 | CDS | 4869039 | 1338 | - | 0.35725 |
mppB | DDB_G0288777 | removes the transit peptide from the precursor form of proteins imported from the cytoplasm across the mitochondrial inner membrane consists of an alpha ( | DDB0232432 | CDS | 1942737 | 1410 | - | 0.358156 |
mppB_ps | DDB_G0288775 | putative pseudogene fragment very similar to | DDB0232432 | CDS | 1938769 | 210 | - | 0.380952 |
mrpRNA | DDB_G0295629 | RNA component of the RNase MRP ribonucleoprotein which is involved in processing of rRNA in the nucleus and replication of mitochondrial DNA | DDB0232432 | CDS | 3919905 | 366 | + | 0.363388 |
mrpl21 | DDB_G0288799 | DDB0232432 | CDS | 1981150 | 519 | - | 0.265896 | |
mrpl3 | DDB_G0288983 | DDB0232432 | CDS | 2204231 | 1056 | - | 0.321023 | |
msrB | DDB_G0291145 | catalyzes the reaction L-methionine oxidized thioredoxin L-methionine R-oxide reduced thioredoxin | DDB0232432 | CDS | 5047547 | 573 | + | 0.267016 |
mut | DDB_G0287563 | catalyzes the reaction (R)-methylmalonyl-CoA succinyl-CoA vitamin B12 dependent based on similarity with other MUT enzymes this protein is truncated at the N-terminus and might not be catalytically active the fragment contains the B12 binding site | DDB0232432 | CDS | 422254 | 921 | - | 0.396308 |
mvpB | DDB_G0291127 | DDB0232432 | CDS | 5070813 | 2541 | + | 0.387249 | |
mybD | DDB_G0287637 | DDB0232432 | CDS | 536098 | 1788 | + | 0.182886 | |
mybG | DDB_G0288783 | DDB0232432 | CDS | 1962158 | 1272 | + | 0.284591 | |
mybI | DDB_G0289151 | DDB0232432 | CDS | 2425624 | 2934 | - | 0.271643 | |
mybO | DDB_G0290787 | bCommunity annotation:b Myb0 appears to be related to both DUO3 of plants and Gon-4 of animals. DUO3 regulates cell cycle progression in developing pollen and appear to be specifically necessary for mitosis as mutant cells accumulate in G2 or become polyploid. DUO3 is expressed in somatic plant tissues mainly in meristerms suggesting a role in cell proliferation though it is apparently has no unique function in this case. In gon-4 (gonadless) mutants of C elegans the gonadal precursors Z1 and Z4 fail to divide. The reason is not known. DUO3 Gon-4 share and MybO share two short sequence motifs called the Gc1 and Gc2 regions. Myb0 has an additional simlarity to DUO3 in the region between 876 and 1031 which is similar to the DUO3-conserved region 2. This is not present in Gon-4 proteins. Myb0 contains an extended myb-like domain at its C-terminus. In this respect MybO resembles Gon-4. Duo3 does not have a myb domain of any kind however it interacts with DUO1 which has an R2R3 class myb do | DDB0232432 | CDS | 4599542 | 3984 | + | 0.259538 |
mybQ | DDB_G0289319 | DDB0232432 | CDS | 2641022 | 2730 | - | 0.334066 | |
mybX | DDB_G0288285 | DDB0232432 | CDS | 1347341 | 4863 | - | 0.282747 | |
myoB | DDB_G0289117 | long tailed class-1 myosin a molecular motor protein that localizes to actin-rich structures at the leading edge of migrating cells | DDB0232432 | CDS | 2410248 | 3336 | + | 0.351619 |
myoE | DDB_G0288679 | (unconventional) class I myosin fast motor molecule involved in phagocytosis | DDB0232432 | CDS | 1829072 | 3018 | - | 0.336978 |
myoF | DDB_G0289177 | DDB0232432 | CDS | 2531958 | 3216 | - | 0.28607 | |
myoH | DDB_G0289447 | DDB0232432 | CDS | 2840200 | 5316 | - | 0.258653 | |
nae1 | DDB_G0287965 | conserved regulatory subunit of the dimeric UBA3-NEA1 E1 enzyme which activates NEDD8 necessary for cell cycle progression through the S-M checkpoint | DDB0232432 | CDS | 887341 | 1563 | + | 0.287268 |
nagC | DDB_G0287597 | DDB0232432 | CDS | 449924 | 1683 | + | 0.24896 | |
nagD | DDB_G0287659 | DDB0232432 | CDS | 447833 | 1695 | + | 0.316814 | |
nat1 | DDB_G0288509 | DDB0232432 | CDS | 1625652 | 921 | + | 0.261672 | |
nat2 | DDB_G0288503 | DDB0232432 | CDS | 1622564 | 978 | + | 0.230061 | |
nat3 | DDB_G0288507 | DDB0232432 | CDS | 1624317 | 900 | + | 0.243333 | |
ncapG2 | DDB_G0288819 | component of the condensin II complex which is involved in physical rigidity of the chromatid axis | DDB0232432 | CDS | 2028467 | 4314 | - | 0.244089 |
ncfA | DDB_G0288773 | homolog of the essential mammalian neutrophil cytosolic factor p67 that functions as an NADPH oxidase activator contains N-terminal TPR repeats and a C-terminal WW domain | DDB0232432 | CDS | 2003648 | 1815 | - | 0.32011 |
ncstn | DDB_G0287801 | component of the gamma-secretase complex which executes the intramembrane proteolysis of type I integral membrane proteins | DDB0232432 | CDS | 721592 | 1980 | - | 0.291414 |
ndrB | DDB_G0288753 | member of the AGC kinase group similar to NDR protein kinases including yeast morphogenesis proteins ORB6 and CBK1 | DDB0232432 | CDS | 1909293 | 1629 | - | 0.324125 |
ndrD | DDB_G0289543 | member of the AGC kinase group NDR family related to mammalian LATS1 and LATS2 (LArge Tumor Suppressor homolog) kinases | DDB0232432 | CDS | 2920470 | 6339 | + | 0.255088 |
ndufa6 | DDB_G0291129 | accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to be not involved in catalysis | DDB0232432 | CDS | 5026489 | 375 | + | 0.290667 |
ndufaf5 | DDB_G0287769 | conserved mitochondrial complex I (CI) assembly factor which when mutated in human leads to mitochondrial disease in Dictyostelium mutations in the ndufaf5 gene cause defects in growth and development and autophagy is increased. | DDB0232432 | CDS | 675763 | 1311 | - | 0.254767 |
ndufv1 | DDB_G0288875 | DDB0232432 | CDS | 2127210 | 1440 | + | 0.359028 | |
ndufv2 | DDB_G0291173 | DDB0232432 | CDS | 5096341 | 744 | - | 0.319892 | |
nek4 | DDB_G0289277 | similar to vertebrate Nek kinases which are involved in regulation of mitosis most similar to Nek4 | DDB0232432 | CDS | 2561379 | 1494 | - | 0.222222 |
nhe4 | DDB_G0290253 | DDB0232432 | CDS | 3840207 | 3027 | - | 0.327387 | |
nipsnap | DDB_G0288989 | DDB0232432 | CDS | 2209540 | 672 | + | 0.269345 | |
nit2 | DDB_G0287939 | DDB0232432 | CDS | 872348 | 987 | - | 0.274569 | |
nmd3_ps | DDB_G0288881 | putative pseudogene fragment similar to D. discoideum gene | DDB0232432 | CDS | 2082521 | 138 | + | 0.347826 |
nola2 | DDB_G0289699 | component of the HACA small nucleolar ribonucleoprotein (HACA snoRNP) complex required for pre-mRNA processing and pseudouridylation | DDB0232432 | CDS | 3120417 | 435 | + | 0.303448 |
nola3 | DDB_G0288347 | component of the HACA small nucleolar ribonucleoprotein (HACA snoRNP) complex required for pre-mRNA processing and pseudouridylation | DDB0232432 | CDS | 1416040 | 195 | + | 0.323077 |
nop14 | DDB_G0287537 | DDB0232432 | CDS | 388563 | 2955 | - | 0.264298 | |
noxA | DDB_G0289653 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation | DDB0232432 | CDS | 3117432 | 1554 | - | 0.310811 |
noxC | DDB_G0291117 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation contains calcium-binding EF hand | DDB0232432 | CDS | 5017189 | 3429 | - | 0.222514 |
npl4 | DDB_G0290227 | ortholog of NPL4 together with ufd1 and cdcD involved in recognition of polyubiquitinated proteins and their presentation to the 26S proteasome for degradation | DDB0232432 | CDS | 3827990 | 1731 | - | 0.312536 |
nubpl | DDB_G0291193 | conserved protein belongs to the MrpNBP35 ATP-binding protein family | DDB0232432 | CDS | 5087724 | 972 | - | 0.304527 |
nudt19 | DDB_G0290277 | ortholog of human NUDT19 a Coenzyme A diphosphatase that mediates the hydrolysis of a wide range of CoA esters | DDB0232432 | CDS | 3853979 | 1089 | + | 0.266299 |
nup133 | DDB_G0287497 | component of the nuclear pore complex which plays a role in RNA export | DDB0232432 | CDS | 329850 | 3621 | + | 0.254073 |
nup155 | DDB_G0291163 | component of the nuclear pore complex may be involved both in binding and translocating proteins | DDB0232432 | CDS | 5077769 | 4728 | - | 0.271151 |
nup210 | DDB_G0288545 | similar to nuclear pore membrane glycoprotein 210 human NUP210 is essential for nuclear pore assembly contains one putative transmembrane domain and a signal sequence | DDB0232432 | CDS | 1669968 | 5751 | + | 0.311076 |
oatA | DDB_G0287913 | catalyzes the reaction L-ornithine a 2-oxo acid L-glutamate 5-semialdehyde an L-amino acid | DDB0232432 | CDS | 841784 | 1251 | + | 0.406875 |
ogdh | DDB_G0288127 | component of the 2-oxoglutarate dehydrogenase complex which catalyzes the conversion of 2-oxoglutarate to succinyl-CoA and COsub2sub | DDB0232432 | CDS | 1102242 | 3042 | + | 0.36785 |
omt10 | DDB_G0290719 | DDB0232432 | CDS | 4487859 | 1314 | + | 0.2793 | |
omt9 | DDB_G0289823 | DDB0232432 | CDS | 3290073 | 1074 | - | 0.286778 | |
osbK | DDB_G0288817 | DDB0232432 | CDS | 2025270 | 1716 | - | 0.321678 | |
ost2 | DDB_G0291049 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST2 and human DAD1 (Defender Against cell Death 1) contains three transmembrane domains | DDB0232432 | CDS | 4827309 | 363 | - | 0.267218 |
oxct | DDB_G0288105 | catalyzes the reaction succinyl-CoA a 3-oxo acid succinate a 3-oxoacyl-CoA defects in human OXCT1 are a cause of ketoacidosis | DDB0232432 | CDS | 1121891 | 1530 | + | 0.357516 |
p2xD | DDB_G0288335 | DDB0232432 | CDS | 1403868 | 1224 | + | 0.269608 | |
p2xE | DDB_G0288061 | member of the Dictyostelium P2X receptor family membrane ion channel activated by ATP may be involved in intracellular calcium signaling | DDB0232432 | CDS | 1030842 | 1167 | + | 0.291345 |
p80 | DDB_G0287297 | endosome phagosome membrane protein contains a putative signal peptide | DDB0232432 | CDS | 134806 | 1593 | - | 0.364093 |
pXi | DDB_G0289119 | CAMK group protein serinethreonine kinase | DDB0232432 | CDS | 2420542 | 2076 | - | 0.25289 |
pabpc1B | DDB_G0290745 | similar to mammalian PABPC1 involved in cytoplasmic regulatory processes of mRNA metabolism binding the poly(A) tail of mRNA contains an additional N-terminal H-rich domain | DDB0232432 | CDS | 4494408 | 2445 | + | 0.325153 |
panC | DDB_G0288935 | catalyzes the reaction ATP (R)-pantoate beta-alanine AMP diphosphate (R)-pantothenate | DDB0232432 | CDS | 2148704 | 903 | + | 0.27021 |
papA | DDB_G0288259 | RNA polymerase that specifically incorporates ATP at the 3' end of mRNA | DDB0232432 | CDS | 1302980 | 2430 | + | 0.327572 |
pcna | DDB_G0287607 | DDB0232432 | CDS | 463300 | 777 | - | 0.352638 | |
pde4 | DDB_G0289121 | DDB0232432 | CDS | 2402421 | 3120 | + | 0.233333 | |
pde7 | DDB_G0289145 | DDB0232432 | CDS | 2414259 | 1278 | - | 0.27856 | |
pdx1 | DDB_G0288299 | DDB0232432 | CDS | 1363519 | 918 | + | 0.37037 | |
pdx2 | DDB_G0288305 | member of the SNO glutamine amidotransferase family predicted to be involved in the pyridoxine (vitamin B6) biosynthetic pathway catalyzes the deamidation of glutamine as part of the synthesis of pyridoxal 5'-phosphate the resulting ammonia molecule is channeled to pdxS | DDB0232432 | CDS | 1361910 | 747 | - | 0.238286 |
pefA | DDB_G0291081 | similar to mammalian apoptosis component ALG-2 contains 5 EF-hand calcium binding domains | DDB0232432 | CDS | 4974992 | 594 | - | 0.340067 |
pemtB | DDB_G0289645 | homolog of mammalian PEMT and S. cerevisiae OPI3 which catalyzes the steps in phosphatidylcholine biosynthesis | DDB0232432 | CDS | 3055772 | 603 | + | 0.263682 |
pex1 | DDB_G0289867 | ortholog of peroxin 1 AAA-family ATPase peroxin required for peroxisome biogenesis mutations in human homolog cause a variety of peroxisomal disorders | DDB0232432 | CDS | 3340420 | 3684 | + | 0.253529 |
pex11 | DDB_G0289623 | ortholog of peroxisomal protein peroxin 11 contains three putative transmembrane domains | DDB0232432 | CDS | 3044413 | 765 | - | 0.287582 |
pfdn1 | DDB_G0287827 | DDB0232432 | CDS | 772980 | 348 | - | 0.238506 | |
pgkA | DDB_G0287595 | catalyzes the reaction 3-phosphoglycerate ATP 3-phospho-D-glyceroyl-phosphate ADP binds and is regulated by calmodulin | DDB0232432 | CDS | 494968 | 1263 | - | 0.364212 |
pgmA | DDB_G0288483 | catalyzes the reaction alpha-D-glucose 1-phosphate alpha-D-glucose 6-phosphate | DDB0232432 | CDS | 1620141 | 1719 | - | 0.34555 |
pgtB | DDB_G0290079 | CAZy family GT24 disruption of this gene results in abolished spore coat lectin-binding and renders spores hypersensitive to plasmolysis | DDB0232432 | CDS | 3623616 | 4017 | + | 0.300971 |
phbA | DDB_G0290123 | ortholog of the yeast Phb1p and other prohibitins that are inner mitochondrial membrane chaperones that stabilize newly synthesized proteins also suggested to play a role in cell senescence | DDB0232432 | CDS | 3692217 | 816 | - | 0.300245 |
phg1c | DDB_G0290159 | DDB0232432 | CDS | 3751345 | 1968 | - | 0.254573 | |
pho2a | DDB_G0290263 | catalytic subunit of protein phosphatase 2A composed of a catalytic subunit (pho2A) a regulatory subunit (phr2AB) and a scaffold subunit (pppA) an additional regulatory B56 (psrA) subunit has been identified | DDB0232432 | CDS | 3933600 | 921 | - | 0.336591 |
pich | DDB_G0288873 | ortholog of human DNA excision repair protein ERCC-6-like (ERCC6L)br bCommunity annotation:b DDB_G0288873 but not ercc6 is strongly overexpressed (6x) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most cells involved in S-phase or mitosis are overexpressed in this strain. Ercc6-like is an essential component of the spindle checkpoint which localizes to the kinetochore in prometaphase it is found on thin threads that stretch between sister kinetochores. It is thought to function as part of the tension sensor the functional core of the spindle checkpoint [see Baumann et al Cell 128 101-114 (2007)]. Other spindle checkpoint components are strongly overexpressed in the rblA null. This suggests that DDB_G0288873 may actually code for the spindle tension sensor in Dicty. Harry MacWilliams May 2010br | DDB0232432 | CDS | 2065550 | 3999 | - | 0.295074 |
pigM | DDB_G0288899 | CAZy family GT50 catalyzes the addition of the first mannose to GPI (glycosylphosphatidylinositol) | DDB0232432 | CDS | 2094858 | 1329 | + | 0.234763 |
pigS | DDB_G0289515 | DDB0232432 | CDS | 2896095 | 1224 | - | 0.253268 | |
pikD | DDB_G0288485 | subunit of PI4K responsible for the phosphorylation of phosphatidylinositol (PI) to PI4P (ATP 1-phosphatidyl-1D-myo-inositol ADP 1-phosphatidyl-1D-myo-inositol 4-phosphate) the first committed step in the generation of phosphatidylinositol 45-bisphosphate (PIP2) a precursor of the second messenger inositol 145-trisphosphate (InsP3) | DDB0232432 | CDS | 1616073 | 3543 | + | 0.269828 |
pikE | DDB_G0289601 | ortholog of yeast VPS34 a phosphatidylinositol 3-kinase | DDB0232432 | CDS | 3005109 | 2451 | - | 0.299878 |
pikH | DDB_G0291093 | putative PI3k putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring unlike other PI3Ks does not contain a ras binding domain but a PH domain and does not localize to the cell cortex upon chemotactic stimulation | DDB0232432 | CDS | 4980832 | 5463 | - | 0.242541 |
pirA | DDB_G0287855 | DDB0232432 | CDS | 727908 | 4011 | + | 0.354026 | |
pitA | DDB_G0290069 | DDB0232432 | CDS | 3651511 | 795 | + | 0.31195 | |
pkgB | DDB_G0290157 | AGC group protein serinethreonine kinase cAMP-activated protein kinase involved in morphogenesis during multicellular development | DDB0232432 | CDS | 3717777 | 1440 | - | 0.324306 |
pkiA | DDB_G0289391 | DDB0232432 | CDS | 2783089 | 384 | + | 0.351562 | |
pks26 | DDB_G0288457 | DDB0232432 | CDS | 1543867 | 7596 | + | 0.253818 | |
pks27 | DDB_G0290467 | DDB0232432 | CDS | 4086338 | 8055 | + | 0.259963 | |
pks28 | DDB_G0290469 | DDB0232432 | CDS | 4095634 | 8073 | + | 0.25703 | |
pks29 | DDB_G0290699 | DDB0232432 | CDS | 4438040 | 9321 | - | 0.239352 | |
pks30 | DDB_G0290701 | DDB0232432 | CDS | 4448854 | 9228 | - | 0.242306 | |
pks31 | DDB_G0290703 | DDB0232432 | CDS | 4460222 | 7872 | - | 0.244538 | |
pks32 | DDB_G0290709 | DDB0232432 | CDS | 4472163 | 9306 | - | 0.239415 | |
pks33 | DDB_G0290729 | DDB0232432 | CDS | 4507516 | 9330 | + | 0.237621 | |
pks34 | DDB_G0290737 | DDB0232432 | CDS | 4522863 | 9237 | - | 0.239472 | |
pks35 | DDB_G0295667 | DDB0232432 | CDS | 4539649 | 7545 | + | 0.249304 | |
pks36 | DDB_G0295659 | DDB0232432 | CDS | 4550115 | 8796 | + | 0.243179 | |
pks38 | DDB_G0290937 | DDB0232432 | CDS | 4772842 | 9402 | - | 0.237184 | |
pks39 | DDB_G0290943 | DDB0232432 | CDS | 4786202 | 9327 | - | 0.237483 | |
pldY | DDB_G0287649 | highly similar to mammalian PLD3 which is of unknown function | DDB0232432 | CDS | 458523 | 1317 | - | 0.290053 |
pno1 | DDB_G0287557 | conserved protein in S. cerevisiae a nucleolar protein required for pre-18S rRNA processing | DDB0232432 | CDS | 417964 | 720 | + | 0.290278 |
ponJ | DDB_G0289919 | DDB0232432 | CDS | 3425059 | 705 | + | 0.296454 | |
ponL | DDB_G0288649 | structurally similar to ponticulins contains a putative signal peptide | DDB0232432 | CDS | 1782283 | 435 | + | 0.271264 |
pop4 | DDB_G0288543 | DDB0232432 | CDS | 1668067 | 759 | - | 0.258235 | |
ppt2 | DDB_G0288807 | very similar to human PPT2 an enzyme which catalyzes the reaction: palmitoyl-protein Hsub2subO palmitate protein | DDB0232432 | CDS | 1997456 | 915 | - | 0.272131 |
prfB | DDB_G0288835 | required for the termination of protein biosynthesis class I release factors bind to ribosomes that have encountered a stop codon at their decoding site and induce release of the nascent polypeptide mediates UAA and UGA-dependent termination in prokaryotes | DDB0232432 | CDS | 2047432 | 1275 | + | 0.28549 |
prmt2 | DDB_G0289445 | DDB0232432 | CDS | 2803733 | 1539 | - | 0.275504 | |
prmt5 | DDB_G0287327 | Skb1 (Shk1 kinase-binding protein 1) family protein ortholog of S. cerevisiae HSL7 and H. sapiens PRMT5 involved in methylation of small nuclear ribonucleoproteins | DDB0232432 | CDS | 141257 | 1929 | - | 0.287714 |
prpD | DDB_G0288681 | DDB0232432 | CDS | 1873609 | 1479 | + | 0.354293 | |
prpD_ps | DDB_G0288721 | putative pseudogene small fragment similar to D. discoideum gene | DDB0232432 | CDS | 1876627 | 147 | + | 0.197279 |
prpf31 | DDB_G0289595 | component of the U4U6-U5 snRNP complex defects in human PRPF31 are the cause of retinitis pigmentosa 11 (RP11) | DDB0232432 | CDS | 2984110 | 1383 | - | 0.295734 |
prpf38b | DDB_G0288401 | DDB0232432 | CDS | 1492016 | 1257 | - | 0.287192 | |
prpf4 | DDB_G0287635 | ortholog of the prp4 splicing factor component of the U4U6-U5 snRNP complex contains 7 WD repeats and a splicing factor motif | DDB0232432 | CDS | 533367 | 1803 | - | 0.297837 |
psiC | DDB_G0290245 | similar to dicA1 contains a signal peptide a PA14 (anthrax protection antigen) domain 3 Dictyostelium (CTDC) repeats expressed in prespore cells | DDB0232432 | CDS | 3769697 | 1551 | + | 0.322373 |
psiD | DDB_G0290925 | similar to dicA1 contains a signal peptide expressed in prespore cells | DDB0232432 | CDS | 4761330 | 1515 | - | 0.342574 |
psiH | DDB_G0289393 | contains a signal peptide a PA14 (anthrax protection antigen) domain 4 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | DDB0232432 | CDS | 2790892 | 2148 | + | 0.341248 |
psiI | DDB_G0288919 | contains a signal peptide a PA14 (anthrax protection antigen) domain 6 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | DDB0232432 | CDS | 2120577 | 2160 | - | 0.316667 |
psiJ | DDB_G0290317 | DDB0232432 | CDS | 3947753 | 2160 | - | 0.319444 | |
psmC4 | DDB_G0289003 | ATPase subunit and regulatory subcomplex of the 26S proteasome developmentally regulated TAT binding protein homolog | DDB0232432 | CDS | 2227887 | 1212 | + | 0.326733 |
psmD1 | DDB_G0287953 | DDB0232432 | CDS | 881632 | 2928 | - | 0.35929 | |
psmD10 | DDB_G0289189 | DDB0232432 | CDS | 2453090 | 699 | - | 0.304721 | |
psmD3 | DDB_G0288621 | DDB0232432 | CDS | 1750413 | 1515 | + | 0.287129 | |
psmG4 | DDB_G0304543 | conserved chaperone protein which promotes assembly of the 20S proteasome may form a dimer with psmG3 and act in concert with psmG1psmG2 | DDB0232432 | CDS | 1134744 | 402 | - | 0.246269 |
pspD_ps | DDB_G0288063 | putative pseudogene simlar to prespore-specific protein pspD | DDB0232432 | CDS | 1037957 | 1068 | - | 0.345506 |
ptcB | DDB_G0288027 | antisense inhibition of ptcB expression leads to slower growth localizes to the mitochondria | DDB0232432 | CDS | 992896 | 1587 | - | 0.236925 |
ptcC | DDB_G0287775 | DDB0232432 | CDS | 679687 | 1836 | - | 0.267429 | |
ptcD | DDB_G0287997 | DDB0232432 | CDS | 944155 | 4218 | + | 0.221669 | |
purB | DDB_G0288333 | catalyzes two reactions in de novo DNA synthesis: 5'-phosphoribosyl-4-(N-succinocarboxamide)-5-aminoimidazole fumarate AICAR and adenylo-succinate fumarate AMP | DDB0232432 | CDS | 1402047 | 1401 | + | 0.33262 |
purD | DDB_G0290121 | bifunctional enzyme of the de novo DNA synthesis pathway contains aminoimidazole ribotide synthetase and glycinamide ribotide synthetase activities | DDB0232432 | CDS | 3683216 | 2448 | + | 0.318219 |
purL | DDB_G0288145 | catayzes the reaction ATP 5'-phosphoribosyl-N-formylglycineamide L-glutamine Hsub2subO ADP phosphate 5-phosphoribosyl-n-formylglycineamidine L-glutamate in de novo DNA synthesis | DDB0232432 | CDS | 1141268 | 4068 | + | 0.342429 |
purN | DDB_G0288985 | catalyzes the reaction N10-formyl-Hsub4subF 5-phospho-ribosyl-glycineamide tetrahydrofolate 5'-phosphoribosyl-N-formylglycineamide in de novo DNA synthesis | DDB0232432 | CDS | 2206145 | 621 | + | 0.275362 |
pus1 | DDB_G0290987 | ortholog of S. cerevisiae PUS1a tRNA:pseudouridine synthase that introduces pseudouridines at positions 26-28 34-36 65 and 67 of tRNA nuclear protein that appears to be involved in tRNA export also acts on U2 snRNA | DDB0232432 | CDS | 4857087 | 1791 | - | 0.289224 |
pus3 | DDB_G0288909 | similar to S. cerevisiae pus3 which introduces pseudouridines at position 38 or 39 in tRNA | DDB0232432 | CDS | 2110038 | 1476 | + | 0.25271 |
pyk3 | DDB_G0289001 | member of the TKL (tyrosine kinase-like) group and the DPYK (Dictyostelium protein tyrosine kinase) family of protein kinases contains two kinase domains one of which is predicted to be inactive the C-terminal kinase domain has tyrosine kinase activitybr bCommunity annotation:b Pyk3 appears to be involved in differentiation pathway choice as the KO shows reduced pstO differentiation and compensatory expansion of the prespore region. Pyk3 has been proposed to act in a pathway involving ptpC and statC effectively potentiating the action of DIF-1. One of the factors that influences pathway choice is cell cycle position classic experiments show that cold-synchronized cells which enter development shortly after warming prefer the stalk pathway. This is due to an increased DIF sensitivity. New results (Strasser Tsang and MacWilliams in preparation) now show that the pyk3 transcript is upregulated roughly fivefold after cold synchronization at a time when cells show strong stalk preference (p | DDB0232432 | CDS | 2269413 | 4017 | - | 0.283047 |
pyrK | DDB_G0287495 | phosphorylates dCMP and dUMP to dCDP and dUDP respectively | DDB0232432 | CDS | 334067 | 588 | + | 0.289116 |
pyroxd1 | DDB_G0289727 | DDB0232432 | CDS | 3170582 | 1641 | + | 0.233394 | |
r31 | DDB_G0295607 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232432 | CDS | 1473461 | 61 | + | 0.344262 |
r58 | DDB_G0295609 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232432 | CDS | 1517413 | 54 | - | 0.314815 |
rab11B | DDB_G0287211 | DDB0232432 | CDS | 41773 | 663 | + | 0.235294 | |
rab18 | DDB_G0289827 | DDB0232432 | CDS | 3292859 | 609 | - | 0.287356 | |
rab7B | DDB_G0287553 | there is another rab7 homolog rab7A | DDB0232432 | CDS | 408133 | 594 | - | 0.294613 |
rabG2 | DDB_G0290783 | DDB0232432 | CDS | 4595466 | 483 | + | 0.335404 | |
rabK1 | DDB_G0290833 | DDB0232432 | CDS | 4609179 | 642 | - | 0.239875 | |
rabK2 | DDB_G0290791 | DDB0232432 | CDS | 4611869 | 444 | - | 0.236486 | |
rabK3 | DDB_G0290831 | DDB0232432 | CDS | 4607175 | 447 | - | 0.272931 | |
rabL | DDB_G0290779 | DDB0232432 | CDS | 4606115 | 615 | - | 0.297561 | |
rabM | DDB_G0290829 | DDB0232432 | CDS | 4605000 | 609 | - | 0.284072 | |
rabN1 | DDB_G0290789 | DDB0232432 | CDS | 4608094 | 651 | - | 0.254992 | |
rabN2 | DDB_G0290793 | DDB0232432 | CDS | 4612672 | 555 | - | 0.27027 | |
rabO | DDB_G0290407 | DDB0232432 | CDS | 4047054 | 657 | + | 0.232877 | |
rabP | DDB_G0290875 | DDB0232432 | CDS | 4703255 | 699 | + | 0.250358 | |
rabggtb | DDB_G0290671 | catalyzes the transfer of a geranyl-geranyl moiety from geranyl-geranyl pyrophosphate to both cysteines in Rab proteins with an -XXCC -XCXC and -CCXX C-terminal forms a hetero-dimer with the | DDB0232432 | CDS | 4317912 | 1020 | + | 0.281373 |
racM | DDB_G0289103 | DDB0232432 | CDS | 2368291 | 570 | - | 0.27193 | |
ragA | DDB_G0288701 | ortholog of S. cerevisiae GTR1 and H. sapiens RagA and RagB a cytoplasmic GTP binding protein | DDB0232432 | CDS | 1844809 | 906 | + | 0.296909 |
ranbp1 | DDB_G0287391 | DDB0232432 | CDS | 246455 | 585 | + | 0.353846 | |
rblA | DDB_G0290551 | putative ortholog of Retinoblastoma protein (Rb) which inhibits progression from G1 to S phase of the cell cycle through interactions with the E2F family of transcription factors expressed in prespore zone seems to work with Btg in cell fate commitment during development | DDB0232432 | CDS | 4252151 | 3939 | - | 0.236101 |
rbx1 | DDB_G0287629 | DDB0232432 | CDS | 496993 | 315 | + | 0.342857 | |
rcdJJ | DDB_G0287213 | DDB0232432 | CDS | 34540 | 861 | - | 0.213705 | |
rdiA | DDB_G0291077 | DDB0232432 | CDS | 4973539 | 594 | + | 0.380471 | |
redC | DDB_G0287983 | similar to the H. sapiens NDOR1 an oxidoreductase that catalyzes the NADP-dependent reduction of cytochrome c and one-electron acceptors | DDB0232432 | CDS | 927535 | 1902 | + | 0.244479 |
rfa1 | DDB_G0289513 | DDB0232432 | CDS | 2891660 | 2040 | + | 0.320098 | |
rft1 | DDB_G0288491 | ortholog of yeast RFT1 an essential integral membrane protein that is required for translocation of Man5GlcNac2-PP-Dol from the cytoplasmic side to the lumenal side of the ER membrane but is not the flippase | DDB0232432 | CDS | 1600467 | 1623 | - | 0.190388 |
rgaA | DDB_G0287585 | DDB0232432 | CDS | 498740 | 2469 | + | 0.357635 | |
rif1 | DDB_G0287899 | ortholog of RIF1 associated with the telomeres and in human required for checkpoint mediated arrest of cell cycle progression in response to DNA damage during S-phase brbr bCommunity annotation:b In budding yeast RIF1 is a telomere-associated protein which has been shown to suppress the recruitment of the ATM DNA-damage signalling complex to the telomere ends and play a role in telomere length regulation (see | DDB0232432 | CDS | 816399 | 3942 | + | 0.236428 |
rliF | DDB_G0288289 | very similar to bacterial beta-xylosidases and also but less similar to mammalian alpha-L-iduronidase repressed after Legionella pneumophila infection | DDB0232432 | CDS | 1354074 | 1473 | + | 0.32315 |
rmp | DDB_G0289477 | DDB0232432 | CDS | 2835235 | 1470 | + | 0.258503 | |
rnu1c | DDB_G0295611 | DDB0232432 | CDS | 1846430 | 163 | + | 0.361963 | |
rnu1d | DDB_G0295613 | DDB0232432 | CDS | 1870152 | 163 | - | 0.368098 | |
rnu2d | DDB_G0295623 | DDB0232432 | CDS | 2747783 | 244 | - | 0.311475 | |
rnu5a | DDB_G0295625 | DDB0232432 | CDS | 3164865 | 118 | - | 0.372881 | |
rnu5b | DDB_G0295627 | DDB0232432 | CDS | 3165224 | 118 | + | 0.364407 | |
roco4 | DDB_G0288251 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains | DDB0232432 | CDS | 1284583 | 5181 | + | 0.332947 |
roco5 | DDB_G0294533 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains RhoGEF PH LRR Roc COR and protein kinase domains | DDB0232432 | CDS | 1439427 | 8403 | - | 0.309413 |
roco9 | DDB_G0288183 | member of the TKL (tyrosine kinase-like) group and ROCO family of protein kinases contains RhoGAP LRR Roc Cor and protein kinase domains | DDB0232432 | CDS | 1219231 | 10098 | - | 0.264706 |
rpa49 | DDB_G0290909 | component of the RNA polymerase I complex weakly similar to S. cerevisiae RPA49 and M. musculus RNA polymerase I associated factor 53 | DDB0232432 | CDS | 4737794 | 1128 | + | 0.265957 |
rpb2 | DDB_G0288257 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB2 | DDB0232432 | CDS | 1296275 | 3513 | - | 0.366354 |
rpb6 | DDB_G0291037 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPO26 | DDB0232432 | CDS | 4838044 | 402 | - | 0.348259 |
rpc11 | DDB_G0287707 | component of the RNA polymerase III complex ortholog of H. sapiens RPC10 and S. cerevisiae RPC11 | DDB0232432 | CDS | 584047 | 336 | + | 0.285714 |
rpc2 | DDB_G0288449 | component of the RNA polymerase III complex ortholog of S. cerevisiae RPC2 | DDB0232432 | CDS | 1494028 | 4827 | + | 0.310131 |
rpl10 | DDB_G0288273 | DDB0232432 | CDS | 1312496 | 654 | - | 0.408257 | |
rpl12 | DDB_G0288295 | DDB0232432 | CDS | 1359447 | 501 | + | 0.411178 | |
rpl22 | DDB_G0288101 | DDB0232432 | CDS | 1106395 | 351 | - | 0.367521 | |
rpl22a | DDB_G0290091 | DDB0232432 | CDS | 3652594 | 351 | - | 0.347578 | |
rpl23 | DDB_G0290315 | DDB0232432 | CDS | 3946402 | 411 | - | 0.420925 | |
rpl35 | DDB_G0288349 | DDB0232432 | CDS | 1418812 | 381 | - | 0.39895 | |
rpl39 | DDB_G0302511 | DDB0232432 | CDS | 657459 | 156 | - | 0.333333 | |
rplp1B | DDB_G0287995 | DDB0232432 | CDS | 942400 | 303 | + | 0.475248 | |
rps17 | DDB_G0290141 | protein component of the small (40S) ribosomal subunit ribosomal protein S17 homolog | DDB0232432 | CDS | 3706333 | 408 | + | 0.377451 |
rps7 | DDB_G0289025 | DDB0232432 | CDS | 2252902 | 582 | - | 0.364261 | |
rps9 | DDB_G0289877 | DDB0232432 | CDS | 3486480 | 558 | + | 0.40681 | |
rrpA | DDB_G0289659 | DDB0232432 | CDS | 3196021 | 7254 | + | 0.263441 | |
sadA | DDB_G0288511 | DDB0232432 | CDS | 1638800 | 2859 | - | 0.349423 | |
scfd1 | DDB_G0288719 | DDB0232432 | CDS | 1870694 | 2022 | - | 0.271019 | |
scsA | DDB_G0289325 | catalyzes the reaction GTP succinate CoA GDP phosphate succinyl-CoA | DDB0232432 | CDS | 2650999 | 948 | - | 0.381857 |
sdhaf1A | DDB_G0289475 | DDB0232432 | CDS | 2834711 | 276 | - | 0.264493 | |
sdrA | DDB_G0290659 | DDB0232432 | CDS | 4286973 | 873 | + | 0.290951 | |
sec61g | DDB_G0287777 | gamma subunit of the SEC61 complex (composed of | DDB0232432 | CDS | 682723 | 210 | + | 0.328571 |
secG | DDB_G0287459 | Arf-guanyl-nucleotide exchange factor of the cytohesin family involved in chemotaxis to cAMP during development and substrate adhesion | DDB0232432 | CDS | 318028 | 2961 | - | 0.372847 |
set1 | DDB_G0289257 | DDB0232432 | CDS | 2551579 | 4461 | + | 0.297467 | |
sevA | DDB_G0289327 | Ca2-dependent F-actin fragmenting protein | DDB0232432 | CDS | 2683596 | 1089 | - | 0.325987 |
sgkD | DDB_G0289343 | DDB0232432 | CDS | 2664172 | 2052 | + | 0.203704 | |
shkB | DDB_G0288617 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232432 | CDS | 1745652 | 1962 | - | 0.331295 |
shkE | DDB_G0290451 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232432 | CDS | 4058161 | 2133 | + | 0.284107 |
sibA | DDB_G0287363 | similar to the integrin beta family cytosolic domain binds talin involved in substrate adhesion and phagocytosisbr bnoteb the sequence in dictyBase has mismatches and does not contain a clear signal sequence whereas the published sequence available from the | DDB0232432 | CDS | 192610 | 5784 | - | 0.331604 |
sibB | DDB_G0288103 | integrin beta family protein cytosolic domain binds talin | DDB0232432 | CDS | 1110992 | 5826 | + | 0.331102 |
sibC | DDB_G0288195 | integrin beta family protein cytosolic domain binds talin expression increases when cells are under conditions that promote adhesiveness | DDB0232432 | CDS | 1194946 | 5865 | - | 0.350725 |
sibD | DDB_G0288197 | integrin beta family protein cytosolic domain binds talin | DDB0232432 | CDS | 1202242 | 5874 | - | 0.312223 |
sibE | DDB_G0288239 | integrin beta family protein cytosolic domain binds talin | DDB0232432 | CDS | 1209765 | 5841 | - | 0.34857 |
sid1 | DDB_G0290761 | ortholog of C. elegans sid1 that enables passive cellular uptake of dsRNA contains 10 transmembrane domains | DDB0232432 | CDS | 4572699 | 1299 | - | 0.265589 |
sigF | DDB_G0289885 | DDB0232432 | CDS | 3500701 | 696 | - | 0.24569 | |
sigG | DDB_G0290071 | DDB0232432 | CDS | 3632186 | 1278 | - | 0.293427 | |
sir2D | DDB_G0289967 | NAD-dependent deacetylase Sirutin 2 family protein that regulates various biological processes by deacetylating histones and other target proteins expressed more highly during vegetative growth | DDB0232432 | CDS | 3383269 | 1629 | - | 0.281768 |
slbp | DDB_G0288225 | binds the stem-loop structure of replication-dependent histone pre-mRNAs and contributes to histone mRNA 3' end processing | DDB0232432 | CDS | 1277134 | 1086 | + | 0.207182 |
slc44a2 | DDB_G0289013 | DDB0232432 | CDS | 2230553 | 1887 | + | 0.325384 | |
slmo | DDB_G0290499 | conserved protein in D. melanogaster lack of SLMO leads to defects in locomotor behavior and die during larval development contains a PRELIMSF1 domain | DDB0232432 | CDS | 4156073 | 687 | + | 0.310044 |
smc5 | DDB_G0290919 | functions in chromosome dynamics heterodimerizes with smc6 | DDB0232432 | CDS | 4745027 | 3396 | - | 0.328033 |
smc6 | DDB_G0288993 | functions in chromosome dynamics heterodimerizes with smc5 | DDB0232432 | CDS | 2211609 | 3558 | - | 0.324902 |
smdA | DDB_G0288495 | DDB0232432 | CDS | 1605485 | 1599 | + | 0.229518 | |
smkA | DDB_G0289067 | suppressor of | DDB0232432 | CDS | 2315722 | 3141 | - | 0.24801 |
smlA | DDB_G0287587 | DDB0232432 | CDS | 461888 | 852 | + | 0.279343 | |
smtA | DDB_G0288907 | DDB0232432 | CDS | 2108749 | 1065 | + | 0.421596 | |
sno12 | DDB_G0295605 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 1152280 | 75 | - | 0.293333 |
sno13 | DDB_G0295621 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2600252 | 80 | - | 0.4375 |
sno16 | DDB_G0295631 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2586031 | 78 | - | 0.333333 |
sno2 | DDB_G0295619 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2599917 | 83 | - | 0.337349 |
sno5 | DDB_G0295617 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2585363 | 81 | - | 0.320988 |
sno7 | DDB_G0295615 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232432 | CDS | 2249624 | 98 | - | 0.438776 |
snrpB2 | DDB_G0288391 | ortholog of human SNRPB2 a component of the U2 snRNP involved in mRNA splicing also similar to human SNRPA | DDB0232432 | CDS | 1486880 | 726 | - | 0.296143 |
snrpE | DDB_G0302414 | conserved SMLSM core protein also known as SME1 associates with U1 U2 U4U6 and U5 snRNP | DDB0232432 | CDS | 1315343 | 279 | - | 0.25448 |
sodE | DDB_G0290343 | very similar to human SOD1 defects in which cause familial amyotrophic lateral sclerosis (ALS) belongs to the Cu-Zn superoxide dismutase family | DDB0232432 | CDS | 3992463 | 459 | + | 0.294118 |
sort1 | DDB_G0290081 | ortholog of S. cerevisiae PEP1 and mammalian sortilin a sorting receptor of the Golgi apparatus | DDB0232432 | CDS | 3627939 | 2316 | - | 0.335924 |
spc3 | DDB_G0290851 | ortholog of the conserved microsomal signal peptidase 23 kDa subunit the signal peptidase complex is a membrane-bound endoproteinase that removes signal peptides from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum contains a putative signal peptide | DDB0232432 | CDS | 4675467 | 513 | + | 0.288499 |
spiA | DDB_G0289075 | regulated by the MADS-box transcription factor SrfA during development expressed in prespore cells | DDB0232432 | CDS | 2352021 | 810 | - | 0.351852 |
spoT | DDB_G0287233 | DDB0232432 | CDS | 32102 | 627 | - | 0.271132 | |
spt5 | DDB_G0287661 | ortholog of the human SUPT5H and S. cerevisiae SPT5 (suppressor of Ty 5) a transcription-elongation factor that is tightly associated in a complex with SPT4 | DDB0232432 | CDS | 473577 | 3396 | - | 0.325383 |
sr | DDB_G0290009 | catalyzes the reaction 78-dihydrobiopterin NADPsupsup sepiapterin NADPH Hsupsup the final step in L-erythro-tetrahydrobiopterin (BH4) biosynthesis a cofactor for aromatic amino acid oxidationbr | DDB0232432 | CDS | 3552302 | 804 | + | 0.238806 |
srr | DDB_G0289463 | converts L-serine into D-serine activated in vitro by Mg as well as Na pyridoxal 5'-phosphate (PLP)-dependent enzyme that catalyzes racemization and dehydration of both isomers of serine | DDB0232432 | CDS | 2816488 | 975 | + | 0.308718 |
srsA | DDB_G0289521 | immidiate-early gene expressed immidiately after nutrition removal involved in starvation response development and spore differentiation there are two transcripts of this gene both contain a putative transmembrane domain | DDB0232432 | CDS | 2911167 | 495 | + | 0.252525 |
ssrp1 | DDB_G0290331 | ortholog of the SSRP1 component of the FACT complex a heterodimer of ssrp1 and spt16 the FACT complex is a general chromatin factor that acts to reorganize nucleosomes involved in multiple processes that require DNA as a template such as mRNA elongation DNA replication and DNA repair | DDB0232432 | CDS | 3969916 | 1584 | - | 0.342172 |
stlB | DDB_G0290853 | belongs to the beta-ketoacyl synthase family type III polyketide synthase responsible for phlorocaprophenone (PCP) production the first step in DIF-1 biosynthesis required for the formation of the outer basal disc and the lower cup | DDB0232432 | CDS | 4652248 | 8907 | + | 0.270461 |
strM | DDB_G0288323 | conserved in other Dictyosteliabr bNomenclature note:b named by colleagues of M. Satre as the protein sequence starts with MSATRE | DDB0232432 | CDS | 1389621 | 894 | + | 0.316555 |
strn | DDB_G0288327 | homolog of mammalians striatins calmodulin-binding proteins expressed in the central nervous system and Drosophila Cka involved in the Jun kinase pathway | DDB0232432 | CDS | 1395012 | 2484 | + | 0.288647 |
swp1 | DDB_G0289479 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae SWP1 and human ribophorin II contains three putative C-terminal transmembrane domains and an N-terminal signal peptide | DDB0232432 | CDS | 2823825 | 2058 | - | 0.336249 |
sybB | DDB_G0290363 | very similar to sybA a gene that is regulated by the MADS-box transcription factor SrfA during development | DDB0232432 | CDS | 3879007 | 306 | + | 0.251634 |
syn1A | DDB_G0289379 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232432 | CDS | 2678322 | 1002 | - | 0.297405 |
syn7A | DDB_G0287733 | member of the SNARE family (Soluble NSF Attachment Protein REceptor) plays a role in endosomal fusion | DDB0232432 | CDS | 617723 | 1071 | + | 0.289449 |
syn8B | DDB_G0288439 | DDB0232432 | CDS | 1539443 | 753 | - | 0.26162 | |
tRNA-Ala-AGC-10 | DDB_G0295297 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 254727 | 73 | - | 0.534247 |
tRNA-Ala-AGC-9 | DDB_G0295239 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2265374 | 73 | + | 0.534247 |
tRNA-Ala-UGC-8 | DDB_G0295267 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3987062 | 96 | - | 0.427083 |
tRNA-Arg-UCU-11 | DDB_G0295257 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3693576 | 73 | + | 0.561644 |
tRNA-Arg-UCU-12 | DDB_G0295281 | transfers an arginine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2593624 | 73 | - | 0.561644 |
tRNA-Asn-GUU-14 | DDB_G0295241 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2321011 | 73 | + | 0.60274 |
tRNA-Asn-GUU-15 | DDB_G0295285 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 1592074 | 73 | - | 0.60274 |
tRNA-Asp-GUC-19 | DDB_G0295263 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 4005478 | 72 | + | 0.569444 |
tRNA-Asp-GUC-20 | DDB_G0295279 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2728188 | 72 | - | 0.569444 |
tRNA-Gln-UUG-12 | DDB_G0295237 | transfers a glutamine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 1989890 | 73 | + | 0.410959 |
tRNA-Glu-UUC-14 | DDB_G0295271 | transfers a glutamic acid residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3245733 | 72 | - | 0.513889 |
tRNA-Gly-GCC-12 | DDB_G0295235 | DDB0232432 | CDS | 284121 | 71 | + | 0.549296 | |
tRNA-Gly-GCC-13 | DDB_G0295291 | DDB0232432 | CDS | 409584 | 71 | - | 0.549296 | |
tRNA-Ile-AAU-11 | DDB_G0295293 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 278611 | 73 | - | 0.589041 |
tRNA-Leu-AAG-6 | DDB_G0295283 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2550132 | 82 | - | 0.463415 |
tRNA-Leu-AAG-7 | DDB_G0295289 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 432078 | 82 | - | 0.463415 |
tRNA-Lys-CUU-7 | DDB_G0295265 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 4947710 | 73 | - | 0.671233 |
tRNA-Lys-UUU-16 | DDB_G0295233 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 40886 | 73 | + | 0.616438 |
tRNA-Lys-UUU-17 | DDB_G0295243 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2727390 | 73 | + | 0.616438 |
tRNA-Lys-UUU-18 | DDB_G0295245 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2768640 | 73 | + | 0.616438 |
tRNA-Lys-UUU-19 | DDB_G0295275 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3113136 | 73 | - | 0.616438 |
tRNA-Met-CAU-13 | DDB_G0295251 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3259687 | 73 | + | 0.493151 |
tRNA-Met-CAU-14 | DDB_G0295261 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3845621 | 73 | + | 0.520548 |
tRNA-Met-CAU-15 | DDB_G0295295 | transfers a methionine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 268971 | 73 | - | 0.493151 |
tRNA-Pro-UGG-13 | DDB_G0295247 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2956680 | 71 | + | 0.492958 |
tRNA-Pro-UGG-14 | DDB_G0295277 | transfers a proline residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 2970447 | 71 | - | 0.492958 |
tRNA-Thr-UGU-5 | DDB_G0295269 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3336512 | 90 | - | 0.455556 |
tRNA-Thr-UGU-6 | DDB_G0295287 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 712716 | 90 | - | 0.455556 |
tRNA-Val-AAC-19 | DDB_G0295273 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3208187 | 74 | - | 0.486486 |
tRNA-Val-UAC-3 | DDB_G0295249 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3061365 | 74 | + | 0.513514 |
tRNA-Val-UAC-4 | DDB_G0295253 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3658887 | 74 | + | 0.540541 |
tRNA-Val-UAC-5 | DDB_G0295255 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3660287 | 74 | + | 0.540541 |
tRNA-Val-UAC-6 | DDB_G0295259 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232432 | CDS | 3761819 | 74 | + | 0.540541 |
taf5 | DDB_G0287337 | subunit of TFIID and SAGA complexes involved in RNA polymerase II transcription initiation and in chromatin modification | DDB0232432 | CDS | 150447 | 2847 | + | 0.316473 |
taf6 | DDB_G0288471 | similar to S. cerevisiae TAF6 subunit of TFIID and SAGA complexes involved in transcription initiation of RNA polymerase II and in chromatin modification | DDB0232432 | CDS | 1566143 | 1629 | - | 0.279926 |
talA | DDB_G0290481 | The bAX4b talin gene has a confirmed stop codon (R. Kay private communication) that terminates the protein after residue 1279 immunohistochemistry shows the presence of a very faint truncated talin (A. Mueller-Taubenberger private communication)br bAX2b talin is the full length homolog of mammalian talin and other proteins of the band 4.1 superfamily all functional data is derived from AX2 involved in cell-substrate adhesion and cytokinesis the AX2 protein sequence is available from the | DDB0232432 | CDS | 4257563 | 3840 | + | 0.33724 |
talB | DDB_G0287505 | talin with an unusual villin headpiece-like domain involved in multicellular development and in autophagic cell death | DDB0232432 | CDS | 376738 | 7845 | + | 0.391714 |
tat | DDB_G0287515 | catalyzes the reaction L-tyrosine 2-oxoglutarate 4-hydroxyphenylpyruvate L-glutamate | DDB0232432 | CDS | 352517 | 1254 | + | 0.297448 |
tgrA_ps6 | DDB_G0289747 | putative pseudogene fragment of immunoglobulin E-set family gene | DDB0232432 | CDS | 3203632 | 611 | - | 0.227496 |
tgrM1 | DDB_G0288711 | DDB0232432 | CDS | 1859437 | 2562 | - | 0.323575 | |
tgrM2 | DDB_G0288709 | DDB0232432 | CDS | 1856022 | 2664 | - | 0.298048 | |
tgrP1 | DDB_G0287605 | DDB0232432 | CDS | 454900 | 1620 | - | 0.169753 | |
thoc2 | DDB_G0291063 | ortholog of human THOC2 and yeast RLR1 which exist in the THO complex required for transcriptional elongation | DDB0232432 | CDS | 4908746 | 6333 | + | 0.291963 |
thoc6 | DDB_G0287653 | ortholog of THOC6 which exists in the THO complex required for transcriptional elongation | DDB0232432 | CDS | 441079 | 1440 | + | 0.271528 |
thrS1 | DDB_G0288267 | catalyzes the reaction ATP L-threonine tRNAThr AMP diphosphate L-threonyl-tRNAThr | DDB0232432 | CDS | 1320046 | 2133 | - | 0.33849 |
thyB | DDB_G0289179 | calmodulin-binding thymidine kinase 1 that is very similar to human TK1 catalyzes the reaction ATP thymidine ADP thymidine 5'-phosphate | DDB0232432 | CDS | 2508266 | 684 | - | 0.330409 |
timm17 | DDB_G0287627 | DDB0232432 | CDS | 494298 | 552 | + | 0.344203 | |
tirA | DDB_G0289237 | DDB0232432 | CDS | 2526970 | 4011 | - | 0.222638 | |
tmcB | DDB_G0289207 | contains two HAT (half a TPR) repeats and 13 predicted transmembrane domains involved in macrocyst formation | DDB0232432 | CDS | 2473231 | 4251 | + | 0.307457 |
tmcC | DDB_G0289253 | contains two HAT (half a TPR) repeats and 13 predicted transmembrane domains null mutant has an increased number of peripheral cells in macrocyst formation | DDB0232432 | CDS | 2544506 | 4167 | - | 0.287257 |
tmc_ps2 | DDB_G0288839 | putative pseudogene similar to a gene family in Dictyostelium including | DDB0232432 | CDS | 2049688 | 2436 | + | 0.267652 |
tmc_ps3 | DDB_G0288843 | putative pseudogene similar to a gene family in Dictyostelium including | DDB0232432 | CDS | 2054056 | 1116 | + | 0.266129 |
tmem120 | DDB_G0288699 | conserved transmembrane protein contains 4 putative transmembrane domains | DDB0232432 | CDS | 1842289 | 1107 | - | 0.311653 |
tmem14A | DDB_G0288759 | one of two Dictyostelium proteins in the eukaryotic transmembrane protein 14 (TMEM14) family contains four putative transmembrane domains | DDB0232432 | CDS | 1930552 | 309 | - | 0.304207 |
tmem164 | DDB_G0287401 | conserved transmembrane protein contains 7 putative transmembrane domains | DDB0232432 | CDS | 257909 | 828 | - | 0.242754 |
tmem167 | DDB_G0289451 | DDB0232432 | CDS | 2806080 | 219 | + | 0.296804 | |
tmem170 | DDB_G0290053 | DDB0232432 | CDS | 3567000 | 387 | - | 0.302326 | |
tmem184E | DDB_G0304961 | TMEM184 family protein contains 7 predicted transmembrane domains | DDB0232432 | CDS | 2986116 | 1689 | - | 0.212552 |
tom1 | DDB_G0290163 | contains a VHS domain and a GAT domain amino terminus is similar to mammalian TOM1 protein which is involved in intracellular protein transport | DDB0232432 | CDS | 3723872 | 1992 | + | 0.316767 |
tpc2 | DDB_G0289105 | similar to human TPC2 a two-pore calcium channel contains Ca2-binding EF-hands and 2 x 5 (10 total) putative transmembrane domains | DDB0232432 | CDS | 2361958 | 6183 | + | 0.253275 |
tpsA | DDB_G0287657 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain enriched in prestalk cells | DDB0232432 | CDS | 444388 | 2202 | - | 0.321072 |
tpsC | DDB_G0290405 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain | DDB0232432 | CDS | 4043666 | 2700 | + | 0.303333 |
trmu | DDB_G0288979 | catalyzes the reaction: S-adenosyl-L-methionine tRNA S-adenosyl-L-homocysteine tRNA containing 5-methylaminomethyl-2-thiouridylate | DDB0232432 | CDS | 2201638 | 1356 | + | 0.266962 |
trxD | DDB_G0287849 | DDB0232432 | CDS | 820586 | 315 | - | 0.260317 | |
trxE | DDB_G0287227 | DDB0232432 | CDS | 23737 | 318 | + | 0.393082 | |
tspE | DDB_G0291177 | has similarity to the mammalian CD9 antigen contains a tetraspanin and 4 putative transmembrane domains | DDB0232432 | CDS | 5101333 | 696 | + | 0.244253 |
tubA | DDB_G0287689 | monomeric subunit of microtubules as most other species Dicty has two alpha-tubulin genes and only one of each beta- and gamma-tubulin the other alpha tubulin gene is | DDB0232432 | CDS | 707217 | 1374 | - | 0.381368 |
tufM | DDB_G0289593 | mitochondrial translation elongation factor Tu highly similar to bacterial elongation factor Tu | DDB0232432 | CDS | 2977521 | 1275 | - | 0.418039 |
uap1 | DDB_G0290055 | catalyzes the reaction UTP N-acetyl-alpha-D-glucosamine 1-phosphate diphosphate UDP-N-acetyl-D-glucosamine | DDB0232432 | CDS | 3567893 | 1464 | - | 0.304645 |
ubc9 | DDB_G0287693 | DDB0232432 | CDS | 688286 | 480 | - | 0.33125 | |
ube2s | DDB_G0289021 | DDB0232432 | CDS | 2250572 | 648 | + | 0.290123 | |
ube2t | DDB_G0291199 | interacts with the Fanconi anaemia complex involved DNA cross-link repair null mutant is sensitive to DNA damaging agents brbr the mammalian Fanconi anaemia nuclear complex includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 Dictyostelium has orthologs for | DDB0232432 | CDS | 5123925 | 879 | - | 0.246871 |
ube3a | DDB_G0290179 | DDB0232432 | CDS | 3742663 | 2163 | - | 0.273694 | |
ubqF | DDB_G0289449 | DDB0232432 | CDS | 2811202 | 1602 | + | 0.359551 | |
ufc1 | DDB_G0289037 | DDB0232432 | CDS | 2284637 | 495 | - | 0.30101 | |
ugt1 | DDB_G0290339 | CAZy family GT28 contains a glycosyltransferase 28 domain and a partial MurG acetylglucosaminetransferase domain | DDB0232432 | CDS | 3987458 | 1197 | + | 0.233918 |
ugt52 | DDB_G0288655 | CAZy family GT1 catalyzes the reaction UDP-glucose a sterol UDP a glucosylsterol | DDB0232432 | CDS | 1802347 | 5094 | - | 0.291323 |
upf1 | DDB_G0288923 | ortholog of yeast NAM7 and the mammalian UPF1 (up-frameshift suppressor 1) or RENT1 protein part of a post-splicing multiprotein complex and involved in nonsense-mediated decay (NMD) of mRNAs containing premature stop codons | DDB0232432 | CDS | 2130048 | 3996 | + | 0.318068 |
uppA | DDB_G0289875 | catalyzes the reaction UTP alpha-D-glucose 1-phosphate diphosphate UDP-glucose | DDB0232432 | CDS | 3439159 | 1536 | - | 0.287109 |
usp12 | DDB_G0290453 | DDB0232432 | CDS | 4071585 | 1428 | - | 0.226891 | |
usp40 | DDB_G0289611 | DDB0232432 | CDS | 3021100 | 5034 | - | 0.283472 | |
vacA | DDB_G0289485 | DDB0232432 | CDS | 2888908 | 1797 | + | 0.341681 | |
valS2 | DDB_G0288939 | catalyzes the reaction ATP L-valine tRNAVal AMP diphosphate L-valyl-tRNAVal | DDB0232432 | CDS | 2152189 | 3156 | + | 0.270279 |
vasP | DDB_G0289541 | DDB0232432 | CDS | 2893954 | 1143 | - | 0.43657 | |
vilA | DDB_G0288557 | DDB0232432 | CDS | 1709022 | 5115 | - | 0.324536 | |
vps29 | DDB_G0288787 | ortholog of VPS29 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | DDB0232432 | CDS | 1965193 | 552 | - | 0.311594 |
vps2A | DDB_G0290087 | putative ortholog of human CHMP2A (Chromatin Modifying Protein 2A) and yeast DID4 (Doa4-Independent Degradation) component of the ESCRT-III complex (endosomal sorting complex required for transport) | DDB0232432 | CDS | 3647628 | 621 | - | 0.299517 |
vps33 | DDB_G0291097 | DDB0232432 | CDS | 4992025 | 1935 | - | 0.328165 | |
vps45 | DDB_G0290213 | putative ortholog of VPS45 involved in vacuolar protein sorting | DDB0232432 | CDS | 3802462 | 1692 | - | 0.278369 |
vps60 | DDB_G0287993 | ortholog of yeast VPS60 and human CHMP5 (CHromatin Modifying Protein 5) which associates with the ESCRT-III complex (endosomal sorting complex required for transport) | DDB0232432 | CDS | 940480 | 648 | - | 0.333333 |
warA | DDB_G0291075 | DDB0232432 | CDS | 5009348 | 2412 | - | 0.283167 | |
wdr18 | DDB_G0288659 | DDB0232432 | CDS | 1790292 | 1683 | + | 0.273321 | |
wdr24 | DDB_G0287817 | DDB0232432 | CDS | 760582 | 3072 | - | 0.277995 | |
wdr5 | DDB_G0287273 | highly similar to WDR5 protein involved in histone H3 K4 methylation | DDB0232432 | CDS | 72820 | 1008 | + | 0.298611 |
wimA_ps1 | DDB_G0288117 | putative pseudogene similar to the wimA gene contains also a short region of similarity with the forC gene | DDB0232432 | CDS | 1065579 | 1581 | - | 0.285895 |
xdh | DDB_G0291047 | catalyzes the reactions xanthine NAD Hsub2subO urate NADH H and xanthine Hsub2subO Osub2sub urate Hsub2subOsub2sub | DDB0232432 | CDS | 4822800 | 4077 | + | 0.347559 |
xpnpep1 | DDB_G0290501 | probable Xaa-Pro aminopeptidase 1 that releases any N-terminal amino acid including proline that is linked to proline even from a dipeptide or tripeptide | DDB0232432 | CDS | 4157355 | 1884 | + | 0.300955 |
xrcc2 | DDB_G0290297 | putative ortholog of XRCC2 which is involved in double-strand break repair interacts with RAD51 | DDB0232432 | CDS | 3921390 | 1167 | + | 0.251928 |
zfaA | DDB_G0290961 | DDB0232432 | CDS | 4810278 | 1383 | - | 0.263919 | |
zfaA_ps | DDB_G0290935 | putative pseudogene similar to a family of D. discoideum zinc finger containing genes including | DDB0232432 | CDS | 4771025 | 543 | - | 0.244936 |
zmpste24 | DDB_G0290849 | proteolytically removes the C-terminal three residues of farnesylated proteins contains 6 putative transmembrane domains and an additional signal peptide | DDB0232432 | CDS | 4673270 | 1281 | - | 0.251366 |