Gene list
Applied filters:
COG category: Carbohydrate transport and metabolism
Number of genes found: 759
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 |
DDB_G0267574 | DDB_G0267574 | DDB0232428 | CDS | 365942 | 678 | + | 0.294985 | |
DDB_G0267582 | DDB_G0267582 | DDB0232428 | CDS | 371018 | 1479 | + | 0.313049 | |
DDB_G0267610 | DDB_G0267610 | there is a paralog of this gene | DDB0232428 | CDS | 411512 | 924 | - | 0.24026 |
DDB_G0267842 | DDB_G0267842 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232428 | CDS | 959377 | 921 | + | 0.327904 |
DDB_G0268184 | DDB_G0268184 | DDB0232428 | CDS | 1619582 | 1536 | - | 0.221354 | |
DDB_G0268206 | DDB_G0268206 | DDB0232428 | CDS | 1686758 | 894 | + | 0.284116 | |
DDB_G0268230 | DDB_G0268230 | DDB0232428 | CDS | 1727069 | 1764 | + | 0.265306 | |
DDB_G0268520 | DDB_G0268520 | DDB0232428 | CDS | 811678 | 3921 | - | 0.217547 | |
DDB_G0269322 | DDB_G0269322 | DDB0232428 | CDS | 2542013 | 864 | - | 0.284722 | |
DDB_G0269964 | DDB_G0269964 | DDB0232428 | CDS | 3938864 | 1998 | + | 0.285285 | |
DDB_G0270074 | DDB_G0270074 | belongs to the glycoside hydrolase 5 (cellulase) family 5 contains a predicted signal sequence | DDB0232428 | CDS | 4187072 | 1530 | - | 0.309804 |
DDB_G0270190 | DDB_G0270190 | similar to bacterial endo-14-beta-glucanase expressed in pstAO cells | DDB0232428 | CDS | 4384621 | 1719 | - | 0.294939 |
DDB_G0270284 | DDB_G0270284 | contains an N-terminal DOMON domain as it occurs in dopamine beta-monooxygenases the Dictyostelium protein is followed by a cytochrome b561 domain which contains 5 putative transmembrane regions in addition the protein contains a putative signal peptide | DDB0232428 | CDS | 4579488 | 1173 | + | 0.277067 |
DDB_G0270304 | DDB_G0270304 | DDB0232428 | CDS | 4607306 | 630 | - | 0.284127 | |
DDB_G0270720 | DDB_G0270720 | DDB0232428 | CDS | 4125800 | 1560 | + | 0.239744 | |
DDB_G0271484 | DDB_G0271484 | DDB0232429 | CDS | 427690 | 1485 | + | 0.256566 | |
DDB_G0272192 | DDB_G0272192 | DDB0232429 | CDS | 1412468 | 1497 | + | 0.329993 | |
DDB_G0272224 | DDB_G0272224 | phosphorylates NAD to NADP | DDB0232429 | CDS | 1711679 | 1389 | + | 0.258459 |
DDB_G0272688 | DDB_G0272688 | DDB0232429 | CDS | 1980098 | 900 | - | 0.31 | |
DDB_G0272839 | DDB_G0272839 | has a short region of similarity to aprataxin a Hint related protein that is mutated in individuals with ataxia with oculomotor apraxia | DDB0232429 | CDS | 2148504 | 1173 | + | 0.224211 |
DDB_G0273195 | DDB_G0273195 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 2690707 | 1764 | - | 0.294218 |
DDB_G0273453 | DDB_G0273453 | there is a second copy of this gene | DDB0232429 | CDS | 2914216 | 2520 | - | 0.265476 |
DDB_G0273565 | DDB_G0273565 | there is a second copy of this gene | DDB0232429 | CDS | 3114676 | 2520 | + | 0.265476 |
DDB_G0273735 | DDB_G0273735 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 3339316 | 1764 | + | 0.294218 |
DDB_G0274161 | DDB_G0274161 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repressionbrbr bCommunity annotation:b DDB_G0274161 is similar to nmr1 originally identified as a Neurospora gene which binds to the transcription factor nit2 and prevents its binding to and activating genes required for nitrogen utilization. The human ortholog is | DDB0232429 | CDS | 4878022 | 927 | + | 0.311758 |
DDB_G0274209 | DDB_G0274209 | DDB0232429 | CDS | 4783187 | 1236 | - | 0.271845 | |
DDB_G0274807 | DDB_G0274807 | DDB0232429 | CDS | 3946871 | 1851 | - | 0.222582 | |
DDB_G0274991 | DDB_G0274991 | DDB0232429 | CDS | 4818450 | 873 | + | 0.229095 | |
DDB_G0275053 | DDB_G0275053 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232429 | CDS | 5239346 | 918 | + | 0.33878 |
DDB_G0275205 | DDB_G0275205 | DDB0232429 | CDS | 5081463 | 1533 | - | 0.270711 | |
DDB_G0275793 | DDB_G0275793 | DDB0232429 | CDS | 5611769 | 1593 | - | 0.2285 | |
DDB_G0275917 | DDB_G0275917 | DDB0232429 | CDS | 6034546 | 3069 | + | 0.289019 | |
DDB_G0276215 | DDB_G0276215 | DDB0232429 | CDS | 6342811 | 1947 | + | 0.313303 | |
DDB_G0276253 | DDB_G0276253 | a bifunctional enzyme that catalyses both the synthesis and the degradation of fructose-2 6-bisphosphate | DDB0232429 | CDS | 6504888 | 1527 | - | 0.301899 |
DDB_G0276293 | DDB_G0276293 | DDB0232429 | CDS | 6559102 | 1473 | - | 0.304141 | |
DDB_G0276429 | DDB_G0276429 | DDB0232429 | CDS | 6932540 | 1422 | - | 0.270042 | |
DDB_G0276473 | DDB_G0276473 | DDB0232429 | CDS | 7015380 | 1092 | - | 0.340659 | |
DDB_G0276625 | DDB_G0276625 | belongs to the drugmetabolite transporter superfamily similar to human SLC35D1 (UDP-glucuronic acidUDP-N-acetylgalactosamine transporter) and S. cerevisiae VRG4 (GDP-mannose transporter 1) contains 8 putative transmembrane domains | DDB0232429 | CDS | 7055459 | 945 | - | 0.271958 |
DDB_G0276661 | DDB_G0276661 | DDB0232429 | CDS | 7093016 | 1377 | + | 0.312273 | |
DDB_G0276801 | DDB_G0276801 | DDB0232429 | CDS | 7352564 | 2265 | - | 0.277263 | |
DDB_G0277007 | DDB_G0277007 | homolog of human SLC35C1 (GDP-fucose transporter 1) defects in human SLC35C1 are the cause of leukocyte adhesion deficiency type II contains 10 putative transmembrane domains | DDB0232429 | CDS | 7200459 | 1107 | + | 0.272809 |
DDB_G0277045 | DDB_G0277045 | DDB0232429 | CDS | 7343113 | 1902 | - | 0.370137 | |
DDB_G0277163 | DDB_G0277163 | DDB0232429 | CDS | 7909800 | 1314 | + | 0.256469 | |
DDB_G0277167 | DDB_G0277167 | DDB0232429 | CDS | 7668593 | 1392 | + | 0.257902 | |
DDB_G0277203 | DDB_G0277203 | members of the NAD-dependent epimerasedehydratase family use nucleotide-sugar substrates for a variety of chemical reactions | DDB0232429 | CDS | 7744744 | 1008 | + | 0.293651 |
DDB_G0277575 | DDB_G0277575 | DDB0232429 | CDS | 8169746 | 387 | - | 0.271318 | |
DDB_G0277669 | DDB_G0277669 | similar to aldose 1-epimerase (mutarotase) the enzyme responsible for the anomeric interconversion of D-glucose and other aldoses between their alpha- and beta-form | DDB0232429 | CDS | 8293206 | 987 | - | 0.261398 |
DDB_G0277763 | DDB_G0277763 | DDB0232429 | CDS | 8471398 | 1350 | - | 0.292593 | |
DDB_G0277773 | DDB_G0277773 | DDB0232429 | CDS | 8461506 | 1395 | - | 0.286022 | |
DDB_G0278059 | DDB_G0278059 | similar to the human acetyl-coenzyme A transporter 1 contains 10 putative transmembrane domains | DDB0232430 | CDS | 207407 | 1857 | - | 0.234787 |
DDB_G0278261 | DDB_G0278261 | similar to the H. sapiens proton myo-inositol cotransporter SLC2A13 contains 10 putative transmembrane domains | DDB0232430 | CDS | 577308 | 1893 | + | 0.270998 |
DDB_G0278575 | DDB_G0278575 | DDB0232430 | CDS | 1095238 | 1539 | - | 0.323587 | |
DDB_G0278631 | DDB_G0278631 | putative ortholog of H. sapiens SLC35D2 UDP-N-acetylglucosamineUDP-glucoseGDP-mannose transporter contains 10 putative transmembrane domains | DDB0232430 | CDS | 462648 | 1149 | + | 0.222802 |
DDB_G0278675 | DDB_G0278675 | DDB0232430 | CDS | 789665 | 1752 | - | 0.261986 | |
DDB_G0278797 | DDB_G0278797 | DDB0232430 | CDS | 1192386 | 1233 | - | 0.316302 | |
DDB_G0279275 | DDB_G0279275 | DDB0232430 | CDS | 1874332 | 1704 | + | 0.286385 | |
DDB_G0279683 | DDB_G0279683 | DDB0232430 | CDS | 2441695 | 819 | + | 0.252747 | |
DDB_G0279943 | DDB_G0279943 | belongs to the major facilitator superefamily contains 12 putative transmembrane domains | DDB0232430 | CDS | 2721717 | 1488 | - | 0.309812 |
DDB_G0280263 | DDB_G0280263 | DDB0232430 | CDS | 3180987 | 825 | - | 0.286061 | |
DDB_G0280761 | DDB_G0280761 | belongs to the major facilitator superefamily contains 12 putative transmembrane domains | DDB0232430 | CDS | 3705496 | 1608 | - | 0.277985 |
DDB_G0280831 | DDB_G0280831 | DDB0232430 | CDS | 1432985 | 1641 | - | 0.313224 | |
DDB_G0281155 | DDB_G0281155 | putative sugar transporter contains 12 putative transmembrane domains | DDB0232430 | CDS | 4113808 | 1614 | + | 0.29368 |
DDB_G0281291 | DDB_G0281291 | DDB0232430 | CDS | 4360504 | 792 | - | 0.285354 | |
DDB_G0281487 | DDB_G0281487 | ortholog of the human NSDHL protein and the yeast ERG26 protein belongs to the 3beta-HSD family | DDB0232430 | CDS | 4603817 | 1050 | + | 0.31619 |
DDB_G0281495 | DDB_G0281495 | DDB0232430 | CDS | 4613870 | 1263 | + | 0.270784 | |
DDB_G0281523 | DDB_G0281523 | DDB0232430 | CDS | 4486206 | 1104 | - | 0.294384 | |
DDB_G0281705 | DDB_G0281705 | DDB0232430 | CDS | 4853137 | 936 | - | 0.314103 | |
DDB_G0281789 | DDB_G0281789 | DDB0232430 | CDS | 4983430 | 1410 | - | 0.367376 | |
DDB_G0281903 | DDB_G0281903 | DDB0232430 | CDS | 5094433 | 1218 | + | 0.254516 | |
DDB_G0282159 | DDB_G0282159 | DDB0232430 | CDS | 5469433 | 1635 | - | 0.327217 | |
DDB_G0282311 | DDB_G0282311 | DDB0232430 | CDS | 5621318 | 1992 | + | 0.314759 | |
DDB_G0282525 | DDB_G0282525 | DDB0232430 | CDS | 5886297 | 1251 | + | 0.243006 | |
DDB_G0282673 | DDB_G0282673 | DDB0232430 | CDS | 6100946 | 1533 | + | 0.300065 | |
DDB_G0282715 | DDB_G0282715 | DDB0232430 | CDS | 6191274 | 2313 | - | 0.316904 | |
DDB_G0282759 | DDB_G0282759 | DDB0232430 | CDS | 5775152 | 1764 | - | 0.361111 | |
DDB_G0282779_ps | DDB_G0282779 | putative pseudogene similar to D. discoideum genes | DDB0232430 | CDS | 5911017 | 2427 | - | 0.261228 |
DDB_G0282945 | DDB_G0282945 | DDB0232431 | CDS | 31559 | 2010 | - | 0.280597 | |
DDB_G0283191 | DDB_G0283191 | DDB0232431 | CDS | 394762 | 1695 | + | 0.277286 | |
DDB_G0283281 | DDB_G0283281 | catalyzes the reaction tryptamine secologanin 3-alpha(S)-strictosidine Hsub2subO in alkaloid biosynthesis | DDB0232431 | CDS | 447879 | 1179 | - | 0.261238 |
DDB_G0283947 | DDB_G0283947 | DDB0232431 | CDS | 1349351 | 1101 | + | 0.297003 | |
DDB_G0283985 | DDB_G0283985 | DDB0232431 | CDS | 1263489 | 1608 | + | 0.250622 | |
DDB_G0284099 | DDB_G0284099 | DDB0232431 | CDS | 1569018 | 1476 | - | 0.249322 | |
DDB_G0284259 | DDB_G0284259 | DDB0232431 | CDS | 1787150 | 2724 | - | 0.335536 | |
DDB_G0284433 | DDB_G0284433 | DDB0232431 | CDS | 1985042 | 960 | + | 0.3375 | |
DDB_G0284557 | DDB_G0284557 | catalyzes the reaction ATP D-gluconate ADP 6-phospho-D-gluconate | DDB0232431 | CDS | 2110678 | 603 | + | 0.238806 |
DDB_G0284737 | DDB_G0284737 | belongs to the haloacid dehalogenase (HAD) hydrolase IIA family similar to human PGP (phosphoglycolate phosphatase) and S. cerevisiae PHO13 (4-nitrophenylphosphatase) | DDB0232431 | CDS | 2397942 | 912 | - | 0.27193 |
DDB_G0284915 | DDB_G0284915 | DDB0232431 | CDS | 2643291 | 696 | - | 0.310345 | |
DDB_G0284943 | DDB_G0284943 | DDB0232431 | CDS | 2669585 | 2082 | - | 0.267531 | |
DDB_G0285511 | DDB_G0285511 | DDB0232431 | CDS | 3331170 | 1683 | - | 0.322638 | |
DDB_G0286079 | DDB_G0286079 | DDB0232431 | CDS | 4034365 | 1554 | - | 0.346847 | |
DDB_G0286605 | DDB_G0286605 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232431 | CDS | 4695789 | 909 | - | 0.275028 |
DDB_G0286749 | DDB_G0286749 | DDB0232431 | CDS | 4924314 | 2643 | + | 0.259554 | |
DDB_G0286833 | DDB_G0286833 | DDB0232431 | CDS | 4956036 | 987 | - | 0.316109 | |
DDB_G0286979 | DDB_G0286979 | DDB0232431 | CDS | 5150412 | 1884 | - | 0.277601 | |
DDB_G0287003 | DDB_G0287003 | DDB0232431 | CDS | 5191304 | 1254 | - | 0.334928 | |
DDB_G0287085 | DDB_G0287085 | there is a paralog of this gene | DDB0232431 | CDS | 5307684 | 948 | - | 0.257384 |
DDB_G0287099 | DDB_G0287099 | DDB0232431 | CDS | 5339911 | 669 | - | 0.227205 | |
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_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_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_G0287843 | DDB_G0287843 | DDB0232432 | CDS | 806278 | 1923 | - | 0.333853 | |
DDB_G0288435 | DDB_G0288435 | DDB0232432 | CDS | 1530778 | 1554 | + | 0.328829 | |
DDB_G0288535 | DDB_G0288535 | DDB0232432 | CDS | 1660756 | 1395 | - | 0.235842 | |
DDB_G0288645 | DDB_G0288645 | DDB0232432 | CDS | 1776536 | 1650 | - | 0.277576 | |
DDB_G0289439 | DDB_G0289439 | DDB0232432 | CDS | 2778983 | 405 | + | 0.367901 | |
DDB_G0289703 | DDB_G0289703 | DDB0232432 | CDS | 3127157 | 2931 | + | 0.247015 | |
DDB_G0289835 | DDB_G0289835 | DDB0232432 | CDS | 3326670 | 708 | + | 0.276836 | |
DDB_G0289953 | DDB_G0289953 | DDB0232432 | CDS | 3505573 | 2313 | - | 0.26243 | |
DDB_G0290153 | DDB_G0290153 | DDB0232432 | CDS | 3712218 | 1545 | - | 0.318447 | |
DDB_G0290423 | DDB_G0290423 | DDB0232432 | CDS | 4067949 | 1743 | + | 0.242111 | |
DDB_G0290691 | DDB_G0290691 | DDB0232432 | CDS | 4421497 | 1581 | - | 0.25933 | |
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_G0291720 | DDB_G0291720 | DDB0232433 | CDS | 721305 | 1278 | - | 0.311424 | |
DDB_G0291722 | DDB_G0291722 | DDB0232433 | CDS | 719367 | 1344 | - | 0.233631 | |
DDB_G0291730 | DDB_G0291730 | DDB0232433 | CDS | 712314 | 1374 | - | 0.235808 | |
DDB_G0291732 | DDB_G0291732 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232433 | CDS | 711008 | 927 | + | 0.326861 |
DDB_G0291758 | DDB_G0291758 | DDB0232433 | CDS | 697440 | 1194 | + | 0.273869 | |
DDB_G0291824 | DDB_G0291824 | DDB0232433 | CDS | 827281 | 1878 | - | 0.300319 | |
DDB_G0291886_ps | DDB_G0291886 | similar to | DDB0232433 | CDS | 881755 | 2151 | + | 0.248257 |
DDB_G0291888 | DDB_G0291888 | DDB0232433 | CDS | 886219 | 1416 | + | 0.214689 | |
DDB_G0292298 | DDB_G0292298 | DDB0232433 | CDS | 1424473 | 501 | - | 0.307385 | |
DDB_G0292432 | DDB_G0292432 | DDB0232433 | CDS | 1610862 | 1815 | - | 0.293113 | |
DDB_G0292440 | DDB_G0292440 | DDB0232433 | CDS | 1632296 | 1068 | - | 0.282772 | |
DDB_G0292442 | DDB_G0292442 | phosphorylates NAD to NADP | DDB0232433 | CDS | 1638801 | 2574 | - | 0.266123 |
DDB_G0292446 | DDB_G0292446 | DDB0232433 | CDS | 1655640 | 3909 | + | 0.294705 | |
DDB_G0292738 | DDB_G0292738 | DDB0232433 | CDS | 2081220 | 900 | + | 0.277778 | |
DDB_G0292750 | DDB_G0292750 | DDB0232433 | CDS | 2064418 | 2055 | + | 0.254988 | |
DDB_G0294567 | DDB_G0294567 | DDB0232430 | CDS | 2439525 | 696 | + | 0.271552 | |
DDB_G0295691 | DDB_G0295691 | shares a region of similarity with proteins of unknown functions contains eight predicted transmembrane domains | DDB0232433 | CDS | 883760 | 1164 | + | 0.256873 |
DDB_G0304561 | DDB_G0304561 | similar to solute carrier family 35 member E4 (SLC35E4) proteins contains 10 predicted transmembrane domains | DDB0232431 | CDS | 2797226 | 1476 | + | 0.278455 |
adk | DDB_G0286057 | catalyzes the reaction ATP adenosine ADP AMP | DDB0232431 | CDS | 4005558 | 1023 | + | 0.396872 |
agl | DDB_G0287569 | DDB0232432 | CDS | 354336 | 4827 | - | 0.311995 | |
ahhA | DDB_G0282009 | highly similar to mammalian adducin 1 expressed in pstO cells and in pstAB pstO and stalk cells during culmination underexpressed in dstA- cells | DDB0232430 | CDS | 5237565 | 807 | - | 0.32342 |
alfA | DDB_G0274391 | Dictyostelium enzyme that hydrolyses O- and S-glycosyl compounds with a preference for cleaving the alpha1-6-O-fucolsyl bonds in fucosylated oligosaccharides secreted during development | DDB0232429 | CDS | 4784888 | 1386 | - | 0.305916 |
alg9 | DDB_G0279349 | CAZy family GT22 catalyzes N-linked mannosylation | DDB0232430 | CDS | 1972184 | 1950 | + | 0.232308 |
amyA | DDB_G0281547 | DDB0232430 | CDS | 4671220 | 1413 | - | 0.357396 | |
aqpA | DDB_G0267378 | similar to aquaporin family of water-channel proteins expressed in prespore cells | DDB0232428 | CDS | 1385036 | 840 | + | 0.365476 |
aqpB | DDB_G0279443 | belongs to the MIP (major intrinsic protein) family contains 6 putative transmembrane domains | DDB0232430 | CDS | 2058202 | 1719 | + | 0.37929 |
athl1 | DDB_G0287109 | DDB0232431 | CDS | 5232785 | 2142 | - | 0.294118 | |
cln3 | DDB_G0291157 | ortholog of Cln3 responsible for Batten's disease a juvenile neurological disorder | DDB0232432 | CDS | 5060161 | 1266 | - | 0.313586 |
clybl | DDB_G0284067 | DDB0232431 | CDS | 1497378 | 1083 | + | 0.279778 | |
comD | DDB_G0283345 | similar to drug resistance transporters contains 14 transmembrane domains | DDB0232431 | CDS | 539820 | 3528 | + | 0.291667 |
dhak | DDB_G0269274 | catalyzes the reaction ATP glycerone ADP glycerone phosphate | DDB0232428 | CDS | 2438501 | 1947 | - | 0.249615 |
enoA | DDB_G0283137 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO enriched in gametes | DDB0232431 | CDS | 225309 | 1305 | - | 0.36092 |
enoB | DDB_G0268214 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO | DDB0232428 | CDS | 1697493 | 1332 | - | 0.327327 |
fba | DDB_G0274375 | catalyzes the reaction fructose-16-bisphosphate dihydroxy-acetone-phosphate D-glyceraldehyde-3-phosphate expressed in pstAB cells and in upper cup during culmination | DDB0232429 | CDS | 3777877 | 1074 | - | 0.385475 |
fbp | DDB_G0270836 | hydrolyses D-fructose 16-bisphosphate to D-fructose 6-phosphate and phosphate (EC 3.1.3.11) | DDB0232428 | CDS | 3681011 | 1041 | + | 0.354467 |
fhit | DDB_G0274257 | ortholog of human FHIT which is a possible tumor suppressor for specific tissues numerous tumor types are associated with aberrant forms of human FHIT protein | DDB0232429 | CDS | 4124527 | 450 | - | 0.311111 |
fslB | DDB_G0270730 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a potential signal sequence | DDB0232428 | CDS | 4235323 | 1929 | - | 0.258683 |
g6pd-1 | DDB_G0273131 | ortholog of the human G6PD defects in G6PD cause chronic non-spherocytic hemolytic anemia (CNSHA) catalyzes the reaction D-glucose 6-phosphate NADPsupsup D-glucono-15-lactone 6-phosphate NADPH Hsupsup there is a second copy of this gene | DDB0232429 | CDS | 2821995 | 1494 | - | 0.32664 |
g6pd-2 | DDB_G0273639 | ortholog of the human G6PD defects in G6PD cause chronic non-spherocytic hemolytic anemia (CNSHA) catalyzes the reaction D-glucose 6-phosphate NADPsupsup D-glucono-15-lactone 6-phosphate NADPH Hsupsup there is a second copy of this gene | DDB0232429 | CDS | 3207904 | 1494 | + | 0.32664 |
gaa | DDB_G0269790 | ortholog of the H. sapiens lysosomal alpha-glucosidase which is essential for the degradation of glygogen to glucose in lysosomes defects in GAA are the cause of glycogen storage disease II a recessive disorder which results in a massive accumulation of glycogen in muscle heart and liver leading to a life expectancy of less than two years | DDB0232428 | CDS | 3563596 | 2604 | + | 0.329493 |
galK | DDB_G0292112 | DDB0232433 | CDS | 1203261 | 1506 | + | 0.317397 | |
ger | DDB_G0270184 | catalyzes the reaction GDP-L-fucose NADP GDP-4-dehydro-6-deoxy-D-mannose NADPH H | DDB0232428 | CDS | 4379266 | 963 | - | 0.284528 |
glb1 | DDB_G0290217 | belongs to glycoside hydrolase family 35 hydrolyzes terminal non-reducing beta-D-galactose residues in beta-D-galactoside has a signal peptide | DDB0232432 | CDS | 3809656 | 2016 | - | 0.312996 |
glb2 | DDB_G0285637 | belongs to glycoside hydrolase family 35 hydrolyzes terminal non-reducing beta-D-galactose residues in beta-D-galactoside has a signal peptide | DDB0232431 | CDS | 3510010 | 2286 | - | 0.279528 |
glgB | DDB_G0274105 | transfers a segment of a 14-alpha-D-glucan chain to a primary hydroxyl group in a similar glucan chain | DDB0232429 | CDS | 4089271 | 2037 | + | 0.348061 |
glk | DDB_G0287631 | catalyzes the reaction ATP D-glucose ADP D-glucose 6-phosphate | DDB0232432 | CDS | 530347 | 1791 | - | 0.319933 |
glpD | DDB_G0291123 | CAZy family GT35 5'-AMP-independent glycogen phosphorylase expressed in late development the combined activities of glpV and glpD results in constant glycogen phosphorylase activity throughout development | DDB0232432 | CDS | 5073815 | 2982 | - | 0.335345 |
glpV | DDB_G0281383 | CAZy family GT35 5'-AMP-dependent glycogen phosphorylase expressed in early development the combined activities of glpV and glpD results in constant glycogen phosphorylase activity throughout development | DDB0232430 | CDS | 4540912 | 2562 | - | 0.366511 |
gluA | DDB_G0292810 | DDB0232433 | CDS | 2240229 | 2466 | - | 0.364152 | |
gnd | DDB_G0277885 | catalyzes the reaction 6-phospho-D-gluconate NADPsupsup D-ribulose 5-phosphate COsub2sub NADPH | DDB0232430 | CDS | 273541 | 1482 | - | 0.398111 |
gnpda1 | DDB_G0278873 | short version of the glucosamine-6-phosphate isomerase similar to fungi and metazoans catalyzes the reaction D-glucosamine 6-phosphate Hsub2subO D-fructose 6-phosphate NHsub3sub | DDB0232430 | CDS | 1321299 | 804 | - | 0.31592 |
gpdA | DDB_G0275153 | DDB0232429 | CDS | 5324765 | 1008 | + | 0.380952 | |
gpi | DDB_G0283673 | catalyzes the reaction D-glucose 6-phosphate D-fructose 6-phosphate | DDB0232431 | CDS | 954966 | 1686 | + | 0.339265 |
gpmA | DDB_G0285311 | catalyzes the reaction 3-phosphoglycerate 2-phosphoglycerate | DDB0232431 | CDS | 3080971 | 750 | - | 0.330667 |
gtr2 | DDB_G0276105 | distant relative of CAZy family GT5 contains a glycosyltransferase domain and an alpha amylase catalytic domain | DDB0232429 | CDS | 6292325 | 7422 | + | 0.325115 |
impa1 | DDB_G0281239 | catalyzes the reaction myo-inositol phosphate Hsub2subO myo-inositol phosphate human IMPA1 is a pharmacological target for Li in the treatment of manic depression | DDB0232430 | CDS | 4261304 | 819 | + | 0.310134 |
manA | DDB_G0292206 | DDB0232433 | CDS | 1355092 | 3033 | - | 0.331355 | |
manB | DDB_G0278259 | DDB0232430 | CDS | 573780 | 3108 | + | 0.298584 | |
manC | DDB_G0268994 | DDB0232428 | CDS | 2093909 | 3240 | + | 0.225926 | |
manD | DDB_G0278653 | DDB0232430 | CDS | 660402 | 3669 | - | 0.24012 | |
manE | DDB_G0278651 | DDB0232430 | CDS | 655951 | 3372 | - | 0.242586 | |
manF | DDB_G0287231 | DDB0232432 | CDS | 28270 | 2985 | - | 0.271692 | |
manG | DDB_G0287577 | DDB0232432 | CDS | 413359 | 3264 | - | 0.321385 | |
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 |
modA | DDB_G0269154 | DDB0232428 | CDS | 3274209 | 2832 | + | 0.328037 | |
mpi | DDB_G0284685 | catalyzes the reaction D-Mannose 6-phosphate D-fructose 6-phosphate | DDB0232431 | CDS | 2341606 | 1359 | - | 0.27741 |
nagA | DDB_G0287033 | DDB0232431 | CDS | 5251113 | 1599 | + | 0.333333 | |
nagB | DDB_G0282539 | DDB0232430 | CDS | 5899632 | 1626 | - | 0.311808 | |
nagB1 | DDB_G0286195 | long version of the glucosamine-6-phosphate isomerase similar to Entamoeba and ciliates catalyzes the reaction D-glucosamine 6-phosphate Hsub2subO D-fructose 6-phosphate NHsub3sub | DDB0232431 | CDS | 4161180 | 2175 | - | 0.316322 |
nagC | DDB_G0287597 | DDB0232432 | CDS | 449924 | 1683 | + | 0.24896 | |
nagD | DDB_G0287659 | DDB0232432 | CDS | 447833 | 1695 | + | 0.316814 | |
nagE | DDB_G0285647 | similar to beta-hexosaminidase but shorter on the amino terminus | DDB0232431 | CDS | 3533871 | 2088 | + | 0.221264 |
ndufa9 | DDB_G0272266 | DDB0232429 | CDS | 1449219 | 1071 | - | 0.323063 | |
padA | DDB_G0286385 | involved in development and cell differentiation modulates the expression of extracellular cAMP relay genes during aggregation | DDB0232431 | CDS | 4393013 | 906 | + | 0.352097 |
pfkA | DDB_G0274111 | catalyzes the reaction ATP D-fructose 6-phosphate ADP D-fructose 16-bisphosphate the Dictyostelium PFK has been found to be a non-allosteric enzyme that binds to tubulin and inhibits tubulin polymerization | DDB0232429 | CDS | 4510635 | 2505 | + | 0.372455 |
pgkA | DDB_G0287595 | catalyzes the reaction 3-phosphoglycerate ATP 3-phospho-D-glyceroyl-phosphate ADP binds and is regulated by calmodulin | DDB0232432 | CDS | 494968 | 1263 | - | 0.364212 |
pgl | DDB_G0292898 | catalyzes the reaction 6-phospho-D-glucono-15-lactone Hsub2subO 6-phospho-D-gluconate | DDB0232433 | CDS | 2232140 | 711 | + | 0.295359 |
pgmA | DDB_G0288483 | catalyzes the reaction alpha-D-glucose 1-phosphate alpha-D-glucose 6-phosphate | DDB0232432 | CDS | 1620141 | 1719 | - | 0.34555 |
pgmB | DDB_G0280897 | ortholog of PGM2 which catalyzes the reaction alpha-D-glucose 1-phosphate alpha-D-glucose 6-phosphate | DDB0232430 | CDS | 3847722 | 1812 | + | 0.334989 |
pkiA | DDB_G0289391 | DDB0232432 | CDS | 2783089 | 384 | + | 0.351562 | |
pyk | DDB_G0283247 | catalyzes the reaction ATP pyruvate ADP phosphoenolpyruvate | DDB0232431 | CDS | 344914 | 1524 | - | 0.358268 |
rbsk | DDB_G0280893 | catalyzes the reaction D-ribose ATP D-ribose-5-phosphate ADP | DDB0232430 | CDS | 3840063 | 957 | + | 0.239289 |
rgn | DDB_G0277535 | similar to regucalcin a calcium binding protein that controls many cellular functions | DDB0232429 | CDS | 7984797 | 897 | + | 0.334448 |
rliA | DDB_G0272783 | twelve transmembrane domain protein that may act as a transporter repressed after Legionella pneumophila infection | DDB0232429 | CDS | 2172067 | 1416 | + | 0.267655 |
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 |
rpe | DDB_G0278275 | catalyzes the reaction D-ribulose 5-phosphate D-xylulose 5-phosphate | DDB0232430 | CDS | 603034 | 678 | - | 0.325959 |
rpiA | DDB_G0276711 | catalyzes the reaction D-ribose 5-phosphate D-ribulose 5-phosphate | DDB0232429 | CDS | 7091221 | 699 | - | 0.311874 |
slc35b2 | DDB_G0269602 | belongs to the drugmetabolite transporter (DMT) superfamily similar to D. melanogaster sll human SLC35B2 contains 8 predicted transmembrane domains | DDB0232428 | CDS | 3110201 | 1080 | - | 0.297222 |
symA | DDB_G0292814 | DDB0232433 | CDS | 2158906 | 1371 | - | 0.33698 | |
tal | DDB_G0280909 | catalyzes the reaction sedoheptulose 7-phosphate D-glyceraldehyde 3-phosphate D-erythrose 4-phosphate D-fructose 6-phosphate | DDB0232430 | CDS | 3865707 | 966 | - | 0.331263 |
tkt-1 | DDB_G0272618 | catalyzes the reaction D-ribose-5-phosphate D-xylulose-5-phosphate D-sedoheptulose-7-phosphate D-glyceraldehyde-3-phosphate there is a second copy of this gene | DDB0232429 | CDS | 2357975 | 1986 | + | 0.39577 |
tkt-2 | DDB_G0274019 | catalyzes the reaction D-ribose-5-phosphate D-xylulose-5-phosphate D-sedoheptulose-7-phosphate D-glyceraldehyde-3-phosphate there is a second copy of this gene | DDB0232429 | CDS | 3671700 | 1986 | - | 0.39577 |
tmem20 | DDB_G0292606 | putative drugmetabolite transporter containing 10 predicted transmembrane domains | DDB0232433 | CDS | 1830985 | 2097 | + | 0.311874 |
tpiA | DDB_G0274471 | catalyzes the reaction D-glyceraldehyde 3-phosphate glycerone phosphate defects in human TPI1 are the cause of triosephosphate isomerase deficiency severe clinical disorder of glycolysis | DDB0232429 | CDS | 4481626 | 774 | + | 0.330749 |
tpsA | DDB_G0287657 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain enriched in prestalk cells | DDB0232432 | CDS | 444388 | 2202 | - | 0.321072 |
tpsB | DDB_G0284975 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain | DDB0232431 | CDS | 2735507 | 2373 | - | 0.307206 |
tpsC | DDB_G0290405 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain | DDB0232432 | CDS | 4043666 | 2700 | + | 0.303333 |
treh | DDB_G0283473 | homolog of human TREH catalyzes the reaction alphaalpha-trehalose H2O 2 D-glucose contains a predicted signal peptide | DDB0232431 | CDS | 746464 | 1785 | + | 0.341737 |
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 |
ugpB | DDB_G0277879 | DDB0232430 | CDS | 140895 | 1509 | - | 0.313453 | |
ugt2 | DDB_G0268540 | CAZy family GT28 highly similar to ugt3 | DDB0232428 | CDS | 1089190 | 1314 | - | 0.227549 |
ugt3 | DDB_G0268544 | CAZy family GT28 highly similar to ugt2 | DDB0232428 | CDS | 1091709 | 1314 | - | 0.225266 |
ugt52 | DDB_G0288655 | CAZy family GT1 catalyzes the reaction UDP-glucose a sterol UDP a glucosylsterol | DDB0232432 | CDS | 1802347 | 5094 | - | 0.291323 |
uppA | DDB_G0289875 | catalyzes the reaction UTP alpha-D-glucose 1-phosphate diphosphate UDP-glucose | DDB0232432 | CDS | 3439159 | 1536 | - | 0.287109 |
wacA | DDB_G0280537 | member of the major intrinsic protein (MIP) family of membrane transporters expressed starting at culmination stage in prespore cells | DDB0232430 | CDS | 3567052 | 825 | + | 0.368485 |
Dictyostelium fasciculatum, SH3 | ||||||||
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g10002 | DFA_10385 | EU5ZYIE02H8LDV-5 | CDS | 1375053 | 1536 | + | 0.369792 | |
g10152 | DFA_10551 | EU5ZYIE02H8LDV-5 | CDS | 1737193 | 1770 | + | 0.342938 | |
g10273 | DFA_10676 | EUAJFUG01CK1KI-5 | CDS | 142216 | 4413 | - | 0.376388 | |
g10313 | DFA_10721 | EUAJFUG01CK1KI-5 | CDS | 246985 | 1806 | - | 0.367663 | |
g10388 | DFA_10802 | EUAJFUG01CK1KI-5 | CDS | 416250 | 1404 | + | 0.352564 | |
g1045 | DFA_01034 | Dfasci-F-a-25c12.r2-5 | CDS | 1796502 | 2325 | + | 0.343656 | |
g10477 | DFA_10893 | EUAJFUG02G6ADK-5 | CDS | 83936 | 594 | + | 0.390572 | |
g10582 | DFA_11003 | EUAJFUG02G6ADK-5 | CDS | 350009 | 792 | + | 0.387626 | |
g10630 | DFA_11049 | EUAJFUG02HR96I-5 | CDS | 73297 | 1584 | + | 0.305556 | |
g10666 | DFA_11081 | EUAJFUG02HR96I-5 | CDS | 151844 | 570 | - | 0.345614 | |
g1079 | DFA_01068 | Dfasci-F-a-25c12.r2-5 | CDS | 1888390 | 1833 | + | 0.444081 | |
g10817 | DFA_11238 | EUAJFUG02HR96I-5 | CDS | 571310 | 1404 | - | 0.399573 | |
g1099 | DFA_01090 | Dfasci-F-a-25c12.r2-5 | CDS | 1943748 | 1266 | - | 0.3594 | |
g11014 | DFA_11431 | EUAJFUG02HR96I-5 | CDS | 1109732 | 912 | - | 0.406798 | |
g11015 | DFA_11432 | EUAJFUG02HR96I-5 | CDS | 1111432 | 909 | - | 0.410341 | |
g11185 | DFA_11605 | EUAJFUG02HR96I-5 | CDS | 1538321 | 1446 | + | 0.355463 | |
g11278 | DFA_11698 | EUAJFUG02HR96I-5 | CDS | 1776208 | 927 | + | 0.277238 | |
g11300 | DFA_11720 | EUAJFUG02HR96I-5 | CDS | 1840608 | 1068 | - | 0.496255 | |
g11306 | DFA_11726 | EUAJFUG02HR96I-5 | CDS | 1855672 | 3159 | - | 0.384299 | |
g1134 | DFA_01129 | Dfasci-F-a-25c12.r2-5 | CDS | 2032109 | 1995 | - | 0.474185 | |
g11395 | DFA_11832 | EUAJFUG02HR96I-5 | CDS | 2117271 | 2682 | - | 0.384787 | |
g11396 | DFA_11835 | EUAJFUG02HR96I-5 | CDS | 2122478 | 1539 | + | 0.380117 | |
g11415 | DFA_11855 | EUAJFUG02HR96I-5 | CDS | 2171108 | 1917 | + | 0.31977 | |
g1146 | DFA_01141 | Dfasci-F-a-25c12.r2-5 | CDS | 2057165 | 666 | - | 0.331832 | |
g11478 | DFA_11935 | EUAJFUG02HR96I-5 | CDS | 2350302 | 996 | - | 0.324297 | |
g11565 | DFA_12027 | EUAJFUG02HR96I-5 | CDS | 2552603 | 888 | - | 0.394144 | |
g11620 | DFA_12086 | EUAJFUG02HR96I-5 | CDS | 2696961 | 1308 | + | 0.327217 | |
g11622 | DFA_12088 | EUAJFUG02HR96I-5 | CDS | 2699899 | 1398 | - | 0.321888 | |
g11718 | DFA_12194 | EUAJFUG02HR96I-5 | CDS | 2962227 | 2502 | - | 0.398881 | |
g11741 | DFA_12217 | EUAJFUG02HR96I-5 | CDS | 3032413 | 876 | - | 0.383562 | |
g11762 | DFA_12239 | EUAJFUG02HR96I-5 | CDS | 3100619 | 1173 | - | 0.335891 | |
g1207 | DFA_01207 | Dfasci-F-a-25c12.r2-5 | CDS | 2207170 | 2145 | + | 0.358508 | |
g1273 | DFA_01273 | Dfasci-F-a-25c12.r2-5 | CDS | 2361571 | 4803 | - | 0.417656 | |
g1290 | DFA_01291 | Dfasci-F-a-25c12.r2-5 | CDS | 2399899 | 1650 | - | 0.323636 | |
g1299 | DFA_01299 | Dfasci-F-a-25c12.r2-5 | CDS | 2415389 | 2757 | + | 0.379398 | |
g1327 | DFA_01327 | Dfasci-F-a-25c12.r2-5 | CDS | 2489371 | 837 | + | 0.457587 | |
g1349 | DFA_01351 | Dfasci-F-a-25c12.r2-5 | CDS | 2540006 | 1464 | - | 0.447404 | |
g139 | DFA_00137 | Dfasci-F-a-11f03.f1-5 | CDS | 400250 | 537 | + | 0.350093 | |
g1468 | DFA_01476 | Dfasci-F-a-25c12.r2-5 | CDS | 2831345 | 1083 | - | 0.374885 | |
g1522 | DFA_01529 | Dfasci-F-a-25c12.r2-5 | CDS | 2970892 | 2481 | - | 0.422007 | |
g1582 | DFA_01587 | Dfasci-F-a-25c12.r2-5 | CDS | 3116778 | 1299 | - | 0.384142 | |
g1594 | DFA_01601 | Dfasci-F-a-25c12.r2-5 | CDS | 3152491 | 1551 | - | 0.426177 | |
g1595 | DFA_01603 | Dfasci-F-a-25c12.r2-5 | CDS | 3157246 | 3315 | + | 0.4727 | |
g1644 | DFA_01658 | Dfasci-F-a-25c12.r2-5 | CDS | 3296038 | 2355 | + | 0.449257 | |
g1662 | DFA_12545 | Dfasci-F-a-25c12.r2-5 | CDS | 3339903 | 1563 | - | 0.420345 | |
g1669 | DFA_01681 | Dfasci-F-a-25c12.r2-5 | CDS | 3355284 | 1371 | - | 0.375638 | |
g1706 | DFA_01720 | Dfasci-F-a-25c12.r2-5 | CDS | 3451830 | 3615 | + | 0.372337 | |
g1721 | DFA_01737 | Dfasci-F-a-25c12.r2-5 | CDS | 3492071 | 1635 | - | 0.36208 | |
g1773 | DFA_01791 | Dfasci-F-a-25c12.r2-5 | CDS | 3629494 | 1026 | - | 0.482456 | |
g1787 | DFA_01804 | Dfasci-F-a-25c12.r2-5 | CDS | 3671281 | 1602 | - | 0.393883 | |
g184 | DFA_00178 | Dfasci-F-a-11f03.f1-5 | CDS | 523651 | 996 | - | 0.446787 | |
g1958 | DFA_01990 | Dfasci-F-a-25c12.r2-5 | CDS | 4120880 | 1068 | - | 0.346442 | |
g2007 | DFA_02039 | Dfasci-G-b-126g04.f1-5 | CDS | 72685 | 1578 | - | 0.391635 | |
g2163 | DFA_02214 | Dfasci-G-b-143d02.r1-5 | CDS | 10829 | 2952 | + | 0.372967 | |
g2176 | DFA_02226 | Dfasci-G-b-143d02.r1-5 | CDS | 37270 | 774 | + | 0.394057 | |
g2270 | DFA_02317 | Dfasci-G-b-143d02.r1-5 | CDS | 269480 | 336 | - | 0.342262 | |
g2396 | DFA_02452 | Dfasci-G-b-143d02.r1-5 | CDS | 591561 | 1536 | + | 0.36263 | |
g2451 | DFA_02500 | Dfasci-G-b-190b03.r1-5 | CDS | 69377 | 1599 | + | 0.395872 | |
g246 | DFA_00238 | Dfasci-F-a-11f03.f1-5 | CDS | 691092 | 930 | - | 0.391398 | |
g2502 | DFA_02552 | Dfasci-G-b-190b03.r1-5 | CDS | 190931 | 849 | - | 0.426384 | |
g2825 | DFA_02887 | Dfasci-G-b-205a01.r1-3 | CDS | 459500 | 1530 | + | 0.439869 | |
g2831 | DFA_02894 | Dfasci-G-b-205a01.r1-3 | CDS | 473459 | 1668 | + | 0.461631 | |
g2852 | DFA_02914 | Dfasci-G-b-205a01.r1-3 | CDS | 535409 | 1518 | - | 0.4361 | |
g2897 | DFA_02964 | Dfasci-G-b-205a01.r1-3 | CDS | 648666 | 1062 | + | 0.311676 | |
g2924 | DFA_02995 | Dfasci-G-b-205a01.r1-3 | CDS | 718895 | 2034 | + | 0.402655 | |
g2950 | DFA_03026 | Dfasci-G-b-205a01.r1-3 | CDS | 789781 | 1611 | + | 0.285537 | |
g2960 | DFA_03039 | Dfasci-G-b-205a01.r1-3 | CDS | 823923 | 2778 | - | 0.404968 | |
g3057 | DFA_03139 | Dfasci-G-b-205a01.r1-3 | CDS | 1049078 | 1083 | - | 0.441367 | |
g3099 | DFA_12672 | Dfasci-G-b-205a01.r1-3 | CDS | 1177259 | 1305 | + | 0.3341 | |
g3279 | DFA_03373 | Dfasci-G-b-205a01.r1-3 | CDS | 1668725 | 1260 | + | 0.335714 | |
g3282 | DFA_03375 | Dfasci-G-b-205a01.r1-3 | CDS | 1672612 | 1617 | + | 0.312307 | |
g3518 | DFA_03630 | Dfasci-G-b-205a01.r1-3 | CDS | 2378889 | 2127 | - | 0.392572 | |
g3520 | DFA_03632 | Dfasci-G-b-205a01.r1-3 | CDS | 2384463 | 1623 | + | 0.333333 | |
g3530 | DFA_03642 | Dfasci-G-b-205a01.r1-3 | CDS | 2414879 | 861 | - | 0.391405 | |
g3657 | DFA_03787 | Dfasci-G-b-285a01.f1-5 | CDS | 259662 | 1866 | - | 0.377278 | |
g3668 | DFA_03802 | Dfasci-G-b-285a01.f1-5 | CDS | 297403 | 1965 | + | 0.366921 | |
g3689 | DFA_03821 | Dfasci-G-b-285a01.f1-5 | CDS | 342052 | 1770 | + | 0.381356 | |
g3709 | DFA_03841 | Dfasci-G-b-285a01.f1-5 | CDS | 391206 | 1365 | + | 0.368498 | |
g3743 | DFA_03882 | Dfasci-G-b-285a01.f1-5 | CDS | 486672 | 1011 | - | 0.341246 | |
g3747 | DFA_03887 | Dfasci-G-b-285a01.f1-5 | CDS | 502797 | 897 | - | 0.478261 | |
g3777 | DFA_03919 | Dfasci-G-b-285a01.f1-5 | CDS | 579882 | 2061 | + | 0.426977 | |
g3827 | DFA_03972 | Dfasci-G-b-285a01.f1-5 | CDS | 715478 | 1377 | - | 0.342774 | |
g387 | DFA_00378 | Dfasci-F-a-25c12.r2-5 | CDS | 102028 | 3021 | + | 0.403509 | |
g4046 | DFA_04211 | Dfasci-G-b-285a01.f1-5 | CDS | 1266251 | 912 | - | 0.35307 | |
g4242 | DFA_04401 | Dfasci-G-o-33e01.r1-3 | CDS | 452740 | 6873 | + | 0.442747 | |
g427 | DFA_00416 | Dfasci-F-a-25c12.r2-5 | CDS | 205038 | 1287 | - | 0.310023 | |
g43 | DFA_00040 | Dfasci-F-a-11f03.f1-5 | CDS | 99846 | 906 | - | 0.362031 | |
g4395 | DFA_04551 | Dfasci-G-o-33e01.r1-3 | CDS | 826456 | 432 | - | 0.358796 | |
g4445 | DFA_04607 | Dfasci-G-o-33e01.r1-3 | CDS | 955427 | 1860 | - | 0.337634 | |
g4600 | DFA_04769 | Dfasci-G-o-33e01.r1-3 | CDS | 1314616 | 708 | + | 0.379943 | |
g4616 | DFA_04785 | Dfasci-G-o-33e01.r1-3 | CDS | 1350495 | 1860 | + | 0.455914 | |
g4724 | DFA_04893 | Dfasci-G-o-80e12.f1-5 | CDS | 182306 | 1029 | + | 0.407191 | |
g4765 | DFA_04938 | Dfasci-G-o-80e12.f1-5 | CDS | 285231 | 1050 | - | 0.304762 | |
g4860 | DFA_05038 | Dfasci-G-o-80e12.f1-5 | CDS | 538613 | 1614 | + | 0.381041 | |
g4894 | DFA_05075 | Dfasci-G-o-80e12.f1-5 | CDS | 641579 | 1698 | + | 0.460542 | |
g4999 | DFA_05186 | Dfasci-G-o-80e12.f1-5 | CDS | 912619 | 1848 | - | 0.362013 | |
g5161 | DFA_05366 | Dfasci-G-o-80e12.f1-5 | CDS | 1368926 | 903 | - | 0.423034 | |
g5214 | DFA_05419 | Dfasci-G-o-80e12.f1-5 | CDS | 1498396 | 996 | - | 0.426707 | |
g5305 | DFA_05514 | Dfasci-G-o-80e12.f1-5 | CDS | 1753623 | 2001 | + | 0.337831 | |
g5307 | DFA_05515 | Dfasci-G-o-80e12.f1-5 | CDS | 1757416 | 1884 | - | 0.445329 | |
g538 | DFA_00519 | Dfasci-F-a-25c12.r2-5 | CDS | 484967 | 744 | + | 0.396505 | |
g5397 | DFA_05608 | Dfasci-G-o-80e12.f1-5 | CDS | 2012942 | 1578 | + | 0.378961 | |
g5404 | DFA_05616 | Dfasci-G-o-80e12.f1-5 | CDS | 2034503 | 1695 | - | 0.40767 | |
g5422 | DFA_05635 | Dfasci-G-o-80e12.f1-5 | CDS | 2089788 | 2412 | + | 0.376866 | |
g5463 | DFA_05675 | Dfasci-G-o-80e12.f1-5 | CDS | 2203893 | 1479 | - | 0.3881 | |
g5524 | DFA_05736 | Dfasci-G-o-80e12.f1-5 | CDS | 2346400 | 1236 | + | 0.385922 | |
g556 | DFA_00538 | Dfasci-F-a-25c12.r2-5 | CDS | 526578 | 1149 | - | 0.369017 | |
g5692 | DFA_05897 | Dfasci-G-p-12c09.r1-3 | CDS | 14547 | 1116 | + | 0.365591 | |
g5759 | DFA_05966 | Dfasci-G-p-12c09.r1-3 | CDS | 194862 | 1839 | + | 0.42795 | |
g5776 | DFA_05983 | Dfasci-G-p-12c09.r1-3 | CDS | 233043 | 948 | - | 0.357595 | |
g5834 | DFA_06043 | Dfasci-G-p-12c09.r1-3 | CDS | 366855 | 1938 | + | 0.452012 | |
g588 | DFA_00568 | Dfasci-F-a-25c12.r2-5 | CDS | 626439 | 690 | + | 0.337681 | |
g5883 | DFA_12875 | Dfasci-G-p-12c09.r1-3 | CDS | 499348 | 1707 | - | 0.422964 | |
g5911 | DFA_06128 | Dfasci-G-p-12c09.r1-3 | CDS | 580189 | 1215 | + | 0.325926 | |
g601 | DFA_00584 | Dfasci-F-a-25c12.r2-5 | CDS | 657741 | 717 | - | 0.308229 | |
g6219 | DFA_06463 | Dfasci-G-p-12c09.r1-3 | CDS | 1392094 | 1308 | - | 0.477829 | |
g6221 | DFA_06465 | Dfasci-G-p-12c09.r1-3 | CDS | 1396295 | 2631 | - | 0.415811 | |
g6311 | DFA_06558 | Dfasci-G-p-12c09.r1-3 | CDS | 1619069 | 1782 | - | 0.383838 | |
g6357 | DFA_06604 | Dfasci-G-p-12c09.r1-3 | CDS | 1740889 | 723 | + | 0.362379 | |
g6364 | DFA_06611 | Dfasci-G-p-12c09.r1-3 | CDS | 1754987 | 1314 | - | 0.328006 | |
g637 | DFA_00620 | Dfasci-F-a-25c12.r2-5 | CDS | 732447 | 1734 | + | 0.374279 | |
g6374 | DFA_06619 | EJPB12P01AWP9W-5 | CDS | 4157 | 3600 | - | 0.369444 | |
g6381 | DFA_06625 | EJPB12P01AWP9W-5 | CDS | 23618 | 1572 | + | 0.397583 | |
g6401 | DFA_06644 | EJPB12P01AWP9W-5 | CDS | 74642 | 1059 | + | 0.338999 | |
g6422 | DFA_06665 | EJPB12P01AWP9W-5 | CDS | 133993 | 1398 | - | 0.378398 | |
g6573 | DFA_06831 | EJPB12P01AWP9W-5 | CDS | 580231 | 954 | - | 0.424528 | |
g6693 | DFA_06948 | ET2XIPL01CNAVH-3 | CDS | 280844 | 1512 | + | 0.439815 | |
g6725 | DFA_06979 | ET2XIPL01CNAVH-3 | CDS | 363581 | 756 | - | 0.443122 | |
g6774 | DFA_07036 | ET2XIPL01CNAVH-3 | CDS | 483039 | 2781 | + | 0.467458 | |
g6799 | DFA_07067 | ET2XIPL01CNAVH-3 | CDS | 560388 | 1506 | - | 0.349934 | |
g6812 | DFA_07080 | ET2XIPL01CNAVH-3 | CDS | 594984 | 1017 | + | 0.355949 | |
g688 | DFA_00671 | Dfasci-F-a-25c12.r2-5 | CDS | 883266 | 2148 | - | 0.4027 | |
g6919 | DFA_07193 | ET2XIPL01CNAVH-3 | CDS | 887936 | 1305 | + | 0.359387 | |
g6999 | DFA_07272 | ET2XIPL01CNAVH-3 | CDS | 1093830 | 825 | - | 0.406061 | |
g7053 | DFA_07326 | ET2XIPL01CNAVH-3 | CDS | 1215856 | 1503 | + | 0.370592 | |
g7112 | DFA_07384 | ET2XIPL01CNAVH-3 | CDS | 1357374 | 879 | + | 0.426621 | |
g7196 | DFA_07463 | ET2XIPL01CNAVH-3 | CDS | 1596003 | 1092 | + | 0.459707 | |
g7249 | DFA_07516 | ET2XIPL01CNAVH-3 | CDS | 1740279 | 1698 | + | 0.377503 | |
g7363 | DFA_07625 | ET2XIPL01COFD4-5 | CDS | 92366 | 3207 | - | 0.304022 | |
g7427 | DFA_07688 | ET2XIPL01COFD4-5 | CDS | 273016 | 1410 | + | 0.383688 | |
g7465 | DFA_07723 | ET2XIPL01COFD4-5 | CDS | 389944 | 639 | + | 0.330203 | |
g7469 | DFA_07728 | ET2XIPL01COFD4-5 | CDS | 398190 | 945 | - | 0.45291 | |
g7571 | DFA_07835 | ET2XIPL01COFD4-5 | CDS | 642030 | 1671 | - | 0.339916 | |
g7601 | DFA_13052 | ET2XIPL01COFD4-5 | CDS | 722971 | 1359 | + | 0.329654 | |
g7711 | DFA_07981 | ET2XIPL01COFD4-5 | CDS | 1017370 | 1686 | + | 0.401542 | |
g7815 | DFA_08090 | ET2XIPL01COFD4-5 | CDS | 1237047 | 1026 | + | 0.375244 | |
g7897 | DFA_13081 | ET2XIPL01COFD4-5 | CDS | 1443249 | 1137 | + | 0.324538 | |
g8032 | DFA_08336 | ET2XIPL01COFD4-5 | CDS | 1820907 | 1224 | - | 0.370915 | |
g8033 | DFA_08337 | ET2XIPL01COFD4-5 | CDS | 1822445 | 1257 | - | 0.473349 | |
g8055 | DFA_08363 | ET2XIPL01COFD4-5 | CDS | 1895918 | 2787 | - | 0.4277 | |
g8079 | DFA_08387 | ET2XIPL01COFD4-5 | CDS | 1957345 | 2043 | - | 0.337249 | |
g8093 | DFA_08398 | ET2XIPL01COFD4-5 | CDS | 2001581 | 912 | - | 0.445175 | |
g8174 | DFA_08473 | ET2XIPL01COFD4-5 | CDS | 2229553 | 327 | - | 0.330275 | |
g8222 | DFA_08518 | ET2XIPL01COFD4-5 | CDS | 2350712 | 1353 | - | 0.410939 | |
g8259 | DFA_08558 | ET2XIPL01COFD4-5 | CDS | 2461453 | 1050 | - | 0.377143 | |
g8339 | DFA_08639 | ET2XIPL01COFD4-5 | CDS | 2674243 | 1515 | + | 0.359076 | |
g8426 | DFA_13125 | ET2XIPL01COFD4-5 | CDS | 2909583 | 1101 | - | 0.411444 | |
g8456 | DFA_08758 | ET2XIPL01COFD4-5 | CDS | 2979802 | 2496 | + | 0.469551 | |
g8500 | DFA_08800 | ET2XIPL01COFD4-5 | CDS | 3085387 | 1917 | - | 0.356808 | |
g8563 | DFA_08869 | ET2XIPL01COFD4-5 | CDS | 3270926 | 969 | + | 0.449948 | |
g8618 | DFA_08929 | ET2XIPL01COFD4-5 | CDS | 3412220 | 1710 | + | 0.419883 | |
g8789 | DFA_13160 | EU5ZYIE01BBABR-5 | CDS | 357906 | 1071 | - | 0.383754 | |
g8807 | DFA_09120 | EU5ZYIE01BBABR-5 | CDS | 405459 | 675 | - | 0.374815 | |
g8831 | DFA_09144 | EU5ZYIE01BBABR-5 | CDS | 453515 | 2556 | - | 0.451487 | |
g8899 | DFA_09217 | EU5ZYIE01DZOHE-5 | CDS | 184592 | 1014 | + | 0.422091 | |
g9017 | DFA_09337 | EU5ZYIE01DZOHE-5 | CDS | 489231 | 1452 | + | 0.417355 | |
g9079 | DFA_09404 | EU5ZYIE01DZOHE-5 | CDS | 649944 | 1605 | + | 0.462305 | |
g9151 | DFA_09486 | EU5ZYIE01EUG8B-5 | CDS | 72257 | 2106 | - | 0.364198 | |
g9441 | DFA_09796 | EU5ZYIE01EUG8B-5 | CDS | 936050 | 1950 | + | 0.381026 | |
g9458 | DFA_09814 | EU5ZYIE02H8LDV-5 | CDS | 33580 | 1764 | + | 0.38322 | |
g9483 | DFA_09841 | EU5ZYIE02H8LDV-5 | CDS | 84471 | 2052 | - | 0.344542 | |
g9517 | DFA_09878 | EU5ZYIE02H8LDV-5 | CDS | 198454 | 2625 | - | 0.366857 | |
g9554 | DFA_09911 | EU5ZYIE02H8LDV-5 | CDS | 287432 | 1569 | - | 0.421925 | |
g9623 | DFA_09984 | EU5ZYIE02H8LDV-5 | CDS | 450536 | 1008 | - | 0.456349 | |
g9681 | DFA_10047 | EU5ZYIE02H8LDV-5 | CDS | 588530 | 4596 | - | 0.366406 | |
g9693 | DFA_10059 | EU5ZYIE02H8LDV-5 | CDS | 624852 | 1410 | - | 0.360284 | |
g9749 | DFA_10122 | EU5ZYIE02H8LDV-5 | CDS | 784468 | 960 | - | 0.405208 | |
g9917 | DFA_10298 | EU5ZYIE02H8LDV-5 | CDS | 1179540 | 885 | + | 0.367232 | |
g9991 | DFA_10375 | EU5ZYIE02H8LDV-5 | CDS | 1348925 | 2172 | - | 0.358195 | |
Dictyostelium lacteum | ||||||||
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g10004 | DLA_11161 | catalyzes the reaction D-ribose 5-phosphate D-ribulose 5-phosphate | GLQOFTK02JL55Q | CDS | 598711 | 714 | - | 0.357143 |
g10006 | DLA_11163 | Dictyostelium enzyme that hydrolyses O- and S-glycosyl compounds with a preference for cleaving the alpha1-6-O-fucolsyl bonds in fucosylated oligosaccharides secreted during development | GLQOFTK02JL55Q | CDS | 600382 | 1398 | + | 0.350501 |
g10032 | DLA_11195 | GLQOFTK02JL55Q | CDS | 663874 | 1269 | - | 0.35067 | |
g10047 | DLA_11210 | GLQOFTK02JL55Q | CDS | 689818 | 1275 | + | 0.347451 | |
g10169 | DLA_11361 | GLQOFTK02JL55Q | CDS | 963978 | 1605 | + | 0.378816 | |
g10188 | DLA_11383 | catalyzes the reaction ATP glycerone ADP glycerone phosphate | GLQOFTK02JL55Q | CDS | 1030200 | 3105 | - | 0.318519 |
g1026 | DLA_01137 | F4PJNLW01A00V1 | CDS | 878684 | 1566 | - | 0.323755 | |
g1196 | DLA_01314 | F4PJNLW01A00V1 | CDS | 1291700 | 1485 | + | 0.319865 | |
g1225 | DLA_01349 | F4PJNLW01A00V1 | CDS | 1374980 | 1335 | + | 0.301873 | |
g1284 | DLA_01408 | F4PJNLW01AQJ8S | CDS | 35153 | 2337 | + | 0.32392 | |
g1359 | DLA_01489 | F4PJNLW01B0TO9 | CDS | 162179 | 2442 | + | 0.379607 | |
g1484 | DLA_01628 | F4PJNLW01B0TO9 | CDS | 425017 | 2556 | + | 0.373631 | |
g1588 | DLA_01742 | catalyzes the reaction fructose-16-bisphosphate dihydroxy-acetone-phosphate D-glyceraldehyde-3-phosphate expressed in pstAB cells and in upper cup during culmination | F4PJNLW01B0TO9 | CDS | 664814 | 1080 | - | 0.393519 |
g159 | DLA_11433 | contig05409_1.exp | CDS | 368849 | 1725 | - | 0.293913 | |
g1604 | DLA_01756 | F4PJNLW01B0TO9 | CDS | 704668 | 921 | + | 0.320304 | |
g1614 | DLA_01767 | F4PJNLW01B0TO9 | CDS | 723057 | 1686 | - | 0.298932 | |
g166 | DLA_00193 | contig05409_1.exp | CDS | 392153 | 2205 | + | 0.350567 | |
g1683 | DLA_01843 | F4PJNLW01B0TO9 | CDS | 880002 | 4254 | + | 0.293371 | |
g181 | DLA_00208 | contig05409_1.exp | CDS | 419599 | 1677 | - | 0.359571 | |
g1901 | DLA_02073 | F4PJNLW01DERRH | CDS | 22421 | 669 | - | 0.331839 | |
g1930 | DLA_02112 | F4PJNLW01DERRH | CDS | 114657 | 1644 | + | 0.340024 | |
g202 | DLA_00227 | contig05409_1.exp | CDS | 476159 | 1665 | - | 0.32973 | |
g2092 | DLA_02306 | F4PJNLW01DERRH | CDS | 476826 | 1020 | + | 0.290196 | |
g2167 | DLA_02386 | F4PJNLW01DERRH | CDS | 648072 | 1086 | + | 0.333333 | |
g2193 | DLA_02414 | F4PJNLW01DERRH | CDS | 696290 | 1455 | - | 0.292783 | |
g2194 | DLA_02415 | F4PJNLW01DERRH | CDS | 698259 | 1287 | + | 0.305361 | |
g2253 | DLA_11522 | F4PJNLW01EE5MJ | CDS | 117818 | 1245 | + | 0.324498 | |
g2336 | DLA_02584 | F4PJNLW01EE5MJ | CDS | 316180 | 1230 | - | 0.321138 | |
g2418 | DLA_02679 | F4PJNLW01EE5MJ | CDS | 484352 | 1005 | + | 0.342289 | |
g2425 | DLA_02686 | F4PJNLW01EE5MJ | CDS | 497320 | 1461 | + | 0.381246 | |
g2477 | DLA_02748 | F4PJNLW01EE5MJ | CDS | 637138 | 1848 | - | 0.33171 | |
g251 | DLA_00279 | contig05409_1.exp | CDS | 571713 | 933 | + | 0.352626 | |
g2574 | DLA_02858 | catalyzes the reaction GDP-L-fucose NADP GDP-4-dehydro-6-deoxy-D-mannose NADPH H | F4PJNLW01EE5MJ | CDS | 858491 | 948 | + | 0.341772 |
g2615 | DLA_02902 | similar to bacterial endo-14-beta-glucanase expressed in pstAO cells | F4PJNLW01EE5MJ | CDS | 960317 | 1725 | + | 0.361739 |
g2652 | DLA_02944 | F4PJNLW01EE5MJ | CDS | 1037367 | 2694 | - | 0.308463 | |
g2668 | DLA_02961 | F4PJNLW01EE5MJ | CDS | 1070320 | 777 | + | 0.328185 | |
g277 | DLA_00307 | contig05409_1.exp | CDS | 639887 | 1617 | - | 0.367965 | |
g287 | DLA_00317 | contig05409_1.exp | CDS | 659718 | 4656 | + | 0.348797 | |
g2980 | DLA_03301 | F4PJNLW02HBBIY | CDS | 232173 | 2199 | - | 0.34925 | |
g3099 | DLA_03431 | hydrolyses D-fructose 16-bisphosphate to D-fructose 6-phosphate and phosphate (EC 3.1.3.11) | F4PJNLW02HBBIY | CDS | 491079 | 1017 | - | 0.347099 |
g3209 | DLA_03557 | GAOABQK02FWKR3 | CDS | 20867 | 1314 | + | 0.266362 | |
g3303 | DLA_03654 | GAOABQK02G6SYV | CDS | 169897 | 792 | + | 0.34596 | |
g3355 | DLA_03711 | GAOABQK02G6SYV | CDS | 277710 | 1317 | + | 0.333333 | |
g3408 | DLA_03769 | GAOABQK02G6SYV | CDS | 384133 | 1446 | + | 0.359613 | |
g3434 | DLA_03797 | GAOABQK02G6SYV | CDS | 454028 | 2922 | + | 0.356605 | |
g3441 | DLA_03805 | GAOABQK02G6SYV | CDS | 467790 | 1587 | - | 0.376812 | |
g3508 | DLA_03886 | GAOABQK02G6SYV | CDS | 622509 | 1536 | - | 0.324219 | |
g3530 | DLA_03909 | transfers a segment of a 14-alpha-D-glucan chain to a primary hydroxyl group in a similar glucan chain | GAOABQK02G6SYV | CDS | 670759 | 2049 | - | 0.348463 |
g3560 | DLA_03942 | GAOABQK02G7M1S | CDS | 44899 | 6978 | - | 0.338062 | |
g3641 | DLA_04038 | GAOABQK02G7M1S | CDS | 243382 | 723 | + | 0.329184 | |
g3686 | DLA_04083 | GAOABQK02G7M1S | CDS | 354857 | 903 | + | 0.301218 | |
g3791 | DLA_04203 | GAOABQK02G7M1S | CDS | 586046 | 1668 | + | 0.374101 | |
g3804 | DLA_04220 | GAOABQK02G7M1S | CDS | 613921 | 1488 | - | 0.373656 | |
g3890 | DLA_04313 | GAOABQK02GQAQJ | CDS | 44882 | 2739 | + | 0.318364 | |
g3896 | DLA_04320 | GAOABQK02GQAQJ | CDS | 57187 | 750 | - | 0.316 | |
g4019 | DLA_04458 | GAOABQK02GQAQJ | CDS | 346864 | 1266 | + | 0.329384 | |
g4026 | DLA_04466 | belongs to the drugmetabolite transporter (DMT) superfamily similar to D. melanogaster sll human SLC35B2 contains 8 predicted transmembrane domains | GAOABQK02GQAQJ | CDS | 363647 | 1137 | - | 0.373791 |
g4222 | DLA_04669 | GAOABQK02GQAQJ | CDS | 763149 | 1296 | + | 0.328704 | |
g427 | DLA_00474 | contig05409_1.exp | CDS | 968607 | 879 | - | 0.32537 | |
g4296 | DLA_04742 | GAOABQK02GQAQJ | CDS | 934578 | 4212 | - | 0.340456 | |
g4514 | DLA_05004 | GAOABQK02H81I9 | CDS | 165813 | 1008 | + | 0.375 | |
g4595 | DLA_05089 | GAOABQK02H81I9 | CDS | 349544 | 1509 | - | 0.355865 | |
g4596 | DLA_05090 | GAOABQK02H81I9 | CDS | 352560 | 1077 | - | 0.312906 | |
g4632 | DLA_05129 | GAOABQK02H81I9 | CDS | 445151 | 1266 | + | 0.325434 | |
g4653 | DLA_05151 | GAOABQK02H81I9 | CDS | 488758 | 999 | + | 0.313313 | |
g4735 | DLA_05242 | GAOABQK02H81I9 | CDS | 688150 | 3072 | + | 0.349284 | |
g4795 | DLA_05307 | GAOABQK02H81I9 | CDS | 831961 | 1068 | - | 0.273408 | |
g4833 | DLA_05351 | GAOABQK02HUB3S | CDS | 18635 | 1593 | + | 0.338983 | |
g4921 | DLA_05448 | GAOABQK02HUB3S | CDS | 229933 | 765 | + | 0.364706 | |
g5134 | DLA_05686 | GAOABQK02HUB3S | CDS | 708017 | 1431 | - | 0.361286 | |
g5161 | DLA_05726 | GAOABQK02HUB3S | CDS | 779799 | 351 | + | 0.2849 | |
g5162 | DLA_05727 | GAOABQK02HUB3S | CDS | 780230 | 2280 | + | 0.339035 | |
g5258 | DLA_05835 | GAOABQK02HUB3S | CDS | 1045122 | 2844 | - | 0.353024 | |
g5287 | DLA_05868 | GAOABQK02HUB3S | CDS | 1127229 | 1563 | - | 0.329495 | |
g5396 | DLA_06005 | GAOABQK02HUB3S | CDS | 1383618 | 2184 | - | 0.340201 | |
g5446 | DLA_06066 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO | GAOABQK02HUB3S | CDS | 1496409 | 1293 | - | 0.369683 |
g5447 | DLA_06067 | GAOABQK02HUB3S | CDS | 1499697 | 2229 | + | 0.336025 | |
g5612 | DLA_06257 | GAOABQK02IBA3P | CDS | 4134 | 1986 | + | 0.330312 | |
g5768 | DLA_06433 | ortholog of human FHIT which is a possible tumor suppressor for specific tissues numerous tumor types are associated with aberrant forms of human FHIT protein | GAOABQK02IBA3P | CDS | 399414 | 435 | + | 0.333333 |
g5777 | DLA_06443 | GAOABQK02IBA3P | CDS | 418948 | 1335 | - | 0.323595 | |
g5794 | DLA_06461 | catalyzes the reaction ATP D-fructose 6-phosphate ADP D-fructose 16-bisphosphate the Dictyostelium PFK has been found to be a non-allosteric enzyme that binds to tubulin and inhibits tubulin polymerization | GAOABQK02IBA3P | CDS | 456155 | 2367 | + | 0.377693 |
g5870 | DLA_06544 | GAOABQK02IBA3P | CDS | 604806 | 876 | - | 0.33105 | |
g5872 | DLA_06546 | GAOABQK02IBA3P | CDS | 607739 | 1356 | + | 0.312684 | |
g5896 | DLA_06569 | GAOABQK02IBA3P | CDS | 673422 | 1083 | - | 0.354571 | |
g5908 | DLA_06583 | GAOABQK02IBA3P | CDS | 721382 | 1710 | - | 0.347368 | |
g6117 | DLA_06812 | GAOABQK02IO52T | CDS | 58106 | 1263 | + | 0.355503 | |
g6186 | DLA_06896 | catalyzes the reaction D-ribose-5-phosphate D-xylulose-5-phosphate D-sedoheptulose-7-phosphate D-glyceraldehyde-3-phosphate there is a second copy of this gene | GAOABQK02IO52T | CDS | 219448 | 1983 | - | 0.395865 |
g62 | DLA_00072 | contig05409_1.exp | CDS | 153753 | 1725 | + | 0.32058 | |
g6226 | DLA_06938 | GAOABQK02IO52T | CDS | 301000 | 1266 | - | 0.345182 | |
g6236 | DLA_06949 | GAOABQK02IO52T | CDS | 322203 | 915 | - | 0.353005 | |
g6275 | DLA_06990 | GAOABQK02IO52T | CDS | 404089 | 1203 | + | 0.334996 | |
g6314 | DLA_07033 | catalyzes the reaction D-glyceraldehyde 3-phosphate glycerone phosphate defects in human TPI1 are the cause of triosephosphate isomerase deficiency severe clinical disorder of glycolysis | GAOABQK02IO52T | CDS | 490529 | 777 | - | 0.365508 |
g6391 | DLA_07112 | GAOABQK02IO52T | CDS | 654391 | 933 | + | 0.301179 | |
g6573 | DLA_07324 | GAOABQK02JOCCH | CDS | 166129 | 657 | - | 0.334855 | |
g6667 | DLA_07428 | GAOABQK02JOCCH | CDS | 383578 | 390 | - | 0.34359 | |
g6690 | DLA_07450 | similar to aquaporin family of water-channel proteins expressed in prespore cells | GAOABQK02JOCCH | CDS | 436199 | 825 | - | 0.386667 |
g6760 | DLA_07530 | GAOABQK02JOCCH | CDS | 601599 | 1413 | + | 0.300778 | |
g6855 | DLA_07641 | GAOABQK02JOCCH | CDS | 809961 | 984 | + | 0.311992 | |
g6886 | DLA_07682 | GLQOFTK02FH5TG | CDS | 4995 | 1023 | + | 0.307918 | |
g6933 | DLA_07730 | GLQOFTK02FH5TG | CDS | 103350 | 1941 | - | 0.320453 | |
g6967 | DLA_07765 | GLQOFTK02FH5TG | CDS | 173393 | 885 | + | 0.362712 | |
g6999 | DLA_07801 | GLQOFTK02FH5TG | CDS | 241685 | 1479 | - | 0.387424 | |
g7087 | DLA_07910 | GLQOFTK02FH5TG | CDS | 474332 | 1572 | + | 0.344148 | |
g7122 | DLA_07952 | GLQOFTK02FH5TG | CDS | 541931 | 2778 | - | 0.364651 | |
g7133 | DLA_07963 | GLQOFTK02FH5TG | CDS | 562162 | 1206 | - | 0.31592 | |
g7214 | DLA_08050 | GLQOFTK02FH5TG | CDS | 734142 | 933 | - | 0.330118 | |
g7221 | DLA_08061 | GLQOFTK02FH5TG | CDS | 756670 | 2181 | - | 0.358551 | |
g7243 | DLA_08081 | GLQOFTK02FH5TG | CDS | 804964 | 879 | - | 0.354949 | |
g7250 | DLA_08089 | GLQOFTK02FH5TG | CDS | 818320 | 984 | - | 0.336382 | |
g7265 | DLA_08110 | phosphorylates NAD to NADP | GLQOFTK02FH5TG | CDS | 854853 | 1323 | - | 0.31746 |
g7272 | DLA_08120 | GLQOFTK02FH5TG | CDS | 869478 | 4377 | + | 0.323966 | |
g7292 | DLA_08145 | similar to aquaporin family of water-channel proteins expressed in prespore cells | GLQOFTK02FH5TG | CDS | 911786 | 825 | + | 0.398788 |
g7382 | DLA_08255 | GLQOFTK02FH5TG | CDS | 1122408 | 1620 | - | 0.312346 | |
g7386 | DLA_08259 | GLQOFTK02FH5TG | CDS | 1130733 | 1926 | + | 0.38162 | |
g749 | DLA_00824 | ortholog of the human G6PD defects in G6PD cause chronic non-spherocytic hemolytic anemia (CNSHA) catalyzes the reaction D-glucose 6-phosphate NADPsupsup D-glucono-15-lactone 6-phosphate NADPH Hsupsup there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 256464 | 1536 | - | 0.373047 |
g7564 | DLA_08460 | GLQOFTK02G2F2O | CDS | 4919 | 1695 | - | 0.321534 | |
g758 | DLA_00835 | F4PJNLW01A00V1 | CDS | 273958 | 909 | - | 0.330033 | |
g7619 | DLA_08523 | GLQOFTK02G2F2O | CDS | 123368 | 948 | + | 0.372363 | |
g7786 | DLA_08702 | GLQOFTK02G2F2O | CDS | 527605 | 957 | + | 0.318704 | |
g8086 | DLA_09037 | GLQOFTK02G2F2O | CDS | 1192492 | 888 | + | 0.261261 | |
g8092 | DLA_09043 | GLQOFTK02G2F2O | CDS | 1202860 | 1071 | - | 0.344538 | |
g8155 | DLA_09114 | GLQOFTK02G2F2O | CDS | 1369393 | 2067 | + | 0.311079 | |
g8176 | DLA_09135 | GLQOFTK02G2F2O | CDS | 1414967 | 1032 | - | 0.378876 | |
g8247 | DLA_09209 | GLQOFTK02G2F2O | CDS | 1564293 | 1893 | + | 0.342842 | |
g8297 | DLA_09258 | GLQOFTK02G2F2O | CDS | 1671893 | 1326 | - | 0.342383 | |
g8353 | DLA_09321 | GLQOFTK02G2F2O | CDS | 1780188 | 693 | - | 0.359307 | |
g8417 | DLA_09386 | GLQOFTK02G2F2O | CDS | 1891326 | 1098 | - | 0.37796 | |
g8609 | DLA_09602 | GLQOFTK02GHM7A | CDS | 283717 | 822 | + | 0.36618 | |
g8685 | DLA_09681 | GLQOFTK02GHM7A | CDS | 461208 | 912 | + | 0.35636 | |
g8705 | DLA_09701 | GLQOFTK02GHM7A | CDS | 505848 | 3387 | - | 0.327428 | |
g8758 | DLA_09754 | members of the NAD-dependent epimerasedehydratase family use nucleotide-sugar substrates for a variety of chemical reactions | GLQOFTK02GHM7A | CDS | 623170 | 1011 | + | 0.339268 |
g877 | DLA_00961 | F4PJNLW01A00V1 | CDS | 546414 | 765 | - | 0.351634 | |
g8843 | DLA_09845 | GLQOFTK02GHM7A | CDS | 843423 | 963 | + | 0.369678 | |
g8865 | DLA_09877 | GLQOFTK02GQ36N | CDS | 13249 | 546 | + | 0.283883 | |
g8883 | DLA_09897 | GLQOFTK02GQ36N | CDS | 42045 | 939 | + | 0.332268 | |
g9000 | DLA_10023 | GLQOFTK02GQ36N | CDS | 311593 | 1686 | + | 0.358837 | |
g9059 | DLA_10081 | GLQOFTK02GQ36N | CDS | 421767 | 1410 | + | 0.353191 | |
g9072 | DLA_10096 | GLQOFTK02GQ36N | CDS | 459748 | 1770 | + | 0.365537 | |
g9113 | DLA_10146 | GLQOFTK02GQ36N | CDS | 577105 | 1857 | - | 0.344103 | |
g9227 | DLA_10280 | GLQOFTK02GUKFG | CDS | 171124 | 1059 | - | 0.352219 | |
g9273 | DLA_10332 | GLQOFTK02GUKFG | CDS | 299129 | 897 | + | 0.376812 | |
g9296 | DLA_10363 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | GLQOFTK02GUKFG | CDS | 350129 | 897 | - | 0.365663 |
g9307 | DLA_10375 | GLQOFTK02GUKFG | CDS | 373057 | 1695 | + | 0.375221 | |
g9314 | DLA_10381 | ortholog of the H. sapiens lysosomal alpha-glucosidase which is essential for the degradation of glygogen to glucose in lysosomes defects in GAA are the cause of glycogen storage disease II a recessive disorder which results in a massive accumulation of glycogen in muscle heart and liver leading to a life expectancy of less than two years | GLQOFTK02GUKFG | CDS | 385590 | 2730 | - | 0.348718 |
g9368 | DLA_10439 | GLQOFTK02GUKFG | CDS | 491811 | 900 | - | 0.313333 | |
g9450 | DLA_10529 | GLQOFTK02IIOHN | CDS | 99402 | 2697 | + | 0.313682 | |
g9640 | DLA_10747 | GLQOFTK02IRMR1 | CDS | 87594 | 4137 | + | 0.32729 | |
g9666 | DLA_10781 | GLQOFTK02IRMR1 | CDS | 154803 | 759 | - | 0.343874 | |
g9721 | DLA_10852 | GLQOFTK02JCFFB | CDS | 91645 | 2967 | + | 0.345804 | |
g9790 | DLA_10924 | GLQOFTK02JL55Q | CDS | 124410 | 3543 | + | 0.338978 | |
g9806 | DLA_10946 | GLQOFTK02JL55Q | CDS | 164996 | 1188 | - | 0.315657 | |
g9999 | DLA_11844 | belongs to the drugmetabolite transporter superfamily similar to human SLC35D1 (UDP-glucuronic acidUDP-N-acetylgalactosamine transporter) and S. cerevisiae VRG4 (GDP-mannose transporter 1) contains 8 putative transmembrane domains | GLQOFTK02JL55Q | CDS | 591072 | 942 | - | 0.321656 |
Polysphondylium pallidum, PN500 | ||||||||
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g1004 | PPL_01167 | DPPA0061d07.r1-5 | CDS | 871355 | 2559 | - | 0.459945 | |
g10067 | PPL_10599 | EXOLTKG01B86TH-3_part2 | CDS | 525060 | 1242 | + | 0.399356 | |
g10070 | PPL_10602 | EXOLTKG01B86TH-3_part2 | CDS | 531410 | 1341 | - | 0.409396 | |
g10082 | PPL_10613 | EXOLTKG01B86TH-3_part2 | CDS | 566168 | 1653 | - | 0.402904 | |
g1012 | PPL_01174 | DPPA0061d07.r1-5 | CDS | 889642 | 1509 | - | 0.417495 | |
g1013 | PPL_01176 | DPPA0061d07.r1-5 | CDS | 895531 | 1098 | - | 0.367942 | |
g10158 | PPL_10688 | similar to aquaporin family of water-channel proteins expressed in prespore cells | EXOLTKG01B86TH-3_part2 | CDS | 794922 | 783 | - | 0.478927 |
g10209 | PPL_10750 | EXOLTKG01B86TH-3y_part1 | CDS | 29751 | 1260 | - | 0.355556 | |
g10381 | PPL_10939 | EXOLTKG01B86TH-3y_part2 | CDS | 66355 | 1680 | - | 0.34881 | |
g10399 | PPL_10958 | EXOLTKG02GJRTE-5 | CDS | 11844 | 882 | - | 0.44898 | |
g10657 | PPL_11247 | PN500-F-W-a08d11.p658-5_part2 | CDS | 255745 | 1020 | + | 0.403922 | |
g10664 | PPL_11255 | PN500-F-W-a08d11.p658-5_part2 | CDS | 274975 | 1491 | - | 0.413816 | |
g10798 | PPL_11388 | PN500-F-W-a08d11.p658-5_part2 | CDS | 684601 | 2172 | + | 0.406998 | |
g10804 | PPL_11393 | PN500-F-W-a08d11.p658-5_part2 | CDS | 699396 | 1587 | + | 0.377442 | |
g11010 | PPL_11757 | PN500-G-d-72b01.r1-5 | CDS | 54493 | 2058 | + | 0.47036 | |
g11058 | PPL_11813 | PN500-G-d-72b01.r1-5 | CDS | 210049 | 1791 | + | 0.428252 | |
g1108 | PPL_01288 | DPPA0061d07.r1-5 | CDS | 1183471 | 696 | - | 0.429598 | |
g11131 | PPL_11885 | PN500-G-d-72b01.r1-5 | CDS | 419322 | 900 | - | 0.354444 | |
g11238 | PPL_11993 | PN500-G-d-72b01.r1-5 | CDS | 708106 | 2010 | + | 0.365174 | |
g11248 | PPL_12005 | PN500-G-d-72b01.r1-5 | CDS | 735411 | 2481 | - | 0.351471 | |
g11250 | PPL_12008 | a bifunctional enzyme that catalyses both the synthesis and the degradation of fructose-2 6-bisphosphate | PN500-G-d-72b01.r1-5 | CDS | 742640 | 1524 | - | 0.446194 |
g11259 | PPL_12017 | PN500-G-d-72b01.r1-5 | CDS | 761753 | 1011 | + | 0.485658 | |
g11373 | PPL_11667 | PN500-G-d-188d09.r1-5 | CDS | 297672 | 2904 | - | 0.460055 | |
g1242 | PPL_01451 | DPPA0090b03.f1-3_x_part2 | CDS | 160968 | 1713 | + | 0.402218 | |
g1308 | PPL_01517 | DPPA0090b03.f1-3_x_part2 | CDS | 364146 | 1716 | + | 0.409674 | |
g1325 | PPL_01536 | DPPA0090b03.f1-3_x_part3 | CDS | 37760 | 4668 | - | 0.448372 | |
g1505 | PPL_01733 | DPPA0090b03.f1-3_x_part3 | CDS | 545453 | 1884 | + | 0.409236 | |
g1536 | PPL_01768 | DPPA0090b03.f1-3_x_part3 | CDS | 634227 | 801 | - | 0.33583 | |
g1538 | PPL_01770 | DPPA0090b03.f1-3_x_part3 | CDS | 640078 | 585 | + | 0.403419 | |
g1548 | PPL_12832 | DPPA0090b03.f1-3_x_part3 | CDS | 669729 | 936 | - | 0.361111 | |
g1549 | PPL_12833 | DPPA0090b03.f1-3_x_part3 | CDS | 671261 | 1134 | - | 0.364198 | |
g1550 | PPL_01785 | DPPA0090b03.f1-3_x_part3 | CDS | 673133 | 1227 | - | 0.393643 | |
g1601 | PPL_01833 | DPPA0090b03.f1-3_x_part3 | CDS | 802402 | 1668 | - | 0.422662 | |
g1606 | PPL_12846 | DPPA0090b03.f1-3_x_part3 | CDS | 815260 | 1446 | + | 0.412172 | |
g1621 | PPL_01857 | DPPA0090b03.f1-3_x_part3 | CDS | 870769 | 387 | + | 0.397933 | |
g163 | PPL_00265 | DPPA0004F08.r1-5_part2 | CDS | 452542 | 1401 | - | 0.449679 | |
g1632 | PPL_01868 | DPPA0090b03.f1-3_x_part3 | CDS | 892648 | 2094 | - | 0.4532 | |
g1715 | PPL_01952 | DPPA0090b03.f1-3_x_part3 | CDS | 1097266 | 2196 | - | 0.434426 | |
g179 | PPL_00284 | DPPA0004F08.r1-5_part2 | CDS | 495323 | 933 | + | 0.353698 | |
g185 | PPL_00290 | DPPA0004F08.r1-5_part2 | CDS | 517343 | 1548 | - | 0.360465 | |
g1859 | PPL_02110 | DPPA0090b03.f1-3_x_part3 | CDS | 1546363 | 1461 | + | 0.379877 | |
g1924 | PPL_02180 | DPPA0090b03.f1-3_x_part3 | CDS | 1758172 | 831 | + | 0.410349 | |
g1945 | PPL_02205 | DPPA0090b03.f1-3_x_part3 | CDS | 1827797 | 726 | + | 0.444904 | |
g1965 | PPL_02224 | DPPA0090b03.f1-3_x_part3 | CDS | 1869117 | 1440 | - | 0.386806 | |
g2038 | PPL_02299 | DPPA0090b03.f1-3_x_part3 | CDS | 2072941 | 1398 | + | 0.404149 | |
g2068 | PPL_02338 | DPPA0090b03.f1-3_x_part3 | CDS | 2184263 | 291 | - | 0.443299 | |
g2071 | PPL_02341 | DPPA0090b03.f1-3_x_part3 | CDS | 2189357 | 1725 | + | 0.395362 | |
g2080 | PPL_02349 | ortholog of the H. sapiens lysosomal alpha-glucosidase which is essential for the degradation of glygogen to glucose in lysosomes defects in GAA are the cause of glycogen storage disease II a recessive disorder which results in a massive accumulation of glycogen in muscle heart and liver leading to a life expectancy of less than two years | DPPA0090b03.f1-3_x_part3 | CDS | 2208477 | 2652 | - | 0.401961 |
g2115 | PPL_12917 | DPPA0090b03.f1-3_x_part3 | CDS | 2300973 | 2178 | - | 0.423324 | |
g2223 | PPL_02515 | highly similar to mammalian adducin 1 expressed in pstO cells and in pstAB pstO and stalk cells during culmination underexpressed in dstA- cells | DPPA0090b03.f1-3_x_part4 | CDS | 178581 | 804 | + | 0.426617 |
g2263 | PPL_02565 | DPPA0090b03.f1-3_x_part4 | CDS | 299376 | 891 | - | 0.418631 | |
g2312 | PPL_02622 | a bifunctional enzyme that catalyses both the synthesis and the degradation of fructose-2 6-bisphosphate | DPPA0090b03.f1-3_y_part1 | CDS | 138301 | 1485 | - | 0.417508 |
g246 | PPL_00357 | DPPA0004F08.r1-5_part2 | CDS | 710510 | 3555 | + | 0.421097 | |
g2480 | PPL_02797 | DPPA0090b03.f1-3_y_part1 | CDS | 564928 | 1287 | + | 0.411033 | |
g2508 | PPL_02827 | DPPA0090b03.f1-3_y_part1 | CDS | 652818 | 1500 | - | 0.428 | |
g2583 | PPL_02907 | DPPA0090b03.f1-3_y_part1 | CDS | 833430 | 1479 | - | 0.446924 | |
g2649 | PPL_02984 | DPPA0090b03.f1-3_y_part1 | CDS | 1025784 | 1626 | - | 0.458795 | |
g2650 | PPL_02985 | DPPA0090b03.f1-3_y_part1 | CDS | 1028382 | 1515 | + | 0.467987 | |
g2858 | PPL_03214 | DPPA0090b03.f1-3_y_part1 | CDS | 1614873 | 2190 | + | 0.407306 | |
g2927 | PPL_03285 | DPPA0090b03.f1-3_y_part1 | CDS | 1786553 | 1620 | + | 0.361728 | |
g2944 | PPL_03303 | DPPA0090b03.f1-3_y_part1 | CDS | 1843700 | 1536 | - | 0.396484 | |
g2961 | PPL_03326 | DPPA0090b03.f1-3_y_part1 | CDS | 1890194 | 2244 | - | 0.441622 | |
g3096 | PPL_03475 | DPPA0090b03.f1-3_y_part1 | CDS | 2256664 | 2820 | + | 0.398227 | |
g3163 | PPL_03585 | DPPA0255d09.f1-5 | CDS | 108410 | 1431 | + | 0.473096 | |
g3216 | PPL_03649 | DPPB0337b12.r1-5 | CDS | 9850 | 1488 | - | 0.376344 | |
g3294 | PPL_03731 | DPPB0337b12.r1-5 | CDS | 221793 | 1011 | - | 0.430267 | |
g3302 | PPL_03738 | DPPB0337b12.r1-5 | CDS | 239988 | 3471 | - | 0.413137 | |
g332 | PPL_00444 | Dictyostelium enzyme that hydrolyses O- and S-glycosyl compounds with a preference for cleaving the alpha1-6-O-fucolsyl bonds in fucosylated oligosaccharides secreted during development | DPPA0004F08.r1-5_part2 | CDS | 952294 | 1389 | - | 0.439165 |
g3349 | PPL_03794 | DPPB0337b12.r1-5 | CDS | 371555 | 3105 | + | 0.386795 | |
g3380 | PPL_03829 | DPPB0337b12.r1-5 | CDS | 461440 | 1464 | + | 0.460383 | |
g3386 | PPL_03837 | DPPB0337b12.r1-5 | CDS | 477285 | 888 | - | 0.406532 | |
g352 | PPL_00466 | DPPA0004F08.r1-5_part2 | CDS | 1021334 | 1446 | - | 0.455048 | |
g3551 | PPL_04016 | similar to Plasmodium falciparum CRT which confers resistance to chloroquine contains 10 predicted transmembrane domains | DPPB0337b12.r1-5 | CDS | 924866 | 1386 | - | 0.417027 |
g3561 | PPL_13080 | catalyzes the reaction GDP-L-fucose NADP GDP-4-dehydro-6-deoxy-D-mannose NADPH H | DPPB0337b12.r1-5 | CDS | 947188 | 963 | + | 0.409138 |
g357 | PPL_00472 | DPPA0004F08.r1-5_part2 | CDS | 1033394 | 1476 | - | 0.441057 | |
g3570 | PPL_04038 | DPPB0337b12.r1-5 | CDS | 974899 | 2427 | - | 0.414916 | |
g3582 | PPL_04050 | DPPB0337b12.r1-5 | CDS | 1017805 | 891 | - | 0.391695 | |
g3682 | PPL_04158 | similar to aquaporin family of water-channel proteins expressed in prespore cells | DPPB0337b12.r1-5 | CDS | 1265637 | 672 | + | 0.391369 |
g3813 | PPL_04308 | DPPB0360e11.f1-5 | CDS | 341773 | 1650 | - | 0.467273 | |
g3822 | PPL_04317 | catalyzes the reaction D-glyceraldehyde 3-phosphate glycerone phosphate defects in human TPI1 are the cause of triosephosphate isomerase deficiency severe clinical disorder of glycolysis | DPPB0360e11.f1-5 | CDS | 366649 | 774 | - | 0.468992 |
g3948 | PPL_04459 | DPPB0360e11.f1-5 | CDS | 749554 | 1743 | - | 0.45611 | |
g4027 | PPL_04547 | DPPB0360e11.f1-5 | CDS | 999195 | 978 | - | 0.370143 | |
g4053 | PPL_04575 | E0KFERV02EE9X2-3_part1 | CDS | 34390 | 1881 | + | 0.43647 | |
g4102 | PPL_04626 | E0KFERV02EE9X2-3_part1 | CDS | 170623 | 1671 | + | 0.432077 | |
g417 | PPL_00537 | DPPA0004F08.r1-5_part2 | CDS | 1220679 | 885 | - | 0.359322 | |
g4240 | PPL_04792 | E0KFERV02EE9X2-3_part1 | CDS | 606383 | 1230 | - | 0.422764 | |
g4295 | PPL_13154 | E0KFERV02EE9X2-3_part1 | CDS | 749836 | 285 | - | 0.477193 | |
g4317 | PPL_04877 | E0KFERV02EE9X2-3_part1 | CDS | 819312 | 795 | - | 0.43522 | |
g4431 | PPL_05025 | E0KFERV02EE9X2-3_part2 | CDS | 228080 | 1038 | - | 0.432563 | |
g448 | PPL_00575 | DPPA0004F08.r1-5_part2 | CDS | 1305039 | 1419 | + | 0.372093 | |
g449 | PPL_00576 | DPPA0004F08.r1-5_part2 | CDS | 1306941 | 1524 | - | 0.417979 | |
g4500 | PPL_05101 | E3JQK7F01CUWUC-3_part1 | CDS | 115942 | 1302 | - | 0.399386 | |
g4505 | PPL_05108 | belongs to the drugmetabolite transporter (DMT) superfamily similar to D. melanogaster sll human SLC35B2 contains 8 predicted transmembrane domains | E3JQK7F01CUWUC-3_part1 | CDS | 128534 | 1095 | - | 0.413699 |
g4506 | PPL_05109 | E3JQK7F01CUWUC-3_part1 | CDS | 130500 | 912 | - | 0.416667 | |
g4527 | PPL_13168 | E3JQK7F01CUWUC-3_part1 | CDS | 195979 | 897 | - | 0.343367 | |
g4531 | PPL_05134 | E3JQK7F01CUWUC-3_part1 | CDS | 205293 | 1029 | + | 0.487852 | |
g4539 | PPL_05142 | E3JQK7F01CUWUC-3_part1 | CDS | 230210 | 1623 | + | 0.32902 | |
g4546 | PPL_05150 | E3JQK7F01CUWUC-3_part1 | CDS | 256468 | 894 | + | 0.385906 | |
g4803 | PPL_05443 | E3JQK7F01EFZL8-5 | CDS | 497213 | 993 | + | 0.434038 | |
g481 | PPL_00613 | DPPA0004F08.r1-5_part2 | CDS | 1408042 | 2610 | + | 0.379693 | |
g4824 | PPL_05463 | E3JQK7F01EFZL8-5 | CDS | 560483 | 4560 | + | 0.391447 | |
g4830 | PPL_05468 | E3JQK7F01EFZL8-5 | CDS | 579011 | 906 | - | 0.373068 | |
g4889 | PPL_05530 | E3JQK7F01EFZL8-5 | CDS | 738814 | 1083 | + | 0.390582 | |
g4998 | PPL_05639 | E3JQK7F01EFZL8-5 | CDS | 1024806 | 1266 | - | 0.399684 | |
g502 | PPL_00633 | DPPA0004F08.r1-5_part2 | CDS | 1470494 | 528 | + | 0.390152 | |
g5055 | PPL_05701 | E3JQK7F01EFZL8-5 | CDS | 1161370 | 933 | + | 0.473741 | |
g5082 | PPL_05730 | E3JQK7F01EFZL8-5 | CDS | 1251577 | 564 | - | 0.381206 | |
g5088 | PPL_05738 | ortholog of the human G6PD defects in G6PD cause chronic non-spherocytic hemolytic anemia (CNSHA) catalyzes the reaction D-glucose 6-phosphate NADPsupsup D-glucono-15-lactone 6-phosphate NADPH Hsupsup there is a second copy of this gene | E3JQK7F01EFZL8-5 | CDS | 1264752 | 1500 | + | 0.399333 |
g5093 | PPL_05743 | E3JQK7F01EFZL8-5 | CDS | 1277892 | 1185 | - | 0.331646 | |
g5138 | PPL_05785 | E3JQK7F01EFZL8-5 | CDS | 1409593 | 1695 | - | 0.422419 | |
g534 | PPL_00669 | DPPA0004F08.r1-5_part3 | CDS | 12073 | 2106 | + | 0.446819 | |
g5491 | PPL_06161 | E3JQK7F02GERJ7-5 | CDS | 113009 | 630 | - | 0.411111 | |
g5525 | PPL_06193 | E3JQK7F02GERJ7-5 | CDS | 200112 | 3090 | - | 0.36699 | |
g5531 | PPL_06197 | E3JQK7F02GERJ7-5 | CDS | 219143 | 3441 | + | 0.439698 | |
g5566 | PPL_06231 | E3JQK7F02HEVRT-5 | CDS | 59570 | 1764 | + | 0.379252 | |
g5764 | PPL_06454 | E3JQK7F02HEVRT-5 | CDS | 683975 | 1308 | - | 0.423547 | |
g577 | PPL_00710 | Dictyostelium enzyme that hydrolyses O- and S-glycosyl compounds with a preference for cleaving the alpha1-6-O-fucolsyl bonds in fucosylated oligosaccharides secreted during development | DPPA0004F08.r1-5_part3 | CDS | 117085 | 1386 | - | 0.388167 |
g5823 | PPL_06518 | E3JQK7F02HP6OU-5 | CDS | 103630 | 711 | - | 0.451477 | |
g5828 | PPL_06525 | E3JQK7F02HP6OU-5 | CDS | 113767 | 1470 | - | 0.441497 | |
g5881 | PPL_06577 | E3JQK7F02HW0LE-5_part2 | CDS | 1372 | 1272 | + | 0.386792 | |
g5935 | PPL_13289 | ortholog of human FHIT which is a possible tumor suppressor for specific tissues numerous tumor types are associated with aberrant forms of human FHIT protein | E3JQK7F02HW0LE-5_part2 | CDS | 142084 | 492 | + | 0.384146 |
g5936 | PPL_06639 | catalyzes the reaction ATP D-fructose 6-phosphate ADP D-fructose 16-bisphosphate the Dictyostelium PFK has been found to be a non-allosteric enzyme that binds to tubulin and inhibits tubulin polymerization | E3JQK7F02HW0LE-5_part2 | CDS | 143143 | 2448 | + | 0.463235 |
g596 | PPL_00730 | catalyzes the reaction D-glyceraldehyde 3-phosphate glycerone phosphate defects in human TPI1 are the cause of triosephosphate isomerase deficiency severe clinical disorder of glycolysis | DPPA0004F08.r1-5_part3 | CDS | 178520 | 777 | + | 0.416988 |
g5994 | PPL_06716 | E3JQK7F02HW0LE-5_part2 | CDS | 307620 | 1761 | - | 0.440091 | |
g6019 | PPL_06742 | E3JQK7F02HW0LE-5_part2 | CDS | 377999 | 1815 | - | 0.426446 | |
g603 | PPL_12712 | DPPA0004F08.r1-5_part3 | CDS | 192383 | 738 | - | 0.341463 | |
g6111 | PPL_06834 | E3JQK7F02HW0LE-5_part2 | CDS | 615035 | 981 | - | 0.343527 | |
g6176 | PPL_06905 | E3JQK7F02HW0LE-5_part2 | CDS | 786372 | 1155 | - | 0.359307 | |
g6181 | PPL_06912 | E3JQK7F02HW0LE-5_part2 | CDS | 804597 | 2184 | + | 0.417582 | |
g6216 | PPL_06947 | E3JQK7F02HW0LE-5_part2 | CDS | 891229 | 1857 | + | 0.383953 | |
g6257 | PPL_06992 | E3JQK7F02HW0LE-5_part2 | CDS | 1012393 | 1095 | - | 0.475799 | |
g6281 | PPL_07017 | E3JQK7F02HW0LE-5_part2 | CDS | 1089078 | 2160 | + | 0.418056 | |
g6320 | PPL_07061 | E3JQK7F02HW0LE-5_part2 | CDS | 1221981 | 1032 | - | 0.439922 | |
g6344 | PPL_07088 | phosphorylates NAD to NADP | E3JQK7F02HW0LE-5_part2 | CDS | 1288589 | 1413 | + | 0.367304 |
g6439 | PPL_07202 | E3JQK7F02HW0LE-5_part2 | CDS | 1569030 | 3132 | - | 0.453065 | |
g6568 | PPL_07342 | E3JQK7F02HW0LE-5_part2 | CDS | 1930564 | 1806 | - | 0.403101 | |
g6584 | PPL_07358 | E3JQK7F02HW0LE-5_part2 | CDS | 1973302 | 1305 | - | 0.383908 | |
g6598 | PPL_07376 | EVG8W8Q01C9YYY-5_part1 | CDS | 34230 | 3291 | - | 0.394713 | |
g665 | PPL_00800 | DPPA0004F08.r1-5_part3 | CDS | 361938 | 1695 | + | 0.339823 | |
g669 | PPL_00805 | DPPA0004F08.r1-5_part3 | CDS | 370686 | 981 | + | 0.405708 | |
g6748 | PPL_07552 | EVG8W8Q01EEF2G-5 | CDS | 69205 | 915 | - | 0.424044 | |
g6779 | PPL_07589 | EVG8W8Q01EEF2G-5 | CDS | 160011 | 1098 | - | 0.441712 | |
g6780 | PPL_07590 | EVG8W8Q01EEF2G-5 | CDS | 161381 | 1254 | + | 0.440989 | |
g684 | PPL_00824 | DPPA0004F08.r1-5_part3 | CDS | 409165 | 927 | - | 0.393743 | |
g69 | PPL_00157 | DPPA0004F08.r1-5_part2 | CDS | 201598 | 1011 | - | 0.436202 | |
g6934 | PPL_07753 | EVG8W8Q02J3HU6-3_part1 | CDS | 254877 | 1614 | - | 0.374226 | |
g6965 | PPL_07790 | EVG8W8Q02J3HU6-3_part1 | CDS | 348167 | 1164 | - | 0.338488 | |
g6974 | PPL_07798 | EVG8W8Q02J3HU6-3_part1 | CDS | 375422 | 1425 | - | 0.388772 | |
g7012 | PPL_07835 | EVG8W8Q02J3HU6-3_part1 | CDS | 486813 | 960 | - | 0.402083 | |
g702 | PPL_00848 | DPPA0061d07.r1-5 | CDS | 3497 | 1887 | - | 0.408585 | |
g7031 | PPL_13374 | EVG8W8Q02J3HU6-3_part1 | CDS | 533368 | 1641 | + | 0.431444 | |
g7060 | PPL_07877 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO | EVG8W8Q02J3HU6-3_part1 | CDS | 611318 | 1311 | + | 0.431731 |
g7097 | PPL_07915 | EVG8W8Q02J3HU6-3_part2 | CDS | 53215 | 1749 | - | 0.375071 | |
g7112 | PPL_07929 | EVG8W8Q02J3HU6-3_part2 | CDS | 88162 | 1398 | + | 0.363376 | |
g7229 | PPL_08062 | EVG8W8Q02J3HU6-3_part3 | CDS | 41890 | 1698 | + | 0.462898 | |
g7247 | PPL_08084 | EVG8W8Q02J3HU6-3_part3 | CDS | 104708 | 2664 | + | 0.392643 | |
g7248 | PPL_08085 | ortholog of the H. sapiens lysosomal alpha-glucosidase which is essential for the degradation of glygogen to glucose in lysosomes defects in GAA are the cause of glycogen storage disease II a recessive disorder which results in a massive accumulation of glycogen in muscle heart and liver leading to a life expectancy of less than two years | EVG8W8Q02J3HU6-3_part3 | CDS | 108029 | 2592 | + | 0.400077 |
g7300 | PPL_08146 | EVG8W8Q02J3HU6-3_part3 | CDS | 257237 | 1506 | - | 0.426959 | |
g7653 | PPL_08555 | EVKQ3GG01CS5PZ-3_part1 | CDS | 25655 | 630 | + | 0.374603 | |
g7731 | PPL_08637 | EVKQ3GG01CS5PZ-3_part1 | CDS | 240391 | 1428 | + | 0.431373 | |
g778 | PPL_00936 | hydrolyses D-fructose 16-bisphosphate to D-fructose 6-phosphate and phosphate (EC 3.1.3.11) | DPPA0061d07.r1-5 | CDS | 247308 | 996 | + | 0.446787 |
g7858 | PPL_08781 | EVKQ3GG01CS5PZ-3_part1 | CDS | 615251 | 1581 | - | 0.424415 | |
g7861 | PPL_08784 | EVKQ3GG01CS5PZ-3_part1 | CDS | 623110 | 1659 | + | 0.455696 | |
g7863 | PPL_08786 | EVKQ3GG01CS5PZ-3_part1 | CDS | 626666 | 2307 | - | 0.385782 | |
g7868 | PPL_08791 | EVKQ3GG01CS5PZ-3_part1 | CDS | 638734 | 1110 | + | 0.454054 | |
g7886 | PPL_08813 | EVKQ3GG01CS5PZ-3_part1 | CDS | 701639 | 1989 | + | 0.340875 | |
g789 | PPL_00950 | DPPA0061d07.r1-5 | CDS | 287448 | 1515 | + | 0.438284 | |
g7901 | PPL_08830 | EVKQ3GG01CS5PZ-3_part1 | CDS | 740785 | 1587 | + | 0.396975 | |
g7985 | PPL_08926 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1018883 | 1302 | - | 0.399386 | |
g8007 | PPL_08950 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1099163 | 1485 | - | 0.410101 | |
g8057 | PPL_08997 | catalyzes the reaction D-ribose 5-phosphate D-ribulose 5-phosphate | EVKQ3GG01CS5PZ-3_part1 | CDS | 1212549 | 696 | - | 0.475575 |
g8073 | PPL_13446 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1255961 | 2004 | - | 0.433134 | |
g8118 | PPL_09063 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1377319 | 1530 | + | 0.381699 | |
g8148 | PPL_09094 | catalyzes the reaction fructose-16-bisphosphate dihydroxy-acetone-phosphate D-glyceraldehyde-3-phosphate expressed in pstAB cells and in upper cup during culmination | EVKQ3GG01CS5PZ-3_part1 | CDS | 1460278 | 1074 | - | 0.504655 |
g8262 | PPL_09211 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1785199 | 1629 | - | 0.411295 | |
g8281 | PPL_09236 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1848876 | 1974 | + | 0.39615 | |
g8302 | PPL_09261 | EVKQ3GG01CS5PZ-3_part2 | CDS | 32349 | 1044 | + | 0.340038 | |
g8320 | PPL_09281 | similar to bacterial endo-14-beta-glucanase expressed in pstAO cells | EVKQ3GG01CS5PZ-3_part2 | CDS | 88404 | 1722 | + | 0.442509 |
g8352 | PPL_09315 | EVKQ3GG01CS5PZ-3_part2 | CDS | 178929 | 963 | - | 0.477674 | |
g8365 | PPL_09330 | EVKQ3GG01CS5PZ-3_part2 | CDS | 209674 | 1353 | - | 0.414634 | |
g8369 | PPL_09334 | EVKQ3GG01CS5PZ-3_part2 | CDS | 218119 | 1515 | - | 0.452805 | |
g8621 | PPL_12253 | EVKQ3GG01DOIJB_part1 | CDS | 558122 | 3648 | - | 0.394737 | |
g8635 | PPL_12269 | EVKQ3GG01DOIJB_part1 | CDS | 599454 | 813 | - | 0.372694 | |
g8708 | PPL_12348 | EVKQ3GG01DOIJB_part1 | CDS | 816967 | 756 | + | 0.493386 | |
g8779 | PPL_12419 | EVKQ3GG01DOIJB_part2 | CDS | 158992 | 2976 | + | 0.398858 | |
g8870 | PPL_12517 | EVKQ3GG01DOIJB_part2 | CDS | 432773 | 906 | - | 0.427152 | |
g8896 | PPL_12544 | EVKQ3GG01DOIJB_part2 | CDS | 516671 | 1938 | - | 0.334365 | |
g8902 | PPL_12550 | EVKQ3GG01DOIJB_part2 | CDS | 534058 | 1434 | + | 0.395397 | |
g895 | PPL_01061 | belongs to the glycoside hydrolase 5 (cellulase) family 5 contains a predicted signal sequence | DPPA0061d07.r1-5 | CDS | 572178 | 1530 | - | 0.413072 |
g8968 | PPL_12629 | EVKQ3GG01DOIJB_part2 | CDS | 759121 | 585 | + | 0.45812 | |
g900 | PPL_01068 | DPPA0061d07.r1-5 | CDS | 589644 | 1182 | + | 0.387479 | |
g9166 | PPL_09596 | EVKQ3GG02I325Y-5_part1 | CDS | 526847 | 873 | - | 0.368843 | |
g9212 | PPL_09641 | EVKQ3GG02I325Y-5_part1 | CDS | 655937 | 1524 | - | 0.431102 | |
g9331 | PPL_09778 | EVKQ3GG02I325Y-5_part1 | CDS | 969927 | 2799 | - | 0.480529 | |
g9396 | PPL_09849 | EVKQ3GG02I325Y-5_part1 | CDS | 1196600 | 2325 | + | 0.406452 | |
g9397 | PPL_09850 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO | EVKQ3GG02I325Y-5_part1 | CDS | 1199713 | 1308 | + | 0.457187 |
g9404 | PPL_09858 | EVKQ3GG02I325Y-5_part1 | CDS | 1212422 | 1062 | + | 0.416196 | |
g9455 | PPL_09914 | EVKQ3GG02I325Y-5_part2_part2 | CDS | 18975 | 2427 | + | 0.404203 | |
g9466 | PPL_09924 | EVKQ3GG02I325Y-5_part2_part2 | CDS | 51306 | 2868 | - | 0.359135 | |
g947 | PPL_01114 | catalyzes the reaction ATP glycerone ADP glycerone phosphate | DPPA0061d07.r1-5 | CDS | 724249 | 1779 | - | 0.412591 |
g9522 | PPL_09995 | transfers a segment of a 14-alpha-D-glucan chain to a primary hydroxyl group in a similar glucan chain | EWNM59D01C4IL7-5_part1 | CDS | 73900 | 2040 | + | 0.452941 |
g9528 | PPL_10002 | EWNM59D01C4IL7-5_part1 | CDS | 88160 | 654 | - | 0.399083 | |
g9537 | PPL_10013 | EWNM59D01C4IL7-5_part1 | CDS | 108788 | 1689 | + | 0.480758 | |
g9596 | PPL_10073 | EWNM59D01C4IL7-5_part1 | CDS | 265841 | 1500 | - | 0.298667 | |
g9615 | PPL_10097 | EWNM59D01C4IL7-5_part1 | CDS | 325677 | 1236 | - | 0.331715 | |
g9619 | PPL_10101 | EWNM59D01C4IL7-5_part1 | CDS | 333298 | 1695 | + | 0.39646 | |
g9655 | PPL_10140 | EWNM59D01C4IL7-5_part1 | CDS | 435035 | 1638 | + | 0.369963 | |
g9693 | PPL_10177 | EWNM59D01C4IL7-5_part1 | CDS | 551934 | 954 | - | 0.425577 | |
g9798 | PPL_10307 | EWNM59D01C4IL7-5_part1 | CDS | 893163 | 2250 | - | 0.425778 | |
g9829 | PPL_10347 | similar to aquaporin family of water-channel proteins expressed in prespore cells | EWNM59D01C4IL7-5_part1 | CDS | 974805 | 825 | + | 0.435152 |
g9982 | PPL_10510 | EXOLTKG01B86TH-3_part2 | CDS | 240902 | 1647 | + | 0.389192 |