Gene list
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COG category: Inorganic ion transport and metabolism
Gene type: CDS
Number of genes found: 504
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_G0267698 | DDB_G0267698 | DDB0232428 | CDS | 623530 | 372 | - | 0.284946 | |
DDB_G0267824 | DDB_G0267824 | DDB0232428 | CDS | 922136 | 1509 | - | 0.266402 | |
DDB_G0267924 | DDB_G0267924 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | DDB0232428 | CDS | 1128799 | 3330 | + | 0.331231 |
DDB_G0268060 | DDB_G0268060 | DDB0232428 | CDS | 1380972 | 2445 | - | 0.312883 | |
DDB_G0268074 | DDB_G0268074 | DDB0232428 | CDS | 1408319 | 2991 | - | 0.251755 | |
DDB_G0268230 | DDB_G0268230 | DDB0232428 | CDS | 1727069 | 1764 | + | 0.265306 | |
DDB_G0268810 | DDB_G0268810 | ortholog of bacterial Mgsup2sup transporter mgtA contains eight transmembrane domains | DDB0232428 | CDS | 2146485 | 2865 | + | 0.339965 |
DDB_G0269332 | DDB_G0269332 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232428 | CDS | 2554441 | 1845 | + | 0.280217 |
DDB_G0269380 | DDB_G0269380 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | DDB0232428 | CDS | 2645714 | 3942 | - | 0.348554 |
DDB_G0269590 | DDB_G0269590 | DDB0232428 | CDS | 3078895 | 4161 | - | 0.280221 | |
DDB_G0269964 | DDB_G0269964 | DDB0232428 | CDS | 3938864 | 1998 | + | 0.285285 | |
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_G0272192 | DDB_G0272192 | DDB0232429 | CDS | 1412468 | 1497 | + | 0.329993 | |
DDB_G0273083 | DDB_G0273083 | member of the Dyp-type peroxidase family lacking a typical heme-binding region does not appear to be present in higher organisms there is a second copy of this gene | DDB0232429 | CDS | 2623576 | 921 | - | 0.334419 |
DDB_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_G0273235 | DDB_G0273235 | contains 8 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 2765356 | 3843 | - | 0.284934 |
DDB_G0273675 | DDB_G0273675 | contains eight transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 3262518 | 3843 | + | 0.284934 |
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_G0273789 | DDB_G0273789 | member of the Dyp-type peroxidase family lacking a typical heme-binding region does not appear to be present in higher organisms there is a second copy of this gene | DDB0232429 | CDS | 3407290 | 921 | + | 0.334419 |
DDB_G0274547 | DDB_G0274547 | DDB0232429 | CDS | 4197500 | 1554 | + | 0.279923 | |
DDB_G0274643 | DDB_G0274643 | DDB0232429 | CDS | 4531583 | 855 | + | 0.352047 | |
DDB_G0274807 | DDB_G0274807 | DDB0232429 | CDS | 3946871 | 1851 | - | 0.222582 | |
DDB_G0275169 | DDB_G0275169 | DDB0232429 | CDS | 5084018 | 3873 | + | 0.268009 | |
DDB_G0275343 | DDB_G0275343 | DDB0232429 | CDS | 5393905 | 1638 | - | 0.234432 | |
DDB_G0275535 | DDB_G0275535 | DDB0232429 | CDS | 5868742 | 3477 | + | 0.300546 | |
DDB_G0275871 | DDB_G0275871 | DDB0232429 | CDS | 5796327 | 3492 | - | 0.286655 | |
DDB_G0276293 | DDB_G0276293 | DDB0232429 | CDS | 6559102 | 1473 | - | 0.304141 | |
DDB_G0276375 | DDB_G0276375 | DDB0232429 | CDS | 6671139 | 3804 | - | 0.226078 | |
DDB_G0276429 | DDB_G0276429 | DDB0232429 | CDS | 6932540 | 1422 | - | 0.270042 | |
DDB_G0276541 | DDB_G0276541 | DDB0232429 | CDS | 6819663 | 5490 | - | 0.298725 | |
DDB_G0276663 | DDB_G0276663 | DDB0232429 | CDS | 7094813 | 2835 | - | 0.292064 | |
DDB_G0277167 | DDB_G0277167 | DDB0232429 | CDS | 7668593 | 1392 | + | 0.257902 | |
DDB_G0277349 | DDB_G0277349 | DDB0232429 | CDS | 7803232 | 759 | - | 0.310935 | |
DDB_G0278047 | DDB_G0278047 | DDB0232430 | CDS | 191972 | 1164 | - | 0.285223 | |
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_G0278265 | DDB_G0278265 | DDB0232430 | CDS | 581627 | 1983 | + | 0.252647 | |
DDB_G0278369 | DDB_G0278369 | DDB0232430 | CDS | 768975 | 1170 | + | 0.22735 | |
DDB_G0278675 | DDB_G0278675 | DDB0232430 | CDS | 789665 | 1752 | - | 0.261986 | |
DDB_G0279275 | DDB_G0279275 | DDB0232430 | CDS | 1874332 | 1704 | + | 0.286385 | |
DDB_G0279943 | DDB_G0279943 | belongs to the major facilitator superefamily contains 12 putative transmembrane domains | DDB0232430 | CDS | 2721717 | 1488 | - | 0.309812 |
DDB_G0281155 | DDB_G0281155 | putative sugar transporter contains 12 putative transmembrane domains | DDB0232430 | CDS | 4113808 | 1614 | + | 0.29368 |
DDB_G0281401 | DDB_G0281401 | DDB0232430 | CDS | 4429232 | 3771 | + | 0.307611 | |
DDB_G0281643 | DDB_G0281643 | DDB0232430 | CDS | 4751182 | 2787 | + | 0.22605 | |
DDB_G0282067 | DDB_G0282067 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232430 | CDS | 5363274 | 1722 | - | 0.349013 |
DDB_G0282285 | DDB_G0282285 | DDB0232430 | CDS | 5511594 | 1578 | - | 0.247148 | |
DDB_G0282311 | DDB_G0282311 | DDB0232430 | CDS | 5621318 | 1992 | + | 0.314759 | |
DDB_G0282945 | DDB_G0282945 | DDB0232431 | CDS | 31559 | 2010 | - | 0.280597 | |
DDB_G0282959 | DDB_G0282959 | DDB0232431 | CDS | 52235 | 4611 | + | 0.25591 | |
DDB_G0283191 | DDB_G0283191 | DDB0232431 | CDS | 394762 | 1695 | + | 0.277286 | |
DDB_G0283629 | DDB_G0283629 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232431 | CDS | 885727 | 1632 | - | 0.321691 |
DDB_G0283985 | DDB_G0283985 | DDB0232431 | CDS | 1263489 | 1608 | + | 0.250622 | |
DDB_G0284605 | DDB_G0284605 | conserved plasma membrane calcium ATPases (PMCA) similar to Dictyostelium PAT1 contains 10 predicted transmembrane domains | DDB0232431 | CDS | 2214347 | 2784 | + | 0.354526 |
DDB_G0284849 | DDB_G0284849 | DDB0232431 | CDS | 2557758 | 3561 | + | 0.298512 | |
DDB_G0284955 | DDB_G0284955 | DDB0232431 | CDS | 2684549 | 4602 | - | 0.27488 | |
DDB_G0285079 | DDB_G0285079 | DDB0232431 | CDS | 2802048 | 603 | + | 0.296849 | |
DDB_G0285511 | DDB_G0285511 | DDB0232431 | CDS | 3331170 | 1683 | - | 0.322638 | |
DDB_G0285541 | DDB_G0285541 | putative family member of integral membrane proteins that are found to increase tolerance to divalent metal ions such as cadmium zinc and cobalt contains 5 predicted transmembrane domains | DDB0232431 | CDS | 3356593 | 1305 | - | 0.314176 |
DDB_G0286043 | DDB_G0286043 | DDB0232431 | CDS | 3989629 | 1887 | + | 0.225755 | |
DDB_G0286611 | DDB_G0286611 | DDB0232431 | CDS | 4704484 | 3666 | - | 0.267321 | |
DDB_G0286639 | DDB_G0286639 | DDB0232431 | CDS | 4771485 | 1107 | - | 0.307136 | |
DDB_G0286727 | DDB_G0286727 | similar to ChaC proteins thought to be associated with the putative ChaA calciumhydrogen cation transport protein in E. coli but with a PUA RNA binding domain fused at the carboxyl terminus | DDB0232431 | CDS | 4900621 | 969 | - | 0.330237 |
DDB_G0286763 | DDB_G0286763 | DDB0232431 | CDS | 4937865 | 1977 | - | 0.195245 | |
DDB_G0286891 | DDB_G0286891 | DDB0232431 | CDS | 5031762 | 3546 | + | 0.227862 | |
DDB_G0286979 | DDB_G0286979 | DDB0232431 | CDS | 5150412 | 1884 | - | 0.277601 | |
DDB_G0287843 | DDB_G0287843 | DDB0232432 | CDS | 806278 | 1923 | - | 0.333853 | |
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_G0288535 | DDB_G0288535 | DDB0232432 | CDS | 1660756 | 1395 | - | 0.235842 | |
DDB_G0289143 | DDB_G0289143 | contains 11 putative transmembrane domains similar to D. purpureum protein | DDB0232432 | CDS | 2407681 | 1719 | + | 0.285049 |
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_G0289621 | DDB_G0289621 | DDB0232432 | CDS | 3043521 | 714 | + | 0.317927 | |
DDB_G0289703 | DDB_G0289703 | DDB0232432 | CDS | 3127157 | 2931 | + | 0.247015 | |
DDB_G0289985 | DDB_G0289985 | similar to human protein KIAA0195 a transmembrane protein contains 8 putative transmembrane domains | DDB0232432 | CDS | 3471284 | 5832 | - | 0.290123 |
DDB_G0290423 | DDB_G0290423 | DDB0232432 | CDS | 4067949 | 1743 | + | 0.242111 | |
DDB_G0291029 | DDB_G0291029 | catalyzes the reaction SOsub4subsup2-sup ATP APS pyrophosphate | DDB0232432 | CDS | 4928744 | 1767 | - | 0.367289 |
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_G0291384 | DDB_G0291384 | DDB0232433 | CDS | 226725 | 1878 | + | 0.256124 | |
DDB_G0291720 | DDB_G0291720 | DDB0232433 | CDS | 721305 | 1278 | - | 0.311424 | |
DDB_G0291722 | DDB_G0291722 | DDB0232433 | CDS | 719367 | 1344 | - | 0.233631 | |
DDB_G0291758 | DDB_G0291758 | DDB0232433 | CDS | 697440 | 1194 | + | 0.273869 | |
DDB_G0291816 | DDB_G0291816 | DDB0232433 | CDS | 805833 | 1002 | - | 0.313373 | |
DDB_G0291824 | DDB_G0291824 | DDB0232433 | CDS | 827281 | 1878 | - | 0.300319 | |
DDB_G0292412 | DDB_G0292412 | similar to S. cerevisiae and S. pombe TRK1 and TRK2 potassium transporters contains 9 predicted transmembrane domains | DDB0232433 | CDS | 1563103 | 1947 | - | 0.260401 |
DDB_G0292432 | DDB_G0292432 | DDB0232433 | CDS | 1610862 | 1815 | - | 0.293113 | |
alg9 | DDB_G0279349 | CAZy family GT22 catalyzes N-linked mannosylation | DDB0232430 | CDS | 1972184 | 1950 | + | 0.232308 |
alp | DDB_G0278495 | catalyzes the reaction a phosphate monoester Hsub2subO an alcohol phosphate exhibits a punctate pattern in immunoflourescence that most likely represents vesicles enzymatic activity is developmentally regulated in a cell type-specific manner | DDB0232430 | CDS | 968065 | 1680 | - | 0.380952 |
amtA | DDB_G0277503 | DDB0232429 | CDS | 8112427 | 1392 | - | 0.35704 | |
amtB | DDB_G0277889 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | DDB0232430 | CDS | 276805 | 1296 | + | 0.364198 |
amtC | DDB_G0267424 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | DDB0232428 | CDS | 1034624 | 1296 | + | 0.350309 |
arsA | DDB_G0293528 | homologous to bacterial genes that are involved in the transport of arsenate selenate and other anionic compounds outside the cell | DDB0232433 | CDS | 3193289 | 990 | - | 0.285859 |
arsB | DDB_G0289879 | has two putative transmembrane domains bacterial homolog associates with ArsA to transport arsenate selenate and other anionic compounds outside the cell | DDB0232432 | CDS | 3431951 | 1692 | + | 0.253546 |
atox1 | DDB_G0284221 | DDB0232431 | CDS | 1705613 | 204 | - | 0.289216 | |
atp7a | DDB_G0284141 | DDB0232431 | CDS | 1486936 | 2958 | - | 0.315416 | |
atp9b | DDB_G0270870 | P-type ATPase (E1-E2) ortholog of human ATP9B and yeast NEO1 which is involved in transport from the Golgi to the ER | DDB0232428 | CDS | 2777615 | 3588 | + | 0.298495 |
cahA | DDB_G0269106 | DDB0232428 | CDS | 4712273 | 831 | + | 0.34657 | |
catA | DDB_G0274595 | catalyzes the reaction 2Hsub2subOsub2sub catalase 2Hsub2subO Osub2sub expressed throughout development expression restricted to prestalk cells during post-aggregationbr bNomenclature conflict:b Do not confuse the acrA gene encoding the late development adenylate cyclase ACR with the genetic locus acrA corresponding to the catA catalase that confers resistance to acriflavin ( | DDB0232429 | CDS | 3823148 | 1491 | + | 0.380952 |
cax1 | DDB_G0279301 | contains 13 transmembrane domains transports Ca2 or other cations using the gradient of H or Na generated by energy-coupled primary transporters | DDB0232430 | CDS | 1901303 | 2340 | + | 0.29188 |
clcA | DDB_G0294096 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers br bNomenclature conflict:b Do not confuse this gene with clc also known as clcA encoding the clathrin light chain | DDB0232429 | CDS | 435997 | 2592 | + | 0.328318 |
clcB | DDB_G0276865 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232429 | CDS | 7525349 | 2448 | - | 0.280637 |
clcC | DDB_G0276229 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232429 | CDS | 6228081 | 2274 | + | 0.311785 |
clcD | DDB_G0278639 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232430 | CDS | 535599 | 3003 | - | 0.360972 |
clcE | DDB_G0286491 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232431 | CDS | 4560350 | 2985 | + | 0.283417 |
clcF | DDB_G0293130 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232433 | CDS | 2574912 | 2430 | + | 0.295885 |
cln3 | DDB_G0291157 | ortholog of Cln3 responsible for Batten's disease a juvenile neurological disorder | DDB0232432 | CDS | 5060161 | 1266 | - | 0.313586 |
comD | DDB_G0283345 | similar to drug resistance transporters contains 14 transmembrane domains | DDB0232431 | CDS | 539820 | 3528 | + | 0.291667 |
ctaA | DDB_G0293004 | DDB0232433 | CDS | 2385585 | 3897 | - | 0.308442 | |
cutc | DDB_G0287539 | DDB0232432 | CDS | 396188 | 843 | - | 0.269276 | |
fmoA | DDB_G0289779 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3265452 | 1578 | - | 0.255387 |
fmoB | DDB_G0271660 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232429 | CDS | 685414 | 1539 | - | 0.237167 |
fmoC | DDB_G0289605 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3016817 | 1566 | - | 0.244572 |
fmoD | DDB_G0289929 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3451742 | 1683 | + | 0.250743 |
fmoE | DDB_G0289931 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3453668 | 1614 | + | 0.245973 |
fmoF | DDB_G0289927 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3449477 | 1590 | + | 0.255346 |
fmoG | DDB_G0289925 | DDB0232432 | CDS | 3446671 | 1611 | + | 0.248293 | |
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 |
fxn | DDB_G0293246 | yeast and human orthologs regulates mitochondrial iron accumulation mutations in human homolog cause Friedrich's ataxia | DDB0232433 | CDS | 2633195 | 582 | - | 0.261168 |
hatA | DDB_G0282141 | histidine-rich pH-dependent actin binding protein N-terminal myristoylation | DDB0232430 | CDS | 5481850 | 357 | + | 0.420168 |
ionA | DDB_G0277269 | expressed in pstAB cells and in pstA cells and upper cup during culmination transports ions across membranes using ATP hydrolysis for energy contains 8 transmembrane domains | DDB0232429 | CDS | 7864423 | 3699 | + | 0.326304 |
ippA | DDB_G0275663 | converts 1D-myo-inositol 14-bisphosphate H2O to 1D-myo-inositol 4-phosphate phosphate | DDB0232429 | CDS | 5791228 | 936 | + | 0.314103 |
ippB | DDB_G0268652 | very similar to A. thaliana AHL and SAL1 phosphatases and S. pombe tol1 (halotolerance protein) all related to the S. cerevisiae HAL2 these proteins are 3'-phosphoadenosine-5'-phosphate (PAP) phosphatases that also act as inositol polyphosphate 1-phosphatases. | DDB0232428 | CDS | 1844690 | 999 | + | 0.274274 |
kcnma1 | DDB_G0269896 | ortholog of the human KCNMA1 a potassium channel activated by both membrane depolarization and increase in cytosolic Ca(2) that mediates export of K() defects in the gene cause generalized epilepsy and paroxysmal dyskinesia (GEPD) | DDB0232428 | CDS | 3812473 | 3735 | - | 0.274431 |
kil2 | DDB_G0279183 | DDB0232430 | CDS | 1731085 | 3477 | + | 0.33132 | |
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 |
nhe1 | DDB_G0275711 | required for cell polarity mediates both Ksupsup facilitation of cell motility and KsupsupNasupsup requirement in chemotactic orientation the genetic interaction between aip1 and nhe1 suggest that defective chemotaxis in nhe1- mutants may be determined by loss of cofilin-dependent actin dynamics | DDB0232429 | CDS | 6042281 | 2025 | - | 0.281481 |
nhe2 | DDB_G0281877 | DDB0232430 | CDS | 5057597 | 2064 | + | 0.228682 | |
nhe3 | DDB_G0292830 | DDB0232433 | CDS | 2111344 | 2361 | - | 0.345616 | |
nhe4 | DDB_G0290253 | DDB0232432 | CDS | 3840207 | 3027 | - | 0.327387 | |
noxB | DDB_G0287101 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation | DDB0232431 | CDS | 5216605 | 2097 | - | 0.244158 |
noxC | DDB_G0291117 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation contains calcium-binding EF hand | DDB0232432 | CDS | 5017189 | 3429 | - | 0.222514 |
nramp1 | DDB_G0276973 | ortholog of the mammalian SLC11a1 transports iron across the phagolysosomal membrane contains 12 transmembrane domains | DDB0232429 | CDS | 7564058 | 1602 | + | 0.314607 |
nramp2 | DDB_G0275815 | NRAMP family protein similar to bacterial manganese transport protein mntH contains 12 transmembrane domains involved in iron homeostasis and resistance to pathogenic bacteria | DDB0232429 | CDS | 5536603 | 1890 | + | 0.292593 |
patA | DDB_G0277861 | P-type ATPase that is up-regulated in calcium-adapted cells contains 10 predicted transmembrane domains | DDB0232430 | CDS | 364618 | 3348 | + | 0.373059 |
patB | DDB_G0282817 | plasma membrane P-type Hsupsup-ATPase that is necessary for survival in acidic environments | DDB0232430 | CDS | 6309404 | 3177 | + | 0.36481 |
potA | DDB_G0282291 | DDB0232430 | CDS | 5660926 | 2934 | + | 0.273347 | |
ppk1 | DDB_G0293524 | similar to bacterial PPK (PPK1 family) which synthesizes poly P a polymer of up to hundreds of phosphate residues | DDB0232433 | CDS | 3029753 | 3162 | - | 0.328906 |
redA | DDB_G0293904 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein involved in the metabolism of compounds that control Dictyostelium cell differentiation | DDB0232433 | CDS | 3580985 | 1896 | - | 0.339135 |
redB | DDB_G0269912 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein similar to the H. sapiens POR protein that is defect in adrenal hyperplasia variant type (AHV) a syndrome with disordered steroidogenesis | DDB0232428 | CDS | 3848909 | 2004 | - | 0.335329 |
redC | DDB_G0287983 | similar to the H. sapiens NDOR1 an oxidoreductase that catalyzes the NADP-dependent reduction of cytochrome c and one-electron acceptors | DDB0232432 | CDS | 927535 | 1902 | + | 0.244479 |
rhgA | DDB_G0283389 | similar to human Rh50 protein a glycoprotein present on the surface of red blood cells contains 10 transmembrane domains | DDB0232431 | CDS | 634252 | 1584 | - | 0.33649 |
rhgB | DDB_G0280059 | DDB0232430 | CDS | 3188254 | 1803 | + | 0.345535 | |
rliA | DDB_G0272783 | twelve transmembrane domain protein that may act as a transporter repressed after Legionella pneumophila infection | DDB0232429 | CDS | 2172067 | 1416 | + | 0.267655 |
slc4 | DDB_G0270422 | DDB0232428 | CDS | 4842234 | 2307 | - | 0.229736 | |
sod2 | DDB_G0271106 | ortholog of the human SOD2 the mitochondrial superoxide dismutase belongs to the ironmanganese superoxide dismutase family | DDB0232429 | CDS | 35093 | 681 | + | 0.325991 |
sodA | DDB_G0267420 | superoxide dismutase of the SOD1 family expressed at constant levels throughout the life cycle and upregulated upon oxidative stress enriched in prespore cells | DDB0232428 | CDS | 338107 | 462 | + | 0.391775 |
sodB | DDB_G0283021 | DDB0232431 | CDS | 167774 | 1284 | - | 0.351246 | |
sodC | DDB_G0282993 | GPI-anchored plasma membrane superoxide dismutase upregulated upon oxidative stress mutants have defects in cytokinesis chemotaxis and localization of several protein during aggregation | DDB0232431 | CDS | 110200 | 1224 | - | 0.332516 |
sodD | DDB_G0281493 | DDB0232430 | CDS | 4612258 | 456 | - | 0.361842 | |
sodE | DDB_G0290343 | very similar to human SOD1 defects in which cause familial amyotrophic lateral sclerosis (ALS) belongs to the Cu-Zn superoxide dismutase family | DDB0232432 | CDS | 3992463 | 459 | + | 0.294118 |
sodF | DDB_G0281461 | DDB0232430 | CDS | 4537876 | 456 | + | 0.346491 | |
symA | DDB_G0292814 | DDB0232433 | CDS | 2158906 | 1371 | - | 0.33698 | |
zntA | DDB_G0268426 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | DDB0232428 | CDS | 1375259 | 1524 | + | 0.256562 |
zntB | DDB_G0286345 | ZIP family zinc transporter LZT subfamily member contains 7 transmembrane domains expressed in pstAB cells | DDB0232431 | CDS | 4327628 | 1119 | + | 0.314567 |
zntC | DDB_G0286049 | ZIP family zinc transporter LZT subfamily member contains 7 transmembrane domains expressed in pstAB cells | DDB0232431 | CDS | 3998261 | 1206 | + | 0.333333 |
zntD | DDB_G0269326 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | DDB0232428 | CDS | 2544681 | 2052 | - | 0.273879 |
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 | |
g10009 | DFA_10391 | EU5ZYIE02H8LDV-5 | CDS | 1391478 | 1824 | - | 0.305921 | |
g10070 | DFA_10459 | EU5ZYIE02H8LDV-5 | CDS | 1523227 | 1572 | + | 0.374682 | |
g10194 | DFA_10600 | EU5ZYIE02H8LDV-5 | CDS | 1844491 | 1362 | - | 0.348018 | |
g10204 | DFA_10609 | EU5ZYIE02H8LDV-5 | CDS | 1871031 | 1275 | + | 0.331765 | |
g10271 | DFA_10674 | EUAJFUG01CK1KI-5 | CDS | 136673 | 4002 | + | 0.455772 | |
g10313 | DFA_10721 | EUAJFUG01CK1KI-5 | CDS | 246985 | 1806 | - | 0.367663 | |
g10722 | DFA_11137 | EUAJFUG02HR96I-5 | CDS | 313846 | 2118 | - | 0.45373 | |
g1079 | DFA_01068 | Dfasci-F-a-25c12.r2-5 | CDS | 1888390 | 1833 | + | 0.444081 | |
g10950 | DFA_11364 | EUAJFUG02HR96I-5 | CDS | 954402 | 204 | - | 0.362745 | |
g10995 | DFA_11414 | EUAJFUG02HR96I-5 | CDS | 1064678 | 882 | + | 0.471655 | |
g11177 | DFA_11598 | EUAJFUG02HR96I-5 | CDS | 1525877 | 1101 | + | 0.360581 | |
g11178 | DFA_11599 | EUAJFUG02HR96I-5 | CDS | 1527407 | 912 | + | 0.410088 | |
g11238 | DFA_11656 | EUAJFUG02HR96I-5 | CDS | 1664398 | 1908 | - | 0.375786 | |
g11452 | DFA_11906 | EUAJFUG02HR96I-5 | CDS | 2284460 | 1386 | - | 0.314574 | |
g11629 | DFA_12097 | EUAJFUG02HR96I-5 | CDS | 2725219 | 666 | + | 0.429429 | |
g1171 | DFA_01169 | Dfasci-F-a-25c12.r2-5 | CDS | 2111468 | 2652 | - | 0.30543 | |
g11733 | DFA_12209 | EUAJFUG02HR96I-5 | CDS | 3010861 | 1293 | + | 0.454756 | |
g11820 | DFA_12300 | EUAJFUG02HR96I-5 | CDS | 3242908 | 2301 | + | 0.461104 | |
g1196 | DFA_01194 | Dfasci-F-a-25c12.r2-5 | CDS | 2170551 | 1569 | + | 0.327597 | |
g1325 | DFA_01325 | Dfasci-F-a-25c12.r2-5 | CDS | 2482994 | 2094 | - | 0.4532 | |
g1360 | DFA_01361 | Dfasci-F-a-25c12.r2-5 | CDS | 2561239 | 1548 | + | 0.354005 | |
g1367 | DFA_01368 | Dfasci-F-a-25c12.r2-5 | CDS | 2577311 | 3213 | - | 0.316527 | |
g1516 | DFA_01522 | Dfasci-F-a-25c12.r2-5 | CDS | 2952614 | 2271 | + | 0.419199 | |
g1582 | DFA_01587 | Dfasci-F-a-25c12.r2-5 | CDS | 3116778 | 1299 | - | 0.384142 | |
g164 | DFA_00160 | Dfasci-F-a-11f03.f1-5 | CDS | 466276 | 2076 | + | 0.343931 | |
g1646 | DFA_01660 | Dfasci-F-a-25c12.r2-5 | CDS | 3301564 | 1035 | + | 0.42029 | |
g1669 | DFA_01681 | Dfasci-F-a-25c12.r2-5 | CDS | 3355284 | 1371 | - | 0.375638 | |
g1701 | DFA_01713 | Dfasci-F-a-25c12.r2-5 | CDS | 3434348 | 3678 | + | 0.420881 | |
g2007 | DFA_02039 | Dfasci-G-b-126g04.f1-5 | CDS | 72685 | 1578 | - | 0.391635 | |
g2096 | DFA_02144 | Dfasci-G-b-126g04.f1-5 | CDS | 331905 | 3708 | + | 0.340615 | |
g2154 | DFA_12579 | Dfasci-G-b-126g04.f1-5 | CDS | 482596 | 2772 | - | 0.395022 | |
g2209 | DFA_02258 | Dfasci-G-b-143d02.r1-5 | CDS | 121469 | 2331 | + | 0.365079 | |
g2249 | DFA_12589 | Dfasci-G-b-143d02.r1-5 | CDS | 217003 | 1512 | + | 0.308201 | |
g2413 | DFA_02467 | Dfasci-G-b-143d02.r1-5 | CDS | 637365 | 1419 | + | 0.403101 | |
g246 | DFA_00238 | Dfasci-F-a-11f03.f1-5 | CDS | 691092 | 930 | - | 0.391398 | |
g2637 | DFA_12630 | Dfasci-G-b-190b03.r1-5 | CDS | 514042 | 1098 | + | 0.361566 | |
g2695 | DFA_02752 | Dfasci-G-b-205a01.r1-3 | CDS | 120305 | 3075 | + | 0.373984 | |
g2813 | DFA_02872 | Dfasci-G-b-205a01.r1-3 | CDS | 426497 | 1722 | - | 0.331591 | |
g2825 | DFA_02887 | Dfasci-G-b-205a01.r1-3 | CDS | 459500 | 1530 | + | 0.439869 | |
g2919 | DFA_02990 | Dfasci-G-b-205a01.r1-3 | CDS | 705953 | 2532 | - | 0.345972 | |
g2953 | DFA_03032 | Dfasci-G-b-205a01.r1-3 | CDS | 802841 | 3795 | + | 0.410277 | |
g2986 | DFA_03071 | Dfasci-G-b-205a01.r1-3 | CDS | 895359 | 2055 | + | 0.367397 | |
g3036 | DFA_03119 | Dfasci-G-b-205a01.r1-3 | CDS | 995219 | 3801 | - | 0.361747 | |
g3069 | DFA_03150 | Dfasci-G-b-205a01.r1-3 | CDS | 1081585 | 1887 | + | 0.338633 | |
g3133 | DFA_03222 | Dfasci-G-b-205a01.r1-3 | CDS | 1277340 | 2361 | + | 0.403643 | |
g3160 | DFA_03251 | Dfasci-G-b-205a01.r1-3 | CDS | 1355107 | 3585 | - | 0.455788 | |
g3177 | DFA_03264 | Dfasci-G-b-205a01.r1-3 | CDS | 1396112 | 4077 | - | 0.410841 | |
g3209 | DFA_03298 | Dfasci-G-b-205a01.r1-3 | CDS | 1501239 | 3897 | + | 0.436746 | |
g3225 | DFA_03314 | Dfasci-G-b-205a01.r1-3 | CDS | 1543493 | 1596 | - | 0.427945 | |
g3262 | DFA_03353 | Dfasci-G-b-205a01.r1-3 | CDS | 1629763 | 1515 | + | 0.304951 | |
g3282 | DFA_03375 | Dfasci-G-b-205a01.r1-3 | CDS | 1672612 | 1617 | + | 0.312307 | |
g3668 | DFA_03802 | Dfasci-G-b-285a01.f1-5 | CDS | 297403 | 1965 | + | 0.366921 | |
g396 | DFA_00386 | Dfasci-F-a-25c12.r2-5 | CDS | 125226 | 600 | + | 0.281667 | |
g4339 | DFA_04497 | Dfasci-G-o-33e01.r1-3 | CDS | 686972 | 1176 | + | 0.294218 | |
g4390 | DFA_04547 | Dfasci-G-o-33e01.r1-3 | CDS | 813429 | 1230 | - | 0.34065 | |
g4452 | DFA_04614 | Dfasci-G-o-33e01.r1-3 | CDS | 968926 | 2868 | - | 0.446304 | |
g4570 | DFA_04735 | Dfasci-G-o-33e01.r1-3 | CDS | 1246645 | 1734 | - | 0.317762 | |
g4713 | DFA_04880 | Dfasci-G-o-80e12.f1-5 | CDS | 152124 | 3288 | + | 0.378954 | |
g4751 | DFA_04922 | Dfasci-G-o-80e12.f1-5 | CDS | 251434 | 1350 | + | 0.283704 | |
g4900 | DFA_05082 | Dfasci-G-o-80e12.f1-5 | CDS | 653816 | 2631 | + | 0.388445 | |
g5022 | DFA_05212 | Dfasci-G-o-80e12.f1-5 | CDS | 976637 | 2943 | - | 0.496772 | |
g5081 | DFA_05287 | Dfasci-G-o-80e12.f1-5 | CDS | 1156155 | 3168 | + | 0.45423 | |
g5194 | DFA_05397 | Dfasci-G-o-80e12.f1-5 | CDS | 1443296 | 741 | - | 0.406208 | |
g5224 | DFA_05429 | Dfasci-G-o-80e12.f1-5 | CDS | 1520826 | 1284 | - | 0.432243 | |
g534 | DFA_00515 | Dfasci-F-a-25c12.r2-5 | CDS | 471671 | 2685 | + | 0.440596 | |
g5465 | DFA_05676 | Dfasci-G-o-80e12.f1-5 | CDS | 2212506 | 1194 | + | 0.464824 | |
g5486 | DFA_05697 | Dfasci-G-o-80e12.f1-5 | CDS | 2254228 | 1080 | + | 0.414815 | |
g5543 | DFA_05754 | Dfasci-G-o-80e12.f1-5 | CDS | 2391715 | 207 | - | 0.381643 | |
g5626 | DFA_05831 | Dfasci-G-o-80e12.f1-5 | CDS | 2596128 | 2733 | + | 0.396634 | |
g5665 | DFA_05869 | Dfasci-G-o-80e12.f1-5 | CDS | 2699005 | 3798 | + | 0.326224 | |
g5683 | DFA_05886 | Dfasci-G-o-80e12.f1-5 | CDS | 2743197 | 600 | + | 0.28 | |
g5692 | DFA_05897 | Dfasci-G-p-12c09.r1-3 | CDS | 14547 | 1116 | + | 0.365591 | |
g5742 | DFA_05945 | Dfasci-G-p-12c09.r1-3 | CDS | 139459 | 3849 | + | 0.415433 | |
g5759 | DFA_05966 | Dfasci-G-p-12c09.r1-3 | CDS | 194862 | 1839 | + | 0.42795 | |
g5762 | DFA_05970 | Dfasci-G-p-12c09.r1-3 | CDS | 202587 | 1902 | - | 0.505258 | |
g5940 | DFA_06156 | Dfasci-G-p-12c09.r1-3 | CDS | 663775 | 1944 | + | 0.345165 | |
g6179 | DFA_06423 | Dfasci-G-p-12c09.r1-3 | CDS | 1292644 | 3372 | + | 0.503262 | |
g6304 | DFA_06552 | Dfasci-G-p-12c09.r1-3 | CDS | 1602405 | 2733 | - | 0.380168 | |
g6340 | DFA_06587 | Dfasci-G-p-12c09.r1-3 | CDS | 1710503 | 2766 | - | 0.413232 | |
g6599 | DFA_06860 | ET2XIPL01CNAVH-3 | CDS | 43891 | 5397 | + | 0.399852 | |
g6756 | DFA_07015 | ET2XIPL01CNAVH-3 | CDS | 440989 | 1194 | - | 0.438023 | |
g676 | DFA_00659 | Dfasci-F-a-25c12.r2-5 | CDS | 846064 | 1041 | + | 0.323727 | |
g6828 | DFA_07095 | ET2XIPL01CNAVH-3 | CDS | 634216 | 3657 | - | 0.378452 | |
g6928 | DFA_07202 | ET2XIPL01CNAVH-3 | CDS | 904901 | 1137 | - | 0.434477 | |
g6929 | DFA_07203 | ET2XIPL01CNAVH-3 | CDS | 907550 | 1053 | - | 0.461538 | |
g7074 | DFA_07347 | ET2XIPL01CNAVH-3 | CDS | 1261971 | 1857 | - | 0.320409 | |
g7084 | DFA_07356 | ET2XIPL01CNAVH-3 | CDS | 1293051 | 705 | - | 0.408511 | |
g7228 | DFA_07494 | ET2XIPL01CNAVH-3 | CDS | 1688204 | 1767 | - | 0.47708 | |
g7239 | DFA_07506 | ET2XIPL01CNAVH-3 | CDS | 1712930 | 1737 | - | 0.455959 | |
g7266 | DFA_07535 | ET2XIPL01CNAVH-3 | CDS | 1778194 | 1284 | + | 0.504673 | |
g7270 | DFA_07538 | ET2XIPL01CNAVH-3 | CDS | 1785413 | 1131 | + | 0.399646 | |
g7354 | DFA_07617 | ET2XIPL01COFD4-5 | CDS | 65377 | 651 | - | 0.411674 | |
g7708 | DFA_07978 | ET2XIPL01COFD4-5 | CDS | 1007380 | 1485 | - | 0.492929 | |
g7711 | DFA_07981 | ET2XIPL01COFD4-5 | CDS | 1017370 | 1686 | + | 0.401542 | |
g8047 | DFA_08356 | ET2XIPL01COFD4-5 | CDS | 1866460 | 2844 | - | 0.40225 | |
g8276 | DFA_08574 | ET2XIPL01COFD4-5 | CDS | 2507049 | 1839 | + | 0.393692 | |
g832 | DFA_00822 | Dfasci-F-a-25c12.r2-5 | CDS | 1268479 | 1569 | - | 0.453155 | |
g8348 | DFA_08647 | ET2XIPL01COFD4-5 | CDS | 2696979 | 3789 | - | 0.449987 | |
g8380 | DFA_08679 | ET2XIPL01COFD4-5 | CDS | 2788774 | 1356 | + | 0.452065 | |
g8402 | DFA_08697 | ET2XIPL01COFD4-5 | CDS | 2829672 | 3222 | - | 0.36468 | |
g8414 | DFA_08715 | ET2XIPL01COFD4-5 | CDS | 2869617 | 4779 | - | 0.409081 | |
g8483 | DFA_08786 | ET2XIPL01COFD4-5 | CDS | 3047882 | 3234 | - | 0.503711 | |
g8500 | DFA_08800 | ET2XIPL01COFD4-5 | CDS | 3085387 | 1917 | - | 0.356808 | |
g8808 | DFA_09121 | EU5ZYIE01BBABR-5 | CDS | 406322 | 3672 | + | 0.404956 | |
g8889 | DFA_09207 | EU5ZYIE01DZOHE-5 | CDS | 143753 | 3243 | - | 0.429849 | |
g8987 | DFA_09305 | EU5ZYIE01DZOHE-5 | CDS | 401487 | 1629 | - | 0.399018 | |
g9187 | DFA_09527 | EU5ZYIE01EUG8B-5 | CDS | 149250 | 2640 | - | 0.404924 | |
g9192 | DFA_09533 | EU5ZYIE01EUG8B-5 | CDS | 159413 | 3696 | - | 0.413961 | |
g9285 | DFA_09636 | EU5ZYIE01EUG8B-5 | CDS | 473354 | 855 | - | 0.31462 | |
g9300 | DFA_09650 | EU5ZYIE01EUG8B-5 | CDS | 522485 | 2895 | + | 0.448359 | |
g9308 | DFA_09659 | EU5ZYIE01EUG8B-5 | CDS | 544364 | 1002 | - | 0.376247 | |
g9319 | DFA_09669 | EU5ZYIE01EUG8B-5 | CDS | 563339 | 984 | - | 0.376016 | |
g9400 | DFA_09755 | EU5ZYIE01EUG8B-5 | CDS | 830507 | 951 | - | 0.371188 | |
g9430 | DFA_09785 | EU5ZYIE01EUG8B-5 | CDS | 907897 | 3438 | + | 0.388307 | |
g9458 | DFA_09814 | EU5ZYIE02H8LDV-5 | CDS | 33580 | 1764 | + | 0.38322 | |
g9574 | DFA_09929 | EU5ZYIE02H8LDV-5 | CDS | 332017 | 2508 | - | 0.398325 | |
g9648 | DFA_10012 | EU5ZYIE02H8LDV-5 | CDS | 508185 | 3075 | + | 0.340813 | |
g9679 | DFA_10045 | EU5ZYIE02H8LDV-5 | CDS | 584898 | 1758 | + | 0.298066 | |
g9690 | DFA_10056 | EU5ZYIE02H8LDV-5 | CDS | 615687 | 2913 | - | 0.406111 | |
g9806 | DFA_10186 | EU5ZYIE02H8LDV-5 | CDS | 916415 | 3351 | - | 0.444345 | |
Dictyostelium lacteum | ||||||||
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g10066 | DLA_11235 | GLQOFTK02JL55Q | CDS | 736563 | 2583 | - | 0.348045 | |
g10141 | DLA_11328 | GLQOFTK02JL55Q | CDS | 908863 | 3234 | - | 0.365801 | |
g1140 | DLA_01258 | superoxide dismutase of the SOD1 family expressed at constant levels throughout the life cycle and upregulated upon oxidative stress enriched in prespore cells | F4PJNLW01A00V1 | CDS | 1151652 | 459 | - | 0.407407 |
g1310 | DLA_01434 | F4PJNLW01B0TO9 | CDS | 44114 | 1947 | + | 0.280431 | |
g1377 | DLA_01509 | F4PJNLW01B0TO9 | CDS | 198101 | 1884 | + | 0.295117 | |
g1585 | DLA_01739 | P-type ATPase (E1-E2) ortholog of human ATP9B and yeast NEO1 which is involved in transport from the Golgi to the ER | F4PJNLW01B0TO9 | CDS | 655356 | 3540 | - | 0.35 |
g1824 | DLA_01989 | F4PJNLW01C9MXC | CDS | 141969 | 2637 | + | 0.332196 | |
g1944 | DLA_02128 | F4PJNLW01DERRH | CDS | 149745 | 2712 | - | 0.344027 | |
g1989 | DLA_02183 | F4PJNLW01DERRH | CDS | 257541 | 3534 | + | 0.338427 | |
g2001 | DLA_02198 | F4PJNLW01DERRH | CDS | 284469 | 3387 | + | 0.317095 | |
g2268 | DLA_02504 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | F4PJNLW01EE5MJ | CDS | 170057 | 2556 | - | 0.330595 |
g2284 | DLA_02526 | F4PJNLW01EE5MJ | CDS | 202874 | 3267 | - | 0.373125 | |
g2340 | DLA_02590 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | F4PJNLW01EE5MJ | CDS | 323676 | 885 | + | 0.281356 |
g2508 | DLA_02781 | F4PJNLW01EE5MJ | CDS | 706288 | 2118 | + | 0.352691 | |
g2579 | DLA_02862 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein similar to the H. sapiens POR protein that is defect in adrenal hyperplasia variant type (AHV) a syndrome with disordered steroidogenesis | F4PJNLW01EE5MJ | CDS | 866908 | 1932 | - | 0.371636 |
g2714 | DLA_03010 | F4PJNLW01EE5MJ | CDS | 1154444 | 4911 | - | 0.321116 | |
g2765 | DLA_03064 | F4PJNLW02GJ9ZB | CDS | 26317 | 3153 | + | 0.338091 | |
g2887 | DLA_03200 | ortholog of bacterial Mgsup2sup transporter mgtA contains eight transmembrane domains | F4PJNLW02HBBIY | CDS | 22158 | 2820 | - | 0.375532 |
g2900 | DLA_03215 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | F4PJNLW02HBBIY | CDS | 55334 | 3594 | + | 0.378687 |
g2931 | DLA_03246 | F4PJNLW02HBBIY | CDS | 116483 | 801 | + | 0.360799 | |
g3044 | DLA_11551 | F4PJNLW02HBBIY | CDS | 382889 | 1017 | - | 0.368732 | |
g3241 | DLA_03589 | GAOABQK02G6SYV | CDS | 27606 | 1335 | - | 0.367041 | |
g3381 | DLA_03738 | GAOABQK02G6SYV | CDS | 334425 | 1299 | - | 0.357198 | |
g3578 | DLA_03962 | GAOABQK02G7M1S | CDS | 93700 | 2844 | + | 0.360408 | |
g3592 | DLA_03983 | GAOABQK02G7M1S | CDS | 133452 | 3414 | - | 0.356766 | |
g367 | DLA_00409 | contig05409_1.exp | CDS | 842702 | 2277 | + | 0.348265 | |
g368 | DLA_00410 | contig05409_1.exp | CDS | 845124 | 1605 | - | 0.290966 | |
g370 | DLA_00412 | contig05409_1.exp | CDS | 849111 | 4869 | + | 0.326761 | |
g3700 | DLA_04099 | GAOABQK02G7M1S | CDS | 390242 | 204 | - | 0.338235 | |
g3834 | DLA_04252 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | GAOABQK02G7M1S | CDS | 688757 | 1176 | - | 0.292517 |
g3883 | DLA_04305 | GAOABQK02GQAQJ | CDS | 32831 | 864 | - | 0.278935 | |
g4075 | DLA_04519 | GAOABQK02GQAQJ | CDS | 466040 | 2841 | - | 0.339317 | |
g4107 | DLA_04553 | GAOABQK02GQAQJ | CDS | 532794 | 1113 | + | 0.327942 | |
g4169 | DLA_04617 | GAOABQK02GQAQJ | CDS | 657047 | 3006 | - | 0.314039 | |
g4210 | DLA_04656 | GAOABQK02GQAQJ | CDS | 733574 | 1152 | - | 0.352431 | |
g424 | DLA_00470 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | contig05409_1.exp | CDS | 959789 | 4086 | + | 0.367107 |
g4240 | DLA_04687 | GAOABQK02GQAQJ | CDS | 801644 | 3270 | + | 0.336391 | |
g4275 | DLA_04720 | GAOABQK02GQAQJ | CDS | 887264 | 1806 | + | 0.330011 | |
g4388 | DLA_04851 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | GAOABQK02GRIAE | CDS | 91802 | 1668 | - | 0.317746 |
g4422 | DLA_04889 | GAOABQK02GRIAE | CDS | 176484 | 1617 | - | 0.303649 | |
g4550 | DLA_05043 | GAOABQK02H81I9 | CDS | 253731 | 1731 | + | 0.33911 | |
g4611 | DLA_05107 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | GAOABQK02H81I9 | CDS | 394523 | 3450 | + | 0.346087 |
g4904 | DLA_05427 | GAOABQK02HUB3S | CDS | 187169 | 1647 | + | 0.352155 | |
g500 | DLA_00553 | contig05409_1.exp | CDS | 1146688 | 912 | + | 0.345395 | |
g5090 | DLA_05638 | GAOABQK02HUB3S | CDS | 607415 | 1278 | + | 0.335681 | |
g5115 | DLA_05664 | very similar to A. thaliana AHL and SAL1 phosphatases and S. pombe tol1 (halotolerance protein) all related to the S. cerevisiae HAL2 these proteins are 3'-phosphoadenosine-5'-phosphate (PAP) phosphatases that also act as inositol polyphosphate 1-phosphatases. | GAOABQK02HUB3S | CDS | 667626 | 1011 | - | 0.339268 |
g5238 | DLA_05812 | GAOABQK02HUB3S | CDS | 1005470 | 1524 | - | 0.322178 | |
g5239 | DLA_05813 | GAOABQK02HUB3S | CDS | 1007273 | 1401 | - | 0.309779 | |
g5251 | DLA_05828 | GAOABQK02HUB3S | CDS | 1033963 | 744 | + | 0.302419 | |
g5276 | DLA_05853 | GAOABQK02HUB3S | CDS | 1086420 | 3279 | + | 0.345837 | |
g5599 | DLA_06244 | GAOABQK02HUB3S | CDS | 1843423 | 1248 | + | 0.329327 | |
g5616 | DLA_06261 | GAOABQK02IBA3P | CDS | 13386 | 1188 | + | 0.319024 | |
g5854 | DLA_06529 | ortholog of the human SOD2 the mitochondrial superoxide dismutase belongs to the ironmanganese superoxide dismutase family | GAOABQK02IBA3P | CDS | 575948 | 660 | - | 0.365152 |
g5997 | DLA_06679 | homologous to bacterial genes that are involved in the transport of arsenate selenate and other anionic compounds outside the cell | GAOABQK02IBA3P | CDS | 944113 | 993 | - | 0.311178 |
g6017 | DLA_06701 | GAOABQK02IBA3P | CDS | 985960 | 2268 | + | 0.338624 | |
g6061 | DLA_06748 | GAOABQK02IBA3P | CDS | 1077036 | 3759 | - | 0.320032 | |
g6218 | DLA_06929 | GAOABQK02IO52T | CDS | 286642 | 1476 | + | 0.348916 | |
g6371 | DLA_07091 | GAOABQK02IO52T | CDS | 612802 | 1539 | - | 0.339181 | |
g6431 | DLA_07156 | GAOABQK02JBK0O | CDS | 40849 | 585 | + | 0.34188 | |
g6489 | DLA_07224 | GAOABQK02JEBFV | CDS | 32112 | 1551 | + | 0.348162 | |
g6537 | DLA_07280 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein involved in the metabolism of compounds that control Dictyostelium cell differentiation | GAOABQK02JOCCH | CDS | 79667 | 1893 | + | 0.384046 |
g6775 | DLA_07547 | GAOABQK02JOCCH | CDS | 625765 | 420 | - | 0.280952 | |
g6776 | DLA_07548 | GAOABQK02JOCCH | CDS | 626390 | 576 | + | 0.289931 | |
g6848 | DLA_07633 | GAOABQK02JOCCH | CDS | 798148 | 1809 | + | 0.310669 | |
g6910 | DLA_07706 | GLQOFTK02FH5TG | CDS | 52915 | 1503 | + | 0.342648 | |
g6911 | DLA_07707 | GLQOFTK02FH5TG | CDS | 54997 | 1104 | + | 0.326087 | |
g692 | DLA_00764 | F4PJNLW01A00V1 | CDS | 123009 | 1257 | + | 0.412888 | |
g693 | DLA_00765 | F4PJNLW01A00V1 | CDS | 124627 | 1254 | + | 0.357257 | |
g7216 | DLA_08052 | contains eight transmembrane domains there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 738361 | 3552 | - | 0.37134 |
g7291 | DLA_08144 | GLQOFTK02FH5TG | CDS | 908615 | 2283 | - | 0.385458 | |
g7322 | DLA_08182 | GLQOFTK02FH5TG | CDS | 986706 | 2640 | - | 0.338636 | |
g7390 | DLA_08263 | NRAMP family protein similar to bacterial manganese transport protein mntH contains 12 transmembrane domains involved in iron homeostasis and resistance to pathogenic bacteria | GLQOFTK02FH5TG | CDS | 1141470 | 1635 | - | 0.313761 |
g7460 | DLA_08345 | member of the Dyp-type peroxidase family lacking a typical heme-binding region does not appear to be present in higher organisms there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 1309398 | 1965 | + | 0.281425 |
g7678 | DLA_08586 | GLQOFTK02G2F2O | CDS | 253171 | 6300 | - | 0.329524 | |
g7767 | DLA_08685 | GLQOFTK02G2F2O | CDS | 487671 | 573 | + | 0.26178 | |
g7860 | DLA_08790 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | GLQOFTK02G2F2O | CDS | 678460 | 3597 | - | 0.352238 |
g7965 | DLA_08900 | GLQOFTK02G2F2O | CDS | 908478 | 1134 | + | 0.386243 | |
g7991 | DLA_08927 | GLQOFTK02G2F2O | CDS | 960624 | 1485 | - | 0.317172 | |
g8236 | DLA_11763 | GLQOFTK02G2F2O | CDS | 1541296 | 1422 | + | 0.331927 | |
g826 | DLA_00906 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers br bNomenclature conflict:b Do not confuse this gene with clc also known as clcA encoding the clathrin light chain | F4PJNLW01A00V1 | CDS | 400235 | 2616 | - | 0.365443 |
g827 | DLA_00907 | F4PJNLW01A00V1 | CDS | 403659 | 1371 | + | 0.391685 | |
g830 | DLA_00910 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | F4PJNLW01A00V1 | CDS | 413597 | 1302 | + | 0.361751 |
g8328 | DLA_09294 | GLQOFTK02G2F2O | CDS | 1731320 | 1677 | - | 0.335122 | |
g8443 | DLA_09415 | GLQOFTK02G2F2O | CDS | 1948145 | 2280 | + | 0.309211 | |
g8658 | DLA_09653 | GLQOFTK02GHM7A | CDS | 402528 | 2721 | + | 0.338111 | |
g8686 | DLA_09682 | GLQOFTK02GHM7A | CDS | 462627 | 2409 | + | 0.350353 | |
g8699 | DLA_09695 | GLQOFTK02GHM7A | CDS | 489002 | 3639 | - | 0.335532 | |
g8704 | DLA_09700 | GLQOFTK02GHM7A | CDS | 504242 | 1575 | + | 0.309841 | |
g8718 | DLA_09714 | catalyzes the reaction 2Hsub2subOsub2sub catalase 2Hsub2subO Osub2sub expressed throughout development expression restricted to prestalk cells during post-aggregationbr bNomenclature conflict:b Do not confuse the acrA gene encoding the late development adenylate cyclase ACR with the genetic locus acrA corresponding to the catA catalase that confers resistance to acriflavin ( | GLQOFTK02GHM7A | CDS | 537522 | 1482 | - | 0.409582 |
g8726 | DLA_09723 | GLQOFTK02GHM7A | CDS | 554712 | 1785 | + | 0.372549 | |
g8757 | DLA_09753 | GLQOFTK02GHM7A | CDS | 621454 | 1257 | - | 0.324582 | |
g9007 | DLA_10029 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | GLQOFTK02GQ36N | CDS | 325674 | 2499 | - | 0.339336 |
g9023 | DLA_10044 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | GLQOFTK02GQ36N | CDS | 353185 | 3483 | - | 0.347402 |
g907 | DLA_01002 | F4PJNLW01A00V1 | CDS | 600317 | 3663 | + | 0.340977 | |
g9223 | DLA_10274 | GLQOFTK02GUKFG | CDS | 160293 | 2016 | + | 0.373512 | |
g9249 | DLA_10304 | GLQOFTK02GUKFG | CDS | 217251 | 2070 | + | 0.329469 | |
g9381 | DLA_10452 | GLQOFTK02GUKFG | CDS | 515519 | 2829 | - | 0.339343 | |
g9484 | DLA_10571 | GLQOFTK02IJPNF | CDS | 6637 | 1104 | - | 0.322464 | |
g9515 | DLA_10605 | GLQOFTK02IJPNF | CDS | 76485 | 993 | - | 0.336354 | |
g9593 | DLA_10695 | GLQOFTK02IJPNF | CDS | 256147 | 768 | - | 0.286458 | |
g9621 | DLA_10725 | GLQOFTK02IRMR1 | CDS | 43505 | 1566 | + | 0.35696 | |
Polysphondylium pallidum, PN500 | ||||||||
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g10082 | PPL_10613 | EXOLTKG01B86TH-3_part2 | CDS | 566168 | 1653 | - | 0.402904 | |
g10159 | PPL_10689 | EXOLTKG01B86TH-3_part2 | CDS | 797843 | 2160 | + | 0.428241 | |
g10264 | PPL_10814 | very similar to A. thaliana AHL and SAL1 phosphatases and S. pombe tol1 (halotolerance protein) all related to the S. cerevisiae HAL2 these proteins are 3'-phosphoadenosine-5'-phosphate (PAP) phosphatases that also act as inositol polyphosphate 1-phosphatases. | EXOLTKG01B86TH-3y_part1 | CDS | 226476 | 1002 | + | 0.423154 |
g10326 | PPL_10878 | EXOLTKG01B86TH-3y_part1 | CDS | 392939 | 2445 | + | 0.361554 | |
g10381 | PPL_10939 | EXOLTKG01B86TH-3y_part2 | CDS | 66355 | 1680 | - | 0.34881 | |
g10557 | PPL_13628 | EXOLTKG02GJRTE-5 | CDS | 454310 | 1086 | - | 0.360958 | |
g10671 | PPL_11263 | ortholog of the human SOD2 the mitochondrial superoxide dismutase belongs to the ironmanganese superoxide dismutase family | PN500-F-W-a08d11.p658-5_part2 | CDS | 289952 | 684 | + | 0.444444 |
g10753 | PPL_11343 | PN500-F-W-a08d11.p658-5_part2 | CDS | 528576 | 4200 | - | 0.443571 | |
g10795 | PPL_11385 | PN500-F-W-a08d11.p658-5_part2 | CDS | 673563 | 3309 | - | 0.458144 | |
g10804 | PPL_11393 | PN500-F-W-a08d11.p658-5_part2 | CDS | 699396 | 1587 | + | 0.377442 | |
g10864 | PPL_11463 | PN500-F-W-a08d11.p658-5_part2 | CDS | 859123 | 1506 | + | 0.460823 | |
g11051 | PPL_11802 | PN500-G-d-72b01.r1-5 | CDS | 184712 | 1554 | + | 0.400257 | |
g11073 | PPL_11828 | PN500-G-d-72b01.r1-5 | CDS | 255915 | 585 | + | 0.329915 | |
g11173 | PPL_11932 | PN500-G-d-72b01.r1-5 | CDS | 533719 | 3600 | + | 0.439444 | |
g11248 | PPL_12005 | PN500-G-d-72b01.r1-5 | CDS | 735411 | 2481 | - | 0.351471 | |
g11293 | PPL_11557 | PN500-G-d-188d09.r1-5 | CDS | 41765 | 3876 | + | 0.386223 | |
g11418 | PPL_00046 | contig_new08661_1.exp-5 | CDS | 120423 | 3867 | + | 0.431084 | |
g1253 | PPL_01462 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers br bNomenclature conflict:b Do not confuse this gene with clc also known as clcA encoding the clathrin light chain | DPPA0090b03.f1-3_x_part2 | CDS | 208249 | 2505 | - | 0.434331 |
g128 | PPL_00227 | superoxide dismutase of the SOD1 family expressed at constant levels throughout the life cycle and upregulated upon oxidative stress enriched in prespore cells | DPPA0004F08.r1-5_part2 | CDS | 364808 | 351 | - | 0.48433 |
g1327 | PPL_01538 | DPPA0090b03.f1-3_x_part3 | CDS | 44498 | 2961 | - | 0.46741 | |
g1392 | PPL_01606 | DPPA0090b03.f1-3_x_part3 | CDS | 224979 | 1212 | + | 0.431518 | |
g1451 | PPL_01672 | DPPA0090b03.f1-3_x_part3 | CDS | 387416 | 1008 | + | 0.46131 | |
g1499 | PPL_01728 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | DPPA0090b03.f1-3_x_part3 | CDS | 527361 | 1272 | + | 0.492138 |
g1608 | PPL_12847 | DPPA0090b03.f1-3_x_part3 | CDS | 821929 | 2769 | + | 0.346334 | |
g1858 | PPL_02109 | DPPA0090b03.f1-3_x_part3 | CDS | 1540562 | 5058 | + | 0.410439 | |
g1868 | PPL_02119 | DPPA0090b03.f1-3_x_part3 | CDS | 1573555 | 1341 | + | 0.416107 | |
g190 | PPL_00295 | DPPA0004F08.r1-5_part2 | CDS | 537130 | 2763 | - | 0.435396 | |
g2062 | PPL_02329 | DPPA0090b03.f1-3_x_part3 | CDS | 2168227 | 4368 | - | 0.389881 | |
g2153 | PPL_02431 | DPPA0090b03.f1-3_x_part3 | CDS | 2406877 | 5463 | - | 0.406004 | |
g2157 | PPL_02435 | DPPA0090b03.f1-3_x_part3 | CDS | 2418494 | 1536 | - | 0.411458 | |
g2224 | PPL_02516 | DPPA0090b03.f1-3_x_part4 | CDS | 180421 | 2160 | + | 0.378241 | |
g2225 | PPL_02517 | P-type ATPase (E1-E2) ortholog of human ATP9B and yeast NEO1 which is involved in transport from the Golgi to the ER | DPPA0090b03.f1-3_x_part4 | CDS | 184436 | 3879 | + | 0.392369 |
g2561 | PPL_02881 | DPPA0090b03.f1-3_y_part1 | CDS | 777401 | 1329 | + | 0.456734 | |
g2652 | PPL_02987 | DPPA0090b03.f1-3_y_part1 | CDS | 1032667 | 834 | - | 0.454436 | |
g2762 | PPL_03111 | homologous to bacterial genes that are involved in the transport of arsenate selenate and other anionic compounds outside the cell | DPPA0090b03.f1-3_y_part1 | CDS | 1356597 | 1026 | - | 0.365497 |
g278 | PPL_00386 | DPPA0004F08.r1-5_part2 | CDS | 806524 | 3240 | - | 0.353704 | |
g2869 | PPL_12998 | DPPA0090b03.f1-3_y_part1 | CDS | 1636403 | 3282 | + | 0.418038 | |
g3042 | PPL_03415 | DPPA0090b03.f1-3_y_part1 | CDS | 2100567 | 2340 | + | 0.382906 | |
g3077 | PPL_03451 | ortholog of bacterial Mgsup2sup transporter mgtA contains eight transmembrane domains | DPPA0090b03.f1-3_y_part1 | CDS | 2187122 | 2808 | - | 0.445157 |
g3108 | PPL_03487 | member of the ZIP (Zrt- and Irt-like Protein) family capable of transporting zinc and other metal ions contains 6 transmembrane domains | DPPA0090b03.f1-3_y_part1 | CDS | 2281990 | 1047 | + | 0.439351 |
g3125 | PPL_03538 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein similar to the H. sapiens POR protein that is defect in adrenal hyperplasia variant type (AHV) a syndrome with disordered steroidogenesis | DPPA0186d03.f1-5 | CDS | 25510 | 1926 | - | 0.441848 |
g3275 | PPL_13048 | DPPB0337b12.r1-5 | CDS | 176828 | 1041 | + | 0.414986 | |
g3307 | PPL_03746 | DPPB0337b12.r1-5 | CDS | 255629 | 1554 | + | 0.433719 | |
g3456 | PPL_03917 | similar to bacterial PPK (PPK1 family) which synthesizes poly P a polymer of up to hundreds of phosphate residues | DPPB0337b12.r1-5 | CDS | 660457 | 3612 | - | 0.419435 |
g3563 | PPL_04029 | DPPB0337b12.r1-5 | CDS | 949786 | 558 | - | 0.342294 | |
g3717 | PPL_04200 | DPPB0360e11.f1-5 | CDS | 45539 | 2874 | - | 0.362909 | |
g3758 | PPL_04245 | DPPB0360e11.f1-5 | CDS | 161115 | 1764 | - | 0.447846 | |
g3774 | PPL_04263 | catalyzes the reaction 2Hsub2subOsub2sub catalase 2Hsub2subO Osub2sub expressed throughout development expression restricted to prestalk cells during post-aggregationbr bNomenclature conflict:b Do not confuse the acrA gene encoding the late development adenylate cyclase ACR with the genetic locus acrA corresponding to the catA catalase that confers resistance to acriflavin ( | DPPB0360e11.f1-5 | CDS | 202680 | 1491 | + | 0.474178 |
g3881 | PPL_04385 | DPPB0360e11.f1-5 | CDS | 567516 | 846 | + | 0.297872 | |
g3948 | PPL_04459 | DPPB0360e11.f1-5 | CDS | 749554 | 1743 | - | 0.45611 | |
g4007 | PPL_04527 | DPPB0360e11.f1-5 | CDS | 945466 | 2085 | + | 0.383213 | |
g4191 | PPL_04728 | E0KFERV02EE9X2-3_part1 | CDS | 441691 | 2904 | + | 0.435262 | |
g4217 | PPL_04764 | E0KFERV02EE9X2-3_part1 | CDS | 537461 | 2418 | - | 0.392887 | |
g4465 | PPL_05062 | E3JQK7F01CUWUC-3_part1 | CDS | 31916 | 2943 | - | 0.348624 | |
g4669 | PPL_05289 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | E3JQK7F01EFZL8-5 | CDS | 98733 | 3096 | + | 0.399871 |
g4782 | PPL_05416 | E3JQK7F01EFZL8-5 | CDS | 432101 | 1674 | - | 0.366189 | |
g4829 | PPL_05467 | E3JQK7F01EFZL8-5 | CDS | 577309 | 1344 | + | 0.446429 | |
g4921 | PPL_05564 | E3JQK7F01EFZL8-5 | CDS | 820710 | 207 | - | 0.425121 | |
g5018 | PPL_05660 | E3JQK7F01EFZL8-5 | CDS | 1074722 | 1155 | + | 0.359307 | |
g5019 | PPL_05661 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | E3JQK7F01EFZL8-5 | CDS | 1076285 | 1659 | + | 0.38698 |
g5058 | PPL_05704 | E3JQK7F01EFZL8-5 | CDS | 1165783 | 2799 | - | 0.413362 | |
g5134 | PPL_05781 | E3JQK7F01EFZL8-5 | CDS | 1398087 | 2784 | + | 0.386853 | |
g5138 | PPL_05785 | E3JQK7F01EFZL8-5 | CDS | 1409593 | 1695 | - | 0.422419 | |
g5185 | PPL_05838 | E3JQK7F02G10GF-5 | CDS | 78319 | 1776 | - | 0.481419 | |
g5196 | PPL_05847 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | E3JQK7F02G10GF-5 | CDS | 108306 | 1290 | - | 0.471318 |
g5216 | PPL_05868 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | E3JQK7F02G10GF-5 | CDS | 172205 | 2241 | - | 0.4083 |
g5245 | PPL_05897 | E3JQK7F02G10GF-5 | CDS | 262512 | 1335 | - | 0.412734 | |
g534 | PPL_00669 | DPPA0004F08.r1-5_part3 | CDS | 12073 | 2106 | + | 0.446819 | |
g5361 | PPL_06017 | E3JQK7F02G10GF-5 | CDS | 581444 | 3102 | - | 0.383623 | |
g5612 | PPL_06276 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | E3JQK7F02HEVRT-5 | CDS | 196082 | 2412 | - | 0.424959 |
g5731 | PPL_06419 | E3JQK7F02HEVRT-5 | CDS | 583758 | 588 | - | 0.394558 | |
g5732 | PPL_06421 | E3JQK7F02HEVRT-5 | CDS | 586330 | 582 | - | 0.402062 | |
g576 | PPL_00709 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | DPPA0004F08.r1-5_part3 | CDS | 107720 | 4014 | - | 0.431241 |
g5881 | PPL_06577 | E3JQK7F02HW0LE-5_part2 | CDS | 1372 | 1272 | + | 0.386792 | |
g5924 | PPL_06625 | E3JQK7F02HW0LE-5_part2 | CDS | 117772 | 3132 | + | 0.450192 | |
g6019 | PPL_06742 | E3JQK7F02HW0LE-5_part2 | CDS | 377999 | 1815 | - | 0.426446 | |
g6069 | PPL_06792 | E3JQK7F02HW0LE-5_part2 | CDS | 501479 | 1128 | - | 0.414894 | |
g6304 | PPL_07043 | E3JQK7F02HW0LE-5_part2 | CDS | 1160215 | 1329 | - | 0.421369 | |
g635 | PPL_12720 | DPPA0004F08.r1-5_part3 | CDS | 282863 | 1014 | - | 0.418146 | |
g6372 | PPL_07119 | E3JQK7F02HW0LE-5_part2 | CDS | 1371353 | 3639 | + | 0.422644 | |
g6418 | PPL_07179 | E3JQK7F02HW0LE-5_part2 | CDS | 1507634 | 2751 | - | 0.39731 | |
g6478 | PPL_07243 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein involved in the metabolism of compounds that control Dictyostelium cell differentiation | E3JQK7F02HW0LE-5_part2 | CDS | 1667506 | 1896 | - | 0.434072 |
g6571 | PPL_07346 | E3JQK7F02HW0LE-5_part2 | CDS | 1941325 | 3393 | - | 0.383142 | |
g665 | PPL_00800 | DPPA0004F08.r1-5_part3 | CDS | 361938 | 1695 | + | 0.339823 | |
g6698 | PPL_07498 | EVG8W8Q01C9YYY-5_part2 | CDS | 126045 | 3090 | + | 0.446602 | |
g6736 | PPL_07539 | EVG8W8Q01EEF2G-5 | CDS | 27100 | 1614 | - | 0.36741 | |
g6775 | PPL_07583 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | EVG8W8Q01EEF2G-5 | CDS | 143632 | 1584 | - | 0.445076 |
g6864 | PPL_07684 | EVG8W8Q02J3HU6-3_part1 | CDS | 81370 | 1884 | + | 0.393312 | |
g6933 | PPL_07752 | EVG8W8Q02J3HU6-3_part1 | CDS | 251108 | 2643 | + | 0.42868 | |
g7025 | PPL_07846 | EVG8W8Q02J3HU6-3_part1 | CDS | 521387 | 1731 | - | 0.370306 | |
g7042 | PPL_07860 | EVG8W8Q02J3HU6-3_part1 | CDS | 562562 | 2283 | + | 0.460797 | |
g7043 | PPL_13375 | EVG8W8Q02J3HU6-3_part1 | CDS | 565004 | 597 | + | 0.422111 | |
g7056 | PPL_07874 | EVG8W8Q02J3HU6-3_part1 | CDS | 603944 | 1479 | + | 0.392833 | |
g7142 | PPL_07960 | EVG8W8Q02J3HU6-3_part2 | CDS | 177257 | 2541 | - | 0.410468 | |
g7233 | PPL_08067 | EVG8W8Q02J3HU6-3_part3 | CDS | 49468 | 2085 | + | 0.370264 | |
g7619 | PPL_08517 | EVG8W8Q02J3HU6-3_part3 | CDS | 1161291 | 1575 | + | 0.415873 | |
g7741 | PPL_08646 | EVKQ3GG01CS5PZ-3_part1 | CDS | 276413 | 1209 | + | 0.497105 | |
g7782 | PPL_08697 | EVKQ3GG01CS5PZ-3_part1 | CDS | 385176 | 1062 | + | 0.449153 | |
g789 | PPL_00950 | DPPA0061d07.r1-5 | CDS | 287448 | 1515 | + | 0.438284 | |
g8065 | PPL_09008 | NRAMP family protein similar to bacterial manganese transport protein mntH contains 12 transmembrane domains involved in iron homeostasis and resistance to pathogenic bacteria | EVKQ3GG01CS5PZ-3_part1 | CDS | 1232876 | 1572 | + | 0.335242 |
g8073 | PPL_13446 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1255961 | 2004 | - | 0.433134 | |
g8111 | PPL_09054 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1360787 | 1380 | + | 0.404348 | |
g8125 | PPL_09071 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1396767 | 2775 | + | 0.456937 | |
g8249 | PPL_09198 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1751263 | 1923 | - | 0.355174 | |
g8281 | PPL_09236 | EVKQ3GG01CS5PZ-3_part1 | CDS | 1848876 | 1974 | + | 0.39615 | |
g8298 | PPL_09257 | EVKQ3GG01CS5PZ-3_part2 | CDS | 23415 | 3672 | - | 0.363017 | |
g8365 | PPL_09330 | EVKQ3GG01CS5PZ-3_part2 | CDS | 209674 | 1353 | - | 0.414634 | |
g8656 | PPL_12290 | EVKQ3GG01DOIJB_part1 | CDS | 669962 | 1248 | + | 0.463141 | |
g8821 | PPL_12462 | EVKQ3GG01DOIJB_part2 | CDS | 276611 | 3354 | + | 0.361956 | |
g8827 | PPL_12470 | EVKQ3GG01DOIJB_part2 | CDS | 292648 | 1818 | + | 0.309131 | |
g8833 | PPL_12476 | EVKQ3GG01DOIJB_part2 | CDS | 310834 | 2274 | + | 0.418206 | |
g888 | PPL_01054 | DPPA0061d07.r1-5 | CDS | 549018 | 1458 | + | 0.432099 | |
g8896 | PPL_12544 | EVKQ3GG01DOIJB_part2 | CDS | 516671 | 1938 | - | 0.334365 | |
g8897 | PPL_12545 | EVKQ3GG01DOIJB_part2 | CDS | 519243 | 2880 | - | 0.441319 | |
g9016 | PPL_09438 | EVKQ3GG02I325Y-5_part1 | CDS | 92763 | 1248 | - | 0.358974 | |
g9090 | PPL_09524 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | EVKQ3GG02I325Y-5_part1 | CDS | 305571 | 3810 | - | 0.447507 |
g9128 | PPL_13520 | EVKQ3GG02I325Y-5_part1 | CDS | 423319 | 1365 | - | 0.454945 | |
g9129 | PPL_13521 | EVKQ3GG02I325Y-5_part1 | CDS | 424769 | 2262 | - | 0.411583 | |
g9301 | PPL_09742 | EVKQ3GG02I325Y-5_part1 | CDS | 877323 | 1884 | - | 0.392781 | |
g9406 | PPL_09861 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | EVKQ3GG02I325Y-5_part1 | CDS | 1218716 | 2475 | + | 0.424646 |
g951 | PPL_01117 | DPPA0061d07.r1-5 | CDS | 737759 | 1560 | + | 0.365385 | |
g964 | PPL_01130 | DPPA0061d07.r1-5 | CDS | 762788 | 3291 | - | 0.45275 | |
g9669 | PPL_10155 | EWNM59D01C4IL7-5_part1 | CDS | 478082 | 681 | - | 0.405286 | |
g9839 | PPL_10356 | EWNM59D01C4IL7-5_part1 | CDS | 1000271 | 744 | + | 0.36828 | |
g9892 | PPL_10414 | EXOLTKG01B86TH-3_part1 | CDS | 97254 | 2595 | - | 0.416185 | |
g9917 | PPL_10442 | converts 1D-myo-inositol 14-bisphosphate H2O to 1D-myo-inositol 4-phosphate phosphate | EXOLTKG01B86TH-3_part2 | CDS | 62907 | 879 | + | 0.450512 |
g9982 | PPL_10510 | EXOLTKG01B86TH-3_part2 | CDS | 240902 | 1647 | + | 0.389192 |