Gene list
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COG category: Cell cycle control, mitosis and meiosis
Organism: Dictyostelium discoideum AX4, AX4
Number of genes found: 243
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium discoideum AX4, AX4 | ||||||||
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Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
DD8-14 | DDB_G0289467 | DDB0232432 | CDS | 2821081 | 1992 | - | 0.317269 | |
DDB_G0267220 | DDB_G0267220 | DDB0232428 | CDS | 37303 | 231 | - | 0.21645 | |
DDB_G0267586 | DDB_G0267586 | DDB0232428 | CDS | 375348 | 1389 | + | 0.267099 | |
DDB_G0267852 | DDB_G0267852 | the Maf protein is a putative inhibitor of septum formation found in eukaryotes bacteria and archaea | DDB0232428 | CDS | 968117 | 651 | - | 0.262673 |
DDB_G0267918 | DDB_G0267918 | DDB0232428 | CDS | 1118591 | 2514 | + | 0.222355 | |
DDB_G0268246 | DDB_G0268246 | DDB0232428 | CDS | 1764265 | 2478 | + | 0.166263 | |
DDB_G0268498 | DDB_G0268498 | DDB0232428 | CDS | 573341 | 2457 | - | 0.334961 | |
DDB_G0269700 | DDB_G0269700 | DDB0232428 | CDS | 3352107 | 2622 | + | 0.249809 | |
DDB_G0269926 | DDB_G0269926 | DDB0232428 | CDS | 3880004 | 2175 | - | 0.306207 | |
DDB_G0269934 | DDB_G0269934 | DDB0232428 | CDS | 3897216 | 6135 | + | 0.351263 | |
DDB_G0270090 | DDB_G0270090 | DDB0232428 | CDS | 4198052 | 774 | + | 0.22093 | |
DDB_G0270092 | DDB_G0270092 | DDB0232428 | CDS | 4199147 | 771 | + | 0.223087 | |
DDB_G0270246 | DDB_G0270246 | DDB0232428 | CDS | 4514326 | 1725 | - | 0.225507 | |
DDB_G0270864 | DDB_G0270864 | DDB0232428 | CDS | 2744495 | 2892 | - | 0.357538 | |
DDB_G0270902 | DDB_G0270902 | DDB0232428 | CDS | 3239824 | 3621 | + | 0.257387 | |
DDB_G0271250 | DDB_G0271250 | DDB0232429 | CDS | 214985 | 1278 | + | 0.234742 | |
DDB_G0271334 | DDB_G0271334 | contains a dilute domain found at the carboxyl terminus of non-muscle myosin V | DDB0232429 | CDS | 87969 | 4518 | + | 0.279991 |
DDB_G0271816 | DDB_G0271816 | DDB0232429 | CDS | 825354 | 3726 | + | 0.318304 | |
DDB_G0272558 | DDB_G0272558 | DDB0232429 | CDS | 1851656 | 3241 | + | 0.294971 | |
DDB_G0272576 | DDB_G0272576 | there is a second copy of this gene | DDB0232429 | CDS | 2466189 | 543 | - | 0.276243 |
DDB_G0272997 | DDB_G0272997 | DDB0232429 | CDS | 2081848 | 3345 | - | 0.23707 | |
DDB_G0273041 | DDB_G0273041 | there is a second copy of this gene | DDB0232429 | CDS | 2381533 | 1344 | - | 0.299851 |
DDB_G0273205 | DDB_G0273205 | contains an EF hand but shows little similarity to other proteins there is a second copy of this gene | DDB0232429 | CDS | 2704086 | 3033 | + | 0.279261 |
DDB_G0273723 | DDB_G0273723 | contains an EF hand but shows little similarity to other proteins there is a second copy of this gene | DDB0232429 | CDS | 3324668 | 3033 | - | 0.279261 |
DDB_G0273927 | DDB_G0273927 | there is a second copy of this gene | DDB0232429 | CDS | 3564872 | 543 | + | 0.276243 |
DDB_G0273997 | DDB_G0273997 | there is a second copy of this gene | DDB0232429 | CDS | 3648910 | 1344 | + | 0.299851 |
DDB_G0274259 | DDB_G0274259 | DDB0232429 | CDS | 4126091 | 3507 | + | 0.260907 | |
DDB_G0274323 | DDB_G0274323 | DDB0232429 | CDS | 3956333 | 840 | - | 0.242857 | |
DDB_G0274695 | DDB_G0274695 | ortholog of human CD2 binding proteinproline-serine-threonine phosphatase-interacting protein 1 | DDB0232429 | CDS | 4207853 | 1170 | + | 0.289744 |
DDB_G0274781 | DDB_G0274781 | contains three EF hands similar to mammalian neuron specific calcium-binding protein hippocalcin belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232429 | CDS | 3825256 | 678 | + | 0.29646 |
DDB_G0274785 | DDB_G0274785 | similar to the H. sapiens TATA element modulatory factor (TMF1) which binds the HIV-1 TATA element and inhibits transcriptional activation by the TATA-binding protein TBP | DDB0232429 | CDS | 3826769 | 3255 | + | 0.2553 |
DDB_G0274789 | DDB_G0274789 | DDB0232429 | CDS | 3841237 | 6309 | + | 0.277223 | |
DDB_G0274893 | DDB_G0274893 | DDB0232429 | CDS | 4359088 | 2748 | - | 0.270742 | |
DDB_G0275331 | DDB_G0275331 | DDB0232429 | CDS | 5365929 | 3147 | + | 0.280902 | |
DDB_G0275401 | DDB_G0275401 | DDB0232429 | CDS | 5385395 | 5256 | + | 0.272831 | |
DDB_G0275505 | DDB_G0275505 | DDB0232429 | CDS | 6018482 | 3393 | + | 0.325965 | |
DDB_G0275783 | DDB_G0275783 | contains a predicted signal anchor contains 3 coiled coil domains | DDB0232429 | CDS | 5653320 | 1734 | + | 0.252018 |
DDB_G0275795 | DDB_G0275795 | DDB0232429 | CDS | 5596338 | 2427 | - | 0.301607 | |
DDB_G0275935 | DDB_G0275935 | DDB0232429 | CDS | 6095467 | 807 | - | 0.2057 | |
DDB_G0276029 | DDB_G0276029 | putative ortholog of H. sapiens CNOT1 and S. cerevisiae CDC39 REMI mutant forms aberrant fruiting bodies (see | DDB0232429 | CDS | 6435703 | 7581 | - | 0.303654 |
DDB_G0276361 | DDB_G0276361 | DDB0232429 | CDS | 6745195 | 2370 | + | 0.332489 | |
DDB_G0276553 | DDB_G0276553 | DDB0232429 | CDS | 6875533 | 2703 | + | 0.260451 | |
DDB_G0276567 | DDB_G0276567 | homolog of S. cerevisiae CDC50 (cell division control protein 50) which is required for polarized cell growth contains two putative transmembrane domains | DDB0232429 | CDS | 6951075 | 939 | - | 0.292865 |
DDB_G0276695 | DDB_G0276695 | DDB0232429 | CDS | 7141543 | 1941 | + | 0.301391 | |
DDB_G0276719 | DDB_G0276719 | DDB0232429 | CDS | 7123870 | 2268 | + | 0.22619 | |
DDB_G0277077 | DDB_G0277077 | contains a UvrBUvrC domain however does not share similarity with UvrB or UvrC | DDB0232429 | CDS | 7466122 | 2190 | + | 0.252968 |
DDB_G0277185 | DDB_G0277185 | DDB0232429 | CDS | 7699060 | 6855 | + | 0.307513 | |
DDB_G0277197 | DDB_G0277197 | DDB0232429 | CDS | 7732529 | 678 | + | 0.205015 | |
DDB_G0277429 | DDB_G0277429 | DDB0232429 | CDS | 8039644 | 2550 | - | 0.296863 | |
DDB_G0277537 | DDB_G0277537 | subunit of PI4K responsible for the phosphorylation of phosphatidylinositol (PI) to PI4P (ATP 1-phosphatidyl-1D-myo-inositol ADP 1-phosphatidyl-1D-myo-inositol 4-phosphate) the first committed step in the generation of phosphatidylinositol 45-bisphosphate (PIP2) a precursor of the second messenger inositol 145-trisphosphate (InsP3) | DDB0232429 | CDS | 7989159 | 7383 | + | 0.301233 |
DDB_G0277675 | DDB_G0277675 | DDB0232429 | CDS | 8331577 | 2112 | - | 0.288826 | |
DDB_G0277807 | DDB_G0277807 | DDB0232429 | CDS | 8439922 | 1833 | + | 0.19749 | |
DDB_G0278073 | DDB_G0278073 | DDB0232430 | CDS | 229027 | 3633 | - | 0.24305 | |
DDB_G0278125 | DDB_G0278125 | DDB0232430 | CDS | 327348 | 2496 | - | 0.333333 | |
DDB_G0278255 | DDB_G0278255 | DDB0232430 | CDS | 568794 | 1545 | - | 0.260841 | |
DDB_G0278351 | DDB_G0278351 | DDB0232430 | CDS | 734436 | 2991 | + | 0.265129 | |
DDB_G0278547 | DDB_G0278547 | DDB0232430 | CDS | 1050062 | 2214 | - | 0.268744 | |
DDB_G0279253 | DDB_G0279253 | DDB0232430 | CDS | 1838283 | 1539 | - | 0.238467 | |
DDB_G0279435 | DDB_G0279435 | DDB0232430 | CDS | 2045716 | 1461 | - | 0.299795 | |
DDB_G0279449 | DDB_G0279449 | DDB0232430 | CDS | 2062975 | 3303 | + | 0.350288 | |
DDB_G0279655 | DDB_G0279655 | similar to Dictyostelium and H. sapiens ppp2r4 (PTPA) the phosphatase 2A regulatory subunit B' | DDB0232430 | CDS | 2376263 | 1407 | - | 0.257996 |
DDB_G0279693 | DDB_G0279693 | contains 1 importin N-terminal domain homolog of human IPO11 (importin-11) and S. cerevisiae KAP120 (importin beta-like protein) both of which function in nuclear protein import as a nuclear transport receptor | DDB0232430 | CDS | 2453262 | 3078 | - | 0.294997 |
DDB_G0279745 | DDB_G0279745 | DDB0232430 | CDS | 2496825 | 1233 | - | 0.25223 | |
DDB_G0279863 | DDB_G0279863 | DDB0232430 | CDS | 2641846 | 3852 | - | 0.314901 | |
DDB_G0280249 | DDB_G0280249 | member of the MAP65ASE1 family of microtubule associated proteins the putative yeast orthologs is an anaphase spindle elongation protein brbr bCommunity annotation:b The provisional identification of this gene as Ase1 is supported by its threefold overexpression in a Dicty strain lacking the Dicty retinoblastoma-like gene rblA (Doquang et al in preparation). Most genes whose products are involved in cell cycle progression are overexpressed in this strain. br Ase1 is a microtubule associated protein resident in the midbody of the mitotic spindle it is phosphorylated by cdk1 during mitotic entry dephosphorylated by the mitotic-exit specific phosphatase cdc14 and degraded by the anaphase promoting complex (see Khmelinskii and Schiebel Cell Cycle 7 283-6 (2008). In budding yeast ase1 is required for spindle elongation and stabilization. br Harry MacWilliams April 2009 | DDB0232430 | CDS | 3162671 | 2316 | - | 0.262522 |
DDB_G0280921 | DDB_G0280921 | contains a PX (phox) domain which is found in various proteins involved in intracellular signaling | DDB0232430 | CDS | 3881788 | 3150 | + | 0.32381 |
DDB_G0281485 | DDB_G0281485 | DDB0232430 | CDS | 4599041 | 4422 | + | 0.246721 | |
DDB_G0281767 | DDB_G0281767 | DDB0232430 | CDS | 4930354 | 2652 | + | 0.255656 | |
DDB_G0281937 | DDB_G0281937 | DDB0232430 | CDS | 5037215 | 594 | + | 0.304714 | |
DDB_G0282101 | DDB_G0282101 | DDB0232430 | CDS | 5369694 | 3006 | + | 0.276114 | |
DDB_G0282471 | DDB_G0282471 | DDB0232430 | CDS | 5811380 | 4041 | + | 0.303885 | |
DDB_G0282633 | DDB_G0282633 | DDB0232430 | CDS | 6031309 | 2760 | + | 0.285507 | |
DDB_G0283369 | DDB_G0283369 | DDB0232431 | CDS | 587429 | 6252 | - | 0.274152 | |
DDB_G0283441 | DDB_G0283441 | DDB0232431 | CDS | 702819 | 2916 | + | 0.284636 | |
DDB_G0283545 | DDB_G0283545 | DDB0232431 | CDS | 794803 | 2850 | + | 0.309474 | |
DDB_G0283681 | DDB_G0283681 | similar to STAG (stromal antigen) proteins which are subunits of a protein complex required for sister chromatid cohesion in eukaryotes | DDB0232431 | CDS | 973798 | 4020 | - | 0.302488 |
DDB_G0283827 | DDB_G0283827 | DDB0232431 | CDS | 1180565 | 2718 | + | 0.307947 | |
DDB_G0283939 | DDB_G0283939 | DDB0232431 | CDS | 1338263 | 3156 | + | 0.290875 | |
DDB_G0284037 | DDB_G0284037 | weakly similar to 26S proteasome regulatory subunit RPN11 (MPR1 protein) REMI mutant forms aberrant fruiting bodies (see | DDB0232431 | CDS | 1593040 | 2148 | + | 0.288175 |
DDB_G0284145 | DDB_G0284145 | DDB0232431 | CDS | 1523365 | 1317 | - | 0.2612 | |
DDB_G0284281 | DDB_G0284281 | DDB0232431 | CDS | 1827185 | 2940 | - | 0.25102 | |
DDB_G0285121 | DDB_G0285121 | DDB0232431 | CDS | 2881701 | 297 | + | 0.228956 | |
DDB_G0285261 | DDB_G0285261 | DDB0232431 | CDS | 3027528 | 1266 | + | 0.239336 | |
DDB_G0285265 | DDB_G0285265 | contains one EF hand similar to calmodulin | DDB0232431 | CDS | 3032493 | 420 | - | 0.292857 |
DDB_G0285305_RTE | DDB_G0285305 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3073434 | 2127 | + | 0.368594 |
DDB_G0285329 | DDB_G0285329 | C-terminal half very similar to nucleotide binding protein 1 belongs to the highly conserved MrpNBP35 ATP-binding protein family | DDB0232431 | CDS | 3094412 | 1497 | - | 0.311289 |
DDB_G0285813 | DDB_G0285813 | belongs to the DUF812 family homolog of human CCDC22 (coiled-coil domain-containing protein 22) contains at least two coiled-coil domains | DDB0232431 | CDS | 3688403 | 1914 | + | 0.293103 |
DDB_G0285851 | DDB_G0285851 | DDB0232431 | CDS | 3717914 | 708 | + | 0.305085 | |
DDB_G0286479 | DDB_G0286479 | DDB0232431 | CDS | 4506469 | 3504 | - | 0.257991 | |
DDB_G0286543 | DDB_G0286543 | contains a RUN domain which is predicted to play a role in Ras-like GTPase signaling pathways | DDB0232431 | CDS | 4611232 | 4086 | + | 0.26603 |
DDB_G0287103 | DDB_G0287103 | similar to timeless which in Drosophila forms a complex at replication forks that plays a role in the DNA damage response and is phosphorylated by cyclin-dependent kinases brbr bCommunity annotation: bDDB G0287103 is induced 11-fold in a | DDB0232431 | CDS | 5268402 | 3981 | + | 0.262999 |
DDB_G0287289 | DDB_G0287289 | DDB0232432 | CDS | 86247 | 4419 | + | 0.283548 | |
DDB_G0287325 | DDB_G0287325 | similar to mammalian EPS15 a clathrin adaptor that binds to the AP2 alpha subunit in mammalian cells | DDB0232432 | CDS | 137312 | 3591 | + | 0.310498 |
DDB_G0287709 | DDB_G0287709 | DDB0232432 | CDS | 584610 | 2652 | - | 0.245098 | |
DDB_G0288013 | DDB_G0288013 | DDB0232432 | CDS | 975395 | 756 | - | 0.244709 | |
DDB_G0288125 | DDB_G0288125 | DDB0232432 | CDS | 1099194 | 795 | - | 0.262893 | |
DDB_G0288539 | DDB_G0288539 | DDB0232432 | CDS | 1648133 | 798 | - | 0.177945 | |
DDB_G0289077 | DDB_G0289077 | DDB0232432 | CDS | 2326670 | 3246 | - | 0.254775 | |
DDB_G0289183 | DDB_G0289183 | DDB0232432 | CDS | 2445521 | 2337 | - | 0.307231 | |
DDB_G0289185 | DDB_G0289185 | DDB0232432 | CDS | 2448283 | 3081 | + | 0.212918 | |
DDB_G0289761 | DDB_G0289761 | DDB0232432 | CDS | 3227434 | 5901 | - | 0.239451 | |
DDB_G0289921 | DDB_G0289921 | DDB0232432 | CDS | 3426110 | 3708 | + | 0.263484 | |
DDB_G0290231 | DDB_G0290231 | DDB0232432 | CDS | 3832338 | 1356 | - | 0.233038 | |
DDB_G0290305 | DDB_G0290305 | DDB0232432 | CDS | 3936242 | 1716 | + | 0.287296 | |
DDB_G0290503 | DDB_G0290503 | DDB0232432 | CDS | 4159418 | 4479 | - | 0.20384 | |
DDB_G0290619 | DDB_G0290619 | DDB0232432 | CDS | 4380155 | 2163 | - | 0.283403 | |
DDB_G0290973 | DDB_G0290973 | similar to Polysphondylium pallidum protein contains at least two predicted coiled-coil domains | DDB0232432 | CDS | 4816558 | 5334 | - | 0.250469 |
DDB_G0291558 | DDB_G0291558 | DDB0232433 | CDS | 503745 | 420 | - | 0.202381 | |
DDB_G0292520 | DDB_G0292520 | DDB0232433 | CDS | 1591188 | 747 | + | 0.322624 | |
DDB_G0292586 | DDB_G0292586 | DDB0232433 | CDS | 1803595 | 1368 | + | 0.29386 | |
DDB_G0292742 | DDB_G0292742 | contains a dilute domain found at the carboxyl terminus of non-muscle myosin V | DDB0232433 | CDS | 2074742 | 2640 | + | 0.267803 |
DDB_G0293216 | DDB_G0293216 | DDB0232433 | CDS | 2689035 | 3537 | - | 0.240317 | |
DDB_G0293342_RTE | DDB_G0293342 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232433 | CDS | 2768512 | 684 | - | 0.342105 |
DDB_G0293548 | DDB_G0293548 | DDB0232433 | CDS | 3018651 | 1998 | - | 0.23974 | |
DDB_G0293620 | DDB_G0293620 | DDB0232433 | CDS | 3157149 | 1728 | - | 0.234375 | |
DDB_G0293628 | DDB_G0293628 | DDB0232433 | CDS | 3167249 | 4926 | + | 0.252944 | |
DDB_G0293756 | DDB_G0293756 | DDB0232433 | CDS | 3283369 | 3300 | - | 0.23 | |
DDB_G0293990 | DDB_G0293990 | DDB0232433 | CDS | 3578831 | 966 | - | 0.219462 | |
DDB_G0295671 | DDB_G0295671 | DDB0232431 | CDS | 4703129 | 1083 | - | 0.237304 | |
DDB_G0295713 | DDB_G0295713 | DDB0232430 | CDS | 4417290 | 2115 | - | 0.249645 | |
DDB_G0346831 | DDB_G0346831 | DDB0232428 | CDS | 4895305 | 2262 | + | 0.229443 | |
DG1113 | DDB_G0280959 | DDB0232430 | CDS | 4213401 | 3474 | - | 0.250144 | |
agnD | DDB_G0281955 | DDB0232430 | CDS | 5166543 | 3888 | + | 0.35571 | |
alxA | DDB_G0275451 | similar to mammalian Alix which interacts with ALG-2 (apoptosis-linked gene 2) contains 1 BRO1 (Bro1-rhophilin) domain 3 coiled-coil regions 1 proline-rich region and a conserved recognition sequence for Src-type tyrosine kinases | DDB0232429 | CDS | 5948745 | 2385 | - | 0.30021 |
anapc10 | DDB_G0268992 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232428 | CDS | 2080758 | 567 | + | 0.257496 |
anapc11 | DDB_G0286909 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232431 | CDS | 5059870 | 264 | - | 0.348485 |
ascc2 | DDB_G0280455 | ortholog of human ASCC2 part of the TRIP4 complex that enhances activation of NF-kappa-B SRF and AP1 | DDB0232430 | CDS | 3375530 | 2826 | + | 0.284501 |
atr1 | DDB_G0291380 | atypical PIKK family protein kinase similar to protein kinase ATR which modulates cell cycle progression and DNA repair in other organisms ATR phosphorylates Rad17 histone H2AX p53 and Nbs1 | DDB0232433 | CDS | 214264 | 9474 | - | 0.259552 |
bloc1s6 | DDB_G0290921 | ortholog of human BLOC1S6 a component of the BLOC-1 complex mutations in human BLOC1S6 have been linked to Hermansky-Pudlak syndrome 9 | DDB0232432 | CDS | 4755734 | 624 | - | 0.213141 |
bre1 | DDB_G0274241 | very similar in the C-terminal RING Zn finger domain belongs to the BRE1 family | DDB0232429 | CDS | 4227111 | 3243 | - | 0.258094 |
bud31 | DDB_G0270360 | a very conserved protein known as G10 protein or BUD31 which in human is suggested to be a nuclear transcription factor and in S. pombe and S. cerevisiae has been shown to be a splicing factor | DDB0232428 | CDS | 4710295 | 666 | - | 0.27027 |
bzpG | DDB_G0282749 | DDB0232430 | CDS | 6241172 | 1119 | - | 0.247542 | |
calA | DDB_G0279407 | calcium-dependent regulatory protein involved in cytokinesis regulated by cytosolic Ca2 fluxes allowing differential binding to target CaM binding proteins (CaMBPs) binds several proteins among them nuclear NumA and Cdk5 | DDB0232430 | CDS | 2244074 | 459 | - | 0.35512 |
calB | DDB_G0269104 | DDB0232428 | CDS | 2981116 | 450 | + | 0.275556 | |
cbpL | DDB_G0288785 | putative Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232432 | CDS | 1964055 | 576 | + | 0.258681 |
cbpM | DDB_G0286371 | putative Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232431 | CDS | 4370399 | 552 | - | 0.277174 |
cdc25 | DDB_G0283617 | similar to mammalian dual specificity protein phosphatases cdc25B and cdc25C involved in the G2M transition through dephosphorylation of cdc2 at Tyr15 and Thr14 | DDB0232431 | CDS | 1053164 | 3162 | - | 0.256799 |
cdc5l | DDB_G0279311 | contains two Myb DNA-binding domains ortholog of human CDC5L and yeast CEF1 may play a role in transcriptional activation and in mRNA splicing | DDB0232430 | CDS | 1918418 | 2403 | - | 0.28506 |
cenA | DDB_G0288427 | similar to human Centrin 2 EF-hand protein localizes to the centromer from which it dissociates during mitosis | DDB0232432 | CDS | 1525659 | 456 | + | 0.245614 |
cenB | DDB_G0279151 | centrin required for nuclear and centrosome stability localizes to the nucleus in interphase but not during mitosis and is involved in the centrosome cycle | DDB0232430 | CDS | 1697579 | 453 | - | 0.258278 |
cepC | DDB_G0290509 | DDB0232432 | CDS | 4173965 | 1413 | - | 0.219391 | |
cepE | DDB_G0275495 | DDB0232429 | CDS | 6003763 | 2400 | - | 0.307083 | |
cepG | DDB_G0278809 | DDB0232430 | CDS | 1225451 | 3894 | + | 0.248074 | |
cnbA | DDB_G0267446 | regulatory subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase contains an EF-hand calcium binding motif | DDB0232428 | CDS | 816934 | 1041 | - | 0.26513 |
cnbB | DDB_G0285999 | contains 3 EF-hands similar to calcineurin B (cnbA) the regulatory subunit of the Ca2calmodulin-dependent serinethreonine protein phosphatase | DDB0232431 | CDS | 3918232 | 552 | + | 0.269928 |
cnrP | DDB_G0279327 | ortholog of importin 9 a nuclear transport receptor that is thought to mediate docking of the importinsubstrate complex to the nuclear pore complex identified as a suppressor of smlA null mutant cnr16 | DDB0232430 | CDS | 1941566 | 3333 | - | 0.311131 |
cog7 | DDB_G0286705 | highly similar to COG7 component of the conserved oligomeric Golgi complex which is composed of eight different subunits Defects in human COG7 are the cause of congenital disorder of glycosylation type 2E (CDG2E) | DDB0232431 | CDS | 4871672 | 2991 | - | 0.252424 |
csnk2b | DDB_G0284601 | ortholog of the CK2 beta chain the regulatory subunit of the ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | DDB0232431 | CDS | 2209637 | 807 | - | 0.281289 |
ctu1 | DDB_G0282921 | ortholog of S. pombe ctu1 (cytosolic thiouridylase subunit 1) with ctu2 required for thiolation of the uridine at the wobble position of Lys(UUU) and Glu(UUC) tRNAs | DDB0232431 | CDS | 190346 | 1083 | - | 0.272391 |
ctu2 | DDB_G0268714 | ortholog of S. pombe ctu2 (cytosolic thiouridylase subunit 2) with ctu1 required for thiolation of the uridine at the wobble position of Lys(UUU) and Glu(UUC) tRNAs | DDB0232428 | CDS | 1986771 | 1572 | - | 0.246819 |
cycA | DDB_G0279085 | weakly similar to cyclin A predicted to interact with the cyclin-dependent kinase CDK12 ( | DDB0232430 | CDS | 1598641 | 1767 | + | 0.254669 |
cycB | DDB_G0275493 | similar to metazoan cyclin B predicted to interact with the cyclin-dependent kinase CDK12 ( | DDB0232429 | CDS | 6000211 | 1311 | - | 0.363844 |
cycC | DDB_G0274139 | similar to metazoan cyclin C predicted to interact with cyclin-dependent kinase | DDB0232429 | CDS | 4921649 | 768 | + | 0.247396 |
cycD | DDB_G0277439 | similar to metazoan and plant type-cyclins of the cell cycle group (G1 subgroup) highest similarity to algal cyclin D predicted to interact with the cyclin-dependent kinase CDK12 ( | DDB0232429 | CDS | 8066558 | 2085 | + | 0.242686 |
cycH | DDB_G0268668 | similar to metazoan cyclin H predicted to interact with cyclin-dependent kinase | DDB0232428 | CDS | 1891354 | 861 | - | 0.190476 |
cycK | DDB_G0286617 | similar to metazoan cyclin K predicted to interact with the cyclin-dependent kinase | DDB0232431 | CDS | 4722525 | 1218 | - | 0.297209 |
cycL | DDB_G0285553 | similar to metazoan and higher plants cyclin Lania-6 predicted to interact with | DDB0232431 | CDS | 3372094 | 822 | - | 0.284672 |
dnapkcs | DDB_G0281167 | atypical PIKK family protein kinase similar to human DNA-PKcs required for the repair of DNA double-strand breaks belongs to the PIKK family of protein kinases | DDB0232430 | CDS | 4132807 | 12900 | + | 0.265504 |
dotA | DDB_G0271626 | H3K79 methyltransferase in Dictyostelium involved in development and DNA repair similar to S. cerevisiae DOT1 which functions in gene silencing at telomeres and DNA repair and is cell cycle regulated Dictyostelium Dot1 however is not cell cycle dependent | DDB0232429 | CDS | 563064 | 5538 | + | 0.267786 |
dynA | DDB_G0280435 | DDB0232430 | CDS | 3347902 | 4620 | - | 0.303896 | |
eb1 | DDB_G0283607 | DDB0232431 | CDS | 912876 | 1521 | + | 0.326759 | |
eif3A | DDB_G0272078 | EIF3A ortholog the eukaryotic initiation factor theta subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232429 | CDS | 1223494 | 3093 | + | 0.38086 |
espl1 | DDB_G0290325 | caspase-like protease also called separin (ESP1) which plays a central role in sister chromosome segregation in yeastbrbr bCommunity annotation:b espl1 is highly similar to separase (aka separin) a widely-conserved peptidase which cleaves the rad21ssc1 non-SMC subunit of cohesin rings remaining at the centromere at metaphase allowing the sister chromatids to separate. Consistent with this homology espl1 is overexpressed fourfold (p6e-14) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes with roles in S-phase or mitosis are overexpressed in this strain and most of the overexpressed genes have identifiable cell cycle functions. espl1 also shows the developmental time course most typical of cell cycle genes.br The separase inhibitor securin conserved between yeast and humans which is broken down at the metaphaseanaphase junction under control of the spindle checkpoint is not recognizable in Dicty. Securin is also unrecognizable plants however whle | DDB0232432 | CDS | 3958340 | 7284 | - | 0.240527 |
forA | DDB_G0279607 | DDB0232430 | CDS | 2388583 | 3657 | + | 0.346185 | |
forG | DDB_G0277175 | DDB0232429 | CDS | 7682673 | 3225 | - | 0.310698 | |
frpA | DDB_G0292068 | contains two N-terminal calponin homology (CH) domains which is similar to fimbrins and a long unrelated C-terminal tail | DDB0232433 | CDS | 1144263 | 3291 | - | 0.267396 |
fszA | DDB_G0277721 | DDB0232429 | CDS | 8463906 | 1554 | + | 0.310811 | |
fszB | DDB_G0269224 | DDB0232428 | CDS | 4529920 | 1101 | + | 0.266122 | |
gacGG | DDB_G0280093 | DDB0232430 | CDS | 2923710 | 3612 | - | 0.295958 | |
gacI | DDB_G0275185 | DDB0232429 | CDS | 5262569 | 2400 | - | 0.281667 | |
gacN | DDB_G0279315 | DDB0232430 | CDS | 1925209 | 1836 | - | 0.259804 | |
gacR | DDB_G0278755 | DDB0232430 | CDS | 1120346 | 2352 | - | 0.306122 | |
gapA | DDB_G0269140 | DDB0232428 | CDS | 3059126 | 2583 | - | 0.297716 | |
gefC | DDB_G0282381 | DDB0232430 | CDS | 6243320 | 4374 | - | 0.299268 | |
gflC | DDB_G0270880 | contains a plant homeodomain (PHD) finger motif no other sequence similarity exists outside this small domain | DDB0232428 | CDS | 2933712 | 5163 | - | 0.270385 |
gnrA | DDB_G0291125 | DDB0232432 | CDS | 5022395 | 3264 | - | 0.324449 | |
gxcC | DDB_G0284845 | plays a role in the regulation of development contains N-terminal armadillo repeats a RhoGEF domain and a C-terminal pleckstrin homology (PH) domain | DDB0232431 | CDS | 2552011 | 3648 | + | 0.347039 |
gxcJJ | DDB_G0275679 | DDB0232429 | CDS | 5709701 | 3522 | - | 0.293583 | |
gxcQ | DDB_G0284501 | DDB0232431 | CDS | 2058245 | 3513 | + | 0.320239 | |
hipA | DDB_G0285703 | clathrin-associated protein involved in spore coat formation and regulated by epsin contains an Epsin N-terminal homology domain (ENTH) and a C-terminal ILWEQ domain that has been shown to bind to F-actin | DDB0232431 | CDS | 3610989 | 2883 | + | 0.367673 |
hook | DDB_G0288691 | similar to C. elegans ZYG-12 and mammalian HOOK proteins which mediates the attachment between the centrosome and the nucleus | DDB0232432 | CDS | 1822874 | 2205 | + | 0.275737 |
hop2 | DDB_G0280989 | DDB0232430 | CDS | 3917295 | 732 | - | 0.260929 | |
iqgC | DDB_G0288977 | contains a rasGAP domain similar to mammalian IQGAP proteins but lacking the calponin domain and the IQ-calmodulin binding region | DDB0232432 | CDS | 2198403 | 2454 | + | 0.347596 |
lmnB | DDB_G0289429 | similar to mammalian lamin B1 localizes to the inner membrane of the nuclear envelope involved in chromatin and centrosome organization and stabilization | DDB0232432 | CDS | 2787284 | 2151 | + | 0.317062 |
mad1 | DDB_G0287755 | conserved component of the spindle-assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate localized to centromeres during mitosis | DDB0232432 | CDS | 658379 | 2460 | - | 0.208537 |
mgp1 | DDB_G0290233 | DDB0232432 | CDS | 3834823 | 2763 | + | 0.287007 | |
mlcC | DDB_G0289563 | light chain that binds to the neck region of myoC contains two calcium-binding EF-hand motifs but does not bind calcium | DDB0232432 | CDS | 2954406 | 225 | - | 0.311111 |
mlcD | DDB_G0277917 | DDB0232430 | CDS | 607477 | 444 | + | 0.304054 | |
mlcE | DDB_G0277859 | component of actin-based molecular motor myosin II (conventional myosin) component | DDB0232430 | CDS | 76885 | 453 | + | 0.364238 |
mlcR | DDB_G0276077 | component of actin-based molecular motor myosin II (conventional myosin) component | DDB0232429 | CDS | 6426413 | 486 | + | 0.31893 |
mnat1 | DDB_G0289079 | DDB0232432 | CDS | 2330339 | 978 | + | 0.293456 | |
mnd1 | DDB_G0291750 | DDB0232433 | CDS | 686426 | 666 | - | 0.252252 | |
mybA | DDB_G0293900 | DDB0232433 | CDS | 3493719 | 3693 | - | 0.25589 | |
mybAA | DDB_G0268368 | DDB0232428 | CDS | 1003245 | 2916 | + | 0.284979 | |
mybQ | DDB_G0289319 | DDB0232432 | CDS | 2641022 | 2730 | - | 0.334066 | |
ncapD2 | DDB_G0293984 | component of the condensin I complex required for conversion of interphase chromatin into mitotic condensed chromosomes | DDB0232433 | CDS | 3563765 | 4212 | - | 0.243115 |
ncapGa | DDB_G0281419 | putative component of the condensin I complex required for conversion of interphase chromatin into mitotic condensed chromosomes There is another putative NCAPG gene in D. discoideum ( | DDB0232430 | CDS | 4452796 | 4611 | - | 0.227933 |
ncapH | DDB_G0292066 | component of the condensin I complex required for conversion of interphase chromatin into mitotic condensed chromosomes | DDB0232433 | CDS | 1141212 | 2637 | + | 0.264316 |
ncsA | DDB_G0275931 | contains four EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232429 | CDS | 6088223 | 561 | - | 0.279857 |
ndc80 | DDB_G0284003 | ortholog of NDC80 (also known as HEC1 and TID3) a subunit of the kinetochore complex involved in microtubule binding and the spindle assembly checkpoint brbr bCommunity annotation: bndc80 is overexpressed 16-fold in a Dictyostelium | DDB0232431 | CDS | 1379527 | 2568 | + | 0.257399 |
ndm | DDB_G0272368 | contains a coiled coil C-terminal BAR-like domain | DDB0232429 | CDS | 1340572 | 5346 | - | 0.245417 |
nubp1 | DDB_G0277437 | ortholog of the human nucleotide binding protein NUBP1 belongs to the highly conserved MrpNBP35 ATP-binding protein family | DDB0232429 | CDS | 8068928 | 948 | - | 0.336498 |
nubp2 | DDB_G0277157 | ortholog of the human nucleotide binding protein NUBP2 belongs to the highly conserved MrpNBP35 ATP-binding protein family contains a Zinc finger C4-type domain | DDB0232429 | CDS | 7917419 | 798 | + | 0.289474 |
nubpl | DDB_G0291193 | conserved protein belongs to the MrpNBP35 ATP-binding protein family | DDB0232432 | CDS | 5087724 | 972 | - | 0.304527 |
nudE | DDB_G0272326 | DDB0232429 | CDS | 1288191 | 1197 | - | 0.265664 | |
nuf2 | DDB_G0279553 | ortholog of NUF2 a component of the evolutionarily conserved kinetochore-associated Ndc80 complex (in S. pombe composed of: Ndc80-Nuf2-Spc24-Spc25) | DDB0232430 | CDS | 2245750 | 1410 | - | 0.289362 |
nup54 | DDB_G0270320 | similar to mammalian Nup54 component of the nuclear pore complex | DDB0232428 | CDS | 4639723 | 1323 | - | 0.312925 |
pikA | DDB_G0278727 | DDB0232430 | CDS | 1154369 | 4716 | + | 0.261026 | |
pikB | DDB_G0283081 | DDB0232431 | CDS | 247398 | 5574 | - | 0.311805 | |
pikC | DDB_G0275011 | DDB0232429 | CDS | 5211773 | 5094 | + | 0.270907 | |
pikD | DDB_G0288485 | subunit of PI4K responsible for the phosphorylation of phosphatidylinositol (PI) to PI4P (ATP 1-phosphatidyl-1D-myo-inositol ADP 1-phosphatidyl-1D-myo-inositol 4-phosphate) the first committed step in the generation of phosphatidylinositol 45-bisphosphate (PIP2) a precursor of the second messenger inositol 145-trisphosphate (InsP3) | DDB0232432 | CDS | 1616073 | 3543 | + | 0.269828 |
pikE | DDB_G0289601 | ortholog of yeast VPS34 a phosphatidylinositol 3-kinase | DDB0232432 | CDS | 3005109 | 2451 | - | 0.299878 |
pikF | DDB_G0268548 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | DDB0232428 | CDS | 1099622 | 4149 | + | 0.291396 |
pikG | DDB_G0282625 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | DDB0232430 | CDS | 6013022 | 5016 | - | 0.234649 |
pikH | DDB_G0291093 | putative PI3k putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring unlike other PI3Ks does not contain a ras binding domain but a PH domain and does not localize to the cell cortex upon chemotactic stimulation | DDB0232432 | CDS | 4980832 | 5463 | - | 0.242541 |
ppp2r4 | DDB_G0270036 | ortholog of the human PPP2R4 (PTPA) that stimulates the phosphotyrosyl phosphatase activity of PP2A in the presence of ATP and Mg(2) in vitro | DDB0232428 | CDS | 4068160 | 978 | + | 0.287321 |
rbx1 | DDB_G0287629 | DDB0232432 | CDS | 496993 | 315 | + | 0.342857 | |
rgaA | DDB_G0287585 | DDB0232432 | CDS | 498740 | 2469 | + | 0.357635 | |
rio1 | DDB_G0280431 | atypical RIO family protein kinase yeast serinethreonine kinase RIO1 plays a role in cell cycle progression | DDB0232430 | CDS | 3344181 | 1725 | - | 0.302609 |
rngB | DDB_G0268860 | DDB0232428 | CDS | 2266964 | 2832 | + | 0.278249 | |
scdA | DDB_G0283375 | DDB0232431 | CDS | 574408 | 2586 | + | 0.287703 | |
sec20 | DDB_G0267646 | DDB0232428 | CDS | 490625 | 732 | + | 0.210383 | |
smc1 | DDB_G0291752 | functions in chromosome dynamics heterodimerizes with smc3 | DDB0232433 | CDS | 688164 | 4122 | + | 0.312712 |
smc2 | DDB_G0284499 | functions in chromosome dynamics heterodimerizes with smc4 | DDB0232431 | CDS | 2051268 | 3555 | - | 0.320394 |
smc3 | DDB_G0276101 | functions in chromosome dynamics heterodimerizes with smc1 | DDB0232429 | CDS | 6321257 | 4314 | - | 0.309458 |
smc4 | DDB_G0286403 | functions in chromosome dynamics heterodimerizes with smc2 | DDB0232431 | CDS | 4414331 | 4248 | - | 0.318974 |
smc5 | DDB_G0290919 | functions in chromosome dynamics heterodimerizes with smc6 | DDB0232432 | CDS | 4745027 | 3396 | - | 0.328033 |
smc6 | DDB_G0288993 | functions in chromosome dynamics heterodimerizes with smc5 | DDB0232432 | CDS | 2211609 | 3558 | - | 0.324902 |
smg1 | DDB_G0275845 | atypical PIKK family protein kinase similar to the PI-3-kinase-related kinase SMG1 which functions in nonsense-mediated mRNA decay belongs to the PIKK family of protein kinases | DDB0232429 | CDS | 5665840 | 7035 | + | 0.267235 |
syf2 | DDB_G0284573 | D. discoideum SYF2 homolog SYF2 proteins are involved in cell cycle progression and pre-mRNA splicing | DDB0232431 | CDS | 2172315 | 882 | + | 0.250567 |
syn10 | DDB_G0284385 | similar to syntaxin a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232431 | CDS | 1923544 | 774 | - | 0.31137 |
syn5 | DDB_G0277565 | similar to syntaxin 5 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232429 | CDS | 8154194 | 909 | - | 0.265127 |
tacc | DDB_G0275391 | promotes microtubule growth localizes to the centromer and has been shown to physically interact with | DDB0232429 | CDS | 5495060 | 4437 | - | 0.320036 |
tbcB | DDB_G0277983 | DDB0232430 | CDS | 98599 | 813 | - | 0.276753 | |
thoc2 | DDB_G0291063 | ortholog of human THOC2 and yeast RLR1 which exist in the THO complex required for transcriptional elongation | DDB0232432 | CDS | 4908746 | 6333 | + | 0.291963 |
tirA | DDB_G0289237 | DDB0232432 | CDS | 2526970 | 4011 | - | 0.222638 | |
tor | DDB_G0281569 | atypical PIKK family FRAP subfamily protein kinase ortholog of tor a protein kinase that plays a central role in response to nutrients stress and intracellular energy state called mTOR in mammals in dTOR in Drosophila | DDB0232430 | CDS | 4934791 | 7143 | - | 0.347893 |
vps52A | DDB_G0293772 | putative ortholog of S. cerevisiae VPS52 component of the GARP (Golgi-associated retrograde protein) complex | DDB0232433 | CDS | 3307775 | 2517 | + | 0.222487 |
vps52B | DDB_G0293496 | similar to S. cerevisiae VPS52 component of the GARP (Golgi-associated retrograde protein) complex | DDB0232433 | CDS | 2961150 | 2631 | - | 0.247815 |
xpo2 | DDB_G0291838 | bCommunity annotation:b DDB_G0291838 is highly similar to cse1 of budding yeast and CAS of metazoans. In yeast this protein has been shown to be essential for the re-export of importin alpha (see Schroeder et al Mol Gen Genet 261 788-795 (1999). CSE stands for | DDB0232433 | CDS | 815672 | 2856 | - | 0.308473 |
xrn1 | DDB_G0276137 | DDB0232429 | CDS | 6232603 | 5250 | - | 0.333333 | |
xrn2 | DDB_G0269922 | DDB0232428 | CDS | 3871046 | 3573 | - | 0.285195 | |
zipA | DDB_G0286985 | DDB0232431 | CDS | 5171363 | 3075 | - | 0.294959 |