Gene list
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Genomic element: DDB0232431
Number of genes found: 2111
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 |
4cl1 | DDB_G0284831 | catalyzes the reaction ATP 4-coumarate CoA AMP diphosphate 4-coumaroyl-CoA | DDB0232431 | CDS | 2416042 | 1656 | - | 0.316425 |
4cl2 | DDB_G0284745 | catalyzes the reaction ATP 4-coumarate CoA AMP diphosphate 4-coumaroyl-CoA | DDB0232431 | CDS | 2413291 | 1656 | - | 0.31401 |
4cl3 | DDB_G0284743 | catalyzes the reaction ATP 4-coumarate CoA AMP diphosphate 4-coumaroyl-CoA | DDB0232431 | CDS | 2409764 | 1656 | - | 0.307971 |
5NT | DDB_G0287199 | catalyzes the reaction a 5'-ribonucleotide Hsub2subO a ribonucleoside phosphate enriched in prestalk cells | DDB0232431 | CDS | 5397049 | 1737 | - | 0.255037 |
D2 | DDB_G0283085 | DDB0232431 | CDS | 276713 | 1608 | + | 0.324627 | |
D7 | DDB_G0284613 | DDB0232431 | CDS | 2275277 | 2553 | - | 0.307873 | |
DD3-3 | DDB_G0283095 | similar to tunicate proteins involved in O-glycosylation as identified by mRNA differential display | DDB0232431 | CDS | 210212 | 1851 | - | 0.399244 |
DDB_G0282917 | DDB_G0282917 | DDB0232431 | CDS | 3257 | 375 | - | 0.333333 | |
DDB_G0282919_TE | DDB_G0282919 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232431 | CDS | 101 | 821 | + | 0.303289 |
DDB_G0282935 | DDB_G0282935 | contains two putative transmembrane domains partial high similarity to D. purpureum protein | DDB0232431 | CDS | 17607 | 930 | - | 0.256989 |
DDB_G0282937 | DDB_G0282937 | DDB0232431 | CDS | 19492 | 312 | - | 0.294872 | |
DDB_G0282939 | DDB_G0282939 | DDB0232431 | CDS | 22195 | 1404 | - | 0.23433 | |
DDB_G0282941 | DDB_G0282941 | DDB0232431 | CDS | 24418 | 1827 | + | 0.307061 | |
DDB_G0282943 | DDB_G0282943 | DDB0232431 | CDS | 28010 | 3210 | + | 0.280685 | |
DDB_G0282945 | DDB_G0282945 | DDB0232431 | CDS | 31559 | 2010 | - | 0.280597 | |
DDB_G0282947 | DDB_G0282947 | DDB0232431 | CDS | 38803 | 3042 | - | 0.273504 | |
DDB_G0282951 | DDB_G0282951 | DDB0232431 | CDS | 45329 | 402 | + | 0.293532 | |
DDB_G0282953 | DDB_G0282953 | family member of conserved eukaryotic proteins of unknown function contains the conserved DUF1671 domain | DDB0232431 | CDS | 45934 | 1953 | - | 0.231439 |
DDB_G0282955 | DDB_G0282955 | DDB0232431 | CDS | 49492 | 903 | + | 0.221484 | |
DDB_G0282957 | DDB_G0282957 | DDB0232431 | CDS | 50957 | 207 | - | 0.251208 | |
DDB_G0282959 | DDB_G0282959 | DDB0232431 | CDS | 52235 | 4611 | + | 0.25591 | |
DDB_G0282961 | DDB_G0282961 | DDB0232431 | CDS | 57054 | 1716 | - | 0.277389 | |
DDB_G0282963 | DDB_G0282963 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats | DDB0232431 | CDS | 60445 | 5286 | + | 0.265796 |
DDB_G0282965 | DDB_G0282965 | DDB0232431 | CDS | 68065 | 972 | - | 0.246914 | |
DDB_G0282971 | DDB_G0282971 | DDB0232431 | CDS | 74287 | 2331 | + | 0.299013 | |
DDB_G0282973 | DDB_G0282973 | DDB0232431 | CDS | 78185 | 876 | + | 0.278539 | |
DDB_G0282975 | DDB_G0282975 | DDB0232431 | CDS | 80707 | 1101 | + | 0.305177 | |
DDB_G0282977 | DDB_G0282977 | DDB0232431 | CDS | 81934 | 3078 | - | 0.254061 | |
DDB_G0282983 | DDB_G0282983 | DDB0232431 | CDS | 99975 | 1746 | + | 0.231959 | |
DDB_G0282985 | DDB_G0282985 | DDB0232431 | CDS | 102023 | 2748 | - | 0.212518 | |
DDB_G0282991 | DDB_G0282991 | DDB0232431 | CDS | 109030 | 1020 | + | 0.227451 | |
DDB_G0282995 | DDB_G0282995 | DDB0232431 | CDS | 113431 | 1077 | + | 0.317549 | |
DDB_G0283003 | DDB_G0283003 | DDB0232431 | CDS | 141272 | 585 | + | 0.312821 | |
DDB_G0283007 | DDB_G0283007 | DDB0232431 | CDS | 147313 | 1230 | + | 0.305691 | |
DDB_G0283011 | DDB_G0283011 | DDB0232431 | CDS | 151994 | 360 | - | 0.286111 | |
DDB_G0283013 | DDB_G0283013 | DDB0232431 | CDS | 153182 | 6882 | + | 0.186574 | |
DDB_G0283015 | DDB_G0283015 | contains 2 putative transmembrane domains contains one putative coiled-coil domain | DDB0232431 | CDS | 161759 | 1599 | - | 0.220763 |
DDB_G0283017 | DDB_G0283017 | DDB0232431 | CDS | 164286 | 2676 | + | 0.246637 | |
DDB_G0283019 | DDB_G0283019 | contains two breast cancer type 2 repeats BRCA2 is a breast tumor suppressor with a potential function in the cellular response to DNA damage | DDB0232431 | CDS | 167136 | 408 | - | 0.264706 |
DDB_G0283025_ps | DDB_G0283025 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 171885 | 2268 | - | 0.27866 |
DDB_G0283031 | DDB_G0283031 | DDB0232431 | CDS | 177075 | 1167 | + | 0.151671 | |
DDB_G0283033 | DDB_G0283033 | DDB0232431 | CDS | 178285 | 2304 | - | 0.268229 | |
DDB_G0283039 | DDB_G0283039 | DDB0232431 | CDS | 196663 | 1341 | - | 0.222968 | |
DDB_G0283041 | DDB_G0283041 | DDB0232431 | CDS | 198610 | 633 | - | 0.276461 | |
DDB_G0283055 | DDB_G0283055 | very similar to the mammalian TBC1 domain family member 20 protein a potential multi-pass membrane protein | DDB0232431 | CDS | 20488 | 1203 | + | 0.261014 |
DDB_G0283057 | DDB_G0283057 | DDB0232431 | CDS | 34226 | 3150 | - | 0.281587 | |
DDB_G0283061 | DDB_G0283061 | DDB0232431 | CDS | 69391 | 1032 | - | 0.293605 | |
DDB_G0283063 | DDB_G0283063 | DDB0232431 | CDS | 115315 | 810 | - | 0.302469 | |
DDB_G0283065 | DDB_G0283065 | putative eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase putative protein serinethreonine kinase related to the GCN2 (general control non-derepressible) family of protein kinases that phosphorylate the alpha subunit of eIF2 | DDB0232431 | CDS | 122741 | 1914 | - | 0.242424 |
DDB_G0283067 | DDB_G0283067 | DDB0232431 | CDS | 138075 | 1203 | + | 0.287614 | |
DDB_G0283069 | DDB_G0283069 | DDB0232431 | CDS | 175065 | 237 | + | 0.350211 | |
DDB_G0283071 | DDB_G0283071 | DDB0232431 | CDS | 181322 | 618 | + | 0.194175 | |
DDB_G0283075 | DDB_G0283075 | ortholog of mammalian MORF4 and S. cerevisiae EAF3 a nonessential component of the NuA4 acetyltransferase complex | DDB0232431 | CDS | 188331 | 1140 | - | 0.25 |
DDB_G0283077 | DDB_G0283077 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 194597 | 1806 | + | 0.268549 |
DDB_G0283079_RTE | DDB_G0283079 | partial ORF2 protein of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232431 | CDS | 199920 | 2053 | - | 0.293717 |
DDB_G0283087 | DDB_G0283087 | similar to butyrylcholinesterase and acetylcholinesterase precursor proteins contains a putative signal peptide | DDB0232431 | CDS | 203029 | 1638 | + | 0.286935 |
DDB_G0283089 | DDB_G0283089 | DDB0232431 | CDS | 205098 | 1434 | - | 0.24477 | |
DDB_G0283091 | DDB_G0283091 | DDB0232431 | CDS | 206705 | 1389 | - | 0.275018 | |
DDB_G0283093 | DDB_G0283093 | DDB0232431 | CDS | 208398 | 1344 | - | 0.274554 | |
DDB_G0283097 | DDB_G0283097 | DDB0232431 | CDS | 214573 | 1221 | + | 0.266994 | |
DDB_G0283099 | DDB_G0283099 | ortholog of the metazoan nipped-B protein which contains the armadillo-like (ARM-like) helical domain and two HEAT repeats the Drosophila protein plays a structural role in chromatin and is involved in sister chromatid cohesion | DDB0232431 | CDS | 217095 | 6192 | + | 0.258398 |
DDB_G0283101 | DDB_G0283101 | DDB0232431 | CDS | 235690 | 660 | + | 0.256061 | |
DDB_G0283103 | DDB_G0283103 | DDB0232431 | CDS | 237163 | 1443 | - | 0.261261 | |
DDB_G0283107 | DDB_G0283107 | DDB0232431 | CDS | 255521 | 1086 | - | 0.291897 | |
DDB_G0283117 | DDB_G0283117 | DDB0232431 | CDS | 267048 | 1032 | - | 0.243217 | |
DDB_G0283121 | DDB_G0283121 | bifunctional enzyme that catalyzes the reactions methylene-tetrahydrofolate NADP NADPH methenyl-Hsub4subF and NADPH methenyl-Hsub4subF methylene-tetrahydrofolate NADP | DDB0232431 | CDS | 275079 | 879 | + | 0.285552 |
DDB_G0283127 | DDB_G0283127 | DDB0232431 | CDS | 283814 | 1287 | - | 0.334887 | |
DDB_G0283129 | DDB_G0283129 | DDB0232431 | CDS | 286809 | 2652 | + | 0.274887 | |
DDB_G0283133_TE | DDB_G0283133 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232431 | CDS | 232444 | 2004 | - | 0.317864 |
DDB_G0283135 | DDB_G0283135 | DDB0232431 | CDS | 223712 | 246 | - | 0.349593 | |
DDB_G0283139 | DDB_G0283139 | mannose-6-phosphate receptors are involved in the transport of lysosomal enzymes from the Golgi complex and the cell surface to lysosomes contains a N-terminal predicted signal sequence and a C-terminal transmembrane domain | DDB0232431 | CDS | 228583 | 2916 | - | 0.250343 |
DDB_G0283143 | DDB_G0283143 | DDB0232431 | CDS | 243331 | 2940 | - | 0.270068 | |
DDB_G0283145 | DDB_G0283145 | DDB0232431 | CDS | 254487 | 771 | - | 0.32166 | |
DDB_G0283147 | DDB_G0283147 | DDB0232431 | CDS | 291263 | 3773 | - | 0.320435 | |
DDB_G0283155 | DDB_G0283155 | DDB0232431 | CDS | 297464 | 780 | + | 0.25641 | |
DDB_G0283159 | DDB_G0283159 | DDB0232431 | CDS | 301718 | 1971 | + | 0.221715 | |
DDB_G0283161 | DDB_G0283161 | DDB0232431 | CDS | 303938 | 405 | - | 0.192593 | |
DDB_G0283169 | DDB_G0283169 | DDB0232431 | CDS | 356370 | 603 | + | 0.258706 | |
DDB_G0283171 | DDB_G0283171 | DDB0232431 | CDS | 358763 | 330 | + | 0.206061 | |
DDB_G0283177 | DDB_G0283177 | DDB0232431 | CDS | 362729 | 1734 | + | 0.198962 | |
DDB_G0283179 | DDB_G0283179 | DDB0232431 | CDS | 366668 | 216 | - | 0.25463 | |
DDB_G0283185 | DDB_G0283185 | DDB0232431 | CDS | 376419 | 1344 | + | 0.145089 | |
DDB_G0283187 | DDB_G0283187 | catalyzes the reaction: A phosphoprotein Hsub2subO a protein phosphate conserved serinethreonine protein phosphatase family protein | DDB0232431 | CDS | 381819 | 939 | + | 0.308839 |
DDB_G0283189 | DDB_G0283189 | similar to DNA polymerase epsilon subunit A in yeast and vertebrates thought to be involved in DNA replication DNA repair and cell-cycle checkpoint control in eukaryotes | DDB0232431 | CDS | 385928 | 7143 | - | 0.297494 |
DDB_G0283191 | DDB_G0283191 | DDB0232431 | CDS | 394762 | 1695 | + | 0.277286 | |
DDB_G0283193 | DDB_G0283193 | DDB0232431 | CDS | 396519 | 1071 | - | 0.264239 | |
DDB_G0283195 | DDB_G0283195 | DDB0232431 | CDS | 400645 | 3024 | + | 0.236442 | |
DDB_G0283197 | DDB_G0283197 | DDB0232431 | CDS | 407180 | 1968 | + | 0.225102 | |
DDB_G0283199 | DDB_G0283199 | DDB0232431 | CDS | 409273 | 645 | - | 0.269767 | |
DDB_G0283201 | DDB_G0283201 | DDB0232431 | CDS | 413865 | 906 | + | 0.210817 | |
DDB_G0283209 | DDB_G0283209 | DDB0232431 | CDS | 364837 | 165 | - | 0.218182 | |
DDB_G0283211_ps | DDB_G0283211 | putative pseudogene belongs to the large D. discoideum zinc-containing alcohol dehydrogenase (ADH) family | DDB0232431 | CDS | 368141 | 768 | - | 0.272135 |
DDB_G0283213 | DDB_G0283213 | DDB0232431 | CDS | 309059 | 783 | - | 0.228608 | |
DDB_G0283215 | DDB_G0283215 | DDB0232431 | CDS | 311593 | 1518 | + | 0.254282 | |
DDB_G0283217_ps | DDB_G0283217 | putative pseudogene similar to a family of Dictyostelium putative mannose-6-phosphate receptors including | DDB0232431 | CDS | 313913 | 915 | + | 0.268852 |
DDB_G0283219_ps | DDB_G0283219 | putative pseudogene fusion fragment similar to parts of | DDB0232431 | CDS | 316554 | 531 | - | 0.312618 |
DDB_G0283221_ps | DDB_G0283221 | putative pseudogene fragment similar to | DDB0232431 | CDS | 317030 | 192 | - | 0.328125 |
DDB_G0283223_ps | DDB_G0283223 | putative pseudogene fragment similar to | DDB0232431 | CDS | 318683 | 696 | + | 0.239943 |
DDB_G0283227 | DDB_G0283227 | DDB0232431 | CDS | 319419 | 2913 | - | 0.240645 | |
DDB_G0283229 | DDB_G0283229 | DDB0232431 | CDS | 324812 | 2925 | - | 0.245128 | |
DDB_G0283231 | DDB_G0283231 | DDB0232431 | CDS | 329911 | 741 | - | 0.234818 | |
DDB_G0283233_ps | DDB_G0283233 | putative pseudogene similar to Dictyostelium genes | DDB0232431 | CDS | 331060 | 2760 | + | 0.238406 |
DDB_G0283235_ps | DDB_G0283235 | putative pseudogene similar to | DDB0232431 | CDS | 335133 | 513 | - | 0.235867 |
DDB_G0283237_ps | DDB_G0283237 | putative pseudogene similar to a family of Dictyostelium genes including | DDB0232431 | CDS | 336082 | 855 | + | 0.25848 |
DDB_G0283241 | DDB_G0283241 | DDB0232431 | CDS | 338450 | 642 | - | 0.23676 | |
DDB_G0283243 | DDB_G0283243 | DDB0232431 | CDS | 339770 | 2898 | + | 0.241201 | |
DDB_G0283245 | DDB_G0283245 | DDB0232431 | CDS | 343211 | 519 | - | 0.22158 | |
DDB_G0283251 | DDB_G0283251 | DDB0232431 | CDS | 377937 | 2190 | - | 0.2621 | |
DDB_G0283253 | DDB_G0283253 | DDB0232431 | CDS | 383852 | 318 | - | 0.289308 | |
DDB_G0283255 | DDB_G0283255 | DDB0232431 | CDS | 398240 | 1713 | + | 0.247519 | |
DDB_G0283259 | DDB_G0283259 | DDB0232431 | CDS | 295136 | 1002 | - | 0.328343 | |
DDB_G0283269 | DDB_G0283269 | has similarity to mammalian threonine aspartase 1 which belongs to the asparaginase 2 family | DDB0232431 | CDS | 428924 | 1770 | - | 0.233333 |
DDB_G0283271 | DDB_G0283271 | 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 | DDB0232431 | CDS | 436406 | 1146 | - | 0.362129 |
DDB_G0283275 | DDB_G0283275 | similar to bacterial 50S ribosomal L4L1e proteins | DDB0232431 | CDS | 442808 | 777 | + | 0.292149 |
DDB_G0283277_ps | DDB_G0283277 | putative pseudogene similar to CAZy family GH9 which catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 443932 | 1299 | - | 0.266359 |
DDB_G0283281 | DDB_G0283281 | catalyzes the reaction tryptamine secologanin 3-alpha(S)-strictosidine Hsub2subO in alkaloid biosynthesis | DDB0232431 | CDS | 447879 | 1179 | - | 0.261238 |
DDB_G0283285 | DDB_G0283285 | DDB0232431 | CDS | 458537 | 4368 | + | 0.278159 | |
DDB_G0283289 | DDB_G0283289 | DDB0232431 | CDS | 465144 | 2178 | + | 0.230946 | |
DDB_G0283291 | DDB_G0283291 | DDB0232431 | CDS | 467526 | 1092 | - | 0.271978 | |
DDB_G0283293 | DDB_G0283293 | catalyzes the reduction of glutamate to delta-1-pyrroline-5-carboxylate a critical step in the de novo biosynthesis of proline and ornithine expressed in pstO cells and in pstO cells and upper cup during culmination | DDB0232431 | CDS | 472326 | 1677 | + | 0.369112 |
DDB_G0283295 | DDB_G0283295 | DDB0232431 | CDS | 476937 | 165 | + | 0.29697 | |
DDB_G0283301 | DDB_G0283301 | DDB0232431 | CDS | 480042 | 1992 | + | 0.254016 | |
DDB_G0283303 | DDB_G0283303 | DDB0232431 | CDS | 497204 | 1404 | + | 0.264245 | |
DDB_G0283305 | DDB_G0283305 | DDB0232431 | CDS | 498765 | 1671 | - | 0.304608 | |
DDB_G0283309 | DDB_G0283309 | similar to the eIF-2B alphabetadelta subunits family | DDB0232431 | CDS | 511242 | 1041 | - | 0.397695 |
DDB_G0283311 | DDB_G0283311 | DDB0232431 | CDS | 512897 | 465 | + | 0.270968 | |
DDB_G0283313 | DDB_G0283313 | DDB0232431 | CDS | 513450 | 1542 | - | 0.295071 | |
DDB_G0283321 | DDB_G0283321 | DDB0232431 | CDS | 527883 | 1863 | - | 0.17284 | |
DDB_G0283325 | DDB_G0283325 | DDB0232431 | CDS | 424767 | 3960 | + | 0.255051 | |
DDB_G0283337 | DDB_G0283337 | DDB0232431 | CDS | 491931 | 3387 | - | 0.219368 | |
DDB_G0283339 | DDB_G0283339 | DDB0232431 | CDS | 501258 | 6369 | - | 0.28152 | |
DDB_G0283347 | DDB_G0283347 | DDB0232431 | CDS | 543684 | 1551 | - | 0.272083 | |
DDB_G0283351 | DDB_G0283351 | DDB0232431 | CDS | 550541 | 4812 | + | 0.209061 | |
DDB_G0283353 | DDB_G0283353 | DDB0232431 | CDS | 558631 | 93 | + | 0.354839 | |
DDB_G0283357 | DDB_G0283357 | DDB0232431 | CDS | 564906 | 3744 | + | 0.276175 | |
DDB_G0283361 | DDB_G0283361 | DDB0232431 | CDS | 572566 | 1557 | + | 0.245986 | |
DDB_G0283369 | DDB_G0283369 | DDB0232431 | CDS | 587429 | 6252 | - | 0.274152 | |
DDB_G0283373 | DDB_G0283373 | contains a predicted signal peptide contains one ERVALR sulphydryl oxidase domain similar to D. purpureum protein | DDB0232431 | CDS | 556576 | 1743 | + | 0.270797 |
DDB_G0283377 | DDB_G0283377 | DDB0232431 | CDS | 578428 | 1326 | + | 0.366516 | |
DDB_G0283379 | DDB_G0283379 | DDB0232431 | CDS | 579956 | 3594 | - | 0.175849 | |
DDB_G0283381 | DDB_G0283381 | contains a weak Spc7 kinetochore protein domain similar to D. purpureum proteinbrbr bCommunity annotation:b DDB_G0283381 appears to be the ortholog of spc7 of Saccharomyces pombe and spc105 of Saccharomyces cerevesiae. Spc105 is a kinetochore component (see Pagliuca et al Plos One 28 e7640m (2009)). Like the conserved kinetochore components spc25 nuf2 and ndc80 DDB_G0283381 is very strongly overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (spc25 30-fold nuf2 18-fold ndc80 16-fold DDB_G0283381 29-fold) (Doquang et al in preparation). This presumably reflects a cell cycle function as most cell cycle genes are overexpressed in this strain and most of the genes strongly overexpressed in the strain have identifiable cell cycle functions. Spc105 forms a complex with kre28 but I could not identify a corresponding gene in Dicty even by using Ashbya as an intermediate. Harry MacWilliams December 2009br | DDB0232431 | CDS | 594665 | 5541 | + | 0.242375 |
DDB_G0283383 | DDB_G0283383 | DDB0232431 | CDS | 603790 | 175 | - | 0.24 | |
DDB_G0283395 | DDB_G0283395 | almost identical to neighboring gene | DDB0232431 | CDS | 606034 | 189 | - | 0.296296 |
DDB_G0283397 | DDB_G0283397 | DDB0232431 | CDS | 606939 | 2757 | - | 0.283642 | |
DDB_G0283399 | DDB_G0283399 | DDB0232431 | CDS | 609993 | 504 | - | 0.18254 | |
DDB_G0283403 | DDB_G0283403 | DDB0232431 | CDS | 615804 | 2241 | + | 0.245872 | |
DDB_G0283407 | DDB_G0283407 | DDB0232431 | CDS | 632298 | 1368 | - | 0.214181 | |
DDB_G0283409 | DDB_G0283409 | DDB0232431 | CDS | 637844 | 387 | - | 0.281654 | |
DDB_G0283413 | DDB_G0283413 | DDB0232431 | CDS | 651190 | 912 | + | 0.267544 | |
DDB_G0283415 | DDB_G0283415 | DDB0232431 | CDS | 652443 | 738 | - | 0.247967 | |
DDB_G0283417 | DDB_G0283417 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232431 | CDS | 654013 | 693 | - | 0.215007 |
DDB_G0283421 | DDB_G0283421 | DDB0232431 | CDS | 663424 | 174 | + | 0.356322 | |
DDB_G0283423 | DDB_G0283423 | DDB0232431 | CDS | 673782 | 4578 | + | 0.189602 | |
DDB_G0283425 | DDB_G0283425 | DDB0232431 | CDS | 683015 | 3312 | - | 0.223732 | |
DDB_G0283427 | DDB_G0283427 | DDB0232431 | CDS | 687466 | 423 | + | 0.262411 | |
DDB_G0283429 | DDB_G0283429 | similar to proteins in bacteria and protozoa COG4271 predicted nucleotide-binding protein containing TIR -like domain (Transcription) | DDB0232431 | CDS | 691392 | 756 | - | 0.276455 |
DDB_G0283431 | DDB_G0283431 | DDB0232431 | CDS | 692545 | 342 | - | 0.122807 | |
DDB_G0283433_ps | DDB_G0283433 | putative pseudogene similar to a large family of D. discoideum proteins including | DDB0232431 | CDS | 694005 | 849 | + | 0.232038 |
DDB_G0283435 | DDB_G0283435 | DDB0232431 | CDS | 696044 | 747 | + | 0.170013 | |
DDB_G0283437 | DDB_G0283437 | DDB0232431 | CDS | 697659 | 621 | + | 0.281804 | |
DDB_G0283439 | DDB_G0283439 | similar to H. sapiens solute carrier family 29 member 1 (SLC29A2) putative ortholog of S. cerevisiae FUN2 | DDB0232431 | CDS | 699253 | 1293 | + | 0.324053 |
DDB_G0283441 | DDB_G0283441 | DDB0232431 | CDS | 702819 | 2916 | + | 0.284636 | |
DDB_G0283443 | DDB_G0283443 | DDB0232431 | CDS | 706025 | 1182 | - | 0.187817 | |
DDB_G0283445 | DDB_G0283445 | DDB0232431 | CDS | 707432 | 1284 | + | 0.221184 | |
DDB_G0283447 | DDB_G0283447 | DDB0232431 | CDS | 709169 | 2019 | + | 0.280832 | |
DDB_G0283449 | DDB_G0283449 | DDB0232431 | CDS | 711483 | 246 | - | 0.378049 | |
DDB_G0283451 | DDB_G0283451 | DDB0232431 | CDS | 712043 | 1215 | - | 0.33251 | |
DDB_G0283455 | DDB_G0283455 | DDB0232431 | CDS | 724620 | 288 | - | 0.284722 | |
DDB_G0283457 | DDB_G0283457 | DDB0232431 | CDS | 726060 | 813 | - | 0.172202 | |
DDB_G0283461 | DDB_G0283461 | DDB0232431 | CDS | 731858 | 195 | + | 0.271795 | |
DDB_G0283463 | DDB_G0283463 | DDB0232431 | CDS | 733335 | 141 | + | 0.312057 | |
DDB_G0283465 | DDB_G0283465 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 734816 | 174 | + | 0.316092 |
DDB_G0283467 | DDB_G0283467 | DDB0232431 | CDS | 735396 | 219 | - | 0.30137 | |
DDB_G0283469 | DDB_G0283469 | DDB0232431 | CDS | 737091 | 444 | + | 0.220721 | |
DDB_G0283471 | DDB_G0283471 | DDB0232431 | CDS | 738038 | 6009 | - | 0.192045 | |
DDB_G0283475 | DDB_G0283475 | DDB0232431 | CDS | 753547 | 7128 | + | 0.317761 | |
DDB_G0283477 | DDB_G0283477 | DDB0232431 | CDS | 763555 | 2520 | - | 0.198016 | |
DDB_G0283481 | DDB_G0283481 | similar to Dictystelium cell surface glycoproteins gp130 and cfrA B C and D (GP138A-D) | DDB0232431 | CDS | 772790 | 1749 | - | 0.238994 |
DDB_G0283485 | DDB_G0283485 | DDB0232431 | CDS | 641115 | 2292 | - | 0.253927 | |
DDB_G0283487 | DDB_G0283487 | DDB0232431 | CDS | 688705 | 2577 | + | 0.177726 | |
DDB_G0283493 | DDB_G0283493 | almost identical to neighboring gene | DDB0232431 | CDS | 605068 | 189 | - | 0.306878 |
DDB_G0283495 | DDB_G0283495 | DDB0232431 | CDS | 611003 | 2319 | + | 0.337214 | |
DDB_G0283499 | DDB_G0283499 | DDB0232431 | CDS | 660137 | 762 | - | 0.229659 | |
DDB_G0283501 | DDB_G0283501 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 665243 | 174 | + | 0.33908 |
DDB_G0283503 | DDB_G0283503 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 666044 | 174 | + | 0.33908 |
DDB_G0283505 | DDB_G0283505 | contains one putative transmembrane domain belongs to a family of small highly conserved genes unique to Dictyostelium discoideum | DDB0232431 | CDS | 666961 | 174 | + | 0.344828 |
DDB_G0283507 | DDB_G0283507 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 667839 | 174 | + | 0.333333 |
DDB_G0283509 | DDB_G0283509 | belongs to a family of small highly conserved genes unique to Dictyostelium discoideum | DDB0232431 | CDS | 668710 | 174 | + | 0.327586 |
DDB_G0283511 | DDB_G0283511 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells and in upper and lower cups during culmination | DDB0232431 | CDS | 669589 | 174 | + | 0.344828 |
DDB_G0283513 | DDB_G0283513 | belongs to a family of small highly conserved genes unique to Dictyostelium discoideum | DDB0232431 | CDS | 670441 | 174 | + | 0.333333 |
DDB_G0283515 | DDB_G0283515 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 671329 | 174 | + | 0.33908 |
DDB_G0283517 | DDB_G0283517 | DDB0232431 | CDS | 672171 | 174 | + | 0.316092 | |
DDB_G0283519 | DDB_G0283519 | DDB0232431 | CDS | 673055 | 174 | + | 0.356322 | |
DDB_G0283521 | DDB_G0283521 | DDB0232431 | CDS | 678402 | 3705 | - | 0.215385 | |
DDB_G0283523 | DDB_G0283523 | DDB0232431 | CDS | 701281 | 375 | + | 0.226667 | |
DDB_G0283527 | DDB_G0283527 | DDB0232431 | CDS | 732951 | 174 | - | 0.189655 | |
DDB_G0283529 | DDB_G0283529 | DDB0232431 | CDS | 760908 | 2349 | - | 0.180077 | |
DDB_G0283531 | DDB_G0283531 | DDB0232431 | CDS | 766653 | 822 | + | 0.304136 | |
DDB_G0283535 | DDB_G0283535 | similar to H. sapiens DMXL1 and DMXL2 and D. melanogaster DmX REMI mutant fails to aggregate see | DDB0232431 | CDS | 837650 | 8379 | - | 0.297291 |
DDB_G0283545 | DDB_G0283545 | DDB0232431 | CDS | 794803 | 2850 | + | 0.309474 | |
DDB_G0283549 | DDB_G0283549 | contains one C2 domain which is is a Ca2-dependent membrane-targeting module found in many cellular proteins involved in signal transduction or membrane trafficking | DDB0232431 | CDS | 803052 | 417 | + | 0.309353 |
DDB_G0283551 | DDB_G0283551 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity highly similar to neighboring gene | DDB0232431 | CDS | 810010 | 3975 | - | 0.255597 |
DDB_G0283553 | DDB_G0283553 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity highly similar to neighboring gene | DDB0232431 | CDS | 815506 | 4545 | - | 0.252805 |
DDB_G0283555 | DDB_G0283555 | contains Dictyostelium spore coat protein N-terminal domain and 7 follistatin-like domains similar to spore coat proteins CotA CotB and CotD expressed in prespore cells | DDB0232431 | CDS | 824798 | 1398 | - | 0.375536 |
DDB_G0283557 | DDB_G0283557 | DDB0232431 | CDS | 827565 | 1848 | + | 0.278139 | |
DDB_G0283559 | DDB_G0283559 | DDB0232431 | CDS | 830931 | 198 | - | 0.328283 | |
DDB_G0283561 | DDB_G0283561 | DDB0232431 | CDS | 831598 | 213 | + | 0.253521 | |
DDB_G0283565 | DDB_G0283565 | DDB0232431 | CDS | 833347 | 3024 | - | 0.305886 | |
DDB_G0283567 | DDB_G0283567 | DDB0232431 | CDS | 836774 | 270 | + | 0.292593 | |
DDB_G0283571 | DDB_G0283571 | DDB0232431 | CDS | 851425 | 318 | - | 0.27673 | |
DDB_G0283573 | DDB_G0283573 | DDB0232431 | CDS | 854108 | 231 | + | 0.363636 | |
DDB_G0283575 | DDB_G0283575 | catalyzes the reaction RX glutathione HX R-S-glutathione enriched in prespore cells | DDB0232431 | CDS | 855359 | 597 | + | 0.303183 |
DDB_G0283577 | DDB_G0283577 | DDB0232431 | CDS | 856410 | 3153 | - | 0.235014 | |
DDB_G0283585 | DDB_G0283585 | DDB0232431 | CDS | 785263 | 4275 | + | 0.340585 | |
DDB_G0283591 | DDB_G0283591 | DDB0232431 | CDS | 783267 | 747 | + | 0.239625 | |
DDB_G0283593 | DDB_G0283593 | DDB0232431 | CDS | 800982 | 1131 | - | 0.218391 | |
DDB_G0283595 | DDB_G0283595 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232431 | CDS | 805455 | 3873 | - | 0.251743 |
DDB_G0283623 | DDB_G0283623 | DDB0232431 | CDS | 873651 | 2988 | + | 0.251339 | |
DDB_G0283625 | DDB_G0283625 | contains a Mob1 motif however it does not cluster with Mob1 proteins | DDB0232431 | CDS | 882607 | 654 | + | 0.310398 |
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_G0283633 | DDB_G0283633 | DDB0232431 | CDS | 889575 | 1416 | - | 0.242232 | |
DDB_G0283639 | DDB_G0283639 | DDB0232431 | CDS | 895310 | 129 | + | 0.286822 | |
DDB_G0283643 | DDB_G0283643 | DDB0232431 | CDS | 896653 | 138 | + | 0.355072 | |
DDB_G0283645 | DDB_G0283645 | very similar to Dictyostelium cbpF cbpG and cbpC contains two EF-hands | DDB0232431 | CDS | 897818 | 516 | - | 0.302326 |
DDB_G0283647 | DDB_G0283647 | DDB0232431 | CDS | 907070 | 228 | - | 0.302632 | |
DDB_G0283649 | DDB_G0283649 | similar to the S. cerevisiae LOT6 a FMN-dependent NAD(P)H:quinone reductase that may be involved in quinone detoxification | DDB0232431 | CDS | 910617 | 600 | - | 0.301667 |
DDB_G0283651 | DDB_G0283651 | tyrosinases are copper monooxygenases that catalyzes the hydroxylation of monophenols and the oxidation of o-diphenols to o-quinols binds two copper ions by 3 conserved His residues there is an almost identical | DDB0232431 | CDS | 918296 | 2451 | - | 0.304774 |
DDB_G0283653 | DDB_G0283653 | tyrosinases are copper monooxygenases that catalyzes the hydroxylation of monophenols and the oxidation of o-diphenols to o-quinols binds two copper ions by 3 conserved His residues there is an almost identical | DDB0232431 | CDS | 921967 | 2463 | - | 0.310597 |
DDB_G0283655 | DDB_G0283655 | DDB0232431 | CDS | 925419 | 1524 | - | 0.224409 | |
DDB_G0283659_ps | DDB_G0283659 | putative pseudogene fragment similar to D. discoideum patatin gene family including | DDB0232431 | CDS | 938852 | 165 | - | 0.248485 |
DDB_G0283665_ps | DDB_G0283665 | putative pseudogene similar to Dictyostelium calcium binding proteins | DDB0232431 | CDS | 945236 | 228 | + | 0.285088 |
DDB_G0283667 | DDB_G0283667 | DDB0232431 | CDS | 946222 | 2400 | + | 0.212917 | |
DDB_G0283669 | DDB_G0283669 | conserved ubiquinol-cytochrome c oxidoreductase subunit a component of the mitochondrial inner membrane electron transport chain | DDB0232431 | CDS | 953002 | 201 | + | 0.368159 |
DDB_G0283675 | DDB_G0283675 | DDB0232431 | CDS | 961972 | 1179 | - | 0.296014 | |
DDB_G0283677 | DDB_G0283677 | DDB0232431 | CDS | 963963 | 882 | + | 0.217687 | |
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_G0283683 | DDB_G0283683 | DDB0232431 | CDS | 978468 | 1566 | - | 0.225415 | |
DDB_G0283687 | DDB_G0283687 | similar to CC1-like splicing factors characterized by an N-terminal arginine-rich low complexity domain followed by three RNA recognition domains similar to human RBM23 and RBM39 | DDB0232431 | CDS | 982205 | 2184 | + | 0.330586 |
DDB_G0283689 | DDB_G0283689 | DDB0232431 | CDS | 985671 | 543 | - | 0.28361 | |
DDB_G0283691 | DDB_G0283691 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D contains a predicted signal peptide | DDB0232431 | CDS | 986987 | 1278 | + | 0.261346 |
DDB_G0283693 | DDB_G0283693 | DDB0232431 | CDS | 990291 | 189 | + | 0.354497 | |
DDB_G0283695 | DDB_G0283695 | DDB0232431 | CDS | 990708 | 1047 | - | 0.221585 | |
DDB_G0283697 | DDB_G0283697 | DDB0232431 | CDS | 992255 | 2562 | + | 0.276347 | |
DDB_G0283703 | DDB_G0283703 | DDB0232431 | CDS | 1003190 | 282 | - | 0.287234 | |
DDB_G0283705 | DDB_G0283705 | DDB0232431 | CDS | 1004930 | 177 | + | 0.338983 | |
DDB_G0283707 | DDB_G0283707 | conserved protein in ciliates and plants contains 9 predicted transmembrane domains including one signal peptide there is an almost identical D. discoideum protein | DDB0232431 | CDS | 1005690 | 1524 | - | 0.377297 |
DDB_G0283711 | DDB_G0283711 | highly similar to other hssA2C7E family proteins | DDB0232431 | CDS | 1011158 | 258 | - | 0.325581 |
DDB_G0283713 | DDB_G0283713 | DDB0232431 | CDS | 1012257 | 261 | + | 0.329502 | |
DDB_G0283715 | DDB_G0283715 | DDB0232431 | CDS | 1012994 | 3216 | - | 0.294154 | |
DDB_G0283719 | DDB_G0283719 | DDB0232431 | CDS | 1023936 | 3963 | - | 0.217007 | |
DDB_G0283721 | DDB_G0283721 | almost identical to the upstream gene | DDB0232431 | CDS | 1029584 | 2190 | + | 0.245205 |
DDB_G0283723 | DDB_G0283723 | almost identical to the downstream gene | DDB0232431 | CDS | 1033128 | 2190 | + | 0.246119 |
DDB_G0283725_ps | DDB_G0283725 | putative pseudogene very similar to pyridoxal phosphate-dependent decarboxylase family genes | DDB0232431 | CDS | 1035645 | 1155 | + | 0.273593 |
DDB_G0283727 | DDB_G0283727 | DDB0232431 | CDS | 1038776 | 756 | + | 0.376984 | |
DDB_G0283729 | DDB_G0283729 | DDB0232431 | CDS | 1039785 | 1530 | - | 0.168627 | |
DDB_G0283731 | DDB_G0283731 | similar to D. purpureum protein contains a histidine rich region | DDB0232431 | CDS | 1041764 | 621 | - | 0.349436 |
DDB_G0283733 | DDB_G0283733 | DDB0232431 | CDS | 1042995 | 1137 | + | 0.278804 | |
DDB_G0283743 | DDB_G0283743 | DDB0232431 | CDS | 934848 | 2514 | + | 0.211615 | |
DDB_G0283745 | DDB_G0283745 | similar to transportin 3 which in human seems to function in nuclear protein import as nuclear transport receptor | DDB0232431 | CDS | 877706 | 2946 | - | 0.243381 |
DDB_G0283747 | DDB_G0283747 | DDB0232431 | CDS | 915081 | 2745 | + | 0.167577 | |
DDB_G0283749 | DDB_G0283749 | DDB0232431 | CDS | 929556 | 4416 | + | 0.217618 | |
DDB_G0283753 | DDB_G0283753 | DDB0232431 | CDS | 1050017 | 1668 | - | 0.285372 | |
DDB_G0283759 | DDB_G0283759 | DDB0232431 | CDS | 1232305 | 3240 | + | 0.274383 | |
DDB_G0283771 | DDB_G0283771 | bCommunity annotation: bDDB_G0283771 shows weak similarities to several kinesin family proteins. The gene is overexpressed sixfold in a Dictyostelium | DDB0232431 | CDS | 1079549 | 2142 | + | 0.280112 |
DDB_G0283773 | DDB_G0283773 | putative GTPase very conserved in protozoa and fungi | DDB0232431 | CDS | 1081883 | 1305 | - | 0.288123 |
DDB_G0283775 | DDB_G0283775 | DDB0232431 | CDS | 1083586 | 3657 | + | 0.178562 | |
DDB_G0283777 | DDB_G0283777 | DDB0232431 | CDS | 1087508 | 249 | - | 0.305221 | |
DDB_G0283781 | DDB_G0283781 | DDB0232431 | CDS | 1089062 | 1107 | + | 0.241192 | |
DDB_G0283783 | DDB_G0283783 | DDB0232431 | CDS | 1091245 | 450 | + | 0.326667 | |
DDB_G0283785 | DDB_G0283785 | contains 2 EGF-like domains a predicted signal sequence and one N-terminal transmembrane domain very similar to it's upstream and downstream neighbors | DDB0232431 | CDS | 1099059 | 3138 | + | 0.271192 |
DDB_G0283787 | DDB_G0283787 | contains 2 EGF-like domains a predicted signal sequence and one N-terminal transmembrane domain very similar to it's two upstream neighbors | DDB0232431 | CDS | 1103072 | 3195 | + | 0.281377 |
DDB_G0283791 | DDB_G0283791 | DDB0232431 | CDS | 1109469 | 1320 | - | 0.238636 | |
DDB_G0283793 | DDB_G0283793 | DDB0232431 | CDS | 1114386 | 2136 | - | 0.305243 | |
DDB_G0283797 | DDB_G0283797 | DDB0232431 | CDS | 1118346 | 1470 | - | 0.267347 | |
DDB_G0283799 | DDB_G0283799 | DDB0232431 | CDS | 1120333 | 1098 | - | 0.211293 | |
DDB_G0283803 | DDB_G0283803 | DDB0232431 | CDS | 1122911 | 582 | + | 0.298969 | |
DDB_G0283807 | DDB_G0283807 | DDB0232431 | CDS | 1128255 | 444 | + | 0.207207 | |
DDB_G0283815 | DDB_G0283815 | DDB0232431 | CDS | 1148242 | 1332 | - | 0.231982 | |
DDB_G0283817 | DDB_G0283817 | DDB0232431 | CDS | 1149949 | 882 | + | 0.314059 | |
DDB_G0283819 | DDB_G0283819 | DDB0232431 | CDS | 1153703 | 1524 | + | 0.349081 | |
DDB_G0283821 | DDB_G0283821 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis | DDB0232431 | CDS | 1155677 | 2826 | - | 0.295824 |
DDB_G0283823 | DDB_G0283823 | DDB0232431 | CDS | 1177277 | 600 | + | 0.273333 | |
DDB_G0283825 | DDB_G0283825 | DDB0232431 | CDS | 1178221 | 1056 | - | 0.24053 | |
DDB_G0283827 | DDB_G0283827 | DDB0232431 | CDS | 1180565 | 2718 | + | 0.307947 | |
DDB_G0283829 | DDB_G0283829 | similar to human ODR4 (odorant response abnormal protein 4) contains one putative transmembrane domain | DDB0232431 | CDS | 1183400 | 1371 | - | 0.190372 |
DDB_G0283831 | DDB_G0283831 | DDB0232431 | CDS | 1185329 | 771 | - | 0.276265 | |
DDB_G0283833 | DDB_G0283833 | DDB0232431 | CDS | 1187328 | 2856 | - | 0.238095 | |
DDB_G0283837 | DDB_G0283837 | proteins containing the actin depolymerisation factor (ADF)cofilin-like domain sever actin filaments and bind to actin monomers | DDB0232431 | CDS | 1195917 | 1860 | + | 0.22957 |
DDB_G0283843 | DDB_G0283843 | DDB0232431 | CDS | 1223477 | 531 | - | 0.306968 | |
DDB_G0283845 | DDB_G0283845 | DDB0232431 | CDS | 1227055 | 540 | + | 0.312963 | |
DDB_G0283847 | DDB_G0283847 | catalyzes the reaction: S-adenosyl-L-methionine phospholipid olefinic fatty acid S-adenosyl-L-homocysteine phospholipid cyclopropane fatty acid underexpressed in | DDB0232431 | CDS | 1228686 | 1293 | + | 0.254447 |
DDB_G0283849 | DDB_G0283849 | DDB0232431 | CDS | 1239874 | 552 | - | 0.282609 | |
DDB_G0283851 | DDB_G0283851 | DDB0232431 | CDS | 1253142 | 750 | - | 0.284 | |
DDB_G0283855 | DDB_G0283855 | DDB0232431 | CDS | 1060450 | 1644 | + | 0.242092 | |
DDB_G0283859 | DDB_G0283859 | DDB0232431 | CDS | 1066871 | 5037 | + | 0.289458 | |
DDB_G0283861 | DDB_G0283861 | DDB0232431 | CDS | 1072483 | 564 | + | 0.289007 | |
DDB_G0283863 | DDB_G0283863 | DDB0232431 | CDS | 1074074 | 1854 | - | 0.244337 | |
DDB_G0283869 | DDB_G0283869 | contains 3 EGF-like domains a predicted signal sequence and one N-terminal transmembrane domain very similar to it's two downstream neighbors | DDB0232431 | CDS | 1094707 | 3405 | + | 0.269016 |
DDB_G0283871 | DDB_G0283871 | DDB0232431 | CDS | 1126533 | 774 | + | 0.289406 | |
DDB_G0283879 | DDB_G0283879 | DDB0232431 | CDS | 1142351 | 591 | - | 0.184433 | |
DDB_G0283885 | DDB_G0283885 | member of a gene family comprising | DDB0232431 | CDS | 1166070 | 1587 | - | 0.21235 |
DDB_G0283887 | DDB_G0283887 | member of a gene family comprising | DDB0232431 | CDS | 1170844 | 1488 | - | 0.217742 |
DDB_G0283889 | DDB_G0283889 | DDB0232431 | CDS | 1174977 | 447 | - | 0.322148 | |
DDB_G0283893 | DDB_G0283893 | DDB0232431 | CDS | 1204398 | 17628 | - | 0.301849 | |
DDB_G0283897 | DDB_G0283897 | DDB0232431 | CDS | 1243225 | 2808 | + | 0.162037 | |
DDB_G0283901 | DDB_G0283901 | DDB0232431 | CDS | 1254332 | 1542 | - | 0.279507 | |
DDB_G0283911 | DDB_G0283911 | highly similar to neighboring gene | DDB0232431 | CDS | 1265347 | 1779 | - | 0.261383 |
DDB_G0283913 | DDB_G0283913 | large molecular weight protein that contains a hsp20 domain highly similar to neighboring gene | DDB0232431 | CDS | 1267681 | 2004 | - | 0.268962 |
DDB_G0283915 | DDB_G0283915 | DDB0232431 | CDS | 1270973 | 702 | + | 0.337607 | |
DDB_G0283919 | DDB_G0283919 | the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232431 | CDS | 1275553 | 3243 | + | 0.30589 |
DDB_G0283923 | DDB_G0283923 | DDB0232431 | CDS | 1301821 | 4350 | - | 0.223448 | |
DDB_G0283925 | DDB_G0283925 | DDB0232431 | CDS | 1306681 | 465 | - | 0.324731 | |
DDB_G0283927 | DDB_G0283927 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232431 | CDS | 1307685 | 1458 | - | 0.226337 |
DDB_G0283935 | DDB_G0283935 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232431 | CDS | 1333704 | 942 | + | 0.284501 |
DDB_G0283939 | DDB_G0283939 | DDB0232431 | CDS | 1338263 | 3156 | + | 0.290875 | |
DDB_G0283941 | DDB_G0283941 | DDB0232431 | CDS | 1341707 | 309 | - | 0.2589 | |
DDB_G0283943 | DDB_G0283943 | catalyzes the reaction aldehyde NADsupsup Hsub2subO an acid NADH Hsupsup | DDB0232431 | CDS | 1342529 | 1488 | - | 0.316532 |
DDB_G0283945 | DDB_G0283945 | DDB0232431 | CDS | 1345149 | 3078 | + | 0.196556 | |
DDB_G0283947 | DDB_G0283947 | DDB0232431 | CDS | 1349351 | 1101 | + | 0.297003 | |
DDB_G0283949 | DDB_G0283949 | DDB0232431 | CDS | 1350512 | 1398 | - | 0.268956 | |
DDB_G0283951 | DDB_G0283951 | contains a predicted signal peptide catalyzes the reaction sn-glycerol 3-phosphate a quinone glycerone phosphate a quinol | DDB0232431 | CDS | 1352908 | 1917 | + | 0.308816 |
DDB_G0283959 | DDB_G0283959 | DDB0232431 | CDS | 1374141 | 837 | + | 0.27957 | |
DDB_G0283961 | DDB_G0283961 | DDB0232431 | CDS | 1375647 | 813 | + | 0.281673 | |
DDB_G0283967 | DDB_G0283967 | DDB0232431 | CDS | 1387840 | 4905 | + | 0.198165 | |
DDB_G0283971 | DDB_G0283971 | contains an N-terminal ubiquitin domain very similar to D. purpureum protein | DDB0232431 | CDS | 1401996 | 2565 | - | 0.329045 |
DDB_G0283973 | DDB_G0283973 | DDB0232431 | CDS | 1405614 | 2154 | + | 0.32637 | |
DDB_G0283975 | DDB_G0283975 | DDB0232431 | CDS | 1408395 | 834 | + | 0.317746 | |
DDB_G0283977 | DDB_G0283977 | DDB0232431 | CDS | 1409294 | 2622 | - | 0.217391 | |
DDB_G0283979 | DDB_G0283979 | DDB0232431 | CDS | 1413537 | 3600 | + | 0.265833 | |
DDB_G0283985 | DDB_G0283985 | DDB0232431 | CDS | 1263489 | 1608 | + | 0.250622 | |
DDB_G0283989 | DDB_G0283989 | one of three paralogs in Dictyostelium (other genes: | DDB0232431 | CDS | 1284281 | 2694 | + | 0.311804 |
DDB_G0283991 | DDB_G0283991 | DDB0232431 | CDS | 1287653 | 1092 | + | 0.308608 | |
DDB_G0283993 | DDB_G0283993 | DDB0232431 | CDS | 1289307 | 3054 | + | 0.270138 | |
DDB_G0283995 | DDB_G0283995 | DDB0232431 | CDS | 1293218 | 2958 | + | 0.260649 | |
DDB_G0283997_ps | DDB_G0283997 | putative pseudogene similar to a family of D. discoideum protein family of unknown function including | DDB0232431 | CDS | 1298443 | 2412 | + | 0.238391 |
DDB_G0283999 | DDB_G0283999 | DDB0232431 | CDS | 1309513 | 1815 | - | 0.284848 | |
DDB_G0284005 | DDB_G0284005 | DDB0232431 | CDS | 1397618 | 285 | - | 0.280702 | |
DDB_G0284007 | DDB_G0284007 | DDB0232431 | CDS | 1398686 | 1059 | - | 0.240793 | |
DDB_G0284011 | DDB_G0284011 | DDB0232431 | CDS | 1429547 | 933 | - | 0.274384 | |
DDB_G0284015 | DDB_G0284015 | DDB0232431 | CDS | 1433731 | 2283 | - | 0.29873 | |
DDB_G0284019 | DDB_G0284019 | DDB0232431 | CDS | 1444241 | 2202 | - | 0.31653 | |
DDB_G0284021 | DDB_G0284021 | DDB0232431 | CDS | 1447496 | 573 | - | 0.280977 | |
DDB_G0284025 | DDB_G0284025 | DDB0232431 | CDS | 1440123 | 2226 | - | 0.269542 | |
DDB_G0284031 | DDB_G0284031 | DDB0232431 | CDS | 1458434 | 846 | + | 0.180851 | |
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_G0284049 | DDB_G0284049 | DDB0232431 | CDS | 1467489 | 3561 | + | 0.243471 | |
DDB_G0284051 | DDB_G0284051 | DDB0232431 | CDS | 1471982 | 1527 | + | 0.333333 | |
DDB_G0284053 | DDB_G0284053 | DDB0232431 | CDS | 1473938 | 714 | + | 0.268908 | |
DDB_G0284055 | DDB_G0284055 | DDB0232431 | CDS | 1474815 | 1335 | - | 0.270412 | |
DDB_G0284057 | DDB_G0284057 | DDB0232431 | CDS | 1478033 | 372 | + | 0.233871 | |
DDB_G0284059 | DDB_G0284059 | DDB0232431 | CDS | 1478818 | 3843 | + | 0.287536 | |
DDB_G0284061 | DDB_G0284061 | DDB0232431 | CDS | 1483793 | 846 | + | 0.241135 | |
DDB_G0284063 | DDB_G0284063 | DDB0232431 | CDS | 1485717 | 825 | + | 0.197576 | |
DDB_G0284069 | DDB_G0284069 | DDB0232431 | CDS | 1498595 | 1281 | - | 0.250585 | |
DDB_G0284073 | DDB_G0284073 | similar to Dictystelium cell surface glycoproteins gp130 and GP138A B C and D | DDB0232431 | CDS | 1506777 | 2643 | + | 0.23496 |
DDB_G0284077 | DDB_G0284077 | DDB0232431 | CDS | 1530962 | 1272 | + | 0.251572 | |
DDB_G0284079 | DDB_G0284079 | contains two ankyrin repeats and an RA domain which plays a role in RasGTP activation in mammals and mating in yeast highly similar to | DDB0232431 | CDS | 1538387 | 912 | + | 0.291667 |
DDB_G0284083 | DDB_G0284083 | DDB0232431 | CDS | 1548205 | 999 | + | 0.209209 | |
DDB_G0284085 | DDB_G0284085 | DDB0232431 | CDS | 1549462 | 1098 | + | 0.175774 | |
DDB_G0284087 | DDB_G0284087 | DDB0232431 | CDS | 1550807 | 3366 | + | 0.229352 | |
DDB_G0284091 | DDB_G0284091 | DDB0232431 | CDS | 1556685 | 723 | - | 0.337483 | |
DDB_G0284095 | DDB_G0284095 | DDB0232431 | CDS | 1559578 | 798 | - | 0.218045 | |
DDB_G0284097 | DDB_G0284097 | DDB0232431 | CDS | 1565830 | 1902 | - | 0.358044 | |
DDB_G0284099 | DDB_G0284099 | DDB0232431 | CDS | 1569018 | 1476 | - | 0.249322 | |
DDB_G0284105 | DDB_G0284105 | DDB0232431 | CDS | 1580531 | 1560 | - | 0.25641 | |
DDB_G0284109 | DDB_G0284109 | DDB0232431 | CDS | 1599639 | 375 | + | 0.293333 | |
DDB_G0284111 | DDB_G0284111 | DDB0232431 | CDS | 1601233 | 375 | + | 0.274667 | |
DDB_G0284115 | DDB_G0284115 | DDB0232431 | CDS | 1607949 | 423 | + | 0.276596 | |
DDB_G0284119 | DDB_G0284119 | contains 3 predicted transmembrane domains and an additional putative signal sequence member of a larger gene family in D. discoideum also present in other dictyostelids | DDB0232431 | CDS | 1614014 | 690 | - | 0.27971 |
DDB_G0284121 | DDB_G0284121 | DDB0232431 | CDS | 1615547 | 945 | - | 0.279365 | |
DDB_G0284125 | DDB_G0284125 | DDB0232431 | CDS | 1617796 | 1131 | - | 0.27763 | |
DDB_G0284127 | DDB_G0284127 | DDB0232431 | CDS | 1619168 | 1389 | + | 0.2455 | |
DDB_G0284131 | DDB_G0284131 | DDB0232431 | CDS | 1625572 | 1989 | + | 0.157366 | |
DDB_G0284133 | DDB_G0284133 | similar to P. pallidum protein weak similarity to PB1 domain in amino terminal region | DDB0232431 | CDS | 1629570 | 3153 | + | 0.290517 |
DDB_G0284135 | DDB_G0284135 | DDB0232431 | CDS | 1634829 | 2763 | + | 0.312704 | |
DDB_G0284137 | DDB_G0284137 | DDB0232431 | CDS | 1638105 | 1461 | - | 0.186858 | |
DDB_G0284139 | DDB_G0284139 | DDB0232431 | CDS | 1640056 | 1743 | - | 0.255307 | |
DDB_G0284143 | DDB_G0284143 | DDB0232431 | CDS | 1490360 | 384 | + | 0.255208 | |
DDB_G0284145 | DDB_G0284145 | DDB0232431 | CDS | 1523365 | 1317 | - | 0.2612 | |
DDB_G0284147 | DDB_G0284147 | DDB0232431 | CDS | 1532512 | 948 | - | 0.186709 | |
DDB_G0284149 | DDB_G0284149 | ortholog of yeast VID24 a peripheral membrane protein located at Vid (vacuole import and degradation) vesicles | DDB0232431 | CDS | 1533705 | 699 | - | 0.296137 |
DDB_G0284151 | DDB_G0284151 | DDB0232431 | CDS | 1536747 | 969 | + | 0.209494 | |
DDB_G0284153 | DDB_G0284153 | DDB0232431 | CDS | 1545923 | 1800 | - | 0.239444 | |
DDB_G0284155 | DDB_G0284155 | contains two PLDc domains has similarity to mammalian phospholipase D2 | DDB0232431 | CDS | 1561847 | 3390 | + | 0.270796 |
DDB_G0284157 | DDB_G0284157 | DDB0232431 | CDS | 1583322 | 3426 | + | 0.28955 | |
DDB_G0284161 | DDB_G0284161 | DDB0232431 | CDS | 1597279 | 312 | + | 0.275641 | |
DDB_G0284163 | DDB_G0284163 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon but the second exon is shorter | DDB0232431 | CDS | 1598186 | 192 | + | 0.322917 |
DDB_G0284165 | DDB_G0284165 | DDB0232431 | CDS | 1606151 | 186 | - | 0.263441 | |
DDB_G0284167 | DDB_G0284167 | DDB0232431 | CDS | 1610129 | 882 | - | 0.422902 | |
DDB_G0284169 | DDB_G0284169 | contains 3 predicted transmembrane domains and an additional putative signal sequence part of a larger gene family in D. discoideum also present in other dictyostelids | DDB0232431 | CDS | 1612603 | 621 | - | 0.322061 |
DDB_G0284173 | DDB_G0284173 | DDB0232431 | CDS | 1652572 | 786 | - | 0.198473 | |
DDB_G0284175 | DDB_G0284175 | similar to S. pombe mus81 in the 3' region also contains DNA polymerase B-like domain SAM domain and SWIM-type zinc finger domains | DDB0232431 | CDS | 1653717 | 2766 | + | 0.240781 |
DDB_G0284177 | DDB_G0284177 | DDB0232431 | CDS | 1658818 | 3171 | + | 0.268054 | |
DDB_G0284179 | DDB_G0284179 | DDB0232431 | CDS | 1643184 | 2079 | - | 0.132275 | |
DDB_G0284189 | DDB_G0284189 | DDB0232431 | CDS | 1669261 | 1044 | + | 0.288314 | |
DDB_G0284191 | DDB_G0284191 | DDB0232431 | CDS | 1670895 | 2205 | + | 0.307483 | |
DDB_G0284193 | DDB_G0284193 | DDB0232431 | CDS | 1673200 | 969 | + | 0.307534 | |
DDB_G0284195 | DDB_G0284195 | bCommunity annotation:b DDB_G0284195 is highly similar in the upstream half to cofactor of BRAC1 also known as COBRA1 which in mammals participates in a four-protein complex called NELF (negative elongation factor). NELF negatively regulates steroid-hormone induced gene regulation. Candidates for other components of the NELF complex are found in Dicty DDB_G0268678 is a clear NELF CD subunit DDB_G0286295 is a possible NELF A subunit DDB_G0276985 is a possible NELF RDBP subunit. Recent work shows that NELF participates in 3' end processing of histone mRNAs in association with the SLBP see Narita et al Mol. Cell 26 349-365 (2007).br DDB G0284195 is strongly (12-fold)overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (Doquang et al in preparation). Most genes with known roles in S-phase or mitosis are overexpressed in this strain. Several other proteins involved in histone mRNA processing are upregulated in the rblA disruptant these include DDB_G0 | DDB0232431 | CDS | 1676837 | 2565 | - | 0.283431 |
DDB_G0284199 | DDB_G0284199 | contains a predicted signal sequence similar to D. purpureum protein | DDB0232431 | CDS | 1682534 | 669 | - | 0.240658 |
DDB_G0284201 | DDB_G0284201 | very similar to RNA polymerase II transcription factor SIII subunit C elongin C or transcription elongation factor B polypeptide 1 (TCEB1) | DDB0232431 | CDS | 1684869 | 330 | + | 0.269697 |
DDB_G0284207 | DDB_G0284207 | DDB0232431 | CDS | 1688943 | 858 | + | 0.284382 | |
DDB_G0284209 | DDB_G0284209 | DDB0232431 | CDS | 1690478 | 876 | - | 0.280822 | |
DDB_G0284211_ps | DDB_G0284211 | putative pseudogene belonging to the short-chain dehydrogenasereductase (SDR) familybrbr bCommunity annotation:b probably a recent pseudogene of the short-chain dehydrogenase family including DDB0185894. The coding sequence share high level of homology with DDB0185894 before and after the stop codon resulting in a truncated and probably non functional protein if that gene is still transcribed. Christophe Anjard May 2007 | DDB0232431 | CDS | 1692886 | 738 | + | 0.298103 |
DDB_G0284213 | DDB_G0284213 | DDB0232431 | CDS | 1693957 | 2109 | - | 0.209578 | |
DDB_G0284217 | DDB_G0284217 | similar to H. sapiens CNOT7 and CNOT8 and S. cerevisiae POP2 which are components of the CCR4-NOT transcription complex | DDB0232431 | CDS | 1700271 | 1104 | - | 0.288043 |
DDB_G0284219 | DDB_G0284219 | member of the MAP65ASE1 family of microtubule associated proteins one of the the yeast homologs is an anaphase spindle elongation protein | DDB0232431 | CDS | 1702610 | 2298 | - | 0.222802 |
DDB_G0284223 | DDB_G0284223 | DDB0232431 | CDS | 1712491 | 1641 | - | 0.322364 | |
DDB_G0284227 | DDB_G0284227 | DDB0232431 | CDS | 1717119 | 4158 | + | 0.246513 | |
DDB_G0284229 | DDB_G0284229 | DDB0232431 | CDS | 1721453 | 222 | - | 0.297297 | |
DDB_G0284231 | DDB_G0284231 | DDB0232431 | CDS | 1721739 | 237 | - | 0.333333 | |
DDB_G0284233 | DDB_G0284233 | DDB0232431 | CDS | 1723068 | 186 | + | 0.333333 | |
DDB_G0284235 | DDB_G0284235 | DDB0232431 | CDS | 1723675 | 1296 | - | 0.206019 | |
DDB_G0284239 | DDB_G0284239 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 1731488 | 2031 | + | 0.356475 |
DDB_G0284241 | DDB_G0284241 | DDB0232431 | CDS | 1733961 | 1293 | + | 0.243619 | |
DDB_G0284243 | DDB_G0284243 | similar to yeast PTC1 type 2C protein phosphatase (PP2C) which is involved in mitochondrial inheritance tRNA splicing sporulation and cell separation | DDB0232431 | CDS | 1735866 | 1212 | - | 0.329208 |
DDB_G0284245 | DDB_G0284245 | contains a single N-terminal RRM domain which is similar to those in human splicing factors arginineserine-rich such as SFRS4 and SFRS6 however these proteins contain two N-terminal RRM domains | DDB0232431 | CDS | 1747466 | 1098 | - | 0.301457 |
DDB_G0284247 | DDB_G0284247 | DDB0232431 | CDS | 1749570 | 1854 | + | 0.228695 | |
DDB_G0284249 | DDB_G0284249 | putative metalloprotease of the peptidase M41 family which belong to a larger family of zinc metalloproteases includes the cell division protein FtsH and the yeast mitochondrial respiratory chain complexes assembly protein | DDB0232431 | CDS | 1751734 | 2295 | - | 0.31329 |
DDB_G0284251 | DDB_G0284251 | kinase domain similar to those of mitogen-activated protein kinases similar to the STE20 family | DDB0232431 | CDS | 1754346 | 1491 | - | 0.273642 |
DDB_G0284253 | DDB_G0284253 | similar to human EI24 (etoposide-induced protein 2.4 homolog) which may play a role in the cellular response to DNA damage andor p53-mediated apoptosis contains 6 putative transmembrane domains | DDB0232431 | CDS | 1758153 | 924 | - | 0.267316 |
DDB_G0284255 | DDB_G0284255 | DDB0232431 | CDS | 1777902 | 2874 | + | 0.292276 | |
DDB_G0284259 | DDB_G0284259 | DDB0232431 | CDS | 1787150 | 2724 | - | 0.335536 | |
DDB_G0284263 | DDB_G0284263 | conserved protein ortholog of human DNAJC11 | DDB0232431 | CDS | 1795281 | 1728 | - | 0.284144 |
DDB_G0284269 | DDB_G0284269 | DDB0232431 | CDS | 1803929 | 411 | + | 0.255474 | |
DDB_G0284271_ps | DDB_G0284271 | putative pseudogene fragment similar to EGF repeat-containing proteins | DDB0232431 | CDS | 1804849 | 915 | + | 0.257923 |
DDB_G0284273 | DDB_G0284273 | DDB0232431 | CDS | 1806777 | 1449 | + | 0.244997 | |
DDB_G0284275 | DDB_G0284275 | DDB0232431 | CDS | 1820423 | 1065 | + | 0.246948 | |
DDB_G0284277 | DDB_G0284277 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232431 | CDS | 1821556 | 870 | - | 0.314943 |
DDB_G0284279_ps | DDB_G0284279 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 1822941 | 3207 | - | 0.225444 |
DDB_G0284281 | DDB_G0284281 | DDB0232431 | CDS | 1827185 | 2940 | - | 0.25102 | |
DDB_G0284283 | DDB_G0284283 | DDB0232431 | CDS | 1832487 | 186 | + | 0.274194 | |
DDB_G0284285 | DDB_G0284285 | DDB0232431 | CDS | 1833130 | 396 | + | 0.282828 | |
DDB_G0284287 | DDB_G0284287 | DDB0232431 | CDS | 1834114 | 456 | - | 0.285088 | |
DDB_G0284289 | DDB_G0284289 | DDB0232431 | CDS | 1835474 | 2166 | - | 0.262696 | |
DDB_G0284303 | DDB_G0284303 | DDB0232431 | CDS | 1792427 | 423 | + | 0.248227 | |
DDB_G0284305_RTE | DDB_G0284305 | 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 | 1664505 | 1593 | + | 0.345888 |
DDB_G0284307 | DDB_G0284307 | conserved ortholog mammalian CAB39 (calcium-binding protein 39) and S. pombe Mo25 involved in cytokinesis | DDB0232431 | CDS | 1707062 | 1092 | + | 0.270147 |
DDB_G0284311 | DDB_G0284311 | DDB0232431 | CDS | 1711370 | 900 | + | 0.257778 | |
DDB_G0284315 | DDB_G0284315 | contains 6 putative transmembrane domains similar to D. purpureum protein | DDB0232431 | CDS | 1728697 | 930 | + | 0.329032 |
DDB_G0284321 | DDB_G0284321 | similar to PTBP1 PTB2 and ROD1 heterogeneous ribonucleoproteins that play a role in pre-mRNA splicing | DDB0232431 | CDS | 1760065 | 2679 | + | 0.267264 |
DDB_G0284325 | DDB_G0284325 | DDB0232431 | CDS | 1809449 | 2103 | + | 0.257252 | |
DDB_G0284337 | DDB_G0284337 | DDB0232431 | CDS | 1851676 | 3819 | + | 0.252946 | |
DDB_G0284343 | DDB_G0284343 | DDB0232431 | CDS | 1860277 | 1104 | - | 0.246377 | |
DDB_G0284351 | DDB_G0284351 | DDB0232431 | CDS | 1869385 | 735 | + | 0.287075 | |
DDB_G0284355 | DDB_G0284355 | DDB0232431 | CDS | 1873789 | 1908 | + | 0.208071 | |
DDB_G0284361 | DDB_G0284361 | DDB0232431 | CDS | 1888546 | 3129 | - | 0.270374 | |
DDB_G0284365 | DDB_G0284365 | DDB0232431 | CDS | 1895020 | 681 | + | 0.287812 | |
DDB_G0284367 | DDB_G0284367 | DDB0232431 | CDS | 1896160 | 816 | - | 0.313726 | |
DDB_G0284369 | DDB_G0284369 | DDB0232431 | CDS | 1898347 | 825 | - | 0.286061 | |
DDB_G0284371 | DDB_G0284371 | DDB0232431 | CDS | 1900513 | 825 | + | 0.266667 | |
DDB_G0284373 | DDB_G0284373 | DDB0232431 | CDS | 1901736 | 1089 | - | 0.240588 | |
DDB_G0284375 | DDB_G0284375 | DDB0232431 | CDS | 1905434 | 1059 | - | 0.266289 | |
DDB_G0284377 | DDB_G0284377 | DDB0232431 | CDS | 1910380 | 1563 | + | 0.213052 | |
DDB_G0284381 | DDB_G0284381 | DDB0232431 | CDS | 1916862 | 3270 | + | 0.307951 | |
DDB_G0284383 | DDB_G0284383 | DDB0232431 | CDS | 1920700 | 2409 | + | 0.288501 | |
DDB_G0284387 | DDB_G0284387 | DDB0232431 | CDS | 1929000 | 3231 | + | 0.263076 | |
DDB_G0284391 | DDB_G0284391 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232431 | CDS | 1935986 | 1761 | - | 0.27314 |
DDB_G0284393 | DDB_G0284393 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232431 | CDS | 1939162 | 1533 | - | 0.296804 |
DDB_G0284395 | DDB_G0284395 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | DDB0232431 | CDS | 1942017 | 1614 | - | 0.296778 |
DDB_G0284397 | DDB_G0284397 | DDB0232431 | CDS | 1944417 | 381 | - | 0.333333 | |
DDB_G0284401 | DDB_G0284401 | conserved hypothetical Dictyostelium protein similar to bacterial ubiquinonemenaquinone biosynthesis methyltransferase ubiE | DDB0232431 | CDS | 1952708 | 879 | - | 0.287827 |
DDB_G0284413 | DDB_G0284413 | DDB0232431 | CDS | 1967001 | 483 | + | 0.300207 | |
DDB_G0284423 | DDB_G0284423 | DDB0232431 | CDS | 1976888 | 1080 | + | 0.201852 | |
DDB_G0284425 | DDB_G0284425 | DDB0232431 | CDS | 1978561 | 240 | + | 0.216667 | |
DDB_G0284427 | DDB_G0284427 | DDB0232431 | CDS | 1979111 | 1335 | - | 0.222472 | |
DDB_G0284429 | DDB_G0284429 | DDB0232431 | CDS | 1981059 | 864 | - | 0.261574 | |
DDB_G0284433 | DDB_G0284433 | DDB0232431 | CDS | 1985042 | 960 | + | 0.3375 | |
DDB_G0284437 | DDB_G0284437 | DDB0232431 | CDS | 1993267 | 987 | + | 0.233029 | |
DDB_G0284439 | DDB_G0284439 | DDB0232431 | CDS | 1994656 | 2079 | + | 0.259259 | |
DDB_G0284441 | DDB_G0284441 | DDB0232431 | CDS | 1997677 | 2505 | - | 0.264271 | |
DDB_G0284443 | DDB_G0284443 | DDB0232431 | CDS | 1858931 | 864 | + | 0.252315 | |
DDB_G0284445_RTE | DDB_G0284445 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 1878838 | 678 | - | 0.340708 |
DDB_G0284451_ps | DDB_G0284451 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 1880019 | 318 | + | 0.251572 |
DDB_G0284453 | DDB_G0284453 | DDB0232431 | CDS | 1903726 | 1056 | - | 0.251894 | |
DDB_G0284455 | DDB_G0284455 | DDB0232431 | CDS | 1906991 | 1917 | - | 0.245696 | |
DDB_G0284457 | DDB_G0284457 | DDB0232431 | CDS | 1974366 | 1104 | + | 0.241848 | |
DDB_G0284459 | DDB_G0284459 | DDB0232431 | CDS | 1986677 | 3675 | + | 0.32 | |
DDB_G0284461 | DDB_G0284461 | DDB0232431 | CDS | 2003252 | 1872 | - | 0.277778 | |
DDB_G0284475 | DDB_G0284475 | DDB0232431 | CDS | 2010250 | 7515 | - | 0.242182 | |
DDB_G0284477 | DDB_G0284477 | DDB0232431 | CDS | 2018714 | 3138 | + | 0.197259 | |
DDB_G0284479 | DDB_G0284479 | DDB0232431 | CDS | 2022587 | 780 | + | 0.346154 | |
DDB_G0284481 | DDB_G0284481 | DDB0232431 | CDS | 2027462 | 3087 | + | 0.288306 | |
DDB_G0284485 | DDB_G0284485 | DDB0232431 | CDS | 2034779 | 846 | - | 0.321513 | |
DDB_G0284487 | DDB_G0284487 | DDB0232431 | CDS | 2036413 | 1587 | + | 0.221172 | |
DDB_G0284491 | DDB_G0284491 | DDB0232431 | CDS | 2041403 | 3639 | - | 0.233855 | |
DDB_G0284493 | DDB_G0284493 | DDB0232431 | CDS | 2045896 | 1209 | + | 0.287014 | |
DDB_G0284497 | DDB_G0284497 | DDB0232431 | CDS | 2050510 | 615 | + | 0.294309 | |
DDB_G0284507 | DDB_G0284507 | putative ortholog of Rad51C which is involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks interacts with XRCC3 | DDB0232431 | CDS | 2070281 | 1146 | - | 0.233857 |
DDB_G0284511 | DDB_G0284511 | DDB0232431 | CDS | 2077506 | 798 | + | 0.29198 | |
DDB_G0284513 | DDB_G0284513 | DDB0232431 | CDS | 2079840 | 4377 | + | 0.275303 | |
DDB_G0284515 | DDB_G0284515 | DDB0232431 | CDS | 2085226 | 1506 | + | 0.241036 | |
DDB_G0284521 | DDB_G0284521 | DDB0232431 | CDS | 2100599 | 771 | - | 0.212711 | |
DDB_G0284523 | DDB_G0284523 | DDB0232431 | CDS | 2102761 | 813 | + | 0.228782 | |
DDB_G0284527 | DDB_G0284527 | DDB0232431 | CDS | 2115024 | 1488 | - | 0.296371 | |
DDB_G0284529 | DDB_G0284529 | DDB0232431 | CDS | 2118136 | 1485 | - | 0.303704 | |
DDB_G0284531 | DDB_G0284531 | DDB0232431 | CDS | 2120826 | 612 | - | 0.254902 | |
DDB_G0284537 | DDB_G0284537 | DDB0232431 | CDS | 2139831 | 906 | - | 0.291391 | |
DDB_G0284539 | DDB_G0284539 | DDB0232431 | CDS | 2152696 | 2997 | - | 0.242576 | |
DDB_G0284541 | DDB_G0284541 | DDB0232431 | CDS | 2025823 | 645 | + | 0.311628 | |
DDB_G0284547 | DDB_G0284547 | DDB0232431 | CDS | 2008237 | 219 | + | 0.255708 | |
DDB_G0284557 | DDB_G0284557 | catalyzes the reaction ATP D-gluconate ADP 6-phospho-D-gluconate | DDB0232431 | CDS | 2110678 | 603 | + | 0.238806 |
DDB_G0284559 | DDB_G0284559 | DDB0232431 | CDS | 2123220 | 1281 | + | 0.238095 | |
DDB_G0284561 | DDB_G0284561 | DDB0232431 | CDS | 2131768 | 2949 | + | 0.232282 | |
DDB_G0284565 | DDB_G0284565 | DDB0232431 | CDS | 2142583 | 4788 | - | 0.267126 | |
DDB_G0284569 | DDB_G0284569 | DDB0232431 | CDS | 2167100 | 2379 | + | 0.226566 | |
DDB_G0284575 | DDB_G0284575 | DDB0232431 | CDS | 2173651 | 1815 | - | 0.344353 | |
DDB_G0284577 | DDB_G0284577 | putative ortholog of H. sapiens CNOT2 and S. cerevisiae CDC36 component of the CCR4-NOT transcription complex | DDB0232431 | CDS | 2176004 | 1740 | - | 0.281034 |
DDB_G0284579 | DDB_G0284579 | DDB0232431 | CDS | 2163129 | 2295 | + | 0.334641 | |
DDB_G0284581 | DDB_G0284581 | DDB0232431 | CDS | 2180042 | 993 | + | 0.193353 | |
DDB_G0284587 | DDB_G0284587 | DDB0232431 | CDS | 2187151 | 1236 | + | 0.231392 | |
DDB_G0284591 | DDB_G0284591 | DDB0232431 | CDS | 2189321 | 3669 | - | 0.270373 | |
DDB_G0284599 | DDB_G0284599 | DDB0232431 | CDS | 2207693 | 1551 | + | 0.320438 | |
DDB_G0284603 | DDB_G0284603 | DDB0232431 | CDS | 2211789 | 1413 | + | 0.208068 | |
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_G0284609_RTE | DDB_G0284609 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 2220278 | 589 | + | 0.271647 |
DDB_G0284615 | DDB_G0284615 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232431 | CDS | 2228341 | 4296 | + | 0.233939 |
DDB_G0284617 | DDB_G0284617 | contains a weak RimK-like ATP-grasp domain which is found in the ribosomal S6 modification enzyme RimK | DDB0232431 | CDS | 2233409 | 1455 | - | 0.236426 |
DDB_G0284619 | DDB_G0284619 | DDB0232431 | CDS | 2237635 | 762 | - | 0.362205 | |
DDB_G0284623 | DDB_G0284623 | DDB0232431 | CDS | 2255880 | 219 | - | 0.305936 | |
DDB_G0284625 | DDB_G0284625 | conserved hypothetical Dictyostelium protein contains one EGF-like type 3 domain | DDB0232431 | CDS | 2257074 | 2667 | - | 0.241095 |
DDB_G0284627 | DDB_G0284627 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains an N-terminal transmembrane domain that might be a signal sequence | DDB0232431 | CDS | 2260399 | 1161 | - | 0.274763 |
DDB_G0284629 | DDB_G0284629 | conserved in Dictyostelids predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) there is a highly similar gene | DDB0232431 | CDS | 2262832 | 339 | + | 0.309735 |
DDB_G0284631 | DDB_G0284631 | conserved in Dictyostelids predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) there is a highly similar gene | DDB0232431 | CDS | 2263474 | 339 | - | 0.306785 |
DDB_G0284633 | DDB_G0284633 | DDB0232431 | CDS | 2264683 | 2184 | + | 0.277473 | |
DDB_G0284635 | DDB_G0284635 | DDB0232431 | CDS | 2267233 | 216 | - | 0.199074 | |
DDB_G0284637 | DDB_G0284637 | DDB0232431 | CDS | 2269967 | 1653 | + | 0.242589 | |
DDB_G0284639_ps | DDB_G0284639 | putative pseudogene nearly identical to the upstream | DDB0232431 | CDS | 2272052 | 1353 | + | 0.24612 |
DDB_G0284641 | DDB_G0284641 | DDB0232431 | CDS | 2274398 | 315 | + | 0.253968 | |
DDB_G0284643 | DDB_G0284643 | DDB0232431 | CDS | 2279720 | 1158 | + | 0.289292 | |
DDB_G0284645 | DDB_G0284645 | DDB0232431 | CDS | 2281332 | 651 | - | 0.394777 | |
DDB_G0284649 | DDB_G0284649 | DDB0232431 | CDS | 2287653 | 2103 | - | 0.258678 | |
DDB_G0284655_ps | DDB_G0284655 | putative pseudogene similar to the large D. discoideum family of FNIP repeat-containing proteins | DDB0232431 | CDS | 2294408 | 1284 | + | 0.288162 |
DDB_G0284657 | DDB_G0284657 | DDB0232431 | CDS | 2303787 | 2301 | + | 0.281617 | |
DDB_G0284661 | DDB_G0284661 | putative protein serinethreonine kinase CAMK group kinase domain similar to mammalian CAM kinase I | DDB0232431 | CDS | 2309177 | 1446 | - | 0.304288 |
DDB_G0284665 | DDB_G0284665 | DDB0232431 | CDS | 2318999 | 171 | - | 0.269006 | |
DDB_G0284671 | DDB_G0284671 | DDB0232431 | CDS | 2323961 | 918 | + | 0.401961 | |
DDB_G0284673_ps | DDB_G0284673 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 2325423 | 180 | - | 0.288889 |
DDB_G0284675 | DDB_G0284675 | DDB0232431 | CDS | 2326080 | 945 | - | 0.27619 | |
DDB_G0284679 | DDB_G0284679 | DDB0232431 | CDS | 2333236 | 1221 | - | 0.30303 | |
DDB_G0284681 | DDB_G0284681 | contains 2 SCP2 (sterol carrier protein) domains contains a predicted peroxisomal targeting signal | DDB0232431 | CDS | 2334842 | 735 | + | 0.327891 |
DDB_G0284683 | DDB_G0284683 | DDB0232431 | CDS | 2336209 | 2649 | - | 0.286523 | |
DDB_G0284687 | DDB_G0284687 | similar to protozoan and bacterial cardiolipin synthetases contains two PLDc domains | DDB0232431 | CDS | 2343826 | 1818 | + | 0.264026 |
DDB_G0284689 | DDB_G0284689 | DDB0232431 | CDS | 2350414 | 5040 | + | 0.22996 | |
DDB_G0284691 | DDB_G0284691 | DDB0232431 | CDS | 2357079 | 867 | + | 0.283737 | |
DDB_G0284693 | DDB_G0284693 | homolog of human COX6B1 and S. cerevisiae COX12 this protein is one of the polypeptide chains of cytochrome c oxidase the terminal oxidase in mitochondrial electron transport | DDB0232431 | CDS | 2358649 | 237 | - | 0.383966 |
DDB_G0284695 | DDB_G0284695 | DDB0232431 | CDS | 2359622 | 1353 | - | 0.27864 | |
DDB_G0284701 | DDB_G0284701 | DDB0232431 | CDS | 2371416 | 1314 | - | 0.269406 | |
DDB_G0284705 | DDB_G0284705 | DDB0232431 | CDS | 2378839 | 1305 | - | 0.308812 | |
DDB_G0284707 | DDB_G0284707 | belongs to a gene family conserved in amoeba similar to bacterial pentalenene synthase contains a putative metal-binding domain | DDB0232431 | CDS | 2388566 | 1086 | + | 0.325967 |
DDB_G0284721 | DDB_G0284721 | DDB0232431 | CDS | 2252387 | 2274 | + | 0.284081 | |
DDB_G0284727 | DDB_G0284727 | DDB0232431 | CDS | 2313169 | 2424 | + | 0.288779 | |
DDB_G0284731 | DDB_G0284731 | DDB0232431 | CDS | 2380797 | 1413 | + | 0.242746 | |
DDB_G0284733_TE | DDB_G0284733 | putative DNA transposon Tdd-4 fragment refer to U57081 for full-length consensus element | DDB0232431 | CDS | 2390943 | 231 | - | 0.277056 |
DDB_G0284737 | DDB_G0284737 | belongs to the haloacid dehalogenase (HAD) hydrolase IIA family similar to human PGP (phosphoglycolate phosphatase) and S. cerevisiae PHO13 (4-nitrophenylphosphatase) | DDB0232431 | CDS | 2397942 | 912 | - | 0.27193 |
DDB_G0284741 | DDB_G0284741 | DDB0232431 | CDS | 2402392 | 4188 | - | 0.298472 | |
DDB_G0284749 | DDB_G0284749 | DDB0232431 | CDS | 2426750 | 3780 | - | 0.234921 | |
DDB_G0284751 | DDB_G0284751 | DDB0232431 | CDS | 2431735 | 1161 | + | 0.228252 | |
DDB_G0284753 | DDB_G0284753 | DDB0232431 | CDS | 2432933 | 1395 | - | 0.276703 | |
DDB_G0284755 | DDB_G0284755 | DDB0232431 | CDS | 2435039 | 1422 | - | 0.262307 | |
DDB_G0284757 | DDB_G0284757 | related to the Ovarian Tumour (OTU) gene of Drosophila function is unknown but conserved cysteine and histidine and possibly the aspartate residues suggests that those not yet recognized as peptidases could possess cysteine protease activity | DDB0232431 | CDS | 2437158 | 2301 | - | 0.303346 |
DDB_G0284763 | DDB_G0284763 | DDB0232431 | CDS | 2448744 | 1185 | - | 0.31308 | |
DDB_G0284765 | DDB_G0284765 | contains a predicted signal peptide there are two similar genes in D. discoideum | DDB0232431 | CDS | 2450678 | 615 | - | 0.273171 |
DDB_G0284767 | DDB_G0284767 | weakly related to ABC transporters does not have transmembrane domains | DDB0232431 | CDS | 2452498 | 2274 | + | 0.228672 |
DDB_G0284773 | DDB_G0284773 | DDB0232431 | CDS | 2467019 | 1581 | + | 0.354839 | |
DDB_G0284777 | DDB_G0284777 | DDB0232431 | CDS | 2472579 | 963 | + | 0.303219 | |
DDB_G0284779 | DDB_G0284779 | DDB0232431 | CDS | 2475500 | 1680 | - | 0.255952 | |
DDB_G0284781 | DDB_G0284781 | DDB0232431 | CDS | 2477533 | 363 | - | 0.22314 | |
DDB_G0284783 | DDB_G0284783 | contains a glutamine-rich region similar to D. purpureum protein | DDB0232431 | CDS | 2479165 | 1812 | + | 0.175497 |
DDB_G0284787 | DDB_G0284787 | DDB0232431 | CDS | 2483195 | 261 | - | 0.218391 | |
DDB_G0284789_ps | DDB_G0284789 | putative pseudogene similar to gene | DDB0232431 | CDS | 2483989 | 1734 | + | 0.258362 |
DDB_G0284793 | DDB_G0284793 | belongs to the PLAC8 family (placenta-specific gene 8 protein) a family of cysteine-rich proteins with highly divergent low complexity amino terminal regions | DDB0232431 | CDS | 2488840 | 330 | - | 0.360606 |
DDB_G0284797_ps | DDB_G0284797 | putative pseudogene similar to | DDB0232431 | CDS | 2492140 | 309 | + | 0.281553 |
DDB_G0284801 | DDB_G0284801 | DDB0232431 | CDS | 2499782 | 600 | + | 0.263333 | |
DDB_G0284805 | DDB_G0284805 | DDB0232431 | CDS | 2500893 | 777 | - | 0.28314 | |
DDB_G0284807 | DDB_G0284807 | DDB0232431 | CDS | 2501891 | 2979 | - | 0.288016 | |
DDB_G0284811 | DDB_G0284811 | DDB0232431 | CDS | 2507767 | 882 | + | 0.31746 | |
DDB_G0284813 | DDB_G0284813 | DDB0232431 | CDS | 2508788 | 258 | - | 0.29845 | |
DDB_G0284815 | DDB_G0284815 | DDB0232431 | CDS | 2517388 | 903 | + | 0.172757 | |
DDB_G0284817 | DDB_G0284817 | DDB0232431 | CDS | 2518687 | 1641 | - | 0.311395 | |
DDB_G0284819 | DDB_G0284819 | DDB0232431 | CDS | 2520967 | 1002 | - | 0.243513 | |
DDB_G0284821 | DDB_G0284821 | DDB0232431 | CDS | 2523362 | 1245 | + | 0.258635 | |
DDB_G0284823 | DDB_G0284823 | DDB0232431 | CDS | 2525345 | 225 | + | 0.377778 | |
DDB_G0284825 | DDB_G0284825 | weakly similar to H. sapiens GARNL1 a RanGAP | DDB0232431 | CDS | 2526025 | 4923 | - | 0.299005 |
DDB_G0284829_TE | DDB_G0284829 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232431 | CDS | 2392075 | 1335 | - | 0.297378 |
DDB_G0284841 | DDB_G0284841 | DDB0232431 | CDS | 2510140 | 2640 | + | 0.273106 | |
DDB_G0284843 | DDB_G0284843 | DDB0232431 | CDS | 2515068 | 729 | + | 0.198903 | |
DDB_G0284847 | DDB_G0284847 | homolog of human SDF2 (stromal cell-derived factor 2) contains 3 MIR domains | DDB0232431 | CDS | 2556090 | 639 | - | 0.317684 |
DDB_G0284849 | DDB_G0284849 | DDB0232431 | CDS | 2557758 | 3561 | + | 0.298512 | |
DDB_G0284853 | DDB_G0284853 | large protein that has similarity to mammalian MYC binding protein 2 (MYCBP2) a putative E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins. | DDB0232431 | CDS | 2532768 | 12495 | + | 0.265146 |
DDB_G0284855 | DDB_G0284855 | DDB0232431 | CDS | 2546123 | 984 | + | 0.300813 | |
DDB_G0284871 | DDB_G0284871 | DDB0232431 | CDS | 2772764 | 1395 | - | 0.321147 | |
DDB_G0284873_RTE | DDB_G0284873 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 2562666 | 423 | - | 0.267139 |
DDB_G0284875 | DDB_G0284875 | DDB0232431 | CDS | 2563672 | 336 | + | 0.366071 | |
DDB_G0284881 | DDB_G0284881 | DDB0232431 | CDS | 2585806 | 612 | + | 0.26634 | |
DDB_G0284885 | DDB_G0284885 | DDB0232431 | CDS | 2588526 | 1503 | - | 0.208916 | |
DDB_G0284887 | DDB_G0284887 | DDB0232431 | CDS | 2599094 | 1245 | - | 0.254618 | |
DDB_G0284889 | DDB_G0284889 | DDB0232431 | CDS | 2600817 | 1215 | - | 0.25679 | |
DDB_G0284893 | DDB_G0284893 | DDB0232431 | CDS | 2604439 | 1080 | - | 0.235185 | |
DDB_G0284895 | DDB_G0284895 | contains an N-terminal SCP domain that occurs in prokaryotic and eukaryotic proteins proposed to be Ca chelating serine proteases also contains two C-terminal WSC domains which are putative carbohydrate binding domains | DDB0232431 | CDS | 2608632 | 2283 | + | 0.297854 |
DDB_G0284899 | DDB_G0284899 | DDB0232431 | CDS | 2613921 | 2838 | + | 0.231501 | |
DDB_G0284901 | DDB_G0284901 | similar to human ISOC2 (isochorismatase domain-containing protein 2 mitochondrial) contains a predicted peroxisomal targeting signal | DDB0232431 | CDS | 2617131 | 621 | - | 0.251208 |
DDB_G0284907 | DDB_G0284907 | DDB0232431 | CDS | 2626851 | 288 | - | 0.277778 | |
DDB_G0284909 | DDB_G0284909 | DDB0232431 | CDS | 2628238 | 1014 | + | 0.204142 | |
DDB_G0284913 | DDB_G0284913 | DDB0232431 | CDS | 2638616 | 4407 | + | 0.276152 | |
DDB_G0284915 | DDB_G0284915 | DDB0232431 | CDS | 2643291 | 696 | - | 0.310345 | |
DDB_G0284917 | DDB_G0284917 | DDB0232431 | CDS | 2644494 | 1533 | - | 0.305936 | |
DDB_G0284919 | DDB_G0284919 | similar to human DHRSX (dehydrogenasereductase SDR family member on chromosome X) and retinol dehydrogenase | DDB0232431 | CDS | 2646442 | 990 | - | 0.233333 |
DDB_G0284921 | DDB_G0284921 | DDB0232431 | CDS | 2648206 | 1515 | + | 0.307591 | |
DDB_G0284925 | DDB_G0284925 | this is one of four almost identical genes on C4 ( | DDB0232431 | CDS | 2654790 | 180 | - | 0.427778 |
DDB_G0284927 | DDB_G0284927 | this is one of four almost identical genes on C4 ( | DDB0232431 | CDS | 2652917 | 180 | - | 0.438889 |
DDB_G0284929 | DDB_G0284929 | DDB0232431 | CDS | 2657638 | 249 | + | 0.293173 | |
DDB_G0284931 | DDB_G0284931 | this is one of four almost identical genes on C4 ( | DDB0232431 | CDS | 2659079 | 174 | + | 0.431034 |
DDB_G0284933 | DDB_G0284933 | DDB0232431 | CDS | 2659670 | 3552 | - | 0.169482 | |
DDB_G0284935 | DDB_G0284935 | DDB0232431 | CDS | 2664011 | 1068 | + | 0.277154 | |
DDB_G0284937 | DDB_G0284937 | DDB0232431 | CDS | 2665360 | 1026 | + | 0.287524 | |
DDB_G0284939 | DDB_G0284939 | DDB0232431 | CDS | 2667885 | 396 | + | 0.282828 | |
DDB_G0284941 | DDB_G0284941 | DDB0232431 | CDS | 2668956 | 381 | + | 0.230971 | |
DDB_G0284943 | DDB_G0284943 | DDB0232431 | CDS | 2669585 | 2082 | - | 0.267531 | |
DDB_G0284949 | DDB_G0284949 | DDB0232431 | CDS | 2677540 | 132 | - | 0.310606 | |
DDB_G0284955 | DDB_G0284955 | DDB0232431 | CDS | 2684549 | 4602 | - | 0.27488 | |
DDB_G0284957 | DDB_G0284957 | DDB0232431 | CDS | 2694222 | 2280 | + | 0.249561 | |
DDB_G0284959 | DDB_G0284959 | ortholog of the conserved OPA3 in H. sapiens defects in OPA3 cause type III 3-methylglutaconic aciduria (MGA type III) also known as optic atrophy plus syndrome | DDB0232431 | CDS | 2698477 | 600 | + | 0.261667 |
DDB_G0284961 | DDB_G0284961 | DDB0232431 | CDS | 2699345 | 534 | - | 0.269663 | |
DDB_G0284963 | DDB_G0284963 | DDB0232431 | CDS | 2700406 | 1275 | + | 0.31451 | |
DDB_G0284965 | DDB_G0284965 | DDB0232431 | CDS | 2702978 | 852 | - | 0.219484 | |
DDB_G0284967 | DDB_G0284967 | DDB0232431 | CDS | 2704245 | 2547 | - | 0.206517 | |
DDB_G0284969 | DDB_G0284969 | DDB0232431 | CDS | 2719814 | 1764 | + | 0.272676 | |
DDB_G0284971 | DDB_G0284971 | DDB0232431 | CDS | 2726690 | 1029 | + | 0.199223 | |
DDB_G0284973 | DDB_G0284973 | DDB0232431 | CDS | 2731379 | 3468 | + | 0.238178 | |
DDB_G0284977 | DDB_G0284977 | DDB0232431 | CDS | 2738670 | 4227 | - | 0.287674 | |
DDB_G0284979 | DDB_G0284979 | DDB0232431 | CDS | 2743512 | 768 | - | 0.33724 | |
DDB_G0284981 | DDB_G0284981 | DDB0232431 | CDS | 2745658 | 1356 | + | 0.30826 | |
DDB_G0284991 | DDB_G0284991 | DDB0232431 | CDS | 2778336 | 3282 | + | 0.241316 | |
DDB_G0284993 | DDB_G0284993 | DDB0232431 | CDS | 2782082 | 129 | - | 0.209302 | |
DDB_G0284995 | DDB_G0284995 | DDB0232431 | CDS | 2782622 | 873 | + | 0.252005 | |
DDB_G0284997 | DDB_G0284997 | DDB0232431 | CDS | 2784039 | 1125 | - | 0.315556 | |
DDB_G0284999 | DDB_G0284999 | DDB0232431 | CDS | 2786060 | 834 | - | 0.306954 | |
DDB_G0285001 | DDB_G0285001 | DDB0232431 | CDS | 2788466 | 1755 | + | 0.249573 | |
DDB_G0285011 | DDB_G0285011 | similar to the fungi mitochondrial transferase caf17 a mitochondrial matrix protein involved in the incorporation of iron-sulfur clusters into mitochondrial aconitase-type proteins | DDB0232431 | CDS | 2814046 | 1227 | - | 0.295029 |
DDB_G0285013 | DDB_G0285013 | DDB0232431 | CDS | 2820652 | 915 | + | 0.253552 | |
DDB_G0285015_ps | DDB_G0285015 | putative pseudogene similar to a Dictyostelium family of genes including | DDB0232431 | CDS | 2822210 | 1053 | - | 0.185185 |
DDB_G0285019 | DDB_G0285019 | DDB0232431 | CDS | 2823631 | 3486 | - | 0.240964 | |
DDB_G0285021 | DDB_G0285021 | belongs to the complex I LYR family similar to human NDUFB9 (NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9) | DDB0232431 | CDS | 2830332 | 321 | - | 0.323988 |
DDB_G0285031 | DDB_G0285031 | DDB0232431 | CDS | 2836987 | 2388 | - | 0.215662 | |
DDB_G0285033 | DDB_G0285033 | belongs to the short-chain dehydrogenasereductase family | DDB0232431 | CDS | 2839925 | 786 | + | 0.307888 |
DDB_G0285035_RTE | DDB_G0285035 | DDB0232431 | CDS | 2841164 | 327 | + | 0.296636 | |
DDB_G0285037 | DDB_G0285037 | DDB0232431 | CDS | 2566569 | 183 | - | 0.262295 | |
DDB_G0285041 | DDB_G0285041 | similar to human ISOC2 (isochorismatase domain-containing protein 2 mitochondrial) contains a predicted peroxisomal targeting signal | DDB0232431 | CDS | 2620294 | 621 | - | 0.243156 |
DDB_G0285043 | DDB_G0285043 | this is one of four almost identical genes on C4 ( | DDB0232431 | CDS | 2656766 | 180 | + | 0.438889 |
DDB_G0285045 | DDB_G0285045 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232431 | CDS | 2573154 | 4140 | - | 0.257005 |
DDB_G0285047 | DDB_G0285047 | DDB0232431 | CDS | 2593257 | 1263 | - | 0.176564 | |
DDB_G0285049 | DDB_G0285049 | DDB0232431 | CDS | 2595117 | 1113 | - | 0.209344 | |
DDB_G0285055 | DDB_G0285055 | DDB0232431 | CDS | 2631798 | 5796 | - | 0.285714 | |
DDB_G0285057 | DDB_G0285057 | DDB0232431 | CDS | 2666993 | 516 | - | 0.261628 | |
DDB_G0285059 | DDB_G0285059 | DDB0232431 | CDS | 2696768 | 1104 | - | 0.181159 | |
DDB_G0285063 | DDB_G0285063 | similar to the H. sapiens HUWE1 an E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins. | DDB0232431 | CDS | 2707152 | 11379 | - | 0.321997 |
DDB_G0285065 | DDB_G0285065 | DDB0232431 | CDS | 2722034 | 1590 | - | 0.272956 | |
DDB_G0285073 | DDB_G0285073 | putative VPS9 ortholog a guanine nucleotide exchange factor involved in vesicle-mediated vacuolar protein transport | DDB0232431 | CDS | 2758636 | 2181 | + | 0.24851 |
DDB_G0285075_ps | DDB_G0285075 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 2776760 | 990 | + | 0.194949 |
DDB_G0285079 | DDB_G0285079 | DDB0232431 | CDS | 2802048 | 603 | + | 0.296849 | |
DDB_G0285081 | DDB_G0285081 | DDB0232431 | CDS | 2808780 | 4416 | + | 0.248188 | |
DDB_G0285083 | DDB_G0285083 | DDB0232431 | CDS | 2815942 | 3063 | + | 0.264447 | |
DDB_G0285085_ps | DDB_G0285085 | putative pseudogene fragment similar to | DDB0232431 | CDS | 2820125 | 1068 | + | 0.243446 |
DDB_G0285087 | DDB_G0285087 | DDB0232431 | CDS | 2827341 | 2205 | - | 0.177778 | |
DDB_G0285089_RTE | DDB_G0285089 | DDB0232431 | CDS | 2841636 | 2991 | + | 0.336342 | |
DDB_G0285091_RTE | DDB_G0285091 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE3-B refer to GenBank AF134170 for full-length consensus element | DDB0232431 | CDS | 2847730 | 216 | - | 0.277778 |
DDB_G0285093 | DDB_G0285093 | DDB0232431 | CDS | 2568202 | 2958 | - | 0.23428 | |
DDB_G0285095 | DDB_G0285095 | DDB0232431 | CDS | 2804851 | 792 | - | 0.306818 | |
DDB_G0285097_RTE | DDB_G0285097 | ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 2848300 | 1119 | + | 0.341376 |
DDB_G0285103 | DDB_G0285103 | DDB0232431 | CDS | 2851187 | 816 | + | 0.253676 | |
DDB_G0285107 | DDB_G0285107 | DDB0232431 | CDS | 2855138 | 492 | + | 0.296748 | |
DDB_G0285109 | DDB_G0285109 | DDB0232431 | CDS | 2862240 | 975 | - | 0.25641 | |
DDB_G0285113 | DDB_G0285113 | similar to human MUDENG (MHD domain-containing death-inducing protein) which induces cell death in cytotoxic T-cells contains one MHD domain (mu homology domain) | DDB0232431 | CDS | 2865898 | 1758 | + | 0.30603 |
DDB_G0285115 | DDB_G0285115 | DDB0232431 | CDS | 2872325 | 639 | + | 0.219092 | |
DDB_G0285119 | DDB_G0285119 | DDB0232431 | CDS | 2877924 | 1566 | + | 0.275862 | |
DDB_G0285121 | DDB_G0285121 | DDB0232431 | CDS | 2881701 | 297 | + | 0.228956 | |
DDB_G0285123 | DDB_G0285123 | DDB0232431 | CDS | 2882150 | 2220 | + | 0.215315 | |
DDB_G0285125 | DDB_G0285125 | DDB0232431 | CDS | 2884598 | 1623 | - | 0.23167 | |
DDB_G0285127 | DDB_G0285127 | DDB0232431 | CDS | 2886739 | 1101 | - | 0.217984 | |
DDB_G0285129 | DDB_G0285129 | DDB0232431 | CDS | 2894961 | 792 | + | 0.257576 | |
DDB_G0285135 | DDB_G0285135 | DDB0232431 | CDS | 2903243 | 660 | - | 0.234848 | |
DDB_G0285143 | DDB_G0285143 | similar to | DDB0232431 | CDS | 2913006 | 1356 | - | 0.272861 |
DDB_G0285145 | DDB_G0285145 | DDB0232431 | CDS | 2915991 | 1305 | + | 0.2659 | |
DDB_G0285149 | DDB_G0285149 | similar to mammalian TNF receptor-associated factors 5 and 6 (TRAF5 TRAF6) | DDB0232431 | CDS | 2888446 | 1284 | - | 0.288162 |
DDB_G0285151 | DDB_G0285151 | DDB0232431 | CDS | 2868305 | 597 | + | 0.293132 | |
DDB_G0285153 | DDB_G0285153 | DDB0232431 | CDS | 2869433 | 939 | + | 0.234292 | |
DDB_G0285155 | DDB_G0285155 | DDB0232431 | CDS | 2891853 | 2406 | - | 0.190357 | |
DDB_G0285157 | DDB_G0285157 | DDB0232431 | CDS | 2898787 | 315 | + | 0.244444 | |
DDB_G0285167 | DDB_G0285167 | DDB0232431 | CDS | 2919389 | 975 | + | 0.222564 | |
DDB_G0285169 | DDB_G0285169 | DDB0232431 | CDS | 2928529 | 2820 | - | 0.197163 | |
DDB_G0285171_ps | DDB_G0285171 | putative pseudogene highly similar to | DDB0232431 | CDS | 2932277 | 516 | + | 0.300388 |
DDB_G0285173 | DDB_G0285173 | DDB0232431 | CDS | 2933402 | 2742 | - | 0.20496 | |
DDB_G0285177 | DDB_G0285177 | DDB0232431 | CDS | 2939040 | 1395 | - | 0.247312 | |
DDB_G0285179 | DDB_G0285179 | DDB0232431 | CDS | 2954586 | 918 | + | 0.27342 | |
DDB_G0285181 | DDB_G0285181 | DDB0232431 | CDS | 2955670 | 414 | - | 0.198068 | |
DDB_G0285183 | DDB_G0285183 | DDB0232431 | CDS | 2957139 | 3534 | + | 0.276174 | |
DDB_G0285185 | DDB_G0285185 | DDB0232431 | CDS | 2960975 | 993 | + | 0.233635 | |
DDB_G0285187 | DDB_G0285187 | DDB0232431 | CDS | 2962656 | 141 | - | 0.375887 | |
DDB_G0285189 | DDB_G0285189 | DDB0232431 | CDS | 2964201 | 462 | - | 0.264069 | |
DDB_G0285191 | DDB_G0285191 | DDB0232431 | CDS | 2965339 | 1785 | - | 0.317647 | |
DDB_G0285201 | DDB_G0285201 | DDB0232431 | CDS | 2968644 | 2385 | - | 0.255765 | |
DDB_G0285203 | DDB_G0285203 | DDB0232431 | CDS | 2941521 | 195 | + | 0.317949 | |
DDB_G0285207_ps | DDB_G0285207 | putative pseudogene highly similar to | DDB0232431 | CDS | 2927541 | 498 | + | 0.297189 |
DDB_G0285209 | DDB_G0285209 | DDB0232431 | CDS | 2951533 | 810 | + | 0.261728 | |
DDB_G0285215 | DDB_G0285215 | DDB0232431 | CDS | 2987082 | 1527 | - | 0.339227 | |
DDB_G0285219 | DDB_G0285219 | DDB0232431 | CDS | 2992421 | 831 | + | 0.311673 | |
DDB_G0285225 | DDB_G0285225 | DDB0232431 | CDS | 3013770 | 1701 | + | 0.218107 | |
DDB_G0285229 | DDB_G0285229 | DDB0232431 | CDS | 3018261 | 555 | - | 0.176577 | |
DDB_G0285233 | DDB_G0285233 | DDB0232431 | CDS | 2981196 | 1893 | - | 0.230851 | |
DDB_G0285235 | DDB_G0285235 | DDB0232431 | CDS | 2989642 | 192 | + | 0.25 | |
DDB_G0285237 | DDB_G0285237 | DDB0232431 | CDS | 2990906 | 705 | + | 0.28227 | |
DDB_G0285243 | DDB_G0285243 | has partial similarity to the S. cerevisiae SEN1 a putative helicase required for RNA polymerase II transcription termination and processing of RNAs | DDB0232431 | CDS | 2998910 | 6210 | + | 0.295169 |
DDB_G0285245 | DDB_G0285245 | DDB0232431 | CDS | 3006660 | 846 | - | 0.328605 | |
DDB_G0285249 | DDB_G0285249 | DDB0232431 | CDS | 3016456 | 828 | - | 0.190821 | |
DDB_G0285255 | DDB_G0285255 | DDB0232431 | CDS | 3020871 | 1140 | + | 0.225439 | |
DDB_G0285259 | DDB_G0285259 | DDB0232431 | CDS | 3024689 | 2052 | - | 0.240253 | |
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_G0285269 | DDB_G0285269 | DDB0232431 | CDS | 3037532 | 930 | + | 0.274194 | |
DDB_G0285271 | DDB_G0285271 | DDB0232431 | CDS | 3042778 | 3132 | + | 0.230204 | |
DDB_G0285273 | DDB_G0285273 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232431 | CDS | 3047069 | 474 | + | 0.308017 |
DDB_G0285275 | DDB_G0285275 | DDB0232431 | CDS | 3047966 | 831 | - | 0.306859 | |
DDB_G0285279 | DDB_G0285279 | DDB0232431 | CDS | 3050725 | 384 | - | 0.265625 | |
DDB_G0285281 | DDB_G0285281 | DDB0232431 | CDS | 3053971 | 774 | + | 0.232558 | |
DDB_G0285283 | DDB_G0285283 | DDB0232431 | CDS | 3058106 | 1854 | - | 0.319849 | |
DDB_G0285285 | DDB_G0285285 | DDB0232431 | CDS | 3060850 | 1323 | - | 0.253212 | |
DDB_G0285287 | DDB_G0285287 | putative ortholog of Rad51D which is involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks | DDB0232431 | CDS | 3062767 | 1065 | - | 0.23662 |
DDB_G0285289 | DDB_G0285289 | DDB0232431 | CDS | 3064118 | 849 | - | 0.332155 | |
DDB_G0285291 | DDB_G0285291 | DDB0232431 | CDS | 3065810 | 1239 | - | 0.34544 | |
DDB_G0285297 | DDB_G0285297 | DDB0232431 | CDS | 3039035 | 3198 | + | 0.262039 | |
DDB_G0285299 | DDB_G0285299 | DDB0232431 | CDS | 3070354 | 1635 | - | 0.310092 | |
DDB_G0285301 | DDB_G0285301 | DDB0232431 | CDS | 3019660 | 434 | - | 0.163594 | |
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_G0285307_RTE | DDB_G0285307 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 3075949 | 1061 | + | 0.321395 |
DDB_G0285309 | DDB_G0285309 | DDB0232431 | CDS | 3077952 | 2850 | + | 0.2 | |
DDB_G0285315_RTE | DDB_G0285315 | 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 | 3088593 | 1362 | - | 0.340675 |
DDB_G0285317_RTE | DDB_G0285317 | 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 | 3090138 | 408 | - | 0.362745 |
DDB_G0285325_RTE | DDB_G0285325 | 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 | 3091037 | 1953 | + | 0.348182 |
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_G0285331 | DDB_G0285331 | DDB0232431 | CDS | 3096169 | 1137 | + | 0.221636 | |
DDB_G0285333 | DDB_G0285333 | DDB0232431 | CDS | 3097865 | 816 | - | 0.310049 | |
DDB_G0285335 | DDB_G0285335 | DDB0232431 | CDS | 3099238 | 1767 | - | 0.203169 | |
DDB_G0285337 | DDB_G0285337 | DDB0232431 | CDS | 3101144 | 1116 | - | 0.243728 | |
DDB_G0285341 | DDB_G0285341 | DDB0232431 | CDS | 3105820 | 1584 | + | 0.332071 | |
DDB_G0285345 | DDB_G0285345 | DDB0232431 | CDS | 3116252 | 228 | - | 0.364035 | |
DDB_G0285347 | DDB_G0285347 | DDB0232431 | CDS | 3118848 | 591 | - | 0.270728 | |
DDB_G0285351 | DDB_G0285351 | DDB0232431 | CDS | 3146811 | 1365 | - | 0.267399 | |
DDB_G0285355 | DDB_G0285355 | DDB0232431 | CDS | 3164414 | 591 | + | 0.203046 | |
DDB_G0285357 | DDB_G0285357 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | DDB0232431 | CDS | 3165268 | 1095 | - | 0.36895 |
DDB_G0285359 | DDB_G0285359 | DDB0232431 | CDS | 3166879 | 630 | - | 0.31746 | |
DDB_G0285361 | DDB_G0285361 | DDB0232431 | CDS | 3169327 | 984 | - | 0.322154 | |
DDB_G0285363 | DDB_G0285363 | DDB0232431 | CDS | 3170836 | 1047 | - | 0.3085 | |
DDB_G0285365 | DDB_G0285365 | DDB0232431 | CDS | 3173380 | 699 | + | 0.296137 | |
DDB_G0285369_ps | DDB_G0285369 | putative pseudogene similar to | DDB0232431 | CDS | 3174564 | 342 | + | 0.230994 |
DDB_G0285377 | DDB_G0285377 | DDB0232431 | CDS | 3204171 | 666 | - | 0.279279 | |
DDB_G0285379 | DDB_G0285379 | DDB0232431 | CDS | 3205403 | 315 | - | 0.209524 | |
DDB_G0285383 | DDB_G0285383 | DDB0232431 | CDS | 3210654 | 138 | - | 0.347826 | |
DDB_G0285385 | DDB_G0285385 | DDB0232431 | CDS | 3211353 | 912 | - | 0.172149 | |
DDB_G0285389 | DDB_G0285389 | putative ortholog of H. sapiens UXT (ubiquitously-expressed transcript) related to prefoldin alpha | DDB0232431 | CDS | 3107718 | 486 | - | 0.201646 |
DDB_G0285397 | DDB_G0285397 | DDB0232431 | CDS | 3149443 | 1437 | - | 0.230341 | |
DDB_G0285401 | DDB_G0285401 | DDB0232431 | CDS | 3154785 | 2763 | + | 0.305465 | |
DDB_G0285403 | DDB_G0285403 | DDB0232431 | CDS | 3157812 | 3108 | - | 0.320463 | |
DDB_G0285405 | DDB_G0285405 | DDB0232431 | CDS | 3175505 | 2772 | - | 0.240981 | |
DDB_G0285409 | DDB_G0285409 | DDB0232431 | CDS | 3184814 | 3579 | - | 0.222408 | |
DDB_G0285411 | DDB_G0285411 | DDB0232431 | CDS | 3189133 | 4317 | + | 0.217049 | |
DDB_G0285413 | DDB_G0285413 | DDB0232431 | CDS | 3199348 | 810 | + | 0.240741 | |
DDB_G0285421 | DDB_G0285421 | has a signal peptide followed by a transmembrane domain conserved in D. purpureum and P. pallidum | DDB0232431 | CDS | 3514189 | 3492 | + | 0.2626 |
DDB_G0285435 | DDB_G0285435 | DDB0232431 | CDS | 3216790 | 4929 | - | 0.313857 | |
DDB_G0285437 | DDB_G0285437 | DDB0232431 | CDS | 3223269 | 969 | + | 0.27451 | |
DDB_G0285439 | DDB_G0285439 | DDB0232431 | CDS | 3224754 | 2421 | + | 0.250723 | |
DDB_G0285441 | DDB_G0285441 | DDB0232431 | CDS | 3227919 | 216 | + | 0.402778 | |
DDB_G0285443 | DDB_G0285443 | DDB0232431 | CDS | 3229422 | 219 | + | 0.39726 | |
DDB_G0285445 | DDB_G0285445 | has the same domain composition as fbxA and | DDB0232431 | CDS | 3230059 | 3537 | - | 0.271699 |
DDB_G0285447 | DDB_G0285447 | conserved protein contains 2 putative transmembrane domains | DDB0232431 | CDS | 3236291 | 918 | - | 0.260349 |
DDB_G0285449 | DDB_G0285449 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232431 | CDS | 3237973 | 2241 | - | 0.253012 |
DDB_G0285459 | DDB_G0285459 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | DDB0232431 | CDS | 3256332 | 786 | + | 0.282443 |
DDB_G0285463 | DDB_G0285463 | member of the TKL (tyrosine kinase-like) group and the CZAK (C-terminal domain of ZakA) family contains 7 putative transmembrane domains | DDB0232431 | CDS | 3259648 | 2076 | - | 0.308285 |
DDB_G0285467 | DDB_G0285467 | DDB0232431 | CDS | 3266519 | 1398 | + | 0.326896 | |
DDB_G0285469 | DDB_G0285469 | DDB0232431 | CDS | 3270785 | 222 | + | 0.193694 | |
DDB_G0285471 | DDB_G0285471 | belongs to the DUF836 family similar to S. cerevisiae glutaredoxin-like protein YDR286C | DDB0232431 | CDS | 3274352 | 327 | + | 0.217125 |
DDB_G0285473 | DDB_G0285473 | DDB0232431 | CDS | 3274945 | 510 | - | 0.186275 | |
DDB_G0285477 | DDB_G0285477 | DDB0232431 | CDS | 3279052 | 282 | - | 0.219858 | |
DDB_G0285481 | DDB_G0285481 | DDB0232431 | CDS | 3294537 | 1533 | - | 0.172864 | |
DDB_G0285483 | DDB_G0285483 | DDB0232431 | CDS | 3297334 | 4668 | + | 0.230291 | |
DDB_G0285485 | DDB_G0285485 | protein family conserved in protozoans fungi and invertebrate animals | DDB0232431 | CDS | 3302460 | 2070 | - | 0.282126 |
DDB_G0285487 | DDB_G0285487 | protein family conserved in protozoans fungi and invertebrate animals | DDB0232431 | CDS | 3305672 | 2205 | - | 0.273016 |
DDB_G0285489 | DDB_G0285489 | similar to human TRMT112 S. cerevisiae TRM112 (multifunctional methyltransferase subunit TRM112) | DDB0232431 | CDS | 3308405 | 387 | + | 0.250646 |
DDB_G0285491 | DDB_G0285491 | DDB0232431 | CDS | 3308999 | 807 | - | 0.262701 | |
DDB_G0285493 | DDB_G0285493 | DDB0232431 | CDS | 3310297 | 1125 | + | 0.255111 | |
DDB_G0285495 | DDB_G0285495 | DDB0232431 | CDS | 3311819 | 1488 | - | 0.252016 | |
DDB_G0285497 | DDB_G0285497 | DDB0232431 | CDS | 3313914 | 525 | + | 0.260952 | |
DDB_G0285499 | DDB_G0285499 | DDB0232431 | CDS | 3314745 | 5034 | + | 0.197855 | |
DDB_G0285501 | DDB_G0285501 | DDB0232431 | CDS | 3320640 | 969 | - | 0.307534 | |
DDB_G0285511 | DDB_G0285511 | DDB0232431 | CDS | 3331170 | 1683 | - | 0.322638 | |
DDB_G0285517 | DDB_G0285517 | DDB0232431 | CDS | 3338968 | 537 | + | 0.268156 | |
DDB_G0285519 | DDB_G0285519 | DDB0232431 | CDS | 3339980 | 867 | - | 0.267589 | |
DDB_G0285525 | DDB_G0285525 | phosphorylates dephospho-CoA to CoA in other organisms this activity is part of a bifunctional enzyme that also has pantetheine-phosphate adenylyltransferase activity in Dictyostelium the latter activity is encoded by | DDB0232431 | CDS | 3344366 | 624 | - | 0.245192 |
DDB_G0285529 | DDB_G0285529 | DDB0232431 | CDS | 3346712 | 1149 | + | 0.252393 | |
DDB_G0285531 | DDB_G0285531 | DDB0232431 | CDS | 3348010 | 1200 | + | 0.245833 | |
DDB_G0285535 | DDB_G0285535 | DDB0232431 | CDS | 3350719 | 1494 | - | 0.240295 | |
DDB_G0285539 | DDB_G0285539 | DDB0232431 | CDS | 3354945 | 1575 | + | 0.233016 | |
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_G0285543 | DDB_G0285543 | DDB0232431 | CDS | 3362096 | 2157 | + | 0.255911 | |
DDB_G0285545 | DDB_G0285545 | similar to H. sapiens solute carrier family 31 member 1 (SLC31A1) or high affinity copper uptake protein 1 contains 3 predicted transmembrane domains | DDB0232431 | CDS | 3364611 | 441 | - | 0.251701 |
DDB_G0285547_RTE | DDB_G0285547 | 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 | 3366450 | 777 | + | 0.332046 |
DDB_G0285549 | DDB_G0285549 | DDB0232431 | CDS | 3370790 | 174 | + | 0.33908 | |
DDB_G0285551 | DDB_G0285551 | DDB0232431 | CDS | 3371635 | 180 | + | 0.316667 | |
DDB_G0285555 | DDB_G0285555 | highly similar to neighboring gene | DDB0232431 | CDS | 3373704 | 1698 | + | 0.287986 |
DDB_G0285557 | DDB_G0285557 | DDB0232431 | CDS | 3378778 | 840 | + | 0.207143 | |
DDB_G0285559 | DDB_G0285559 | DDB0232431 | CDS | 3380070 | 3711 | + | 0.221234 | |
DDB_G0285563 | DDB_G0285563 | DDB0232431 | CDS | 3385916 | 852 | - | 0.246479 | |
DDB_G0285565_ps | DDB_G0285565 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 3389420 | 1143 | + | 0.304462 |
DDB_G0285567 | DDB_G0285567 | DDB0232431 | CDS | 3392571 | 222 | - | 0.396396 | |
DDB_G0285569 | DDB_G0285569 | DDB0232431 | CDS | 3393304 | 219 | + | 0.406393 | |
DDB_G0285573_ps | DDB_G0285573 | putative pseudogene similar to short-chain dehydrogenasereductase (SDR) family proteins | DDB0232431 | CDS | 3394833 | 402 | + | 0.278607 |
DDB_G0285577 | DDB_G0285577 | DDB0232431 | CDS | 3396934 | 1275 | - | 0.219608 | |
DDB_G0285581 | DDB_G0285581 | DDB0232431 | CDS | 3402388 | 3645 | - | 0.249108 | |
DDB_G0285583 | DDB_G0285583 | DDB0232431 | CDS | 3409194 | 282 | - | 0.212766 | |
DDB_G0285585 | DDB_G0285585 | DDB0232431 | CDS | 3409926 | 2799 | - | 0.302608 | |
DDB_G0285587 | DDB_G0285587 | DDB0232431 | CDS | 3413814 | 1170 | - | 0.275214 | |
DDB_G0285595 | DDB_G0285595 | DDB0232431 | CDS | 3427765 | 573 | + | 0.249564 | |
DDB_G0285603 | DDB_G0285603 | DDB0232431 | CDS | 3435392 | 168 | + | 0.309524 | |
DDB_G0285605 | DDB_G0285605 | DDB0232431 | CDS | 3453352 | 1362 | - | 0.24743 | |
DDB_G0285607 | DDB_G0285607 | DDB0232431 | CDS | 3454900 | 1086 | - | 0.200737 | |
DDB_G0285609 | DDB_G0285609 | DDB0232431 | CDS | 3456501 | 2034 | - | 0.212881 | |
DDB_G0285611 | DDB_G0285611 | DDB0232431 | CDS | 3459087 | 1167 | + | 0.24593 | |
DDB_G0285613 | DDB_G0285613 | DDB0232431 | CDS | 3463966 | 1338 | + | 0.254111 | |
DDB_G0285617 | DDB_G0285617 | highly similar to | DDB0232431 | CDS | 3471998 | 1431 | + | 0.322851 |
DDB_G0285619 | DDB_G0285619 | DDB0232431 | CDS | 3474787 | 744 | + | 0.346774 | |
DDB_G0285621 | DDB_G0285621 | conserved Dictyostelium protein contains a putative signal sequence and one C-terminal transmembrane domain | DDB0232431 | CDS | 3475963 | 1665 | + | 0.282282 |
DDB_G0285623 | DDB_G0285623 | DDB0232431 | CDS | 3480410 | 801 | - | 0.273408 | |
DDB_G0285627 | DDB_G0285627 | DDB0232431 | CDS | 3486954 | 1422 | + | 0.268636 | |
DDB_G0285629 | DDB_G0285629 | DDB0232431 | CDS | 3488592 | 801 | - | 0.264669 | |
DDB_G0285631 | DDB_G0285631 | conserved Dictyostelium protein contains one putative transmembrane domain and an additional putative signal sequence | DDB0232431 | CDS | 3493674 | 1872 | - | 0.313034 |
DDB_G0285633 | DDB_G0285633 | DDB0232431 | CDS | 3496907 | 780 | + | 0.248718 | |
DDB_G0285635 | DDB_G0285635 | DDB0232431 | CDS | 3498174 | 3117 | - | 0.235804 | |
DDB_G0285639 | DDB_G0285639 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232431 | CDS | 3518236 | 462 | + | 0.25974 |
DDB_G0285645 | DDB_G0285645 | DDB0232431 | CDS | 3531932 | 957 | - | 0.256008 | |
DDB_G0285649 | DDB_G0285649 | the protein phosphatase 2C-related domain occurs in protein phosphatase 2C (PPC2) as well as in other proteins such as pyruvate dehydrogenase (lipoamide)]-phosphatase and adenylate cyclase | DDB0232431 | CDS | 3536200 | 1197 | - | 0.345029 |
DDB_G0285651 | DDB_G0285651 | DDB0232431 | CDS | 3544377 | 183 | - | 0.278689 | |
DDB_G0285653 | DDB_G0285653 | DDB0232431 | CDS | 3545567 | 1605 | + | 0.270405 | |
DDB_G0285655 | DDB_G0285655 | DDB0232431 | CDS | 3547353 | 3402 | - | 0.288948 | |
DDB_G0285657 | DDB_G0285657 | DDB0232431 | CDS | 3551340 | 1260 | + | 0.246032 | |
DDB_G0285659 | DDB_G0285659 | DDB0232431 | CDS | 3553333 | 630 | + | 0.185714 | |
DDB_G0285663 | DDB_G0285663 | conserved protozoa protein that are putative permeases involved in the transport of lipids contains 10 putative transmembrane domains | DDB0232431 | CDS | 3554545 | 3456 | - | 0.308738 |
DDB_G0285665 | DDB_G0285665 | DDB0232431 | CDS | 3559921 | 3723 | - | 0.235831 | |
DDB_G0285667 | DDB_G0285667 | DDB0232431 | CDS | 3564751 | 3594 | - | 0.238175 | |
DDB_G0285669 | DDB_G0285669 | DDB0232431 | CDS | 3569277 | 3756 | - | 0.236954 | |
DDB_G0285671 | DDB_G0285671 | DDB0232431 | CDS | 3574096 | 555 | - | 0.212613 | |
DDB_G0285673 | DDB_G0285673 | DDB0232431 | CDS | 3575375 | 255 | - | 0.270588 | |
DDB_G0285675 | DDB_G0285675 | DDB0232431 | CDS | 3576296 | 774 | + | 0.21447 | |
DDB_G0285677 | DDB_G0285677 | DDB0232431 | CDS | 3577440 | 4140 | + | 0.251932 | |
DDB_G0285681 | DDB_G0285681 | DDB0232431 | CDS | 3584332 | 708 | - | 0.289548 | |
DDB_G0285685 | DDB_G0285685 | DDB0232431 | CDS | 3590065 | 1152 | + | 0.265625 | |
DDB_G0285687 | DDB_G0285687 | DDB0232431 | CDS | 3591605 | 1089 | - | 0.24977 | |
DDB_G0285689 | DDB_G0285689 | DDB0232431 | CDS | 3593584 | 1908 | - | 0.22065 | |
DDB_G0285691 | DDB_G0285691 | DDB0232431 | CDS | 3596207 | 975 | + | 0.212308 | |
DDB_G0285693 | DDB_G0285693 | DDB0232431 | CDS | 3597715 | 2736 | + | 0.240863 | |
DDB_G0285695 | DDB_G0285695 | conserved in Dictyostelium contains weak match to FNIP repeat regions | DDB0232431 | CDS | 3600764 | 1572 | - | 0.276081 |
DDB_G0285697 | DDB_G0285697 | DDB0232431 | CDS | 3603409 | 1389 | + | 0.36933 | |
DDB_G0285699 | DDB_G0285699 | DDB0232431 | CDS | 3605127 | 1839 | + | 0.269712 | |
DDB_G0285701 | DDB_G0285701 | DDB0232431 | CDS | 3607268 | 2649 | + | 0.177803 | |
DDB_G0285705 | DDB_G0285705 | contains a RING-finger that is a specialised type of Zn-finger domain which in some cases has been shown to be involved in ubiquitin E3 ligase activity contains 14 putative transmembrane domains | DDB0232431 | CDS | 3615364 | 3267 | + | 0.296602 |
DDB_G0285707 | DDB_G0285707 | DDB0232431 | CDS | 3619487 | 2613 | + | 0.202067 | |
DDB_G0285709 | DDB_G0285709 | DDB0232431 | CDS | 3622848 | 1554 | + | 0.341055 | |
DDB_G0285711 | DDB_G0285711 | the phox domain has been associated with diverse functions such as cell signalling vesicular trafficking protein sorting and lipid modification and the C2 domain is a Ca2-dependent membrane-targeting module found in many cellular proteins involved in signal transduction or membrane trafficking similar to D. purpureum protein | DDB0232431 | CDS | 3625722 | 990 | + | 0.256566 |
DDB_G0285715 | DDB_G0285715 | DDB0232431 | CDS | 3630133 | 873 | - | 0.234822 | |
DDB_G0285721 | DDB_G0285721 | DDB0232431 | CDS | 3632780 | 213 | + | 0.2723 | |
DDB_G0285723 | DDB_G0285723 | DDB0232431 | CDS | 3633398 | 2304 | - | 0.224392 | |
DDB_G0285729 | DDB_G0285729 | DDB0232431 | CDS | 3466396 | 1875 | + | 0.301333 | |
DDB_G0285735 | DDB_G0285735 | DDB0232431 | CDS | 3214213 | 2166 | + | 0.220683 | |
DDB_G0285737 | DDB_G0285737 | DDB0232431 | CDS | 3228708 | 222 | - | 0.396396 | |
DDB_G0285739 | DDB_G0285739 | DDB0232431 | CDS | 3251052 | 999 | - | 0.25025 | |
DDB_G0285743 | DDB_G0285743 | DDB0232431 | CDS | 3271863 | 2334 | - | 0.222793 | |
DDB_G0285745_ps | DDB_G0285745 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 3279817 | 3096 | - | 0.295866 |
DDB_G0285749 | DDB_G0285749 | DDB0232431 | CDS | 3360351 | 1407 | + | 0.180526 | |
DDB_G0285751 | DDB_G0285751 | DDB0232431 | CDS | 3367805 | 2289 | + | 0.187418 | |
DDB_G0285753_ps | DDB_G0285753 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 3388026 | 975 | + | 0.29641 |
DDB_G0285755_ps | DDB_G0285755 | putative pseudogene similar to cyclin-like F-box containing proteins | DDB0232431 | CDS | 3393941 | 645 | - | 0.317829 |
DDB_G0285757_ps | DDB_G0285757 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3406976 | 126 | + | 0.277778 |
DDB_G0285761 | DDB_G0285761 | contains a growth factor receptor domain contains a predicted signal peptide and a putative C-terminal transmembrane domain | DDB0232431 | CDS | 3436262 | 1560 | - | 0.364744 |
DDB_G0285763 | DDB_G0285763 | DDB0232431 | CDS | 3439404 | 1161 | + | 0.282515 | |
DDB_G0285765 | DDB_G0285765 | DDB0232431 | CDS | 3445107 | 2346 | - | 0.252771 | |
DDB_G0285767 | DDB_G0285767 | DDB0232431 | CDS | 3448354 | 4086 | + | 0.254772 | |
DDB_G0285769 | DDB_G0285769 | highly similar to agglutinin domain-containing protein | DDB0232431 | CDS | 3460993 | 1425 | - | 0.311579 |
DDB_G0285771 | DDB_G0285771 | DDB0232431 | CDS | 3478635 | 1413 | + | 0.257608 | |
DDB_G0285773 | DDB_G0285773 | conserved Dictyostelium protein contains one putative transmembrane domain | DDB0232431 | CDS | 3482506 | 1851 | - | 0.310103 |
DDB_G0285775 | DDB_G0285775 | conserved Dictyostelium protein contains one putative transmembrane domain | DDB0232431 | CDS | 3490502 | 1758 | - | 0.300341 |
DDB_G0285779 | DDB_G0285779 | DDB0232431 | CDS | 3507070 | 174 | - | 0.321839 | |
DDB_G0285781 | DDB_G0285781 | DDB0232431 | CDS | 3508114 | 468 | + | 0.288462 | |
DDB_G0285787 | DDB_G0285787 | DDB0232431 | CDS | 3526607 | 207 | - | 0.130435 | |
DDB_G0285791 | DDB_G0285791 | DDB0232431 | CDS | 3503514 | 771 | + | 0.203632 | |
DDB_G0285795_RTE | DDB_G0285795 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3658983 | 900 | + | 0.4 |
DDB_G0285797 | DDB_G0285797 | DDB0232431 | CDS | 3638134 | 16644 | + | 0.222603 | |
DDB_G0285799 | DDB_G0285799 | DDB0232431 | CDS | 3663997 | 1467 | + | 0.220859 | |
DDB_G0285801 | DDB_G0285801 | DDB0232431 | CDS | 3665650 | 1035 | + | 0.310145 | |
DDB_G0285803 | DDB_G0285803 | belongs to the GNAT family homolog of S. cerevisiae MAK3 (maintenance of killer protein 3) | DDB0232431 | CDS | 3673056 | 558 | + | 0.250896 |
DDB_G0285805 | DDB_G0285805 | DDB0232431 | CDS | 3681493 | 2529 | + | 0.232503 | |
DDB_G0285807 | DDB_G0285807 | DDB0232431 | CDS | 3686003 | 735 | + | 0.220408 | |
DDB_G0285811 | DDB_G0285811 | DDB0232431 | CDS | 3686858 | 660 | - | 0.295455 | |
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_G0285819_ps | DDB_G0285819 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3700169 | 531 | + | 0.350282 |
DDB_G0285823 | DDB_G0285823 | DDB0232431 | CDS | 3703536 | 1521 | + | 0.331361 | |
DDB_G0285825 | DDB_G0285825 | DDB0232431 | CDS | 3705430 | 468 | - | 0.273504 | |
DDB_G0285827 | DDB_G0285827 | DDB0232431 | CDS | 3706474 | 1002 | + | 0.251497 | |
DDB_G0285831 | DDB_G0285831 | DDB0232431 | CDS | 3709396 | 522 | + | 0.260536 | |
DDB_G0285833 | DDB_G0285833 | DDB0232431 | CDS | 3684831 | 246 | + | 0.268293 | |
DDB_G0285835_RTE | DDB_G0285835 | 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 | 3661035 | 1953 | + | 0.343574 |
DDB_G0285837 | DDB_G0285837 | DDB0232431 | CDS | 3674059 | 6603 | - | 0.283356 | |
DDB_G0285839 | DDB_G0285839 | DDB0232431 | CDS | 3698143 | 1359 | + | 0.178808 | |
DDB_G0285841_RTE | DDB_G0285841 | 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 | 3710715 | 539 | + | 0.369202 |
DDB_G0285851 | DDB_G0285851 | DDB0232431 | CDS | 3717914 | 708 | + | 0.305085 | |
DDB_G0285861 | DDB_G0285861 | DDB0232431 | CDS | 3733661 | 1101 | - | 0.234332 | |
DDB_G0285863 | DDB_G0285863 | DDB0232431 | CDS | 3736082 | 210 | + | 0.309524 | |
DDB_G0285865 | DDB_G0285865 | DDB0232431 | CDS | 3737676 | 2679 | + | 0.196342 | |
DDB_G0285867 | DDB_G0285867 | DDB0232431 | CDS | 3740816 | 189 | - | 0.222222 | |
DDB_G0285869 | DDB_G0285869 | DDB0232431 | CDS | 3741819 | 1299 | - | 0.282525 | |
DDB_G0285871 | DDB_G0285871 | DDB0232431 | CDS | 3745815 | 588 | - | 0.290816 | |
DDB_G0285873 | DDB_G0285873 | DDB0232431 | CDS | 3747167 | 552 | + | 0.199275 | |
DDB_G0285875 | DDB_G0285875 | DDB0232431 | CDS | 3748302 | 6714 | + | 0.260798 | |
DDB_G0285879 | DDB_G0285879 | DDB0232431 | CDS | 3762999 | 1614 | - | 0.228005 | |
DDB_G0285885_ps | DDB_G0285885 | putative pseudogene very similar to large conserved family of Dictyostelium EGF-like domain-containing proteins | DDB0232431 | CDS | 3776481 | 1125 | - | 0.251556 |
DDB_G0285887 | DDB_G0285887 | DDB0232431 | CDS | 3778774 | 825 | + | 0.242424 | |
DDB_G0285889 | DDB_G0285889 | DDB0232431 | CDS | 3780014 | 780 | + | 0.265385 | |
DDB_G0285893 | DDB_G0285893 | similar to other Dictyostelium hypothetical proteins contains a putative signal peptide | DDB0232431 | CDS | 3788417 | 1101 | + | 0.326975 |
DDB_G0285897 | DDB_G0285897 | DDB0232431 | CDS | 3798877 | 1701 | + | 0.280423 | |
DDB_G0285899 | DDB_G0285899 | catalyzes the reaction L-alanine 2-oxoglutarate pyruvate L-glutamate | DDB0232431 | CDS | 3800826 | 1605 | - | 0.332087 |
DDB_G0285901 | DDB_G0285901 | contains a Vps53-like N-terminal domain Vps53 complexes with Vps52 and Vps54 to form a multi-subunit complex which might be involved in regulating membrane trafficking events | DDB0232431 | CDS | 3805604 | 2517 | + | 0.294795 |
DDB_G0285903 | DDB_G0285903 | DDB0232431 | CDS | 3808445 | 792 | - | 0.27399 | |
DDB_G0285905 | DDB_G0285905 | DDB0232431 | CDS | 3809647 | 843 | - | 0.204033 | |
DDB_G0285907 | DDB_G0285907 | related to the Ovarian Tumour (OTU) gene of Drosophila function is unknown but conserved cysteine and histidine and possibly the aspartate residues suggests that those not yet recognized as peptidases could possess cysteine protease activity | DDB0232431 | CDS | 3810828 | 1614 | - | 0.254027 |
DDB_G0285909 | DDB_G0285909 | catalyzes the removal of a phosphate group attached to a tyrosine residue ortholog of S. cerevisiae SIW14 that plays a role in actin filament organization and endocytosis | DDB0232431 | CDS | 3812938 | 546 | + | 0.287546 |
DDB_G0285911 | DDB_G0285911 | DDB0232431 | CDS | 3814964 | 3186 | + | 0.27307 | |
DDB_G0285913 | DDB_G0285913 | DDB0232431 | CDS | 3818293 | 3525 | - | 0.217305 | |
DDB_G0285917 | DDB_G0285917 | DDB0232431 | CDS | 3827611 | 618 | - | 0.300971 | |
DDB_G0285919 | DDB_G0285919 | homolog of human TIPRL and S. cerevisiae TIP41 (TAP42-interacting protein 1) TIP41 interacts with TAP42 and negatively regulates the TOR signaling pathway TIPRL is a putative MAPK-activating protein | DDB0232431 | CDS | 3828991 | 825 | - | 0.255758 |
DDB_G0285923 | DDB_G0285923 | DDB0232431 | CDS | 3831998 | 2388 | - | 0.356784 | |
DDB_G0285927 | DDB_G0285927 | similar to mammalian AASDHPPT that transfers the 4'-phosphopantetheine moiety from coenzyme A to a serine residue of a broad range of acceptors | DDB0232431 | CDS | 3839546 | 891 | - | 0.216611 |
DDB_G0285929 | DDB_G0285929 | DDB0232431 | CDS | 3845153 | 246 | - | 0.292683 | |
DDB_G0285933 | DDB_G0285933 | DDB0232431 | CDS | 3854532 | 2721 | + | 0.247336 | |
DDB_G0285935 | DDB_G0285935 | DDB0232431 | CDS | 3859998 | 465 | - | 0.236559 | |
DDB_G0285941 | DDB_G0285941 | DDB0232431 | CDS | 3873726 | 1392 | - | 0.255747 | |
DDB_G0285943 | DDB_G0285943 | ortholg of mammalian transmembrane protein 87A (TMEM87A) contains seven transmembrane domains | DDB0232431 | CDS | 3726406 | 1737 | - | 0.279217 |
DDB_G0285945 | DDB_G0285945 | DDB0232431 | CDS | 3759550 | 126 | + | 0.380952 | |
DDB_G0285951_RTE | DDB_G0285951 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3715691 | 1080 | - | 0.414815 |
DDB_G0285953 | DDB_G0285953 | DDB0232431 | CDS | 3743951 | 1569 | + | 0.281708 | |
DDB_G0285955 | DDB_G0285955 | DDB0232431 | CDS | 3767530 | 6150 | + | 0.218537 | |
DDB_G0285959 | DDB_G0285959 | DDB0232431 | CDS | 3842242 | 2313 | + | 0.280588 | |
DDB_G0285965 | DDB_G0285965 | contains a AWS domain (Associated With SET) but not SET domain contains a signal peptide and a C-terminal transmembrane domain | DDB0232431 | CDS | 3879686 | 753 | - | 0.245684 |
DDB_G0285967 | DDB_G0285967 | tensin family protein (related to the tumor suppressor PTEN) contains a a lipid phosphatase domain and a C2-like domain and a C-terminal LIM domain (absent from PTEN) | DDB0232431 | CDS | 3881074 | 2997 | - | 0.265933 |
DDB_G0285969 | DDB_G0285969 | putative cysteine protease member of the DJ-1ThiJPfpI family which includes human PARK7 associated with Parkinson's disease | DDB0232431 | CDS | 3885433 | 618 | - | 0.305825 |
DDB_G0285973 | DDB_G0285973 | DDB0232431 | CDS | 3894503 | 1404 | + | 0.289174 | |
DDB_G0285975 | DDB_G0285975 | DDB0232431 | CDS | 3896573 | 2754 | + | 0.265432 | |
DDB_G0285979_ps | DDB_G0285979 | putative pseudogene similar to Dictyostelium genes | DDB0232431 | CDS | 3899815 | 834 | + | 0.226619 |
DDB_G0285981 | DDB_G0285981 | similar to the vertebrate loss of heterozygosity 11 chromosomal region 2 gene A | DDB0232431 | CDS | 3901446 | 2496 | + | 0.276843 |
DDB_G0285983 | DDB_G0285983 | DDB0232431 | CDS | 3904475 | 633 | - | 0.339652 | |
DDB_G0285985 | DDB_G0285985 | contains 7 predicted transmembrane domains very similar to D. purpureum protein | DDB0232431 | CDS | 3906524 | 936 | - | 0.258547 |
DDB_G0285987 | DDB_G0285987 | DDB0232431 | CDS | 3908514 | 1293 | - | 0.2529 | |
DDB_G0285989 | DDB_G0285989 | DDB0232431 | CDS | 3911476 | 3705 | + | 0.239676 | |
DDB_G0285991 | DDB_G0285991 | DDB0232431 | CDS | 3915272 | 882 | - | 0.25737 | |
DDB_G0286001 | DDB_G0286001 | DDB0232431 | CDS | 3920731 | 366 | + | 0.262295 | |
DDB_G0286003 | DDB_G0286003 | DDB0232431 | CDS | 3925023 | 3213 | + | 0.304077 | |
DDB_G0286017_ps | DDB_G0286017 | putative pseudogene similar to ubiquitin domain-containing proteins especially | DDB0232431 | CDS | 3946482 | 564 | - | 0.308511 |
DDB_G0286021 | DDB_G0286021 | DDB0232431 | CDS | 3953660 | 657 | + | 0.305936 | |
DDB_G0286023 | DDB_G0286023 | DDB0232431 | CDS | 3954952 | 264 | - | 0.32197 | |
DDB_G0286025 | DDB_G0286025 | similar to bacterial cellulase celA expressed in pstAB pstA and pstO cells | DDB0232431 | CDS | 3964324 | 1653 | + | 0.351482 |
DDB_G0286029_ps | DDB_G0286029 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3967753 | 345 | - | 0.194203 |
DDB_G0286039 | DDB_G0286039 | DDB0232431 | CDS | 3986273 | 1083 | - | 0.288089 | |
DDB_G0286043 | DDB_G0286043 | DDB0232431 | CDS | 3989629 | 1887 | + | 0.225755 | |
DDB_G0286045 | DDB_G0286045 | one of many putative Dictyostelium potassium channels contains 3 pentapeptide repeats | DDB0232431 | CDS | 3992727 | 2226 | + | 0.27044 |
DDB_G0286047 | DDB_G0286047 | DDB0232431 | CDS | 3995156 | 198 | + | 0.282828 | |
DDB_G0286053 | DDB_G0286053 | DDB0232431 | CDS | 4001619 | 744 | - | 0.327957 | |
DDB_G0286055 | DDB_G0286055 | conserved in Dictyostelids contains also a SCP-like extracellular domain | DDB0232431 | CDS | 4003428 | 1293 | + | 0.317092 |
DDB_G0286061 | DDB_G0286061 | DDB0232431 | CDS | 4010233 | 1629 | - | 0.327808 | |
DDB_G0286063 | DDB_G0286063 | DDB0232431 | CDS | 4014322 | 939 | - | 0.280085 | |
DDB_G0286065 | DDB_G0286065 | DDB0232431 | CDS | 4016707 | 1554 | + | 0.276062 | |
DDB_G0286067 | DDB_G0286067 | DDB0232431 | CDS | 4019113 | 3573 | + | 0.240974 | |
DDB_G0286071 | DDB_G0286071 | DDB0232431 | CDS | 4026106 | 339 | - | 0.233038 | |
DDB_G0286073 | DDB_G0286073 | DDB0232431 | CDS | 4028900 | 1638 | + | 0.281441 | |
DDB_G0286079 | DDB_G0286079 | DDB0232431 | CDS | 4034365 | 1554 | - | 0.346847 | |
DDB_G0286081 | DDB_G0286081 | DDB0232431 | CDS | 4036084 | 462 | - | 0.25974 | |
DDB_G0286083 | DDB_G0286083 | the SWIM domain is found in variety of prokaryotic and eukaryotic proteins it is predicted to have DNA-binding and protein-protein interaction functions in different contexts similar to D. purpureum protein | DDB0232431 | CDS | 4038588 | 486 | + | 0.244856 |
DDB_G0286085 | DDB_G0286085 | DDB0232431 | CDS | 4039412 | 1188 | - | 0.222222 | |
DDB_G0286087 | DDB_G0286087 | DDB0232431 | CDS | 4041102 | 189 | + | 0.354497 | |
DDB_G0286089 | DDB_G0286089 | DDB0232431 | CDS | 4041536 | 1113 | - | 0.253369 | |
DDB_G0286091 | DDB_G0286091 | DDB0232431 | CDS | 4045722 | 4077 | + | 0.201128 | |
DDB_G0286093 | DDB_G0286093 | DDB0232431 | CDS | 4055353 | 477 | - | 0.32914 | |
DDB_G0286097_RTE | DDB_G0286097 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 3948218 | 1335 | + | 0.307865 |
DDB_G0286101_RTE | DDB_G0286101 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 3944436 | 860 | - | 0.40814 |
DDB_G0286103 | DDB_G0286103 | DDB0232431 | CDS | 3961629 | 480 | - | 0.245833 | |
DDB_G0286105 | DDB_G0286105 | DDB0232431 | CDS | 3980260 | 1230 | - | 0.233333 | |
DDB_G0286109 | DDB_G0286109 | similar to latrophilin-like receptor lrlA a G-protein-coupled receptor (GPCR) family protein contains four predicted transmembrane domains and is significantly shorter than lrlA | DDB0232431 | CDS | 3983688 | 603 | + | 0.28524 |
DDB_G0286113_ps | DDB_G0286113 | putative pseudogene fragment similar to | DDB0232431 | CDS | 4044149 | 603 | + | 0.233831 |
DDB_G0286115 | DDB_G0286115 | PIP5K catalyze the formation of phosphoinositol-45-bisphosphate via the phosphorylation of phosphatidylinositol-4-phosphate a precursor in the phosphinositide signaling pathway | DDB0232431 | CDS | 4051045 | 3816 | + | 0.277778 |
DDB_G0286129 | DDB_G0286129 | similar to mammalian F-boxWD repeat-containing protein 7 which is part to the E3 ubiquitin-protein ligase complex | DDB0232431 | CDS | 4060377 | 2220 | + | 0.263514 |
DDB_G0286133 | DDB_G0286133 | DDB0232431 | CDS | 4074134 | 996 | + | 0.257028 | |
DDB_G0286135 | DDB_G0286135 | DDB0232431 | CDS | 4075230 | 1239 | - | 0.256659 | |
DDB_G0286137 | DDB_G0286137 | ortholog of human HPS1 mutations in human HPS1 have been linked to Hermansky-Pudlak syndrome 1 | DDB0232431 | CDS | 4107413 | 3030 | + | 0.244884 |
DDB_G0286139 | DDB_G0286139 | DDB0232431 | CDS | 4110771 | 675 | - | 0.197037 | |
DDB_G0286141 | DDB_G0286141 | DDB0232431 | CDS | 4121354 | 291 | - | 0.329897 | |
DDB_G0286143 | DDB_G0286143 | DDB0232431 | CDS | 4126891 | 1035 | + | 0.28599 | |
DDB_G0286145 | DDB_G0286145 | DDB0232431 | CDS | 4130109 | 1128 | + | 0.25266 | |
DDB_G0286151 | DDB_G0286151 | similar to H. sapiens solute carrier family 2 facilitated glucose transporter member 1 (SLC2A1) | DDB0232431 | CDS | 4135325 | 1371 | + | 0.301969 |
DDB_G0286153 | DDB_G0286153 | DDB0232431 | CDS | 4137733 | 2769 | + | 0.216324 | |
DDB_G0286155_ps | DDB_G0286155 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 4140756 | 3867 | + | 0.221102 |
DDB_G0286157 | DDB_G0286157 | DDB0232431 | CDS | 4145918 | 1047 | + | 0.335244 | |
DDB_G0286161 | DDB_G0286161 | DDB0232431 | CDS | 4152139 | 1269 | + | 0.291568 | |
DDB_G0286163 | DDB_G0286163 | DDB0232431 | CDS | 4153623 | 1959 | - | 0.270036 | |
DDB_G0286165 | DDB_G0286165 | DDB0232431 | CDS | 4105304 | 1455 | + | 0.181443 | |
DDB_G0286167 | DDB_G0286167 | DDB0232431 | CDS | 4119612 | 1410 | - | 0.312057 | |
DDB_G0286173 | DDB_G0286173 | DDB0232431 | CDS | 4103161 | 1461 | + | 0.251882 | |
DDB_G0286175 | DDB_G0286175 | DDB0232431 | CDS | 4122107 | 1164 | - | 0.257732 | |
DDB_G0286177_ps | DDB_G0286177 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 4147632 | 2766 | + | 0.238612 |
DDB_G0286193 | DDB_G0286193 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | DDB0232431 | CDS | 4160391 | 174 | - | 0.356322 |
DDB_G0286197 | DDB_G0286197 | DDB0232431 | CDS | 4164497 | 1557 | + | 0.344894 | |
DDB_G0286201_ps | DDB_G0286201 | putative pseudogene similar to a Dictyostelid family of oxidoreductases including | DDB0232431 | CDS | 4168246 | 846 | + | 0.239953 |
DDB_G0286203 | DDB_G0286203 | DDB0232431 | CDS | 4169821 | 1026 | + | 0.24269 | |
DDB_G0286205 | DDB_G0286205 | DDB0232431 | CDS | 4173358 | 1683 | + | 0.312537 | |
DDB_G0286207 | DDB_G0286207 | DDB0232431 | CDS | 4176726 | 1320 | + | 0.282576 | |
DDB_G0286209 | DDB_G0286209 | DDB0232431 | CDS | 4178618 | 2700 | + | 0.236667 | |
DDB_G0286211 | DDB_G0286211 | DDB0232431 | CDS | 4189884 | 2700 | + | 0.23963 | |
DDB_G0286213_ps | DDB_G0286213 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 4193633 | 594 | + | 0.215488 |
DDB_G0286215_ps | DDB_G0286215 | putative pseudogene fragment very similar to | DDB0232431 | CDS | 4194622 | 408 | - | 0.183824 |
DDB_G0286217_ps | DDB_G0286217 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 4195341 | 1722 | + | 0.263066 |
DDB_G0286219 | DDB_G0286219 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog highly similar to mammalian TBP-associated factor 172 (TAF-172BTAF1) and yeast MOT1 | DDB0232431 | CDS | 4198019 | 6018 | + | 0.302758 |
DDB_G0286223 | DDB_G0286223 | contains up to 13 WD40 repeats very similar to D. purpureum protein | DDB0232431 | CDS | 4210540 | 2304 | + | 0.291667 |
DDB_G0286225 | DDB_G0286225 | similar to D. purpureum protein contains an N-terminal signal sequence | DDB0232431 | CDS | 4213306 | 393 | - | 0.24173 |
DDB_G0286227 | DDB_G0286227 | DDB0232431 | CDS | 4214477 | 1329 | - | 0.24304 | |
DDB_G0286231 | DDB_G0286231 | DDB0232431 | CDS | 4221429 | 267 | + | 0.322097 | |
DDB_G0286235 | DDB_G0286235 | DDB0232431 | CDS | 4229393 | 900 | - | 0.222222 | |
DDB_G0286237 | DDB_G0286237 | DDB0232431 | CDS | 4231345 | 2271 | + | 0.231616 | |
DDB_G0286239 | DDB_G0286239 | DDB0232431 | CDS | 4234344 | 1080 | + | 0.316667 | |
DDB_G0286243 | DDB_G0286243 | DDB0232431 | CDS | 4239634 | 3012 | + | 0.285193 | |
DDB_G0286245 | DDB_G0286245 | DDB0232431 | CDS | 4243076 | 1338 | + | 0.190583 | |
DDB_G0286249 | DDB_G0286249 | DDB0232431 | CDS | 4245484 | 1125 | - | 0.205333 | |
DDB_G0286255_ps | DDB_G0286255 | putative pseudogene very similar to | DDB0232431 | CDS | 4255797 | 240 | - | 0.325 |
DDB_G0286259 | DDB_G0286259 | protein conserved in bacteria and plants D. discoideum contains a second highly similar protein ( | DDB0232431 | CDS | 4259863 | 537 | + | 0.258845 |
DDB_G0286261 | DDB_G0286261 | DDB0232431 | CDS | 4260842 | 1266 | + | 0.269352 | |
DDB_G0286263 | DDB_G0286263 | DDB0232431 | CDS | 4262351 | 1776 | + | 0.197072 | |
DDB_G0286265 | DDB_G0286265 | DDB0232431 | CDS | 4264645 | 648 | + | 0.310185 | |
DDB_G0286267 | DDB_G0286267 | DDB0232431 | CDS | 4265901 | 639 | + | 0.29108 | |
DDB_G0286269 | DDB_G0286269 | DDB0232431 | CDS | 4267268 | 3276 | - | 0.284188 | |
DDB_G0286271 | DDB_G0286271 | DDB0232431 | CDS | 4271583 | 1893 | + | 0.255151 | |
DDB_G0286277 | DDB_G0286277 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 4282916 | 1716 | + | 0.322844 |
DDB_G0286279 | DDB_G0286279 | DDB0232431 | CDS | 4287649 | 5016 | - | 0.203748 | |
DDB_G0286281 | DDB_G0286281 | DDB0232431 | CDS | 4293465 | 1311 | - | 0.156369 | |
DDB_G0286283 | DDB_G0286283 | DDB0232431 | CDS | 4297454 | 924 | + | 0.199134 | |
DDB_G0286285 | DDB_G0286285 | DDB0232431 | CDS | 4298472 | 231 | - | 0.281385 | |
DDB_G0286287 | DDB_G0286287 | DDB0232431 | CDS | 4298931 | 1293 | - | 0.234339 | |
DDB_G0286289 | DDB_G0286289 | DDB0232431 | CDS | 4300974 | 1836 | + | 0.26634 | |
DDB_G0286291 | DDB_G0286291 | DDB0232431 | CDS | 4305951 | 648 | - | 0.259259 | |
DDB_G0286295 | DDB_G0286295 | DDB0232431 | CDS | 4317522 | 2910 | + | 0.306873 | |
DDB_G0286297 | DDB_G0286297 | DDB0232431 | CDS | 4322636 | 354 | - | 0.251412 | |
DDB_G0286299 | DDB_G0286299 | lysin-rich threonine-rich repetitive protein sequence | DDB0232431 | CDS | 4324089 | 1356 | + | 0.368732 |
DDB_G0286305 | DDB_G0286305 | DDB0232431 | CDS | 4332234 | 1017 | - | 0.360865 | |
DDB_G0286307 | DDB_G0286307 | DDB0232431 | CDS | 4334492 | 696 | + | 0.267241 | |
DDB_G0286309 | DDB_G0286309 | DDB0232431 | CDS | 4335795 | 1026 | + | 0.337232 | |
DDB_G0286311 | DDB_G0286311 | DDB0232431 | CDS | 4337464 | 4422 | + | 0.313433 | |
DDB_G0286313 | DDB_G0286313 | DDB0232431 | CDS | 4342189 | 744 | - | 0.198925 | |
DDB_G0286315 | DDB_G0286315 | conserved protein contains a signal peptide and 11 transmembrane domains | DDB0232431 | CDS | 4343761 | 2028 | + | 0.296844 |
DDB_G0286317 | DDB_G0286317 | DDB0232431 | CDS | 4186251 | 2646 | + | 0.238473 | |
DDB_G0286321 | DDB_G0286321 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 4294974 | 1674 | - | 0.295699 |
DDB_G0286323 | DDB_G0286323 | DDB0232431 | CDS | 4348548 | 4242 | + | 0.244932 | |
DDB_G0286325_ps | DDB_G0286325 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 4171531 | 354 | + | 0.262712 |
DDB_G0286327 | DDB_G0286327 | DDB0232431 | CDS | 4175501 | 759 | + | 0.210804 | |
DDB_G0286329 | DDB_G0286329 | DDB0232431 | CDS | 4182511 | 2691 | + | 0.239316 | |
DDB_G0286331 | DDB_G0286331 | DDB0232431 | CDS | 4205671 | 2769 | + | 0.283135 | |
DDB_G0286333 | DDB_G0286333 | DDB0232431 | CDS | 4247436 | 1866 | + | 0.219185 | |
DDB_G0286341 | DDB_G0286341 | highly similar to bacterial glutathione S-transferase catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232431 | CDS | 4285901 | 975 | + | 0.300513 |
DDB_G0286343 | DDB_G0286343 | DDB0232431 | CDS | 4316449 | 282 | + | 0.230496 | |
DDB_G0286347 | DDB_G0286347 | DDB0232431 | CDS | 4346922 | 1293 | + | 0.225058 | |
DDB_G0286351 | DDB_G0286351 | similar to the cudA transcriptional regulator REMI mutant forms aberrant fruiting bodies (see | DDB0232431 | CDS | 4526380 | 1824 | - | 0.279057 |
DDB_G0286361 | DDB_G0286361 | DDB0232431 | CDS | 4357070 | 1545 | - | 0.248544 | |
DDB_G0286363 | DDB_G0286363 | DDB0232431 | CDS | 4359667 | 1233 | + | 0.301703 | |
DDB_G0286365 | DDB_G0286365 | DDB0232431 | CDS | 4361252 | 2802 | + | 0.210564 | |
DDB_G0286367 | DDB_G0286367 | DDB0232431 | CDS | 4364169 | 1488 | - | 0.190188 | |
DDB_G0286369 | DDB_G0286369 | DDB0232431 | CDS | 4366711 | 2475 | - | 0.192323 | |
DDB_G0286373 | DDB_G0286373 | DDB0232431 | CDS | 4372108 | 1011 | + | 0.228487 | |
DDB_G0286375 | DDB_G0286375 | DDB0232431 | CDS | 4381593 | 1650 | + | 0.276364 | |
DDB_G0286377 | DDB_G0286377 | DDB0232431 | CDS | 4383620 | 2157 | - | 0.251275 | |
DDB_G0286379 | DDB_G0286379 | DDB0232431 | CDS | 4386579 | 1125 | + | 0.265778 | |
DDB_G0286381 | DDB_G0286381 | DDB0232431 | CDS | 4388115 | 1494 | - | 0.305221 | |
DDB_G0286383 | DDB_G0286383 | DDB0232431 | CDS | 4391636 | 708 | + | 0.237288 | |
DDB_G0286387 | DDB_G0286387 | DDB0232431 | CDS | 4394653 | 1521 | - | 0.279421 | |
DDB_G0286393 | DDB_G0286393 | DDB0232431 | CDS | 4403606 | 843 | - | 0.339265 | |
DDB_G0286397 | DDB_G0286397 | DDB0232431 | CDS | 4407676 | 1281 | - | 0.225605 | |
DDB_G0286401 | DDB_G0286401 | DDB0232431 | CDS | 4410583 | 1149 | - | 0.238468 | |
DDB_G0286405 | DDB_G0286405 | DDB0232431 | CDS | 4419066 | 966 | - | 0.161491 | |
DDB_G0286407_ps | DDB_G0286407 | putative pseudogene similar to family of D. discoideum genes including | DDB0232431 | CDS | 4424245 | 213 | + | 0.248826 |
DDB_G0286409 | DDB_G0286409 | DDB0232431 | CDS | 4425235 | 936 | + | 0.252137 | |
DDB_G0286413 | DDB_G0286413 | DDB0232431 | CDS | 4443400 | 903 | + | 0.299003 | |
DDB_G0286417 | DDB_G0286417 | DDB0232431 | CDS | 4458209 | 3048 | - | 0.271982 | |
DDB_G0286421 | DDB_G0286421 | DDB0232431 | CDS | 4468376 | 231 | + | 0.30303 | |
DDB_G0286423 | DDB_G0286423 | DDB0232431 | CDS | 4468953 | 1521 | - | 0.275477 | |
DDB_G0286429 | DDB_G0286429 | DDB0232431 | CDS | 4478853 | 828 | + | 0.27657 | |
DDB_G0286431 | DDB_G0286431 | contains a predicted signal peptide conserved in Dictyostelium | DDB0232431 | CDS | 4480269 | 1596 | - | 0.275689 |
DDB_G0286435_ps | DDB_G0286435 | putative pseudogene similar to upstream EGF-like domain-containing proteins | DDB0232431 | CDS | 4482591 | 2133 | - | 0.241444 |
DDB_G0286437 | DDB_G0286437 | DDB0232431 | CDS | 4495367 | 2814 | - | 0.25693 | |
DDB_G0286439 | DDB_G0286439 | DDB0232431 | CDS | 4502152 | 213 | + | 0.220657 | |
DDB_G0286441 | DDB_G0286441 | DDB0232431 | CDS | 4511137 | 1749 | - | 0.276158 | |
DDB_G0286443 | DDB_G0286443 | DDB0232431 | CDS | 4513273 | 675 | - | 0.244444 | |
DDB_G0286445 | DDB_G0286445 | DDB0232431 | CDS | 4518430 | 840 | + | 0.230952 | |
DDB_G0286447 | DDB_G0286447 | DDB0232431 | CDS | 4520436 | 1566 | - | 0.292465 | |
DDB_G0286449 | DDB_G0286449 | DDB0232431 | CDS | 4523376 | 2082 | - | 0.207493 | |
DDB_G0286459 | DDB_G0286459 | contains one C1 domain (protein kinase C conserved region 1) which is involved in phorbol esterdiacylglycerol binding contains one coiled-coil domain | DDB0232431 | CDS | 4373322 | 4896 | - | 0.252247 |
DDB_G0286463 | DDB_G0286463 | DDB0232431 | CDS | 4380273 | 318 | + | 0.367925 | |
DDB_G0286465 | DDB_G0286465 | DDB0232431 | CDS | 4420447 | 3666 | + | 0.261866 | |
DDB_G0286467 | DDB_G0286467 | DDB0232431 | CDS | 4434479 | 3645 | + | 0.273251 | |
DDB_G0286469 | DDB_G0286469 | DDB0232431 | CDS | 4466916 | 1269 | - | 0.153664 | |
DDB_G0286475 | DDB_G0286475 | DDB0232431 | CDS | 4504352 | 156 | - | 0.25641 | |
DDB_G0286477 | DDB_G0286477 | DDB0232431 | CDS | 4505969 | 165 | + | 0.181818 | |
DDB_G0286479 | DDB_G0286479 | DDB0232431 | CDS | 4506469 | 3504 | - | 0.257991 | |
DDB_G0286481 | DDB_G0286481 | putative protein serinethreonine kinase similar to casein kinase II the alpha chain of a ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | DDB0232431 | CDS | 4514745 | 1818 | - | 0.264026 |
DDB_G0286485 | DDB_G0286485 | DDB0232431 | CDS | 4551311 | 1197 | + | 0.235589 | |
DDB_G0286487 | DDB_G0286487 | conserved protein ortholog of mammalian GPR108 contains a signal peptide and 7 transmembrane domains | DDB0232431 | CDS | 4553269 | 1350 | - | 0.275556 |
DDB_G0286489 | DDB_G0286489 | DDB0232431 | CDS | 4557644 | 2172 | + | 0.219613 | |
DDB_G0286493 | DDB_G0286493 | DDB0232431 | CDS | 4549634 | 156 | - | 0.275641 | |
DDB_G0286497_RTE | DDB_G0286497 | ORF2 protein fragment of tRNA-specific non-long terminal repeat retrotransposon TRE3-A refer to GenBank AF134169 for full-length consensus element | DDB0232431 | CDS | 4563823 | 360 | - | 0.330556 |
DDB_G0286503_RTE | DDB_G0286503 | ORF of tRNA-specific long terminal repeat retrotransposon DGLT-A refer to AF298204 for full-length element | DDB0232431 | CDS | 4566580 | 1558 | + | 0.290757 |
DDB_G0286505 | DDB_G0286505 | DDB0232431 | CDS | 4570772 | 1404 | + | 0.255698 | |
DDB_G0286507 | DDB_G0286507 | contains an RNA recognition motif (RRM) a putative RNA binding domain and a thioesterase domain | DDB0232431 | CDS | 4572284 | 1899 | - | 0.296998 |
DDB_G0286511 | DDB_G0286511 | similar to human ubiquitin-conjugating enzyme E2 J2 (UBE2J2) and yeast ubiquitin-conjugating 6 (UBC6) | DDB0232431 | CDS | 4575968 | 726 | - | 0.311295 |
DDB_G0286513 | DDB_G0286513 | DDB0232431 | CDS | 4577203 | 1683 | + | 0.236482 | |
DDB_G0286515 | DDB_G0286515 | DDB0232431 | CDS | 4579041 | 3036 | - | 0.244401 | |
DDB_G0286523 | DDB_G0286523 | DDB0232431 | CDS | 4588407 | 1884 | + | 0.306794 | |
DDB_G0286527_ps | DDB_G0286527 | putative pseudogene similar to a Dictyostelid family of putative SAM-dependent methyltransferases including | DDB0232431 | CDS | 4594246 | 561 | - | 0.247772 |
DDB_G0286531_RTE | DDB_G0286531 | ORF2 protein encoding endonuclease and reverse transcriptase of tRNA-specific non-long terminal repeat retrotransposon TRE5-B refer to GenBank AF298209 for consensus full-length element | DDB0232431 | CDS | 4596405 | 1318 | - | 0.383156 |
DDB_G0286533 | DDB_G0286533 | DDB0232431 | CDS | 4607142 | 2370 | + | 0.302532 | |
DDB_G0286537 | DDB_G0286537 | DDB0232431 | CDS | 4631120 | 1092 | - | 0.333333 | |
DDB_G0286539 | DDB_G0286539 | has limited similarity to mammalian p53 binding protein 1 (e.g. human TP53BP1) which plays a role in the response to DNA damagebrbr bCommunity annotation:b DDB G0286539 is similar (first blast hit both ways) to metazoan p53 binding protein. The homology is mostly within the BRCT domain but several additional small islands of homology are recognized by Blast2Sequences scattered along most of the length of the molecules. p53 binding protein aka 53BP1 is thought to mediate between sensors of double strand breaks and effectors of repair processes cell cycle arrest and apoptosis (see Fitzgerald et al Biochemical Society Transactions 37 897-904 (2009).br The Dicty gene is overexpressed fourfold (p2e-17)in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes whose products have roles in cell cycle progression are overexpressed in this strain this includes a number of genes for replication-coupled DNA repair (Doquang et al in preparation) and more specifical | DDB0232431 | CDS | 4632777 | 2724 | + | 0.270558 |
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_G0286547_RTE | DDB_G0286547 | 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 | 4637483 | 2117 | - | 0.344355 |
DDB_G0286565 | DDB_G0286565 | DDB0232431 | CDS | 4641695 | 396 | + | 0.257576 | |
DDB_G0286567 | DDB_G0286567 | DDB0232431 | CDS | 4642679 | 1848 | + | 0.237554 | |
DDB_G0286569 | DDB_G0286569 | DDB0232431 | CDS | 4644643 | 345 | - | 0.173913 | |
DDB_G0286571 | DDB_G0286571 | DDB0232431 | CDS | 4645438 | 285 | + | 0.189474 | |
DDB_G0286575 | DDB_G0286575 | similar to retinol dehydrogenase and eukaryotic proteins of the short chain dehydrogenasesreductases family | DDB0232431 | CDS | 4647468 | 873 | + | 0.218786 |
DDB_G0286577 | DDB_G0286577 | DDB0232431 | CDS | 4648951 | 483 | + | 0.258799 | |
DDB_G0286581 | DDB_G0286581 | DDB0232431 | CDS | 4651768 | 915 | + | 0.285246 | |
DDB_G0286583 | DDB_G0286583 | DDB0232431 | CDS | 4653100 | 2169 | + | 0.262333 | |
DDB_G0286585 | DDB_G0286585 | DDB0232431 | CDS | 4657116 | 414 | + | 0.311594 | |
DDB_G0286587 | DDB_G0286587 | DDB0232431 | CDS | 4659532 | 414 | + | 0.318841 | |
DDB_G0286589 | DDB_G0286589 | DDB0232431 | CDS | 4670086 | 825 | - | 0.220606 | |
DDB_G0286591 | DDB_G0286591 | DDB0232431 | CDS | 4672737 | 2370 | - | 0.225738 | |
DDB_G0286593 | DDB_G0286593 | DDB0232431 | CDS | 4675755 | 1425 | + | 0.188772 | |
DDB_G0286595 | DDB_G0286595 | DDB0232431 | CDS | 4677268 | 1824 | - | 0.209978 | |
DDB_G0286597 | DDB_G0286597 | DDB0232431 | CDS | 4679470 | 525 | + | 0.260952 | |
DDB_G0286601 | DDB_G0286601 | DDB0232431 | CDS | 4687512 | 648 | - | 0.302469 | |
DDB_G0286603 | DDB_G0286603 | catalyzes the reaction L-glutamine D-fructose 6-phosphate L-glutamate D-glucosamine 6-phosphate | DDB0232431 | CDS | 4689118 | 1950 | - | 0.334359 |
DDB_G0286605 | DDB_G0286605 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | DDB0232431 | CDS | 4695789 | 909 | - | 0.275028 |
DDB_G0286611 | DDB_G0286611 | DDB0232431 | CDS | 4704484 | 3666 | - | 0.267321 | |
DDB_G0286613 | DDB_G0286613 | DDB0232431 | CDS | 4708744 | 7692 | - | 0.303952 | |
DDB_G0286615 | DDB_G0286615 | DDB0232431 | CDS | 4721350 | 453 | - | 0.273731 | |
DDB_G0286619 | DDB_G0286619 | DDB0232431 | CDS | 4727396 | 1386 | - | 0.345599 | |
DDB_G0286625 | DDB_G0286625 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232431 | CDS | 4749168 | 1566 | - | 0.308429 |
DDB_G0286627 | DDB_G0286627 | putative protein serinethreonine kinase belongs to the STE group the kinase domain is similar to yeast BCK1 a mitogen-activated protein (MAP) kinase kinase kinase | DDB0232431 | CDS | 4756048 | 2016 | - | 0.251984 |
DDB_G0286629 | DDB_G0286629 | DDB0232431 | CDS | 4758841 | 312 | + | 0.224359 | |
DDB_G0286635 | DDB_G0286635 | DDB0232431 | CDS | 4764695 | 198 | - | 0.237374 | |
DDB_G0286637 | DDB_G0286637 | bifunctional enzyme catalyzes the reactions 510-methylenetetrahydrofolate 3-methyl-2-oxobutanoate tetrahydrofolate 2-dehydropantoate and (R)-pantoate NADP 2-dehydropantoate NADPH H | DDB0232431 | CDS | 4765267 | 2502 | - | 0.289369 |
DDB_G0286639 | DDB_G0286639 | DDB0232431 | CDS | 4771485 | 1107 | - | 0.307136 | |
DDB_G0286641 | DDB_G0286641 | putative GTPase that has high similarity to NOG1GTPBP4 GTPases which in S. cerevisiae associates with free 60S ribosomal subunits in the nucleolus this D. discoideumprotein is only about half the length and lacks the NOG1 C-terminal domain | DDB0232431 | CDS | 4774707 | 1044 | + | 0.198276 |
DDB_G0286649 | DDB_G0286649 | DDB0232431 | CDS | 4789671 | 867 | - | 0.314879 | |
DDB_G0286655 | DDB_G0286655 | DDB0232431 | CDS | 4795283 | 4173 | - | 0.22358 | |
DDB_G0286657 | DDB_G0286657 | contains a predicted signal peptide and two transmembrane domains highly similar to the neighboring gene | DDB0232431 | CDS | 4800131 | 303 | - | 0.306931 |
DDB_G0286659 | DDB_G0286659 | contains a predicted signal peptide and two transmembrane domains highly similar to the neighboring gene | DDB0232431 | CDS | 4800814 | 318 | - | 0.292453 |
DDB_G0286661 | DDB_G0286661 | bCommunity annotation:b DDB G0286661 is weakly similar to the histone chaperone chromatin-assembly factor caf1. DDB G0286661 and another caf1-related gene DDB_G0269800 are overexpressed in the Dicty rblA-null (fourfold and sevenfold respectively). Most genes associated with cell cycle progression are overexpressed in this strain. In addition DDB_G0269800 has a PIP (PCNA_interacting) domain (QKKLTSFF) as does human caf1. These observations support the idea that DDB_G0269800 is actually involved in replication-coupled chromatin assembly. br Harry MacWilliams September 2009 brbr bNote:b Do not confuse this gene with | DDB0232431 | CDS | 4801886 | 1485 | + | 0.261279 |
DDB_G0286667 | DDB_G0286667 | highly similar to | DDB0232431 | CDS | 4812413 | 267 | - | 0.348315 |
DDB_G0286669 | DDB_G0286669 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub | DDB0232431 | CDS | 4814848 | 2004 | - | 0.335329 |
DDB_G0286673 | DDB_G0286673 | DDB0232431 | CDS | 4821852 | 3297 | + | 0.234152 | |
DDB_G0286675 | DDB_G0286675 | DDB0232431 | CDS | 4825895 | 222 | - | 0.396396 | |
DDB_G0286677 | DDB_G0286677 | DDB0232431 | CDS | 4835533 | 4689 | + | 0.307955 | |
DDB_G0286679 | DDB_G0286679 | acyl carrier protein (ACP) is an essential cofactor in the synthesis of fatty acids in bacteria and plants in addition ACP is involved in many other reactions that require acyl transfer steps such as the synthesis of polyketide antibiotics phosphopantetheine is the prosthetic group of ACPs in some multienzyme complexes where it serves as a 'swinging arm' for the attachment of activated fatty acid and amino-acid groups | DDB0232431 | CDS | 4840734 | 258 | - | 0.232558 |
DDB_G0286681 | DDB_G0286681 | DDB0232431 | CDS | 4841268 | 2442 | - | 0.304668 | |
DDB_G0286683 | DDB_G0286683 | DDB0232431 | CDS | 4844701 | 618 | + | 0.190939 | |
DDB_G0286685 | DDB_G0286685 | DDB0232431 | CDS | 4845533 | 204 | - | 0.279412 | |
DDB_G0286687 | DDB_G0286687 | DDB0232431 | CDS | 4848740 | 132 | - | 0.19697 | |
DDB_G0286689 | DDB_G0286689 | DDB0232431 | CDS | 4852457 | 195 | + | 0.271795 | |
DDB_G0286691 | DDB_G0286691 | DDB0232431 | CDS | 4852997 | 408 | + | 0.25 | |
DDB_G0286695 | DDB_G0286695 | DDB0232431 | CDS | 4856852 | 735 | - | 0.285714 | |
DDB_G0286697 | DDB_G0286697 | DDB0232431 | CDS | 4858448 | 3414 | - | 0.227006 | |
DDB_G0286699 | DDB_G0286699 | DDB0232431 | CDS | 4862450 | 747 | + | 0.301205 | |
DDB_G0286701 | DDB_G0286701 | DDB0232431 | CDS | 4868445 | 1659 | + | 0.229656 | |
DDB_G0286707 | DDB_G0286707 | DDB0232431 | CDS | 4875042 | 2937 | + | 0.243105 | |
DDB_G0286713 | DDB_G0286713 | DDB0232431 | CDS | 4882439 | 693 | - | 0.277056 | |
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_G0286729 | DDB_G0286729 | DDB0232431 | CDS | 4902848 | 786 | + | 0.328244 | |
DDB_G0286731 | DDB_G0286731 | DDB0232431 | CDS | 4904757 | 543 | + | 0.292818 | |
DDB_G0286735 | DDB_G0286735 | DDB0232431 | CDS | 4909097 | 2085 | + | 0.317026 | |
DDB_G0286737 | DDB_G0286737 | DDB0232431 | CDS | 4911744 | 1629 | + | 0.206262 | |
DDB_G0286739 | DDB_G0286739 | DDB0232431 | CDS | 4913488 | 591 | - | 0.182741 | |
DDB_G0286741 | DDB_G0286741 | DDB0232431 | CDS | 4914735 | 1260 | + | 0.307937 | |
DDB_G0286745 | DDB_G0286745 | DDB0232431 | CDS | 4920445 | 1449 | - | 0.285714 | |
DDB_G0286749 | DDB_G0286749 | DDB0232431 | CDS | 4924314 | 2643 | + | 0.259554 | |
DDB_G0286751 | DDB_G0286751 | DDB0232431 | CDS | 4927372 | 540 | - | 0.157407 | |
DDB_G0286755 | DDB_G0286755 | catalyzes the reaction NADPH 78-dihydrofolate NADP tetrahydrofolate in folate biosynthesis and formylTHF biosynthesis | DDB0232431 | CDS | 4931449 | 615 | - | 0.260163 |
DDB_G0286757 | DDB_G0286757 | DDB0232431 | CDS | 4933318 | 1227 | + | 0.321108 | |
DDB_G0286759 | DDB_G0286759 | similar to the mammalian KRTCAP2 (keratinocytes-associated protein 2) contains 4 putative transmembrane domains | DDB0232431 | CDS | 4935044 | 384 | - | 0.294271 |
DDB_G0286761 | DDB_G0286761 | DDB0232431 | CDS | 4936897 | 915 | + | 0.239344 | |
DDB_G0286763 | DDB_G0286763 | DDB0232431 | CDS | 4937865 | 1977 | - | 0.195245 | |
DDB_G0286765 | DDB_G0286765 | similar to BCS1 a mitochondrial chaperone required for assembly of cytochrome BC(1) complex expressed in pstA and pstO cells and in the upper and lower cups during culmination | DDB0232431 | CDS | 4940455 | 1725 | + | 0.276522 |
DDB_G0286767 | DDB_G0286767 | DDB0232431 | CDS | 4943773 | 255 | + | 0.313726 | |
DDB_G0286769 | DDB_G0286769 | DDB0232431 | CDS | 4945147 | 624 | - | 0.211538 | |
DDB_G0286775_ps | DDB_G0286775 | putative pseudogene fragment similar to gene | DDB0232431 | CDS | 4660931 | 444 | + | 0.198198 |
DDB_G0286779 | DDB_G0286779 | weakly similar to hssA2C7E family protein has a similar gene structure with a N terminal 13 nt exon | DDB0232431 | CDS | 4846920 | 195 | - | 0.230769 |
DDB_G0286781 | DDB_G0286781 | DDB0232431 | CDS | 4849724 | 195 | - | 0.282051 | |
DDB_G0286783 | DDB_G0286783 | DDB0232431 | CDS | 4929423 | 129 | - | 0.170543 | |
DDB_G0286787 | DDB_G0286787 | DDB0232431 | CDS | 4655553 | 639 | - | 0.214397 | |
DDB_G0286789 | DDB_G0286789 | DDB0232431 | CDS | 4662033 | 624 | + | 0.328526 | |
DDB_G0286791 | DDB_G0286791 | DDB0232431 | CDS | 4668476 | 1419 | + | 0.188865 | |
DDB_G0286793 | DDB_G0286793 | DDB0232431 | CDS | 4671665 | 576 | + | 0.291667 | |
DDB_G0286795 | DDB_G0286795 | DDB0232431 | CDS | 4684750 | 2076 | - | 0.186416 | |
DDB_G0286799 | DDB_G0286799 | DDB0232431 | CDS | 4720383 | 183 | - | 0.229508 | |
DDB_G0286801 | DDB_G0286801 | DDB0232431 | CDS | 4733206 | 282 | + | 0.255319 | |
DDB_G0286805 | DDB_G0286805 | DDB0232431 | CDS | 4742371 | 2757 | - | 0.261153 | |
DDB_G0286807 | DDB_G0286807 | DDB0232431 | CDS | 4751624 | 2067 | - | 0.195936 | |
DDB_G0286809 | DDB_G0286809 | DDB0232431 | CDS | 4768925 | 1560 | - | 0.253205 | |
DDB_G0286811 | DDB_G0286811 | DDB0232431 | CDS | 4773313 | 1191 | - | 0.25105 | |
DDB_G0286813_ps | DDB_G0286813 | putative pseudogene fragment similar to large EGF domain-containing proteins such as | DDB0232431 | CDS | 4811831 | 327 | + | 0.229358 |
DDB_G0286815_ps | DDB_G0286815 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 4826644 | 246 | + | 0.247967 |
DDB_G0286817 | DDB_G0286817 | DDB0232431 | CDS | 4863743 | 3132 | - | 0.24106 | |
DDB_G0286821 | DDB_G0286821 | DDB0232431 | CDS | 4918278 | 2088 | + | 0.198755 | |
DDB_G0286823_RTE | DDB_G0286823 | 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 | 4639700 | 1392 | - | 0.355603 |
DDB_G0286827_ps | DDB_G0286827 | putative pseudogene similar to | DDB0232431 | CDS | 4953029 | 363 | - | 0.261708 |
DDB_G0286829 | DDB_G0286829 | DDB0232431 | CDS | 4954349 | 585 | + | 0.217094 | |
DDB_G0286831 | DDB_G0286831 | DDB0232431 | CDS | 4955377 | 324 | - | 0.29321 | |
DDB_G0286833 | DDB_G0286833 | DDB0232431 | CDS | 4956036 | 987 | - | 0.316109 | |
DDB_G0286835 | DDB_G0286835 | DDB0232431 | CDS | 4957742 | 1602 | + | 0.182896 | |
DDB_G0286841 | DDB_G0286841 | member of the AGC kinase group similar to the kinase domains of MAST kinases (Microtubule-Associated SerineThreonine kinase) | DDB0232431 | CDS | 4966020 | 1389 | - | 0.218143 |
DDB_G0286845 | DDB_G0286845 | DDB0232431 | CDS | 4972112 | 885 | + | 0.277966 | |
DDB_G0286847 | DDB_G0286847 | DDB0232431 | CDS | 4973256 | 2538 | - | 0.215524 | |
DDB_G0286849 | DDB_G0286849 | similar to bacterial short-chain dehydrogenasereductase family proteins and human RDH8 (retinol dehydrogenase 8) | DDB0232431 | CDS | 4977120 | 870 | - | 0.28046 |
DDB_G0286853 | DDB_G0286853 | DDB0232431 | CDS | 4990193 | 714 | + | 0.277311 | |
DDB_G0286861 | DDB_G0286861 | DDB0232431 | CDS | 4978558 | 885 | + | 0.275706 | |
DDB_G0286863_RTE | DDB_G0286863 | DDB0232431 | CDS | 4996972 | 1293 | + | 0.288476 | |
DDB_G0286865 | DDB_G0286865 | DDB0232431 | CDS | 5001179 | 171 | - | 0.245614 | |
DDB_G0286867 | DDB_G0286867 | conserved Dictyostelium protein contains a putative N-terminal signal sequence a C-terminal anchoring transmembrane domain and one EGF-like domain | DDB0232431 | CDS | 5001922 | 4224 | - | 0.253788 |
DDB_G0286869 | DDB_G0286869 | DDB0232431 | CDS | 5007468 | 1266 | + | 0.259084 | |
DDB_G0286871 | DDB_G0286871 | DDB0232431 | CDS | 5008976 | 573 | + | 0.233857 | |
DDB_G0286873 | DDB_G0286873 | DDB0232431 | CDS | 5009906 | 1077 | + | 0.257196 | |
DDB_G0286877 | DDB_G0286877 | DDB0232431 | CDS | 5013005 | 4725 | - | 0.205291 | |
DDB_G0286879 | DDB_G0286879 | DDB0232431 | CDS | 5018337 | 561 | - | 0.210339 | |
DDB_G0286881 | DDB_G0286881 | DDB0232431 | CDS | 5019240 | 2853 | + | 0.278654 | |
DDB_G0286883 | DDB_G0286883 | DDB0232431 | CDS | 5022922 | 573 | - | 0.277487 | |
DDB_G0286885 | DDB_G0286885 | DDB0232431 | CDS | 5024349 | 1764 | + | 0.384354 | |
DDB_G0286887 | DDB_G0286887 | DDB0232431 | CDS | 5026472 | 372 | - | 0.271505 | |
DDB_G0286891 | DDB_G0286891 | DDB0232431 | CDS | 5031762 | 3546 | + | 0.227862 | |
DDB_G0286897 | DDB_G0286897 | DDB0232431 | CDS | 5040461 | 4215 | - | 0.308422 | |
DDB_G0286899 | DDB_G0286899 | DDB0232431 | CDS | 5047649 | 3129 | + | 0.230745 | |
DDB_G0286901 | DDB_G0286901 | DDB0232431 | CDS | 5050966 | 2181 | - | 0.200367 | |
DDB_G0286911 | DDB_G0286911 | DDB0232431 | CDS | 5061049 | 1503 | + | 0.29674 | |
DDB_G0286913 | DDB_G0286913 | DDB0232431 | CDS | 5070335 | 2940 | + | 0.187755 | |
DDB_G0286915 | DDB_G0286915 | DDB0232431 | CDS | 5073666 | 237 | - | 0.409283 | |
DDB_G0286917 | DDB_G0286917 | DDB0232431 | CDS | 5074484 | 1932 | + | 0.201346 | |
DDB_G0286921 | DDB_G0286921 | DDB0232431 | CDS | 5081040 | 1605 | - | 0.28162 | |
DDB_G0286923 | DDB_G0286923 | DDB0232431 | CDS | 5085448 | 1203 | - | 0.335827 | |
DDB_G0286925 | DDB_G0286925 | DDB0232431 | CDS | 5087989 | 990 | + | 0.363636 | |
DDB_G0286929 | DDB_G0286929 | DDB0232431 | CDS | 5090123 | 651 | + | 0.27957 | |
DDB_G0286931 | DDB_G0286931 | DDB0232431 | CDS | 5091515 | 15669 | + | 0.264535 | |
DDB_G0286933 | DDB_G0286933 | DDB0232431 | CDS | 5107749 | 2073 | + | 0.239267 | |
DDB_G0286935 | DDB_G0286935 | DDB0232431 | CDS | 5114045 | 1605 | + | 0.189408 | |
DDB_G0286937 | DDB_G0286937 | DDB0232431 | CDS | 5117554 | 126 | + | 0.222222 | |
DDB_G0286939 | DDB_G0286939 | DDB0232431 | CDS | 5118438 | 834 | + | 0.252998 | |
DDB_G0286941 | DDB_G0286941 | DDB0232431 | CDS | 5119924 | 2415 | + | 0.291511 | |
DDB_G0286943 | DDB_G0286943 | DDB0232431 | CDS | 5123987 | 156 | + | 0.275641 | |
DDB_G0286947 | DDB_G0286947 | DDB0232431 | CDS | 5126978 | 5022 | + | 0.258662 | |
DDB_G0286949 | DDB_G0286949 | DDB0232431 | CDS | 5132153 | 285 | + | 0.252632 | |
DDB_G0286951 | DDB_G0286951 | DDB0232431 | CDS | 5136274 | 3333 | + | 0.259826 | |
DDB_G0286955 | DDB_G0286955 | DDB0232431 | CDS | 5145533 | 1125 | - | 0.277333 | |
DDB_G0286957 | DDB_G0286957 | DDB0232431 | CDS | 5147352 | 249 | - | 0.39759 | |
DDB_G0286959 | DDB_G0286959 | DDB0232431 | CDS | 5154310 | 1710 | - | 0.261404 | |
DDB_G0286963 | DDB_G0286963 | DDB0232431 | CDS | 5110525 | 2316 | + | 0.269862 | |
DDB_G0286965 | DDB_G0286965 | DDB0232431 | CDS | 5117185 | 300 | + | 0.243333 | |
DDB_G0286969 | DDB_G0286969 | DDB0232431 | CDS | 5063512 | 6240 | + | 0.356731 | |
DDB_G0286973 | DDB_G0286973 | DDB0232431 | CDS | 5142082 | 1713 | - | 0.253357 | |
DDB_G0286975_ps | DDB_G0286975 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 5144135 | 969 | - | 0.283798 |
DDB_G0286977 | DDB_G0286977 | DDB0232431 | CDS | 5148727 | 1143 | - | 0.276465 | |
DDB_G0286979 | DDB_G0286979 | DDB0232431 | CDS | 5150412 | 1884 | - | 0.277601 | |
DDB_G0286981 | DDB_G0286981 | DDB0232431 | CDS | 5158045 | 5043 | + | 0.17906 | |
DDB_G0286983 | DDB_G0286983 | DDB0232431 | CDS | 5163425 | 1503 | - | 0.302728 | |
DDB_G0286987_RTE | DDB_G0286987 | ORF1 of tRNA-specific non-long terminal repeat retrotransposon TRE5-A formerly known as DRE | DDB0232431 | CDS | 5166703 | 1335 | - | 0.307116 |
DDB_G0286989 | DDB_G0286989 | DDB0232431 | CDS | 5175729 | 402 | + | 0.310945 | |
DDB_G0286991 | DDB_G0286991 | DDB0232431 | CDS | 5177493 | 1380 | + | 0.33913 | |
DDB_G0286993 | DDB_G0286993 | DDB0232431 | CDS | 5169198 | 1524 | - | 0.211942 | |
DDB_G0286995 | DDB_G0286995 | DDB0232431 | CDS | 5179444 | 1834 | + | 0.23337 | |
DDB_G0286999 | DDB_G0286999 | DDB0232431 | CDS | 5181860 | 1561 | + | 0.305573 | |
DDB_G0287001 | DDB_G0287001 | member of the TKL (tyrosine kinase-like) group contains zinc-binding LIM domain | DDB0232431 | CDS | 5188585 | 1953 | - | 0.28213 |
DDB_G0287003 | DDB_G0287003 | DDB0232431 | CDS | 5191304 | 1254 | - | 0.334928 | |
DDB_G0287005 | DDB_G0287005 | similar to the H. sapiens eukaryotic translation initiation factor 3 subunit M (EIF3M) | DDB0232431 | CDS | 5193960 | 1206 | + | 0.27529 |
DDB_G0287013 | DDB_G0287013 | DDB0232431 | CDS | 5205106 | 1026 | - | 0.346979 | |
DDB_G0287015 | DDB_G0287015 | DDB0232431 | CDS | 5207077 | 414 | + | 0.345411 | |
DDB_G0287017 | DDB_G0287017 | belongs to the HAD-like hydrolase superfamily similar to human HDHD3 (haloacid dehalogenase-like hydrolase domain-containing protein 3) | DDB0232431 | CDS | 5207898 | 858 | - | 0.221445 |
DDB_G0287023 | DDB_G0287023 | DDB0232431 | CDS | 5202818 | 669 | + | 0.139013 | |
DDB_G0287025 | DDB_G0287025 | DDB0232431 | CDS | 5203841 | 984 | + | 0.251016 | |
DDB_G0287027 | DDB_G0287027 | DDB0232431 | CDS | 5209927 | 3015 | - | 0.242454 | |
DDB_G0287037 | DDB_G0287037 | DDB0232431 | CDS | 5215181 | 978 | + | 0.274029 | |
DDB_G0287039 | DDB_G0287039 | DDB0232431 | CDS | 5219424 | 1599 | - | 0.202001 | |
DDB_G0287041 | DDB_G0287041 | DDB0232431 | CDS | 5221229 | 1827 | + | 0.181719 | |
DDB_G0287043 | DDB_G0287043 | DDB0232431 | CDS | 5225371 | 1083 | + | 0.263158 | |
DDB_G0287047 | DDB_G0287047 | DDB0232431 | CDS | 5227447 | 249 | - | 0.405622 | |
DDB_G0287051 | DDB_G0287051 | DDB0232431 | CDS | 5231470 | 777 | + | 0.235521 | |
DDB_G0287059 | DDB_G0287059 | DDB0232431 | CDS | 5272697 | 2523 | - | 0.200159 | |
DDB_G0287061 | DDB_G0287061 | contains a Rab GTPase domain but due to its predicted molecular weight (1836 amino acids) it is not a small GTPase | DDB0232431 | CDS | 5278698 | 5511 | + | 0.245328 |
DDB_G0287063 | DDB_G0287063 | DDB0232431 | CDS | 5285069 | 1296 | + | 0.266975 | |
DDB_G0287065 | DDB_G0287065 | DDB0232431 | CDS | 5286829 | 480 | + | 0.258333 | |
DDB_G0287067 | DDB_G0287067 | DDB0232431 | CDS | 5289082 | 393 | - | 0.29771 | |
DDB_G0287069 | DDB_G0287069 | DDB0232431 | CDS | 5289970 | 1167 | + | 0.264782 | |
DDB_G0287071 | DDB_G0287071 | DDB0232431 | CDS | 5291519 | 1101 | + | 0.248865 | |
DDB_G0287073 | DDB_G0287073 | contains a single HMG12 box | DDB0232431 | CDS | 5293321 | 1053 | + | 0.296296 |
DDB_G0287075 | DDB_G0287075 | DDB0232431 | CDS | 5294660 | 1419 | - | 0.317829 | |
DDB_G0287077 | DDB_G0287077 | DDB0232431 | CDS | 5299968 | 1221 | + | 0.22932 | |
DDB_G0287079 | DDB_G0287079 | DDB0232431 | CDS | 5302047 | 1824 | + | 0.247259 | |
DDB_G0287081 | DDB_G0287081 | DDB0232431 | CDS | 5304055 | 840 | - | 0.24881 | |
DDB_G0287083 | DDB_G0287083 | DDB0232431 | CDS | 5305570 | 1755 | + | 0.211966 | |
DDB_G0287085 | DDB_G0287085 | there is a paralog of this gene | DDB0232431 | CDS | 5307684 | 948 | - | 0.257384 |
DDB_G0287089 | DDB_G0287089 | DDB0232431 | CDS | 5311879 | 489 | - | 0.255624 | |
DDB_G0287091 | DDB_G0287091 | DDB0232431 | CDS | 5313189 | 492 | - | 0.288618 | |
DDB_G0287093 | DDB_G0287093 | DDB0232431 | CDS | 5314330 | 471 | - | 0.248408 | |
DDB_G0287097 | DDB_G0287097 | contains 4 FNIP repeats conserved in Dictyostelium | DDB0232431 | CDS | 5338338 | 1497 | + | 0.263193 |
DDB_G0287099 | DDB_G0287099 | DDB0232431 | CDS | 5339911 | 669 | - | 0.227205 | |
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_G0287105 | DDB_G0287105 | DDB0232431 | CDS | 5213175 | 1323 | - | 0.250189 | |
DDB_G0287107 | DDB_G0287107 | DDB0232431 | CDS | 5223614 | 1176 | - | 0.261054 | |
DDB_G0287111 | DDB_G0287111 | DDB0232431 | CDS | 5266193 | 765 | + | 0.235294 | |
DDB_G0287113 | DDB_G0287113 | DDB0232431 | CDS | 5275365 | 2301 | - | 0.280748 | |
DDB_G0287115 | DDB_G0287115 | DDB0232431 | CDS | 5287659 | 1137 | - | 0.284081 | |
DDB_G0287117_TE | DDB_G0287117 | putative DNA transposon Tdd-4 refer to U57081 for full-length consensus element | DDB0232431 | CDS | 5315241 | 3150 | - | 0.275238 |
DDB_G0287123 | DDB_G0287123 | DDB0232431 | CDS | 5341430 | 5022 | + | 0.175627 | |
DDB_G0287129 | DDB_G0287129 | DDB0232431 | CDS | 5352426 | 420 | - | 0.292857 | |
DDB_G0287133 | DDB_G0287133 | DDB0232431 | CDS | 5355378 | 2250 | - | 0.211556 | |
DDB_G0287135 | DDB_G0287135 | DDB0232431 | CDS | 5361475 | 1197 | - | 0.185464 | |
DDB_G0287139 | DDB_G0287139 | DDB0232431 | CDS | 5368411 | 816 | + | 0.280637 | |
DDB_G0287145 | DDB_G0287145 | DDB0232431 | CDS | 5377683 | 213 | - | 0.211268 | |
DDB_G0287149 | DDB_G0287149 | similar to mammalian DNA polymerase kappa (POLK) and E. coli dinB a translesion DNA repair polymerase | DDB0232431 | CDS | 5382189 | 1554 | - | 0.240026 |
DDB_G0287151 | DDB_G0287151 | similar to retinol dehydrogenase and eukaryotic short chain dehydrogenasesreductases family proteins | DDB0232431 | CDS | 5393798 | 930 | - | 0.224731 |
DDB_G0287153 | DDB_G0287153 | DDB0232431 | CDS | 5400400 | 480 | + | 0.308333 | |
DDB_G0287155 | DDB_G0287155 | DDB0232431 | CDS | 5407048 | 495 | + | 0.161616 | |
DDB_G0287157 | DDB_G0287157 | DDB0232431 | CDS | 5407710 | 4575 | - | 0.261639 | |
DDB_G0287161 | DDB_G0287161 | DDB0232431 | CDS | 5415608 | 1059 | - | 0.266289 | |
DDB_G0287163 | DDB_G0287163 | DDB0232431 | CDS | 5419077 | 819 | - | 0.191697 | |
DDB_G0287165 | DDB_G0287165 | similar to spastin (spastic paraplegia 4 protein) a mammalian ATP-dependent microtubule severing protein | DDB0232431 | CDS | 5420537 | 1968 | + | 0.269817 |
DDB_G0287167 | DDB_G0287167 | DDB0232431 | CDS | 5422690 | 4314 | - | 0.248725 | |
DDB_G0287169 | DDB_G0287169 | DDB0232431 | CDS | 5428138 | 693 | - | 0.265512 | |
DDB_G0287171 | DDB_G0287171 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232431 | CDS | 5429343 | 5619 | + | 0.2399 |
DDB_G0287173_ps | DDB_G0287173 | putative pseudogene similar to protein kinases but does not contain the consensus sequences required for kinase function | DDB0232431 | CDS | 5444697 | 834 | - | 0.27458 |
DDB_G0287175_ps | DDB_G0287175 | putative pseudogene similar to a D. discoideum gene family including | DDB0232431 | CDS | 5376601 | 354 | + | 0.285311 |
DDB_G0287177 | DDB_G0287177 | DDB0232431 | CDS | 5445848 | 339 | - | 0.277286 | |
DDB_G0287179 | DDB_G0287179 | DDB0232431 | CDS | 5446279 | 294 | - | 0.20068 | |
DDB_G0287183_ps | DDB_G0287183 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 5446818 | 720 | + | 0.323611 |
DDB_G0287185 | DDB_G0287185 | contains one ML (MD-2-related lipid recognition) domain similar to fungal proteins of the NPC2 family contains a predicted signal peptide | DDB0232431 | CDS | 5448496 | 456 | - | 0.263158 |
DDB_G0287187 | DDB_G0287187 | DDB0232431 | CDS | 5359561 | 1791 | + | 0.156896 | |
DDB_G0287189 | DDB_G0287189 | DDB0232431 | CDS | 5363024 | 624 | - | 0.192308 | |
DDB_G0287191 | DDB_G0287191 | DDB0232431 | CDS | 5366531 | 219 | + | 0.493151 | |
DDB_G0287193 | DDB_G0287193 | DDB0232431 | CDS | 5388100 | 3177 | + | 0.251495 | |
DDB_G0287195 | DDB_G0287195 | DDB0232431 | CDS | 5391671 | 1593 | + | 0.244821 | |
DDB_G0287201 | DDB_G0287201 | DDB0232431 | CDS | 5401496 | 1863 | - | 0.243156 | |
DDB_G0287205 | DDB_G0287205 | DDB0232431 | CDS | 5405589 | 168 | - | 0.27381 | |
DDB_G0287207 | DDB_G0287207 | large protein (1685 amino acids) containing a Rab domain Rab small GTPases are usually around 200 amino acids in length | DDB0232431 | CDS | 5437470 | 5058 | + | 0.217477 |
DDB_G0294559 | DDB_G0294559 | DDB0232431 | CDS | 1421546 | 1047 | - | 0.281757 | |
DDB_G0294563 | DDB_G0294563 | EGF domain similar to the EGF-like repeats found in subtilisin-like serine peptidase tenascin X and WIF (Wnt inhibitory factor) | DDB0232431 | CDS | 2282608 | 2265 | - | 0.236645 |
DDB_G0294589 | DDB_G0294589 | DDB0232431 | CDS | 4603487 | 882 | + | 0.276644 | |
DDB_G0294593 | DDB_G0294593 | DDB0232431 | CDS | 470714 | 624 | - | 0.219551 | |
DDB_G0294595 | DDB_G0294595 | multi-domain protein the TPR superhelical structures present a surface that is well suited to binding large substrates such as proteins and nucleic acids | DDB0232431 | CDS | 1785353 | 1542 | + | 0.217899 |
DDB_G0294621 | DDB_G0294621 | contains three Sel1-like repeats which are related to tetratricopeptide (TPR) repeats | DDB0232431 | CDS | 86151 | 1854 | + | 0.304207 |
DDB_G0294631 | DDB_G0294631 | similar to Entamoeba histolytica XP_650568 contains no conserved functional domains | DDB0232431 | CDS | 4158602 | 765 | - | 0.267974 |
DDB_G0295481_ps | DDB_G0295481 | putative pseudogene fragment very similar to Dictyostelium ppiD | DDB0232431 | CDS | 944514 | 243 | + | 0.283951 |
DDB_G0295485 | DDB_G0295485 | DDB0232431 | CDS | 3666930 | 5076 | - | 0.310481 | |
DDB_G0295671 | DDB_G0295671 | DDB0232431 | CDS | 4703129 | 1083 | - | 0.237304 | |
DDB_G0295717 | DDB_G0295717 | DDB0232431 | CDS | 2373104 | 2466 | - | 0.242092 | |
DDB_G0295719 | DDB_G0295719 | DDB0232431 | CDS | 2369310 | 1851 | + | 0.415451 | |
DDB_G0295733 | DDB_G0295733 | DDB0232431 | CDS | 4157569 | 480 | - | 0.277083 | |
DDB_G0295781 | DDB_G0295781 | weakly similar to S. cerevisiae DUG3 involved in degradation of glutathione (GSH) and other peptides containing a gamma-glu-X bond in an alternative pathway to GSH degradation by gamma-glutamyl transpeptidase | DDB0232431 | CDS | 4542261 | 1125 | - | 0.330667 |
DDB_G0295783 | DDB_G0295783 | DDB0232431 | CDS | 4538199 | 156 | - | 0.24359 | |
DDB_G0295785 | DDB_G0295785 | DDB0232431 | CDS | 4536016 | 1086 | + | 0.252302 | |
DDB_G0295789 | DDB_G0295789 | shares a short region of similarity with GRP1 (general receptor for phosphoinositides 1)-associated scaffold protein contains one transmembrane domain | DDB0232431 | CDS | 3213388 | 480 | - | 0.279167 |
DDB_G0295823 | DDB_G0295823 | DDB0232431 | CDS | 3559137 | 111 | + | 0.369369 | |
DDB_G0304561 | DDB_G0304561 | similar to solute carrier family 35 member E4 (SLC35E4) proteins contains 10 predicted transmembrane domains | DDB0232431 | CDS | 2797226 | 1476 | + | 0.278455 |
DDB_G0304886 | DDB_G0304886 | DDB0232431 | CDS | 5267330 | 372 | + | 0.317204 | |
DDB_G0307042 | DDB_G0307042 | DDB0232431 | CDS | 4491401 | 2778 | - | 0.257019 | |
DDB_G0307043 | DDB_G0307043 | DDB0232431 | CDS | 4487639 | 2757 | - | 0.228509 | |
DDB_G0347783 | DDB_G0347783 | DDB0232431 | CDS | 989598 | 174 | + | 0.281609 | |
DDB_G0348373 | DDB_G0348373 | DDB0232431 | CDS | 2073118 | 135 | - | 0.281481 | |
DDB_G0348374 | DDB_G0348374 | DDB0232431 | CDS | 2071986 | 195 | - | 0.333333 | |
DDB_G0348834 | DDB_G0348834 | DDB0232431 | CDS | 3284415 | 4749 | + | 0.217098 | |
DDB_G0348835 | DDB_G0348835 | DDB0232431 | CDS | 3289563 | 4740 | + | 0.221097 | |
DDB_G0349073_ps | DDB_G0349073 | putative pseudogene fragment similar to a D. discoideum gene family including | DDB0232431 | CDS | 241054 | 1427 | - | 0.28171 |
DDB_G0349530 | DDB_G0349530 | DDB0232431 | CDS | 1603328 | 2448 | - | 0.33701 | |
DG2044 | DDB_G0285423 | DDB0232431 | CDS | 3504616 | 1833 | + | 0.228587 | |
Dd5P2 | DDB_G0284187 | DDB0232431 | CDS | 1813905 | 5403 | - | 0.294281 | |
H1 | DDB_G0285319 | linker histone H1H5 family protein plays a role in formation of 30 nm chromatin fiber | DDB0232431 | CDS | 3145643 | 543 | + | 0.401473 |
H2AZ | DDB_G0286747 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H2B | DDB0232431 | CDS | 4922308 | 432 | - | 0.293981 |
H2Bv3 | DDB_G0286509 | DDB0232431 | CDS | 4575107 | 465 | + | 0.393548 | |
aass | DDB_G0284835 | bifunctional enzyme: lysine-ketoglutarate reductase (lysine alpha-ketoglutarate NADPH saccharopine) and saccharopine dehydrogenase (catalyzes the reaction saccharopine L-glutamate 2-aminoadipate 6-semialdehyde NADH Hsupsup) there is a related monofunctional saccharopine reductase | DDB0232431 | CDS | 2456087 | 2730 | + | 0.342125 |
abcA10 | DDB_G0283387 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232431 | CDS | 620087 | 2664 | + | 0.267643 |
abcB6 | DDB_G0282931 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232431 | CDS | 9046 | 2037 | - | 0.300442 |
abcC5 | DDB_G0286559 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232431 | CDS | 4828905 | 4383 | - | 0.281314 |
abcC8 | DDB_G0284867 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232431 | CDS | 2579815 | 4782 | - | 0.31765 |
abcC9 | DDB_G0285165 | full transporter consisting of two ABC domains and two transmembrane domains | DDB0232431 | CDS | 2942482 | 4038 | + | 0.23477 |
abcF1 | DDB_G0285997 | DDB0232431 | CDS | 3922084 | 2127 | - | 0.381758 | |
abcF2 | DDB_G0284047 | DDB0232431 | CDS | 1542455 | 1782 | - | 0.335578 | |
abcH4 | DDB_G0283479 | DDB0232431 | CDS | 768532 | 2649 | - | 0.254058 | |
abkD | DDB_G0284897 | atypical protein serinethreonine kinase contains ABC1 kinase (protein kinase-like) domain yeast ABC1 essential for the electron transfer in the BC(1) complex E.coli homolog required for ubiquinone biosynthesis | DDB0232431 | CDS | 2611033 | 2088 | - | 0.273946 |
acadsb | DDB_G0282967 | mammalian ACADSB has highest activity toward short branched chain acyl-CoA derivative such as (s)-2-methylbutyryl-CoA isobutyryl-CoA and 2-methylhexanoyl-CoA as well as toward short straight chain butyryl-CoA and hexanoyl-CoA in human defects in ACADSB cause shortbranched-chain acyl-CoA dehydrogenase deficiency (SBCADD) also called 2-methylbutyryl-CoA dehydrogenase deficiency or 2-methylbutyryl glycinuria | DDB0232431 | CDS | 70875 | 1242 | + | 0.329308 |
acmsd | DDB_G0286525 | catalyzes the reaction: 2-amino-3-(3-oxoprop-1-en-1-yl)but-2-enedioate 2-aminomuconate semialdehyde CO2 | DDB0232431 | CDS | 4592587 | 1080 | + | 0.340741 |
acoA | DDB_G0283261 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2subbr bNomenclature conflict:b Do not confuse this gene with aco the oxidoreductase or aco1 and aco2 the aconitases | DDB0232431 | CDS | 449907 | 2064 | + | 0.307655 |
act29 | DDB_G0286893 | has 56 | DDB0232431 | CDS | 5035700 | 1164 | - | 0.265464 |
adcD | DDB_G0286693 | DDB0232431 | CDS | 4853622 | 2358 | - | 0.242578 | |
adk | DDB_G0286057 | catalyzes the reaction ATP adenosine ADP AMP | DDB0232431 | CDS | 4005558 | 1023 | + | 0.396872 |
adkA | DDB_G0283805 | catalyzes the reaction AMP ATP ADP ADP in de novo DNA synthesis | DDB0232431 | CDS | 1124176 | 831 | - | 0.32491 |
agps | DDB_G0286183 | catalyses the reaction: 1-acyl-glycerone 3-phosphate a long-chain alcohol 1-alkyl-glycerone 3-phosphate a long-chain acid anion in ether lipid biosynthesis mutations in the human ortholog AGPS causes peroxisomal disorders | DDB0232431 | CDS | 4303510 | 1836 | + | 0.345316 |
agtA | DDB_G0283005 | likely catalyzes the alpha addition of galactose to Fuc-Gal-GlcNAc-HyPro143-Skp1 (FpaAFpaB) | DDB0232431 | CDS | 143819 | 1947 | - | 0.214689 |
aifB | DDB_G0285005 | similar to H. sapiens AIFM2 a caspase-independent mitochondrial effector of apoptotic cell death | DDB0232431 | CDS | 2794340 | 1164 | - | 0.287801 |
aifC | DDB_G0285003 | similar to H. sapiens AIFM2 a caspase-independent mitochondrial effector of apoptotic cell death | DDB0232431 | CDS | 2790283 | 1227 | - | 0.235534 |
aifD | DDB_G0286241 | similar to H. sapiens AIFM2 a caspase-independent mitochondrial effector of apoptotic cell death | DDB0232431 | CDS | 4236868 | 1194 | + | 0.329983 |
alg1 | DDB_G0286011 | CAZy family GT33 catalyzes N-linked mannosylation | DDB0232431 | CDS | 3960039 | 1482 | + | 0.279352 |
alg6 | DDB_G0283841 | CAZy family GT57 catalyzes N-linked glucosylation | DDB0232431 | CDS | 1202486 | 1557 | + | 0.242775 |
alkB | DDB_G0285575 | DDB0232431 | CDS | 3395637 | 1182 | + | 0.307953 | |
alrB | DDB_G0285053 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2618768 | 936 | - | 0.318376 |
alrD | DDB_G0285027 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2833891 | 873 | - | 0.266896 |
alrE | DDB_G0285025 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2832495 | 870 | - | 0.301149 |
alrF | DDB_G0285023 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2831142 | 918 | - | 0.238562 |
alyL | DDB_G0286229 | amoeba lysozyme family protein (aly) but divergent compared to alyA-D | DDB0232431 | CDS | 4218365 | 1719 | + | 0.401396 |
anapc1 | DDB_G0285349 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232431 | CDS | 3135215 | 6810 | - | 0.22467 |
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 |
anapc4 | DDB_G0285223 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232431 | CDS | 3010019 | 2514 | + | 0.234686 |
anapc6 | DDB_G0286233 | putative ortholog of cdc16 a conserved protein containing several TPRs (tetratrico peptide repeats) | DDB0232431 | CDS | 4222260 | 2598 | - | 0.234411 |
ap4b1 | DDB_G0283319 | putative ortholog of H. sapiens AP4B1 member of a complex that mediates protein sorting | DDB0232431 | CDS | 525048 | 2517 | + | 0.247517 |
ap4s1 | DDB_G0284905 | DDB0232431 | CDS | 2625777 | 420 | - | 0.240476 | |
aplA | DDB_G0284043 | DDB0232431 | CDS | 1521553 | 1569 | + | 0.303378 | |
aplB | DDB_G0286651 | DDB0232431 | CDS | 4791776 | 1005 | + | 0.371144 | |
aplC | DDB_G0286561 | DDB0232431 | CDS | 4793559 | 474 | + | 0.303797 | |
aplN | DDB_G0284339 | DDB0232431 | CDS | 1855900 | 882 | + | 0.263039 | |
aplO | DDB_G0286653 | DDB0232431 | CDS | 4794405 | 555 | + | 0.27027 | |
arfrp1 | DDB_G0283631 | DDB0232431 | CDS | 888563 | 651 | + | 0.271889 | |
argC | DDB_G0286257 | contains both N-acetyl-gamma-glutamyl-phosphate reductase and acetylglutamate kinase activities catalyzes the reactions N-acetyl-L-glutamate 5-semialdehyde NADPsupsup phosphate N-acetyl-L-glutamyl 5-phosphate NADPH Hsupsup bandb ATP N-acetyl-L-glutamate ADP N-acetyl-L-glutamate 5-phosphate | DDB0232431 | CDS | 4256396 | 2544 | - | 0.331368 |
arl8 | DDB_G0283525 | DDB0232431 | CDS | 729167 | 558 | + | 0.284946 | |
arpC | DDB_G0283755 | component of the Dictyostelium Arp2Arp3 complex | DDB0232431 | CDS | 1135639 | 1257 | - | 0.381862 |
arpF | DDB_G0287007 | ortholog of the conserved actin related protein ARP6 in mammalian called ACTR6 a putative component of a chromatin-remodeling complex | DDB0232431 | CDS | 5196102 | 1473 | + | 0.260014 |
asf1 | DDB_G0285513 | DDB0232431 | CDS | 3334165 | 465 | - | 0.301075 | |
asns | DDB_G0286059 | catalyzes the reaction Hsub2subO L-glutamine L-aspartate ATP - L-glutamate L-asparagine pyrophosphate AMP | DDB0232431 | CDS | 4007481 | 1674 | - | 0.367981 |
atg12 | DDB_G0282929 | DDB0232431 | CDS | 160759 | 375 | - | 0.269333 | |
atg18 | DDB_G0285375 | ortholog of the conserved fungi ATG18 and very similar to the mammalian WIPI2 and WIPI1 proteins contains 2 WD-40 repeats | DDB0232431 | CDS | 3197399 | 1119 | - | 0.2958 |
atg8 | DDB_G0286191 | DDB0232431 | CDS | 4321108 | 369 | - | 0.319783 | |
atg9 | DDB_G0285323 | Dictyostelium homolog of yeast atg9 involved in phagocytosis growth development and the response to pathogen bacteria contains 6 predicted transmembrane domains | DDB0232431 | CDS | 3194807 | 2100 | + | 0.279048 |
athl1 | DDB_G0287109 | DDB0232431 | CDS | 5232785 | 2142 | - | 0.294118 | |
atox1 | DDB_G0284221 | DDB0232431 | CDS | 1705613 | 204 | - | 0.289216 | |
atp5O | DDB_G0283283 | DDB0232431 | CDS | 456147 | 891 | + | 0.342312 | |
atp7a | DDB_G0284141 | DDB0232431 | CDS | 1486936 | 2958 | - | 0.315416 | |
bcaA | DDB_G0285509 | catalyzes the reaction 2-keto-3-methyl-valerate L-glutamate L-iso-leucine | DDB0232431 | CDS | 3329709 | 1137 | + | 0.35708 |
bdp1 | DDB_G0283405 | TFIIIB subunit interacts with the non LTR retrotransposon TRE5-Abrbr bCommunity annotation:b Bdp1 is a subunit of TFIIIB a factor necessary for the initiation of transcription by RNA polIII and thus for the production of tRNA and several other small RNAs. TFIIIB is overexpressed in a wide variety of cancers see White Oncogene 23 3208-3216 (2004). In healthy cells TFIIIB interacts with and is inhibited by the tumor-suppressor Rb. Interestingly bdp1 is overexpressed (threefold p6e-10) in a Dicty strain in which the rb-like gene rblA has been disrupted. The TFIIIB-Rb antagonism thus predates the development of organisms that have tumors. The function of this interaction remains to be explained. Harry MacWilliams September 2009 | DDB0232431 | CDS | 618312 | 1374 | - | 0.275837 |
bkdA | DDB_G0286335 | catalyzes the reaction 3-methyl-2-oxobutanoate lipoamide S-(2-methylpropanoyl)-dihydrolipoamide COsub2sub E1 component of branched-chain keto acid dehydrogenase | DDB0232431 | CDS | 4250107 | 1326 | + | 0.337858 |
bloc1s7 | DDB_G0283001 | ortholog of human SNAPINBLOC1S7 a component of the BLOC-1 complex that is required for normal biogenesis of lysosome-related organelles | DDB0232431 | CDS | 139924 | 669 | - | 0.275037 |
btg | DDB_G0285069 | interacts with RblA to control cell fate commitment during development homolog of mammalian BTG2 | DDB0232431 | CDS | 2748189 | 1272 | + | 0.327044 |
bxdc5 | DDB_G0285829 | ortholog of S. cerevisiae RPF1 and H. sapiens BXDC5 a nucleolar protein involved in the assembly of the large ribosomal subunit | DDB0232431 | CDS | 3708077 | 954 | - | 0.292453 |
bzpL | DDB_G0284023 | DDB0232431 | CDS | 1449089 | 1593 | - | 0.252354 | |
bzpN | DDB_G0286411 | DDB0232431 | CDS | 4426368 | 3000 | - | 0.301667 | |
cad3 | DDB_G0285817 | very similar to cadA (cad1) a calcium-binding cell-cell adhesion molecule | DDB0232431 | CDS | 3695620 | 642 | - | 0.366044 |
cadA | DDB_G0285793 | calcium-dependent cell-cell adhesion protein lacks a signal sequence and is transported through the contractile vacuole to the plasma membrane for either secretion or cell surface presentation abcb4 has been identified as the anchor on the membranebr bNomenclature conflict:b Do not confuse the cadA gene encoding a calcium-dependent cell adhesion molecule with the cadA locus associated with resistance to cadmium ( | DDB0232431 | CDS | 3656149 | 642 | + | 0.333333 |
cbpB | DDB_G0283533 | DDB0232431 | CDS | 829856 | 423 | + | 0.283688 | |
cbpC | DDB_G0283613 | DDB0232431 | CDS | 904975 | 501 | - | 0.287425 | |
cbpD1 | DDB_G0283153 | contains four EF-hands expressed in post-aggregation stage of development | DDB0232431 | CDS | 347658 | 489 | - | 0.292434 |
cbpD2 | DDB_G0283083 | contains four EF-hands expressed in post-aggregation stage of development | DDB0232431 | CDS | 279175 | 948 | - | 0.299578 |
cbpD3_ps | DDB_G0285475 | putative pseudogene very similar to Dicyostelium cbpD1 and cbpD2 but missing their conserved N-terminal 15 amino acids | DDB0232431 | CDS | 3277201 | 438 | - | 0.289954 |
cbpF | DDB_G0283611 | DDB0232431 | CDS | 899345 | 525 | - | 0.312381 | |
cbpG | DDB_G0283609 | DDB0232431 | CDS | 901731 | 510 | - | 0.296078 | |
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 |
cdc20 | DDB_G0285601 | ortholog of CDC20 a cell-cycle regulated activator of anaphase-promoting complexcyclosome (APCC) which is required for metaphaseanaphase transition directs ubiquitination of mitotic cyclins | DDB0232431 | CDS | 3433247 | 1500 | + | 0.346 |
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 |
cdipt | DDB_G0284857 | similar to human CDIPT and S. cerevisiae PIS1 (phosphatidylinositol synthase) catalyzes the reaction CDP-diacylglycerol myo-inositol CMP phosphatidyl-1D-myo-inositol contains 4 putative transmembrane domains | DDB0232431 | CDS | 2547724 | 624 | + | 0.298077 |
cdk11 | DDB_G0283279 | very similar to human CDL1 (PITSLRE serinethreonine-protein kinase CDC2L1) which appears to play multiple roles in cell cycle progression cytokinesis and apoptosis predicted to interact with | DDB0232431 | CDS | 446640 | 1077 | - | 0.338904 |
cdk7 | DDB_G0285417 | putative ortholog of CDK7 and CTK1 which phosphorylates the C-terminal repeated domain of the RNA polymerase II large subunit predicted to be activated by | DDB0232431 | CDS | 3627427 | 1083 | + | 0.307479 |
cepD | DDB_G0283111 | DDB0232431 | CDS | 261195 | 1959 | - | 0.244002 | |
cepH | DDB_G0285313 | DDB0232431 | CDS | 3082073 | 5757 | - | 0.266806 | |
cf60 | DDB_G0284363 | regulates aggregate size and number component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) similar to histidine acid phosphatase but does not possess phosphatase activity | DDB0232431 | CDS | 1892663 | 1251 | - | 0.347722 |
chdA | DDB_G0284171 | CHD gene family protein containing a chromodomain a helicase domain and a DNA-binding domain similar to H. sapiens chromodomain-helicase-DNA-binding protein 2 (CHD-2) (SwissProt: O14647) chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232431 | CDS | 1645755 | 5754 | - | 0.310219 |
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 |
clp1 | DDB_G0285507 | ortholog of the conserved CLP1 protein S. cerevisiae CLP1 is involved in both the endonucleolytic cleavage and polyadenylation steps of mRNA 3'-end maturation Mammalian CLP1 is a subunit of cleavage complex IIA which is required for cleavage but not for polyadenylation of pre-mRNA | DDB0232431 | CDS | 3327387 | 1380 | - | 0.322464 |
clybl | DDB_G0284067 | DDB0232431 | CDS | 1497378 | 1083 | + | 0.279778 | |
cmbC_ps1 | DDB_G0283131 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 290287 | 246 | + | 0.333333 |
cmbl | DDB_G0285591 | DDB0232431 | CDS | 3421735 | 768 | - | 0.303385 | |
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 |
cnrB | DDB_G0283115 | identified as a suppressor of smlA null mutant cnr2 contains six predicted transmembrane domains | DDB0232431 | CDS | 264436 | 1860 | - | 0.277419 |
cofE | DDB_G0283367 | similar to cofA a 15 kDa protein with actin filament severing activity contains an actin-binding cofilintropomyosin type domain | DDB0232431 | CDS | 586631 | 408 | - | 0.267157 |
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 |
colD | DDB_G0284983 | DDB0232431 | CDS | 2752867 | 2778 | + | 0.311375 | |
comD | DDB_G0283345 | similar to drug resistance transporters contains 14 transmembrane domains | DDB0232431 | CDS | 539820 | 3528 | + | 0.291667 |
commd2 | DDB_G0284879 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232431 | CDS | 2578442 | 603 | - | 0.220564 |
commd3 | DDB_G0283795 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232431 | CDS | 1117216 | 588 | - | 0.231293 |
commd6 | DDB_G0286077 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | DDB0232431 | CDS | 4032914 | 231 | + | 0.25974 |
copB | DDB_G0284735 | beta subunit of the coatomer complex essential for the secretory pathway colocalizes with comitin at the Golgi | DDB0232431 | CDS | 2394561 | 2739 | + | 0.316174 |
cotD | DDB_G0283149 | DDB0232431 | CDS | 411746 | 1668 | + | 0.413669 | |
cpnC | DDB_G0284791 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | DDB0232431 | CDS | 2486260 | 1620 | - | 0.296914 |
cprC | DDB_G0283867 | DDB0232431 | CDS | 1092858 | 1014 | + | 0.302761 | |
crlC | DDB_G0283619 | belongs to the serpentineG-protein coupled receptor family | DDB0232431 | CDS | 927333 | 1086 | - | 0.281768 |
crlD | DDB_G0283579 | similar to serpentineG-protein coupled receptors contains 7 putative transmembrane domains | DDB0232431 | CDS | 861957 | 1413 | + | 0.194621 |
crlE | DDB_G0286301 | similar to serpentineG-protein coupled receptors contains 7 putative transmembrane domains | DDB0232431 | CDS | 4326009 | 993 | + | 0.2286 |
crtA | DDB_G0283539 | Ca2-binding protein with chaperone activity in the endoplasmic reticulum plays a role in phagocytosis | DDB0232431 | CDS | 820858 | 1275 | - | 0.374902 |
cryS | DDB_G0285419 | DDB0232431 | CDS | 3375645 | 1653 | - | 0.329704 | |
csn1 | DDB_G0283587 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232431 | CDS | 822737 | 1377 | - | 0.284677 |
csn5 | DDB_G0284597 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232431 | CDS | 2205667 | 999 | - | 0.304304 |
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 |
cstf3 | DDB_G0286645 | component of the CSTF complex which in mammalian is required for polyadenylation and 3'-end cleavage of pre-mRNAs | DDB0232431 | CDS | 4781245 | 3198 | + | 0.329894 |
ctnnA | DDB_G0285939 | cateninvinculin family protein binds to aardvark the Dictyostelium beta-catenin related protein required for the formation of a polarized epithelium at the culminant tip and thus for stalk formation during culmination | DDB0232431 | CDS | 3870921 | 2529 | + | 0.356267 |
ctsB | DDB_G0283921 | member of the papain cysteine protease family which has a wide range of specificities | DDB0232431 | CDS | 1297288 | 936 | + | 0.353632 |
ctsZ | DDB_G0283401 | member of the papain cysteine protease family which has a wide range of specificities | DDB0232431 | CDS | 613897 | 891 | + | 0.367003 |
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 |
cudA | DDB_G0284465 | required for culmination expressed in prespore and pstA cells exists as a homodimer | DDB0232431 | CDS | 2091815 | 2409 | - | 0.275633 |
culC | DDB_G0284903 | very similar to mammalian cullin 3 (CUL3) acts as scaffold for ubiquitin ligases (E3) involved in ubiquitin-mediated protein degradation | DDB0232431 | CDS | 2621558 | 2310 | - | 0.290476 |
cutA | DDB_G0283621 | DDB0232431 | CDS | 908845 | 1551 | + | 0.359768 | |
cwc2 | DDB_G0284563 | similar to S. pombe and S. cerevisiae CWC2 which are involved in pre-mRNA splicing | DDB0232431 | CDS | 2134830 | 1587 | - | 0.308129 |
cyb5r1 | DDB_G0285399 | catalyzes the reaction NADH 2 ferricytochrome b5 NAD() H() 2 ferrocytochrome involved in desaturation and elongation of fatty acids cholesterol biosynthesis and drug metabolism | DDB0232431 | CDS | 3151723 | 861 | + | 0.341463 |
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 |
cyp508A4 | DDB_G0284535 | DDB0232431 | CDS | 2137636 | 1506 | + | 0.288181 | |
cyp513B1 | DDB_G0287087 | DDB0232431 | CDS | 5309664 | 1464 | - | 0.262295 | |
cyp517A1 | DDB_G0283929 | DDB0232431 | CDS | 1320998 | 1452 | + | 0.274793 | |
cyp517A2 | DDB_G0284647 | DDB0232431 | CDS | 2285672 | 1533 | - | 0.241357 | |
cyp517A4 | DDB_G0283933 | DDB0232431 | CDS | 1331360 | 1452 | + | 0.270661 | |
cyp519B1 | DDB_G0284089 | DDB0232431 | CDS | 1554448 | 1530 | - | 0.241176 | |
cyp519E1 | DDB_G0286419 | DDB0232431 | CDS | 4464134 | 1521 | - | 0.272847 | |
cyp554A1 | DDB_G0284923 | DDB0232431 | CDS | 2649920 | 1509 | - | 0.222001 | |
cyp555A1 | DDB_G0286743 | DDB0232431 | CDS | 4916138 | 1455 | - | 0.187629 | |
cyp556A1 | DDB_G0284345 | DDB0232431 | CDS | 1862286 | 1974 | + | 0.238095 | |
cysS | DDB_G0287159 | catalyzes the reaction ATP L-cysteine tRNACys AMP diphosphate L-cysteinyl-tRNACys | DDB0232431 | CDS | 5412959 | 1983 | - | 0.328795 |
dagA | DDB_G0285161 | DDB0232431 | CDS | 2973018 | 2097 | - | 0.314258 | |
dcp2 | DDB_G0283315 | ortholog of the conserved mRNA-decapping enzyme 2 necessary for the degradation of mRNAs | DDB0232431 | CDS | 515744 | 1863 | + | 0.31723 |
dcp2_ps | DDB_G0283809 | putative pseudogene similar to | DDB0232431 | CDS | 1130346 | 258 | - | 0.325581 |
dct | DDB_G0283767 | DDB0232431 | CDS | 1132285 | 1065 | + | 0.383099 | |
dduE | DDB_G0284357 | underexpressed in | DDB0232431 | CDS | 1881383 | 2076 | - | 0.276493 |
dduF | DDB_G0284549 | contains a predicted signal peptide (cleavage site not optimal) downregulated in the uninfected | DDB0232431 | CDS | 2024271 | 777 | + | 0.36036 |
ddx10 | DDB_G0284017 | DDB0232431 | CDS | 1436851 | 2637 | + | 0.277209 | |
ddx3 | DDB_G0283661 | conserved RNA helicase very similar to mammalian DDX3X and DDX3Y and yeast DBP1 | DDB0232431 | CDS | 939305 | 2139 | - | 0.370266 |
ddx3_ps | DDB_G0283657 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 937904 | 180 | + | 0.355556 |
derl2 | DDB_G0285131 | component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins contains 5 putative transmembrane domains | DDB0232431 | CDS | 2896240 | 765 | - | 0.28366 |
dgcA | DDB_G0283453 | Dictyostelium diguanylate cyclase synthesizes cyclic-di-GMP from 2 molecules of GTP expressed at the slug and fruiting body tip responsible for stalk differentiation | DDB0232431 | CDS | 715640 | 1566 | - | 0.210089 |
dgtB | DDB_G0286519 | CAZy family GT2 catalytic subunit forms a complex with DPM1 and DPM2 catalyzes the reaction GDP-mannose dolichyl phosphate GDP dolichyl D-mannosyl phosphate | DDB0232431 | CDS | 4586343 | 765 | - | 0.299346 |
dhkG | DDB_G0284045 | DDB0232431 | CDS | 1509861 | 10299 | - | 0.239441 | |
dhkL | DDB_G0282927 | DDB0232431 | CDS | 127874 | 5130 | + | 0.280507 | |
dhps | DDB_G0285725 | catalyzes the first step in the formation of deoxyhypusine: [eIF5A]-lysine spermidine [eIF5A]-deoxyhypusine propane-13-diamine an essential post-translational modification only found in mature eIF5A factor the second reaction is catalyzed by Dohh | DDB0232431 | CDS | 3636502 | 1131 | + | 0.318302 |
dhx15 | DDB_G0285213 | DDB0232431 | CDS | 2984261 | 2184 | + | 0.330128 | |
dhx16 | DDB_G0285937 | DEADDEAH box helicases are involved in various aspects of RNA metabolism including nuclear pre-mRNA splicing | DDB0232431 | CDS | 3866187 | 3321 | + | 0.311352 |
dia1 | DDB_G0285431 | specifically expressed during the transition from growth to development serine-rich protein possibly anchored to the plasma membranebr bNomenclature conflict:b Do not confuse this gene with forF often called Ddia1 encoding a diaphanous formin | DDB0232431 | CDS | 3246902 | 1368 | - | 0.315058 |
dimt1l | DDB_G0283789 | essential protein that dimethylates two adjacent adenosines in the loop of a conserved hairpin near the 3'-end of 18S rRNA in the 40S particle in S. cerevisiae | DDB0232431 | CDS | 1107655 | 945 | + | 0.285714 |
dlcA | DDB_G0284589 | dynein is a multisubunit microtubule-dependent motor enzyme that acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules belongs to the T-complex testis-specific protein 1 family | DDB0232431 | CDS | 2178851 | 336 | + | 0.285714 |
dlcC | DDB_G0285855 | dynein is a multisubunit microtubule-dependent motor enzyme that acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules belongs to the roadblockLC7 family | DDB0232431 | CDS | 3725623 | 294 | + | 0.234694 |
dlpB | DDB_G0285931 | DDB0232431 | CDS | 3850259 | 2427 | - | 0.309848 | |
dnaja5 | DDB_G0286579 | conserved eukaryotic protein of unknown function contains DNAJ domain and two C2H2-like Zinc finger domains | DDB0232431 | CDS | 4649529 | 1902 | - | 0.268665 |
dnajc13 | DDB_G0286293 | very similar to the mammalian DnaJ homolog subfamily C member 13 required in D. melanogaster (Rme-8) for receptor-mediated endocytosis 8 | DDB0232431 | CDS | 4307439 | 7779 | - | 0.331919 |
dnajc19 | DDB_G0283735 | putative component of the PAM complex required for the ATP-dependent translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix defects in DNAJC19 in human cause dilated cardiomyopathy with ataxia (DCMA) contains one putative N-terminal signal sequence | DDB0232431 | CDS | 1046052 | 342 | + | 0.304094 |
dnajc3 | DDB_G0286251 | DnaJ (Hsp40) homolog subfamily C member 3 which in H. sapiens is a interferon-induced double-stranded RNA-activated protein kinase inhibitor | DDB0232431 | CDS | 4252375 | 1509 | + | 0.319417 |
dng1 | DDB_G0284411 | DDB0232431 | CDS | 1965235 | 975 | + | 0.322051 | |
dnpep | DDB_G0286149 | DDB0232431 | CDS | 4132917 | 1455 | - | 0.327148 | |
docD | DDB_G0284725 | DDB0232431 | CDS | 2297325 | 5775 | + | 0.29316 | |
dph1 | DDB_G0284257 | ortholog to the conserved DPH1 which in S. cerevisiae is required for synthesis of diphthamide a modified histidine residue of translation elongation factor 2 | DDB0232431 | CDS | 1781348 | 1419 | - | 0.319239 |
dus2l | DDB_G0283877 | ortholog of S. cerevisiae SMM1 and the animal DUS2L catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of tRNAs | DDB0232431 | CDS | 1134008 | 1209 | + | 0.276261 |
dutA | DDB_G0294515 | untranslatable RNA overexpression of dutA segments suppresses the culmination mutant phenotype of STATa (dstA) revealing an inhibitory role of dutA in culmination accordingly dutA expression ceases with the onset of culmination dutA segment overexpression is also correlated with increased tyrosine phosphorylation of STATa | DDB0232431 | CDS | 2979542 | 1060 | + | 0.162264 |
dynB | DDB_G0285503 | DDB0232431 | CDS | 3322100 | 1293 | + | 0.269142 | |
e2f | DDB_G0284129 | bCommunity annotation: b Dicty's single E2F is likely to be an | DDB0232431 | CDS | 1622284 | 2592 | + | 0.296682 |
eIF2a | DDB_G0284267 | EIF2A ortholog the eukaryotic initiation factor 2A that binds Met-tRNA | DDB0232431 | CDS | 1799493 | 1827 | - | 0.363437 |
eIF5 | DDB_G0286753 | EIF5 ortholog the eukaryotic initiation factor 5 catalyzes the hydrolysis of GTP bound to the 40S ribosomal initiation complex | DDB0232431 | CDS | 4930004 | 1182 | + | 0.337563 |
eb1 | DDB_G0283607 | DDB0232431 | CDS | 912876 | 1521 | + | 0.326759 | |
echs1 | DDB_G0285071 | conserved protein catalyzes the reaction (3S)-3-hydroxyacyl-CoA trans-2(or 3)-enoyl-CoA Hsub2subO | DDB0232431 | CDS | 2750152 | 834 | + | 0.333333 |
ecmC | DDB_G0286663 | forms a heterodimer sheathin 62 also forms a heterotrimer sheathin 68 with ecmB and ecmE | DDB0232431 | CDS | 4806034 | 831 | - | 0.299639 |
ecmD | DDB_G0286647 | forms a 68 kDa heterodimer with ecmB sheathin 55 and a homodimer sheathin 53 | DDB0232431 | CDS | 4787507 | 822 | - | 0.309002 |
efa1B | DDB_G0284035 | DDB0232431 | CDS | 1535647 | 651 | + | 0.391705 | |
efa1G | DDB_G0282979 | component of the eukaryotic translation elongation factor EF-1 which plays a role in attaching aminoacyl-tRNAs to the ribosome | DDB0232431 | CDS | 88701 | 1233 | + | 0.400649 |
eftud2 | DDB_G0283359 | highly conserved U5 small nuclear ribonucleoprotein subunit that is similar to elongation factor Tu ortholog of yeast SNU114 and human EFTUD2 | DDB0232431 | CDS | 569125 | 3057 | - | 0.328099 |
eif2b5 | DDB_G0283163 | EIF2B5 ortholog the eukaryotic initiation factor 2B epsilon subunit guanyl nucleotide exchange factor for eIF2 defects are linked to leukoencephalopathy with vanishing white matter | DDB0232431 | CDS | 349612 | 2124 | - | 0.303672 |
eif3B | DDB_G0283597 | EIF3B ortholog the eukaryotic initiation factor eta 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 | DDB0232431 | CDS | 847464 | 2013 | + | 0.350224 |
eif3I | DDB_G0285683 | EIF3I ortholog the eukaryotic initiation factor beta 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 | DDB0232431 | CDS | 3586013 | 996 | - | 0.348394 |
eif5a | DDB_G0284861 | DDB0232431 | CDS | 2766075 | 480 | + | 0.395833 | |
elmoC | DDB_G0282949 | DDB0232431 | CDS | 42516 | 1857 | - | 0.268713 | |
elof1 | DDB_G0287203 | ortholog of the conserved elongation factor 1 a transcription elongation factor that contains a conserved zinc finger domain implicated in chromatin structure maintenance in actively transcribed regions in S. cerevisiae | DDB0232431 | CDS | 5404659 | 243 | - | 0.366255 |
elp1 | DDB_G0284075 | similar to S. cerevisiae IKI3 subunit of the RNA polymerase II elongator complex and mammalian IKAP proteins | DDB0232431 | CDS | 1525708 | 4173 | + | 0.306255 |
enoA | DDB_G0283137 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO enriched in gametes | DDB0232431 | CDS | 225309 | 1305 | - | 0.36092 |
eppA | DDB_G0283327 | putative substrate for erkB highly repetitive protein contains a possible eggshell domain first identified in the human parasite Schistosome mansoni | DDB0232431 | CDS | 431083 | 1209 | + | 0.404467 |
erg24 | DDB_G0284407 | catalyzes the reaction 44-dimethyl-5-alpha-cholesta-824-dien-3-beta-ol NADP() 44-dimethyl-5-alpha-cholesta-81424-trien-3-beta-ol NADPH | DDB0232431 | CDS | 1962362 | 1389 | + | 0.398848 |
eriA | DDB_G0283113 | similar to C. elegans eri-1 RNA exonuclease that acts as a negative regulator of RNA interference (RNAi) contains one exonuclease domainbrbr bCommunity annotation:b EriA codes for a multifunctional RNA exonuclease which has been identified with negative regulation of RNAi and in processing the 5.8s ribosomal RNA. The gene is nearly 8-fold overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA is disrupted. Other genes overexpressed in this strain include virtually all those with unique or major functions in S-phase or mitosis. Neither RNAi nor ribosomal processing obviously fits into this class. However it has recently been shown in mammalian cells that eriA under the pseudonym 3'hExo stably associates with histone pre-mRNAs and participates in a complex that determines the site of their cleavage (see Yang et al Mol Cell Biol 29 4045-4056 (2009). Another protein in this complex is the histone stem-loop binding protein DDB_G0277383 which is threefold upregulated in t | DDB0232431 | CDS | 263707 | 663 | + | 0.273002 |
erkA | DDB_G0286353 | DDB0232431 | CDS | 4355028 | 1590 | + | 0.303774 | |
erkB | DDB_G0283903 | DDB0232431 | CDS | 1385123 | 1110 | - | 0.323423 | |
esd | DDB_G0283037 | very similar to human ESD and to S. cerevisiae S-formylglutathione hydrolase (YJL068C) which seems to be involved in formaldehyde detoxification | DDB0232431 | CDS | 192516 | 858 | + | 0.264569 |
exoc1 | DDB_G0285067 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232431 | CDS | 2728155 | 2640 | - | 0.285606 |
exoc4 | DDB_G0284833 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232431 | CDS | 2418843 | 3549 | - | 0.272753 |
expl2 | DDB_G0284677 | similar to plant expansins which modify the cell wall to allow expansion during cell growth contains a predicted signal peptide | DDB0232431 | CDS | 2331829 | 1224 | + | 0.363562 |
fadA | DDB_G0285211 | DDB0232431 | CDS | 2993554 | 1395 | - | 0.341219 | |
fam18B | DDB_G0286703 | DDB0232431 | CDS | 4870527 | 786 | + | 0.300254 | |
fam32 | DDB_G0283963 | DDB0232431 | CDS | 1382400 | 339 | - | 0.230089 | |
fam96B | DDB_G0283801 | DDB0232431 | CDS | 1121919 | 492 | + | 0.264228 | |
fhkD | DDB_G0285963 | CAMK group RAD53 family protein kinase similar to mammalian cell cycle checkpoint kinases chk2 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteins | DDB0232431 | CDS | 3876403 | 2250 | - | 0.286667 |
fia | DDB_G0284389 | composed of a DUF292 domain at the amino terminus two filaminABP280 repeats and an actin domain at the carboxyl terminus | DDB0232431 | CDS | 1932445 | 2835 | - | 0.337919 |
flpA | DDB_G0286549 | DDB0232431 | CDS | 4784977 | 2148 | + | 0.268622 | |
fncJ | DDB_G0286621 | ortholog of Fanconi anaemia complementation group protein involved DNA cross-link repair also known as BRIP1 (BRCA1 Interacting Protein 1) however the Dicty gene appears to be missing the region that interacts with BRCA1 in the human protein unlike other members of the complex null mutant is not sensitive to DNA damaging agents brbr mammalian ortholog is part of the Fanconi anaemia nuclear complex that includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 in human mutations in this gene cause Fanconi anaemia an autosomal recessive disorder affecting all bone marrow elements Dictyostelium has orthologs for | DDB0232431 | CDS | 4729555 | 3237 | + | 0.296262 |
fntA | DDB_G0283053 | catalyzes the transfer of a farnesyl group or a geranylgeranyl group via a thioether linkage (-C-S-C-) to a cysteine at or near the carboxyl terminus of the protein forms a heterodimer with the | DDB0232431 | CDS | 15565 | 969 | - | 0.28483 |
forH | DDB_G0285589 | required for filopodia formation and maintenance through removal of capping protein and actin polymerization also important for spherical cell morphology and resulting pseudopod orientation towards a cAMP gradient | DDB0232431 | CDS | 3415704 | 3264 | + | 0.321078 |
forI | DDB_G0284519 | DDB0232431 | CDS | 2097497 | 2808 | + | 0.275641 | |
fpgt | DDB_G0285257 | ortholog of the fucose-1-phosphate guanylyltransferase conserved among higher eukaryotes and in Dictyostelium catalyzes the reaction: GTP beta-L-fucose 1-phosphate diphosphate GDP-L-fucose | DDB0232431 | CDS | 3022479 | 1884 | + | 0.234607 |
fscB | DDB_G0282989 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins but does not contain the N-terminal CRD (cysteine rich domain) domain predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232431 | CDS | 107175 | 1311 | + | 0.234935 |
fsjC | DDB_G0284945 | RrmJFtsJ ribosomal RNA methyltransferase family member well conserved heat shock proteins present in prokaryotes archaea and eukaryotes this is the ortholog of H. sapiens FTSJ3 involved in rRNA processing and 60S ribosomal subunit maturation (yeast) | DDB0232431 | CDS | 2672551 | 2502 | - | 0.321343 |
fslA | DDB_G0284761 | similar to G-protein-coupled receptors contains 7 putative transmembrane domains and a potential signal sequence | DDB0232431 | CDS | 2445394 | 1785 | - | 0.270588 |
fslK | DDB_G0284729 | similar to G-protein-coupled receptors predicted to have 7 transmembrane domains and a putative signal peptide | DDB0232431 | CDS | 2327899 | 1743 | + | 0.27883 |
fslL | DDB_G0284585 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a potential signal sequence | DDB0232431 | CDS | 2184288 | 1860 | + | 0.254301 |
fslP | DDB_G0286607 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins predicted to have 7 transmembrane domains | DDB0232431 | CDS | 4697072 | 1764 | - | 0.250567 |
fslQ | DDB_G0286609 | similar to G-protein-coupled receptors and to frizzled and smoothened proteins predicted to have 7 transmembrane domains | DDB0232431 | CDS | 4699815 | 1737 | - | 0.242948 |
fut1 | DDB_G0284467 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2125012 | 1170 | + | 0.249573 |
fut10 | DDB_G0286889 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 5027996 | 1998 | - | 0.287287 |
fut2 | DDB_G0284775 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2469559 | 2334 | + | 0.212939 |
fut4 | DDB_G0284551 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2055453 | 1398 | - | 0.288984 |
fut5 | DDB_G0284505 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2066316 | 1389 | + | 0.267819 |
fut6 | DDB_G0284503 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 2064096 | 1392 | + | 0.295259 |
fut7 | DDB_G0283287 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | DDB0232431 | CDS | 463265 | 1485 | + | 0.246465 |
gacC | DDB_G0284571 | DDB0232431 | CDS | 2170033 | 1200 | - | 0.288333 | |
gacG | DDB_G0283955 | DDB0232431 | CDS | 1364111 | 3939 | - | 0.25311 | |
gacJ | DDB_G0285641 | DDB0232431 | CDS | 3519879 | 2721 | + | 0.299522 | |
gacK | DDB_G0285915 | DDB0232431 | CDS | 3822394 | 2913 | - | 0.296601 | |
gacT | DDB_G0285163 | weakly similar to similar to RalA binding protein 1 REMI mutant forms aberrant fruiting bodies see | DDB0232431 | CDS | 2946825 | 3030 | - | 0.313531 |
gatA | DDB_G0286875 | catalyzes the reaction ATP L-glutamyl-tRNA(Gln) L-glutamine ADP phosphate L-glutaminyl-tRNA(Gln) L-glutamate | DDB0232431 | CDS | 5011319 | 1653 | + | 0.260738 |
gatC | DDB_G0284291 | catalyzes the reaction ATP L-glutamyl-tRNA(Gln) L-glutamine ADP phosphate L-glutaminyl-tRNA(Gln) L-glutamate | DDB0232431 | CDS | 1839037 | 300 | - | 0.276667 |
gcdh | DDB_G0283411 | catalyzes the reaction glutaryl-CoA acceptor crotonoyl-CoA COsub2sub reduced acceptor belongs to the acyl-CoA dehydrogenase family | DDB0232431 | CDS | 638800 | 1263 | - | 0.374505 |
gcn5 | DDB_G0283459 | DDB0232431 | CDS | 727119 | 1239 | - | 0.284907 | |
gcsA | DDB_G0284651 | catalyzes the reaction ATP L-glutamate L-cysteine ADP phosphate gamma-L-glutamyl-L-cysteine the first and limiting step in glutathione (GSH) biosynthesis | DDB0232431 | CDS | 2291954 | 1881 | + | 0.289739 |
gdap2 | DDB_G0284349 | ortholog of the human GDAP2 protein contains an Appr-1-p processing domain and a C-terminal cellular retinaldehyde-bindingtriple function domain | DDB0232431 | CDS | 1866926 | 1707 | - | 0.246632 |
gdt3_ps | DDB_G0285891 | putative pseudogene member of the TKL (tyrosine kinase-like) group and the GDT family belongs to the MLK protein kinase family | DDB0232431 | CDS | 3781232 | 5880 | - | 0.234014 |
gdt5 | DDB_G0285895 | highly similar to other Dictyostelium GDT proteins however it does not contain a protein kinase domain | DDB0232431 | CDS | 3790076 | 3531 | - | 0.296233 |
gefA | DDB_G0284329 | guanine nucleotide exchange factor for RasC promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form required for adenylyl cyclase activation | DDB0232431 | CDS | 1926792 | 1818 | + | 0.338834 |
gerE | DDB_G0286551 | contains numerous TETP repeats expressed specifically in spores | DDB0232431 | CDS | 4754201 | 1374 | - | 0.306405 |
gflB | DDB_G0286773 | similar to son of sevenless contains RhoGAP and RasGEF domains | DDB0232431 | CDS | 4946624 | 4806 | - | 0.332501 |
gghA | DDB_G0286535 | DDB0232431 | CDS | 4609676 | 954 | - | 0.328092 | |
glb2 | DDB_G0285637 | belongs to glycoside hydrolase family 35 hydrolyzes terminal non-reducing beta-D-galactose residues in beta-D-galactoside has a signal peptide | DDB0232431 | CDS | 3510010 | 2286 | - | 0.279528 |
gloB1 | DDB_G0285717 | catalyzes the reaction S-lactoyl-glutathione H2O reduced glutathione D-lactate | DDB0232431 | CDS | 3631211 | 807 | - | 0.275093 |
glod5 | DDB_G0286857 | conserved protein ortholog of human GLOD5 | DDB0232431 | CDS | 4996053 | 390 | - | 0.269231 |
glyS | DDB_G0284583 | catalyzes the reaction ATP glycine tRNAGly AMP diphosphate glycyl-tRNAGly | DDB0232431 | CDS | 2181616 | 2037 | + | 0.354934 |
gmd | DDB_G0284553 | catalyzes the reaction GDP-mannose GDP-4-dehydro-6-deoxy-D-mannose Hsub2subO | DDB0232431 | CDS | 2061934 | 1071 | - | 0.327731 |
gmsA | DDB_G0286015 | homologous to the Chlamydomonas reinhardtii a2gene enriched in gametes | DDB0232431 | CDS | 3951359 | 1347 | - | 0.368226 |
gnl1 | DDB_G0285371 | DDB0232431 | CDS | 3179167 | 2541 | - | 0.283747 | |
gnl3 | DDB_G0287147 | similar to the conserved guanine nucleotide-binding protein-like 3 also called nucleostemin in mammals a protein in the nucleolus of most stem cells and many tumor cells involved in cell-cycle progression | DDB0232431 | CDS | 5379967 | 1848 | - | 0.318182 |
gnt14 | DDB_G0284567 | CAZy family GT49 similar to vertebrate acetylglucosaminyltransferase-like protein | DDB0232431 | CDS | 2159197 | 1923 | + | 0.237129 |
gpaA | DDB_G0283349 | DDB0232431 | CDS | 547836 | 1071 | + | 0.323996 | |
gpaC | DDB_G0287031 | subunit of the heterotrimeric G protein that has GTPase activity has N-terminal pleckstrin homology (PH) domain | DDB0232431 | CDS | 5297647 | 1713 | + | 0.27087 |
gpaD | DDB_G0285425 | subunit of the heterotrimeric G protein that has GTPase activity involved in the chemotactic response to folate | DDB0232431 | CDS | 3541732 | 1038 | + | 0.313102 |
gpaE | DDB_G0286185 | subunit of the heterotrimeric G protein that has GTPase activity involved in the chemotactic response to folate | DDB0232431 | CDS | 4227524 | 1044 | + | 0.285441 |
gpaF | DDB_G0283151 | DDB0232431 | CDS | 306164 | 1044 | - | 0.251916 | |
gpaH | DDB_G0284469 | DDB0232431 | CDS | 2128349 | 1212 | - | 0.284653 | |
gpaI | DDB_G0283419 | DDB0232431 | CDS | 656137 | 1029 | - | 0.284742 | |
gpi | DDB_G0283673 | catalyzes the reaction D-glucose 6-phosphate D-fructose 6-phosphate | DDB0232431 | CDS | 954966 | 1686 | + | 0.339265 |
gpmA | DDB_G0285311 | catalyzes the reaction 3-phosphoglycerate 2-phosphoglycerate | DDB0232431 | CDS | 3080971 | 750 | - | 0.330667 |
gpn3 | DDB_G0285197 | DDB0232431 | CDS | 2952647 | 858 | + | 0.29021 | |
gpt1 | DDB_G0285815 | very similar to the mammalian N-acetylglucosamine-1-phosphotransferase alphabeta subunit (GNPTAB) precursor a central part of the Dictyostelium protein is not conserved in humans the precursor is cleaved and contributes to a | DDB0232431 | CDS | 3691117 | 3717 | + | 0.286252 |
gpt8 | DDB_G0286711 | DDB0232431 | CDS | 4880623 | 1236 | - | 0.242718 | |
gpt9 | DDB_G0286709 | DDB0232431 | CDS | 4878583 | 1131 | - | 0.236074 | |
grlD | DDB_G0286895 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232431 | CDS | 5037852 | 2376 | + | 0.280724 |
grlM | DDB_G0286643 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232431 | CDS | 4778203 | 2250 | + | 0.317333 |
grlN | DDB_G0283839 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232431 | CDS | 1198222 | 2676 | - | 0.230568 |
grn | DDB_G0283671 | very similar to H. sapiens granulins1-7 which are products of the precurser gene GRN defects in GRN cause the ubiquitin-positive frontotemporal dementia (UP-FTD) | DDB0232431 | CDS | 953712 | 393 | - | 0.279898 |
grpE | DDB_G0283763 | similar to S. cerevisiae MGE1 and H. sapiens GrpE involved in protein import into mitochondria | DDB0232431 | CDS | 1238328 | 642 | - | 0.302181 |
gtaD | DDB_G0286855 | DDB0232431 | CDS | 4992545 | 1593 | - | 0.170747 | |
gtaL | DDB_G0285139 | DDB0232431 | CDS | 2908294 | 1923 | + | 0.24909 | |
gtaM | DDB_G0286837 | DDB0232431 | CDS | 4960352 | 1527 | + | 0.207597 | |
gtaN | DDB_G0287057 | DDB0232431 | CDS | 5258336 | 2862 | - | 0.264151 | |
gtaQ | DDB_G0286843 | DDB0232431 | CDS | 4968885 | 1071 | - | 0.340803 | |
gtaW | DDB_G0286839 | DDB0232431 | CDS | 4963061 | 888 | + | 0.315315 | |
gtf2a2 | DDB_G0285343 | important but not essential for transcriptional activation functioning as either an antirepressor or a coactivator | DDB0232431 | CDS | 3114831 | 348 | + | 0.284483 |
gtf2f2 | DDB_G0287131 | DDB0232431 | CDS | 5353824 | 726 | - | 0.287879 | |
gtr3 | DDB_G0286945 | distant relative of CAZy family GT8 similar to glycogenin and galactinol synthase | DDB0232431 | CDS | 5125247 | 1116 | + | 0.312724 |
guaB | DDB_G0283701 | catalyzes the reaction Hsub2subO NAD IMP xanthosine-5-phosphate NADH the first step of GMP biosynthesis | DDB0232431 | CDS | 1000722 | 1548 | - | 0.386305 |
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 |
gxcFF | DDB_G0284739 | DDB0232431 | CDS | 2399480 | 2226 | - | 0.260108 | |
gxcP | DDB_G0285859 | DDB0232431 | CDS | 3730680 | 2916 | + | 0.281207 | |
gxcQ | DDB_G0284501 | DDB0232431 | CDS | 2058245 | 3513 | + | 0.320239 | |
gxcR | DDB_G0285303 | DDB0232431 | CDS | 3051378 | 1653 | - | 0.268603 | |
hbs1 | DDB_G0283769 | DDB0232431 | CDS | 1138835 | 2190 | + | 0.306393 | |
hbx10 | DDB_G0284293 | DDB0232431 | CDS | 1841189 | 1917 | + | 0.27856 | |
hbx11 | DDB_G0295787 | DDB0232431 | CDS | 4544537 | 669 | - | 0.2571 | |
hbx12 | DDB_G0286733 | DDB0232431 | CDS | 4905654 | 2541 | - | 0.27194 | |
hcpA | DDB_G0283023 | contains two Chromo domains locates to the centromere and plays a role in growth and mitosis forms a heterodimer with hcpB | DDB0232431 | CDS | 170065 | 678 | - | 0.297935 |
hcpB | DDB_G0282987 | contains two Chromo domains locates to the centromere and plays a role in growth forms a homodimer or a heterodimer with hcpA | DDB0232431 | CDS | 105576 | 735 | + | 0.308844 |
hdaC_ps2 | DDB_G0285625 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3485870 | 171 | + | 0.421053 |
helD | DDB_G0285843 | conserved RNA helicase S. cerevisiae prp16 involved in the second catalytic step of splicing exhibits ATP-dependent RNA unwinding activity | DDB0232431 | CDS | 3861549 | 4164 | + | 0.307157 |
hemC | DDB_G0284697 | DDB0232431 | CDS | 2361299 | 978 | + | 0.294479 | |
hemD | DDB_G0285009 | catalyzes the reaction hydroxymethylbilane uroporphyrinogen III Hsub2subO in heme biosynthesis | DDB0232431 | CDS | 2803238 | 1152 | - | 0.171875 |
hfnA | DDB_G0283983 | contains an N-terminal filaminABP280 repeat and a C-terminal HECT (Homologous to the E6-AP Carboxyl Terminus) domain the latter common in ubiquitin ligases | DDB0232431 | CDS | 1259472 | 3363 | + | 0.223313 |
hgd | DDB_G0283765 | reduction of homogentisic acid reductase results in accumulation of an intermediate in the tyrosine degradative pathway homogentisic acid which is spontaneously oxidized resulting in a brown phenotype catalyzes the reaction homogentisate Osub2sub 4-maleylacetoacetate | DDB0232431 | CDS | 1151090 | 1299 | - | 0.34719 |
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 |
hmgL | DDB_G0283813 | catalyzes the reaction 3-hydroxy-3-methyl-glutaryl-CoA acetoacetate acetyl-CoA | DDB0232431 | CDS | 1145359 | 1221 | - | 0.354627 |
hprT | DDB_G0285193 | catalyzes the reaction PRPP hypoxanthine pyrophosphate IMP in the salvage pathways of purine nucleosides br overexpressed in dstB (STATb) null mutants | DDB0232431 | CDS | 2972049 | 543 | + | 0.281768 |
hus1 | DDB_G0285353 | similar to Hus1 a component of a heterotrimeric clamp (the 9-1-1 complex) that recognizes damaged DNA and initiates signal transduction for repair | DDB0232431 | CDS | 3152730 | 816 | - | 0.265931 |
iksA | DDB_G0283109 | similar to fungal kinases contains an IQ calmodulin-binding region | DDB0232431 | CDS | 257953 | 2940 | + | 0.272449 |
iliA | DDB_G0285615 | contains a putative N-terminal signal sequence regulated by | DDB0232431 | CDS | 3469352 | 768 | + | 0.278646 |
iliB | DDB_G0284409 | induced by Legionella pneumophila infection | DDB0232431 | CDS | 1964242 | 597 | + | 0.278057 |
iliG | DDB_G0284295 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages induced by Legionella pneumophila infection | DDB0232431 | CDS | 1844275 | 1443 | + | 0.369369 |
iliJ | DDB_G0286041 | contains a central large T4 RNA ligase RnlA-like domain a property shared by a related gene | DDB0232431 | CDS | 3987715 | 1332 | - | 0.250751 |
immp | DDB_G0283049 | in other organisms there are two subunits for this enzyme with relatively high sequence similarity to each other Dictyostelium appear to have a single gene | DDB0232431 | CDS | 142399 | 972 | + | 0.220165 |
impA | DDB_G0285455 | highly similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates the impA promoter is shared with and inversely regulated with dia1 during the growth-development transition | DDB0232431 | CDS | 3249271 | 585 | + | 0.324786 |
impA_ps | DDB_G0285457 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 3250615 | 261 | + | 0.314176 |
ino1 | DDB_G0285505 | catalyzes the reaction D-glucose 6-phosphate 1D-myo-inositol 3-phosphate enzyme activity is reduced by valproate | DDB0232431 | CDS | 3324153 | 1536 | - | 0.363932 |
ints1 | DDB_G0285393 | ortholog of integrator complex subunit 1 component of a multiprotein mediator of small nuclear RNA processing | DDB0232431 | CDS | 3120198 | 7494 | - | 0.243662 |
ints4 | DDB_G0286633 | ortholog of integrator complex subunit 4 component of a multiprotein mediator of small nuclear RNA processing | DDB0232431 | CDS | 4760652 | 3702 | + | 0.23852 |
ints7 | DDB_G0284483 | ortholog of integrator complex subunit 7 component of a multiprotein mediator of small nuclear RNA processing | DDB0232431 | CDS | 2030962 | 3075 | - | 0.227967 |
isca2 | DDB_G0284809 | DDB0232431 | CDS | 2506040 | 630 | - | 0.249206 | |
isy1 | DDB_G0285521 | ortholog of human and yeast ISY1 which plays a role in mRNA splicing | DDB0232431 | CDS | 3341295 | 900 | + | 0.261111 |
itpa | DDB_G0286495 | ortholog of human ITPA and S. cerevisiae HAM1 hydrolyzes ITP and dITP to their respective monophosphate derivatives defects in human ITPA cause inosine triphosphate pyrophosphohydrolase deficiency characterized by an abnormal accumulation of inosine triphosphate in erythrocytes however pathological symptoms are not known | DDB0232431 | CDS | 4555858 | 585 | - | 0.309402 |
jcdC | DDB_G0286391 | DDB0232431 | CDS | 4401925 | 1248 | + | 0.208333 | |
kif4 | DDB_G0285101 | belongs to the CENP-E subfamily predicted to play a role in mitosis has a putative nuclear localization signal C-terminal to its motor domain | DDB0232431 | CDS | 2856191 | 5769 | + | 0.268677 |
kif8 | DDB_G0284471 | DDB0232431 | CDS | 2103969 | 5622 | - | 0.284596 | |
kinX | DDB_G0283391 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family similar to LIM kinases which regulate actin dynamics | DDB0232431 | CDS | 749416 | 3285 | + | 0.312329 |
kmo | DDB_G0283173 | catalyzes the reaction L-kynurenine NADPH H Osub2sub 3-hydroxy-L-kynurenine NADP Hsub2subO during nicotinic acid biosynthesis | DDB0232431 | CDS | 359274 | 1383 | - | 0.31598 |
krsA | DDB_G0284181 | putative protein serinethreonine kinase belongs to the protein kinase MST subfamily similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase involved in signal transduction and hyperosmotic response | DDB0232431 | CDS | 1697612 | 1386 | - | 0.313853 |
ku70 | DDB_G0286069 | regulatory subunit of the DNA-dependent protein kinase complex DNA-PK which consists of Ku70 Ku80 and DNA-PKcs | DDB0232431 | CDS | 4023180 | 2730 | + | 0.277656 |
ku80 | DDB_G0286303 | subunit of the DNA-dependent protein kinase complex DNA-PK which consists of Ku70 Ku80 and DNA-PKcs | DDB0232431 | CDS | 4329334 | 2391 | + | 0.288164 |
kynu | DDB_G0284203 | catalyzes the reaction L-kynurenine Hsub2subO anthranilate L-alanine during nicotinic acid biosynthesis | DDB0232431 | CDS | 1685557 | 1356 | - | 0.314897 |
leo1 | DDB_G0286051 | component of the conserved Paf1 complex a multifunctional complex involved in histone methylation and plays a role in RNA elongation and processing | DDB0232431 | CDS | 3999753 | 1464 | - | 0.301913 |
leuS | DDB_G0285451 | catalyzes the reaction ATP L-leucine tRNALeu AMP diphosphate L-leucyl-tRNALeu | DDB0232431 | CDS | 3240792 | 3177 | + | 0.352849 |
lig3 | DDB_G0283857 | ATP-dependent DNA ligase contains the BRCT domain which is also found in BRCA1 interacts with XRCC1 | DDB0232431 | CDS | 1062604 | 3528 | + | 0.289399 |
limA | DDB_G0283599 | DDB0232431 | CDS | 968949 | 3552 | - | 0.290259 | |
limB | DDB_G0284863 | DDB0232431 | CDS | 2691906 | 1662 | + | 0.353791 | |
lin9 | DDB_G0286665 | putative ortholog of the C. elegans abnormal cell lineage protein Lin-9 the Drosophila ortholog aly is a member of a multiprotein complex containing retinoblastoma and RbAp48 (the ortholog of Dicty RbbD) which localizes to and stabilizes heterochromatin | DDB0232431 | CDS | 4807662 | 3000 | - | 0.269667 |
lmpB | DDB_G0287035 | DDB0232431 | CDS | 5254629 | 2268 | + | 0.351852 | |
lrlA | DDB_G0286037 | similar to latrophilins that are a family of secretin-like G-protein-coupled receptors (GPCRs) contains 7 putative transmembrane domains | DDB0232431 | CDS | 3985122 | 921 | + | 0.243214 |
lsm4 | DDB_G0287053 | DDB0232431 | CDS | 5235945 | 534 | - | 0.35206 | |
lvsE | DDB_G0282925 | DDB0232431 | CDS | 90982 | 6579 | + | 0.286518 | |
lvsF | DDB_G0284333 | similar to mammalian FAN human LYST and mouse Beige proteins | DDB0232431 | CDS | 1946519 | 3465 | - | 0.278788 |
lyrm5 | DDB_G0284341 | belongs to a family of short proteins that includes ndufa6 from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | DDB0232431 | CDS | 1857300 | 474 | + | 0.204641 |
maea | DDB_G0284463 | DDB0232431 | CDS | 2005913 | 1272 | - | 0.272799 | |
maoD | DDB_G0282999 | catalyzes the reaction RCHsub2subNHsub2sub Hsub2subO Osub2sub RCHO ammonia Hsub2subOsub2sub acts on primary amines as well as on some secondary and tertiary amines | DDB0232431 | CDS | 133295 | 1665 | - | 0.255255 |
masB | DDB_G0282969 | catalyzes the reaction acetyl-CoA Hsub2subO glyoxylate malate coenzyme A | DDB0232431 | CDS | 72206 | 1629 | - | 0.267649 |
mcfB | DDB_G0285599 | similar to the H. sapiens calcium-dependent mitochondrial aspartate and glutamate carriers SLC25A24 and SLC25A25 contains two EF-handsbrbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 3430845 | 1305 | + | 0.28046 |
mcfC | DDB_G0287009 | putative orthlolog of H. sapiens SLC25A24 calcium-dependent mitochondrial ATP-MgPi carrier contains four N-terminal EF-handsbrbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 5197882 | 1419 | - | 0.284708 |
mcfM | DDB_G0283751 | ortholog of SLC25A32 involved in transport of folate across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 1044239 | 921 | - | 0.261672 |
mcfO | DDB_G0283329 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane very similar to the calcium-dependent mitochondrial aspartate and glutamate carrier aralar1 (slc25A12) the human protein may have a function in the urea cyclebrbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 432962 | 2319 | - | 0.329021 |
mcfR | DDB_G0283811 | similar to Grave disease carrier protein (slc25a16) belongs to the substrate carrier proteins that are involved in transport of molecules across the mitochondrial membrane may transport coenzyme A brbr bCommunity annotation:b Overview of the | DDB0232431 | CDS | 1144131 | 981 | + | 0.280326 |
mcm2 | DDB_G0286623 | similar to MCM2 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | DDB0232431 | CDS | 4745862 | 3027 | + | 0.320449 |
mcm7 | DDB_G0282933 | similar to MCM7 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | DDB0232431 | CDS | 12867 | 2370 | + | 0.319409 |
mcm8 | DDB_G0283009 | DDB0232431 | CDS | 149067 | 2439 | - | 0.304633 | |
mcm9 | DDB_G0286035 | DDB0232431 | CDS | 3976133 | 3828 | + | 0.299373 | |
med18 | DDB_G0285713 | ortholog of the mediator of RNA polymerase II transcription subunit 18 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 3629117 | 756 | + | 0.313492 |
med25 | DDB_G0286967 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 25 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 5053310 | 4661 | - | 0.297576 |
med29 | DDB_G0284719 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 29 (metazoa) or 2 (fungi) the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 2245895 | 1665 | + | 0.253453 |
med31 | DDB_G0285221 | ortholog of the mediator of RNA polymerase II transcription subunit 31 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 2996613 | 531 | - | 0.265537 |
med6 | DDB_G0284421 | ortholog of the mediator of RNA polymerase II transcription subunit 6 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 1975693 | 804 | - | 0.257463 |
med9 | DDB_G0287019 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 9 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 5209121 | 594 | + | 0.274411 |
memo1 | DDB_G0284869 | ortholog of the H. sapiens MEMO1 a mediator of ErbB2-driven cell motility | DDB0232431 | CDS | 2629450 | 873 | - | 0.293242 |
mgp4 | DDB_G0283899 | DDB0232431 | CDS | 1248575 | 2730 | + | 0.296337 | |
mhcA | DDB_G0286355 | myosin II heavy chain component of the actin-based molecular motor (conventional myosin) has actin-activated ATPase activity myosin II consists of two heavy chains and one essential (mlcE) and one regulatory light chain (mlcR) respectively | DDB0232431 | CDS | 4451077 | 6351 | + | 0.377893 |
migA | DDB_G0283263 | DDB0232431 | CDS | 453096 | 2592 | + | 0.275077 | |
mipp1 | DDB_G0285339 | enzyme that hydrolyzes 23 bisphosphoglycerate to yield 2-phosphoglycerate | DDB0232431 | CDS | 3103340 | 1908 | + | 0.284591 |
mkcA | DDB_G0285427 | similar to MAP cascade kinases belonging to the PAK sub-family of the STE20 serinethreonine kinases partial suppressor of tagB mutation | DDB0232431 | CDS | 3440715 | 2583 | - | 0.275648 |
mkkA | DDB_G0283265 | developmentally regulated MEKK | DDB0232431 | CDS | 530684 | 3804 | + | 0.287066 |
mlh3 | DDB_G0283883 | MLH3 ortholog required for DNA mismatch repair | DDB0232431 | CDS | 1160700 | 4977 | + | 0.279687 |
mlysS | DDB_G0286517 | catalyzes the reaction ATP L-lysine tRNALys AMP diphosphate L-lysyl-tRNALys | DDB0232431 | CDS | 4584316 | 1848 | + | 0.267316 |
mmetS | DDB_G0285759 | catalyzes the reaction ATP L-methionine tRNAMet AMP diphosphate L-methionyl-tRNAMet | DDB0232431 | CDS | 3423740 | 1728 | + | 0.305556 |
mmm1 | DDB_G0285921 | similar to S. cerevisiae MMM1 (maintenance of mitochondrial morphology protein 1) MMM1 is a component of the endoplasmic reticulum-mitochondria encounter structure which is essential for maintaining the structure of mitochondria contains one putative transmembrane domain | DDB0232431 | CDS | 3830484 | 1080 | + | 0.251852 |
mocs1 | DDB_G0285137 | DDB0232431 | CDS | 2905081 | 1893 | + | 0.24617 | |
mocs2s | DDB_G0285133 | DDB0232431 | CDS | 2902514 | 261 | - | 0.275862 | |
mpi | DDB_G0284685 | catalyzes the reaction D-Mannose 6-phosphate D-fructose 6-phosphate | DDB0232431 | CDS | 2341606 | 1359 | - | 0.27741 |
mrd1 | DDB_G0284663 | ortholog of yeast MRD1 and mammalian RBM19 yeast MRD1 binds to the 35S pre-rRNA and the U3 snoRNA and is involved in pre-rRNA processing contains 5 RRM domains | DDB0232431 | CDS | 2315842 | 2688 | - | 0.278646 |
mrfA | DDB_G0284183 | regulates gene expression in pstA cells ortholog of mouse myelin-gene transcription factor | DDB0232431 | CDS | 1846274 | 2799 | - | 0.272955 |
mrkB | DDB_G0285643 | CAMKL family protein kinase similar to SNF1 kinases MARK kinases and AMPK kinases | DDB0232431 | CDS | 3523048 | 2148 | - | 0.284916 |
mrpl15 | DDB_G0284405 | DDB0232431 | CDS | 1955406 | 756 | + | 0.308201 | |
mrpl51 | DDB_G0283273 | homolog of S. cerevisiae MRPL51 protein component of the mitochondrial large ribosomal subunit | DDB0232431 | CDS | 441777 | 375 | - | 0.277333 |
msh4 | DDB_G0283957 | DDB0232431 | CDS | 1370478 | 3126 | - | 0.240883 | |
msh5 | DDB_G0284747 | DDB0232431 | CDS | 2423376 | 2643 | - | 0.239879 | |
mtr | DDB_G0284699 | multifunctional folate synthesis enzyme catlayzes the reaction 5-methyltetrahydrofolate L-homocysteine tetrahydrofolate L-methionine. | DDB0232431 | CDS | 2362420 | 3783 | - | 0.358181 |
mybL | DDB_G0285373 | DDB0232431 | CDS | 3182160 | 2568 | + | 0.264798 | |
mybU | DDB_G0283953 | DDB0232431 | CDS | 1355165 | 7146 | - | 0.29625 | |
mybY | DDB_G0284399 | DDB0232431 | CDS | 1950553 | 1719 | + | 0.272833 | |
mybZ | DDB_G0284103 | DDB0232431 | CDS | 1573183 | 2181 | - | 0.289775 | |
nadsyn1 | DDB_G0285877 | catalyzes the reaction ATP deamido-NAD L-glutamine Hsub2subO AMP diphosphate NAD L-glutamate | DDB0232431 | CDS | 3760460 | 2142 | + | 0.351074 |
nagA | DDB_G0287033 | DDB0232431 | CDS | 5251113 | 1599 | + | 0.333333 | |
nagB1 | DDB_G0286195 | long version of the glucosamine-6-phosphate isomerase similar to Entamoeba and ciliates catalyzes the reaction D-glucosamine 6-phosphate Hsub2subO D-fructose 6-phosphate NHsub3sub | DDB0232431 | CDS | 4161180 | 2175 | - | 0.316322 |
nagE | DDB_G0285647 | similar to beta-hexosaminidase but shorter on the amino terminus | DDB0232431 | CDS | 3533871 | 2088 | + | 0.221264 |
nat4 | DDB_G0287121 | DDB0232431 | CDS | 5328050 | 837 | - | 0.222222 | |
ncbp2 | DDB_G0287197 | ortholog of mammalian NCPB2 and yeast CBP2 small subunit of the heterodimeric cap binding complex involved in mediating U snRNA export from the nucleus | DDB0232431 | CDS | 5395993 | 705 | + | 0.299291 |
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 |
ndrC | DDB_G0284839 | member of the AGC kinase group NDR family related to mammalian LATS1 and LATS2 (LArge Tumor Suppressor homolog) kinases | DDB0232431 | CDS | 2493584 | 3939 | + | 0.307692 |
ndufa12 | DDB_G0285783 | DDB0232431 | CDS | 3508802 | 417 | + | 0.326139 | |
ndufa8 | DDB_G0284799 | accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to be not involved in catalysis | DDB0232431 | CDS | 2498543 | 315 | - | 0.330159 |
ndufs7 | DDB_G0285239 | DDB0232431 | CDS | 2997614 | 537 | - | 0.374302 | |
nedd8l2 | DDB_G0286927 | similar to the conserved NEDD8 (neddylin) protein however this is the most divergent member of the family in Dictyostelium | DDB0232431 | CDS | 5089206 | 243 | - | 0.255144 |
nfu1 | DDB_G0285593 | ortholog of S. cerevisiae NFU1 involved in iron metabolism in mitochondria | DDB0232431 | CDS | 3425659 | 945 | - | 0.238095 |
nhej1 | DDB_G0284785 | DDB0232431 | CDS | 2481017 | 1596 | - | 0.196742 | |
nog1 | DDB_G0285465 | very similar to NOG1GTPBP4 GTPases which in S. cerevisiae associates with free 60S ribosomal subunits in the nucleolus and is involved in their biogenesis | DDB0232431 | CDS | 3263032 | 2025 | - | 0.342222 |
nol5a | DDB_G0285679 | ortholog of H. sapiens NOL5A and S. cerevisiae SIK1 SIK1 is a component of the box CD snoRNP complex involved in rRNA processing | DDB0232431 | CDS | 3582121 | 1623 | + | 0.325323 |
noxB | DDB_G0287101 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation | DDB0232431 | CDS | 5216605 | 2097 | - | 0.244158 |
nudc | DDB_G0286159 | DDB0232431 | CDS | 4151188 | 516 | - | 0.257752 | |
nup107 | DDB_G0285579 | component of the nuclear pore complex which plays a role in RNA export | DDB0232431 | CDS | 3398560 | 2958 | - | 0.251859 |
nup85 | DDB_G0285415 | similar to the conserved Nup85 component of the nuclear pore complex | DDB0232431 | CDS | 3200903 | 2673 | + | 0.259259 |
nxf | DDB_G0286455 | nxf bNbuclear RNA ebXbport bFbactor | DDB0232431 | CDS | 4446182 | 1665 | + | 0.308108 |
nxnB | DDB_G0284261 | type I annexins inhibit phospholipase A2 following dephosphorylation by protein kinases involved in the signal transduction pathway may also associate with the cell cytoskeleton by binding to F-actin | DDB0232431 | CDS | 1793617 | 1464 | + | 0.230191 |
oplah | DDB_G0284953 | catalyzes the reaction ATP 5-oxo-L-proline 2 Hsub2subO ADP phosphate L-glutamate | DDB0232431 | CDS | 2680203 | 3798 | - | 0.322012 |
orcA | DDB_G0283073 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232431 | CDS | 182130 | 1896 | - | 0.2827 |
orcF | DDB_G0284771 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232431 | CDS | 2460990 | 1410 | + | 0.28156 |
osbG | DDB_G0283035 | DDB0232431 | CDS | 184491 | 1269 | - | 0.3026 | |
osbH | DDB_G0283709 | DDB0232431 | CDS | 1009391 | 1209 | + | 0.34574 | |
osbI | DDB_G0284353 | DDB0232431 | CDS | 1870805 | 1287 | - | 0.311577 | |
osbJ | DDB_G0285141 | DDB0232431 | CDS | 2910487 | 1173 | - | 0.289855 | |
ost3 | DDB_G0285537 | subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST3 and human N33 (tumor suppressor candidate 3) contains four C-terminal transmembrane domain and an N-terminal signal peptide | DDB0232431 | CDS | 3352785 | 1056 | - | 0.287879 |
oxaA | DDB_G0284883 | similar to OXA1 a conserved inner mitochondrial membrane protein that is required for the activity and assembly of cytochrome oxidase and for the insertion of integral membrane proteins into the mitochondrial inner membrane there is a second putative oxidase assembly protein in D. discoideum | DDB0232431 | CDS | 2586982 | 1191 | + | 0.260285 |
pRNA | DDB_G0295593 | RNA component of ribonuclease P (RNase P) involved in generating mature 5' ends of tRNA | DDB0232431 | CDS | 2775844 | 369 | - | 0.330623 |
padA | DDB_G0286385 | involved in development and cell differentiation modulates the expression of extracellular cAMP relay genes during aggregation | DDB0232431 | CDS | 4393013 | 906 | + | 0.352097 |
pdkB | DDB_G0284489 | member of the AGC kinase group similar to mammalian PDK (phosphoinositide-dependent protein kinase) known to phosphorylate AktPKB | DDB0232431 | CDS | 2038480 | 2727 | + | 0.260726 |
pdsA | DDB_G0285995 | DDB0232431 | CDS | 3929775 | 1359 | - | 0.339956 | |
pex12 | DDB_G0285523 | ortholog of peroxin 12 a RING-finger peroxisomal membrane peroxin that plays an essential role in peroxisome biogenesis and peroxisomal matrix protein import forms translocation subcomplex with peroxin 2 and peroxin 10 mutations in human homolog cause a variety of peroxisomal disorders | DDB0232431 | CDS | 3342493 | 1380 | - | 0.25 |
pex5 | DDB_G0286033 | ortholog of peroxin 5 peroxisomal membrane signal receptor for C-terminal tripeptide signal sequence (PTS1) of peroxisomal matrix proteins required for peroxisomal matrix protein importmutations in human homolog cause a variety of peroxisomal disorders | DDB0232431 | CDS | 3973237 | 1926 | - | 0.336449 |
pfdn3 | DDB_G0286473 | DDB0232431 | CDS | 4502996 | 588 | - | 0.268707 | |
pfdn6 | DDB_G0286147 | DDB0232431 | CDS | 4132037 | 423 | + | 0.255319 | |
pgtA | DDB_G0283761 | catalyzes the beta13 addition of galactose to GlcNAc-Skp1 and the alpha12 addition of fucose to GalBeta13GlcNAc-Skp1 (FpaAFpaB) | DDB0232431 | CDS | 1235916 | 2310 | + | 0.208225 |
pgtC | DDB_G0284107 | CAZy family GT24 contains two glycosyltransferase domains | DDB0232431 | CDS | 1589376 | 3198 | - | 0.22733 |
phaZ | DDB_G0284359 | similar to PHB depolymerase which catalyzes the reaction: H2O poly[(R)-3-hydroxybutanoate](n) poly[(R)-3-hydroxybutanoate](x) poly[(R)-3-hydroxybutanoate](n-x) where x is between 1 and 5 units polyhydroxyalkanoates (PHAs) are typical storage compounds of carbon and energy and are widely found in prokaryotes the most common PHA is poly(3-hydroxybutyrate) (PHB) | DDB0232431 | CDS | 1884053 | 1023 | - | 0.289345 |
phbB | DDB_G0284117 | ortholog of the yeast Phb2p and other prohibitins that are inner mitochondrial membrane chaperones that stabilize newly synthesized proteins also suggested to play a role in cell senescence | DDB0232431 | CDS | 1608856 | 882 | + | 0.290249 |
phdA | DDB_G0285845 | DDB0232431 | CDS | 3755842 | 855 | - | 0.294737 | |
phesA | DDB_G0287141 | catalyzes the reaction ATP L-phenylalanine tRNAPhe AMP diphosphate L-phenylalanyl-tRNAPhe in S. cerevisiae acts as a tetramer composed of two alpha and two beta subunits | DDB0232431 | CDS | 5374001 | 1464 | + | 0.295082 |
phf5a | DDB_G0284403 | DDB0232431 | CDS | 1954324 | 333 | - | 0.318318 | |
phg2 | DDB_G0283699 | serinethreonine kinase regulating cell substrate adhesion phagocytosis motility and actin organization member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats | DDB0232431 | CDS | 995559 | 4164 | - | 0.304275 |
phlp2 | DDB_G0285433 | DDB0232431 | CDS | 3253005 | 720 | + | 0.297222 | |
phr2aB | DDB_G0283905 | regulatory subunit of protein phosphatase 2A composed of a catalytic subunit (pho2A) a regulatory subunit (phr2AB) and a scaffold subunit (pppA) an additional regulatory B56 (psrA) subunit has been identified | DDB0232431 | CDS | 1423354 | 1452 | - | 0.331267 |
pigA | DDB_G0283965 | CAZy family GT4 subunit of the transferase that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-N-acetylglucosamine to phosphatidylinositol (PI) | DDB0232431 | CDS | 1382938 | 1572 | + | 0.268448 |
pigB | DDB_G0284435 | CAZy family GT22 catalyzes the addition of the third mannose to GPI (glycosylphosphatidylinositol) | DDB0232431 | CDS | 1990910 | 1644 | + | 0.230535 |
pigC | DDB_G0286221 | putative glycosyltransferase involved in GPI biosynthesis subunit of the transferase that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-N-acetylglucosamine to phosphatidylinositol (PI) | DDB0232431 | CDS | 4208827 | 1038 | - | 0.256262 |
pigF | DDB_G0284667 | involved in GPI biosynthesis functions with PigO to transfer ethanolamine phosphate to the third mannose of GPI (glycosylphosphatidylinositol) | DDB0232431 | CDS | 2319957 | 660 | + | 0.265152 |
pigK | DDB_G0285461 | DDB0232431 | CDS | 3257355 | 1341 | - | 0.266219 | |
pigW | DDB_G0286111 | DDB0232431 | CDS | 3995640 | 1479 | - | 0.257606 | |
pigX | DDB_G0283717 | DDB0232431 | CDS | 1018005 | 1785 | - | 0.222409 | |
pikB | DDB_G0283081 | DDB0232431 | CDS | 247398 | 5574 | - | 0.311805 | |
pkaC | DDB_G0283907 | AGC group PKA family protein kinase protein serinethreonine kinase regulates spore cell differentiation | DDB0232431 | CDS | 1394958 | 1947 | + | 0.333847 |
pkgC | DDB_G0286125 | serinethreonine protein kinase of the AGC group similar to mammalian ribosomal protein S6 kinase | DDB0232431 | CDS | 4067973 | 2733 | - | 0.312843 |
pkgD | DDB_G0284029 | AGC group protein serinethreonine kinase similar to cAMP-activated protein kinase catalytic subunits | DDB0232431 | CDS | 1459718 | 2979 | - | 0.28231 |
pks22 | DDB_G0284001 | DDB0232431 | CDS | 1312340 | 7500 | - | 0.264533 | |
pks23 | DDB_G0283931 | DDB0232431 | CDS | 1322762 | 7500 | - | 0.2616 | |
pks24 | DDB_G0287119 | DDB0232431 | CDS | 5319738 | 7416 | - | 0.237325 | |
pks25 | DDB_G0287095 | DDB0232431 | CDS | 5330551 | 7143 | + | 0.235475 | |
plbC | DDB_G0286095 | highly similar to | DDB0232431 | CDS | 4056446 | 1698 | + | 0.269729 |
plbD | DDB_G0284449 | highly similar to | DDB0232431 | CDS | 1876303 | 1710 | + | 0.287134 |
pms1 | DDB_G0283981 | ortholog of H. sapiens PMS2 and S. cerevisiae PMS1 required for DNA mismatch repair | DDB0232431 | CDS | 1418066 | 3069 | - | 0.273053 |
polA4 | DDB_G0285853 | ortholog of the DNA primase small subunit of the DNA polymerase alpha-primase complex required for the initiation of DNA replication | DDB0232431 | CDS | 3724070 | 1230 | - | 0.281301 |
polB | DDB_G0284713 | similar to yeast Pol4 and mammalian DNA polymerase beta involved in repair of DNA double-strand breaks by non-homologous end joining (NHEJ) | DDB0232431 | CDS | 2376164 | 1530 | - | 0.261438 |
polD1 | DDB_G0285381 | required for chromomsomal DNA replication contains a polymerase and a 3'-5' exonuclease domain | DDB0232431 | CDS | 3206066 | 3315 | - | 0.332428 |
ponB | DDB_G0286247 | protein structurally similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane expressed in bacterially grown vegetative and fusion-competent cells | DDB0232431 | CDS | 4244481 | 438 | - | 0.33105 |
ponC1 | DDB_G0286717 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to 1 downstream and 3 upstream genes | DDB0232431 | CDS | 4885049 | 444 | - | 0.34009 |
ponC2 | DDB_G0286715 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to the 4 upstream genes | DDB0232431 | CDS | 4883827 | 444 | - | 0.331081 |
ponC3 | DDB_G0286721 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to 2 downstream and 2 upstream genes | DDB0232431 | CDS | 4887442 | 444 | - | 0.335586 |
ponC4 | DDB_G0286719 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to 3 downstream and 1 upstream gene | DDB0232431 | CDS | 4886230 | 444 | - | 0.34009 |
ponC5 | DDB_G0286723 | similar to ponticulin (ponA) a protein that anchors the actin cytoskeleton to the plasma membrane almost identical to the 4 downstream genes | DDB0232431 | CDS | 4888589 | 444 | - | 0.333333 |
ponF | DDB_G0286631 | structurally similar to ponticulins contains a putative signal peptide | DDB0232431 | CDS | 4759468 | 516 | - | 0.381783 |
ponH | DDB_G0286573 | structurally similar to ponticulins contains a putative signal peptide | DDB0232431 | CDS | 4646321 | 612 | + | 0.372549 |
ppa1 | DDB_G0284265 | inorganic pyrophosphatase 1 (PPAse) cytoplasmic enzyme in yeast IPP1 catalyzes the rapid exchange of oxygens from Pi with water | DDB0232431 | CDS | 1798190 | 840 | + | 0.333333 |
ppan | DDB_G0285515 | ortholog of the Drosophila Peter Pan gene that when mutated results in larvae that do not grow and show minimal DNA replication | DDB0232431 | CDS | 3335964 | 1281 | + | 0.299766 |
ppiD | DDB_G0283663 | ortholog of the mammalian PPID peptidyl-prolyl cis-trans isomerase (PPIase) accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232431 | CDS | 943186 | 1065 | + | 0.293897 |
ppil2 | DDB_G0284323 | DDB0232431 | CDS | 1783122 | 1845 | + | 0.266125 | |
ppp5C | DDB_G0283157 | DDB0232431 | CDS | 299093 | 1545 | - | 0.307443 | |
pppA | DDB_G0283601 | scaffold subunit of the serinethreonine protein phosphatase 2A composed of a catalytic subunit (pho2A) a regulatory subunit (phr2AB) and a scaffold subunit (pppA) an additional regulatory B56 (psrA) subunit has been identified | DDB0232431 | CDS | 949430 | 1755 | - | 0.312251 |
pprA | DDB_G0284039 | DDB0232431 | CDS | 1595576 | 1011 | - | 0.2364 | |
ppt1 | DDB_G0285533 | ortholog of the human PPT1 an enzyme which catalyzes the reaction: palmitoyl-protein Hsub2subO palmitate protein defects in PPT1 are the cause of infantile neuronal ceroid lipofuscinosis 1 a progressive neurodegenerative disease | DDB0232431 | CDS | 3349371 | 912 | - | 0.262061 |
prafB | DDB_G0285007 | belongs to a conserved family of multi-pass transmembrane proteins contains 4 predicted transmembrane domains | DDB0232431 | CDS | 2796145 | 477 | - | 0.285115 |
prdx5 | DDB_G0285741 | DDB0232431 | CDS | 3255042 | 519 | + | 0.358382 | |
prfA | DDB_G0283175 | required for the termination of protein biosynthesis class I release factors bind to ribosomes that have encountered a stop codon at their decoding site and induce release of the nascent polypeptide mediates UAA and UAG-dependent termination in prokaryotes | DDB0232431 | CDS | 360952 | 1293 | + | 0.329466 |
proA | DDB_G0287125 | G-actin binding protein very similar to proB involved in F-actin regulation cytokinesis and development | DDB0232431 | CDS | 5417279 | 381 | - | 0.377953 |
proB | DDB_G0286187 | G-actin binding protein very similar to proA involved in F-actin regulation cytokinesis and development | DDB0232431 | CDS | 4278216 | 375 | - | 0.429333 |
proS | DDB_G0284197 | catalyzes the reaction ATP L-proline tRNAPro AMP diphosphate L-prolyl-tRNAPro | DDB0232431 | CDS | 1680128 | 1647 | + | 0.375228 |
prp40 | DDB_G0283543 | ortholog of prp40 which in yeast is a U1 snRNP protein involved in splicing | DDB0232431 | CDS | 792074 | 2046 | - | 0.280547 |
prpf39 | DDB_G0283307 | contains a putative HAT (Half A TPR) repeat PRP39 in yeast is involved in mRNA splicing | DDB0232431 | CDS | 508620 | 2100 | - | 0.25 |
prsA | DDB_G0284669 | ortholog of PRS involved in nucleotide histidine and tryptophan biosynthesis | DDB0232431 | CDS | 2322296 | 954 | + | 0.318658 |
prsC | DDB_G0283627 | highly similar to PRS involved in nucleotide histidine and tryptophan biosynthesis | DDB0232431 | CDS | 883884 | 966 | - | 0.284679 |
psiM | DDB_G0284759 | contains a signal peptide a PA14 domain and 4 Dictyostelium (slime mold) repeats enriched in gametes | DDB0232431 | CDS | 2442205 | 2202 | + | 0.336512 |
psmB7 | DDB_G0283679 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232431 | CDS | 967091 | 801 | - | 0.340824 |
psmC3 | DDB_G0284415 | DDB0232431 | CDS | 1968066 | 1266 | + | 0.347551 | |
psmC6 | DDB_G0284517 | DDB0232431 | CDS | 2090141 | 1182 | + | 0.335871 | |
psmD13 | DDB_G0285105 | DDB0232431 | CDS | 2852779 | 1158 | + | 0.273748 | |
psmE3 | DDB_G0285099 | PA28 activator subunit of the 20S proteasome animals contain 3 different subunits: alpha beta and gamma the alpha and beta subunits are only present in animals possessing an adaptive immune system Dictyostelium has the gamma ortholog only PsmE3 is localized to the nucleus similar to the gamma class of REG proteasome activator in metazoans | DDB0232431 | CDS | 2880074 | 678 | + | 0.261062 |
pspE | DDB_G0286905 | DDB0232431 | CDS | 5076581 | 468 | - | 0.348291 | |
pspG | DDB_G0286499 | DDB0232431 | CDS | 4569135 | 741 | - | 0.330634 | |
pten | DDB_G0286557 | DDB0232431 | CDS | 4733890 | 1602 | - | 0.315855 | |
purA | DDB_G0285429 | catalyzes the reaction L-aspartate IMP GTP adenylo-succinate phosphate GDP in de novo DNA synthesis | DDB0232431 | CDS | 3358729 | 1284 | + | 0.348131 |
purC%2FE | DDB_G0283987 | bifunctional enzyme composed of SAICAR synthase and AIR carboxylase that catalyze steps in de novo DNA synthesis | DDB0232431 | CDS | 1280148 | 2994 | + | 0.325985 |
pwp2 | DDB_G0284621 | DDB0232431 | CDS | 2240813 | 2769 | - | 0.298664 | |
pyk | DDB_G0283247 | catalyzes the reaction ATP pyruvate ADP phosphoenolpyruvate | DDB0232431 | CDS | 344914 | 1524 | - | 0.358268 |
r21 | DDB_G0294415 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 956823 | 55 | - | 0.4 |
r22 | DDB_G0295571 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 960281 | 58 | - | 0.344828 |
r23A | DDB_G0295585 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1668807 | 57 | - | 0.368421 |
r23B | DDB_G0295579 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1666945 | 57 | - | 0.368421 |
r23C | DDB_G0295575 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1662690 | 57 | - | 0.368421 |
r24A | DDB_G0295577 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1663884 | 58 | + | 0.413793 |
r24B | DDB_G0295587 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1675652 | 58 | - | 0.413793 |
r26 | DDB_G0295583 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 1668202 | 58 | + | 0.396552 |
r32 | DDB_G0295599 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 2793917 | 55 | + | 0.327273 |
r34 | DDB_G0295601 | small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends localizes to the cytoplasm | DDB0232431 | CDS | 3575039 | 50 | + | 0.4 |
r48 | DDB_G0295563 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 77659 | 43 | - | 0.395349 |
r49 | DDB_G0295565 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 958244 | 58 | - | 0.37931 |
r50 | DDB_G0295567 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 959090 | 57 | - | 0.333333 |
r51 | DDB_G0295569 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 959587 | 58 | - | 0.413793 |
r52 | DDB_G0295573 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 961592 | 58 | + | 0.431034 |
r53 | DDB_G0295581 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 1667874 | 32 | + | 0.40625 |
r54 | DDB_G0295589 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 1675966 | 56 | + | 0.339286 |
r55 | DDB_G0295591 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 2757052 | 94 | + | 0.255319 |
r56 | DDB_G0295595 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 2792181 | 58 | - | 0.344828 |
r57 | DDB_G0295597 | predicted class I RNA a small non-coding RNA (55-65 nt) containing highly conserved 5' and 3' ends | DDB0232431 | CDS | 2793529 | 49 | + | 0.367347 |
rab1A | DDB_G0283757 | DDB0232431 | CDS | 1241175 | 609 | - | 0.326765 | |
rab1D | DDB_G0284985 | DDB0232431 | CDS | 2756032 | 615 | - | 0.304065 | |
rab21 | DDB_G0286553 | DDB0232431 | CDS | 4804109 | 639 | + | 0.309859 | |
rab32A | DDB_G0283603 | DDB0232431 | CDS | 965063 | 660 | - | 0.309091 | |
rab32D | DDB_G0285051 | DDB0232431 | CDS | 2597422 | 687 | + | 0.263464 | |
rabZ | DDB_G0286169 | DDB0232431 | CDS | 4062977 | 690 | - | 0.298551 | |
racA | DDB_G0286555 | RhoBTB subfamily protein which have a unique domain architecture composed of a N-terminal GTPase domain two bric a brac domains (BTB and a conserved C-terminal domain there are orthoolgs in several eukaryotes including mammals but are absent from fungi and plants in Dictyostelium appears to be involved in the regulation of the actin cytoskeleton | DDB0232431 | CDS | 4692759 | 1797 | - | 0.327212 |
racP | DDB_G0285453 | DDB0232431 | CDS | 3245052 | 1131 | + | 0.312113 | |
rad54 | DDB_G0282997 | similar to RAD54 DNA repair protein chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232431 | CDS | 118731 | 2796 | + | 0.33226 |
rad54b | DDB_G0285117 | similar to RAD54b DNA repair protein chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | DDB0232431 | CDS | 2873116 | 2970 | - | 0.278788 |
rae1 | DDB_G0283835 | DDB0232431 | CDS | 1191439 | 1029 | + | 0.308066 | |
ragC | DDB_G0284495 | ortholog of S. cerevisiae GTR2 and H. sapiens RagC a cytoplasmic GTP binding protein | DDB0232431 | CDS | 2047442 | 1083 | - | 0.277008 |
rapgap9 | DDB_G0284065 | similar to H. sapiens Rap1GAP involved in morphogenesis development and cell adhesion | DDB0232431 | CDS | 1493285 | 1101 | - | 0.348774 |
rasS | DDB_G0283537 | DDB0232431 | CDS | 849934 | 585 | - | 0.305983 | |
rbbE | DDB_G0285847 | DDB0232431 | CDS | 3858078 | 1578 | + | 0.292142 | |
rbm8A | DDB_G0286007 | conserved protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance the human ortholog has been shown to interact with | DDB0232431 | CDS | 3939784 | 564 | - | 0.281915 |
rbrA | DDB_G0286961 | required for cell type proportioning contains two IBR (In Between Ring fingers) domains | DDB0232431 | CDS | 5132945 | 1563 | - | 0.31286 |
rcbA | DDB_G0286357 | DDB0232431 | CDS | 4412389 | 1029 | + | 0.371234 | |
rcdII | DDB_G0284041 | DDB0232431 | CDS | 1500251 | 1395 | - | 0.26595 | |
rdeA | DDB_G0282923 | DDB0232431 | CDS | 67134 | 765 | + | 0.299346 | |
regA | DDB_G0284331 | contains a 3'5'-cyclic nucleotide phosphodiesterase and an RR domain found in two-component signal transduction systems | DDB0232431 | CDS | 1956975 | 2382 | - | 0.290932 |
repE | DDB_G0286013 | ortholog of H. sapiens | DDB0232431 | CDS | 3955941 | 3546 | - | 0.278624 |
repG | DDB_G0284987 | similar to H. sapiens xeroderma pigmentosum group G (XPG) M. musculus ERCC5 and S. pombe RAD2 cleaves 5' overhang flap structure generated when DNA polymerase encounters the 5'end of a downstream Okazaki fragment | DDB0232431 | CDS | 2762877 | 1155 | - | 0.309091 |
rfc1 | DDB_G0285961 | ortholog of H. sapiens RFC 140 kDa subunit | DDB0232431 | CDS | 3845828 | 4206 | + | 0.3136 |
rfc4 | DDB_G0286027 | ortholog of H. sapiens RFC4 (37 kDa subunit) and S. cerevisiae RFC2 | DDB0232431 | CDS | 3966261 | 1044 | + | 0.314176 |
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 |
ripA | DDB_G0284611 | component of the TORC2 (Tor complex 2) with Tor Lst8 and PiaA that plays a role in regulation of adenylate cyclase (ACA) and protein kinase B (PKB) activation during aggregation | DDB0232431 | CDS | 2346926 | 5055 | + | 0.321464 |
rnrA | DDB_G0284071 | catalyzes the reaction 2'-deoxyribonucleoside diphosphate thioredoxin disulfide Hsub2subO ribonucleoside diphosphate reduced thioredoxin | DDB0232431 | CDS | 1503516 | 2613 | + | 0.381554 |
roco8 | DDB_G0286127 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains DEP LRR Roc COR and protein kinase domains | DDB0232431 | CDS | 4112361 | 5604 | - | 0.267131 |
romo1 | DDB_G0286181 | conserved mitochondrial protein ROMO1 in H. sapiens and MGR2 (Mitochondrial Genome Required) in S. cerevisiae involved in reactive oxygen species production contains 2 predicted transmembrane domains | DDB0232431 | CDS | 4077065 | 387 | + | 0.27907 |
rpb12 | DDB_G0283365 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPC10 | DDB0232431 | CDS | 585874 | 141 | + | 0.347518 |
rpb7 | DDB_G0284891 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB7 | DDB0232431 | CDS | 2602996 | 519 | + | 0.306358 |
rpc9 | DDB_G0286521 | DDB0232431 | CDS | 4587626 | 393 | - | 0.239186 | |
rpkA | DDB_G0283615 | DDB0232431 | CDS | 1020192 | 2487 | - | 0.291516 | |
rpl17 | DDB_G0285277 | DDB0232431 | CDS | 3049805 | 543 | + | 0.412523 | |
rpl18a | DDB_G0285881 | DDB0232431 | CDS | 3775456 | 516 | + | 0.395349 | |
rpl26 | DDB_G0283741 | DDB0232431 | CDS | 1048980 | 420 | + | 0.390476 | |
rpl34 | DDB_G0286389 | DDB0232431 | CDS | 4400738 | 369 | - | 0.365854 | |
rpl37 | DDB_G0285971 | DDB0232431 | CDS | 3886590 | 276 | + | 0.42029 | |
rplP0 | DDB_G0286501 | DDB0232431 | CDS | 4590677 | 918 | - | 0.418301 | |
rplP2 | DDB_G0283393 | DDB0232431 | CDS | 661727 | 321 | - | 0.485981 | |
rps10 | DDB_G0286117 | protein component of the small (40S) ribosomal subunit highly expressed in vegetative cells and in early development | DDB0232431 | CDS | 4072416 | 465 | - | 0.415054 |
rps12 | DDB_G0284237 | protein component of the small (40S) ribosomal subunit ribosomal protein S12 homolog | DDB0232431 | CDS | 1729814 | 411 | - | 0.413625 |
rps13 | DDB_G0284533 | protein component of the small (40S) ribosomal subunit ribosomal protein S13 homolog | DDB0232431 | CDS | 2127182 | 456 | - | 0.388158 |
rps15 | DDB_G0285561 | protein component of the small (40S) ribosomal subunit ribosomal protein S15 homolog | DDB0232431 | CDS | 3385002 | 435 | + | 0.402299 |
rps16 | DDB_G0284093 | protein component of the small (40S) ribosomal subunit ribosomal protein S16 homolog | DDB0232431 | CDS | 1558362 | 444 | + | 0.387387 |
rps28 | DDB_G0285597 | protein component of the small (40S) ribosomal subunit ribosomal protein S28 homolog | DDB0232431 | CDS | 3428530 | 219 | - | 0.429224 |
rps5 | DDB_G0286075 | DDB0232431 | CDS | 4031568 | 573 | + | 0.418848 | |
rsc43 | DDB_G0285251 | DDB0232431 | CDS | 3035959 | 771 | - | 0.293126 | |
rsmA | DDB_G0283547 | DDB0232431 | CDS | 800136 | 660 | + | 0.260606 | |
samkB | DDB_G0284859 | putative protein kinase containing a SAM (sterile alpha motif) homology domain a putative protein interaction module | DDB0232431 | CDS | 2549067 | 1782 | + | 0.251403 |
samkB_ps2 | DDB_G0284851 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 2551418 | 183 | + | 0.295082 |
samkE_ps1 | DDB_G0283165 | putative pseudogene SAMK (SAM domain-containing kinase) family | DDB0232431 | CDS | 352482 | 1272 | - | 0.26022 |
samkE_ps2 | DDB_G0283257 | putative pseudogene SAMK (SAM domain-containing kinase) family does not contain the consensus sequences required for kinase function | DDB0232431 | CDS | 404751 | 624 | + | 0.280449 |
scdA | DDB_G0283375 | DDB0232431 | CDS | 574408 | 2586 | + | 0.287703 | |
scrA | DDB_G0285253 | adaptor protein that couples Rho GTPases and the Arp23 complex to stimulate actin polymerization | DDB0232431 | CDS | 3055336 | 1332 | + | 0.388889 |
sdh | DDB_G0285267 | catalyzes the reaction saccharopine NADsupsup Hsub2subO L-glutamate 2-aminoadipate 6-semialdehyde NADH Hsupsup there is also a bifunctional enzyme ( | DDB0232431 | CDS | 3034209 | 1443 | + | 0.348579 |
sec1 | DDB_G0283937 | highly similar to mammalian Sec1 (also known as syntaxin binding protein 1) which plays a role in vesicle transport by binding to t-SNAREs expressed in prespore cells involved in osmoregulation and hence cell motility | DDB0232431 | CDS | 1335851 | 1797 | + | 0.329994 |
sec63 | DDB_G0286131 | similar to the widely conserved SEC63 which seems to be required for integral membrane and secreted preprotein translocation across the endoplasmic reticulum membrane | DDB0232431 | CDS | 4064803 | 2445 | - | 0.350102 |
sf3b2 | DDB_G0284555 | DDB0232431 | CDS | 2068357 | 1878 | + | 0.305112 | |
sfxn | DDB_G0285029 | very similar to mammalian sideroflexins especially SFXN 5 and SFXN3 and to S. cerevisieae FSF1 contains five putative transmembrane domains | DDB0232431 | CDS | 2834988 | 990 | - | 0.279798 |
sgkB | DDB_G0284545 | homolog of human Sphk2 phosphorylates sphinganine to sphinganine 1-phosphate | DDB0232431 | CDS | 2087340 | 2283 | + | 0.251862 |
shkA | DDB_G0283267 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain negative regulator of phosphoinositol signaling | DDB0232431 | CDS | 438511 | 1584 | + | 0.318182 |
sigD_ps | DDB_G0284317 | putative pseudogene fragment similar to D. discoideum gene | DDB0232431 | CDS | 1740402 | 387 | + | 0.361757 |
sigM | DDB_G0286563 | regulated by the MADS-box transcription factor SrfA during development contains two EGF domains | DDB0232431 | CDS | 4725803 | 1491 | + | 0.298457 |
sir2A | DDB_G0283917 | NAD-dependent deacetylase Sirutin 2 family protein that regulates various biological processes by deacetylating histones and other target proteins expressed more highly during vegetative growth | DDB0232431 | CDS | 1272110 | 1539 | + | 0.293047 |
sir2B | DDB_G0286671 | N-terminus has several ankyrin repeats C-terminus has a Sirutin (Sir2) domain a NAD-dependent deacetylase that regulates various biological processes by deacetylating histones and other target proteins expressed more highly during development localized to prestalk and rearguard region of the slug and to the apical disc and upper and lower cups in the culminant (similar expression pattern as sir2E) | DDB0232431 | CDS | 4818681 | 2337 | + | 0.267009 |
sir2C | DDB_G0284795 | NAD-dependent deacetylase Sirutin 2 family protein that regulates various biological processes by deacetylating histones and other target proteins expressed more highly during vegetative growth | DDB0232431 | CDS | 2489743 | 1371 | - | 0.231947 |
smc2 | DDB_G0284499 | functions in chromosome dynamics heterodimerizes with smc4 | DDB0232431 | CDS | 2051268 | 3555 | - | 0.320394 |
smc4 | DDB_G0286403 | functions in chromosome dynamics heterodimerizes with smc2 | DDB0232431 | CDS | 4414331 | 4248 | - | 0.318974 |
snf2a | DDB_G0285205 | SNF2 family protein similar to human SMARCA4 putative regulator of chromatin | DDB0232431 | CDS | 2921996 | 4815 | + | 0.304673 |
sno15 | DDB_G0295561 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232431 | CDS | 59280 | 113 | + | 0.362832 |
sno8 | DDB_G0295603 | expressed non-coding RNA CD box snoRNAs are involved in rRNA processing and methylation | DDB0232431 | CDS | 4444849 | 88 | - | 0.397727 |
snpA | DDB_G0285111 | DDB0232431 | CDS | 2863727 | 876 | - | 0.3379 | |
snrpA1 | DDB_G0284101 | ortholog of human SNRPA1 a component of the U2 snRNP involved in mRNA splicing | DDB0232431 | CDS | 1571395 | 735 | + | 0.240816 |
snrpD2 | DDB_G0285395 | DDB0232431 | CDS | 3142648 | 339 | - | 0.294985 | |
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 |
spc25 | DDB_G0284013 | ortholog of Spc25 which interacts with Ndc80 in the attachment of microtubules to kinetochores brbr bCommunity annotation: b spc25 is overexpressed 16-fold in a | DDB0232431 | CDS | 1432537 | 975 | + | 0.220513 |
spc97 | DDB_G0285849 | DDB0232431 | CDS | 3719511 | 4008 | + | 0.262974 | |
spc98 | DDB_G0283909 | DDB0232431 | CDS | 1376667 | 2442 | - | 0.269042 | |
splA | DDB_G0283385 | dual-specificity protein kinase involved in spore coat formation and morphogenesis member of the TKL (tyrosine kinase-like) group and the CZAK (C-terminal domain of ZakA) family | DDB0232431 | CDS | 623097 | 7233 | + | 0.323655 |
splB | DDB_G0285321 | member of the TKL (tyrosine kinase-like) group activates the transcriptional regulator STATc | DDB0232431 | CDS | 3131349 | 3468 | + | 0.27797 |
spt4 | DDB_G0285293 | ortholog of the human SUPT4H1 and S. cerevisiae SPT4 (suppressor of Ty 4) a transcription-elongation factor that is tightly associated in a complex with SPT5 | DDB0232431 | CDS | 3068070 | 276 | + | 0.344203 |
spyA | DDB_G0285263 | CAZy family GT41 contains 7 TPRs (Tetratrico Peptide Repeats) | DDB0232431 | CDS | 3029506 | 2595 | - | 0.246243 |
srfD | DDB_G0283483 | DDB0232431 | CDS | 775937 | 1341 | - | 0.246831 | |
srp68 | DDB_G0285821 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232431 | CDS | 3701203 | 1845 | + | 0.280217 |
srpA | DDB_G0294413 | signal recognition particle (SRP) RNA forms the SRP complex with the SRP 72 68 54 19 14 and 9 proteins | DDB0232431 | CDS | 2767691 | 278 | + | 0.471223 |
srrm1 | DDB_G0286425 | very similar to the mammalian serinearginine repetitive matrix protein 1 (SRRM1) which is part of pre- and post-splicing multiprotein mRNP complexes involved in numerous pre-mRNA processing events | DDB0232431 | CDS | 4471381 | 1812 | + | 0.291943 |
sslA1 | DDB_G0284335 | mutation in the sslA1 gene increases the fruiting body size of smlA mutants positively regulates group size there is an identical gene on chromosome 3 | DDB0232431 | CDS | 1885441 | 1737 | - | 0.270581 |
ssr1 | DDB_G0283497 | DDB0232431 | CDS | 648667 | 711 | - | 0.331927 | |
strap | DDB_G0286457 | ortholog of the serine-threonine kinase receptor-associated protein STRAP an inhibitor of TGF-beta signaling contains 7 WD40 repeats | DDB0232431 | CDS | 4462466 | 882 | - | 0.349206 |
stt3 | DDB_G0285159 | CAZy family GT66 subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST1 contains 13 transmembrane domains | DDB0232431 | CDS | 2899851 | 2145 | + | 0.359441 |
sumo | DDB_G0286189 | sumoylates the MAP kinase kinase Mek1 (mekA) sumoylation is involved in cellular translocation after cAMP stimulation and activation of the kinase | DDB0232431 | CDS | 4217038 | 297 | + | 0.356902 |
sunB | DDB_G0285925 | SUN-like protein with a centrally located domain contains a predicted N-terminal signal sequence | DDB0232431 | CDS | 3835569 | 3837 | + | 0.250195 |
svkA | DDB_G0286359 | very similar to mammalian ST25 kinase (SOK1) and other STE20-like kinases stress-responsive kinase phosphorylates severin essential for cell separation during cytokinesis | DDB0232431 | CDS | 4476218 | 1437 | + | 0.343076 |
swip | DDB_G0283355 | DDB0232431 | CDS | 559359 | 3408 | - | 0.314847 | |
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 |
sympk | DDB_G0284319 | in mammals symplekin is a component of the tight junction plaque but has also been detected in a wide range of cell types that do not form tight junctions may be required for pre-mRNA polyadenylation | DDB0232431 | CDS | 1741477 | 4482 | + | 0.280455 |
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 |
syn6 | DDB_G0284185 | similar to syntaxin a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232431 | CDS | 1791019 | 696 | + | 0.178161 |
tRNA-Ala-AGC-8 | DDB_G0295209 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3947721 | 73 | - | 0.534247 |
tRNA-Ala-UGC-7 | DDB_G0295207 | transfers an alanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 4682789 | 96 | - | 0.427083 |
tRNA-Asn-GUU-13 | DDB_G0295217 | transfers an asparagine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3320206 | 73 | - | 0.60274 |
tRNA-Asp-GUC-12 | DDB_G0295175 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2841024 | 72 | + | 0.569444 |
tRNA-Asp-GUC-13 | DDB_G0295177 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3073029 | 72 | + | 0.569444 |
tRNA-Asp-GUC-14 | DDB_G0295185 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3942404 | 72 | + | 0.569444 |
tRNA-Asp-GUC-15 | DDB_G0295213 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3919822 | 72 | - | 0.569444 |
tRNA-Asp-GUC-16 | DDB_G0295221 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3057091 | 72 | - | 0.569444 |
tRNA-Asp-GUC-17 | DDB_G0295223 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3029253 | 72 | - | 0.569444 |
tRNA-Asp-GUC-18 | DDB_G0295225 | transfers an aspartic acid residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2845703 | 72 | - | 0.569444 |
tRNA-Gly-GCC-11 | DDB_G0295219 | DDB0232431 | CDS | 3320060 | 71 | - | 0.549296 | |
tRNA-Ile-AAU-10 | DDB_G0295169 | transfers an isoleucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 1879566 | 73 | + | 0.589041 |
tRNA-Leu-AAG-4 | DDB_G0295199 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5435309 | 82 | + | 0.463415 |
tRNA-Leu-AAG-5 | DDB_G0295201 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5435936 | 82 | + | 0.463415 |
tRNA-Leu-UAA-11 | DDB_G0295195 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5168273 | 83 | + | 0.481928 |
tRNA-Leu-UAA-12 | DDB_G0295203 | transfers a leucine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5226859 | 83 | - | 0.481928 |
tRNA-Lys-UUU-14 | DDB_G0295187 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3970863 | 73 | + | 0.616438 |
tRNA-Lys-UUU-15 | DDB_G0295229 | transfers a lysine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 1802373 | 73 | - | 0.616438 |
tRNA-Phe-GAA-11 | DDB_G0295173 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2563537 | 74 | + | 0.554054 |
tRNA-Phe-GAA-12 | DDB_G0295189 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 4598294 | 74 | + | 0.554054 |
tRNA-Phe-GAA-13 | DDB_G0295193 | transfers a phenylalanine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 4999193 | 74 | + | 0.554054 |
tRNA-Sec-UGA | DDB_G0302695 | transfers an selenocysteine residue to a growing polypeptide chain during protein synthesis opposite some TGA codons there are several selenoproteins in Dictyostelium | DDB0232431 | CDS | 2475153 | 81 | + | 0.506173 |
tRNA-Ser-GCU-10 | DDB_G0295171 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2227631 | 81 | + | 0.592593 |
tRNA-Ser-GCU-11 | DDB_G0295227 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 2220197 | 81 | - | 0.592593 |
tRNA-Ser-UGA-7 | DDB_G0295211 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3945723 | 82 | - | 0.52439 |
tRNA-Ser-UGA-8 | DDB_G0295231 | transfers a serine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 1589109 | 82 | - | 0.52439 |
tRNA-Thr-UGU-3 | DDB_G0295183 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3710357 | 90 | + | 0.466667 |
tRNA-Thr-UGU-4 | DDB_G0295215 | transfers a threonine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3717164 | 90 | - | 0.455556 |
tRNA-Tyr-GUA-5 | DDB_G0295179 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3366227 | 83 | + | 0.493976 |
tRNA-Tyr-GUA-6 | DDB_G0295181 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 3658459 | 83 | + | 0.493976 |
tRNA-Tyr-GUA-7 | DDB_G0295191 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 4844157 | 84 | + | 0.488095 |
tRNA-Tyr-GUA-8 | DDB_G0295197 | transfers a tyrosine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5312947 | 83 | + | 0.518072 |
tRNA-Val-AAC-18 | DDB_G0295205 | transfers a valine residue to a growing polypeptide chain during protein synthesis | DDB0232431 | CDS | 5047177 | 74 | - | 0.486486 |
tagB | DDB_G0286119 | amino terminus has a serine protease domain carboxyl terminus consists of a half-transporter of the ABCB family | DDB0232431 | CDS | 4091463 | 5721 | + | 0.301695 |
tagC | DDB_G0286121 | amino terminus has a serine protease domain carboxy terminus consists of a half-transporter of the ABCB family | DDB0232431 | CDS | 4085057 | 5226 | + | 0.293724 |
tagD | DDB_G0286123 | amino terminus has a serine protease domain carboxy terminus consists of a half-transporter of the ABCB family | DDB0232431 | CDS | 4078435 | 5478 | + | 0.288244 |
tbcC | DDB_G0284313 | DDB0232431 | CDS | 1725990 | 1263 | - | 0.200317 | |
tfb1m | DDB_G0286199 | DDB0232431 | CDS | 4166229 | 1458 | - | 0.268176 | |
tgrA_ps10 | DDB_G0349532 | putative pseudogene fragment of immunoglobulin E-set family genes including | DDB0232431 | CDS | 1602101 | 832 | - | 0.253606 |
tgrD1 | DDB_G0286825 | contains three immunolubulin-like folds (IPTTIG domains) | DDB0232431 | CDS | 4985657 | 2688 | + | 0.289062 |
tgrE1 | DDB_G0286851 | conserved hypothetical protein contains an IPTTIG domain found in cell surface receptors | DDB0232431 | CDS | 4982216 | 2739 | - | 0.319825 |
tgrE_ps | DDB_G0285217 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 2989226 | 216 | - | 0.291667 |
tgrH1 | DDB_G0283323 | DDB0232431 | CDS | 482981 | 3369 | - | 0.240427 | |
tgrH_ps1 | DDB_G0283341 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 518010 | 1107 | - | 0.257453 |
tgrH_ps2 | DDB_G0283183 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 373477 | 999 | + | 0.248248 |
tgrI1 | DDB_G0283335 | DDB0232431 | CDS | 487136 | 2568 | + | 0.222741 | |
tgrI2 | DDB_G0283317 | DDB0232431 | CDS | 522108 | 2553 | + | 0.221308 | |
tgrI3 | DDB_G0283249 | DDB0232431 | CDS | 370291 | 2559 | - | 0.221962 | |
tgrI_ps1 | DDB_G0283873 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 1129091 | 492 | - | 0.21748 |
tgrI_ps2 | DDB_G0282981 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 98815 | 459 | - | 0.230937 |
tgrI_ps3 | DDB_G0283299 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 477747 | 285 | - | 0.238596 |
tgrL1 | DDB_G0284659 | DDB0232431 | CDS | 2306298 | 2214 | - | 0.266486 | |
tgrT_ps1 | DDB_G0283029 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 175761 | 552 | - | 0.320652 |
tgrT_ps2 | DDB_G0283027 | putative pseudogene immunoglobulin E-set family gene | DDB0232431 | CDS | 174707 | 234 | - | 0.282051 |
timm10 | DDB_G0284911 | conserved component of the mitochondrial intermembrane space forms a complex with Timm9 which mediates insertion of hydrophobic proteins at the inner membrane. | DDB0232431 | CDS | 2631200 | 267 | - | 0.348315 |
timm22 | DDB_G0283865 | DDB0232431 | CDS | 1077530 | 537 | - | 0.340782 | |
timm23 | DDB_G0286541 | DDB0232431 | CDS | 4635713 | 495 | - | 0.339394 | |
tmem184A | DDB_G0284525 | similar to H. sapiens TMEM184A and B contains 7 predicted transmembrane domains | DDB0232431 | CDS | 2111778 | 1482 | - | 0.2861 |
tmem184F | DDB_G0284327 | TMEM184 family protein the long splice variant contains 6 putative transmembrane domains and an additional signal sequence the short splice variant contains 4 putative transmembrane domains | DDB0232431 | CDS | 1812405 | 1863 | + | 0.263017 |
tmem33 | DDB_G0286009 | DDB0232431 | CDS | 3940845 | 873 | + | 0.293242 | |
top1 | DDB_G0283205 | ortholog of TOP1 a nuclear topoisomerase responsible for relaxing single-stranded supercoiled DNA | DDB0232431 | CDS | 416900 | 2682 | + | 0.35123 |
tpsB | DDB_G0284975 | CAZy family GT20 contains an N-terminal glycosyltransferase domain and a C-terminal trehalose-phosphatase domain | DDB0232431 | CDS | 2735507 | 2373 | - | 0.307206 |
treh | DDB_G0283473 | homolog of human TREH catalyzes the reaction alphaalpha-trehalose H2O 2 D-glucose contains a predicted signal peptide | DDB0232431 | CDS | 746464 | 1785 | + | 0.341737 |
trmt11 | DDB_G0283969 | DDB0232431 | CDS | 1400103 | 1524 | + | 0.270341 | |
tsfm | DDB_G0286399 | DDB0232431 | CDS | 4409316 | 1068 | + | 0.305243 | |
tsg101 | DDB_G0286797 | DDB0232431 | CDS | 4717096 | 1437 | - | 0.314544 | |
tsnax | DDB_G0284837 | ortholog of human TSNAX interacts with translin (TSN) may be involved in RNA metabolism | DDB0232431 | CDS | 2473632 | 855 | - | 0.247953 |
ttc4 | DDB_G0286253 | DDB0232431 | CDS | 4254280 | 1194 | - | 0.278057 | |
u2af1 | DDB_G0285077 | small subunit of the U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) which is a splicing factor that forms a heterodimer with | DDB0232431 | CDS | 2799520 | 1416 | + | 0.366525 |
u2af2 | DDB_G0286395 | large subunit of the U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) which is a splicing factor that forms a heterodimer with | DDB0232431 | CDS | 4405482 | 2016 | + | 0.361607 |
uba2 | DDB_G0286919 | conserved protein forms a heterodimer with sae1 acts as a E1 ligase for sumo | DDB0232431 | CDS | 5077667 | 1986 | - | 0.302618 |
ubcB | DDB_G0284865 | high similarity to E2ubiquitin-conjugating enzymes from yeast metazoans and plants ubiquitin-conjugating enzymes (EC: 6.3.2.19) (UBC or E2 enzymes) catalyze the covalent attachment of ubiquitin to target proteins | DDB0232431 | CDS | 2571519 | 447 | - | 0.340045 |
ubcC | DDB_G0284009 | DDB0232431 | CDS | 1428069 | 708 | + | 0.310734 | |
ube1c | DDB_G0283891 | conserved catalytic subunit of the dimeric UBE1C-APPBP1 E1 enzyme which activates NEDD8 necessary for cell cycle progression through the S-M checkpoint | DDB0232431 | CDS | 1193106 | 1329 | - | 0.311512 |
ubl5 | DDB_G0284205 | ortholog of human UBL5 and yeast HUB1 human UBL5 interacts with cyclin-dependent kinase CLK4 | DDB0232431 | CDS | 1687407 | 204 | - | 0.289216 |
ubqD | DDB_G0286907 | DDB0232431 | CDS | 5083931 | 690 | - | 0.327536 | |
ubqP | DDB_G0286031 | DDB0232431 | CDS | 3971817 | 939 | - | 0.28754 | |
uch2 | DDB_G0285527 | catalyzes the thiol-dependent hydrolysis of ester thiolester amide peptide and isopeptide bonds formed by the C-terminal Gly of ubiquitin most closely related to human BAP1 and UCHL5 genes | DDB0232431 | CDS | 3345269 | 1032 | + | 0.26938 |
ucpB | DDB_G0283333 | ortholog of slc25a30 that belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane | DDB0232431 | CDS | 469001 | 885 | - | 0.309605 |
ucpC | DDB_G0284225 | ortholog of slc25a11 catalyzes the transport of 2-oxoglutarate across the inner mitochondrial membrane in an electroneutral exchange for malate or other dicarboxylic acids plays a role in several metabolic processes such as the malate-aspartate shuttle the oxoglutaratesocitrate shuttle in gluconeogenesis from lactate and in nitrogen metabolism | DDB0232431 | CDS | 1714783 | 957 | + | 0.315569 |
ucr | DDB_G0284947 | conserved ubiquinol-cytochrome c oxidoreductase subunit a component of the mitochondrial inner membrane electron transport chain | DDB0232431 | CDS | 2675998 | 645 | + | 0.384496 |
udkC | DDB_G0283371 | contains a N-terminal uridine kinase domaine domain and a C-terminal adenylate cyclase domain like the UdkD protein and other plant proteins | DDB0232431 | CDS | 600577 | 1350 | - | 0.297778 |
udpA | DDB_G0284431 | catalyzes the reaction phosphate uridine ribose-1-phosphate uracil in salvage pathways of pyrimidine ribonucleotides and deoxyribose phosphate degradation | DDB0232431 | CDS | 1983105 | 750 | - | 0.4 |
uduD2 | DDB_G0283125 | upregulated in the uninfected | DDB0232431 | CDS | 281753 | 1455 | + | 0.285911 |
uduG | DDB_G0286953 | upregulated in the uninfected | DDB0232431 | CDS | 5140537 | 957 | + | 0.406479 |
uox | DDB_G0286427 | catalyzes the reaction urate Osub2sub Hsub2subO 5-hydroxyisourate Hsub2subOsub2sub | DDB0232431 | CDS | 4473628 | 864 | - | 0.366898 |
uqcrb | DDB_G0286171 | ortholog of mammalian UQCRB a component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex) which is part of the mitochondrial respiratory chain | DDB0232431 | CDS | 4097397 | 330 | - | 0.30303 |
urm1 | DDB_G0283737 | homolog of human and S. cerevisiae URM1 yeast URM1 is involved in tRNA modification and is alsoindirectly involved in oxidative stress response and regulation of budding and haploid invasive growth | DDB0232431 | CDS | 1046828 | 291 | - | 0.261168 |
utp15 | DDB_G0283581 | DDB0232431 | CDS | 863530 | 1590 | - | 0.3 | |
utp23 | DDB_G0283685 | putative U3 snoRNP protein ortholog of H. sapiens C8orf53 and S. cerevisiae UTP23 | DDB0232431 | CDS | 980287 | 1320 | + | 0.266667 |
vamp7A | DDB_G0284951 | member of the SNARE family (Soluble NSF Attachment Protein REceptor) localizes to endosome and interacts with syn7A | DDB0232431 | CDS | 2678890 | 651 | + | 0.288786 |
vatA | DDB_G0287127 | ortholog of the A subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the A subunit is part of the V1 subunit | DDB0232431 | CDS | 5370324 | 1857 | - | 0.367798 |
vatA_ps | DDB_G0287137 | putative pseudogene small fragment almost identical with parts of | DDB0232431 | CDS | 5367030 | 285 | - | 0.322807 |
vatC | DDB_G0284473 | ortholog of the C subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the C subunit is part of the V1 subunit | DDB0232431 | CDS | 2149008 | 1107 | - | 0.31346 |
vmp1 | DDB_G0285175 | conserved protein required for biogenesis of the contractile vacuole in response to osmotic stress contains 8 predicted transmembrane domains | DDB0232431 | CDS | 2937306 | 1212 | + | 0.291254 |
vps13A | DDB_G0286725 | putative ortholog of S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 4889609 | 10122 | - | 0.30488 |
vps13D | DDB_G0286545 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 4616198 | 13779 | - | 0.252994 |
vps13F | DDB_G0287055 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 5237174 | 12741 | - | 0.271172 |
vps20 | DDB_G0287021 | component of the ESCRT-III complex (endosomal sorting complex required for transport) putative ortholog of human CHMP6 (Chromatin Modifying Protein 6) and yeast VPS20 | DDB0232431 | CDS | 5201277 | 657 | - | 0.284627 |
vps22 | DDB_G0283203 | component of the ELL complex an RNA polymerase II transcription factor and of the ESCRT-II complex (endosomal sorting complex required for transport) | DDB0232431 | CDS | 415279 | 741 | + | 0.25641 |
vps24 | DDB_G0284769 | DDB0232431 | CDS | 2459478 | 624 | - | 0.304487 | |
vps28 | DDB_G0285295 | DDB0232431 | CDS | 3068985 | 867 | - | 0.229527 | |
vps4 | DDB_G0284347 | DDB0232431 | CDS | 1865073 | 1335 | + | 0.326592 | |
vps41 | DDB_G0286803 | DDB0232431 | CDS | 4738365 | 3264 | - | 0.33701 | |
vti1B | DDB_G0283363 | DDB0232431 | CDS | 584359 | 810 | + | 0.308642 | |
wdr89 | DDB_G0283635 | DDB0232431 | CDS | 891645 | 1080 | + | 0.285185 | |
xacC | DDB_G0285391 | DDB0232431 | CDS | 3109098 | 4134 | - | 0.341558 | |
xpf | DDB_G0284419 | DDB0232431 | CDS | 1971161 | 2895 | + | 0.245596 | |
xpo5 | DDB_G0284379 | DDB0232431 | CDS | 1912156 | 3408 | - | 0.289319 | |
xpot | DDB_G0283119 | DDB0232431 | CDS | 269911 | 3267 | - | 0.277319 | |
xpr1 | DDB_G0285957 | ortholog of XPR1 which in mammals confers susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | DDB0232431 | CDS | 3794131 | 2760 | - | 0.294203 |
xrcc3 | DDB_G0283637 | putative ortholog of XRCC3 which is involved in double-strand break repair interacts with RAD51 | DDB0232431 | CDS | 893273 | 1695 | + | 0.220059 |
yakA | DDB_G0283605 | belongs to the CMGC group of protein kinases putative protein serinethreonine kinase | DDB0232431 | CDS | 868454 | 4377 | + | 0.303404 |
yipf5 | DDB_G0283541 | very similar to Yip1 domain family member 5 (YIPF5) in yeast YIP1 localizes to the Golgi and interacts with GTPases contains four putative transmembrane domains | DDB0232431 | CDS | 791068 | 639 | + | 0.273865 |
zipA | DDB_G0286985 | DDB0232431 | CDS | 5171363 | 3075 | - | 0.294959 | |
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 |