Gene list
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COG category: Intracellular trafficking and secretion
Organism: Dictyostelium lacteum
Number of genes found: 117
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium lacteum | ||||||||
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Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g10068 | DLA_11239 | GLQOFTK02JL55Q | CDS | 744417 | 1392 | + | 0.34842 | |
g10121 | DLA_11301 | GLQOFTK02JL55Q | CDS | 861962 | 600 | - | 0.32 | |
g10131 | DLA_11314 | GLQOFTK02JL55Q | CDS | 883525 | 1353 | - | 0.316334 | |
g10184 | DLA_11379 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) there is a second copy of this gene | GLQOFTK02JL55Q | CDS | 1021400 | 1650 | + | 0.330909 |
g10209 | DLA_11406 | newcontig00824_1.exp | CDS | 21406 | 1950 | - | 0.316923 | |
g1346 | DLA_01475 | F4PJNLW01B0TO9 | CDS | 131246 | 558 | + | 0.306452 | |
g1431 | DLA_01571 | F4PJNLW01B0TO9 | CDS | 311263 | 1335 | - | 0.28764 | |
g1493 | DLA_01638 | F4PJNLW01B0TO9 | CDS | 445215 | 936 | + | 0.356838 | |
g1564 | DLA_01716 | F4PJNLW01B0TO9 | CDS | 618733 | 624 | + | 0.301282 | |
g1640 | DLA_01795 | F4PJNLW01B0TO9 | CDS | 777633 | 1689 | - | 0.316163 | |
g1804 | DLA_11505 | F4PJNLW01C9MXC | CDS | 95206 | 1290 | - | 0.306202 | |
g188 | DLA_00213 | contig05409_1.exp | CDS | 431852 | 564 | + | 0.296099 | |
g2054 | DLA_02259 | F4PJNLW01DERRH | CDS | 398942 | 468 | - | 0.260684 | |
g2235 | DLA_02469 | F4PJNLW01EE5MJ | CDS | 78419 | 2289 | - | 0.351682 | |
g2251 | DLA_02488 | F4PJNLW01EE5MJ | CDS | 109636 | 4569 | + | 0.33968 | |
g2357 | DLA_02607 | F4PJNLW01EE5MJ | CDS | 354640 | 645 | - | 0.339535 | |
g2366 | DLA_02616 | F4PJNLW01EE5MJ | CDS | 373247 | 591 | + | 0.279188 | |
g2458 | DLA_02727 | F4PJNLW01EE5MJ | CDS | 588955 | 3414 | - | 0.347393 | |
g2481 | DLA_02752 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | F4PJNLW01EE5MJ | CDS | 642626 | 11559 | + | 0.33541 |
g2488 | DLA_02759 | F4PJNLW01EE5MJ | CDS | 667342 | 6816 | + | 0.359008 | |
g2591 | DLA_02874 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | F4PJNLW01EE5MJ | CDS | 898216 | 14703 | - | 0.327484 |
g2606 | DLA_02891 | contains Sec23Sec24 zinc finger trunk and helical domains yeast Sec23Sec24 is a component of COPII (coat protein complex II) involved in ER to Golgi transport | F4PJNLW01EE5MJ | CDS | 943766 | 2277 | + | 0.317523 |
g2708 | DLA_03003 | endoplasmic reticulum receptor for the KDEL signal sequence of proteins resident in the endoplasmic reticulum believed to cycle between the cis side of the Golgi apparatus and the ER | F4PJNLW01EE5MJ | CDS | 1143920 | 663 | + | 0.266968 |
g2724 | DLA_03020 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | F4PJNLW01EE5MJ | CDS | 1181808 | 477 | + | 0.333333 |
g2779 | DLA_03076 | F4PJNLW02GJ9ZB | CDS | 56201 | 2220 | - | 0.340991 | |
g2824 | DLA_03127 | F4PJNLW02GJ9ZB | CDS | 146833 | 2541 | - | 0.245179 | |
g2853 | DLA_03160 | F4PJNLW02GJ9ZB | CDS | 213172 | 4545 | + | 0.256106 | |
g2871 | DLA_03182 | F4PJNLW02GJ9ZB | CDS | 266560 | 510 | + | 0.235294 | |
g2942 | DLA_03260 | F4PJNLW02HBBIY | CDS | 138381 | 11952 | + | 0.347808 | |
g3021 | DLA_03347 | F4PJNLW02HBBIY | CDS | 321833 | 1110 | + | 0.341441 | |
g3156 | DLA_03498 | GAOABQK02FRRQV | CDS | 39437 | 1425 | - | 0.30386 | |
g3207 | DLA_03555 | GAOABQK02FWKR3 | CDS | 17848 | 1452 | - | 0.278926 | |
g3316 | DLA_03667 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GAOABQK02G6SYV | CDS | 194474 | 921 | + | 0.324647 |
g3329 | DLA_03680 | GAOABQK02G6SYV | CDS | 221699 | 456 | - | 0.29386 | |
g3336 | DLA_03689 | GAOABQK02G6SYV | CDS | 231693 | 1032 | - | 0.304264 | |
g3395 | DLA_03755 | GAOABQK02G6SYV | CDS | 363597 | 558 | + | 0.320789 | |
g344 | DLA_00386 | contig05409_1.exp | CDS | 787271 | 429 | + | 0.379953 | |
g359 | DLA_00401 | contig05409_1.exp | CDS | 830609 | 1770 | - | 0.337853 | |
g3782 | DLA_04192 | GAOABQK02G7M1S | CDS | 559788 | 3381 | - | 0.359065 | |
g3807 | DLA_04222 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | GAOABQK02G7M1S | CDS | 617133 | 4275 | - | 0.349942 |
g3816 | DLA_04233 | GAOABQK02G7M1S | CDS | 656435 | 1044 | - | 0.304598 | |
g3851 | DLA_04271 | GAOABQK02G7M1S | CDS | 737197 | 1590 | + | 0.267925 | |
g4130 | DLA_04578 | belongs to the synaptobrevin family ortholog of human SEC22B contains a longin domain and a v-snare coiled-coil domain contains 1 predicted transmembrane domain | GAOABQK02GQAQJ | CDS | 570431 | 627 | - | 0.283892 |
g4157 | DLA_04604 | GAOABQK02GQAQJ | CDS | 627845 | 1929 | + | 0.365993 | |
g4267 | DLA_04713 | GAOABQK02GQAQJ | CDS | 860607 | 1854 | - | 0.340345 | |
g4555 | DLA_05048 | GAOABQK02H81I9 | CDS | 262440 | 1518 | - | 0.373518 | |
g4596 | DLA_05090 | GAOABQK02H81I9 | CDS | 352560 | 1077 | - | 0.312906 | |
g4680 | DLA_05181 | GAOABQK02H81I9 | CDS | 553088 | 1659 | + | 0.335744 | |
g4800 | DLA_05313 | GAOABQK02H81I9 | CDS | 839363 | 3039 | - | 0.336624 | |
g4830 | DLA_05348 | GAOABQK02HUB3S | CDS | 11346 | 1809 | - | 0.319514 | |
g486 | DLA_00538 | contig05409_1.exp | CDS | 1115144 | 207 | - | 0.338164 | |
g5070 | DLA_05615 | GAOABQK02HUB3S | CDS | 553749 | 6030 | - | 0.315091 | |
g5085 | DLA_05630 | GAOABQK02HUB3S | CDS | 588330 | 2022 | - | 0.333828 | |
g5285 | DLA_05866 | GAOABQK02HUB3S | CDS | 1120661 | 2448 | - | 0.330474 | |
g5598 | DLA_06243 | GAOABQK02HUB3S | CDS | 1842440 | 417 | - | 0.270983 | |
g5662 | DLA_06308 | GAOABQK02IBA3P | CDS | 127226 | 600 | + | 0.343333 | |
g572 | DLA_00632 | contig05409_1.exp | CDS | 1311038 | 1035 | - | 0.296618 | |
g5739 | DLA_06401 | GAOABQK02IBA3P | CDS | 327191 | 3069 | - | 0.358749 | |
g5952 | DLA_06631 | GAOABQK02IBA3P | CDS | 824711 | 705 | - | 0.307801 | |
g6112 | DLA_06805 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) | GAOABQK02IO52T | CDS | 49054 | 1587 | + | 0.360428 |
g632 | DLA_00700 | F4PJNLW01A00V1 | CDS | 1619 | 1938 | + | 0.31063 | |
g6433 | DLA_07159 | GAOABQK02JBK0O | CDS | 45121 | 2970 | - | 0.306734 | |
g6436 | DLA_07162 | GAOABQK02JBK0O | CDS | 55174 | 2730 | + | 0.323077 | |
g6467 | DLA_07196 | GAOABQK02JBK0O | CDS | 131417 | 2556 | + | 0.321205 | |
g6552 | DLA_07297 | GAOABQK02JOCCH | CDS | 107432 | 1428 | - | 0.338235 | |
g6599 | DLA_07351 | GAOABQK02JOCCH | CDS | 228160 | 1170 | - | 0.315385 | |
g6607 | DLA_07358 | GAOABQK02JOCCH | CDS | 240004 | 12681 | - | 0.328365 | |
g6614 | DLA_07365 | GAOABQK02JOCCH | CDS | 270577 | 426 | - | 0.284038 | |
g6686 | DLA_07446 | GAOABQK02JOCCH | CDS | 428514 | 2859 | - | 0.317943 | |
g6710 | DLA_07472 | GAOABQK02JOCCH | CDS | 467845 | 2673 | - | 0.329592 | |
g6711 | DLA_07474 | GAOABQK02JOCCH | CDS | 471109 | 7059 | - | 0.374982 | |
g6720 | DLA_07485 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GAOABQK02JOCCH | CDS | 494830 | 1011 | - | 0.318497 |
g6777 | DLA_07549 | GAOABQK02JOCCH | CDS | 627098 | 894 | - | 0.332215 | |
g6937 | DLA_04686 | GLQOFTK02FH5TG | CDS | 112858 | 411 | - | 0.29927 | |
g6969 | DLA_07767 | GLQOFTK02FH5TG | CDS | 179062 | 2796 | - | 0.363019 | |
g6985 | DLA_07786 | GLQOFTK02FH5TG | CDS | 212046 | 747 | + | 0.298527 | |
g73 | DLA_00084 | contig05409_1.exp | CDS | 173780 | 2514 | + | 0.356404 | |
g7346 | DLA_08210 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GLQOFTK02FH5TG | CDS | 1043861 | 1017 | + | 0.281219 |
g7430 | DLA_08309 | GLQOFTK02FH5TG | CDS | 1244453 | 2094 | - | 0.330946 | |
g7470 | DLA_08357 | GLQOFTK02FH5TG | CDS | 1338085 | 3267 | - | 0.329966 | |
g7475 | DLA_08365 | GLQOFTK02FH5TG | CDS | 1349218 | 11601 | - | 0.325403 | |
g7486 | DLA_08378 | GLQOFTK02FH5TG | CDS | 1383522 | 3045 | + | 0.314286 | |
g7539 | DLA_08433 | there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 1491296 | 2943 | + | 0.321441 |
g7566 | DLA_08462 | GLQOFTK02G2F2O | CDS | 8848 | 1590 | - | 0.31195 | |
g7576 | DLA_08474 | GLQOFTK02G2F2O | CDS | 31480 | 675 | - | 0.371852 | |
g7724 | DLA_08642 | GLQOFTK02G2F2O | CDS | 383694 | 4512 | - | 0.359043 | |
g7747 | DLA_08662 | conserved protein mainly among fungi and plants | GLQOFTK02G2F2O | CDS | 436087 | 2898 | + | 0.333333 |
g7934 | DLA_08869 | GLQOFTK02G2F2O | CDS | 837751 | 234 | + | 0.25641 | |
g7936 | DLA_08871 | GLQOFTK02G2F2O | CDS | 840428 | 2337 | + | 0.286264 | |
g8143 | DLA_09100 | GLQOFTK02G2F2O | CDS | 1346133 | 1419 | + | 0.384778 | |
g8197 | DLA_09154 | GLQOFTK02G2F2O | CDS | 1451518 | 3885 | - | 0.351351 | |
g8416 | DLA_09385 | GLQOFTK02G2F2O | CDS | 1890456 | 453 | + | 0.335541 | |
g8477 | DLA_09450 | SNARE protein interacts with AP180 (clmA) which retrieves Vamp7B from the contractile vacuole | GLQOFTK02G2F2O | CDS | 2028516 | 690 | + | 0.291304 |
g8508 | DLA_09484 | GLQOFTK02GHM7A | CDS | 38320 | 2019 | + | 0.301139 | |
g852 | DLA_00932 | F4PJNLW01A00V1 | CDS | 470736 | 10092 | + | 0.339279 | |
g8531 | DLA_09510 | GLQOFTK02GHM7A | CDS | 98002 | 2253 | + | 0.377275 | |
g8593 | DLA_09585 | GLQOFTK02GHM7A | CDS | 246755 | 4185 | + | 0.314934 | |
g8608 | DLA_09601 | GLQOFTK02GHM7A | CDS | 279919 | 3174 | - | 0.371456 | |
g891 | DLA_00983 | F4PJNLW01A00V1 | CDS | 569380 | 1380 | - | 0.301449 | |
g9041 | DLA_10062 | GLQOFTK02GQ36N | CDS | 387355 | 1842 | + | 0.290988 | |
g9098 | DLA_10129 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | GLQOFTK02GQ36N | CDS | 538065 | 4770 | - | 0.341719 |
g9158 | DLA_10199 | GLQOFTK02GUKFG | CDS | 11171 | 471 | - | 0.314225 | |
g9210 | DLA_10261 | GLQOFTK02GUKFG | CDS | 129499 | 4644 | + | 0.343239 | |
g9236 | DLA_10289 | GLQOFTK02GUKFG | CDS | 189555 | 1299 | + | 0.326405 | |
g9240 | DLA_10294 | GLQOFTK02GUKFG | CDS | 198640 | 1005 | + | 0.321393 | |
g9259 | DLA_10316 | GLQOFTK02GUKFG | CDS | 240693 | 10326 | + | 0.328879 | |
g9262 | DLA_10320 | GLQOFTK02GUKFG | CDS | 258563 | 918 | - | 0.262527 | |
g9270 | DLA_10328 | GLQOFTK02GUKFG | CDS | 292343 | 2208 | - | 0.347373 | |
g9339 | DLA_10412 | GLQOFTK02GUKFG | CDS | 436075 | 3642 | + | 0.354201 | |
g9445 | DLA_10523 | GLQOFTK02IIOHN | CDS | 85920 | 4386 | + | 0.332421 | |
g9499 | DLA_10589 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention in D. discoideum involved in early development and tip formation | GLQOFTK02IJPNF | CDS | 37254 | 10056 | - | 0.289081 |
g963 | DLA_01066 | F4PJNLW01A00V1 | CDS | 736130 | 7947 | - | 0.317227 | |
g9819 | DLA_10960 | GLQOFTK02JL55Q | CDS | 195158 | 1359 | + | 0.309051 | |
g9834 | DLA_10974 | GLQOFTK02JL55Q | CDS | 223375 | 3783 | + | 0.317209 | |
g9932 | DLA_11079 | GLQOFTK02JL55Q | CDS | 449060 | 2265 | + | 0.335099 | |
g9983 | DLA_11136 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GLQOFTK02JL55Q | CDS | 557966 | 924 | - | 0.311688 |
g9999 | DLA_11844 | belongs to the drugmetabolite transporter superfamily similar to human SLC35D1 (UDP-glucuronic acidUDP-N-acetylgalactosamine transporter) and S. cerevisiae VRG4 (GDP-mannose transporter 1) contains 8 putative transmembrane domains | GLQOFTK02JL55Q | CDS | 591072 | 942 | - | 0.321656 |