ID: 57231 | sorting nexin 14 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (85505496..85593858, complement) | RGS-PX2, SCAR20 | 616105 |
ID: 10401 | protein inhibitor of activated STAT 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (145848522..145859081, complement) | ZMIZ5 | 605987 |
ID: 57448 | baculoviral IAP repeat containing 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (32357023..32618878) | APOLLON, BRUCE | 605638 |
ID: 23623 | RUN and SH3 domain containing 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155320894..155331118) | NESCA | 617318 |
ID: 6993 | dynein light chain Tctex-type 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (158636474..158644743, complement) | CW-1, TCTEL1, TCTEX1, tctex-1 | 601554 |
ID: 113444 | small integral membrane protein 12 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (34850362..34859749, complement) | C1orf212 | |
ID: 28988 | drebrin like [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (44044702..44069456) | ABP1, HIP-55, HIP55, SH3P7 | 610106 |
ID: 51374 | all-trans retinoic acid induced differentiation factor [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27212041..27217183) | APR--3, APR-3, APR3, C2orf28, HSPC013, PRO240, p18 | 619682 |
ID: 27032 | ATPase secretory pathway Ca2+ transporting 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (130850595..131016712) | ATP2C1A, BCPM, HHD, PMR1, SPCA1, hSPCA1 | 604384 |
ID: 3978 | DNA ligase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (48115445..48170344, complement) | IMD96, LIGI, hLig1 | 126391 |
ID: 476 | ATPase Na+/K+ transporting subunit alpha 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (116373244..116404774) | CMT2DD, HOMGSMR2 | 182310 |
ID: 79780 | coiled-coil domain containing 82 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (96352773..96389912, complement) | HSPC048 | 619870 |
ID: 8833 | guanine monophosphate synthase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (155869430..155944020) | GATD7 | 600358 |
ID: 100134934 | TEN1 subunit of CST complex [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (75979240..76000586) | C17orf106 | 613130 |
ID: 26503 | solute carrier family 17 member 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (73593379..73653992, complement) | AST, ISSD, NSD, SD, SIALIN, SIASD, SLD, VEAT | 604322 |
ID: 5906 | RAP1A, member of RAS oncogene family [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (111542009..111716691) | C21KG, G-22K, KREV-1, KREV1, RAP1, SMGP21 | 179520 |
ID: 165918 | ring finger protein 168 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196468783..196503768, complement) | RIDL, hRNF168 | 612688 |
ID: 57558 | ubiquitin specific peptidase 35 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (78188919..78237219) | | |
ID: 8493 | protein phosphatase, Mg2+/Mn2+ dependent 1D [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (60600193..60666280) | IDDGIP, JDVS, PP2C-DELTA, WIP1 | 605100 |
ID: 11273 | ataxin 2 like [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (28822999..28837232) | A2D, A2LG, A2LP, A2RP | 607931 |