ID: 283219 | potassium channel tetramerization domain containing 21 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (78171249..78188626, complement) | KCASH2 | 618790 |
ID: 3978 | DNA ligase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (48115445..48170344, complement) | IMD96, LIGI, hLig1 | 126391 |
ID: 63933 | mitochondrial calcium uniporter regulator 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (13786557..13814557, complement) | C6orf79, CCDC90A, FMP32 | 616952 |
ID: 112611 | RWD domain containing 2A [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83193357..83198935) | RWDD2, dJ747H23.2 | |
ID: 5238 | phosphoglucomutase 3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83148705..83193900, complement) | AGM1, IMD23, PAGM, PGM 3 | 172100 |
ID: 8976 | WASP like actin nucleation promoting factor [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (123681943..123749003, complement) | N-WASP, NWASP, WASPB | 605056 |
ID: 8635 | ribonuclease T2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (166922113..166956550, complement) | RNASE6PL, bA514O12.3 | 612944 |
ID: 79677 | structural maintenance of chromosomes 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (17663812..17753810, complement) | SMC-6L1, hSMC6, SMC6 | 609387 |
ID: 23052 | endonuclease domain containing 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (95089846..95132645) | | 619568 |
ID: 84299 | migration and invasion enhancer 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39728510..39730532, complement) | C17orf37, C35, ORB3, RDX12, XTP4 | 611802 |
ID: 57558 | ubiquitin specific peptidase 35 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (78188919..78237219) | | 620959 |
ID: 54677 | carnitine O-octanoyltransferase [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (87345664..87399794) | COT | 606090 |
ID: 7706 | tripartite motif containing 25 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56887909..56914049, complement) | EFP, RNF147, Z147, ZNF147 | 600453 |
ID: 55654 | transmembrane protein 127 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (96248514..96265997, complement) | | 613403 |
ID: 22835 | ZFP30 zinc finger protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (37631006..37656261, complement) | ZNF745 | 617317 |
ID: 6760 | SS18 subunit of BAF chromatin remodeling complex [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (26016253..26091219, complement) | SMARCL1, SSXT, SYT | 600192 |
ID: 9747 | TRPM8 channel associated factor 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (143851375..143902176, complement) | FAM115A, GATD9A | 616251 |
ID: 533 | ATPase H+ transporting V0 subunit b [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43974960..43978295) | ATP6F, HATPL, VMA16 | 603717 |
ID: 63916 | engulfment and cell motility 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (46366050..46406615, complement) | CED-12, CED12, Ced-12A, ELMO-2, VMPI | 606421 |
ID: 64224 | HERPUD family member 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (35632659..35695135, complement) | | 620829 |