ID: 55958 | kelch like family member 9 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (21329665..21335404, complement) | | 611201 |
ID: 5347 | polo like kinase 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (23678889..23690367) | PLK, STPK13 | 602098 |
ID: 8878 | sequestosome 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179806393..179838078) | A170, DMRV, EBIAP, FTDALS3, NADGP, OSIL, PDB3, ZIP3, p60, p62, p62B | 601530 |
ID: 203228 | C9orf72-SMCR8 complex subunit [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (27546546..27573866, complement) | ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1 | 614260 |
ID: 3667 | insulin receptor substrate 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (226731312..226799820, complement) | HIRS-1 | 147545 |
ID: 65018 | PTEN induced kinase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (20633458..20651511) | BRPK, PARK6 | 608309 |
ID: 9212 | aurora kinase B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (8204731..8210575, complement) | AIK2, AIM-1, AIM1, ARK-2, ARK2, AurB, IPL1, PPP1R48, STK-1, STK12, STK5, aurkb-sv1, aurkb-sv2 | 604970 |
ID: 1051 | CCAAT enhancer binding protein beta [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50190583..50192690) | C/EBP-beta, IL6DBP, NF-IL6, TCF5 | 189965 |
ID: 4625 | myosin heavy chain 7 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (23412740..23435660, complement) | CMD1S, CMH1, CMYO7A, CMYO7B, CMYP7A, CMYP7B, MPD1, MYHCB, SPMD, SPMM | 160760 |
ID: 3814 | KiSS-1 metastasis suppressor [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (204190341..204196491, complement) | HH13, KiSS-1 | 603286 |
ID: 7321 | ubiquitin conjugating enzyme E2 D1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (58335006..58370748) | E2(17)KB1, SFT, UBC4/5, UBCH5, UBCH5A | 602961 |
ID: 9978 | ring-box 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (40951378..40973309) | BA554C12.1, RNF75, ROC1 | 603814 |
ID: 2120 | ETS variant transcription factor 6 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (11649674..11895377) | TEL, TEL/ABL, THC5 | 600618 |
ID: 8452 | cullin 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (224470150..224585363, complement) | CUL-3, NEDAUS, PHA2E | 603136 |
ID: 8451 | cullin 4A [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113208193..113267108) | | 603137 |
ID: 10987 | COP9 signalosome subunit 5 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (67043079..67062133, complement) | CSN5, JAB1, MOV-34, SGN5 | 604850 |
ID: 89780 | Wnt family member 3A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (228006998..228061271) | | 606359 |
ID: 7432 | vasoactive intestinal peptide [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (152750797..152759760) | PHM27 | 192320 |
ID: 4738 | NEDD8 ubiquitin like modifier [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (24216857..24232367, complement) | NEDD-8 | 603171 |
ID: 3191 | heterogeneous nuclear ribonucleoprotein L [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38836370..38852347, complement) | HNRPL, P/OKcl.14, hnRNP-L | 603083 |