ID: 56893 | ubiquilin 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156031247..156053798, complement) | A1U, A1Up, C1orf6, CIP75, UBIN | 605440 |
ID: 9441 | mediator complex subunit 26 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (16574919..16628204, complement) | CRSP7, CRSP70 | 605043 |
ID: 23118 | TGF-beta activated kinase 1 (MAP3K7) binding protein 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (149217926..149411607) | CHTD2, MAP3K7IP2, TAB-2 | 605101 |
ID: 1108 | chromodomain helicase DNA binding protein 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6570082..6607379, complement) | CHD-4, Mi-2b, Mi2-BETA, SIHIWES | 603277 |
ID: 80148 | solute carrier family 66 member 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79902420..79951653, complement) | PQLC1 | |
ID: 10174 | sorbin and SH3 domain containing 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22544973..22575788) | SCAM-1, SCAM1, SH3D4 | 610795 |
ID: 10134 | B cell receptor associated protein 31 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (153700492..153724387, complement) | 6C6-AG, BAP31, CDM, DDCH, DELXQ28, DXS1357E, MICRODELXq28 | 300398 |
ID: 1508 | cathepsin B [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (11842524..11868087, complement) | APPS, CPSB, KWE, RECEUP | 116810 |
ID: 6573 | solute carrier family 19 member 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45502517..45563025, complement) | CHMD, FOLT, IFC-1, IFC1, IMD114, MEGAF, REFC, RFC, RFC1, RFT-1, hRFC, hSLC19A1 | 600424 |
ID: 136895 | sperm microtubule inner protein 4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (25125772..25180354, complement) | C7orf31 | 616071 |
ID: 9841 | zinc finger and BTB domain containing 24 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (109462594..109483219, complement) | BIF1, ICF2, PATZ2, ZNF450 | 614064 |
ID: 10494 | serine/threonine kinase 25 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241492670..241509572, complement) | SOK1, YSK1 | 602255 |
ID: 10207 | PATJ crumbs cell polarity complex component [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (61742480..62163915) | Cipp, INADL, InaD-like, hINADL | 603199 |
ID: 1509 | cathepsin D [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (1752755..1763927, complement) | CLN10, CPSD, HEL-S-130P | 116840 |
ID: 1892 | enoyl-CoA hydratase, short chain 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (133362485..133373354, complement) | ECHS1D, SCEH, mECH, mECH1 | 602292 |
ID: 79869 | cleavage and polyadenylation specific factor 7 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (61402729..61429975, complement) | CFIm59 | |
ID: 55861 | dysbindin domain containing 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45405993..45410610) | C20orf35, CK1BP, HSMNP1 | 611453 |
ID: 9189 | zinc finger BED-type containing 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (2486435..2500976, complement); Chromosome Y, NC_000024.10 (2486435..2500976, complement) | ALTE, DREF, TRAMP, hDREF | 300178 |
ID: 2879 | glutathione peroxidase 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1103994..1106779) | GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx, snPHGPx | 138322 |
ID: 84255 | solute carrier family 37 member 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (140333752..140398530, complement) | SPX3 | 619137 |