ID: 1353 | cytochrome c oxidase copper chaperone COX11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (54951902..54968785, complement) | COX11P, MC4DN23 | 603648 |
ID: 140468 | COX11 pseudogene 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (28446920..28447630) | COX11, COX11P | |
ID: 672 | BRCA1 DNA repair associated [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43044295..43170327, complement) | BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4, PPP1R53, PSCP, RNF53 | 113705 |
ID: 675 | BRCA2 DNA repair associated [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (32315077..32400268) | BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD, FANCD1, GLM3, PNCA2, XRCC11 | 600185 |
ID: 2100 | estrogen receptor 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64226707..64338613, complement) | ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2, ODG8 | 601663 |
ID: 7316 | ubiquitin C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (124911646..124914650, complement) | HMG20 | 191340 |
ID: 5770 | protein tyrosine phosphatase non-receptor type 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50510383..50585241) | PTP1B | 176885 |
ID: 407008 | microRNA 223 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (66018870..66018979) | MIRN223, miRNA223, mir-223 | 300694 |
ID: 4544 | melatonin receptor 1B [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (92969651..92984960) | FGQTL2, MEL-1B-R, MT2 | 600804 |
ID: 5903 | RAN binding protein 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (108719482..109842301) | ADANE, ANE1, IIAE3, NUP358, TRP1, TRP2 | 601181 |
ID: 2071 | ERCC excision repair 3, TFIIH core complex helicase subunit [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127257290..127294144, complement) | BTF2, GTF2H, RAD25, Ssl2, TFIIH, TTD2, XPB | 133510 |
ID: 3187 | heterogeneous nuclear ribonucleoprotein H1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179614178..179634784, complement) | HNRPH, HNRPH1, NEDCDS, hnRNPH | 601035 |
ID: 4543 | melatonin receptor 1A [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186533655..186555567, complement) | MEL-1A-R, MT1 | 600665 |
ID: 25818 | kallikrein related peptidase 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50943303..50953038, complement) | KLK-L2, KLKL2, SCTE | 605643 |
ID: 23274 | C-type lectin domain containing 16A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10944564..11182186) | Gop-1, KIAA0350 | 611303 |
ID: 8604 | solute carrier family 25 member 12 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171783405..171894244, complement) | AGC1, ARALAR, DEE39, EIEE39 | 603667 |
ID: 6143 | ribosomal protein L19 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39200283..39204732) | L19, eL19 | 180466 |
ID: 23545 | ATPase H+ transporting V0 subunit a2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123712353..123761755) | A2, ARCL, ARCL2A, ATP6A2, ATP6N1D, J6B7, RTF, STV1, TJ6, TJ6M, TJ6S, VPH1, WSS, a2V | 611716 |
ID: 55750 | acylglycerol kinase [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (141551410..141655244) | CATC5, CTRCT38, MTDPS10, MULK | 610345 |
ID: 6016 | Ras like without CAAX 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155897808..155911349, complement) | NS8, RIBB, RIT, ROC1 | 609591 |