ID: 4696 | NADH:ubiquinone oxidoreductase subunit A3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (54102855..54107568) | B9, CI-B9 | 603832 |
ID: 2950 | glutathione S-transferase pi 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (67583812..67586653) | DFN7, FAEES3, GST3, GSTP, HEL-S-22, PI | 134660 |
ID: 183 | angiotensinogen [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230702523..230745583, complement) | ANHU, SERPINA8, hFLT1 | 106150 |
ID: 4582 | mucin 1, cell surface associated [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155185824..155192915, complement) | ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3, EMA, H23AG, KL-6, MAM6, MCD, MCKD, MCKD1, MUC-1, MUC-1/SEC, MUC-1/X/ZD, PEM, PEMT, PUM, MUC1 | 158340 |
ID: 3084 | neuregulin 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (31639245..32774046) | ARIA, GGF, GGF2, HGL, HRG, HRG1, HRGA, MST131, MSTP131, NDF-IT2, SMDF, NRG1 | 142445 |
ID: 3956 | galectin 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37675636..37679802) | GAL1, GBP | 150570 |
ID: 2214 | Fc gamma receptor IIIa [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161541759..161550737, complement) | CD16, CD16-II, CD16A, FCG3, FCGR3, FCGRIII, FCR-10, FCRIII, FCRIIIA, FcGRIIIA, IGFR3, IMD20 | 146740 |
ID: 4627 | myosin heavy chain 9 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36281280..36387967, complement) | BDPLT6, DFNA17, EPSTS, FTNS, MATINS, MHA, NMHC-II-A, NMMHC-IIA, NMMHCA | 160775 |
ID: 2289 | FKBP prolyl isomerase 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (35573590..35728583, complement) | AIG61, FKBP54, P54, PPIase, Ptg-10, FKBP5 | 602623 |
ID: 10643 | insulin like growth factor 2 mRNA binding protein 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (23310209..23470491, complement) | CT98, IMP-3, IMP3, KOC, KOC1, VICKZ3 | 608259 |
ID: 360 | aquaporin 3 (Gill blood group) [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (33441160..33447593, complement) | AQP-3, GIL | 600170 |
ID: 7879 | RAB7A, member RAS oncogene family [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (128726183..128814798) | CMT2B, PRO2706, RAB7 | 602298 |
ID: 4001 | lamin B1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (126776623..126837020) | ADLD, LMN, LMN2, LMNB, MCPH26 | 150340 |
ID: 56606 | solute carrier family 2 member 9 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (9771025..10040270, complement) | GLUT9, GLUTX, UAQTL2, URATv1 | 606142 |
ID: 445 | argininosuccinate synthase 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130444707..130501274) | ASS, CTLN1 | 603470 |
ID: 3030 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26190635..26244632, complement) | ECHA, GBP, HADH, LCEH, LCHAD, MTPA, TP-ALPHA | 600890 |
ID: 10935 | peroxiredoxin 3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (119167720..119178812, complement) | AOP-1, AOP1, HBC189, MER5, PPPCD, PRO1748, SCAR32, SP-22, prx-III | 604769 |
ID: 3113 | major histocompatibility complex, class II, DP alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33064569..33080748, complement) | DP(W3), DP(W4), DPA1, HLA-DP1A, HLA-DPA, HLA-DPB1, HLADP, HLASB, PLT1 | 142880 |
ID: 6583 | solute carrier family 22 member 4 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (132294394..132344190) | DFNB60, ETTh, OCTN1 | 604190 |
ID: 506 | ATP synthase F1 subunit beta [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (56638175..56645984, complement) | ATP5B, ATPMB, ATPSB, HEL-S-271, HUMOP2 | 102910 |