ID: 220001 | von Willebrand factor C and EGF domains [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (61258286..61295316, complement) | URG11, VWC1 | 611115 |
ID: 3309 | heat shock protein family A (Hsp70) member 5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (125234853..125241343, complement) | BIP, GRP78, HEL-S-89n | 138120 |
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: 3303 | heat shock protein family A (Hsp70) member 1A [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31815543..31817942) | HEL-S-103, HSP70, HSP70-1, HSP70-1A, HSP70-2, HSP70.1, HSP70.2, HSP70I, HSP72, HSPA1 | 140550 |
ID: 3115 | major histocompatibility complex, class II, DP beta 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33075990..33089696) | DPB1, HLA-DP, HLA-DP1B, HLA-DPB | 142858 |
ID: 7078 | TIMP metallopeptidase inhibitor 3 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (32801705..32863041) | HSMRK222, K222, K222TA2, SFD | 188826 |
ID: 3416 | insulin degrading enzyme [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92451684..92574093, complement) | INSULYSIN | 146680 |
ID: 9401 | RecQ like helicase 4 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144511288..144517833, complement) | RECQ4 | 603780 |
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: 4052 | latent transforming growth factor beta binding protein 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (32946953..33399509) | ARCL2E | 150390 |
ID: 3198 | homeobox A1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (27092993..27096000, complement) | BSAS, HOX1, HOX1F | 142955 |
ID: 80198 | MUS81 structure-specific endonuclease subunit [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65859674..65867653) | SLX3 | 606591 |
ID: 51162 | EGF like domain multiple 7 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136658856..136672678) | NEU1, VE-STATIN, ZNEU1 | 608582 |
ID: 2201 | fibrillin 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128257909..128538245, complement) | CCA, DA9, EOMD | 612570 |
ID: 5277 | phosphatidylinositol glycan anchor biosynthesis class A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (15319451..15335554, complement) | GPI3, MCAHS2, NEDEPH, PIG-A, PNH1 | 311770 |
ID: 10009 | zinc finger and BTB domain containing 33 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (120250812..120258398) | ZNF-kaiso, ZNF348 | 300329 |
ID: 8535 | chromobox 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (79833156..79839440, complement) | NBP16, PC2 | 603079 |
ID: 3913 | laminin subunit beta 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49121114..49133050, complement) | LAMS, NPHS5, PIERS | 150325 |
ID: 5442 | RNA polymerase mitochondrial [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (617221..633537, complement) | APOLMT, COXPD55, MTRNAP, MTRPOL, h-mtRPOL | 601778 |
ID: 8425 | latent transforming growth factor beta binding protein 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40593166..40629820) | ARCL1C, LTBP-4L, LTBP4S, LTBP4 | 604710 |