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: 3146 | high mobility group box 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (30456704..30617597, complement) | HMG-1, HMG1, HMG3, SBP-1 | 163905 |
ID: 5925 | RB transcriptional corepressor 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (48303751..48481890) | OSRC, PPP1R130, RB, p105-Rb, p110-RB1, pRb, pp110 | 614041 |
ID: 2706 | gap junction protein beta 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20187470..20192938, complement) | BAPS, CX26, DFNA3, DFNA3A, DFNB1, DFNB1A, HID, KID, NSRD1, PPK | 121011 |
ID: 2322 | fms related receptor tyrosine kinase 3 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (28003274..28100576, complement) | CD135, FLK-2, FLK2, STK1 | 136351 |
ID: 2321 | fms related receptor tyrosine kinase 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (28300346..28495128, complement) | FLT, FLT-1, VEGFR-1, VEGFR1 | 165070 |
ID: 3356 | 5-hydroxytryptamine receptor 2A [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (46831546..46898082, complement) | 5-HT2A, HTR2 | 182135 |
ID: 2308 | forkhead box O1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40555667..40666641, complement) | FKH1, FKHRA, FOXO1 | 136533 |
ID: 8600 | TNF superfamily member 11 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (42562736..42608013) | CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B, TRANCE, hRANKL2, sOdf | 602642 |
ID: 9365 | klotho [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (33016243..33066143) | HFTC3A, KL | 604824 |
ID: 10673 | TNF superfamily member 13b [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (108269629..108308484) | BAFF, BLYS, CD257, DTL, TALL-1, TALL1, THANK, TNFSF20, TNLG7A, ZTNF4 | 603969 |
ID: 2155 | coagulation factor VII [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113105788..113120685) | SPCA | 613878 |
ID: 10631 | periostin [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37562585..37598768, complement) | OSF-2, OSF2, PDLPOSTN, PN | 608777 |
ID: 540 | ATPase copper transporting beta [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51932669..52012132, complement) | PWD, WC1, WD, WND | 606882 |
ID: 1045 | caudal type homeobox 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27960918..27969315, complement) | CDX-3/AS, CDX3, CDX2 | 600297 |
ID: 2159 | coagulation factor X [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113122799..113149529) | FX, FXA | 613872 |
ID: 1361 | carboxypeptidase B2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (46053186..46105033, complement) | CPU, PCPB, TAFI | 603101 |
ID: 2073 | ERCC excision repair 5, endonuclease [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102846032..102875995) | COFS3-201, ERCM2, UVDR, XPG, XPGC, ERCC5 | 133530 |
ID: 688 | KLF transcription factor 5 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73054976..73077538) | BTEB2, CKLF, IKLF | 602903 |
ID: 1910 | endothelin receptor type B [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (77895487..77975527, complement) | ABCDS, ET-B, ET-BR, ETB, ETB1, ETBR, ETRB, HSCR, HSCR2, WS4A | 131244 |