ID: 1559 | cytochrome P450 family 2 subfamily C member 9 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (94938658..94990091) | CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9 | 601130 |
ID: 6822 | sulfotransferase family 2A member 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47870467..47886315, complement) | DHEA-ST, DHEA-ST8, DHEAS, HST, ST2, ST2A1, ST2A3, STD, SULT2A3, hSTa | 125263 |
ID: 2165 | coagulation factor XIII B chain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (197038741..197067260, complement) | FXIIIB | 134580 |
ID: 6360 | C-C motif chemokine ligand 16 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (35976499..35981497, complement) | CKb12, HCC-4, ILINCK, LCC-1, LEC, LMC, Mtn-1, NCC-4, NCC4, SCYA16, SCYL4 | 601394 |
ID: 1558 | cytochrome P450 family 2 subfamily C member 8 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (95036772..95069497, complement) | CPC8DM, CYPIIC8, MP-12/MP-20, CYP2C8 | 601129 |
ID: 570 | bile acid-CoA:amino acid N-acyltransferase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (101360417..101385006, complement) | BACAT, BACD1, BAT, HCHO | 602938 |
ID: 3026 | hyaluronan binding protein 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (113550831..113589602) | FSAP, HABP, HGFAL, NMTC5, PHBP | 603924 |
ID: 388646 | guanylate binding protein 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (89131742..89176003, complement) | GBP4L | 612468 |
ID: 1361 | carboxypeptidase B2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (46053186..46105033, complement) | CPU, PCPB, TAFI | 603101 |
ID: 85320 | ATP binding cassette subfamily C member 11 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (48164819..48247539, complement) | EWWD, MRP8, WW | 607040 |
ID: 1369 | carboxypeptidase N subunit 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100042193..100081869, complement) | CPN, SCPN | 603103 |
ID: 256394 | serpin family A member 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94442464..94452800, complement) | | 619619 |
ID: 1562 | cytochrome P450 family 2 subfamily C member 18 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (94683729..94736190) | CPCI, CYP2C, CYP2C17, P450-6B/29C, P450IIC17 | 601131 |
ID: 8608 | retinol dehydrogenase 16 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (56951431..56957608, complement) | RODH-4, RODH4, SDR9C8, hRDH-E | 620043 |
ID: 6554 | solute carrier family 10 member 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69775416..69797241, complement) | FHCA2, NTCP | 182396 |
ID: 335 | apolipoprotein A1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116835751..116837622, complement) | AMYLD3, HPALP2, apo(a) | 107680 |
ID: 2822 | glycosylphosphatidylinositol specific phospholipase D1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (24423969..24495287, complement) | GPIPLD, GPIPLDM, PIGPLD, PIGPLD1, PLD | 602515 |
ID: 462 | serpin family C member 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (173903800..173917327, complement) | AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2, THPH7 | 107300 |
ID: 1581 | cytochrome P450 family 7 subfamily A member 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (58490178..58500163, complement) | CP7A, CYP7, CYPVII | 118455 |
ID: 1565 | cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene) [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (42126499..42130810, complement) | CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 | 124030 |