ID: 64240 | ATP binding cassette subfamily G member 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (43806211..43839231, complement) | STSL, STSL2 | 605459 |
ID: 64241 | ATP binding cassette subfamily G member 8 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (43838971..43882988) | GBD4, STSL, STSL1 | 605460 |
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: 335 | apolipoprotein A1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116835751..116837622, complement) | AMYLD3, HPALP2, apo(a) | 107680 |
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: 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: 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 |
ID: 345 | apolipoprotein C3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116829907..116833072) | APOCIII, Apo-C3, ApoC-3 | 107720 |
ID: 91828 | exocyst complex component 3 like 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (103094174..103110559) | C14orf73 | |
ID: 7448 | vitronectin [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28367284..28370307, complement) | V75, VN, VNT | 193190 |
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: 85320 | ATP binding cassette subfamily C member 11 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (48164819..48247539, complement) | EWWD, MRP8, WW | 607040 |
ID: 2155 | coagulation factor VII [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113105788..113120685) | SPCA | 613878 |
ID: 8608 | retinol dehydrogenase 16 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (56951431..56957608, complement) | RODH-4, RODH4, SDR9C8, hRDH-E | 620043 |
ID: 432 | asialoglycoprotein receptor 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7173431..7179370, complement) | ASGPR, ASGPR1, CLEC4H1, HL-1 | 108360 |
ID: 336 | apolipoprotein A2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161222292..161223628, complement) | Apo-AII, ApoA-II, apoAII | 107670 |
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: 256394 | serpin family A member 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94442464..94452800, complement) | | 619619 |
ID: 2165 | coagulation factor XIII B chain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (197038741..197067260, complement) | FXIIIB | 134580 |
ID: 6554 | solute carrier family 10 member 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69775416..69797241, complement) | FHCA2, NTCP | 182396 |