ID: 345 | apolipoprotein C3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116829907..116833072) | APOCIII, Apo-C3, ApoC-3 | 107720 |
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: 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: 7448 | vitronectin [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28367284..28370307, complement) | V75, VN, VNT | 193190 |
ID: 64240 | ATP binding cassette subfamily G member 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (43806211..43839231, complement) | STSL, STSL2 | 605459 |
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: 2161 | coagulation factor XII [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (177402141..177409564, complement) | HAE3, HAEX, HAF | 610619 |
ID: 1565 | cytochrome P450 family 2 subfamily D member 6 [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: 256394 | serpin family A member 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94442464..94452800, complement) | | 619619 |
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: 64241 | ATP binding cassette subfamily G member 8 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (43838971..43882988) | GBD4, STSL, STSL1 | 605460 |
ID: 23562 | claudin 14 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (36460621..36576569, complement) | DFNB29 | 605608 |
ID: 6554 | solute carrier family 10 member 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69775416..69797241, complement) | FHCA2, NTCP | 182396 |
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: 1548 | cytochrome P450 family 2 subfamily A member 6 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40843541..40850447, complement) | CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB | 122720 |
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: 10747 | MBL associated serine protease 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11026523..11047239, complement) | MAP-2, MAP19, MASP-2, MASP1P1, sMAP | 605102 |
ID: 91828 | exocyst complex component 3 like 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (103094174..103110559) | C14orf73 | |
ID: 2165 | coagulation factor XIII B chain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (197038741..197067260, complement) | FXIIIB | 134580 |
ID: 3263 | hemopexin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (6431049..6440987, complement) | HX | 142290 |