ID: 2328 | flavin containing dimethylaniline monoxygenase 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (171090905..171117819) | FMOII, TMAU, dJ127D3.1 | 136132 |
ID: 388646 | guanylate binding protein 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (89131742..89176003, complement) | GBP4L | 612468 |
ID: 2998 | glycogen synthase 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21532577..21604847, complement) | | 138571 |
ID: 10246 | solute carrier family 17 member 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (25912754..25930691, complement) | NPT3 | 611049 |
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: 2822 | glycosylphosphatidylinositol specific phospholipase D1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (24423969..24495287, complement) | GPIPLD, GPIPLDM, PIGPLD, PIGPLD1, PLD | 602515 |
ID: 420 | ADP-ribosyltransferase 4 (inactive) (Dombrock blood group) [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (14825569..14843526, complement) | ARTC4, CD297, DO, DO/ART4, DOK1 | 110600 |
ID: 9970 | nuclear receptor subfamily 1 group I member 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161229669..161238203, complement) | CAR, CAR1, MB67 | 603881 |
ID: 2165 | coagulation factor XIII B chain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (197038741..197067260, complement) | FXIIIB | 134580 |
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: 3053 | serpin family D member 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20774113..20787720) | D22S673, HC2, HCF2, HCII, HLS2, LS2, THPH10 | 142360 |
ID: 730262 | peptidylprolyl isomerase A like 4E [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (144372875..144373634, complement) | COAS2, PPIAL4F | 608608 |
ID: 199920 | FYN binding protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (56718789..56826914, complement) | ARAP, C1orf168 | 618478 |
ID: 81494 | complement factor H related 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (196975034..197009678) | CFHL5D, FHR-5, FHR5, CFHR5 | 608593 |
ID: 6580 | solute carrier family 22 member 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (160121815..160158718) | HOCT1, OCT1, oct1_cds | 602607 |
ID: 10400 | phosphatidylethanolamine N-methyltransferase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17505563..17592142, complement) | PEAMT, PEMPT2, PLMT, PNMT, PEMT | 602391 |
ID: 763 | carbonic anhydrase 5A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87881549..87936529, complement) | CA5D, CAV, CAVA, GS1-21A4.1, CA5A | 114761 |
ID: 2267 | fibrinogen like 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17864389..17895538, complement) | HFREP1, HP-041, HPS, LFIRE-1, LFIRE1 | 605776 |
ID: 1361 | carboxypeptidase B2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (46053186..46105033, complement) | CPU, PCPB, TAFI | 603101 |
ID: 8647 | ATP binding cassette subfamily B member 11 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (168915390..169031324, complement) | ABC16, BRIC2, BSEP, PFIC-2, PFIC2, PGY4, SPGP | 603201 |