ID: 6694 | secreted phosphoprotein 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (234050702..234077134) | SPP-244, SPP2 | 602637 |
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 |
ID: 3950 | leukocyte cell derived chemotaxin 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (135946904..135954983, complement) | chm-II, chm2 | 602882 |
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: 622 | 3-hydroxybutyrate dehydrogenase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197509783..197573343, complement) | BDH, SDR9C1 | 603063 |
ID: 3263 | hemopexin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (6431049..6440987, complement) | HX | 142290 |
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: 85320 | ATP binding cassette subfamily C member 11 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (48164819..48247539, complement) | EWWD, MRP8, WW | 607040 |
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: 10599 | solute carrier organic anion transporter family member 1B1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21131194..21239796) | HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 | 604843 |
ID: 388646 | guanylate binding protein 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (89131742..89176003, complement) | GBP4L | 612468 |
ID: 81494 | complement factor H related 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (196975034..197009678) | CFHL5D, FHR-5, FHR5, CFHR5 | 608593 |
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: 6554 | solute carrier family 10 member 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69775416..69797241, complement) | FHCA2, NTCP | 182396 |
ID: 7363 | UDP glucuronosyltransferase family 2 member B4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (69480165..69526014, complement) | HLUG25, UDPGT2B4, UDPGTH1, UDPGTh-1, UGT2B11 | 600067 |
ID: 735 | complement C9 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (39284140..39364495, complement) | ARMD15D, C9 | 120940 |
ID: 2147 | coagulation factor II, thrombin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (46719213..46739506) | PT, RPRGL2, THPH1 | 176930 |
ID: 83597 | receptor transporter protein 3 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (46497976..46500950) | LTM1, TMEM7, Z3CXXC3 | 607181 |
ID: 2266 | fibrinogen gamma chain [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154604136..154612656, complement) | | 134850 |
ID: 3698 | inter-alpha-trypsin inhibitor heavy chain 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (7703316..7749520) | H2P, ITI-HC2, SHAP | 146640 |