ID: 28234 | solute carrier organic anion transporter family member 1B3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (20810705..20916911) | HBLRR, LST-2, LST-3TM13, LST3, OATP-8, OATP1B3, OATP8, SLC21A8 | 605495 |
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: 3698 | inter-alpha-trypsin inhibitor heavy chain 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (7703316..7749520) | H2P, ITI-HC2, SHAP | 146640 |
ID: 622 | 3-hydroxybutyrate dehydrogenase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197509783..197573343, complement) | BDH, SDR9C1 | 603063 |
ID: 3950 | leukocyte cell derived chemotaxin 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (135946904..135954983, complement) | chm-II, chm2 | 602882 |
ID: 387775 | solute carrier family 22 member 10 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63289903..63363144) | OAT5, hOAT5 | 607580 |
ID: 256394 | serpin family A member 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94442464..94452800, complement) | | 619619 |
ID: 1361 | carboxypeptidase B2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (46053186..46105033, complement) | CPU, PCPB, TAFI | 603101 |
ID: 2165 | coagulation factor XIII B chain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (197038741..197067260, complement) | FXIIIB | 134580 |
ID: 6898 | tyrosine aminotransferase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71565660..71577092, complement) | | 613018 |
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: 3263 | hemopexin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (6431049..6440987, complement) | HX | 142290 |
ID: 3026 | hyaluronan binding protein 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (113550831..113589602) | FSAP, HABP, HGFAL, NMTC5, PHBP | 603924 |
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: 732 | complement C8 beta chain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (56929207..56966015, complement) | C82 | 120960 |
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: 6291 | serum amyloid A4, constitutive [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (18231355..18236802, complement) | C-SAA, CSAA | 104752 |
ID: 114770 | peptidoglycan recognition protein 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (15468645..15479501, complement) | HMFT0141, PGLYRPL, PGRP-L, PGRPL, TAGL-like, tagL, tagL-alpha, tagl-beta | 608199 |
ID: 319 | apolipoprotein F [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (56360568..56362857, complement) | Apo-F, LTIP | 107760 |
ID: 1373 | carbamoyl-phosphate synthase 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (210477685..210679107) | CPSASE1, GATD6, PHN | 608307 |