Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
54578 | UGT1A6 | UDP glucuronosyltransferase family 1 member A6 | |
54579 | UGT1A5 | UDP glucuronosyltransferase family 1 member A5 | |
54600 | UGT1A9 | UDP glucuronosyltransferase family 1 member A9 | |
54657 | UGT1A4 | UDP glucuronosyltransferase family 1 member A4 | |
54658 | UGT1A1 | UDP glucuronosyltransferase family 1 member A1 | |
54659 | UGT1A3 | UDP glucuronosyltransferase family 1 member A3 | |
56886 | UGGT1 | UDP-glucose glycoprotein glucosyltransferase 1 | |
57511 | COG6 | component of oligomeric golgi complex 6 | |
64132 | XYLT2 | xylosyltransferase 2 | |
80270 | HSD3B7 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 |
Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
35105 | Ugt301D1 | UDP-glycosyltransferase family 301 member D1 | |
35137 | Ugt36F1 | UDP-glycosyltransferase family 36 member F1 | |
35138 | Ugt36D1 | UDP-glycosyltransferase family 36 member D1 | |
35139 | Ugt36E1 | UDP-glycosyltransferase family 36 member E1 | |
40079 | Ugt316A1 | UDP-glycosyltransferase family 316 member A1 | |
41334 | Ugt35A1 | UDP-glycosyltransferase family 35 member A1 | |
41574 | Ugt37A3 | UDP-glycosyltransferase family 37 member A3 | |
42538 | Ugt49B2 | UDP-glycosyltransferase family 49 member B2 | |
53501 | Ugt304A1 | UDP-glycosyltransferase family 304 member A1 | |
53502 | Ugt302K1 | UDP-glycosyltransferase family 302 member K1 |
UniProt ID | Protein Name | Source |
---|---|---|
O60656 | UDP-glucuronosyltransferase 1A9 | |
P00558 | Phosphoglycerate kinase 1 | |
P05062 | Fructose-bisphosphate aldolase B | |
P06858 | Lipoprotein lipase | |
P07954 | Fumarate hydratase, mitochondrial | |
P09104 | Gamma-enolase | |
P11172 | Uridine 5'-monophosphate synthase | |
P11413 | Glucose-6-phosphate 1-dehydrogenase | |
P16109 | P-selectin | |
P16442 | Histo-blood group ABO system transferase |
HPO ID | HPO Term |
---|---|
HP:0000952 | Jaundice |
HP:0002910 | Elevated circulating hepatic transaminase concentration |
HP:0000007 | Autosomal recessive inheritance |
HP:0008282 | Unconjugated hyperbilirubinemia |
HP:0001399 | Hepatic failure |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024