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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
UDP glucuronosyltransferase family 1 member A5
Summary
- Gene Symbol
-
- UGT1A5
- Aliases
-
- UGT1E
- Organism
- Homo sapiens (human)
Annotation
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cellular glucuronidation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| enzyme binding | ||
| protein homodimerization activity | ||
| protein heterodimerization activity | ||
| glucuronosyltransferase activity |
GO Hierarchy
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:2383 | neonatal jaundice | |
| DOID:2739 | Gilbert syndrome | |
| DOID:2741 | bilirubin metabolic disorder | |
| DOID:2752 | glycogen storage disease II | |
| DOID:305 | carcinoma | |
| DOID:3803 | Crigler-Najjar syndrome | |
| DOID:4015 | sarcomatoid carcinoma | |
| DOID:409 | liver disease | |
| DOID:4766 | embryoma | |
| DOID:615 | leukopenia |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115608461 | STRHB03216 | ||
| 115608795 | STRHB03216 |
