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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
UDP glucuronosyltransferase family 1 member A1
Summary
- Gene Symbol
-
- UGT1A1
- Aliases
-
- UGT1A
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Cytoplasm
- Disease variant
- Endoplasmic reticulum
- Glycoprotein
- Glycosyltransferase
- Lipid metabolism
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| biphenyl catabolic process | ||
| animal organ regeneration | ||
| response to lipopolysaccharide | ||
| flavonoid glucuronidation | ||
| bilirubin conjugation |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| plasma membrane | ||
| endoplasmic reticulum chaperone complex | ||
| perinuclear region of cytoplasm |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| steroid binding | ||
| protein homodimerization activity | ||
| enzyme binding | ||
| enzyme inhibitor activity | ||
| retinoic acid binding |
GO Hierarchy
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:13739 | nutmeg liver | |
| DOID:1380 | endometrial cancer | |
| DOID:14221 | abdominal obesity-metabolic syndrome 1 | |
| DOID:1443 | cerebral degeneration | |
| DOID:14499 | Fabry disease | |
| DOID:14525 | Reye syndrome | |
| DOID:1485 | cystic fibrosis | |
| DOID:1520 | colon carcinoma | |
| DOID:1588 | thrombocytopenia | |
| DOID:1612 | breast cancer |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001392 | Abnormality of the liver |
| HP:0001399 | Hepatic failure |
| HP:0002354 | Memory impairment |
| HP:0002910 | Elevated circulating hepatic transaminase concentration |
| HP:0003265 | Neonatal hyperbilirubinemia |
| HP:0003577 | Congenital onset |
| HP:0003623 | Neonatal onset |
| HP:0006579 | Prolonged neonatal jaundice |
| HP:0008176 | Neonatal unconjugated hyperbilirubinemia |
| HP:0008282 | Unconjugated hyperbilirubinemia |
| Disease ID | Disease Name |
|---|---|
| ORPHA:79234 |
|
| ORPHA:79235 |
|
| OMIM:237900 |
|
| OMIM:218800 |
|
| OMIM:143500 |
|
| OMIM:606785 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 109096697 | CYPCA51496 | ||
| 116446652 | CORMO24175 | ||
| 103258345 | CARSF21068 | ||
| 115608460 | STRHB03216 | ||
| 115608461 | STRHB03216 | ||
| 115608795 | STRHB03216 |
