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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 |
|---|---|---|
| steroid metabolic process | ||
| xenobiotic metabolic process | ||
| cellular response to estradiol stimulus | ||
| estrogen metabolic process |
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:10825 | essential hypertension | |
| DOID:10914 | amnestic disorder | |
| DOID:10923 | sickle cell anemia | |
| DOID:10965 | spastic diplegia | |
| DOID:10968 | spastic monoplegia | |
| DOID:10969 | hemiplegia | |
| DOID:10970 | spastic quadriplegic cerebral palsy | |
| DOID:1099 | alpha thalassemia | |
| DOID:11054 | urinary bladder cancer | |
| DOID:1107 | esophageal carcinoma |
- 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 |
|---|---|---|---|
| 185500 | WB:WBGene00018206 | ||
| 35105 | FB:FBgn0032684 | ||
| 35137 | FB:FBgn0027074 | ||
| 35138 | FB:FBgn0032713 | ||
| 35139 | FB:FBgn0027070 | ||
| 40079 | FB:FBgn0036842 | ||
| 41333 | FB:FBgn0026314 | ||
| 41334 | FB:FBgn0026315 | ||
| 41574 | FB:FBgn0038083 | ||
| 42538 | FB:FBgn0038886 |
