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MIRAGE
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 |
|---|---|---|
| liver development | ||
| bilirubin conjugation | ||
| xenobiotic metabolic process | ||
| xenobiotic metabolic process | ||
| xenobiotic metabolic process |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytochrome complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| retinoic acid binding | ||
| enzyme inhibitor activity | ||
| enzyme inhibitor activity | ||
| steroid binding | ||
| protein binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- glucuronosyltransferase
- Functional Category
-
- G: Carbohydrate transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| UDP-glycosyltransferase activity |
| transferase activity |
| InterPro |
|---|
| UDP-glucuronosyl/UDP-glucosyltransferase |
| UDP-glycosyltransferase family, conserved site |
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:10211 | cholelithiasis | |
| DOID:11151 | cholecystolithiasis | |
| DOID:1380 | endometrial cancer | |
| DOID:1612 | breast cancer | |
| DOID:2043 | hepatitis B | |
| DOID:2394 | ovarian cancer | |
| DOID:2739 | Gilbert syndrome | |
| DOID:2741 | bilirubin metabolic disorder | |
| DOID:3803 | Crigler-Najjar syndrome | |
| DOID:3908 | lung non-small cell carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000365 | Hearing impairment |
| HP:0000750 | Delayed speech and language development |
| HP:0000952 | Jaundice |
| HP:0001080 | Biliary tract abnormality |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| HP:0001298 | Encephalopathy |
| HP:0001337 | Tremor |
| HP:0001343 | Kernicterus |
| Disease ID | Disease Name |
|---|---|
| OMIM:218800 |
|
| OMIM:606785 |
|
| ORPHA:79234 |
|
| ORPHA:79235 |
|
| OMIM:143500 |
|
| OMIM:237900 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 7363 | FB:FBgn0040261 | ||
| 7364 | FB:FBgn0040261 | ||
| 7365 | FB:FBgn0040261 | ||
| 7366 | FB:FBgn0040261 | ||
| 7367 | FB:FBgn0040261 | ||
| 7368 | FB:FBgn0040261 | ||
| 10720 | FB:FBgn0040261 | ||
| 10941 | FB:FBgn0040261 | ||
| 22236 | Xenbase:XB-GENE-998849 | ||
| 22238 | WB:WBGene00018206 |
