Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
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:0110757 | type 1 diabetes mellitus 20 | |
| DOID:0110758 | type 1 diabetes mellitus 21 | |
| DOID:0110759 | type 1 diabetes mellitus 22 | |
| DOID:0110760 | type 1 diabetes mellitus 23 | |
| DOID:0110761 | type 1 diabetes mellitus 24 | |
| DOID:0110845 | xeroderma pigmentosum group D | |
| DOID:0110892 | inflammatory bowel disease 1 | |
| DOID:0111029 | hemochromatosis type 1 | |
| DOID:0111414 | trichohepatoenteric syndrome | |
| DOID:0111415 | trichohepatoenteric syndrome 1 |
- 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 |
|---|---|
| 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 |
|---|---|---|---|
| 24861 | RGD:3935 | ||
| 100025642 | MONDO13171 | ||
| 102443979 | PELSI04246 | ||
| 100552049 | ANOCA00897 | ||
| 110198831 | PHACI30779 | ||
| 100229734 | TAEGU27645 | ||
| 101817057 | FICAL14143 | ||
| 114582812 | PODMU07548 | ||
| 105813987 | PROCO20590 | ||
| 850886 | SGD:S000004179 |
