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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
UDP-glucuronosyltransferase 1A1
Summary
- UniProt ID
- P22309
- Gene Symbol
-
- UGT1A1
- GNT1
- UGT1
- Organism
- Homo sapiens (human)
External Links
- GlyConnect
- GlyGen
- P22309
- PubChem
- P22309
- SwissLipids
- The Human Metabolome Database
- HMDBP00483
- O-GlcNAcAtlas
- P22309
Annotation
- Keyword
-
- Alternative splicing
- Cytoplasm
- Disease variant
- Endoplasmic reticulum
- Glycoprotein
- Glycosyltransferase
- Lipid metabolism
- Reference proteome
- Signal
- Transmembrane helix
- Gene Ontology (GO)
Sequence
MAVESQGGRPLVLGLLLCVLGPVVSHAGKILLIPVDGSHWLSMLGAIQQLQQRGHEIVVLAPDASLYIRDGAFYTLKTYPVPFQREDVKESFVSLGHNVFENDSFLQRVIKTYKKIKKDSAMLLSGCSHLLHNKELMASLAESSFDVMLTDPFLPCSPIVAQYLSLPTVFFLHALPCSLEFEATQCPNPFSYVPRPLSSHSDHMTFLQRVKNMLIAFSQNFLCDVVYSPYATLASEFLQREVTVQDLLSSASVWLFRSDFVKDYPRPIMPNMVFVGGINCLHQNPLSQEFEAYINASGEHGIVVFSLGSMVSEIPEKKAMAIADALGKIPQTVLWRYTGTRPSNLANNTILVKWLPQNDLLGHPMTRAFITHAGSHGVYESICNGVPMVMMPLFGDQMDNAKRMETKGAGVTLNVLEMTSEDLENALKAVINDKSYKENIMRLSSLHKDRPVEPLDLAVFWVEFVMRHKGAPHLRPAAHDLTWYQYHSLDVIGFLLAVVLTVAFITFKCCAYGYRKCLGKKGRVKKAHKSKTH
Glycosylation Sites
G49108TO
G39188ZX
G14669DU
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| APAP ADME | Homo sapiens |
| Aspirin ADME | Homo sapiens |
| Defective UGT1A1 causes hyperbilirubinemia | Homo sapiens |
| Glucuronidation | Homo sapiens |
| Heme degradation | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:2047 | hepatitis D | |
| DOID:0040085 | bacterial sepsis | |
| DOID:0050387 | nonpapillary renal cell carcinoma | |
| DOID:0050471 | Carney complex | |
| DOID:0050589 | inflammatory bowel disease | |
| DOID:0050590 | severe congenital neutropenia | |
| DOID:0050782 | Zollinger-Ellison syndrome | |
| DOID:0050830 | peripheral artery disease | |
| DOID:0050865 | tongue squamous cell carcinoma | |
| DOID:0060041 | autism spectrum disorder |
