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
Sequence
MAVESQGGRPLVLGLLLCVLGPVVSHAGKILLIPVDGSHWLSMLGAIQQLQQRGHEIVVLAPDASLYIRDGAFYTLKTYPVPFQREDVKESFVSLGHNVFENDSFLQRVIKTYKKIKKDSAMLLSGCSHLLHNKELMASLAESSFDVMLTDPFLPCSPIVAQYLSLPTVFFLHALPCSLEFEATQCPNPFSYVPRPLSSHSDHMTFLQRVKNMLIAFSQNFLCDVVYSPYATLASEFLQREVTVQDLLSSASVWLFRSDFVKDYPRPIMPNMVFVGGINCLHQNPLSQEFEAYINASGEHGIVVFSLGSMVSEIPEKKAMAIADALGKIPQTVLWRYTGTRPSNLANNTILVKWLPQNDLLGHPMTRAFITHAGSHGVYESICNGVPMVMMPLFGDQMDNAKRMETKGAGVTLNVLEMTSEDLENALKAVINDKSYKENIMRLSSLHKDRPVEPLDLAVFWVEFVMRHKGAPHLRPAAHDLTWYQYHSLDVIGFLLAVVLTVAFITFKCCAYGYRKCLGKKGRVKKAHKSKTH
Glycosylation Sites
Displaying all 4 entries
Position Description PubMed ID GlyTouCan ID Source
102 N-linked (GlcNAc...) asparagine
295 N-linked (GlcNAc...) asparagine
338
347 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 5 entries
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
Displaying entries 1 - 10 of 257 in total
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

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024