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MGP Database

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MGP003269

Ontology/Pathway Information

Entrez Gene ID	7368
Gene Name	UDP glycosyltransferase 8
Gene Symbol	UGT8
Species	Homo sapiens

Gene Ontology (GO Annotations)

GO ID	Source	Type	Description
GO:0016021	IEA:UniProtKB-KW	C	integral component of membrane
GO:0043231	IBA:GO_Central	C	intracellular membrane-bounded organelle
GO:0003851	IEA:UniProtKB-EC	F	2-hydroxyacylsphingosine 1-beta-galactosyltransferase activity
GO:0015020	IBA:GO_Central	F	glucuronosyltransferase activity
GO:0008489	TAS:ProtInc	F	UDP-galactose:glucosylceramide beta-1,4-galactosyltransferase activity
GO:0008088	IEA:Ensembl	P	axon cargo transport
GO:0032870	IBA:GO_Central	P	cellular response to hormone stimulus
GO:0007417	TAS:ProtInc	P	central nervous system development
GO:0007010	IEA:Ensembl	P	cytoskeleton organization
GO:0009813	IBA:GO_Central	P	flavonoid biosynthetic process
GO:0052696	IBA:GO_Central	P	flavonoid glucuronidation
GO:0006682	IEA:UniProtKB-UniPathway	P	galactosylceramide biosynthetic process
GO:0048812	IEA:Ensembl	P	neuron projection morphogenesis
GO:0030913	IEA:Ensembl	P	paranodal junction assembly
GO:0007422	TAS:ProtInc	P	peripheral nervous system development
GO:0002175	IEA:Ensembl	P	protein localization to paranode region of axon

SMP Pathway Links

SMP ID	Description
SMP00525	Fabry disease
SMP00349	Gaucher Disease
SMP00348	Globoid Cell Leukodystrophy
SMP00526	Krabbe disease
SMP00347	Metachromatic Leukodystrophy (MLD)
SMP00034	Sphingolipid Metabolism