POGLUT1

Last Update:2022-01-07

POGLUT1 encodes protein O-glucosyltransferase 1. POGLUT1 transfer Glc directly toward Ser in epidermal growth factor-like (EGF) repeats domains of Notch receptors. POGLUT1 was first identified as rumi, the gene responsible for the Notch phenotype of drosophila. Like POFUT1/2, POGLUT1 has an ER-retaining sequence at its C-terminus, and this reaction is also occured in the endoplasmic reticulum. In addition to Glc-T activity, POGLUT1 also possesses Xly-T activity using UDP-Xyl as a sugar donor substrate. It is the causative gene of Dowling-Degos disease 4, a human hereditary skin disease.

Keyword: Dowling-Degos disease ,  EGF-like repeat ,  O-glucose


GGDB Symbol POGLUT1    Alias
Designationprotein O-glucosyltransferase 1
OrganismHomo sapiens
GeneID 56983
HGNC POGLUT1 (22954)
mRNA NM_152305
map
Protein NP_689518
EC#    
CAZy
GlyCosmos Glycogenes POGLUT1
OMIM 615618
Disease name
GDGDB
Human Protein Atlas ENSG00000163389
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Orthologous Gene

Acceptor Substrates (Reference)

Acceptor Substrates (KEM-C)

Expression

RNA Expression from Human Protein Atlas
This RNA expression data uses "HPA data" from the Human Protein Atlas. Tissue RNA Expression

data available from v22.proteinatlas.org

Expression (Reference)

Gene Ontology

This page does not indicate all of the enzymatic reaction, and expression of "POGLUT1".