DPAGT1

Last Update:2017-03-27

The enzyme, which is encoded by this gene, is the enzyme involved in the first step of the synthesis of the dolichol phosphate-linked oligosaccharides in the synthesis of the glycoproteins (N-linked glycans) (GlcNAc-1-P transferase, ALG7). Its enzymatic activity is the transfer the N-acetylglucosamine from the sugar nucleotide UDP-GlcNAc (UDP-N-acetylglucosamine), which is a donor substrate, to the dolichol phosphate, as an acceptor substrate. Biosynthesis is performed on the cytoplasmic side of the endoplasmic reticulum membrane. It has become clear that a mutation of this gene results in congenital disorder of glycosylation type Ij.

Keyword: congenital disorders of glycosylation ,  lipid-linked oligosaccharide
dolichol-phosphate
UDP-GlcNAc
GlcNAc-PP-dolichol

N-Acetylglucosaminyltransferase


GGDB Symbol DPAGT1    Alias
DesignationUDP-GlcNAc:Dolichol phosphate N-acetylglucosaminephosphotransferase
OrganismHomo sapiens
GeneID 1798
HGNC DPAGT1 (2995)
mRNA NM_001382
map11q23.3
Protein NP_001373
EC# 2.7.8.15   
CAZy
GlyCosmos Glycogenes DPAGT1
OMIM 191350
Disease name CDG Ij ,  Congenital Disorder of Glycosylation type Ij
GDGDB CON00352   
Human Protein Atlas ENSG00000172269
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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 "DPAGT1".