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
HGNC Symbol
|
: |
DPAGT1
|
historical
|
: |
ALG7 DGPT DPAGT DPAGT2 G1PT GPT UAGT UGAT
|
related terminology
|
: |
CDG-Ij CDG1J
|
allelic
|
: |
CDG-Ij CDG1J
|
unknown
|
: |
D11S366
|
|
|
|
Designation | UDP-GlcNAc:Dolichol phosphate N-acetylglucosaminephosphotransferase |
Organism | Homo sapiens |
GeneID |
1798
|
HGNC |
DPAGT1
(2995)
|
mRNA |
NM_001382
|
map | 11q23.3 |
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
|
This page does not indicate all of the enzymatic reaction, and expression of "DPAGT1".