XB-GENEPAGE-6257495
???displayGene.symbol???:
mpdu1
???displayGene.name???:
mannose-P-dolichol utilization defect 1
???displayGene.synonyms???
cdgif
,
hbebp2bpa
,
lec35
,
my008
,
pp3958
,
pqlc5
[+]
(
Nomenclature history )
AI Protein Function
:
mpdu1 encodes an endoplasmic reticulum membrane protein that participates in dolichol‑linked oligosaccharide biosynthesis and is required for protein N‑glycosylation; the protein is localized to the ER...[+]
???displayGene.geneInteractants???
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Diseases:
Disease Ontology:
congenital disorder of glycosylation type I
MIM:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If; CDG1F
External Links:
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