XB-GENEPAGE-5911792
???displayGene.symbol???:
mogs
???displayGene.name???:
mannosyl-oligosaccharide glucosidase
???displayGene.synonyms???
(
Nomenclature history )
???displayGene.geneFunction???
Glucosidase I
AI Protein Function
:
mogs encodes an endoplasmic reticulum membrane‑bound glucosidase I that catalyzes removal of the terminal glucose from N‑linked oligosaccharides during protein N‑glycosylation; the protein localizes to...[+]
InterPro
:
???displayGene.geneInteractants???
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Diseases:
Disease Ontology:
congenital disorder of glycosylation type II
MIM:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIb; CDG2B
External Links:
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| ???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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