Anti-ALG9

This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. Protein function: Catalyzes the transfer of mannose from Dol-P-Man to lipid-linked oligosaccharides. [The UniProt Consortium]