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ALG9

Official Full Name
ALG9 alpha-1,2-mannosyltransferase
Organism
Homo sapiens
GeneID
79796
Background
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. [provided by RefSeq, Dec 2008]
Synonyms
CDG1L; DIBD1; GIKANIS; LOH11CR1J;

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