NCBI Description of 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.|
Community Annotation of ALG9 Add / Edit ALG9: Annotations
No community annotations yet for ALG9.
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