rs185264895
This variant is located in the ALG9 gene.
▶ClinVar annotation
About 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. [provided by RefSeq, Dec 2008]
View all ALG9 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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