{"symbol":"ALG9","synonyms":["CDG1L","LOH11CR1J","DIBD1","GIKANIS"],"name":"ALG9, alpha-1,2-mannosyltransferase","description":"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]","ncbiEntrezGeneId":79796,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/79796","proteins":[{"symbol":"ALG9_HUMAN","href":"/api/1.0/protein/ALG9_HUMAN"}],"hgncRootFamilies":[{"name":"Glycosyltransferases","href":"/api/1.0/gene_family/Glycosyltransferases"}]}