{"symbol":"ALG3","synonyms":["NOT56L","CDG1D","D16ERTD36E","CDGS6","CDGS4","NOT56"],"name":"ALG3, alpha-1,3- mannosyltransferase","description":"This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","ncbiEntrezGeneId":10195,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/10195","proteins":[{"symbol":"ALG3_HUMAN","href":"/api/1.0/protein/ALG3_HUMAN"}],"hgncRootFamilies":[{"name":"Glycosyltransferases","href":"/api/1.0/gene_family/Glycosyltransferases"}]}