ALG9 ALG9 alpha-1,2-mannosyltransferase [ Homo sapiens (human) ] - Gene - Data resources

79796

ALG9 ALG9 alpha-1,2-mannosyltransferase [ Homo sapiens (human) ]
Source: NCBI Gene (ID 79796)

Symbol: ALG9

Full name: ALG9 alpha-1,2-mannosyltransferase

Gene type: protein coding

RefSeq status: REVIEWED

Also known as: CDG1L; DIBD1; GIKANIS; LOH11CR1J

Summary: 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]

Expression: Ubiquitous expression in testis (RPKM 3.4), thyroid (RPKM 3.0) and 25 other tissues

Orthologs: mouse

Gene size: 103557bp

Exon count: 27