MAN2A1
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
Alpha-mannosidase 2 is an enzyme that in humans is encoded by the MAN2A1 gene.[5][6][7]
External IDsOMIM: 154582; MGI: 104669; HomoloGene: 1777; GeneCards: MAN2A1; OMA:MAN2A1 - orthologs
Function
This gene encodes a protein which is a member of family 38 of the glycosyl hydrolases. The protein is located in the Golgi apparatus and catalyzes the final hydrolytic step in the asparagine-linked oligosaccharide (N-linked glycosylation) maturation pathway. Mutations in the mouse homolog of this gene have been shown to cause a systemic autoimmune disease similar to human systemic lupus erythematosus.[7]