Protein-coding gene in the species Homo sapiens
Alpha-mannosidase 2 is an enzyme that in humans is encoded by the MAN2A1 gene .[ 5] [ 6] [ 7]
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]
^ a b c GRCh38: Ensembl release 89: ENSG00000112893 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024085 – Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Moremen KW, Robbins PW (Dec 1991). "Isolation, characterization, and expression of cDNAs encoding murine alpha-mannosidase II, a Golgi enzyme that controls conversion of high mannose to complex N-glycans" . The Journal of Cell Biology . 115 (6): 1521–34. doi :10.1083/jcb.115.6.1521 . PMC 2289207 . PMID 1757461 .
^ Oka T, Ungar D, Hughson FM, Krieger M (May 2004). "The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins" . Molecular Biology of the Cell . 15 (5): 2423–35. doi :10.1091/mbc.E03-09-0699 . PMC 404034 . PMID 15004235 .
^ a b "Entrez Gene: MAN2A1 mannosidase, alpha, class 2A, member 1" .
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