This gene encodes the first enzyme in the N-linked oligosaccharide processing pathway. The enzyme cleaves the distal alpha-1,2-linked glucose residue from the Glc(3)-Man(9)-GlcNAc(2) oligosaccharide precursor. This protein is located in the lumen of the endoplasmic reticulum. Defects in this gene are a cause of type IIb congenital disorder of glycosylation (CDGIIb). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MOGS-20-RE | 20 (40 μL) | 200 μL |  |
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| MOGS-20-OR | 20 (40 μL) | 200 μL |  |
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| MOGS-20-GO | 20 (40 μL) | 200 μL |  |
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| MOGS-20-GR | 20 (40 μL) | 200 μL |  |
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| MOGS-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes the first enzyme in the N-linked oligosaccharide processing pathway. The enzyme cleaves the distal alpha-1,2-linked glucose residue from the Glc(3)-Man(9)-GlcNAc(2) oligosaccharide precursor. This protein is located in the lumen of the endoplasmic reticulum. Defects in this gene are a cause of type IIb congenital disorder of glycosylation (CDGIIb). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
Gene Symbol : MOGS
Gene Name : Mannosyl-oligosaccharide glucosidase
Chromosome : CHR 2: 744,654,09-744,610,56
Locus : 2p13.1
Alt. Genes : AKAP9
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