This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation. [provided by RefSeq, Jul 2008]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
ALG12-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation. [provided by RefSeq, Jul 2008]
Gene Symbol : ALG12
Gene Name : ALG12, alpha-1,6-mannosyltransferase
Chromosome : CHR 22: 499,184,68-498,601,62
Locus : 22q13.33
Alt. Genes : ENAM
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