This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition of the second glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation of proteins. Mutations in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ih). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ALG8-20-RE | 20 (40 μL) | 200 μL |  |
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| ALG8-20-OR | 20 (40 μL) | 200 μL |  |
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| ALG8-20-GO | 20 (40 μL) | 200 μL |  |
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| ALG8-20-GR | 20 (40 μL) | 200 μL |  |
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| ALG8-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition of the second glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation of proteins. Mutations in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ih). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Symbol : ALG8
Gene Name : ALG8, alpha-1,3-glucosyltransferase
Chromosome : CHR 11: 781,396,59-781,009,41
Locus : 11q14.1
Alt. Genes : FEM1B
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