This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ALG2-20-RE | 20 (40 μL) | 200 μL |  |
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| ALG2-20-OR | 20 (40 μL) | 200 μL |  |
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| ALG2-20-GO | 20 (40 μL) | 200 μL |  |
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| ALG2-20-GR | 20 (40 μL) | 200 μL |  |
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| ALG2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]
Gene Symbol : ALG2
Gene Name : ALG2, alpha-1,3/1,6-mannosyltransferase
Chromosome : CHR 9: 992,219,63-992,164,24
Locus : 9q22.33
Alt. Genes : LRPPRC
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