This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ALG9-20-RE | 20 (40 μL) | 200 μL |  |
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| ALG9-20-OR | 20 (40 μL) | 200 μL |  |
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| ALG9-20-GO | 20 (40 μL) | 200 μL |  |
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| ALG9-20-GR | 20 (40 μL) | 200 μL |  |
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| ALG9-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Symbol : ALG9
Gene Name : ALG9, alpha-1,2-mannosyltransferase
Chromosome : CHR 11: 111,871,580-111,776,095
Locus : 11q23.1
Alt. Genes : PREB
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