This gene encodes an endoplasmic reticulum membrane protein that is required for utilization of the mannose donor mannose-P-dolichol in the synthesis of lipid-linked oligosaccharides and glycosylphosphatidylinositols. Mutations in this gene result in congenital disorder of glycosylation type If. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MPDU1-20-RE | 20 (40 μL) | 200 μL |  |
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| MPDU1-20-OR | 20 (40 μL) | 200 μL |  |
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| MPDU1-20-GO | 20 (40 μL) | 200 μL |  |
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| MPDU1-20-GR | 20 (40 μL) | 200 μL |  |
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| MPDU1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an endoplasmic reticulum membrane protein that is required for utilization of the mannose donor mannose-P-dolichol in the synthesis of lipid-linked oligosaccharides and glycosylphosphatidylinositols. Mutations in this gene result in congenital disorder of glycosylation type If. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]
Gene Symbol : MPDU1
Gene Name : Mannose-P-dolichol utilization defect 1
Chromosome : CHR 17: 758,364,6-758,821,1
Locus : 17p13.1
Alt. Genes : SUGP2
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