This gene encodes an enzyme which catalyzes the translocation of the Man(5)GlcNAc (2)-PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type In.[provided by RefSeq, Dec 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RFT1-20-RE | 20 (40 μL) | 200 μL |  |
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| RFT1-20-OR | 20 (40 μL) | 200 μL |  |
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| RFT1-20-GO | 20 (40 μL) | 200 μL |  |
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| RFT1-20-GR | 20 (40 μL) | 200 μL |  |
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| RFT1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an enzyme which catalyzes the translocation of the Man(5)GlcNAc (2)-PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type In.[provided by RefSeq, Dec 2008]
Gene Symbol : RFT1
Gene Name : RFT1 homolog
Chromosome : CHR 3: 531,304,68-530,711,50
Locus : 3p21.1
Alt. Genes : OPTN
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