6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PGD-20-RE | 20 (40 μL) | 200 μL |  |
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| PGD-20-OR | 20 (40 μL) | 200 μL |  |
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| PGD-20-GO | 20 (40 μL) | 200 μL |  |
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| PGD-20-GR | 20 (40 μL) | 200 μL |  |
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| PGD-20-AQ | 20 (40 μL) | 200 μL |  |
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6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]
Gene Symbol : PGD
Gene Name : Phosphogluconate dehydrogenase
Chromosome : CHR 1: 103,989,91-104,205,10
Locus : 1p36.22
Alt. Genes : LRPPRC
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