This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15. [provided by RefSeq, May 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| HADH-20-RE | 20 (40 μL) | 200 μL |  |
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| HADH-20-OR | 20 (40 μL) | 200 μL |  |
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| HADH-20-GO | 20 (40 μL) | 200 μL |  |
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| HADH-20-GR | 20 (40 μL) | 200 μL |  |
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| HADH-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15. [provided by RefSeq, May 2010]
Gene Symbol : HADH
Gene Name : Hydroxyacyl-CoA dehydrogenase
Chromosome : CHR 4: 107,989,713-108,035,174
Locus : 4q25
Alt. Genes : PREB
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