Your search for "hadh" returned 468 TaqMan® SNP Genotyping Assays
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]
AA409008, AU019341, AW742602, HAD, HADH, HADH1, HADHSC, HCDH, HHF4, MSCHAD, SCHAD
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