The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| EHHADH-20-RE | 20 (40 μL) | 200 μL |  |
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| EHHADH-20-OR | 20 (40 μL) | 200 μL |  |
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| EHHADH-20-GO | 20 (40 μL) | 200 μL |  |
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| EHHADH-20-GR | 20 (40 μL) | 200 μL |  |
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| EHHADH-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
Gene Symbol : EHHADH
Gene Name : Enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
Chromosome : CHR 3: 185,282,885-185,190,623
Locus : 3q27.2
Alt. Genes : PREB
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