EHHADH: Difference between revisions
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Latest revision as of 19:24, 5 July 2018
| enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase | |
|---|---|
| Identifiers | |
| Symbol | EHHADH |
| Alt. symbols | ECHD |
| Entrez | 1962 |
| HUGO | 3247 |
| OMIM | 607037 |
| Other data | |
| EC number | 4.2.1.17 |
| Locus | Chr. 3 q26.3-q28 |
EHHADH is a human gene that encodes for a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. Mutations of the gene are a cause of peroxisomal disorders such as Zellweger syndrome. [1]
See also
References
- ↑ "EHHADH enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase [ Homo sapiens (human) ]". NCBI. 6 September 2017. Retrieved 12 September 2017.
 | This article on a gene on human chromosome 3 is a stub. You can help Wikipedia by expanding it. |