Gene: EHHADH

Alternate names for this Gene: ECHD|FRTS3|L-PBE|LBFP|LBP|MFE1|PBFE

Gene Summary: 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.

Gene is located in Chromosome: 3

Location in Chromosome : 3q27.2

Description of this Gene: enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase

Type of Gene: protein-coding

Gene: EHHADH-AS1

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene: