enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase (EHHADH)

Name: EHHADH
Description: enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase
Orgname: Homo sapiens
Status: 0
CurrentID: 0
Chromosome: 3
GeneticSource: genomic
MapLocation: 3q26.3-q28
OtherAliases: ECHD, L-PBE, LBFP, LBP, MGC120586, PBFE
OtherDesignations: 3,2-trans-enoyl-CoA isomerase|L-3-hydroxyacyl-CoA dehydrogenase|L-bifunctional protein, peroxisomal|peroxisomal enoyl-CoA hydratase
NomenclatureSymbol: EHHADH
NomenclatureName: enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase
NomenclatureStatus: Official
TaxID: 9606
Mim:
GenomicInfo:
GeneWeight: 2496
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. [provided by RefSeq]
ChrSort: 03
ChrStart: 184908411

UniProtein db: EHHADH UniProt protein knowledge database
Ensembl db: EHHADH Ensembl genome database

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