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ECHS1 mutant hexamer [mitochondrial matrix]
Stable Identifier
R-HSA-9916711
Type
Complex
Species
Homo sapiens
Compartment
mitochondrial matrix
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of branched-chain amino acid catabolism (Homo sapiens)
Mitochondrial short-chain enoyl-CoA hydratase deficiency 1 (Homo sapiens)
ECHS1 mutants don't synthesize beta-hydroxyisobutyryl-CoA (Homo sapiens)
ECHS1 mutant hexamer [mitochondrial matrix] (Homo sapiens)
Participants
components
x 6
ECHS1 mutants [mitochondrial matrix]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
mitochondrial short-chain enoyl-CoA hydratase 1 deficiency
DOID:0070540
ECHS1D
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