Literature summary extracted from

Battisti, C.; Forte, F.; Molinelli, M.; Funghini, S.; Pasquini, E.; Tassini, M.; Dotti, M.T.; Federico, A.
A new case of short-chain acyl-CoA dehydrogenase deficiency: clinical, biochemical, genetic and (1)H-NMR spectroscopic studies (2007), Neurol. Sci., 28, 328-330.

Application

EC Number	Application	Comment	Organism
1.3.8.1	medicine	short-chain-acyl-CoA-dehydrogenase deficiency is an inborn error of mitochondrial fatty acid metabolism caused by rare mutations as well as common susceptibility variations in the SCAD gene	Homo sapiens

Organism

EC Number	Organism	UniProt	Comment	Textmining
1.3.8.1	Homo sapiens	-	-	-

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
1.3.8.1	butyryl-CoA + electron acceptor	-	Homo sapiens	2-butenoyl-CoA + reduced acceptor	-	?

Synonyms

EC Number	Synonyms	Comment	Organism
1.3.8.1	SCAD	-	Homo sapiens
1.3.8.1	short-chain acyl-CoA dehydrogenase	-	Homo sapiens

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Release 2023.1 (January 2023)