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Symbol
Name
ID

Acad9
acyl-Coenzyme A dehydrogenase family, member 9
MGI:1914272

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Hypotonia	Generalized hypotonia	EMG: myopathic abnormalities	Muscle weakness	Fatigable weakness	Generalized muscle weakness	Myopathy
Disease(s) Associated with ACAD9
nuclear type mitochondrial complex I deficiency 20

Mouse Phenotypes		myocardial fiber disarray	decreased cardiac muscle contractility	cardiomyopathy	abnormal muscle morphology	centrally nucleated skeletal muscle fibers	muscle weakness
Availability	Mouse Genotype	myocardial fiber disarray	decreased cardiac muscle contractility	cardiomyopathy	abnormal muscle morphology	centrally nucleated skeletal muscle fibers	muscle weakness
	Acad9^{tm1c(KOMP)Wtsi}/Acad9^{tm1c(KOMP)Wtsi} Tg(ACTA1-cre)79Jme/0 (conditional)
	Acad9^{tm1c(KOMP)Wtsi}/Acad9^{tm1c(KOMP)Wtsi} Tg(Myh6-cre)2182Mds/0 (conditional)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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