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Symbol
Name
ID

Acadvl
acyl-Coenzyme A dehydrogenase, very long chain
MGI:895149

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Hypotonia	Infantile muscular hypotonia	Muscle spasm	Muscle stiffness	Muscle weakness	Exercise-induced rhabdomyolysis
Disease(s) Associated with ACADVL
very long chain acyl-CoA dehydrogenase deficiency

Mouse Phenotypes		abnormal myocardial fiber morphology	myocardial fiber degeneration	dilated cardiomyopathy	decreased ventricle muscle contractility	cardiomyopathy	abnormal skeletal muscle fiber morphology
Availability	Mouse Genotype	abnormal myocardial fiber morphology	myocardial fiber degeneration	dilated cardiomyopathy	decreased ventricle muscle contractility	cardiomyopathy	abnormal skeletal muscle fiber morphology
	Acadvl^tm1Vje/Acadvl^tm1Vje
	Acadvl^tm1Zkhu/Acadvl^tm1Zkhu Tg(Myh6-cre)1Jmk/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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