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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
Muscular hypotonia
Generalized hypotonia
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
Acadvltm1Vje/Acadvltm1Vje
Acadvltm1Zkhu/Acadvltm1Zkhu
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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last database update
02/04/2020
MGI 6.14
The Jackson Laboratory