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Symbol
Name
ID
Acadvl
acyl-Coenzyme A dehydrogenase, very long chain
MGI:895149
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Decreased plasma carnitine
Elevated serum creatine kinase
Nonketotic hypoglycemia
Dicarboxylic aciduria
Exercise-induced myoglobinuria
Disease(s) Associated with ACADVL
very long chain acyl-CoA dehydrogenase deficiency

Mouse Phenotypes
abnormal adaptive thermogenesis
impaired adaptive thermogenesis
abnormal amino acid level
increased circulating carnitine level
decreased circulating glucose level
hypoglycemia
decreased core body temperature
decreased respiratory quotient
impaired glucose tolerance
decreased glycogen level
abnormal lipid homeostasis
abnormal enzyme/coenzyme activity
Availability Mouse Genotype
Acadvltm1Uab/Acadvltm1Uab
Acadvltm1Vje/Acadvltm1Vje
Acadvltm1Vje/Acadvl+
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
02/18/2020
MGI 6.14
The Jackson Laboratory