About   Help   FAQ
Symbol
Name
ID
Acadm
acyl-Coenzyme A dehydrogenase, medium chain
MGI:87867
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Distal arthrogryposis
Hypotonia
Generalized hypotonia
Muscle spasm
Fatigable weakness
Fatigable weakness of neck muscles
Proximal muscle weakness
Skeletal muscle atrophy
Myopathy
Disease(s) Associated with ACADM
medium chain acyl-CoA dehydrogenase deficiency

Mouse Phenotypes
abnormal myocardial fiber morphology
myocardial fiber degeneration
cardiomyopathy
Availability Mouse Genotype
Acadmtm1Uab/Acadmtm1Uab

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory