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Symbol
Name
ID
Etfdh
electron transferring flavoprotein, dehydrogenase
MGI:106100
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Scapular winging
Increased intramyocellular lipid droplets
Hypotonia
Difficulty climbing stairs
Exercise-induced muscle fatigue
Muscle weakness
Fatigable weakness of neck muscles
Poor head control
Proximal muscle weakness
Skeletal muscle atrophy
Rhabdomyolysis
Disease(s) Associated with ETFDH
multiple acyl-CoA dehydrogenase deficiency

Mouse Phenotypes
abnormal skeletal muscle fiber mitochondrial morphology
abnormal muscle physiology
myopathy
Availability Mouse Genotype
Etfdhtm1c(EUCOMM)Hmgu/Etfdhtm1c(EUCOMM)Hmgu
Tg(ACTA1-rtTA,tetO-cre)102Monk/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
04/23/2024
MGI 6.23
The Jackson Laboratory