Symbol Name ID |
Etfdh
electron transferring flavoprotein, dehydrogenase MGI:106100 |
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 |
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Availability | Mouse Genotype | |||
Etfdhtm1c(EUCOMM)Hmgu/Etfdhtm1c(EUCOMM)Hmgu Tg(ACTA1-rtTA,tetO-cre)102Monk/0 (conditional) |
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 |
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