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Symbol Name ID |
Etfdh
electron transferring flavoprotein, dehydrogenase MGI:106100 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased circulating carnitine concentration |
Electron transfer flavoprotein-ubiquinone oxidoreductase defect |
| Disease(s) Associated with ETFDH | ||
| multiple acyl-CoA dehydrogenase deficiency |
| Mouse Phenotypes | abnormal skeletal muscle fiber mitochondrial morphology |
abnormal oxidative phosphorylation |
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| Availability | Mouse Genotype | ||
| Etfdhtm1c(EUCOMM)Hmgu/Etfdhtm1c(EUCOMM)Hmgu Tg(ACTA1-rtTA,tetO-cre)102Monk/0 (conditional) |
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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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