Symbol Name ID |
Atp5f1a
ATP synthase F1 subunit alpha MGI:88115 |
Darker colors indicate more annotations |
Human Phenotypes | Failure to thrive |
Intrauterine growth retardation |
Disease(s) Associated with ATP5F1A | ||
combined oxidative phosphorylation deficiency 22 | ||
mitochondrial complex V (ATP synthase) deficiency nuclear type 4A |
Mouse Phenotypes | decreased lean body mass |
decreased body weight |
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Availability | Mouse Genotype | ||
Atp5f1atm1a(EUCOMM)Wtsi/Atp5f1a+ |
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 04/16/2024 MGI 6.23 |
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