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Symbol
Name
ID
Atp5f1a
ATP synthase F1 subunit alpha
MGI:88115
Phenotype annotations related to growth/size/body
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
Availability Mouse Genotype
Atp5f1atm1a(EUCOMM)Wtsi/Atp5f1a+

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
04/16/2024
MGI 6.23
The Jackson Laboratory