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Symbol
Name
ID
Foxp3
forkhead box P3
MGI:1891436
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Splenomegaly
Failure to thrive in infancy
Cachexia
Disease(s) Associated with FOXP3
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome

Mouse Phenotypes
scaly ears
small ears
thick ears
decreased body weight
weight loss
cachexia
decreased body size
postnatal growth retardation
distended abdomen
Availability Mouse Genotype
Foxp3tm3(DTR/GFP)Ayr/Foxp3tm3(DTR/GFP)Ayr
Foxp3m1Btlr/Y
Foxp3sf/Y
Foxp3tm1.1Ayr/Y
Foxp3tm2Flv/Y
Foxp3tm1Ayr/Y
Tg(Cd4-cre)1Cwi/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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Funding Information
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory