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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	Failure to thrive in infancy	Cachexia
Disease(s) Associated with FOXP3
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome

Mouse Phenotypes

enlarged heart

scaly ears

small ears

thick ears

decreased body weight

cachexia

decreased body size

postnatal growth retardation

distended abdomen

enlarged liver

enlarged spleen

increased spleen weight

Availability

Mouse Genotype

Foxp3^tm1.1Ayr/Foxp3^tm1.1Ayr

Foxp3^m1Btlr/Y

Foxp3^sf/Y

Foxp3^tm1.1Ayr/Y

Foxp3^tm1Tch/Y

Foxp3^tm2Flv/Y

Foxp3^tm3Tch/Y

Foxp3^tm1Ayr/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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