FOXP3

(redirected from forkhead box P3)
Also found in: Wikipedia.

FOXP3

A gene on chromosome Xp11.23 that encodes a member of the forkhead/winged-helix family of transcriptional regulators.

Molecular pathology
FOXP3 mutations cause immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) (X-linked autoimmunity-immunodeficiency syndrome).
References in periodicals archive ?
The new test is based on the RNA genetic markers forkhead box P3 (FoxP3), granzyme B (GZMB), and perforin (PRF1) licensed exclusively from Boston-based Beth Israel Deaconess Medical Center (BIDMC), a teaching hospital of Harvard Medical School, and New York City-based Weill Cornell Medical College, the medical school of Cornell University, among other markers.