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FOXP3

—Forkhead Box P3

Chromosome: X

Location: X:49250436-49264800

OMIM: 300292

Ensembl: ENSG00000049768

Official·OMIM:300292 Official·ENSG00000049768

Encodes regulatory T cell transcription factor. Mutations cause IPEX syndrome.

Treatment Roadmap — FOXP3

Preclinical

Phase 1

8 trial

Phase 2

14 trial

Phase 3

3 trial

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

IPEX Syndrome

X-Linked RecessivePrevalence: 1/1000000immunologic

Official·OMIM:304790 Official·ORPHA37042

Summary

Clinical Trial

Approved Therapy

Registered Variant