Welcome - FOXP1 Community

What is FOXP1 ?

FOXP1 (forkhead box P1) is a gene located on chromosome 3 that everybody carries and is important for the normal functioning of the body. The FOXP1 gene is translated (transcribed) into FOXP1-RNA and then into the FOXP1-protein which carries out the normal body functions of the gene. The FOXP1 gene is a member of a family of transcription factors that control the levels of proteins important for normal development of the embryo before birth and the immune and neurological systems after birth. 

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FOXP1 Resources

More members stories

Latest Member Stories

Our 10.5 months old son was diagnosed with FOXP1 mutation

by heather-itz published 3 months ago
2 comments

Our son, Eythan, is 10.5 months old suffers from general developmental delay. Last week we received the whole-exom sequencing results that indicate...

Results for whole-exome FOXP1 exam arrived

by vkcf published 4 months ago
3 comments

I, Vasco, and my wife have a son named Nickolas who turned four years old in March. We only discovered the causes for his delayed development recen...

Partners and Patient Groups

RareConnect is a patient-led initiative. Patient organisations partner with EURORDIS, itself an international patient organisation, to create communities and provide moderators from within their network. The following patient groups are official partners of this community.