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.FOXP1 Resources
Latest Member Stories
Our son, Eythan, is 10.5 months old suffers from general developmental delay. Last week we received the whole-exom sequencing results that indicate...
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.