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.
by RareConnect team
published about 1 month ago
Rare Disease Day takes place on the last day of February each year.
The main objective of Rare Disease Day is to raise awareness amongst the gen...
published 4 months ago
So.... Hi! I'm Mindy, Kolbe's mom. Kolbe received a diagnosis of FOXP1 mutation a year ago, tomorrow. He is the most wonderfully loving, engaging, ...
Partners and Patient Groups
RareConnect is a joint venture of EURORDIS and NORD. The following patient groups are official partners of this community.