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. 

Read more

FOXP1 Resources

More members stories

Latest Member Stories

Recently diagnosed

by Kcottrell07 published 4 days ago
No comment

Our now 5 year old son was recently diagnosed with a FOXP1 mutation and UPF3B mutation. He came to our family through foster care at 4 months old. ...

Christopher's Story

by anond8d4d4c7 published 8 days ago
4 comments

Our son Christopher was born in 2000, he just turned 16. He was a happy, healthy baby and met his developmental milestones until his first birthday...

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.