Reviewed May 2008
What is the official name of the FOXP3 gene?
The official name of this gene is “forkhead box P3.”
FOXP3 is the gene's official symbol. The FOXP3 gene is also known by other names, listed below.
What is the normal function of the FOXP3 gene?
The FOXP3 gene provides instructions for producing the forkhead box P3 (FOXP3) protein. The FOXP3 protein attaches (binds) to specific regions of DNA and helps control the activity of genes that are involved in regulating the immune system. On the basis of this role, the FOXP3 protein is called a transcription factor. This protein is essential for the production and normal function of certain immune cells called regulatory T cells, which play an important role in preventing autoimmunity. Autoimmunity occurs when the body attacks its own tissues and organs by mistake. The FOXP3 protein is found primarily in an immune system gland called the thymus, where regulatory T cells are produced.
Does the FOXP3 gene share characteristics with other genes?
The FOXP3 gene belongs to a family of genes called FOX (Forkhead box genes).
A gene family is a group of genes that share important characteristics. Classifying individual genes into families helps researchers describe how genes are related to each other. For more information, see What are gene families? in the Handbook.
How are changes in the FOXP3 gene related to health conditions?
-
immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome - caused by mutations in the FOXP3 gene
-
At least 21 mutations in the FOXP3 gene have been found to cause immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome. Most mutations change one protein building block (amino acid) in the region of the FOXP3 protein that binds to DNA or lead to the production of an abnormally short, nonfunctional protein. Mutations in the FOXP3 gene result in reduced numbers or a complete absence of regulatory T cells. Without the proper number of regulatory T cells, the body cannot control immune responses. Normal body tissues and organs are attacked, causing the multiple autoimmune disorders present in people with IPEX syndrome.
Where is the FOXP3 gene located?
Cytogenetic Location: Xp11.23
Molecular Location on the X chromosome: base pairs 48,994,353 to 49,008,231
The FOXP3 gene is located on the short (p) arm of the X chromosome at position 11.23.
More precisely, the FOXP3 gene is located from base pair 48,994,353 to base pair 49,008,231 on the X chromosome.
See How do geneticists indicate the location of a gene? in the Handbook.
Where can I find additional information about FOXP3?
What other names do people use for the FOXP3 gene or gene products?
- AIID
- DIETER
- FOXP3_HUMAN
- immune dysregulation, polyendocrinopathy, enteropathy, X-linked
- immunodeficiency, polyendocrinopathy, enteropathy, X-linked
- IPEX
- JM2
- MGC141961
- MGC141963
- PIDX
- scurfin
- XPID
Where can I find general information about genes?
The Handbook provides basic information about genetics in clear language.
These links provide additional genetics resources that may be useful.
What glossary definitions help with understanding FOXP3?
The resources on this site should not be used as a substitute for
professional medical care or advice. Users seeking information about
a personal genetic disease, syndrome, or condition should consult with a qualified
healthcare professional.
See How can I find a genetics professional in my area? in the Handbook.
Indicates a page outside Genetics Home Reference.
