FOXG1

Forkhead box protein G1 is a protein that in humans is encoded by the FOXG1 gene.

Function

This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in the development of the brain and telencephalon.

Cajal Retzius Cell development is regulated by Foxg1

FOXG1 syndrome

FOXG1 syndrome is characterized by microcephaly and brain malformations. It affects most aspects of development. FOXG1 syndrome is classified as an Autism Spectrum Disorder and was previously considered a variant of Rett Syndrome.

Interactions

FOXG1 has been shown to interact with JARID1B.

See also

References

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.