FOXG1
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). Forkhead box protein G1 is a protein that in humans is encoded by the FOXG1 gene.[1][2][3]
Contents
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.[3]
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 and can cause seizures. FOXG1 syndrome is classified as an Autism Spectrum Disorder and was previously considered a variant of Rett Syndrome.[4][5]
Interactions
FOXG1 has been shown to interact with JARID1B.[6]
See also
References
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- ↑ 3.0 3.1 Lua error in package.lua at line 80: module 'strict' not found.
- ↑ http://ghr.nlm.nih.gov/condition/foxg1-syndrome
- ↑ http://dnatesting.uchicago.edu/blog/foxg1-syndrome-more-congenital-variant-rett-syndrome
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
Further reading
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External links
- FOXG1B protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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