Английская Википедия:FOXG1

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Версия от 03:42, 6 марта 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Short description|Protein-coding gene in the species Homo sapiens}} {{Infobox_gene}} '''Forkhead box protein G1''' is a protein that in humans is encoded by the ''FOXG1'' gene.<ref name="pmid7959731">{{cite journal | vauthors = Murphy DB, Wiese S, Burfeind P, Schmundt D, Mattei MG, Schulz-Schaeffer W, Thies U | title = Human brain factor 1, a new member of the fork head gene...»)
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Шаблон:Short description Шаблон:Infobox gene Forkhead box protein G1 is a protein that in humans is encoded by the FOXG1 gene.[1][2][3]

Function

This gene belongs to the forkhead family of transcription factors that is characterized by a distinct forkhead domain. The complete function of this gene has not yet been determined; however, it has been shown to play a role in the development of the brain and telencephalon. Mutations of FOXG1 are the cause of FoxG1 syndrome.[4]

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.[5][6]

Interactions

FOXG1 has been shown to interact with JARID1B.[7]

See also

References

Шаблон:Reflist

Further reading

Шаблон:Refbegin

Шаблон:Refend

External links

Шаблон:Transcription factors

Шаблон:NLM content


Шаблон:Gene-14-stub

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  1. ↑ Шаблон:Cite journal
  2. ↑ Шаблон:Cite journal
  3. ↑ Шаблон:Cite web
  4. ↑ Шаблон:Cite journal
  5. ↑ Шаблон:Cite web
  6. ↑ Шаблон:Cite web
  7. ↑ Шаблон:Cite journal
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