Structured Summary
Abstract
A forkhead box transcription factor that is expressed in the developing eyelid and during very early development of the gonad, prior to sex determination. It is essential for development of the ovary and inhibits SOX9 TRANSCRIPTION FACTOR to prevent differentiation to testes. It also induces APOPTOSIS in ovarian cells. Mutations in the FOXL2 gene are associated with BLEPHAROPHIMOSIS; Ptosis, and Epicanthus inversus (BPES with ovarian failure).
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Synonyms
2 entry terms
- FOXL2 Protein
- Forkhead Box L2 Protein
MeSH Record
Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2018
MeSH Record
Previous Indexing
- Forkhead Transcription Factors (2006-2017)
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AMA Style
References
- National Library of Medicine. Forkhead Box Protein L2. Medical Subject Headings (MeSH). 2026. Unique ID D000074842. http://id.nlm.nih.gov/mesh/2026/D000074842
- Forkhead Box Protein L2. In: Wikipedia. https://en.wikipedia.org/wiki/Forkhead_Box_Protein_L2
- Forkhead Box Protein L2. In: Wikidata. https://www.wikidata.org/wiki/Q65089657