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FOXL2

FOXL2
Identifiers
Aliases FOXL2, BPES, BPES1, PFRK, PINTO, POF3, forkhead box L2
External IDs MGI: 1349428 HomoloGene: 74992 GeneCards: FOXL2
Gene location (Human)
Chromosome 3 (human)
Chr. Chromosome 3 (human)
Chromosome 3 (human)
Genomic location for FOXL2
Genomic location for FOXL2
Band 3q22.3 Start 138,944,224 bp
End 138,947,140 bp
RNA expression pattern
PBB GE FOXL2 220102 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_023067

NM_012020

RefSeq (protein)

NP_075555

NP_036150

Location (UCSC) Chr 3: 138.94 – 138.95 Mb Chr 3: 98.96 – 98.96 Mb
PubMed search

NM_023067

NM_012020

NP_075555

NP_036150

Forkhead box protein L2 is a protein that in humans is encoded by the FOXL2 gene.

FOXL2 is a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and plays a role in ovarian development and function. FoxL2 is a marker for ovarian differentiation, and is required for granulosa cell differentiation. In addition, the foxl2 protein will prevent the formation of testes by suppressing expression of SOX9.

In postnatal ovaries FOXL2 regulates granulosa cell differentiation and also supports the growth of the pre-ovulatory follicles during adult life.

FOXL2 has several post-translational modifications that modulate its stability, subcellular localization and pro-apoptotic activity. By a yeast-two-hybrid screening, 10 novel protein partners of FOXL2 are discovered. The interactions were confirmed by co-immunoprecipitation experiments between FOXL2 and CXXC4 (IDAX), CXXC5 (RINF/WID), CREM, GMEB1 (P96PIF), NR2C1 (TR2), SP100, RPLP1, BAF (BANF1), XRCC6 (KU70) and SIRT1.


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