foxl2 Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description forkhead box L2|This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jun 2009] (NCBI Entrez Gene Database, 668)
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Genes

26 genes co-occuring with the biological term foxl2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
CLU clusterin
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
ESR1 estrogen receptor 1
FOXD1 forkhead box D1
FOXL2 forkhead box L2
FOXO1 forkhead box O1
FOXP3 forkhead box P3
FSHB follicle stimulating hormone, beta polypeptide
FST follistatin
GATA4 GATA binding protein 4
GDF9 growth differentiation factor 9
INHBA inhibin, beta A
NOBOX NOBOX oogenesis homeobox
NOTCH1 notch 1
NR5A1 nuclear receptor subfamily 5, group A, member 1
PIAS1 protein inhibitor of activated STAT, 1
PISRT1 polled intersex syndrome regulated transcript 1 (non-protein coding RNA)
PTTG1 pituitary tumor-transforming 1
RSPO1 R-spondin 1
SIRT1 sirtuin 1
SMAD3 SMAD family member 3
SOX9 SRY (sex determining region Y)-box 9
STAR steroidogenic acute regulatory protein
UBE2I ubiquitin-conjugating enzyme E2I
WNT4 wingless-type MMTV integration site family, member 4