FOXL2

Information FOXL2

Description

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. Expansion of a polyalanine repeat region and other mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jul 2016]

Full Name

forkhead box L2

Source NCBI

Species

Homo sapiens [tax_id: 9606]

Genome

hg38

ReMap Statistics

Datasets
8
Biotypes
3
Peaks
242,237
Non-redundant peaks
118,194

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

NCBI Gene
668
Official Gene Name
FOXL2
JASPAR
Ensembl
ENSG00000183770
UniProt
P58012
Genevisible
P58012
RefSeq
NM_023067
Aliases
BPES; BPES1; PFRK; PINTO; POF3
All peaks FOXL2
Download BED file
Non redundant peaks FOXL2
Download BED file
SEQUENCES FOXL2
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for FOXL2

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
FOXL2 SVOG-3e no-DOX-mut GEO Homo sapiens GSE126171 258
FOXL2 SVOG-3e DOX-WT GEO Homo sapiens GSE126171 21,658
FOXL2 KGN 1513 GEO Homo sapiens GSE138496 47,797
FOXL2 KGN 1512 GEO Homo sapiens GSE138496 36,069
FOXL2 HGrC1 C134W-TGF GEO Homo sapiens GSE138496 77,242
FOXL2 HGrC1 C134W-TGF_parental GEO Homo sapiens GSE138496 55,078
FOXL2 HGrC1 EV-TGF GEO Homo sapiens GSE138496 3,234
FOXL2 HGrC1 EV GEO Homo sapiens GSE138496 901
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks