NR2F1

Information NR2F1

Description

The protein encoded by this gene is a nuclear hormone receptor and transcriptional regulator. The encoded protein acts as a homodimer and binds to 5'-AGGTCA-3' repeats. Defects in this gene are a cause of Bosch-Boonstra optic atrophy syndrome (BBOAS). [provided by RefSeq, Apr 2014]

Full Name

nuclear receptor subfamily 2 group F member 1

Source NCBI

Species

Homo sapiens [tax_id: 9606]

Genome

hg38

ReMap Statistics

Datasets
3
Biotypes
3
Peaks
95,303
Non-redundant peaks
82,440

TF Classification

Super Class
Zinc-coordinating DNA-binding domains
Class
Nuclear receptors with C4 zinc fingers
Familly
RXR-related receptors (NR2)
Sub Familly
COUP-like receptors (NR2F)

Source TFClass

External IDs

NCBI Gene
7025
Official Gene Name
NR2F1
JASPAR
MA0017
Ensembl
ENSG00000175745
UniProt
P10589
Genevisible
P10589
RefSeq
NM_005654
Aliases
BBOAS; BBSOAS; COUP-TFI; COUPTF1; EAR-3; EAR3; ERBAL3; SVP44; TCFCOUP1; TFCOUP1

External links
All peaks NR2F1
Download BED file
Non redundant peaks NR2F1
Download BED file
SEQUENCES NR2F1
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for NR2F1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
NR2F1 K-562 ENCODE Homo sapiens ENCSR970NKQ 48,340
NR2F1 GM12878 ENCODE Homo sapiens ENCSR514VYD 41,489
NR2F1 neuron-progenitor GEO Homo sapiens GSE132965 5,474
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks