ReMap 2018 v1.2

An integrative ChIP-seq analysis of regulatory regions

NR2F1

Function : nuclear receptor subfamily 2 group F member 1
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]

Classification  

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

External references

Ensembl ENSG00000175745
RefSeq NP_005645
Uniprot P10589
Aliases BBOAS, BBSOAS, COUP-TFI, EAR-3, EAR3, ERBAL3, NR2F2, SVP44, TCFCOUP1, TFCOUP1
UCSC Gene coordinates chr5:93583336-93594612

External Links

JASPAR MA0017.2
Wikipedia NR2F1
WikiGenes NR2F1
Transcription Factor Encylopedia NR2F1
GeneCards NR2F1
FactorBook NR2F1


Genomic visualization & Analyses for MACS

Datasets
quality
DNA constraint
Motifs UCSC genome
browser

Downloading peaks and sequences for MACS

All peaks BED file
Merged peaks
(non-redundant peaks)
BED file
Peak sequences FASTA file

MACS - Datasets retained for NR2F1

Genomic visualization & Analyses for JAMM

Datasets
quality
DNA constraint
Motifs UCSC genome
browser

Downloading peaks and sequences for JAMM

All peaks BED file
Merged peaks
(non-redundant peaks)
BED file
Peak sequences FASTA file

JAMM - Datasets retained for NR2F1