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
ReMap Statistics
- Datasets
- 3
- Biotypes
- 3
- Peaks
- 204,841
- Non-redundant peaks
- 175,072
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
- JASPAR
- MA0017
- Ensembl
- ENSG00000175745
- UniProt
- P10589
- Genevisible
- P10589
- RefSeq
- NM_005654
- Aliases
- BBOAS; BBSOAS; COUP-TFI; COUPTF1; EAR-3; EAR3; ERBAL3; SVP44; TCFCOUP1; TFCOUP1
Datasets Table for NR2F1
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| NR2F1 | GM12878 | ENCODE | Homo sapiens | ENCSR514VYD | 41,844 | |||
| NR2F1 | K-562 | ENCODE | Homo sapiens | ENCSR970NKQ | 49,039 | |||
| NR2F1 | MCF-7 | GEO | Homo sapiens | GSE41561 | 113,958 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |