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 |
