NR2F1

GENE INFORMATION

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Gene name

NR2F1 (HGNC Symbol)

Synonyms

COUP-TFI, EAR-3, ERBAL3, SVP44, TCFCOUP1, TFCOUP1

Description

Nuclear receptor subfamily 2, group F, member 1 (HGNC Symbol)

Entrez gene summary

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]

Chromosome

5

Cytoband

q15

Chromosome location (bp)

93583337 - 93594615

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000175745 (version 78.38)

Entrez gene

7025

UniProt

P10589 (UniProt - Evidence at protein level)

neXtProt

NX_P10589

Antibodypedia

NR2F1 antibodies
 

PROTEIN VIEW

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NR2F1-001
 
NR2F1-201
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

NR2F1-001 ENSP00000325819
ENST00000327111
P10589
Show all »
Show » Show » 423 46.2 No 0
NR2F1-201 ENSP00000481517
ENST00000615873
F1DAL9
Show all »
Show » Show » 398 43.9 No 0