NR2F1, nuclear receptor subfamily 2 group F member 1

NR2F1, nuclear receptor subfamily 2 group F member 1

• 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]

• Gene Synonyms (COUP transcription factor 1, COUP transcription factor I, COUP-TF I, COUP-TF1, V-erbA-related protein 3, chicken ovalbumin upstream promoter-transcription factor I, transcription factor COUP 1 (chicken ovalbumin upstream promoter 1, v-erb-a homolog-like 3), BBOAS, BBSOAS, COUP-TFI, COUPTF1, EAR-3, EAR3, ERBAL3, SVP44, TCFCOUP1, TFCOUP1,)
• NCBI Gene ID: 7025
• Species: Homo sapiens (Human)
• UNIPROT ID#>>P10589
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

nuclear receptor subfamily 2 group F member 1 interacts with:

• BAF chromatin remodeling complex subunit BCL11A
  BAF chromatin remodeling complex subunit BCL11B
  chromobox 5
  COP9 signalosome subunit 2
  H4 clustered histone 1
  limb development membrane protein 1 like
  microcephalin 1
  nuclear receptor binding SET domain protein 1
  nuclear receptor coactivator 1
  nuclear receptor coactivator 2
  nuclear receptor coactivator 3
  nuclear receptor corepressor 2
  pleckstrin homology domain containing A4
  prohibitin 2
  ring finger protein 13
  TEA domain transcription factor 2
  thyroid hormone receptor alpha
  TNFAIP3 interacting protein 2

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.