POU4F3, POU class 4 homeobox 3

POU4F3, POU class 4 homeobox 3

• This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15. [provided by RefSeq, Mar 2009]

• Gene Synonyms (POU domain, class 4, transcription factor 3, brain-3C, brain-specific homeobox/POU domain protein 3C, brn-3C, deafness, autosomal dominant 42, BRN3C, DFNA15, DFNA42, DFNA52,)
• NCBI Gene ID: 5459
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q15319
• 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.

POU class 4 homeobox 3 interacts with:

• aurora kinase A
  dual specificity phosphatase 21
  keratin associated protein 6-3
  NHL repeat containing 4
  phospholipase A2 group X

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.