SIX5, SIX homeobox 5

SIX5, SIX homeobox 5

• The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2. [provided by RefSeq, Jul 2009]

• Gene Synonyms (BOR2, DMAHP, homeobox protein SIX5, DM locus-associated homeodomain protein, dystrophia myotonica-associated homeodomain protein, sine oculis homeobox homolog 5,)
• NCBI Gene ID: 147912
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q8N196
• 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.

SIX homeobox 5 interacts with:

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.