BBS12, Bardet-Biedl syndrome 12

BBS12, Bardet-Biedl syndrome 12

• The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]

• Gene Synonyms (Bardet-Biedl syndrome 12 protein, truncated Bardet-Biedl syndrome 12 protein, C4orf24,)
• NCBI Gene ID: 166379
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q6ZW61
• 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.

Bardet-Biedl syndrome 12 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.