NP_001171478.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
79,085 Da
NCBI Official Full Name
Bardet-Biedl syndrome 12 protein
NCBI Official Synonym Full Names
Bardet-Biedl syndrome 12
NCBI Official Synonym Symbols
NCBI Protein Information
Bardet-Biedl syndrome 12 protein
UniProt Protein Name
Bardet-Biedl syndrome 12 protein
UniProt Synonym Gene Names
NCBI Summary for BBS12
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]
UniProt Comments for BBS12
Probable molecular chaperone. Assists the folding of proteins upon ATP hydrolysis. As part of the BBS/CCT complex may play a role in the assembly of BBSome, a complex involved in ciliogenesis regulating transports vesicles to the cilia. Involved in adipogenic differentiation.
Research Articles on BBS12
Precautions
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Disclaimer
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Products associated with BBS12 recombinant protein
Pathways associated with BBS12 recombinant protein
Diseases associated with BBS12 recombinant protein
Organs/Tissues associated with BBS12 recombinant protein
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