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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| BBS12-20-RE | 20 (40 μL) | 200 μL |  |
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| BBS12-20-OR | 20 (40 μL) | 200 μL |  |
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| BBS12-20-GO | 20 (40 μL) | 200 μL |  |
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| BBS12-20-GR | 20 (40 μL) | 200 μL |  |
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| BBS12-20-AQ | 20 (40 μL) | 200 μL |  |
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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 Symbol : BBS12
Gene Name : Bardet-Biedl syndrome 12
Chromosome : CHR 4: 122,700,436-122,744,942
Locus : 4q27
Alt. Genes : PREB
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