This gene encodes gamma butyrobetaine hydroxylase which catalyzes the formation of L-carnitine from gamma-butyrobetaine, the last step in the L-carnitine biosynthetic pathway. Carnitine is essential for the transport of activated fatty acids across the mitochondrial membrane during mitochondrial beta-oxidation.
A synthesized peptide derived from human BBS10, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human 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.
A synthesized peptide derived from human BBS2, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human BBS3, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human BBS4, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human BBS5, corresponding to a region within C-terminal amino acids.
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