BBS2
Bardet–Biedl syndrome 2 protein is a protein that in humans is encoded by the BBS2 gene.
This gene encodes a protein of unknown function. Mutations in this gene have been observed in patients with Bardet–Biedl [syndrome type 2]. Bardet–Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation, and mental retardation.