Bardet–Biedlov sindrom 10, poznat i kao BBS10 je genetički kodiran.[5]
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Zatvori
Protein Bardet-Biedlov sindroma 10 ima udaljenu homologiju sekvence tipa II šaperonina. Kao molekulski šaperon, ovaj protein može uticati na presavijanje ili stabilnost drugih proteina cilijskih ili baznih tijela. Inhibicija ekspresije ovog proteina narušava ciliogenezu u preadipocitima.[6][7]
Mutacije u ovom genu povezane su sa Bardet-Biedlovim sindromom.[5]
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