Additionally, a mouse knockout model of BBS5 developed a cone-rod dystrophy as well as displayed mislocalization of cone-specific proteins such as OPN1SW, OPN1MW and GNAT2 (Bales et al., 2020); we report that OPN1MW and GNAT2 are mislocalized in Bbs10−/− mice. The gene discussed is OPN1SW; the disease is cone-rod dystrophy.