A recent flurry of papers identified multiple Arl3 variants that cause either dominant or recessive retinal disease (Alkanderi et al., 2018; Fu et al., 2021; Holtan et al., 2019; Ratnapriya et al., 2021; Sheikh et al., 2019; Strom et al., 2016). The gene discussed is ARL3; the disease is Abnormal retinal morphology.