Patients harboring homozygous TRIM32 missense variants displayed Bardet–Biedl syndrome (a form of syndromic RP), including obesity, RP, hypogonadism, and cognitive impairment.[32] Interestingly, TRIM49, a member of the TRIM family, shows retina‐specific mRNA expression in humans (GeneCards‐ SAGE, https://www.genecards.org/) but has not yet been functionally characterized. The gene discussed is TRAT1; the disease is retinitis pigmentosa 1.