Indeed, in the hCOR list (excluding shared genes), 7 genes (AHI1, ATXN7, KCNV2, PROM1, RD3, RPGRIP1) have been linked to human CRD or Leber’s congenital amaurosis (LCA) diseases, while mCOR list only contains one such gene (GUCA1A). The gene discussed is RPGRIP1; the disease is cone-rod dystrophy.