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). This evidence concerns the gene ATXN7 and cone-rod dystrophy.