Based on putative function and/or involvement in retinal disease (see Table S5), we selected 16 genes – Bach2, Cdr2, Dusp12, Esrrb, Gpsm2, Haus1, Kdm5b, Lman1, Lrp11, Lrrc2, Ncoa2, Plekha2, Ppargc1b, Trim36, Wisp1 and Zdhhc14. This evidence concerns the gene PPARGC1B and Abnormal retinal morphology.