Coding regions, intron-exon boundaries and untranslated exons of Clusterin-like 1 (CLUL1), elastin microfibril interfacer 2 (EMILIN2), lipin 2 (LPIN2), myomesin 1 (MYOM1), myosin regulatory light chain 3 (MRCL3), myosin regulatory light chain 2 (MRLC2), transforming growth β-induced factor (TGIFβ), large Drosophila homolog associated protein 1 (DLGAP1), and zinc finger protein 161 homolog (ZFP161) were sequenced, but mutation analysis did not identify sequence alterations associated with high myopia [11]. The gene discussed is MYL12A; the disease is myopia.