The result that UBIAD1 did not localize with a marker for endoplasmic reticulum (Figure 4) while wild type and N102S mutant UBIAD1 did co-localize with a mitochondrial marker, OXPHOS complex (Figure 4F), demonstrates that mislocalization of N102S mutant protein is not a factor in SCD. The gene discussed is UBIAD1; the disease is Schnyder corneal dystrophy.