We also inspected the distribution of CEP290, known to localize along the CC from super-resolution microscopy [20], and Lebercilin (LCA5), a proposed FAM161A interactor [10], mutations in which have been linked to Leber congenital amaurosis, a retinopathy causing severe visual deficiency from the first year after birth [21,22]. The gene discussed is CEP290; the disease is Leber congenital amaurosis.