Ciliopathy

特許 係属中 A ciliopathy is a genetic disorder of the cellular cilia or the cilia anchoring structures, the basal bodies,[1] or of ciliary function.[2] Although ciliopathies are usually considered to involve proteins that localize to motile and/or immotile (primary) cilia or centrosomes, it is possible for ciliopathies to be associated with proteins such as XPNPEP3, which localizes to mitochondria but is believed to affect ciliary function through proteolytic cleavage of ciliary proteins.