IFT80 and ciliopathy: This was indeed confirmed by a large screen from the Anton lab, where mouse in utero electroporation of a shRNA library of 30 known ciliopathy genes revealed cortical migration defects for as many as 17 of them, such as BBS1 (Bardet–Biedl syndrome protein 1) and IFT80 (Intraflagellar transport 80) (see Table 1) [10].