Consistent with the localisation of NUP88 to the axoneme of ciliated cells (Figs. 6d, 8), NUP88 appears to be part of the Bardet-Biedl Syndrome (BBSome) coat complex, in complex with DYNLT1, and the WDR19/IFT-A complex38. The gene discussed is WDR19; the disease is Bardet-Biedl syndrome.