Finally, SHIP164 was reported to be a Parkinson’s disease candidate gene (Jansen et al., 2017), and loss-of-function mutations in VPS13C, another chorein motif lipid transport protein (Fig. 7 A), implicated in the endocytic/lysosome pathway are responsible for familial forms of Parkinson’s disease (Lesage et al., 2016). The gene discussed is BLTP3B; the disease is Parkinson disease.