Automated description from the Alliance of Genome Resources (Release 7.5.0)
Predicted to enable kinesin binding activity. Predicted to be involved in several processes, including autophagosome-lysosome fusion; late endosome to lysosome transport; and natural killer cell mediated cytotoxicity. Predicted to be located in autolysosome and lysosomal membrane. Predicted to be active in endosome membrane. Orthologous to human PLEKHM2 (pleckstrin homology and RUN domain containing M2).
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