PLEKHM2 pleckstrin homology and RUN domain containing M2 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 23207)
Source: NCBI Gene (ID 23207)
Symbol: PLEKHM2
Full name: pleckstrin homology and RUN domain containing M2
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: SKIP
Summary: This gene encodes a protein that binds the plus-end directed microtubule motor protein kinesin, together with the lysosomal GTPase Arl8, and is required for lysosomes to distribute away from the microtubule-organizing center. The encoded protein belongs to the multisubunit BLOC-one-related complex that regulates lysosome positioning. It binds a Salmonella effector protein called Salmonella induced filament A and is a critical host determinant in Salmonella pathogenesis. It has a domain architecture consisting of an N-terminal RPIP8, UNC-14, and NESCA (RUN) domain that binds kinesin-1 as well as the lysosomal GTPase Arl8, and a C-terminal pleckstrin homology domain that binds the Salmonella induced filament A effector protein. Naturally occurring mutations in this gene lead to abnormal localization of lysosomes, impaired autophagy flux and are associated with recessive dilated cardiomyopathy and left ventricular noncompaction. [provided by RefSeq, Feb 2017]
Expression: Ubiquitous expression in bone marrow (RPKM 21.8), testis (RPKM 21.5) and 25 other tissues
Orthologs: mouse
Gene size: 53264bp
Exon count: 22