PLEKHM2 Chromosome 1

Pleckstrin homology and RUN domain containing M2
7 variants 7 Health Risk

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What This Gene Does
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]
Gene Info
Gene Group
Pleckstrin homology domain containing
Locus Type
gene with protein product
Location
1p36.21
Ensembl
ENSG00000116786
Associated Conditions (1)
PLEKHM2-related disorder
Key Variants
All Variants (7)
RSID Category Clinical Significance Conditions
RS181186746 Health Risk Conflicting classifications of pathogenicity —
RS199578594 Health Risk Conflicting classifications of pathogenicity PLEKHM2-related disorder, PLEKHM2-related disorder
RS200329773 Health Risk Conflicting classifications of pathogenicity —
RS201370265 Health Risk Conflicting classifications of pathogenicity —
RS376758113 Health Risk Conflicting classifications of pathogenicity —
RS764775012 Health Risk Conflicting classifications of pathogenicity —
RS779397937 Health Risk Conflicting classifications of pathogenicity —
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