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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