MYOZ2 Chromosome 4

Myozenin 2
12 variants 12 Health Risk

Upload your DNA to see your personal genotypes for variants in MYOZ2.

What This Gene Does
The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder. [provided by RefSeq, Aug 2011]
Gene Info
Gene Group
Myozenins
Locus Type
gene with protein product
Location
4q26
Ensembl
ENSG00000172399
Associated Conditions (6)
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 16
Restrictive cardiomyopathy
Cardiomyopathy
MYOZ2-related disorder
Key Variants
RS143345726
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy 16
Health Risk
RS148908208
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy, Cardiomyopathy, Cardiovascular phenotype
Health Risk
RS201476980
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Hypertrophic cardiomyopathy, Cardiovascular phenotype
Health Risk
RS201971682
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy 16, Cardiovascular phenotype, Hypertrophic cardiomyopathy 16
Health Risk
RS372215131
Conflicting classifications of pathogenicity
Cardiomyopathy, Hypertrophic cardiomyopathy, Cardiovascular phenotype
Health Risk
RS397517289
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy, Cardiomyopathy, Cardiovascular phenotype
Health Risk
RS536009604
Conflicting classifications of pathogenicity
Cardiomyopathy, Hypertrophic cardiomyopathy, Cardiomyopathy
Health Risk
RS554299359
Conflicting classifications of pathogenicity
Cardiomyopathy, Hypertrophic cardiomyopathy, Cardiovascular phenotype
Health Risk
RS748809573
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy, Cardiovascular phenotype, Hypertrophic cardiomyopathy
Health Risk
RS774202003
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy, Cardiovascular phenotype, MYOZ2-related disorder
Health Risk
RS774333721
Conflicting classifications of pathogenicity
Cardiomyopathy, Cardiovascular phenotype, Cardiomyopathy
Health Risk
RS199476398
Likely pathogenic
Hypertrophic cardiomyopathy 16, Hypertrophic cardiomyopathy 16
Health Risk
All Variants (12)
RSID Category Clinical Significance Conditions
RS143345726 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy 16
RS148908208 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiomyopathy, Cardiovascular phenotype
RS201476980 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Hypertrophic cardiomyopathy, Cardiovascular phenotype
RS201971682 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 16, Cardiovascular phenotype, Hypertrophic cardiomyopathy 16
RS372215131 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Hypertrophic cardiomyopathy, Cardiovascular phenotype
RS397517289 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiomyopathy, Cardiovascular phenotype
RS536009604 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Hypertrophic cardiomyopathy, Cardiomyopathy
RS554299359 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Hypertrophic cardiomyopathy, Cardiovascular phenotype
RS748809573 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiovascular phenotype, Hypertrophic cardiomyopathy
RS774202003 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiovascular phenotype, MYOZ2-related disorder
RS774333721 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Cardiomyopathy
RS199476398 Health Risk Likely pathogenic Hypertrophic cardiomyopathy 16, Hypertrophic cardiomyopathy 16
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