MYH10 Chromosome 17

Myosin heavy chain 10
7 variants 7 Health Risk

Upload your DNA to see your personal genotypes for variants in MYH10.

What This Gene Does
This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin; it should not be confused with the unconventional myosin-10 (MYO10). Myosins are actin-dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene have been associated with May-Hegglin anomaly and developmental defects in brain and heart. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Gene Info
Gene Group
Myosin heavy chains, class II
Locus Type
gene with protein product
Location
17p13.1
Ensembl
ENSG00000133026
Associated Conditions (5)
See cases
Complex neurodevelopmental disorders
7 conditions
6 conditions
Inborn genetic diseases
Key Variants
All Variants (7)
RSID Category Clinical Significance Conditions
RS2151813002 Health Risk Conflicting classifications of pathogenicity See cases, See cases
RS2082452725 Health Risk Likely pathogenic
RS2544384657 Health Risk Likely pathogenic
RS2544245567 Health Risk Pathogenic Complex neurodevelopmental disorders, Complex neurodevelopmental disorders
RS2544300043 Health Risk Pathogenic See cases, See cases
RS755969165 Health Risk Pathogenic 7 conditions, 6 conditions, 7 conditions
RS797044880 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
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