ACTA1 Chromosome 1

Actin alpha 1, skeletal muscle
197 variants 197 Health Risk

Upload your DNA to see your personal genotypes for variants in ACTA1.

What This Gene Does
The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause a variety of myopathies, including nemaline myopathy, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects with manifestations such as hypotonia. [provided by RefSeq, Sep 2019]
Gene Info
Gene Group
Actins
Locus Type
gene with protein product
Location
1q42.13
Ensembl
ENSG00000143632
Associated Conditions (34)
Actin accumulation myopathy
Familial restrictive cardiomyopathy
Congenital myopathy with fiber type disproportion
ACTA1-related disorder
Congenital myopathy 4A
autosomal dominant
Progressive scapulohumeroperoneal distal myopathy
Congenital myopathy 2c
severe infantile
Abnormality of the musculature
Alpha-actinopathy
Myopathy
Nemaline myopathy
Inborn genetic diseases
Neuromuscular disease
ACTA1-related myopathies
Congenital myopathy
Centronuclear myopathy
Nemaline myopathy 3
autosomal dominant or recessive
+14 more conditions
Key Variants
RS1253964609
Conflicting classifications of pathogenicity
Actin accumulation myopathy, Actin accumulation myopathy
Health Risk
RS140074813
Conflicting classifications of pathogenicity
Familial restrictive cardiomyopathy, Actin accumulation myopathy, Congenital myopathy with fiber type disproportion
Health Risk
RS141030526
Conflicting classifications of pathogenicity
Actin accumulation myopathy, Congenital myopathy with fiber type disproportion, Familial restrictive cardiomyopathy
Health Risk
RS143948837
Conflicting classifications of pathogenicity
Actin accumulation myopathy, Familial restrictive cardiomyopathy, Congenital myopathy with fiber type disproportion
Health Risk
RS1553255361
Conflicting classifications of pathogenicity
Actin accumulation myopathy, Congenital myopathy 4A, autosomal dominant
Health Risk
RS1558081797
Conflicting classifications of pathogenicity
Actin accumulation myopathy, Congenital myopathy 2c, severe infantile
Health Risk
RS1659932688
Conflicting classifications of pathogenicity
Actin accumulation myopathy, Familial restrictive cardiomyopathy, Congenital myopathy with fiber type disproportion
Health Risk
RS1659945481
Conflicting classifications of pathogenicity
Actin accumulation myopathy, Actin accumulation myopathy
Health Risk
RS1659954399
Conflicting classifications of pathogenicity
Abnormality of the musculature, Actin accumulation myopathy, Abnormality of the musculature
Health Risk
RS1659962077
Conflicting classifications of pathogenicity
Congenital myopathy with fiber type disproportion, Actin accumulation myopathy, Congenital myopathy with fiber type disproportion
Health Risk
RS1659986880
Conflicting classifications of pathogenicity
Actin accumulation myopathy, Actin accumulation myopathy
Health Risk
RS371410845
Conflicting classifications of pathogenicity
Progressive scapulohumeroperoneal distal myopathy, Actin accumulation myopathy, Congenital myopathy with fiber type disproportion
Health Risk
All Variants (197)
RSID Category Clinical Significance Conditions
RS1253964609 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Actin accumulation myopathy
RS140074813 Health Risk Conflicting classifications of pathogenicity Familial restrictive cardiomyopathy, Actin accumulation myopathy, Congenital myopathy with fiber type disproportion
RS141030526 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Congenital myopathy with fiber type disproportion, Familial restrictive cardiomyopathy
RS143948837 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Familial restrictive cardiomyopathy, Congenital myopathy with fiber type disproportion
RS1553255361 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Congenital myopathy 4A, autosomal dominant
RS1558081797 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Congenital myopathy 2c, severe infantile
RS1659932688 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Familial restrictive cardiomyopathy, Congenital myopathy with fiber type disproportion
RS1659945481 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Actin accumulation myopathy
RS1659954399 Health Risk Conflicting classifications of pathogenicity Abnormality of the musculature, Actin accumulation myopathy, Abnormality of the musculature
RS1659962077 Health Risk Conflicting classifications of pathogenicity Congenital myopathy with fiber type disproportion, Actin accumulation myopathy, Congenital myopathy with fiber type disproportion
RS1659986880 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Actin accumulation myopathy
RS371410845 Health Risk Conflicting classifications of pathogenicity Progressive scapulohumeroperoneal distal myopathy, Actin accumulation myopathy, Congenital myopathy with fiber type disproportion
RS371799971 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Actin accumulation myopathy
RS373785144 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, ACTA1-related disorder, Actin accumulation myopathy
RS375945657 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Actin accumulation myopathy
RS551585351 Health Risk Conflicting classifications of pathogenicity Congenital myopathy with fiber type disproportion, Actin accumulation myopathy, Familial restrictive cardiomyopathy
RS727503798 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Congenital myopathy 2c, severe infantile
RS748592740 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Actin accumulation myopathy
RS770931836 Health Risk Conflicting classifications of pathogenicity Congenital myopathy with fiber type disproportion, Familial restrictive cardiomyopathy, Actin accumulation myopathy
RS878854374 Health Risk Conflicting classifications of pathogenicity Actin accumulation myopathy, Actin accumulation myopathy
RS886044062 Health Risk Conflicting classifications of pathogenicity
RS1057518493 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy, Actin accumulation myopathy
RS1057519311 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1057520216 Health Risk Likely pathogenic Actin accumulation myopathy, Alpha-actinopathy, Myopathy
RS1064795075 Health Risk Likely pathogenic
RS1085308014 Health Risk Likely pathogenic Actin accumulation myopathy, Alpha-actinopathy, Actin accumulation myopathy
RS112919437 Health Risk Likely pathogenic
RS1175339508 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1180279387 Health Risk Likely pathogenic ACTA1-related disorder, ACTA1-related disorder
RS121909524 Health Risk Likely pathogenic Congenital myopathy 2c, severe infantile, autosomal dominant
RS121909526 Health Risk Likely pathogenic Actin accumulation myopathy, Alpha-actinopathy, Actin accumulation myopathy
RS121909528 Health Risk Likely pathogenic Alpha-actinopathy, Actin accumulation myopathy, Alpha-actinopathy
RS121909530 Health Risk Likely pathogenic Congenital myopathy with fiber type disproportion, Actin accumulation myopathy, Congenital myopathy 2c
RS142311664 Health Risk Likely pathogenic Actin accumulation myopathy, Familial restrictive cardiomyopathy, Congenital myopathy with fiber type disproportion
RS1553255301 Health Risk Likely pathogenic Actin accumulation myopathy, Alpha-actinopathy, Actin accumulation myopathy
RS1553255360 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1553255501 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1553255502 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy, Actin accumulation myopathy
RS1558081384 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1558081804 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1571892193 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1571892196 Health Risk Likely pathogenic Actin accumulation myopathy, Alpha-actinopathy, Actin accumulation myopathy
RS1571892209 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1571892703 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1571892988 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
RS1571893783 Health Risk Likely pathogenic
RS1571894217 Health Risk Likely pathogenic Actin accumulation myopathy, Alpha-actinopathy, Actin accumulation myopathy
RS1659954132 Health Risk Likely pathogenic Nemaline myopathy, Nemaline myopathy
RS1659961434 Health Risk Likely pathogenic Neuromuscular disease, Neuromuscular disease
RS1659962016 Health Risk Likely pathogenic Actin accumulation myopathy, Actin accumulation myopathy
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