TPM1 Chromosome 15

Tropomyosin 1
125 variants 125 Health Risk

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What This Gene Does
This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy and dilated cardiomyopathy 1Y. [provided by RefSeq, Jun 2022]
Gene Info
Gene Group
Tropomyosins
Locus Type
gene with protein product
Location
15q22.2
Ensembl
ENSG00000140416
Associated Conditions (23)
Hypertrophic cardiomyopathy 3
Dilated cardiomyopathy 1Y
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
Primary familial hypertrophic cardiomyopathy
TPM1-related disorder
Primary dilated cardiomyopathy
Uterine corpus endometrial carcinoma
Gastric cancer
Hypertrophic cardiomyopathy 1
Left ventricular noncompaction 9
Hypertrophic cardiomyopathy 21
Long QT syndrome
Paroxysmal familial ventricular fibrillation
See cases
Left ventricular noncompaction cardiomyopathy
Pulmonary atresia with intact ventricular septum
Atrial septal defect 1
Catecholaminergic polymorphic ventricular tachycardia
+3 more conditions
Key Variants
RS1032357917
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy 3, Dilated cardiomyopathy 1Y, Hypertrophic cardiomyopathy 3
Health Risk
RS104894505
Conflicting classifications of pathogenicity
Dilated cardiomyopathy 1Y, Hypertrophic cardiomyopathy, Cardiovascular phenotype
Health Risk
RS1060501866
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy, Cardiovascular phenotype, Hypertrophic cardiomyopathy
Health Risk
RS1131003
Conflicting classifications of pathogenicity
Cardiomyopathy, Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy 3
Health Risk
RS113759732
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy, Cardiomyopathy, Cardiovascular phenotype
Health Risk
RS1350935943
Conflicting classifications of pathogenicity
Dilated cardiomyopathy 1Y, Hypertrophic cardiomyopathy 3, Hypertrophic cardiomyopathy
Health Risk
RS139159081
Conflicting classifications of pathogenicity
Cardiomyopathy, Cardiomyopathy
Health Risk
RS141757680
Conflicting classifications of pathogenicity
Primary familial hypertrophic cardiomyopathy, Cardiomyopathy, TPM1-related disorder
Health Risk
RS143922069
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy 3, Dilated cardiomyopathy 1Y
Health Risk
RS144451403
Conflicting classifications of pathogenicity
Cardiomyopathy, Cardiomyopathy
Health Risk
RS149659674
Conflicting classifications of pathogenicity
Cardiomyopathy, Hypertrophic cardiomyopathy, Dilated cardiomyopathy 1Y
Health Risk
RS1555408679
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy, Cardiomyopathy, Cardiovascular phenotype
Health Risk
All Variants (125)
RSID Category Clinical Significance Conditions
RS2542806797 Health Risk Likely pathogenic Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS371680410 Health Risk Likely pathogenic Catecholaminergic polymorphic ventricular tachycardia, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1
RS397516363 Health Risk Likely pathogenic Primary dilated cardiomyopathy, Dilated cardiomyopathy 1Y, Cardiomyopathy
RS397516364 Health Risk Likely pathogenic Primary dilated cardiomyopathy, Primary dilated cardiomyopathy
RS397516370 Health Risk Likely pathogenic Primary dilated cardiomyopathy, Primary dilated cardiomyopathy
RS397516371 Health Risk Likely pathogenic Primary dilated cardiomyopathy, Primary dilated cardiomyopathy
RS397516386 Health Risk Likely pathogenic Cardiomyopathy, Cardiomyopathy
RS727504264 Health Risk Likely pathogenic Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS727504389 Health Risk Likely pathogenic Primary dilated cardiomyopathy, Primary dilated cardiomyopathy
RS754664923 Health Risk Likely pathogenic Cardiovascular phenotype, Hypertrophic cardiomyopathy, Dilated cardiomyopathy 1Y
RS876657662 Health Risk Likely pathogenic Primary dilated cardiomyopathy, Primary dilated cardiomyopathy
RS879253758 Health Risk Likely pathogenic Effort-induced polymorphic ventricular tachycardia, Effort-induced polymorphic ventricular tachycardia
RS886037905 Health Risk Likely pathogenic Dilated cardiomyopathy 1Y, Dilated cardiomyopathy 1Y
RS104894503 Health Risk Pathogenic Hypertrophic cardiomyopathy 3, Primary familial hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS199476317 Health Risk Pathogenic Primary dilated cardiomyopathy, Hypertrophic cardiomyopathy, Dilated cardiomyopathy 1Y
RS199476319 Health Risk Pathogenic Left ventricular noncompaction 9, Left ventricular noncompaction 9
RS2140974070 Health Risk Pathogenic Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS730881157 Health Risk Pathogenic
RS104894504 Health Risk Pathogenic/Likely pathogenic Hypertrophic cardiomyopathy 3, Hypertrophic cardiomyopathy, Cardiovascular phenotype
RS199476306 Health Risk Pathogenic/Likely pathogenic Hypertrophic cardiomyopathy, Cardiovascular phenotype, Hypertrophic cardiomyopathy 3
RS199476311 Health Risk Pathogenic/Likely pathogenic Primary dilated cardiomyopathy, Dilated cardiomyopathy 1Y, Hypertrophic cardiomyopathy
RS199476315 Health Risk Pathogenic/Likely pathogenic Left ventricular noncompaction 9, Primary familial hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS199476316 Health Risk Pathogenic/Likely pathogenic Cardiomyopathy, Primary familial hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS397516373 Health Risk Pathogenic/Likely pathogenic Primary dilated cardiomyopathy, Cardiomyopathy, Hypertrophic cardiomyopathy
RS730881131 Health Risk Pathogenic/Likely pathogenic Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy 3, Hypertrophic cardiomyopathy
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