CAV3 Chromosome 3

Caveolin 3
53 variants 53 Health Risk

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What This Gene Does
This gene encodes a caveolin family member, which functions as a component of the caveolae plasma membranes found in most cell types. Caveolin proteins are proposed to be scaffolding proteins for organizing and concentrating certain caveolin-interacting molecules. Mutations identified in this gene lead to interference with protein oligomerization or intra-cellular routing, disrupting caveolae formation and resulting in Limb-Girdle muscular dystrophy type-1C (LGMD-1C), hyperCKemia or rippling muscle disease (RMD). Alternative splicing has been identified for this locus, with inclusion or exclusion of a differentially spliced intron. In addition, transcripts utilize multiple polyA sites and contain two potential translation initiation sites. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Caveolins
Locus Type
gene with protein product
Location
3p25.3
Ensembl
ENSG00000182533
Associated Conditions (22)
Caveolinopathy
Long QT syndrome
CAV3-related disorder
Cardiomyopathy
Long QT syndrome 1
Cardiovascular phenotype
See cases
Rippling muscle disease 2
Limb-girdle muscular dystrophy
Hypertrophic cardiomyopathy 1
Elevated circulating creatine kinase concentration
Distal myopathy
Tateyama type
Long QT syndrome 9
autosomal recessive
Long QT syndrome 2/9
digenic
Hypertrophic cardiomyopathy
Abnormality of the musculature
Myopathy with tubular aggregates
+2 more conditions
Key Variants
RS1052106103
Conflicting classifications of pathogenicity
Caveolinopathy, Caveolinopathy
Health Risk
RS1060502318
Conflicting classifications of pathogenicity
Long QT syndrome, CAV3-related disorder, Long QT syndrome
Health Risk
RS112626848
Conflicting classifications of pathogenicity
Long QT syndrome, Cardiomyopathy, Long QT syndrome 1
Health Risk
RS116840776
Conflicting classifications of pathogenicity
Rippling muscle disease 2, Limb-girdle muscular dystrophy, Cardiovascular phenotype
Health Risk
RS116840778
Conflicting classifications of pathogenicity
Elevated circulating creatine kinase concentration, Rippling muscle disease 2, Distal myopathy
Health Risk
RS116840795
Conflicting classifications of pathogenicity
Long QT syndrome, Cardiomyopathy, Cardiovascular phenotype
Health Risk
RS1182984115
Conflicting classifications of pathogenicity
Long QT syndrome, Cardiovascular phenotype, Long QT syndrome
Health Risk
RS121909281
Conflicting classifications of pathogenicity
Long QT syndrome 9, Cardiovascular phenotype, Cardiomyopathy
Health Risk
RS139786391
Conflicting classifications of pathogenicity
Long QT syndrome, Cardiovascular phenotype, Long QT syndrome
Health Risk
RS140575619
Conflicting classifications of pathogenicity
Long QT syndrome, Caveolinopathy, Cardiomyopathy
Health Risk
RS147250678
Conflicting classifications of pathogenicity
Cardiomyopathy, Long QT syndrome, Caveolinopathy
Health Risk
RS148846096
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Long QT syndrome, CAV3-related disorder
Health Risk
All Variants (53)
RSID Category Clinical Significance Conditions
RS116840789 Health Risk Pathogenic/Likely pathogenic Rippling muscle disease 2, Elevated circulating creatine kinase concentration, Long QT syndrome
RS2124988406 Health Risk Pathogenic/Likely pathogenic Long QT syndrome, Long QT syndrome
RS104893714 Health Risk risk factor Long QT syndrome 9, acquired, susceptibility to
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