| Gene Symbol | CAVEOLIN3 |
| Aliases | CAVEOLIN3PROTEIN |
| Function | Caveolin-3 is essential for muscle health, and mutations in CAV3 cause several inherited muscle disorders including limb-girdle muscular dystrophy type 1C (LGMDR1C), rippling muscle disease, and fa... |
| Subcellular Localization | </strong></td><td>Muscle caveolae, Neuromuscular junction, Sarcolemma</td></tr> |
| GeneCards | CAVEOLIN3 |
| Human Protein Atlas | CAVEOLIN3 |
| LGMDR1C | Autosomal recessive limb-girdle muscular dystrophy |
| Rippling muscle disease | Autosomal dominant condition with muscle hyperexcitability |
| Hypertrophic cardiomyopathy | Familial form with marked ventricular hypertrophy |
| Distal myopathy | Affecting distal muscle groups |
| Membrane organization | Concentrating signaling receptors and effectors |
| Mechanotransduction | Sensing mechanical stress in muscle fibers |
| Endocytosis/exocytosis | Regulating vesicle trafficking |
| Cholesterol homeostasis | Managing cellular cholesterol pools |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
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