Uniprot AC	Entrez ID	Gene Name	Disease	Cell Type	PTM Type	State	Position	PMID
P56539	859	CAV3	Sudden infant death syndrome		Ubiquitination	N	K15	
P56539	859	CAV3	HyperCKmia		Ubiquitination	N	K30	
P56539	859	CAV3	Myopathy		Ubiquitination	N	K30	
P56539	859	CAV3	Rippling muscle disease		Ubiquitination	N	K30	
P56539	859	CAV3	Myopathy		SUMOylation	N	K38