GM27131
                                                
                                                LCL from B-Lymphocyte
                                                
                                                
                                             
                                            
                                                
                                                    
                                                         Description:
                                                    
                                                    
                                                         
                                                            
                                                            CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 
                                                            
                                                            MYOSIN-BINDING PROTEIN C, CARDIAC; MYBPC3 
                                                            
                                                    
                                                 
                                                
                                                
                                                
                                                
                                             
                                         
                                     
                                    
                                        
                                            
                                            
                                            
                                            
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
                                                                    
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                                                                            NIGMS Human Genetic Cell Repository
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	| Subcollection | 
	Heritable Diseases PIGI Consented Sample | 
 
                                                                
                                                                
                                                                
                                                                
                                                                
                                                                
                                                                
                                                                    
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                                                                            Biopsy Source
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                                                                            Peripheral vein
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                                                                            Cell Type
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                                                                            B-Lymphocyte
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                                                                            Tissue Type
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                                                                            Blood
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                                                                            Transformant
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                                                                            Epstein-Barr Virus
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                                                                            Sample Source
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                                                                            LCL from B-Lymphocyte
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                                                                            Race
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                                                                            White
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                                                                            Ethnicity
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                                                                            Not Hispanic/Latino
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                                                                            Ethnicity
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                                                                            German, Irish
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                                                                            Country of Origin
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                                                                            USA
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                                                                            Family History
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                                                                            Y
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                                                                            Relation to Proband
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                                                                            proband
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                                                                            Confirmation
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                                                                            Molecular characterization before cell line submission to CCR
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                                                                            Species
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                                                                            Homo sapiens
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                                                                            Common Name
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                                                                            Human
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                                                                            Remarks
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	| IDENTIFICATION OF SPECIES OF ORIGIN | 
	Species of Origin Confirmed by LINE assay | 
 
	|   | 
 
                                                                
	| Gene | 
	MYBPC3 | 
 
	| Chromosomal Location | 
	11p11.2 | 
 
	| Allelic Variant 1 | 
	p.Cys528ThrfsX4; CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 | 
 
	| Identified Mutation | 
	c.1577_1580dupCACT (p.C528TfsX4) | 
 
                                                                
                                                                
                                                                
                                                                
                                                                
                                                                
                                                             
                                                         
                                                     
                                                 
                                                
                                                    
                                                        
                                                            
                                                            
                                                            
                                                                
	| Remarks | 
	Clinically affected; Symptoms onset at age 25 including exertional chest pain, echocardiography shows stable morphology, cardiac function at the low end of normal range; Treatment: beta-blocker and Ca-channel blockers were not effective in managing chest pain and are no longer being taken, moderate-intensity exercise only; Sequencing revealed a heterozygous genetic variant in MYBPC3 gene (c.1577_1580dupCACT) resulting in a shift of reading frame starting at codon Cysteine 528 (p.Cys528ThrfsX4); Several family members share the same MYBPC3 mutation; Pedigree established: carrier heterozygote father, carrier heterozygote paternal grandfather who died from idiopathic pulmonary fibrosis and underwent quadruple coronary bypass surgery, 2 carrier paternal aunts (1 of which with preclinical HCM), 1 HCM clinically affected cousin, and 1 preclinical HCM carrier cousin. Same donor as GM29381 iPSC. | 
 
                                                                
                                                             
                                                            
                                                            
                                                         
                                                     
                                                 
                                                
                                                
                                                
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
	| Split Ratio | 
	1:6 | 
 
	| Temperature | 
	37 C | 
 
	| Percent CO2 | 
	5% | 
 
	| Percent O2 | 
	AMBIENT | 
 
	| Medium | 
	Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent | 
 
	| Serum | 
	15% fetal bovine serum Not Inactivated | 
 
	| Substrate | 
	None specified | 
 
	| Subcultivation Method | 
	dilution - add fresh medium | 
 
	| Supplement | 
	- | 
 
                                                                
                                                                
                                                             
                                                         
                                                     
                                                 
                                             
                                         
                                     
                                 
                                
                             
                         
                     
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