FIGURE
            Fig 1
- ID
 - ZDB-FIG-221216-68
 - Publication
 - Liu et al., 2022 - LOF variants identifying candidate genes of laterality defects patients with congenital heart disease
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                        Fig 1
                    
                    
                
                
            
        
        
    
        
            
            
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 Schematic of the methodology applied to identify candidate genes. 
        
    
                        
                    
                
            
            
            
            
            
            The results of ES performed on 70 patients were screened according to a series of criteria. 10226 rare variants were screened out. Among them, 776 LOF variants were selected for further analysis. 39 genes were identified from LOF variants for function and homology analysis. Finally, TRIP11, DNHD1, CFAP74, and EGR4 were selected as candidate genes for further study.  | 
    
                
                    
                        Expression Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Expression Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Antibody Labeling
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Phenotype Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Acknowledgments
                    
                    
                
                
            
        
        
    
        
            
            
                
                    
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      Full text @ PLoS Genet.