FIGURE
            Figure 2
- ID
 - ZDB-FIG-220430-98
 - Publication
 - Yan et al., 2022 - Functional Study of TMEM163 Gene Variants Associated with Hypomyelination Leukodystrophy
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                        Figure 2
                    
                    
                
                
            
        
        
    
        
            
            
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  Figure 2. Intracellular zinc flux assay of HeLa cells stably expressing wild-type and variant TMEM163 proteins. The HLD-linked variant TMEM163-L76P showed significantly enhanced zinc efflux, while the TMEM163-L76R variant displayed marked loss of zinc efflux activity that mimicked the inactive TMEM163-D124A-D128A mutant. Unmodified HeLa cells and stable cells expressing the TMEM163-E286K mutant were included as additional controls. Significance testing was performed using ANOVA with repeated measures followed by a post-hoc analysis using Tukey’s multiple comparisons test (p < 0.0001, n = 4 independent trials). Data are represented as means ± SEM. A.U., arbitrary unit.  
        
    
                        
                    
                
            
            
            
            
            
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                        Expression Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Expression Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Antibody Labeling
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Phenotype Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Acknowledgments
                    
                    
                
                
            
        
        
    
        
            
            
                
                    
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