FIGURE
            Fig. S14
- ID
 - ZDB-FIG-141007-56
 - Publication
 - Bielczyk-Maczyńska et al., 2014 - A loss of function screen of identified genome-wide association study Loci reveals new genes controlling hematopoiesis
 - Other Figures
 - All Figure Page
 - Back to All Figure Page
 
                
                    
                        Fig. S14
                    
                    
                
                
            
        
        
    
        
            
            
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 All the erythrocytes present in circulation of 2 dpf zebrafish embryos derive from the primitive wave of hematopoiesis. In order to assess the primitive erythropoiesis, MO injected embryos were stained with O-dianisidine at 2 dpf (arrow). Knockdown of 12 out of 15 candidate genes, namely: akap10, brf1a, brf1b, kalrn1, mfn2, pdia5, psmd13, rcor1, satb1, waspla, wasplb and wdr66, resulted in no observable phenotype. Depletion of brd3a, kalrn2 and kif1b resulted in a severe reduction in the number of primitive erythrocytes. All the embryos are positioned anterior up and dorsal to the back.  | 
    
                
                    
                        Expression Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Expression Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Antibody Labeling
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Phenotype Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Acknowledgments
                    
                    
                
                
            
        
        
    
        
            
            
                
                    
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      Full text @ PLoS Genet.