ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
ddb1
- ID
 - ZDB-GENE-040426-1272
 - Name
 - damage-specific DNA binding protein 1
 - Symbol
 - ddb1 Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- zgc:63840
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 18 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Predicted to enable nucleic acid binding activity. Acts upstream of or within negative regulation of apoptotic process and regulation of cell cycle process. Predicted to be active in nucleus and site of double-strand break. Is expressed in blastomere; endoderm; nervous system; pharyngeal arch; and somite. Human ortholog(s) of this gene implicated in communication disorder. Orthologous to human DDB1 (damage specific DNA binding protein 1).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 2 figures from Hu et al., 2015
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
 - No data available
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| White-Kernohan syndrome | 619426 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Cleavage/polyadenylation specificity factor, A subunit, C-terminal | RSE1/DDB1/CFT1/CPSF1 | RSE1/DDB1/CPSF1, first beta-propeller domain | WD40/YVTN repeat-like-containing domain superfamily | 
|---|---|---|---|---|---|---|
| UniProtKB:Q6PGT6 | InterPro | 897 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers