ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
deaf1
- ID
- ZDB-GENE-081022-163
- Name
- DEAF1 transcription factor
- Symbol
- deaf1 Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - zgc:194895
 
- Type
- protein_coding_gene
- Location
- Chr: 25 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. Human ortholog(s) of this gene implicated in Vulto-van Silfout-de Vries syndrome. Orthologous to human DEAF1 (DEAF1 transcription factor).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Vulto-van Silfout-de Vries syndrome | Alliance | Vulto-van Silfout-de Vries syndrome | 615828 | 
| Neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures | 617171 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | SAND domain | SAND-like domain superfamily | Transcription factor DEAF-1 | Zinc finger, MYND-type | 
|---|---|---|---|---|---|---|
| UniProtKB:A0A8M2BLH6 | InterPro | 532 | ||||
| UniProtKB:B3DHN2 | InterPro | 528 | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
