ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
zic1
- ID
 - ZDB-GENE-000208-4
 - Name
 - zic family member 1 (odd-paired homolog, Drosophila)
 - Symbol
 - zic1 Nomenclature History
 - Previous Names
 - Type
 - protein_coding_gene
 - Location
 - Chr: 24 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and zinc ion binding activity. Acts upstream of or within brain development and embryonic retina morphogenesis in camera-type eye. Predicted to be active in nucleus. Is expressed in several structures, including central nervous system; neural keel; neural plate; neural rod; and presumptive neural plate. Human ortholog(s) of this gene implicated in Dandy-Walker syndrome and craniosynostosis 6. Orthologous to human ZIC1 (Zic family member 1).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 76 figures from 47 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
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- MGC:76803 (26 images)
 
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| craniosynostosis 6 | Alliance | ?Craniosynostosis 6 | 616602 | 
| Structural brain anomalies with impaired intellectual development and craniosynostosis | 618736 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | C2H2-type zinc-finger protein GLI-like | ZIC1-5/GLI1-3like, C2H2 zinc finger | ZIC protein, zinc finger domain | Zinc finger C2H2 superfamily | Zinc finger C2H2-type | 
|---|---|---|---|---|---|---|---|
| UniProtKB:O93311 | InterPro | 442 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers