ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
gli2a
- ID
 - ZDB-GENE-990706-8
 - Name
 - GLI family zinc finger 2a
 - Symbol
 - gli2a Nomenclature History
 - Previous Names
 - Type
 - protein_coding_gene
 - Location
 - Chr: 9 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Enables sequence-specific DNA binding activity. Acts upstream of or within several processes, including digestive tract morphogenesis; kidney development; and nervous system development. Located in non-motile cilium and nucleus. Is expressed in several structures, including central nervous system; digestive system; head; mesoderm; and neural plate. Human ortholog(s) of this gene implicated in Culler-Jones syndrome; holoprosencephaly 9; and spina bifida. Orthologous to human GLI2 (GLI family zinc finger 2).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 34 figures from 25 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
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- eu801 (22 images)
 
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
 - 47 figures from 29 publications
 - Cross-Species Comparison
 - Alliance
 
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Culler-Jones syndrome | Alliance | Culler-Jones syndrome | 615849 | 
| holoprosencephaly 9 | Alliance | Holoprosencephaly 9 | 610829 | 
                
                    
                        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 | Zinc finger C2H2 superfamily | Zinc finger C2H2-type | 
|---|---|---|---|---|---|---|
| UniProtKB:Q9YGS4 | InterPro | 1439 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
        
    
    
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers