ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
fgf3
- ID
 - ZDB-GENE-980526-178
 - Name
 - fibroblast growth factor 3
 - Symbol
 - fgf3 Nomenclature History
 - Previous Names
 - Type
 - protein_coding_gene
 - Location
 - Chr: 7 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Enables fibroblast growth factor receptor binding activity. Acts upstream of with a negative effect on Wnt signaling pathway. Acts upstream of or within with a positive effect on hypothalamus development. Acts upstream of or within several processes, including embryonic morphogenesis; nervous system development; and positive regulation of cell differentiation. Located in extracellular matrix and extracellular space. Is expressed in several structures, including brain; mesoderm; neural rod; pharynx; and sensory system. Orthologous to human FGF3 (fibroblast growth factor 3).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 145 figures from 108 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
 - No data available
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
 - 32 figures from 17 publications
 - Cross-Species Comparison
 - Alliance
 
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Deafness, congenital with inner ear agenesis, microtia, and microdontia | 610706 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Cytokine IL1/FGF | Fibroblast growth factor family | 
|---|---|---|---|---|
| UniProtKB:P48802 | InterPro | 256 | ||
| UniProtKB:B3DHR1 | InterPro | 256 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers