ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
nog3
- ID
- ZDB-GENE-990714-8
- Name
- noggin 3
- Symbol
- nog3 Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - zNog3
- noggin
 
- Type
- protein_coding_gene
- Location
- Chr: 12 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Acts upstream of or within several processes, including cloaca development; embryonic viscerocranium morphogenesis; and regionalization. Predicted to be located in extracellular region. Predicted to be active in extracellular space. Is expressed in cartilage element; fin; head; and otic vesicle. Human ortholog(s) of this gene implicated in Huntington's disease; bone disease (multiple); cleft lip; and hyperopia. Orthologous to human NOG (noggin).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- 12 figures from 7 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
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        - eu301 (4 images)
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 1 Figure from Ning et al., 2013
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| brachydactyly type B2 | Alliance | Brachydactyly, type B2 | 611377 | 
| multiple synostoses syndrome 1 | Alliance | Multiple synostoses syndrome 1 | 186500 | 
| proximal symphalangism 1 | Alliance | Symphalangism, proximal, 1A | 185800 | 
| tarsal-carpal coalition syndrome | Alliance | Tarsal-carpal coalition syndrome | 186570 | 
| Stapes ankylosis with broad thumbs and toes | 184460 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Cystine-knot cytokine | Noggin | 
|---|---|---|---|---|
| UniProtKB:Q9YHV3 | InterPro | 223 | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
