ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
clrn2
- ID
- ZDB-GENE-061207-64
- Name
- clarin 2
- Symbol
- clrn2 Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - si:dkey-245p14.5
 
- Type
- protein_coding_gene
- Location
- Chr: 1 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Involved in auditory receptor cell stereocilium organization and sensory perception of sound. Acts upstream of or within auditory receptor cell morphogenesis. Located in cell hair. Is expressed in several structures, including gill; inner ear; integument; notochord; and testis. Used to study autosomal recessive nonsyndromic deafness. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness. Orthologous to human CLRN2 (clarin 2).
- Genome Resources
- Note
- None
- Comparative Information
- 
    
        
        
              
- All Expression Data
- 1 figure from Vona et al., 2021
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 1 Figure from Vona et al., 2021
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Deafness, autosomal recessive 117 | 619174 | 
| Human Disease | Fish | Conditions | Citations | 
|---|---|---|---|
| autosomal recessive nonsyndromic deafness | WT + CRISPR3-clrn2 + CRISPR4-clrn2 + CRISPR5-clrn2 + CRISPR6-clrn2 + CRISPR7-clrn2 | standard conditions | Vona et al., 2021 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Type | InterPro ID | Name | 
|---|---|---|
| Family | IPR026748 | Clarin | 
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Clarin | 
|---|---|---|---|
| UniProtKB:B8A5K7 | InterPro | 233 | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
