ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
bsnd
- ID
 - ZDB-GENE-070705-548
 - Name
 - barttin CLCNK type accessory subunit beta
 - Symbol
 - bsnd Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- im:7136367
 - si:dkeyp-51f12.4
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 20 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Enables chloride transmembrane transporter activity. Predicted to be involved in chloride transport. Predicted to be located in membrane. Predicted to be active in basolateral plasma membrane. Is expressed in pronephric duct. Human ortholog(s) of this gene implicated in Bartter disease; Bartter disease type 4a; and sensorineural hearing loss. Orthologous to human BSND (barttin CLCNK type accessory subunit beta).
 - Genome Resources
 - Note
 - None
 - Comparative Information
 - 
    
        
        
            
        
    
    
    
 
- All Expression Data
 - 6 figures from 4 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
 - 
    
        
    
    
        
        
- IMAGE:7136367 (2 images)
 
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
 - No data available
 - Cross-Species Comparison
 - Alliance
 
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Bartter disease type 4a | Alliance | Bartter syndrome, type 4a | 602522 | 
| Bartter disease type 4a | Alliance | Sensorineural deafness with mild renal dysfunction | 602522 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Type | InterPro ID | Name | 
|---|---|---|
| Family | IPR029181 | Barttin | 
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Barttin | 
|---|---|---|---|
| UniProtKB:E7F4W6 | InterPro | 175 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers