ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
slc6a6b
- ID
- ZDB-GENE-030131-3077
- Name
- solute carrier family 6 member 6b
- Symbol
- slc6a6b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 22 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Enables taurine:sodium symporter activity. Acts upstream of or within taurine transmembrane transport. Predicted to be located in membrane. Predicted to be active in cell projection and plasma membrane. Is expressed in several structures, including blastomere; cardiovascular system; nervous system; optic vesicle; and presumptive neural retina. Orthologous to human SLC6A6 (solute carrier family 6 member 6).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- 4 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 2 figures from Kozlowski et al., 2008
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Hypotaurinemic retinal degeneration and cardiomyopathy | 145350 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Sodium:neurotransmitter symporter | Sodium:neurotransmitter symporter superfamily | Sodium:neurotransmitter symporter, taurine | 
|---|---|---|---|---|---|
| UniProtKB:Q2VRP7 | InterPro | 625 | 
- Genome Browsers
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis | 
|---|---|---|---|---|---|
| mRNA | slc6a6b-201
                             (1) | Ensembl | 1,725 nt | 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
