ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
slc30a10
- ID
- ZDB-GENE-060608-2
- Name
- solute carrier family 30 member 10
- Symbol
- slc30a10 Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - ZnT10 (1)
 
- Type
- protein_coding_gene
- Location
- Chr: 13 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable zinc ion transmembrane transporter activity. Acts upstream of or within manganese ion homeostasis and manganese ion transport. Predicted to be active in membrane. Is expressed in brain; liver; and yolk syncytial layer. Human ortholog(s) of this gene implicated in hypermanganesemia with dystonia 1. Orthologous to human SLC30A10 (solute carrier family 30 member 10).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- 1 figure from Xia et al., 2017
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 5 figures from Xia et al., 2017
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| hypermanganesemia with dystonia 1 | Alliance | Hypermanganesemia with dystonia 1 | 613280 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Cation efflux protein | Cation efflux transmembrane domain superfamily | 
|---|---|---|---|---|
| UniProtKB:A8WFU0 | InterPro | 385 | ||
| UniProtKB:A0A0R4IEQ2 | InterPro | 385 | 
- Genome Browsers
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis | 
|---|---|---|---|---|---|
| mRNA | slc30a10-201
                             (1) | Ensembl | 2,067 nt | 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
