ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
tk2
- ID
 - ZDB-GENE-040718-243
 - Name
 - thymidine kinase 2
 - Symbol
 - tk2 Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- zgc:100948
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 7 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Predicted to enable deoxynucleoside kinase activity. Predicted to act upstream of or within phosphorylation. Predicted to be active in mitochondrion. Is expressed in exocrine pancreas and pectoral fin. Human ortholog(s) of this gene implicated in autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3 and mitochondrial DNA depletion syndrome 2. Orthologous to human TK2 (thymidine kinase 2).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 5 figures from 4 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
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- IMAGE:7146682 (1 image)
 
 
                
                    
                        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 | 
|---|---|---|---|
| autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3 | Alliance | ?Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3 | 617069 | 
| mitochondrial DNA depletion syndrome 2 | Alliance | Mitochondrial DNA depletion syndrome 2 (myopathic type) | 609560 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Deoxynucleoside kinase domain | Deoxyribonucleoside Kinase | P-loop containing nucleoside triphosphate hydrolase | 
|---|---|---|---|---|---|
| UniProtKB:A0A8M1N0Z5 | InterPro | 268 | |||
| UniProtKB:A0AB32TZF0 | InterPro | 268 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers