ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
dct
- ID
- ZDB-GENE-000508-1
- Name
- dopachrome tautomerase
- Symbol
- dct Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - TRP-2
- trp2
- tyrosinase-related protein-2
- zgc:109860
 
- Type
- protein_coding_gene
- Location
- Chr: 9 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable dopachrome isomerase activity. Acts upstream of or within melanin metabolic process. Predicted to be located in melanosome membrane. Predicted to be active in melanosome. Is expressed in several structures, including eye; female organism; immature eye; integument; and neural crest. Used to study oculocutaneous albinism. Human ortholog(s) of this gene implicated in oculocutaneous albinism. Orthologous to human DCT (dopachrome tautomerase).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- 105 figures from 76 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 1 Figure from Pennamen et al., 2020
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Oculocutaneous albinism, type VIII | 619165 | 
| Human Disease | Fish | Conditions | Citations | 
|---|---|---|---|
| oculocutaneous albinism | WT + MO1-dct | standard conditions | Pennamen et al., 2020 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Di-copper centre-containing domain superfamily | Tyrosinase and Hemocyanin | Tyrosinase copper-binding domain | 
|---|---|---|---|---|---|
| UniProtKB:A1L1Y0 | InterPro | 513 | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
