ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
tap2c
- ID
 - ZDB-GENE-990415-260
 - Name
 - transporter associated with antigen processing, subunit type c
 - Symbol
 - tap2c Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- tap2 (1)
 - abcb3
 - si:dz179b20.3
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 19 Mapping Details/Browsers
 - Genome Assembly
 - Unknown
 - Annotation Status
 - Not in current annotation release
 - Description
 - Acts upstream of or within response to methylmercury. Is expressed in brain; liver; and musculature system. Human ortholog(s) of this gene implicated in several diseases, including aspirin-induced respiratory disease; autoimmune disease (multiple); cervical cancer (multiple); dengue hemorrhagic fever; and systemic scleroderma (multiple). Orthologous to human TAP2 (transporter 2, ATP binding cassette subfamily B member).
 - Genome Resources
 - 
    
        
    
    
        
        
- Alliance (1)
 - Gene:30695 (1)
 - VEGA:OTTDARG00000001710 (1)
 
 - Note
 - 
    
        
        
    
        
            No gene match in Ensembl GRCz11.
 - Comparative Information
 - 
    
        
        
            
        
    
    
    
 
- All Expression Data
 - 3 figures from Gonzalez et al., 2005
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
 - No data available
 
                
                    
                        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 | 
|---|---|---|---|
| MHC class I deficiency 2 | 620813 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
    
        
    
No data available
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
    
        
    
No data available
    
            
        
    
    
    - Genome Browsers
 - No data available
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
 - No data available
 
- Comparative Orthology
 - Alliance