ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
uqcrb
- ID
 - ZDB-GENE-050522-542
 - Name
 - ubiquinol-cytochrome c reductase binding protein
 - Symbol
 - uqcrb Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- im:6900881
 - zgc:109893
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 19 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Acts upstream of or within angiogenesis. Predicted to be located in mitochondrial inner membrane. Predicted to be part of respiratory chain complex III. Is expressed in several structures, including adaxial cell; alar plate midbrain region; digestive system; optic tectum; and pronephric duct. Human ortholog(s) of this gene implicated in inherited metabolic disorder and mitochondrial complex III deficiency nuclear type 3. Orthologous to human UQCRB (ubiquinol-cytochrome c reductase binding protein).
 - Genome Resources
 - Note
 - None
 - Comparative Information
 - 
    
        
        
            
        
    
    
    
 
- All Expression Data
 - 6 figures from Thisse et al., 2004
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
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- IMAGE:6900881 (10 images)
 
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
 - 3 figures from Cho et al., 2013
 - Cross-Species Comparison
 - Alliance
 
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| mitochondrial complex III deficiency nuclear type 3 | Alliance | Mitochondrial complex III deficiency, nuclear type 3 | 615158 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Cytochrome b-c1 complex subunit 7 | Cytochrome b-c1 complex subunit 7 superfamily | 
|---|---|---|---|---|
| UniProtKB:Q4VBV1 | InterPro | 111 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers