ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
atp5po
- ID
 - ZDB-GENE-050522-147
 - Name
 - ATP synthase peripheral stalk subunit OSCP
 - Symbol
 - atp5po Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- atp5o
 - un-named hi3619
 - unm hi3619
 - wu:fk86d05
 - zgc:109976
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 9 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in proton motive force-driven mitochondrial ATP synthesis. Predicted to act upstream of or within proton motive force-driven ATP synthesis and proton transmembrane transport. Predicted to be located in membrane. Is expressed in several structures, including alar plate midbrain region; gut; optic tectum; optic vesicle; and retina. Human ortholog(s) of this gene implicated in mitochondrial complex V (ATP synthase) deficiency nuclear type 7. Orthologous to human ATP5PO (ATP synthase peripheral stalk subunit OSCP).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 8 figures from 3 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
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- IMAGE:6910463 (9 images)
 
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| mitochondrial complex V (ATP synthase) deficiency nuclear type 7 | Alliance | Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7 | 620359 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | ATPase, OSCP/delta subunit | F1F0 ATP synthase OSCP/delta subunit, N-terminal domain superfamily | 
|---|---|---|---|---|
| UniProtKB:Q6DRD1 | InterPro | 209 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers