Entity Details
    
        
          
        
      
            
                    
                        
                            | Primary name | PLPL8_HUMAN | 
                        
                            | Entity type | UniProt | 
                        
                            | Source | Source Link | 
                    
             
            
            
                Details
                
                    
	
		| Accession | Q9NP80 | 
		| EntryName | PLPL8_HUMAN | 
		| FullName | Calcium-independent phospholipase A2-gamma | 
		| TaxID | 9606 | 
		| Evidence | evidence at protein level | 
		| Length | 782 | 
		| SequenceStatus | complete | 
		| DateCreated | 2007-09-11 | 
		| DateModified | 2021-06-02 | 
                 
             
            
            
            
                       
            
            
                Subcellular Location
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		| Subcellular Location | 
		| Endoplasmic reticulum membrane | 
		| Microsome membrane | 
		| Mitochondrion membrane | 
		| Peroxisome membrane | 
                 
              
            
                Domains
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		| Domain | Name | Category | Type | 
		| IPR002641 | Patatin-like phospholipase domain | Domain | Domain | 
		| IPR016035 | Acyl transferase/acyl hydrolase/lysophospholipase | Family | Homologous superfamily | 
                 
             
            
             
                Diseases
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		| Disease ID | Source | Name | Description | 
		| 251950 | OMIM | Mitochondrial myopathy with lactic acidosis (MMLA) | An autosomal recessive disorder characterized by progressive muscle weakness, hypotonia, seizures, poor weight gain, lactic acidosis, and elevated serum pyruvate concentration. Some patients manifest growth failure and moderate neural deafness. The disease is caused by variants affecting the gene represented in this entry. | 
                 
               
                        
                       
            
                Interactions
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