ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
mrap
- ID
 - ZDB-GENE-060503-387
 - Name
 - melanocortin 2 receptor accessory protein
 - Symbol
 - mrap Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- MRAP1 (1)
 - si:ch211-152c12.3
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 15 Mapping Details/Browsers
 - Genome Assembly
 - GRCz11
 - Annotation Status
 - Unknown
 - Description
 - Enables melanocortin receptor binding activity and peptide hormone binding activity. Contributes to corticotropin receptor activity. Acts upstream of or within positive regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway and protein localization to cell surface. Located in plasma membrane. Is expressed in adipose tissue; head kidney; liver; and ovary. Human ortholog(s) of this gene implicated in familial glucocorticoid deficiency. Orthologous to human MRAP (melanocortin 2 receptor accessory protein).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 3 figures from 3 publications
 - 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 | 
|---|---|---|---|
| Glucocorticoid deficiency 2 | 607398 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
    
        
    
No data available
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
    
        
    
No data available
    
            
        
    
    
    
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers