ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
mecom
- ID
 - ZDB-GENE-050208-123
 - Name
 - MDS1 and EVI1 complex locus
 - Symbol
 - mecom Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- evi1
 - im:7140716
 - prdm3 (1)
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 15 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Acts upstream of or within several processes, including embryonic cranial skeleton morphogenesis; endothelial to hematopoietic transition; and pronephric nephron development. Predicted to be active in nucleus. Is expressed in several structures, including brain; dorsal aorta; head; mesoderm; and pronephros. Human ortholog(s) of this gene implicated in myeloid neoplasm. Orthologous to human MECOM (MDS1 and EVI1 complex locus).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 27 figures from 16 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
 - No data available
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
 - 20 figures from 6 publications
 - Cross-Species Comparison
 - Alliance
 
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 | 616738 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | SET domain | SET domain superfamily | Zinc finger | Zinc finger C2H2 superfamily | Zinc finger C2H2-type | 
|---|---|---|---|---|---|---|---|
| UniProtKB:A0A8M6YSJ7 | InterPro | 1257 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers