After several years of serving the research community, our ActiveDriverDB database will be retired on May 1st 2026. Please make sure to download any data you need and update your links or workflows before that date.
We want to sincerely thank all our users for their support, feedback, and collaboration over the years — your contributions have been invaluable to this project. A special thank you to Dr. Michal Krassowski for leading the development of our open-source software and database.
For any questions or assistance, please contact Jüri Reimand (juri.reimand@utoronto.ca).
EHMT1 (NM_024757) - euchromatic histone lysine methyltransferase 1
Histone-Lysine N-Methyltransferase Ehmt1 Isoform 1
Legend
                Mutation impacts
                
  
    
    
  
              
                
                Sites
                
  
    
    
  
              
                  -    C-linked
 -    N-linked
 -    O-linked
 -    S-linked
 
-    SARS-CoV-2
 
Others
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              Mutations Visualisation
              
  
    
    
  
            
          
        Protein summary
        
  
    
    
  
      
    The protein encoded by this gene is a histone methyltransferase that methylates the lysine-9 position of histone H3. This action marks the genomic region packaged with these methylated histones for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017].
- Strand
 - +
 - Chromosome
 - 9
 
- Protein
 - 1298 residues
 - All mutations
 - 379
 
- PTM sites
 - 51
 - CDS
 - 140,513,480 - 140,729,405
 - Transcription
 - 140,513,443 - 140,730,578