EHMT1 (euchromatic histone-lysine N-methyltransferase 1) is a protein-coding gene. Diseases associated with EHMT1 include kleefstra syndrome, and kleefstra syndrome due to 9q34 microdeletion. GO annotations related to this gene include methyltransferase activity and histone-lysine N-methyltransferase activity. An important paralog of this gene is NSD1.
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