KMT2A (Lysine Methyltransferase 2A) is a Protein Coding gene. Diseases associated with KMT2A include Wiedemann-Steiner Syndrome and Cornelia De Lange Syndrome 1. Among its related pathways are Circadian rythm related genes and Chromatin organization. Gene Ontology (GO) annotations related to this gene include DNA binding transcription factor activity and identical protein binding. An important paralog of this gene is KMT2B.