KMT2A, lysine methyltransferase 2A, 4297

N. diseases: 535; N. variants: 65
Disease: Autosome Abnormalities ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004403
Disease: Autosome Abnormalities
Autosome Abnormalities 		0.300 Biomarker group CTD_human MLL fusion-driven activation of CDK6 potentiates proliferation in MLL-rearranged infant ALL. 24736461 2014