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KMT2A
Genelysine methyltransferase 2A
Encodes
The protein product this gene encodes, reached through the canonical GENE→PROTEIN (encodes) relation. Its biology, drugs, indications, trials and therapeutic evidence live on the protein's own page.
Also known as
Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.
MLL · TRX1 · HRX · ALL-1 · HTRX1 · CXXC7 · MLL1A · MLL1 · ALL1 · HTRX
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MLL
TRX1, HRX, ALL-1, HTRX1, CXXC7, MLL1A, MLL1, ALL1, HTRX
myeloid/lymphoid or mixed-lineage leukemia (trithorax (Drosophila) homolog), myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila), lysine (K)-specific methyltransferase 2A, Trithorax-like protein, CXXC-type zinc finger protein 7, Acute lymphocytic 1
Histone-lysine N-methyltransferase 2A
Associated diseases
Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.
Gene family
HGNC gene-group membership.
PHD finger proteinsZinc fingers CXXC-typeHistone lysine methyltransferasesBromodomain containingSET domain containing
Provenance
HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.