Lysine-specific methyltransferase 2a

Preferred Label : Lysine-specific methyltransferase 2a;

Symbol : KMT2A;

CISMeF acronym : KMT2A;

Type : Gene;

Alternative titles and symbols : Myeloid/lymphoid leukemia gene; All1 gene; Mixed lineage leukemia gene; Trithorax, drosophila, homolog of; Cxxc finger protein 7; Myeloid/lymphoid or mixed lineage leukemia gene; MLL1; TRX1; MLL; ALL1; CXXC7; HRX;

Included titles and symbols : Mll/cdk6 fusion gene; Mll/cip29 fusion gene; Mll/gmps fusion gene; Mll/gph fusion gene; Mll/lasp1 fusion gene; Mll/cbl fusion gene; Mll/af4 fusion gene; Mll/fbp17 fusion gene; Mll/af9 fusion gene; Mll/af10 fusion gene; Mll/maml2 fusion gene; Mll/abi1 fusion gene; Mll/graf fusion gene; Mll/laf4 fusion gene; Mll/af15q14 fusion gene; Mll/pnutl1 fusion gene; Mll/af6 fusion gene; Mll/kiaa1524 fusion gene; Mll/enl fusion gene; Mll/larg fusion gene; Mll/lpp fusion gene; Mll/sept6 fusion gene; Mll/mpfyve fusion gene;

Ensembl ID : ENSG00000118058;

Prefixed ID : *159555;

Details

Origin ID

159555;

UMLS CUI

C0919528;

Automatic exact mappings (from CISMeF team)
- Histone-Lysine N-Methyltransferase 2A [NCIt concept]
- KMT2A Gene [NCIt concept]
- KMT2A wt Allele [NCIt concept]
- Thioredoxin [NCIt concept]
HGNC gene
- lysine methyltransferase 2A [HGNC gene]
Phenotypes related
- Wiedemann-steiner syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KMT2A Gene [NCIt concept]
- MLL gene [LOINC component]
- lysine methyltransferase 2A [ORDO Gene]
- lysine methyltransferase 2A [HGNC gene]

Keyword's position in hierarchy(ies) :

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