Lysine-specific methyltransferase 2b

Preferred Label : Lysine-specific methyltransferase 2b;

Symbol : KMT2B;

CISMeF acronym : KMT2B;

Type : Gene;

Alternative titles and symbols : Myeloid/lymphoid or mixed-lineage leukemia 4; Myeloid/lymphoid or mixed-lineage leukemia 2; Trithorax, drosophila, homolog of, 2; MLL4; MLL2; TRX2; KIAA0304;

Ensembl ID : ENSG00000272333;

Prefixed ID : *606834;

Détails

Origin ID

606834;

UMLS CUI

C1847413;

Automatic exact mappings (from CISMeF team)
- Histone-Lysine N-Methyltransferase 2B [NCIt concept]
- Histone-Lysine N-Methyltransferase 2D [NCIt concept]
- KMT2B Gene [NCIt concept]
- KMT2B wt Allele [NCIt concept]
- KMT2D Gene [NCIt concept]
- KMT2D wt Allele [NCIt concept]
- lysine methyltransferase 2B [HGNC gene]
- lysine methyltransferase 2D [ORDO Gene]
HGNC gene
- lysine methyltransferase 2B [HGNC gene]
NCIt concept(s)
- Histone-Lysine N-Methyltransferase 2B [NCIt concept]
- KMT2B Gene [NCIt concept]
- KMT2B wt Allele [NCIt concept]
ORDO concept(s)
- lysine methyltransferase 2B [ORDO Gene]
Phenotypes related
- Dystonia 28, childhood-onset [OMIM Phenotype]
- Intellectual developmental disorder, autosomal dominant 68 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KMT2B Gene [NCIt concept]
- lysine methyltransferase 2B [HGNC gene]

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