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KMT2A gene

Known as: LYSINE-SPECIFIC METHYLTRANSFERASE 2A, KMT2A, CXXC FINGER PROTEIN 7 
This gene is involved in transcriptional regulation and alterations in the gene are associated with acute lymphoblastic leukemia.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
The rearrangements of the MLL located on the chromosome 11q23 are the major cause of mixed-lineage leukemia. The translocation… 
2015
2015
Wiedemann–Steiner syndrome (WSS) is an autosomal dominant congenital anomaly syndrome characterized by hairy elbows, dysmorphic… 
2013
2013
This study was purposed to establish a retrovirus-mediated murine model with MLL-AF9 leukemia, so as to provide a basis for… 
2005
2005
Proteases from digestive fluid of Nang-lai strains of the Thai silkworm, Bombyx mori were partially purified by 40% ammonium… 
Review
2002
Review
2002
We identified and characterized the Drosophila gene ear (ENL/AF9-related), which is closely related to mammalian genes that have… 
Review
1998
Review
1998
We examined the MLL genomic translocation breakpoint in acute myeloid leukemia of infant twins. Southern blot analysis in both… 
1994
1994
Seven patients with acute leukemia and translocation involving band 11q23 have been studied by fluorescence in situ hybridization…