KMT2A, lysine methyltransferase 2A, 4297

N. diseases: 535; N. variants: 65
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 Biomarker disease BEFREE We established a reporter system to systematically quantitate and stratify the potential for such compounds to promote chromosomal translocations between the MLL and AF9 bcrs analogous to those in infant leukemia. 30387535 2019
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Excess congenital non-synonymous variation in leukemia-associated genes in MLL- infant leukemia: a Children's Oncology Group report. 24301523 2014
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Because of the unfavorable outcome associated with MLL rearrangements in infant leukemia, we intensified postremission treatment according to the Interfant-06 study protocol. 24635731 2014
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE The mixed lineage leukemia (MLL) gene is commonly rearranged in infant leukemia (IL). 22422485 2013
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE This review highlights the key clinical, pathologic, and epidemiologic features of infant leukemia, including the high frequency of mixed lineage leukemia (MLL) gene rearrangements. 24319237 2013
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE MLL gene rearrangements in infant leukemia vary with age at diagnosis and selected demographic factors: a Children's Oncology Group (COG) study. 21800415 2012
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Rearrangements of the Mixed-Lineage Leukemia (MLL) gene are found in > 70% of infant leukemia, ~ 10% of adult acute myelogenous leukemia (AML), and many cases of secondary acute leukemias. 22160057 2011
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 Biomarker disease BEFREE Nebulette is the second member of the nebulin family fused to the MLL gene in infant leukemia. 20362230 2010
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE The clinical features and molecular analyses for the fusion transcripts of mixed lineage leukemia (MLL) gene rearrangement in infant leukemia have not been well documented in the Chinese population. 20979094 2010
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE MLL rearrangements are hallmark genetic abnormalities in infant leukemia known to arise in utero. 19587093 2009
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Outcome of recurrent or refractory acute lymphoblastic leukemia in infants with MLL gene rearrangements: A report from the Japan Infant Leukemia Study Group. 19229974 2009
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 Biomarker disease BEFREE MLL associated leukemias account for the majority of infant leukemia, approximately 10% of adult de novo leukemia and approximately 33% of therapy related acute leukemia with a balanced chromosome translocation. 19729989 2009
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 Biomarker disease BEFREE Infant leukemia (IL) is characterised by the presence of MLL rearrangements and a poor outcome. 19052976 2008
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Infant leukemia associated with rearrangement of the MLL gene typically presents with high-risk clinical features. 19131787 2008
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Definitive diagnosis of coexisting pro-B cell infant leukemia with cryptic MLL rearrangement was delayed by the transient regeneration of normal hematopoiesis and reduction of abnormal blastoid cells in the bone marrow following immunoglobulin administration. 16814860 2007
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Molecular characterization of a rare MLL-AF4 (MLL-AFF1) fusion rearrangement in infant leukemia. 17889710 2007
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 Biomarker disease BEFREE Other variables of interest were not notably associated with infant leukemia regardless of MLL status. 17220341 2007
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 Biomarker disease BEFREE Infants with acute lymphoblastic leukemia and a germline MLL gene are highly curable with use of chemotherapy alone: results from the Japan Infant Leukemia Study Group. 16478880 2006
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 Biomarker disease BEFREE MLL chimeric protein activation renders cells vulnerable to chromosomal damage: an explanation for the very short latency of infant leukemia. 16688745 2006
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE However, whereas the genomic breakpoints in MLL tend to cluster in the 5' portion of the 8.3 kb breakpoint cluster region (BCR) in de novo and adult patients and in the 3' portion in infant leukemia patients and t-AML patients, those in both the AML1 and ETO genes occur in the same clustered regions in both de novo and t-AML patients. 16893685 2006
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Leukemias with MLL translocations have been the topic of intense interest because of the unusual, biphenotypic immunophenotype of these leukemias, because of the unique clinical presentation of some MLL translocations (infant leukemia and therapy-related leukemia), and because of the large number of different chromosomal loci that partner with MLL in these translocations. 16797254 2006
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE Analysis of the outcome among ALL infants with MLL gene rearrangements registered in the Japan Infant Leukemia Study between 1996 and 1999 showed the event-free survival of patients with t(9;11) was not different from that of those with other 11q23 translocations. 16158826 2005
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 GeneticVariation disease BEFREE In previous studies, genotypes conferring lower NQO1 activity have been associated with an increased risk of acute leukemia, particularly infant leukemia carrying MLL/AF4 fusion genes. 15590400 2004
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 Biomarker disease BEFREE This report demonstrates that chromosomal insertion of MLL sequences is a rare but recurrent abnormality associated with infant leukemia. 12759932 2003
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
0.100 PosttranslationalModification disease BEFREE The role of the MLL gene in infant leukemia. 14704031 2003