Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.080 GeneticVariation disease BEFREE Identification of a Cryptic Insertion ins(11;X)(q23;q28q12) Resulting in a KMT2A-FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic Leukemia. 28253492 2016
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.080 GeneticVariation disease BEFREE Southern blot analysis did not reveal any abnormality of ATM, nor of MLL, which is also located on 11q23 and is involved in t(1;11)(q21;q23) in acute myelomonocytic leukemia. 14499692 2003
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.080 GeneticVariation disease BEFREE Fusion of MLL and MSF in adult de novo acute myelomonocytic leukemia (M4) with t(11;17)(q23;q25). 12095151 2002
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.080 GeneticVariation disease BEFREE We report amplification of the MLL gene region (11q23-->11qter) in a 72-year-old woman with myelodysplastic syndrome progressing to acute myelomonocytic leukemia and in a 51-year-old man with a history of hairy cell leukemia and secondary myelodysplasia progressing to acute myelogenous leukemia. 11063808 2000
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.080 GeneticVariation disease BEFREE He achieved complete remission, but developed acute myelomonocytic leukemia (AML, FAB M4) with t(9;11)(p22;q23) in March 1997 and a rearrangement of the MLL gene was also recognized. 9846019 1998
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.080 GeneticVariation disease BEFREE We have characterized two t(1;11)(q21;q23) translocations that fuse the MLL gene to a novel gene, AF1q on chromosomal band 1q21, in two infants with acute myelomonocytic leukemia (AMMOL). 7833468 1995
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.080 Biomarker disease BEFREE Acute myelomonocytic leukemia after treatment with chronic oral etoposide: are MLL and LTG9 genes targets for etoposide? 7948964 1994
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.080 GeneticVariation disease BEFREE We describe a case of acute myelomonocytic leukemia (AMML; FAB type M4) with t(10;11)(p13;q23) in which the breakpoint at 11q23 was centromeric to the MLL gene and distinct from the breakpoint seen in promyelocytic leukemias with t(11;17)(q23;q22), thus providing further evidence of heterogeneity of breakpoints in 11q23 in acute leukemia. 7529550 1994