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: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 Biomarker disease BEFREE Rearrangements of the human trithorax gene (MLL, HRX, Htrx-1, All-1) were studied by Southern blotting in blast cells stored at presentation from 65 adults with de novo acute myelomonocytic (AML-M4) and acute monocytic leukemia (AML-M5). 7949133 1994
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE A case of acute monocytic leukemia with t(11;17) involving a rearrangement of MLL-1 and a region proximal to the RARA gene. 8194047 1994
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 Biomarker disease CTD_human Molecular rearrangements of the MLL gene are present in most cases of infant acute myeloid leukemia and are strongly correlated with monocytic or myelomonocytic phenotypes. 8282816 1994
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE In the present study, we isolated chimeric cDNAs between the MLL and a gene designated MLLT3 at 9p22 from a cDNA library of an IMS-M1 cell line with a t(9;11)(p22;q23) translocation, a representative karyotypic abnormality seen in acute monocytic leukemia. 8414510 1993
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE In this study, 29 cases of adult acute myeloid leukemia (AML) were analyzed to determine the frequency of MLL gene rearrangement. 8616778 1996
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Of 16 acute myeloid leukemia patients with trisomy 11 and rearrangement of MLL reported, our patient was the youngest in age and the only one with AMoL. 9209466 1997
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Two acute monocytic leukemia (AML-M5a) cell lines (MOLM-13 and MOLM-14) with interclonal phenotypic heterogeneity showing MLL-AF9 fusion resulting from an occult chromosome insertion, ins(11;9)(q23;p22p23). 9305600 1997
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Progression from myelodysplastic syndrome with monosomy 7 to acute monoblastic leukemia with MLL gene rearrangement. 9594441 1998
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE The mixed lineage leukemia (MLL) gene located at chromosome band 11q23 is frequently rearranged in patients with therapy-related acute monocytic leukemia who received topoisomerase II inhibitors. 10648423 2000
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Analysis of MLL-derived transcripts in infant acute monocytic leukemia with a complex translocation (1;11;4)(q21;q23;p16). 10700861 2000
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Molecular analysis of the rearranged genome and chimeric mRNAs caused by the t(6;11)(q27;q23) chromosome translocation involving MLL in an infant acute monocytic leukemia. 10719372 2000
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AML. 10803509 2000
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Following the development of therapy-related leukemia after 1 year, evolution of therapy-related AML-M4 with t(11;17)(q23;q25) and the rearrangement of the MLL gene were observed, while AML/MTG8 disappeared. 10905055 2000
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Cytogenetic and molecular analysis of the acute monocytic leukemia cell line THP-1 with an MLL-AF9 translocation. 11066077 2000
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE We analyzed one patient with de novo acute monoblastic leukemia with t(11;14)(q23;q24) and identified that a human homologue of gephyrin (human gephyrin) fused with MLL. 11289145 2001
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 Biomarker disease BEFREE These genetic subgroups seem to display biological heterogeneity: MLL copy gain or amplification in association with 5q- was detected only in AML patients and was significantly associated with extremely short survival (median overall survival: 30 days, P = 0.0102). 11746988 2002
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Combined present results and literatures suggest that AML with the MLL-SEPTIN6 fusion gene is a subset of infant AML, which differentiate into the myeloid lineage, although AML with other MLL fusion genes is capable of differentiating into the myelomonocytic or monocytic lineage. 11809673 2002
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 Biomarker disease BEFREE MLLT10 (previously called AF10) is a moderately common MLL fusion partner predominantly occurring in acute monoblastic leukemia (AML-M5). 11896537 2002
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Fluorescence in situ hybridization (FISH) analysis in a case of infant acute monocytic leukemia M5 revealed a complex rearrangement between chromosomes 10 and 11, leading to the disruption of the MLL gene. 12127405 2002
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE We report a case of secondary acute myelogenous leukemia (AML) with 11q23 cytogenetic abnormality and mixed lymphoid leukemia (MLL) gene expression in a patient treated with Y90 labeled anti-CD20 antibody (Zevalin). 12539741 2002
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Is t(10;11)(p11.2;q23) involving MLL and ABI-1 genes associated with congenital acute monocytic leukemia? 12547160 2002
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 Biomarker disease LHGDN Is t(10;11)(p11.2;q23) involving MLL and ABI-1 genes associated with congenital acute monocytic leukemia? 12547160 2002
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: almost identical MLL breakpoints in therapy-related AML after treatment without etoposides. 12619163 2003
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 Biomarker disease BEFREE FLT3 and MLL intragenic abnormalities in AML reflect a common category of genotoxic stress. 12791658 2003
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 Biomarker disease BEFREE AML with 11q23/MLL abnormalities as defined by the WHO classification: incidence, partner chromosomes, FAB subtype, age distribution, and prognostic impact in an unselected series of 1897 cytogenetically analyzed AML cases. 12805060 2003