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 GeneticVariation disease BEFREE Among them, the translocation t(9;11)(p22;q23), KMT2A-MLLT3, is the most common abnormality accounting for approximately 22% of KMT2A rearrangements in infant AML cases. 28595195 2017
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE This case report helps to better understand the rare but potentially severe impact of KMT2A- FLNA fusions in infants with AML to improve prognostic stratification of therapy and clinical management. 28253492 2016
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Translocations involving the mixed lineage leukemia (MLL) gene, localized at 11q23, frequently occur in pediatric acute myeloid leukemia (AML). 20861917 2010
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 Rearrangement of MLL in a patient with congenital acute monoblastic leukemia and granulocytic sarcoma associated with a t(1;11)(p36;q23) translocation. 15621793 2005
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 Gene expression profiles of t(8;16)(p11;p13) pediatric AML cases clustered close to, but distinct from, MLL-rearranged AML. 23974201 2013
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 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 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 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 GeneticVariation disease BEFREE Here, we report a second case--an infant acute monocytic leukemia (AML M5b)--with an MLL/GRAF fusion. 15382263 2004
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 The coexpression of the MLL partial tandem duplication (PTD) and the FLT3 internal tandem duplication (ITD) mutations associate with a poor outcome in cytogenetically normal acute myeloid leukemia (AML). 24085765 2013
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 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: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Rearrangements of the MLL (11q23) gene in AML are usually related to the morphological phenotype FAB M5. 16044313 2005
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Karyotyping detected abnormal chromosome 11 only in 4/43 patients and Classical t(4:11) in one AML patient but combination of Painting FISH and LS-FISH confirmed ALL-1 gene alteration in 17/18 cases. 12860012 2003
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE AML with chromosomal translocations involving the mixed lineage leukemia (MLL) gene are usually associated with poor survival. 23798388 2013
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 GeneticVariation disease BEFREE We have identified a new mixed lineage leukemia (MLL) gene fusion partner in a patient with treatment-related acute myeloid leukemia (AML) presenting a t(2;11)(q37;q23) as the only cytogenetic abnormality. 16682951 2006
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Both patients with IDH1 mutations had AML-M0 subtype and MLL-partial tandem duplication. 23365461 2013
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.400 GeneticVariation disease BEFREE Translocations involving the mixed-lineage leukemia (MLL) gene, localized at 11q23, comprise 15 to 20% of all pediatric acute myeloid leukemia (AML) cases. 21566656 2011
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 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 Analysis of MLL-derived transcripts in infant acute monocytic leukemia with a complex translocation (1;11;4)(q21;q23;p16). 10700861 2000