ATM, ATM serine/threonine kinase, 472

N. diseases: 684; N. variants: 974
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease BEFREE Inhibition of novel GCN5-ATM axis restricts the onset of acquired drug resistance in leukemia. 29297932 2018
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease RGD A rat model of ataxia-telangiectasia: evidence for a neurodegenerative phenotype. 28007901 2017
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease GENOMICS_ENGLAND Germline Genetic Predisposition to Hematologic Malignancy. 28297620 2017
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease BEFREE Collectively, these data indicated that ATR or ATM inhibition represent potential therapeutic strategies for the treatment of AML, especially MLL-driven leukemias. 27625305 2016
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE Both A-T and T-cell prolymphoblastic leukemia patients with somatic mutations of ATM frequently carry inv(14;14) between the T-cell receptor α/δ (TCRα/δ) and immunoglobulin H loci, but the molecular origin of this translocation remains elusive. 25721125 2015
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE Biallelic inactivation of the ATM gene causes ataxia-telangiectasia (A-T), a complex neurological disease associated with a high risk of leukaemias and lymphomas. 19404735 2010
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE The mutations in the ATM gene may be involved in the development of some subtypes of sporadic lymphomas and leukemias. 17516749 2007
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE We show that the residual ATM allele is mutated in 36% of CLLs with an 11q deletion and that these leukemias demonstrate an impaired cellular response to irradiation or cytotoxic drug exposure in vitro. 17968022 2007
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease LHGDN Promyelocytic leukemia nuclear bodies behave as DNA damage sensors whose response to DNA double-strand breaks is regulated by NBS1 and the kinases ATM, Chk2, and ATR. 17030982 2006
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE ATM mutations have been reported in adult sporadic lymphoma and leukaemia. 14735203 2004
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE Inherited biallelic mutations of the ATM (ataxia-telangiectasia mutated) gene cause ataxia-telangiectasia, a rare autosomal recessive disorder associated with a high incidence of childhood leukaemias and lymphomas, suggesting that ATM gene alterations may be involved in lymphomagenesis. 14628072 2004
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease BEFREE Our finding in this patient suggests that altered function of ATM plays some pathogenic roles in the development of MLL(+) leukemia. 12511424 2003
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease LHGDN Our finding in this patient suggests that altered function of ATM plays some pathogenic roles in the development of MLL(+) leukemia. 12511424 2003
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE This, coupled with a possibly increased risk of leukaemia in relatives of patients with Ataxia Telangiectasia, led us to question whether the ATM gene is involved in familial cases of CLL. 10516748 1999
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE A role for ATM in the development of sporadic T-cell chronic leukemias is supported by the finding of loss of heterozygosity at 11q22-23 and ATM mutations in leukemias carrying TCL-1 rearrangements. 9892178 1999
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE T-prolymphocytic leukaemia (T-PLL) is a rare, sporadic leukaemia similar to a mature T-cell leukaemia seen in some patients with Ataxia Telangiectasia (A-T), a recessive multisystem disorder caused by mutations of the ATM gene at chromosome 11q23. 9488043 1998
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease BEFREE The absence of somatic nucleotide changes in ATM in T-ALL as compared with T-PLL suggests a distinct pattern of genetic events in the development of the two leukemias. 9622061 1998
CUI: C0023418
Disease: leukemia
leukemia
0.900 GeneticVariation disease BEFREE ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer. 9463314 1998
CUI: C0023418
Disease: leukemia
leukemia
0.900 CausalMutation disease CGI
CUI: C0023418
Disease: leukemia
leukemia
0.900 Biomarker disease HPO
CUI: C0023418
Disease: leukemia
leukemia
0.900 GenomicAlterations disease CGI