TCF3, transcription factor 3, 6929

N. diseases: 244; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
0.600 Biomarker disease GENOMICS_ENGLAND Epistatic interactions between mutations of TACI (TNFRSF13B) and TCF3 result in a severe primary immunodeficiency disorder and systemic lupus erythematosus. 29114388 2017
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
0.600 Biomarker disease CTD_human
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
0.600 Biomarker disease HPO
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 Biomarker disease BEFREE Strikingly, we did not detect recurrent mutations in genes of the ID3-TCF3 axis or the SWI/SNF complex that are frequently altered in BL, or in genes frequently mutated in germinal center-derived B-cell lymphomas like <i>KMT2D</i> or <i>CREBBP</i> An exception is <i>GNA13</i>, which was mutated in 7 of 15 cases. 30567752 2019
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 Biomarker disease BEFREE A total of four TFs (E2F1, NFKB1, E2F4 and TCF3) exhibit complicated regulation associations in BL-associated networks. 30127896 2018
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 Biomarker disease BEFREE In conclusion, <i>ID3-TCF3-CCND3</i> pathway genes are mutated in more than 88% of <i>MYC</i>-rearranged pediatric B-cell non-Hodgkin lymphoma and the pathway may represent a highly relevant second hit of Burkitt lymphoma pathogenesis, especially in children and adolescents. 28209658 2017
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 AlteredExpression disease BEFREE Since no definitive data are available on the genetic landscape of endemic Burkitt (eBL), we first assessed the mutation frequency of TCF3/ID3 in eBL compared with sBL and subsequently the somatic hypermutation status of the BCR to answer whether an extrinsic activation of BCR signaling could also be demonstrated in Burkitt lymphoma. 26712879 2016
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 Biomarker disease BEFREE TCF-3 promotes antigen-independent (tonic) B-cell-receptor signaling in Burkitt lymphoma by transactivating immunoglobulin heavy- and light-chain genes while repressing PTPN6, which encodes the phosphatase SHP-1, a negative regulator of B-cell-receptor signaling. 24492847 2014
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 AlteredExpression disease BEFREE In particular, mutations in the transcription factors ID3 and TCF3, leading to overexpression of B-cell receptor components such as VPREB3, have been shown to be specific for Burkitt lymphoma (BL) and play an important tumourigenic role by mediating the activation of the pro-survival phosphatidylinositol-3-OH kinase pathway. 24493312 2014
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 GeneticVariation disease BEFREE Two studies in this issue identify the landscape of somatic mutations in Burkitt lymphoma and highlight the pathogenic and clinical relevance of inactivating mutations of ID3, an inhibitor of the TCF3 transcription factor. 23192177 2012
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 AlteredExpression disease BEFREE TCF3 activated the pro-survival phosphatidylinositol-3-OH kinase pathway in BL, in part by augmenting tonic B-cell receptor signalling. 22885699 2012
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 Biomarker disease CTD_human B-cell development fails in the absence of the Pbx1 proto-oncogene. 17244677 2007
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 Biomarker disease CTD_human Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. 1967982 1990
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
0.580 FusionGene disease ORPHANET
Childhood Acute Lymphoblastic Leukemia
0.400 GeneticVariation disease BEFREE The <i>ERG</i> risk genotype was underrepresented in ALL with the <i>ETV6-RUNX1</i> fusion (<i>P</i> < .0005) but enriched in the <i>TCF3-PBX1</i> subtype (<i>P</i> < .05). 30510082 2019
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.400 GeneticVariation disease BEFREE t(17;19)(q21-q22;p13), responsible for TCF3-HLF fusion, is a rare translocation in childhood B-cell precursor acute lymphoblastic leukemia(BCP-ALL). t(1;19)(q23;p13), producing TCF3-PBX1 fusion, is a common translocation in childhood BCP-ALL. 31305009 2019
Childhood Acute Lymphoblastic Leukemia
0.400 Biomarker disease BEFREE To determine whether methylation differences between mostly fatal TCF3-HLF and curable TCF3-PBX1 pediatric acute lymphoblastic leukemia subtypes can be associated with differential gene expression and remission. 29334255 2018
Childhood Acute Lymphoblastic Leukemia
0.400 GeneticVariation disease BEFREE Pediatric acute lymphoblastic leukemia with t(1;19)/TCF3-PBX1 in Taiwan. 28436581 2017
AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT
0.400 Biomarker disease GENOMICS_ENGLAND Epistatic interactions between mutations of TACI (TNFRSF13B) and TCF3 result in a severe primary immunodeficiency disorder and systemic lupus erythematosus. 29114388 2017
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.400 AlteredExpression disease BEFREE We reviewed the roles of miRNA here with emphasis on their function in human leukemia and the mechanisms of the TEL/AML1, BCR/ABL, MLL/AF4 and TCF3/PBX1 oncoproteins on miRNAs expression in acute lymphoblastic leukemia. 27431573 2016
Childhood Acute Lymphoblastic Leukemia
0.400 Biomarker disease BEFREE Drug response profiling of matched patient-derived xenografts revealed a distinct profile for TCF3-HLF ALL with resistance to conventional chemotherapeutics but sensitivity to glucocorticoids, anthracyclines and agents in clinical development. 26214592 2015
Childhood Acute Lymphoblastic Leukemia
0.400 Biomarker disease CTD_human Drug response profiling of matched patient-derived xenografts revealed a distinct profile for TCF3-HLF ALL with resistance to conventional chemotherapeutics but sensitivity to glucocorticoids, anthracyclines and agents in clinical development. 26214592 2015
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.400 GeneticVariation disease BEFREE Clinical features and prognostic significance of TCF3-PBX1 fusion gene in Chinese children with acute lymphoblastic leukemia by using a modified ALL-BFM-95 protocol. 25551271 2015
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.400 Biomarker disease BEFREE Investigation for TCF3(E2A)-PBX1 rearrangements may be useful in BCL6-positive B-lymphoblastic leukemia. 25780007 2015
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.400 Biomarker disease CTD_human Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options. 26214592 2015