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BCL6 and lymphoma are reported together in 6 articles.
Gene
BCL6
- HGNC
- HGNC:1001
8articles
8mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Lymphoma
428articles
428mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
6 records shown · first 60Rare aggressive presentation of primary cutaneous diffuse large B-Cell lymphoma, leg type, in the upper arm with concurrent non-small cell lung cancer.
PMID 40449942 | DOI 10.1136/bcr-2024-264401 · BMJ case reports · 2025 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | BCL6 | “Histopathological analysis revealed dense dermal lymphoid infiltrate with a non-germinal centre phenotype (CD20+, MUM1+, BCL2+, BCL6+, CD10-).” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “Rare aggressive presentation of primary cutaneous diffuse large B-Cell lymphoma, leg type, in the upper arm with concurrent non-small cell lung cancer.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | BCL2 | “Histopathological analysis revealed dense dermal lymphoid infiltrate with a non-germinal centre phenotype (CD20+, MUM1+, BCL2+, BCL6+, CD10-).” | 0.98 | hgnc_dict_v1 |
| phenotype | lung cancer | “Rare aggressive presentation of primary cutaneous diffuse large B-Cell lymphoma, leg type, in the upper arm with concurrent non-small cell lung cancer.” | 0.98 | phenotype_alias_lexicon_v2 |
Molecular carcinogenesis in Hodgkin lymphoma: Interplay between B lymphocyte mutations and NF-κB pathway dysregulation.
PMID 40738056 | DOI 10.1016/j.prp.2025.156145 · Pathology, research and practice · 2025 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | BCL6 | “Particular focus is drawn to genetic mutations concerning Epstein-Barr virus (EBV)-related proteins, such as BCL6 and CREBBP, which are reported to cause disruptions in normal B cell formation and support aberrant cell growth.” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “Molecular carcinogenesis in Hodgkin lymphoma: Interplay between B lymphocyte mutations and NF-κB pathway dysregulation.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | CREBBP | “Particular focus is drawn to genetic mutations concerning Epstein-Barr virus (EBV)-related proteins, such as BCL6 and CREBBP, which are reported to cause disruptions in normal B cell formation and support aberrant cell growth.” | 0.98 | hgnc_dict_v1 |
Molecular complexity of diffuse large B-cell lymphoma: a molecular perspective and therapeutic implications.
PMID 38001281 | DOI 10.1007/s13353-023-00804-5 · Journal of applied genetics · 2024 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | BCL6 | “Genetic investigations, led by high-throughput sequencing, have unveiled recurrent mutations in genes such as MYC, BCL2, and BCL6, casting light on the underlying genetic chaos propelling DLBCL's aggressiveness.” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “Molecular complexity of diffuse large B-cell lymphoma: a molecular perspective and therapeutic implications.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | MYC | “Genetic investigations, led by high-throughput sequencing, have unveiled recurrent mutations in genes such as MYC, BCL2, and BCL6, casting light on the underlying genetic chaos propelling DLBCL's aggressiveness.” | 0.98 | hgnc_dict_v1 |
| gene | BCL2 | “Genetic investigations, led by high-throughput sequencing, have unveiled recurrent mutations in genes such as MYC, BCL2, and BCL6, casting light on the underlying genetic chaos propelling DLBCL's aggressiveness.” | 0.98 | hgnc_dict_v1 |
Dysregulation of miRNAs in DLBCL: Causative Factor for Pathogenesis, Diagnosis and Prognosis.
PMID 34679437 | PMCID PMC8535125 | DOI 10.3390/diagnostics11101739 · Diagnostics (Basel, Switzerland) · 2021 · 7 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | BCL6 | “These genetic mutations are involved in epigenetic modification, ability to escape immunosurveillance, impaired BCL6 and NF-κβ signaling pathways and blocking terminal differentiation.” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “Diffuse large B-cell lymphoma (DLBCL) is an aggressive non-Hodgkin's lymphoma (NHL), arising from different stages of B-cell differentiation whose pathogenesis involves miRNAs.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | MYC | “Recently miRNAs were also identified to act either as oncogenes or tumor suppressors in DLBCL pathology by altering the expression levels of some of the known DLBCL related oncogenes. i.e., miR-155, miR-17-92 and miR-21 act as oncogenes by altering the expression levels of MYC, SHIP and FOXO1, respectively, conversely; miR-34a, mir-144 and miR-181a act as tumor suppressors by altering the expression levels of SIRT1, BCL6 and CARD11, respectively.” | 0.98 | hgnc_dict_v1 |
| gene | FOXO1 | “Recently miRNAs were also identified to act either as oncogenes or tumor suppressors in DLBCL pathology by altering the expression levels of some of the known DLBCL related oncogenes. i.e., miR-155, miR-17-92 and miR-21 act as oncogenes by altering the expression levels of MYC, SHIP and FOXO1, respectively, conversely; miR-34a, mir-144 and miR-181a act as tumor suppressors by altering the expression levels of SIRT1, BCL6 and CARD11, respectively.” | 0.98 | hgnc_dict_v1 |
Comprehensive Genomic Analysis of Noonan Syndrome and Acute Myeloid Leukemia in Adults: A Review and Future Directions.
PMID 32541138 | DOI 10.1159/000505715 · Acta haematologica · 2020 · 7 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | BCL6 | “Here, we describe a young adult patient with a novel combined germline PTPN11 and somatic NPM1, IDH1,and BCL6 mutations who presented with fatal AML.” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “While mutations in the transcriptional repressor BCL6 are known to contribute to the pathogenesis of diffuse large B cell lymphoma (DLBCL) and chronic lymphocytic leukemia (CLL), its novel identification in this patient suggests an expanded role in aggressive AML.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | PTPN11 | “Germline mutations in PTPN11 are the most common cause of NS.” | 0.98 | hgnc_dict_v1 |
| gene | NPM1 | “Somatic mutations in NPM1 occur frequently in AML.” | 0.98 | hgnc_dict_v1 |
COO and MYC/BCL2 status do not predict outcome among patients with stage I/II DLBCL: a retrospective multicenter study.
PMID 31285189 | PMCID PMC6616265 | DOI 10.1182/bloodadvances.2019000251 · Blood advances · 2019 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | BCL6 | “In advanced-stage diffuse large B-cell lymphoma (DLBCL), the presence of an activated B-cell phenotype or a non-germinal center (GCB) phenotype, coexpression of MYC and BCL2 by immunohistochemistry, and the cooccurrence of MYC and BCL2 or BCL6 rearrangements are associated with inferior outcomes.” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “In advanced-stage diffuse large B-cell lymphoma (DLBCL), the presence of an activated B-cell phenotype or a non-germinal center (GCB) phenotype, coexpression of MYC and BCL2 by immunohistochemistry, and the cooccurrence of MYC and BCL2 or BCL6 rearrangements are associated with inferior outcomes.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | BCL2 | “COO and MYC/BCL2 status do not predict outcome among patients with stage I/II DLBCL: a retrospective multicenter study.” | 0.98 | hgnc_dict_v1 |