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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

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FOXO1 and lymphoma are reported together in 1 article.

Gene

FOXO1

HGNC
HGNC:3819
32articles
32mentions
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

1 records shown · first 60

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
TypeEntitySource evidenceConfidenceExtractor
geneFOXO1“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.”0.98hgnc_dict_v1
phenotypelymphoma“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.”0.98phenotype_alias_lexicon_v2
geneBCL6“These genetic mutations are involved in epigenetic modification, ability to escape immunosurveillance, impaired BCL6 and NF-κβ signaling pathways and blocking terminal differentiation.”0.98hgnc_dict_v1
geneMYC“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.”0.98hgnc_dict_v1