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TP53 and gastric cancer are reported together in 3 articles.

Gene

TP53

HGNC
HGNC:11998
219articles
219mentions
7variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
106articles
106mentions
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

3 records shown · first 60

STK11 and DNA Repair Gene Mutations Define Hereditary Subset of Middle Eastern Papillary Thyroid Cancer.

PMID 41898519 | PMCID PMC13026885 | DOI 10.3390/ijms27062656 · International journal of molecular sciences · 2026 · 16 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneTP53“Eleven patients (4.5%) harbored germline PVs/LPVs in cancer susceptibility genes including STK11, TP53, BRCA1, BRCA2, FANCA, SLX4, RAD50, MSH6, POLD1 and NF1.”0.98hgnc_dict_v1
phenotypegastric cancer“A TP53 hotspot mutation (p.R175H) was identified in a patient with a personal history of gastric cancer, a malignancy associated with Li-Fraumeni syndrome.”0.98phenotype_alias_lexicon_v2
geneSTK11“STK11 and DNA Repair Gene Mutations Define Hereditary Subset of Middle Eastern Papillary Thyroid Cancer.”0.98hgnc_dict_v1
geneBRCA1“Eleven patients (4.5%) harbored germline PVs/LPVs in cancer susceptibility genes including STK11, TP53, BRCA1, BRCA2, FANCA, SLX4, RAD50, MSH6, POLD1 and NF1.”0.98hgnc_dict_v1

P53-associated lncRNAs regulate immune functions and RNA-modifiers in gastric cancer.

PMID 39166030 | PMCID PMC11334848 | DOI 10.1016/j.heliyon.2024.e35228 · Heliyon · 2024 · 13 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneTP53“TP53, a guardian of the genome, suppresses or enhances tumors through various regulatory pathways.”0.98hgnc_dict_v1
phenotypegastric cancer“P53-associated lncRNAs regulate immune functions and RNA-modifiers in gastric cancer.”0.98phenotype_alias_lexicon_v2
geneZC3H13“Similarly, significant differences in immune function (APC_co_stimulation, CCR, and checkpoint) and m6A modification (FTO, ZC3H13, YTHDC1, and RBM15), and m5C modification (NOP2 and TET1) between both groups were also observed.”0.98hgnc_dict_v1
geneYTHDC1“Similarly, significant differences in immune function (APC_co_stimulation, CCR, and checkpoint) and m6A modification (FTO, ZC3H13, YTHDC1, and RBM15), and m5C modification (NOP2 and TET1) between both groups were also observed.”0.98hgnc_dict_v1

Li-Fraumeni Syndrome with Unusual Synchronous Malignancies: A Case Report.

PMID 38188481 | PMCID PMC10769503 | DOI 10.1159/000535099 · Case reports in oncology · 2024 · 3 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneTP53“INTRODUCTION: Li-Fraumeni syndrome (LFS) is a rare autosomal dominant disorder brought on by pathogenic mutations in the TP53 tumor suppressor gene.”0.98hgnc_dict_v1
phenotypegastric cancer“CONCLUSION: Gastric cancer and neuroendocrine tumors are not usually associated with LFS.”0.98phenotype_alias_lexicon_v2
phenotypeleukemia“CASE PRESENTATION: We are presenting a 48-year-old male with a diagnosis of LFS that was confirmed by a genetic test triggered by the patient's son's diagnosis of LFS and leukemia.”0.98phenotype_alias_lexicon_v2