Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4361
Gene Symbol: MRE11
MRE11
0.010 Biomarker disease BEFREE BRCA1 negativity was associated with decreased overall survival in sporadic GC (p = 0.002), and MRE11 negativity 31127894 2019
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
0.010 Biomarker disease BEFREE BRCA1 negativity was associated with decreased overall survival in sporadic GC (p = 0.002), and MRE11 negativity 31127894 2019
Entrez Id: 406991
Gene Symbol: MIR21
MIR21
0.010 AlteredExpression disease BEFREE Spasmolytic polypeptide-expressing metaplasia associated with higher expressions of miR-21, 155, and 223 can be regressed by Helicobacter pylori eradication in the gastric cancer familial relatives. 30990573 2019
Entrez Id: 7032
Gene Symbol: TFF2
TFF2
0.010 AlteredExpression disease BEFREE Spasmolytic polypeptide-expressing metaplasia associated with higher expressions of miR-21, 155, and 223 can be regressed by Helicobacter pylori eradication in the gastric cancer familial relatives. 30990573 2019
Entrez Id: 6765
Gene Symbol: ST8
ST8
0.010 Biomarker disease BEFREE A narrative review of PubMed/MEDLINE was performed, focusing on the health-related quality-of-life implications of surgery for hereditary breast and ovarian cancer, familial adenomatous polyposis and hereditary diffuse gastric cancer. 29341149 2018
Entrez Id: 1045
Gene Symbol: CDX2
CDX2
0.010 Biomarker disease BEFREE The absence of CDX2 in HDGC suggests that it may develop along a carcinogenetic pathway different from that of SDGC. 29307626 2018
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.010 GeneticVariation disease BEFREE Clinically defined HDGC families can harbor mutations in genes (ie, BRCA2) with different clinical ramifications from CDH1. 26182300 2015
Entrez Id: 11080
Gene Symbol: DNAJB4
DNAJB4
0.010 AlteredExpression disease BEFREE Increased expression of DNAJB4 leads to stabilization of WT Ecad in the plasma membrane, while it induces premature degradation of unfolded HDGC mutants in the proteasome. 24293545 2014
Entrez Id: 1500
Gene Symbol: CTNND1
CTNND1
0.010 Biomarker disease BEFREE Germline mutations in CTNNA1, CTNNB1, JUP, or CTNND1 are unlikely to play a major role in HDGC. 23071139 2012
Entrez Id: 3728
Gene Symbol: JUP
JUP
0.010 Biomarker disease BEFREE Germline mutations in CTNNA1, CTNNB1, JUP, or CTNND1 are unlikely to play a major role in HDGC. 23071139 2012
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
0.010 GeneticVariation disease BEFREE We examined replication error (RER) of six microsatellite markers and screened mutations of the 10-(A) repeat sequence in the transforming growth factor-beta receptor type II (TGF-betaRII) gene in individuals from seven unrelated FGC families. 11399952 2001
Entrez Id: 1828
Gene Symbol: DSG1
DSG1
0.010 Biomarker disease BEFREE Genes coding for DGI (DSG1) and HDGC (DSG2) have previously been assigned to human chromosome 18. 1601426 1992
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
0.020 AlteredExpression disease BEFREE Different CDH1 genotypes were associated with different intracellular signalling activation levels including different p-ERK, p-mTOR and β-catenin levels in early submucosal T1a lesions of HDGC families with different CDH1 variants. 30745422 2019
Entrez Id: 79728
Gene Symbol: PALB2
PALB2
0.020 Biomarker disease BEFREE From these studies, PALB2 has emerged as a new familial gastric cancer gene. 30507471 2018
Entrez Id: 79728
Gene Symbol: PALB2
PALB2
0.020 GeneticVariation disease BEFREE The results of this study suggest a role for the known cancer predisposition gene PALB2 in families with hereditary diffuse gastric cancer and no detected pathogenic CDH1 variants. 29706558 2018
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
0.020 GeneticVariation disease BEFREE Germline mutations in CTNNA1, CTNNB1, JUP, or CTNND1 are unlikely to play a major role in HDGC. 23071139 2012
Entrez Id: 51343
Gene Symbol: FZR1
FZR1
0.020 GeneticVariation disease BEFREE In the latter group, a syndrome which has been well characterised is hereditary diffuse gastric cancer; this is specifically associated with CDH1 (E-cadherin) germline mutations in about 30% of families. 17513507 2008
Entrez Id: 1829
Gene Symbol: DSG2
DSG2
0.020 GeneticVariation disease BEFREE In this study, we investigated whether alterations of Dsg2 are involved in gastric carcinogenesis and whether germline mutations contribute to a genetic predisposition in familial gastric cancer patients with no germline mutations in the E-cadherin gene. 16025435 2005
Entrez Id: 51343
Gene Symbol: FZR1
FZR1
0.020 GeneticVariation disease BEFREE Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families. 11729114 2001
Entrez Id: 1829
Gene Symbol: DSG2
DSG2
0.020 Biomarker disease BEFREE Genes coding for DGI (DSG1) and HDGC (DSG2) have previously been assigned to human chromosome 18. 1601426 1992
Entrez Id: 4360
Gene Symbol: MRC1
MRC1
0.030 GeneticVariation disease BEFREE Because of the low incidence, mutation analysis of MMR gene might be considered in MSI-H familial GC with diffuse type only. 23555086 2013
Entrez Id: 4360
Gene Symbol: MRC1
MRC1
0.030 GeneticVariation disease BEFREE It is well known that germ line mutations in the cis-element of tumor suppressor genes such as mismatch repair (MMR) genes, the adenomatous polyposis coli (APC) gene and the E-cadherin (CDH1) gene are involved in Lynch syndrome, familial adenomatous polyposis and hereditary diffuse gastric cancer, respectively. 21134075 2011
Entrez Id: 4360
Gene Symbol: MRC1
MRC1
0.030 GeneticVariation disease BEFREE Germline mutations and polymorphic variants in MMR, E-cadherin and MYH genes associated with familial gastric cancer in Jiangsu of China. 16929514 2006
Entrez Id: 4292
Gene Symbol: MLH1
MLH1
0.040 PosttranslationalModification disease BEFREE In MSI-H GC, MLH1 promoter methylation was slightly higher in sporadic GC than familial GC (50% versus 23.1%), while the frequency of MMR gene mutation was slightly higher in familial GC than in sporadic GC (15.4% versus 3.1%). 23555086 2013
Entrez Id: 4292
Gene Symbol: MLH1
MLH1
0.040 GeneticVariation disease BEFREE A new familial gastric cancer-related gene polymorphism: T1151A in the mismatch repair gene hMLH1. 20177793 2011