Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 GeneticVariation disease BEFREE PSCA rs2294008 C-allele was associated with per allele OR of 1.34 (95% CI, 1.18-1.51; P=2.28×10<sup>-6</sup>) for the risk of DU. 31839644 2019
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 GeneticVariation disease BEFREE Recently, three genome-wide association studies have identified the PSCA (prostate stem cell antigen) rs2294008 polymorphism (C > T) associated with susceptibility to gastric cancer, bladder cancer, and duodenal ulcers, highlighting its critical role in disease pathogenesis. 27001215 2016
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 GeneticVariation disease BEFREE Frequency of PSCA rs2294008 C/C genotype in duodenal ulcer was 36.1%, which was significantly higher than those with gastric cancer (12.4%), gastric ulcer (19.0%), gastritis (10.7%), and H. pylori-negatives (19.5%) (p < .001). 25582162 2015
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 GeneticVariation disease BEFREE From these results we conclude that the PSCA rs2294008 polymorphism is involved in the susceptibility to GC and DU, as well as in the prognosis of the diffuse-type of GC in Caucasians. 25721731 2015
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 GeneticVariation disease BEFREE Recently we conducted the genome wide association study for duodenal ulcer and identified disease susceptibility variations at two genetic loci corresponding to the Prostate stem cell antigen (PSCA) gene and the ABO blood group (ABO) gene. 23704932 2013
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 GeneticVariation disease GWASDB The C allele of rs2294008 at PSCA was associated with increased risk of duodenal ulcer (odds ratio (OR) = 1.84; P = 3.92 × 10(-33)) in a recessive model but was associated with decreased risk of gastric cancer (OR = 0.79; P = 6.79 × 10(-12)), as reported previously. 22387998 2012
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 Biomarker disease CTD_human The C allele of rs2294008 at PSCA was associated with increased risk of duodenal ulcer (odds ratio (OR) = 1.84; P = 3.92 × 10(-33)) in a recessive model but was associated with decreased risk of gastric cancer (OR = 0.79; P = 6.79 × 10(-12)), as reported previously. 22387998 2012
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 GeneticVariation disease BEFREE The C allele of rs2294008 at PSCA was associated with increased risk of duodenal ulcer (odds ratio (OR) = 1.84; P = 3.92 × 10(-33)) in a recessive model but was associated with decreased risk of gastric cancer (OR = 0.79; P = 6.79 × 10(-12)), as reported previously. 22387998 2012
Entrez Id: 8000
Gene Symbol: PSCA
PSCA
0.460 GeneticVariation disease GWASCAT The C allele of rs2294008 at PSCA was associated with increased risk of duodenal ulcer (odds ratio (OR) = 1.84; P = 3.92 × 10(-33)) in a recessive model but was associated with decreased risk of gastric cancer (OR = 0.79; P = 6.79 × 10(-12)), as reported previously. 22387998 2012
Entrez Id: 28
Gene Symbol: ABO
ABO
0.430 GeneticVariation disease BEFREE Recently we conducted the genome wide association study for duodenal ulcer and identified disease susceptibility variations at two genetic loci corresponding to the Prostate stem cell antigen (PSCA) gene and the ABO blood group (ABO) gene. 23704932 2013
Entrez Id: 28
Gene Symbol: ABO
ABO
0.430 Biomarker disease CTD_human The T allele of rs2294008 encodes a translation initiation codon upstream of the reported site and changes protein localization from the cytoplasm to the cell surface. rs505922 at ABO was also associated with duodenal ulcer in a recessive model (OR = 1.32; P = 1.15 × 10(-10)). 22387998 2012
Entrez Id: 28
Gene Symbol: ABO
ABO
0.430 GeneticVariation disease GWASCAT The T allele of rs2294008 encodes a translation initiation codon upstream of the reported site and changes protein localization from the cytoplasm to the cell surface. rs505922 at ABO was also associated with duodenal ulcer in a recessive model (OR = 1.32; P = 1.15 × 10(-10)). 22387998 2012
Entrez Id: 28
Gene Symbol: ABO
ABO
0.430 GeneticVariation disease GWASDB The T allele of rs2294008 encodes a translation initiation codon upstream of the reported site and changes protein localization from the cytoplasm to the cell surface. rs505922 at ABO was also associated with duodenal ulcer in a recessive model (OR = 1.32; P = 1.15 × 10(-10)). 22387998 2012
Entrez Id: 28
Gene Symbol: ABO
ABO
0.430 GeneticVariation disease BEFREE The T allele of rs2294008 encodes a translation initiation codon upstream of the reported site and changes protein localization from the cytoplasm to the cell surface. rs505922 at ABO was also associated with duodenal ulcer in a recessive model (OR = 1.32; P = 1.15 × 10(-10)). 22387998 2012
Entrez Id: 28
Gene Symbol: ABO
ABO
0.430 Biomarker disease BEFREE Hereditary aspects of duodenal ulceration: pepsin 1 secretion in relation to ABO blood groups and ABH secretor status. 119857 1979
Entrez Id: 5321
Gene Symbol: PLA2G4A
PLA2G4A
0.410 GeneticVariation disease BEFREE Bleeding diathesis and gastro-duodenal ulcers in inherited cytosolic phospholipase-A2 alpha deficiency. 25102815 2014
Entrez Id: 5321
Gene Symbol: PLA2G4A
PLA2G4A
0.410 Biomarker disease CTD_human Inherited human cPLA(2alpha) deficiency is associated with impaired eicosanoid biosynthesis, small intestinal ulceration, and platelet dysfunction. 18451993 2008
Entrez Id: 5321
Gene Symbol: PLA2G4A
PLA2G4A
0.410 Biomarker disease HPO
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
0.320 GeneticVariation disease BEFREE A significant difference (P = 0.04) in the distribution of rare haplotypes of the TGF-beta1 gene between patients with duodenal ulcer and healthy controls has been found. 17376051 2007
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
0.320 GeneticVariation disease BEFREE Our results show that the TGFB1 T+869C gene polymorphism is involved in the susceptibility to DU and provide further evidence that host genetic factors play a key role in the pathogenesis of H. pylori-related diseases. 16971953 2006
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
0.320 GeneticVariation disease LHGDN Our results show that the TGFB1 T+869C gene polymorphism is involved in the susceptibility to DU and provide further evidence that host genetic factors play a key role in the pathogenesis of H. pylori-related diseases. 16971953 2006
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
0.320 Therapeutic disease CTD_human Effect of exogenous administration of transforming growth factor-beta and famotidine on the healing of duodenal ulcer under the impact of indomethacin. 12868675 2003
Entrez Id: 4843
Gene Symbol: NOS2
NOS2
0.300 Biomarker disease CTD_human Role of endogenous nitric oxide (NO) and NO synthases in healing of indomethacin-induced intestinal ulcers in rats. 17045617 2007
Entrez Id: 5743
Gene Symbol: PTGS2
PTGS2
0.300 Biomarker disease CTD_human Healing of duodenal ulcers is not impaired by indomethacin or rofecoxib, the selective COX-2 inhibitor, in rats. 12481160 2002
Entrez Id: 4843
Gene Symbol: NOS2
NOS2
0.300 Biomarker disease CTD_human We investigated the effects of COX and NOS inhibitors on the healing of duodenal ulcers, in comparison with gastric ulcers, in rats. 12481160 2002