MUC1, mucin 1, cell surface associated, 4582

N. diseases: 594; N. variants: 18
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease BEFREE Our results confirm an association between gastric cancer in Europeans and three loci previously reported in Asians, MUC1, PRKAA1 and PSCA, refine the association signal at PRKAA1 and support a pathogenic role for the tandem repeat identified in MUC1. 26098866 2015
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease BEFREE Associations of genetic variants in the PSCA, MUC1 and PLCE1 genes with stomach cancer susceptibility in a Chinese population. 25658482 2015
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease BEFREE We also confirmed a previously reported association for rs4072037 in MUC1 with p=6.59×10(-8) for total gastric cancer and similar estimates for cardia and non-cardia cancers. 26129866 2016
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease GWASCAT Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours. 26129866 2016
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease BEFREE Those subjects with both the risk alleles MUC1 rs9841504 and ZBTB20 rs4072037 had a greater than 3-fold increased risk of gastric cancer. 27127881 2016
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease BEFREE In summary, these results suggest that the MUC1 rs4072037G allele may be a low-penetrating protection factor for GCa risk in Chinese populations. 26910281 2016
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease BEFREE However, subtype-specific associations were observed for gastric cardia adenocarcinomas at MUC1/TRIM46/1q22 rs2070803 [HRAA versus GA+GG = 2.16; 95% confidence interval (CI) = 1.24-3.78; P = 0.0068] and LTA/TNF/6p21.33 rs1799724 (HRTT+CT versus CC = 1.30; 95% CI = 1.07-1.57; P = 0.0077), and for diffuse-type GC at PSCA/8q24.3 rs2294008 (HRTT versus CT+CC = 1.99; 95% CI = 1.33-2.97; P = 7.8E-04). 29028942 2017
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease BEFREE In conclusion, this meta-analysis suggested that rs4245739 polymorphism in the MUC1 gene may play a pivotal role in the pathogenesis of GC, especially for white populations. 28561882 2017
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease GWASCAT Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies. 26701879 2017
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 Biomarker disease BEFREE The surface marker expression suggested a tumor origin of the cells, and indicated the intestinal phenotype of a GC (CD10<sup>+</sup>, MUC1). 29552124 2018
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.200 GeneticVariation disease BEFREE Our study confirms the protective effect of MUC1 rs4072037 polymorphism on the risk of GC under the dominant model. 28489708 2018