Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 GeneticVariation disease BEFREE Stomach cancer-derived del223V-226L mutation of the STCH gene causes loss of sensitization to TRAIL-mediated apoptosis. 18793616 2008
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 GeneticVariation disease BEFREE Stomach cancer-derived del223V-226L mutation of the STCH gene causes loss of sensitization to TRAIL-mediated apoptosis. 18793616 2008
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 Biomarker disease BEFREE We found a significant association of five SNPs in the stress70 protein chaperon family member STCH gene with gastric cancer, especially with the non-cardia localization subgroup (P=0.0005-0.02, odds ratio=1.44-1.72). 16087163 2005
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 Biomarker disease BEFREE We found a significant association of five SNPs in the stress70 protein chaperon family member STCH gene with gastric cancer, especially with the non-cardia localization subgroup (P=0.0005-0.02, odds ratio=1.44-1.72). 16087163 2005
CUI: C0795875
Disease: Chromosome 21 monosomy
Chromosome 21 monosomy
0.010 GeneticVariation disease BEFREE Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region. 25803843 2015
CUI: C1297882
Disease: Partial Trisomy
Partial Trisomy
0.010 Biomarker disease BEFREE Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region. 25803843 2015
CUI: C0013080
Disease: Down Syndrome
Down Syndrome
0.010 Biomarker disease BEFREE The Tc1 human chromosome 21 (Hsa21) transchromosomic mouse model of Down syndrome is trisomic for many Hsa21 genes including Hspa13 and following Chandler/Rocky Mountain Laboratory (RML) prion inoculation, shows a 4% reduction in incubation time. 22869728 2012
CUI: C0162534
Disease: Prion Diseases
Prion Diseases
0.010 GeneticVariation group BEFREE Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice. 22869728 2012
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome
0.010 Biomarker disease BEFREE The Tc1 human chromosome 21 (Hsa21) transchromosomic mouse model of Down syndrome is trisomic for many Hsa21 genes including Hspa13 and following Chandler/Rocky Mountain Laboratory (RML) prion inoculation, shows a 4% reduction in incubation time. 22869728 2012
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.010 Biomarker group LHGDN A genetic variant in the gene encoding the stress70 protein chaperone family member STCH is associated with gastric cancer in the Japanese population. 16087163 2005