PRSS2, serine protease 2, 5645

N. diseases: 66; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 GeneticVariation disease BEFREE In this study, we evaluated the association of claudin2 and PRSS1-PRSS2 polymorphisms with idiopathic RAP and CP. 26110235 2015
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 GeneticVariation disease BEFREE It has been recently shown that a loss-of-function variant, c.571G>A (p.G191R), in the anionic trypsinogen (PRSS2) gene protects against chronic pancreatitis in European populations. 19052022 2009
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 GeneticVariation disease BEFREE However mutations in cationic and anionic trypsinogen gene do not play an important role in causing CP in Asia Pacific region. 21323990 2011
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 Biomarker disease CTD_human A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis. 16699518 2006
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 GeneticVariation disease BEFREE A genome-wide association study reported an association of chronic pancreatitis (CP) with variants in PRSS1-PRSS2 (rs10273639; near the gene encoding cationic trypsinogen) and CLDN2-MORC4 loci (rs7057398 in RIPPLY1 and rs12688220 in MORC4). 25253127 2015
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 AlteredExpression disease LHGDN A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis. 16699518 2006
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 GeneticVariation disease BEFREE A recent genome-wide association study (GWAS) identified association with variants in X-linked CLDN2 and MORC4, and PRSS1-PRSS2 loci with chronic pancreatitis (CP) in North American patients of European ancestry. 26820620 2016
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 Biomarker disease CTD_human Hereditary chronic pancreatitis. 18206817 2008
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 Biomarker disease HPO
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 GeneticVariation disease BEFREE Here we analysed whether common variants in the CLDN2-MORC4 and the PRSS1-PRSS2 locus that increase recurrent AP and CP risk associate with AP. 29884332 2018
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 GeneticVariation disease BEFREE In conclusion, the G191R variant of PRSS2 mitigates intrapancreatic trypsin activity and thereby protects against chronic pancreatitis. 16699518 2006
CUI: C0376670
Disease: Pancreatitis, Alcoholic
Pancreatitis, Alcoholic
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. 28754779 2018
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.140 GeneticVariation disease BEFREE These individuals and 100 patients with pHPT without pancreatitis were analysed for CTRC (p.R254W and p.K247_R254del) and PRSS2 (p.G191R) mutations using melting curve analysis and DNA sequencing or PCR and gel electrophoresis (in case of p.K247_R254del CTRC). 20625975 2011
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.140 Biomarker disease HPO
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.140 Biomarker disease LHGDN Hereditary pancreatitis caused by a double gain-of-function trypsinogen mutation. 18461367 2008
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.140 GeneticVariation disease BEFREE Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. 23143602 2012
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.140 GeneticVariation disease BEFREE In contrast, no pancreatitis-associated mutations have been found in the anionic trypsinogen gene (PRSS2), suggesting that this isoform might play a relatively unimportant role in pancreatitis. 14695529 2004
CUI: C0030299
Disease: Pancreatic Pseudocyst
Pancreatic Pseudocyst
0.100 Biomarker disease HPO
CUI: C0810032
Disease: Pancreatic disorders (not diabetes)
Pancreatic disorders (not diabetes)
0.010 GeneticVariation group BEFREE A loss-of-function p.G191R variant in the anionic trypsinogen (PRSS2) gene in Japanese patients with pancreatic disorders. 19052022 2009
CUI: C0030286
Disease: Pancreatic Diseases
Pancreatic Diseases
0.010 AlteredExpression group BEFREE Taken together, the observations indicate that up-regulation of anionic trypsinogen in pancreatic diseases does not affect physiological trypsinogen activation, but significantly limits trypsin generation under potential pathological conditions. 12709065 2003
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.020 Biomarker disease BEFREE Among these proteins, three (SYCN, REG1B, and PRSS2) were previously reported as circulating candidate biomarkers of pancreatic cancer. 31538697 2019
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.020 Biomarker disease BEFREE Hyperexpression of the PRSS2 gene and hypermethylation of ELA3B gene promoter were associated with PC, raising the possibility of their application as new biomarkers in PC diagnosis and screening. 20428826 2010
CUI: C1842406
Disease: Pancreatic calcification
Pancreatic calcification
0.100 Biomarker phenotype HPO
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis
0.010 AlteredExpression disease BEFREE Analysis of Parkinson's disease cases alone indicated that serpin-A5 and serpin-A13, and trypsin-2 expression in midbrain and cerebral cortex was different in cases with a high incidence of L-DOPA-induced dyskinesia and psychosis compared to those with low levels of these treatment-induced side effects. 25982926 2015
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 Biomarker group BEFREE Tumor-associated trypsin-2 and matrix metalloprotease-9 (MMP-9) are associated with cancer, particularly with invasive squamous cell carcinomas. 18062964 2008