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 LHGDN Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl. 15776435 2005
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: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.070 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 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: C0238339
Disease: Hereditary pancreatitis
Hereditary pancreatitis
0.630 GeneticVariation disease ORPHANET Here we demonstrate a heterozygous hybrid PRSS2 (encoding anionic trypsinogen)/PRSS1 gene in a French white family with hereditary pancreatitis, by means of quantitative fluorescent multiplex PCR and RT-PCR analyses. 18461367 2008
CUI: C0238339
Disease: Hereditary pancreatitis
Hereditary pancreatitis
0.630 GeneticVariation disease BEFREE Here we demonstrate a heterozygous hybrid PRSS2 (encoding anionic trypsinogen)/PRSS1 gene in a French white family with hereditary pancreatitis, by means of quantitative fluorescent multiplex PCR and RT-PCR analyses. 18461367 2008
CUI: C2938901
Disease: Tropical infectious disease
Tropical infectious disease
0.010 GeneticVariation disease BEFREE Here, we characterize the structural and proteolytic attributes of serine protease 2 (SmSP2) from Schistosoma mansoni, one of the major species responsible for the tropical infectious disease, schistosomiasis. 29677188 2018
CUI: C2931073
Disease: Collagenopathy, type 2 alpha 1
Collagenopathy, type 2 alpha 1
0.010 Biomarker disease BEFREE Here, we show that human trypsin-2 is also capable of cleaving the triple helix of human cartilage collagen type II. 16192646 2005
CUI: C0149521
Disease: Pancreatitis, Chronic
Pancreatitis, Chronic
0.490 Biomarker disease CTD_human Hereditary chronic pancreatitis. 18206817 2008
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.140 Biomarker disease LHGDN Hereditary pancreatitis caused by a double gain-of-function trypsinogen mutation. 18461367 2008
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: 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: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
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: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.070 Biomarker disease BEFREE In a prospective cohort, urinary trypsinogen-2 level > 500 μg/L independently predicted local complications of AP. 31039289 2019
CUI: C0558353
Disease: Tongue Carcinoma
Tongue Carcinoma
0.010 AlteredExpression disease BEFREE In conclusion, trypsin-2 over-expression enhanced tongue carcinoma cell invasion by various genetic and proteolytic mechanisms. 22909050 2012
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: 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: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
0.010 AlteredExpression disease LHGDN In infants who subsequently developed BPD (n = 18), we detected significantly higher concentrations of trypsinogen-2 during postnatal days 5 to 10 compared with those who survived without it. 12949286 2003
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: C0000737
Disease: Abdominal Pain
Abdominal Pain
0.120 Biomarker phenotype BEFREE It is important to know the diagnostic accuracy of serum amylase, serum lipase, urinary trypsinogen-2, and urinary amylase for the diagnosis of acute pancreatitis, so that an informed decision can be made as to whether the person with abdominal pain has acute pancreatitis. 28431198 2017
CUI: C0042769
Disease: Virus Diseases
Virus Diseases
0.010 Biomarker group BEFREE Mannan-binding lectin (MBL) - associated serine protease 2 (MASP-2) co-activates the lectin pathway of complement in response to several viral infections. 27588826 2016
Infection caused by Human T-lymphotropic virus
0.010 GeneticVariation disease BEFREE Mannose binding lectin and mannose binding lectin-associated serine protease-2 genes polymorphisms in human T-lymphotropic virus infection. 23861212 2013
CUI: C0032285
Disease: Pneumonia
Pneumonia
0.010 Biomarker disease BEFREE Mannose-binding lectin and mannose-binding lectin-associated serine protease 2 in susceptibility, severity, and outcome of pneumonia in adults. 18582923 2008