Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE SPINK1 c.194+2T>C mutation had a higher occurrence in juvenile ICP patients than in adult group and typically presented with recurrent acute pancreatitis. 28348582 2017
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE The haplotype harboring the SPINK1 c.101A>G (p.Asn34Ser) variant (also known as rs17107315:T>C) represents the most important heritable risk factor for idiopathic chronic pancreatitis identified to date. 28556356 2017
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE PRSS1 (R122H) mutations were detected in one (1.3%) patient with ICP and SPINK1 (N34S) mutations were present in one (4.1%) patient with ACP. 29641165 2017
Entrez Id: 5644
Gene Symbol: PRSS1
PRSS1
0.100 GeneticVariation disease BEFREE PRSS1 (R122H) mutations were detected in one (1.3%) patient with ICP and SPINK1 (N34S) mutations were present in one (4.1%) patient with ACP. 29641165 2017
Entrez Id: 5644
Gene Symbol: PRSS1
PRSS1
0.100 GeneticVariation disease BEFREE In this study, we have demonstrated the association of claudin2 (rs7057398) polymorphism with IRAP and progression of IRAP to CP, and PRSS1 (rs10273639) polymorphism with IRAP and ICP. 26110235 2015
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 Biomarker disease BEFREE Serine Protease Inhibitor Kazal Type 1 (SPINK1) c.194+2T > C Mutation May Predict Long-term Outcome of Endoscopic Treatments in Idiopathic Chronic Pancreatitis. 26632706 2015
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE Mutation analysis of PRSS1, SPINK1 and CFTR gene in patients with alcoholic and idiopathic chronic pancreatitis: A single center study. 25835118 2015
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE The serine protease inhibitor Kazal type 1 c.194+2T>C variant was present in 44.9% of patients with idiopathic chronic pancreatitis. 23017645 2013
Entrez Id: 5644
Gene Symbol: PRSS1
PRSS1
0.100 Biomarker disease BEFREE A conservative assessment of the major genetic causes of idiopathic chronic pancreatitis: data from a comprehensive analysis of PRSS1, SPINK1, CTRC and CFTR genes in 253 young French patients. 23951356 2013
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE Tropical pancreatitis associates with SPINK1 and/or CFTR gene mutations in approximately 50% of patients, similar to the frequency in idiopathic chronic pancreatitis. 21844753 2011
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE Coinheritance of p.R75Q or CF causing CFTR variants with SPINK1 variants significantly increases the risk of ICP. 20977904 2011
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE The prevalence of cationic trypsinogen (PRSS1) and serine protease inhibitor, Kazal type 1 (SPINK1) gene mutations in Polish patients with alcoholic and idiopathic chronic pancreatitis. 20676769 2011
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE Tropical pancreatitis associates with SPINK1 and/or CFTR gene mutations in approximately 50% of patients, similar to the frequency in idiopathic chronic pancreatitis. 21844753 2011
Entrez Id: 5644
Gene Symbol: PRSS1
PRSS1
0.100 GeneticVariation disease BEFREE The prevalence of cationic trypsinogen (PRSS1) and serine protease inhibitor, Kazal type 1 (SPINK1) gene mutations in Polish patients with alcoholic and idiopathic chronic pancreatitis. 20676769 2011
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE Coinheritance of p.R75Q or CF causing CFTR variants with SPINK1 variants significantly increases the risk of ICP. 20977904 2011
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE CFTR mutations enhance susceptibility for idiopathic chronic pancreatitis (ICP) and congenital bilateral absence of the vas deferens (CBAVD); however, it is unknown why CFTR heterozygotes are at increased disease risk. 21520337 2011
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations. 20551465 2010
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations. 20551465 2010
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 Biomarker disease BEFREE Some other genes, such as SPINK1 or CFTR, have been associated with familial idiopathic chronic pancreatitis. 19944211 2009
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE Thus, the CFTR gene mutation, especially the 5T genotype, appears to have some relationship to ICP prevalence in Japanese patients independent of cystic fibrosis. 19383231 2009
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE Abnormal CFTR allele was found to be thrice as frequent in ICP patients as in controls (22/156 vs 19/400, p < 0.0001). 17539902 2007
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 Biomarker disease BEFREE These findings indicate that PSTI is a modifier gene for CFTR-related ICP and have implications for the diagnosis and pathogenesis of pancreatitis. 15758663 2005
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE At least one CFTR mutation or variant was carried in 18 of 40 patients (45%) with idiopathic chronic pancreatitis and in 6 of 16 patients (38%) with idiopathic recurrent acute pancreatitis but in only 11 of the 50 controls (22%, P=0.005). 16193325 2005
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
0.100 GeneticVariation disease BEFREE Heterozygous SPINK1 mutations were detected in eight ICP patients (15% v 1% in controls) but only one also carried an additional mild CFTR mutation. 15987793 2005
Entrez Id: 1080
Gene Symbol: CFTR
CFTR
0.100 GeneticVariation disease BEFREE Heterozygous SPINK1 mutations were detected in eight ICP patients (15% v 1% in controls) but only one also carried an additional mild CFTR mutation. 15987793 2005