CORIN, corin, serine peptidase, 10699

N. diseases: 55; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE This study aims to investigate the association of 2 single nucleotide polymorphisms (SNPs) in CORIN (rs2271037 and rs3749585) with hypertension, as well as their potential interactions with some risk factors of hypertension in a Han population of northeastern China. 29391274 2018
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE To understand the prevalence and functional significance of CORIN variants in hypertension, we sequenced CORIN exons in 300 normal and 401 hypertensive individuals in a Chinese population and identified nine nonsynonymous variants, of which eight were not characterized previously. 28861913 2017
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE CORIN variants and mutations impairing corin activation have been identified in people with hypertension and pre-eclampsia. 26259032 2015
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE CORIN variants have been associated with hypertension and heart disease in African Americans. 25488193 2014
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE Here, we report a new mutation in exon 12 of the CORIN gene identified in a family of patients with hypertension. 23372161 2013
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE A corin gene variant (T555I/Q568P) was identified in blacks with hypertension and cardiac hypertrophy. 22987923 2012
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE In humans, single nucleotide polymorphisms in the corin gene have been identified in African Americans with hypertension and cardiac hypertrophy. 18716601 2009
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group LHGDN Thus, our results show that the corin gene SNPs associated with hypertension and cardiac hypertrophy impair corin zymogen activation and natriuretic peptide processing activity. 18669922 2008
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 Biomarker group BEFREE Thus, our results show that the corin gene SNPs associated with hypertension and cardiac hypertrophy impair corin zymogen activation and natriuretic peptide processing activity. 18669922 2008
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE We recently identified a minor allele in the corin gene defined by 2 highly linked single nucleotide polymorphisms (T555I and Q568P), which was associated with hypertension in blacks. 17296875 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group LHGDN We recently identified a minor allele in the corin gene defined by 2 highly linked single nucleotide polymorphisms (T555I and Q568P), which was associated with hypertension in blacks. 17296875 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE More recently, single nucleotide polymorphisms (SNPs) are found in the human corin gene, which are associated with an increased risk for hypertension and cardiac hypertrophy. 17485366 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group LHGDN Corin gene minor allele defined by 2 missense mutations is common in blacks and associated with high blood pressure and hypertension. 16216958 2005
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 GeneticVariation group BEFREE Corin gene minor allele defined by 2 missense mutations is common in blacks and associated with high blood pressure and hypertension. 16216958 2005
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 Biomarker group BEFREE The demonstrated corin protein expression by heart myocytes supports its proposed role as the pro-ANP convertase, and thus a potentially critical mediator of major cardiovascular diseases including hypertension and congestive heart failure. 11082206 2000
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.200 Biomarker group HPO