GP6, glycoprotein VI platelet, 51206

N. diseases: 89; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 Biomarker disease CLINGEN An adenine insertion in exon 6 of human GP6 generates a truncated protein associated with a bleeding disorder in four Chilean families. 23815599 2013
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 GermlineCausalMutation disease ORPHANET A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorder. 19552682 2009
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 GeneticVariation disease UNIPROT Absence of collagen-induced platelet activation caused by compound heterozygous GPVI mutations. 19549989 2009
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 GeneticVariation disease UNIPROT A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorder. 19552682 2009
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 GermlineCausalMutation disease ORPHANET Absence of collagen-induced platelet activation caused by compound heterozygous GPVI mutations. 19549989 2009
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 Biomarker disease CLINGEN Absence of collagen-induced platelet activation caused by compound heterozygous GPVI mutations. 19549989 2009
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 Biomarker disease CLINGEN A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorder. 19552682 2009
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 Biomarker disease GENOMICS_ENGLAND Absence of collagen-induced platelet activation caused by compound heterozygous GPVI mutations. 19549989 2009
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 Biomarker disease CLINGEN The contribution of glycoprotein VI to stable platelet adhesion and thrombus formation illustrated by targeted gene deletion. 12738669 2003
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 Biomarker disease CLINGEN A crucial role of glycoprotein VI for platelet recruitment to the injured arterial wall in vivo. 12515812 2003
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 Biomarker disease CLINGEN Cloning, characterization, and functional studies of human and mouse glycoprotein VI: a platelet-specific collagen receptor from the immunoglobulin superfamily. 10961879 2000
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency
0.600 Biomarker disease CTD_human
Finding of Mean Corpuscular Hemoglobin
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 AlteredExpression disease BEFREE Platelet GPVI surface expression is enhanced following acute ischemic events like myocardial infarction and cerebral stroke, serves as an imminent diagnostic tool independent of markers of tissue necrosis, and is associated with poor prognosis. 27753514 2017
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.100 GeneticVariation phenotype GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
Platelet Component Distribution Width Measurement
0.100 GeneticVariation phenotype GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 AlteredExpression disease BEFREE Increased GPVI levels are associated with poor clinical outcome and are an early indicator for imminent myocardial infarction in patients with chest pain. 24553806 2014
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 Biomarker disease BEFREE Also, treatment of mice undergoing experimental myocardial infarction with αCD133-GPVI-labeled progenitor cells reduces infarction size and preserves myocardial function. 22448969 2012
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 GeneticVariation disease BEFREE The impact of platelet collagen receptor polymorphisms in the pathogenesis of myocardial infarction at young age remains unknown. 22627583 2012
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 GeneticVariation disease BEFREE A significant association between GP VI 13254C allele carriers and premature MI was found (p=0.025). 19786296 2010
CUI: C0032176
Disease: Platelet aggregation
Platelet aggregation
0.100 GeneticVariation phenotype GWASDB Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. 20526338 2010
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 GeneticVariation disease BEFREE The combined ThrThr/TT haplotype of GPIbalpha as well as the AA genotype of GPIV seem to decrease the risk of fatal MI among men during early middle-age. 17619827 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 Biomarker disease BEFREE Our preliminary data suggests that platelet collagen receptor density, when measured directly, may be related to prior myocardial infarction. 15874887 2005