Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 351
Gene Symbol: APP
APP
0.700 GeneticVariation disease UNIPROT Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP. 20697050 2010
Entrez Id: 351
Gene Symbol: APP
APP
0.700 Biomarker disease GENOMICS_ENGLAND Iowa variant of familial Alzheimer's disease: accumulation of posttranslationally modified AbetaD23N in parenchymal and cerebrovascular amyloid deposits. 20228223 2010
Entrez Id: 351
Gene Symbol: APP
APP
0.700 GeneticVariation disease UNIPROT A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy. 16178030 2005
Entrez Id: 351
Gene Symbol: APP
APP
0.700 GeneticVariation disease UNIPROT Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutation. 12654973 2003
Entrez Id: 351
Gene Symbol: APP
APP
0.700 GeneticVariation disease UNIPROT Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy. 11409420 2001
Entrez Id: 351
Gene Symbol: APP
APP
0.700 Biomarker disease CTD_human Substitutions at codon 22 of Alzheimer's abeta peptide induce diverse conformational changes and apoptotic effects in human cerebral endothelial cells. 10821838 2000
Entrez Id: 351
Gene Symbol: APP
APP
0.700 Biomarker disease GENOMICS_ENGLAND Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. 2111584 1990
Entrez Id: 351
Gene Symbol: APP
APP
0.700 Biomarker disease CTD_human Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. 2111584 1990
Entrez Id: 351
Gene Symbol: APP
APP
0.700 GeneticVariation disease UNIPROT Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. 2111584 1990
Entrez Id: 351
Gene Symbol: APP
APP
0.700 CausalMutation disease CLINVAR