Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
0.070 Biomarker disease BEFREE Novel neuroimaging findings were two patients had typical neuroimaging abnormalities of CJD and frontotemporal dementia, respectively. 29569252 2018
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
0.070 Biomarker disease BEFREE Mutational analysis of PRNP in Alzheimer's disease and frontotemporal dementia in China. 27910931 2016
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
0.070 GeneticVariation disease BEFREE To evaluate the proton magnetic resonance (MR) spectroscopy ((1) H MRS) changes in carriers of a novel octapeptide repeat insertion in the prion protein gene (PRNP) and family history of frontotemporal dementia with ataxia. 22612156 2013
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
0.070 GeneticVariation disease BEFREE The V363I variation was associated with frontotemporal dementia only in the proband which was also homozygous for the A allele of the progranulin single-nucleotide polymorphism rs9897526 and for methionine at codon 129 of the prion protein gene. 21343707 2011
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
0.070 Biomarker disease BEFREE This kindred has a unique combination of clinical and neuropathologic features associated with the largest base pair insertion identified to date in PRNP and underscores the need to consider familial prion disease in the differential diagnosis of a familial frontotemporal dementia-like syndrome. 21911696 2011
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
0.070 GeneticVariation disease BEFREE We found no association between PGRN polymorphisms, APOE and microtubule-associated protein tau genotypes, and age at onset of the disease; whereas we report evidence for an association between PRNP codon 129 polymorphism and age at onset of disease in frontotemporal dementia-PGRN(+) patients. 20711061 2011
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
0.070 Biomarker disease BEFREE Variably protease-sensitive prionopathy (VPSPr) is a novel disease involving the prion protein (PrP) that has clinical similarities with non-Alzheimer's dementias especially frontotemporal dementia, diffuse Lewis body disease, and normal pressure hydrocephalus. 21584652 2011