rs63750416, MAPT

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism. 9736786 1998
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. 9641683 1998
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Accelerated filament formation from tau protein with specific FTDP-17 missense mutations. 10214944 1999
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT A distinct familial presenile dementia with a novel missense mutation in the tau gene. 10208578 1999
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration. 10489057 1999
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation. 10553987 1999
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau. 10374757 1999
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT A Japanese patient with frontotemporal dementia and parkinsonism by a tau P301S mutation. 11071507 2000
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation. 11117541 2000
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene. 10802785 2000
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Effects of FTDP-17 mutations on the in vitro phosphorylation of tau by glycogen synthase kinase 3beta identified by mass spectrometry demonstrate certain mutations exert long-range conformational changes. 11278002 2001
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation BEFREE Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells. 11585254 2001
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells. 11585254 2001
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
0.020 GeneticVariation BEFREE Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells. 11585254 2001
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
0.010 GeneticVariation BEFREE We report a 62-year-old Japanese man with familial frontotemporal dementia and a novel missense mutation (N296H) in exon 10 of the tau gene. 11585254 2001
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
0.010 GeneticVariation BEFREE Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells. 11585254 2001
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Functional effects of tau gene mutations deltaN296 and N296H. 11906000 2002
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Early-onset, rapidly progressive familial tauopathy with R406W mutation. 11889249 2002
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Clinical and genetic studies of families with the tau N279K mutation (FTDP-17). 12473774 2002
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation. 11921059 2002
Dementia in Parkinson's disease
CUI: C0349081
Disease: Dementia in Parkinson's disease
0.010 GeneticVariation BEFREE Two of these mutations, N296N and N296H, lead to a clinical syndrome similar to autosomal dominant fronto-temporal dementia with Parkinsonism linked to chromosome 17. 11911984 2002
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology. 12509859 2003
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe. 14517953 2003
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT Phenotypic heterogeneity within a new family with the MAPT p301s mutation. 16240366 2005
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
0.720 GeneticVariation UNIPROT A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease. 15883319 2005