rs63750129
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Our strategy was to use the natural tau promoter for expressing the human-tau (htau) gene with two mutations K257T/P301S (double mutant, DM) associated with severe phenotypes of frontotemporal-dementia in humans.
|
18490011 |
2008 |
rs63750129
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.
|
11891833 |
2002 |
rs63750512
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.
|
11891833 |
2002 |
rs63750129
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Pick's disease associated with the novel Tau gene mutation K369I.
|
11601501 |
2001 |
rs63750512
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Pick's disease associated with the novel Tau gene mutation K369I.
|
11601501 |
2001 |
rs63750129
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Taken together, the present findings indicate that the K257T mutation in Tau can cause a dementing condition similar to Pick's disease.
|
11089577 |
2000 |
rs63750129
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Pick's disease is associated with mutations in the tau gene.
|
11117542 |
2000 |
rs63750129
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Taken together, the present findings indicate that the K257T mutation in Tau can cause a dementing condition similar to Pick's disease.
|
11089577 |
2000 |
rs63750512
|
|
|
0.820 |
GeneticVariation |
BEFREE |
The present findings indicate that the G389R mutation in Tau can cause a dementia similar to that in Pick's disease.
|
11193177 |
2000 |
rs63750512
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Pick's disease is associated with mutations in the tau gene.
|
11117542 |
2000 |
rs63750512
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Tau gene mutation K257T causes a tauopathy similar to Pick's disease.
|
11089577 |
2000 |
rs63750129
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.
|
10604746 |
1999 |
rs63750512
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Taken together, the present findings indicate that the G389R mutation in Tau can cause a dementing condition that closely resembles Pick's disease.
|
10604746 |
1999 |
rs63750512
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Taken together, the present findings indicate that the G389R mutation in Tau can cause a dementing condition that closely resembles Pick's disease.
|
10604746 |
1999 |
rs63750129
|
|
C |
0.820 |
CausalMutation |
CLINVAR |
|
|
|
rs63750512
|
|
A |
0.820 |
CausalMutation |
CLINVAR |
|
|
|
rs63751068
|
|
|
0.810 |
GeneticVariation |
BEFREE |
The G183V mutation possibly causing Pick disease causes production of aberrant transcripts truncating the open reading frame after exon 5 sequence.
|
24101600 |
2014 |
rs63750635
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.
|
11891833 |
2002 |
rs63750635
|
|
|
0.810 |
GeneticVariation |
BEFREE |
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.
|
11891833 |
2002 |
rs63750635
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Pick's disease associated with the novel Tau gene mutation K369I.
|
11601501 |
2001 |
rs63751264
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Taken together, results indicate that the K369I mutation in Tau can cause a dementing disease with a neuropathology like that of Pick's disease.
|
11601501 |
2001 |
rs63750635
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Pick's disease is associated with mutations in the tau gene.
|
11117542 |
2000 |
rs63750635
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Tau gene mutation K257T causes a tauopathy similar to Pick's disease.
|
11089577 |
2000 |
rs63750635
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.
|
10604746 |
1999 |
rs63750635
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
|
|
|