rs387907098
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
Ataxia, Spinocerebellar
0.010
GeneticVariation
BEFREE
We further confirmed our finding by identifying another missense mutation c.980A-G transition (D327G ) in exon seven of TGM6 in an additional spinocerebellar ataxia family, which also cosegregated with the phenotype.
21106500
2010
rs201964784
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
C
0.800
CausalMutation
CLINVAR
rs372250159
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
T
0.800
CausalMutation
CLINVAR
rs387907097
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
G
0.800
CausalMutation
CLINVAR
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
21106500
2010
rs387907098
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
G
0.800
CausalMutation
CLINVAR
rs387907097
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
Leukemia, Myelocytic, Acute
G
0.700
CausalMutation
CLINVAR
rs793888526
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
A
0.700
CausalMutation
CLINVAR
rs34972666
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
Alzheimer's Disease
0.800
GeneticVariation
GWASCAT
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
23535033
2014
rs6114027
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
Tuberculosis
C
0.700
GeneticVariation
GWASCAT
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese.
30287856
2018
rs34972666
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
Alzheimer's Disease
0.800
GeneticVariation
GWASDB
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
23535033
2014
rs201964784
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization.
25253745
2014
rs201964784
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
21106500
2010
rs201964784
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
29053796
2017
rs201964784
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Whole exome sequencing identifies a novel mutation in the transglutaminase 6 gene for spinocerebellar ataxia in a Chinese family.
22554020
2013
rs201964784
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis.
23206699
2013
rs372250159
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
29053796
2017
rs372250159
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Whole exome sequencing identifies a novel mutation in the transglutaminase 6 gene for spinocerebellar ataxia in a Chinese family.
22554020
2013
rs372250159
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization.
25253745
2014
rs372250159
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
21106500
2010
rs372250159
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis.
23206699
2013
rs387907097
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
21106500
2010
rs387907097
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization.
25253745
2014
rs387907097
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis.
23206699
2013
rs387907097
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Whole exome sequencing identifies a novel mutation in the transglutaminase 6 gene for spinocerebellar ataxia in a Chinese family.
22554020
2013
rs387907097
×
Entrez Id:
343641
Gene Symbol:
TGM6
TGM6
SPINOCEREBELLAR ATAXIA 35
0.800
GeneticVariation
UNIPROT
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
29053796
2017