TGM6, transglutaminase 6, 343641

N. diseases: 54; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201964784
rs201964784
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. 29053796 2017
dbSNP: rs372250159
rs372250159
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. 29053796 2017
dbSNP: rs387907097
rs387907097
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. 29053796 2017
dbSNP: rs387907098
rs387907098
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. 29053796 2017
dbSNP: rs201964784
rs201964784
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization. 25253745 2014
dbSNP: rs34972666
rs34972666
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C0002395
Disease:
Alzheimer's Disease 		0.800 GeneticVariation GWASDB Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033 2014
dbSNP: rs34972666
rs34972666
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C0002395
Disease:
Alzheimer's Disease 		0.800 GeneticVariation GWASCAT Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033 2014
dbSNP: rs372250159
rs372250159
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization. 25253745 2014
dbSNP: rs387907097
rs387907097
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization. 25253745 2014
dbSNP: rs387907098
rs387907098
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization. 25253745 2014
dbSNP: rs201964784
rs201964784
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
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
dbSNP: rs201964784
rs201964784
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis. 23206699 2013
dbSNP: rs372250159
rs372250159
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
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
dbSNP: rs372250159
rs372250159
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis. 23206699 2013
dbSNP: rs387907097
rs387907097
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis. 23206699 2013
dbSNP: rs387907097
rs387907097
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
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
dbSNP: rs387907098
rs387907098
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
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
dbSNP: rs387907098
rs387907098
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis. 23206699 2013
dbSNP: rs201964784
rs201964784
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. 21106500 2010
dbSNP: rs372250159
rs372250159
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. 21106500 2010
dbSNP: rs387907097
rs387907097
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		G 0.800 CausalMutation CLINVAR TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. 21106500 2010
dbSNP: rs387907097
rs387907097
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. 21106500 2010
dbSNP: rs387907098
rs387907098
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		0.800 GeneticVariation UNIPROT TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. 21106500 2010
dbSNP: rs201964784
rs201964784
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		C 0.800 CausalMutation CLINVAR
dbSNP: rs372250159
rs372250159
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
CUI: C3888031
Disease:
SPINOCEREBELLAR ATAXIA 35 		T 0.800 CausalMutation CLINVAR