FUS, FUS RNA binding protein, 2521

N. diseases: 301; N. variants: 39
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909668
rs121909668
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 19251628 2009
dbSNP: rs121909668
rs121909668
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. 19251627 2009
dbSNP: rs121909668
rs121909668
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China. 27604643 2016
dbSNP: rs121909668
rs121909668
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. 19861302 2010
dbSNP: rs121909668
rs121909668
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Genetic contribution of FUS to frontotemporal lobar degeneration. 20124201 2010
dbSNP: rs121909669
rs121909669
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 19251628 2009
dbSNP: rs121909669
rs121909669
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China. 27604643 2016
dbSNP: rs121909669
rs121909669
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Genetic contribution of FUS to frontotemporal lobar degeneration. 20124201 2010
dbSNP: rs121909669
rs121909669
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. 19251627 2009
dbSNP: rs121909669
rs121909669
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. 19861302 2010
dbSNP: rs121909671
rs121909671
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. 19251627 2009
dbSNP: rs121909671
rs121909671
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China. 27604643 2016
dbSNP: rs121909671
rs121909671
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 19251628 2009
dbSNP: rs121909671
rs121909671
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Genetic contribution of FUS to frontotemporal lobar degeneration. 20124201 2010
dbSNP: rs121909671
rs121909671
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. 19861302 2010
dbSNP: rs267606831
rs267606831
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 19251628 2009
dbSNP: rs267606831
rs267606831
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Genetic contribution of FUS to frontotemporal lobar degeneration. 20124201 2010
dbSNP: rs267606831
rs267606831
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China. 27604643 2016
dbSNP: rs267606831
rs267606831
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. 19861302 2010
dbSNP: rs267606831
rs267606831
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. 19251627 2009
dbSNP: rs267606832
rs267606832
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. 19251627 2009
dbSNP: rs267606832
rs267606832
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. 19861302 2010
dbSNP: rs267606832
rs267606832
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C3539195
Disease:
TREMOR, HEREDITARY ESSENTIAL, 4
0.800 GeneticVariation UNIPROT Exome sequencing identifies FUS mutations as a cause of essential tremor. 22863194 2012
dbSNP: rs267606832
rs267606832
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Genetic contribution of FUS to frontotemporal lobar degeneration. 20124201 2010
dbSNP: rs267606832
rs267606832
Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 19251628 2009