Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
|
19251627 |
2009 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
|
19251627 |
2009 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
|
19251628 |
2009 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
GeneticVariation
|
disease |
UNIPROT |
Genetic contribution of FUS to frontotemporal lobar degeneration.
|
20124201 |
2010 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
|
20577002 |
2010 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
GeneticVariation
|
disease |
UNIPROT |
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.
|
19861302 |
2010 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
Biomarker
|
disease |
BEFREE |
Our results indicated that changing FUS/TLS to an insoluble form may be a common process in polyQ diseases and ALS6.
|
19833157 |
2010 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.
|
20668259 |
2010 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import.
|
20606625 |
2010 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis.
|
22055719 |
2012 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
GeneticVariation
|
disease |
BEFREE |
Mutations in FUS/TLS (fused in sarcoma/translated in liposarcoma) cause an inheritable form of amyotrophic lateral sclerosis (ALS6).
|
21965298 |
2012 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq.
|
23577159 |
2013 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation.
|
24204307 |
2013 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
Activity-dependent FUS dysregulation disrupts synaptic homeostasis.
|
25324524 |
2014 |
Entrez Id: |
2521 |
Gene Symbol: |
FUS |
FUS
|
0.430 |
CausalMutation
|
disease |
CLINVAR |
Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis.
|
24908169 |
2014 |
Entrez Id: |
157807 |
Gene Symbol: |
CLVS1 |
CLVS1
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
|
24529757 |
2014 |
KRT18P55
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
|
24256812 |
2014 |
Entrez Id: |
283383 |
Gene Symbol: |
ADGRD1 |
ADGRD1
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
|
24529757 |
2014 |
Entrez Id: |
5648 |
Gene Symbol: |
MASP1 |
MASP1
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
|
24529757 |
2014 |
Entrez Id: |
2066 |
Gene Symbol: |
ERBB4 |
ERBB4
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
|
24529757 |
2014 |
Entrez Id: |
203228 |
Gene Symbol: |
C9orf72 |
C9orf72
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
|
24256812 |
2014 |
Entrez Id: |
8821 |
Gene Symbol: |
INPP4B |
INPP4B
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
|
24529757 |
2014 |
METTL21A
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
|
24529757 |
2014 |
SLC25A12
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
|
24529757 |
2014 |
Entrez Id: |
3680 |
Gene Symbol: |
ITGA9 |
ITGA9
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
|
24529757 |
2014 |