Entrez Id: |
1501 |
Gene Symbol: |
CTNND2 |
CTNND2
|
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: |
79104 |
Gene Symbol: |
MEG8 |
MEG8
|
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: |
23503 |
Gene Symbol: |
ZFYVE26 |
ZFYVE26
|
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: |
10242 |
Gene Symbol: |
KCNMB2 |
KCNMB2
|
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: |
10562 |
Gene Symbol: |
OLFM4 |
OLFM4
|
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: |
288 |
Gene Symbol: |
ANK3 |
ANK3
|
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: |
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 |
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 |
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 |
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 |