|
| 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 |
Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
|
27604643 |
2016 |
|
| 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 |
GeneticVariation
|
disease |
UNIPROT |
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.
|
19861302 |
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 |
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 |
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
|
19251628 |
2009 |
|
| 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 |
|
| 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: |
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 |
|
| Entrez Id: |
3236 |
| Gene Symbol: |
HOXD10 |
HOXD10
|
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: |
9619 |
| Gene Symbol: |
ABCG1 |
ABCG1
|
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: |
4978 |
| Gene Symbol: |
OPCML |
OPCML
|
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: |
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 |