×
Entrez Id:
6647
Gene Symbol:
SOD1
SOD1
0.300
Biomarker
disease
MGD
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity.
25468678
2015
×
Entrez Id:
6647
Gene Symbol:
SOD1
SOD1
0.300
CausalMutation
disease
CLINVAR
×
Entrez Id:
51542
Gene Symbol:
VPS54
VPS54
0.200
Biomarker
disease
MGD
Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS.
20643756
2011
×
Entrez Id:
7422
Gene Symbol:
VEGFA
VEGFA
0.200
Biomarker
disease
MGD
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death.
12847526
2003
×
Entrez Id:
7422
Gene Symbol:
VEGFA
VEGFA
0.200
Biomarker
disease
MGD
Loss of HIF-2alpha and inhibition of VEGF impair fetal lung maturation, whereas treatment with VEGF prevents fatal respiratory distress in premature mice.
12053176
2002
×
Entrez Id:
7422
Gene Symbol:
VEGFA
VEGFA
0.200
Biomarker
disease
MGD
Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration.
11381259
2001
×
Entrez Id:
6648
Gene Symbol:
SOD2
SOD2
0.200
Biomarker
disease
MGD
Ocular pathology in mitochondrial superoxide dismutase (Sod2)-deficient mice.
11527927
2001
×
Entrez Id:
6648
Gene Symbol:
SOD2
SOD2
0.200
Biomarker
disease
MGD
A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase.
9462746
1998
×
Entrez Id:
6623
Gene Symbol:
SNCG
SNCG
0.200
Biomarker
disease
MGD
×
Entrez Id:
23025
Gene Symbol:
UNC13A
UNC13A
0.100
GeneticVariation
disease
GWASCAT
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
28931804
2017
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
0.100
GeneticVariation
disease
GWASCAT
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
28931804
2017
×
Entrez Id:
203228
Gene Symbol:
C9orf72
C9orf72
0.100
GeneticVariation
disease
GWASCAT
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
28931804
2017
×
Entrez Id:
23098
Gene Symbol:
SARM1
SARM1
0.100
GeneticVariation
disease
GWASCAT
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
28931804
2017
×
Entrez Id:
285195
Gene Symbol:
SLC9A9
SLC9A9
0.100
GeneticVariation
disease
GWASCAT
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
27244217
2016
×
Entrez Id:
23362
Gene Symbol:
PSD3
PSD3
0.100
GeneticVariation
disease
GWASCAT
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
27244217
2016
×
Entrez Id:
3416
Gene Symbol:
IDE
IDE
0.100
GeneticVariation
disease
GWASCAT
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
27244217
2016
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
0.100
GeneticVariation
disease
GWASCAT
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
27244217
2016
×
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:
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:
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:
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
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:
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
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