Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6647
Gene Symbol: SOD1
SOD1 		0.300 CausalMutation disease CLINVAR
Entrez Id: 6623
Gene Symbol: SNCG
SNCG 		0.200 Biomarker disease MGD
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: 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: 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 VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death. 12847526 2003
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: 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
Entrez Id: 284085
Gene Symbol: KRT18P55
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
Entrez Id: 151194
Gene Symbol: METTL21A
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
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: 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: 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: 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: 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: 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: 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
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