Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
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
Entrez Id: 2521
Gene Symbol: FUS
FUS 		0.430 GeneticVariation disease BEFREE Due to mutation, FUS protein became more rigid in nature and might alter the structural and functional behavior of protein and play a major role in inducing ALS6. 24738488 2015
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: 2521
Gene Symbol: FUS
FUS 		0.430 CausalMutation disease CLINVAR Activity-dependent FUS dysregulation disrupts synaptic homeostasis. 25324524 2014
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: 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: 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: 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: 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: 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: 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: 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