Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
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 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 GeneticVariation disease UNIPROT Genetic contribution of FUS to frontotemporal lobar degeneration. 20124201 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 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 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: 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: 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: 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: 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 A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 24256812 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: 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: 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: 8604
Gene Symbol: SLC25A12
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: 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: 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: 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: 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