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 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 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 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 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 CausalMutation disease CLINVAR Activity-dependent FUS dysregulation disrupts synaptic homeostasis. 25324524 2014
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 Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq. 23577159 2013
Entrez Id: 2521
Gene Symbol: FUS
FUS 		0.430 CausalMutation disease CLINVAR Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia. 20668259 2010
Entrez Id: 2521
Gene Symbol: FUS
FUS 		0.430 CausalMutation disease CLINVAR ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation. 24204307 2013
Entrez Id: 2521
Gene Symbol: FUS
FUS 		0.430 CausalMutation disease CLINVAR FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 22055719 2012
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 CausalMutation disease CLINVAR ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import. 20606625 2010
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