Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
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: 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 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: 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