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 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 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 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 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 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 Genetic contribution of FUS to frontotemporal lobar degeneration. 20124201 2010
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 GeneticVariation disease UNIPROT Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. 19861302 2010
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 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 fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import. 20606625 2010
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 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 GeneticVariation disease UNIPROT Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 19251628 2009
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
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