Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
0.600 | CausalMutation | disease | CLINVAR | Activity-dependent FUS dysregulation disrupts synaptic homeostasis. | 25324524 | 2014 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis. | 24908169 | 2014 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq. | 23577159 | 2013 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation. | 24204307 | 2013 | ||||
|
0.600 | GeneticVariation | disease | UNIPROT | Exome sequencing identifies FUS mutations as a cause of essential tremor. | 22863194 | 2012 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. | 22055719 | 2012 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import. | 20606625 | 2010 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. | 20577002 | 2010 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia. | 20668259 | 2010 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. | 19251627 | 2009 | ||||
|
0.600 | Biomarker | disease | CTD_human |