Variant: rs121909668

present in Gene: FUS present in Chromosome: 16 Position on Chromosome: 31191418 Alleles of this Variant: C/A;G;T

rs121909668 in FUS gene and AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) PMID 20668259 2010 Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.

PMID 27604643 2016 Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.

PMID 24908169 2014 Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis.

PMID 25324524 2014 Activity-dependent FUS dysregulation disrupts synaptic homeostasis.

PMID 22055719 2012 FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis.

PMID 20577002 2010 SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.

PMID 20606625 2010 ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import.

PMID 20124201 2010 Genetic contribution of FUS to frontotemporal lobar degeneration.

PMID 24204307 2013 ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation.

PMID 19861302 2010 Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.

PMID 19251627 2009 Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

PMID 23577159 2013 Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq.

PMID 19251628 2009 Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.

rs121909668 in FUS gene and TREMOR, HEREDITARY ESSENTIAL, 4 PMID 23577159 2013 Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq.

PMID 24204307 2013 ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation.

PMID 20606625 2010 ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import.

PMID 25324524 2014 Activity-dependent FUS dysregulation disrupts synaptic homeostasis.

PMID 22055719 2012 FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis.

PMID 20577002 2010 SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.

PMID 24908169 2014 Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis.

PMID 19251627 2009 Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

PMID 20668259 2010 Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.