Variant: rs1161032867 

    present in Gene: FUS
    present in Chromosome: 16
    Position on Chromosome: 31191070
    Alleles of this Variant: G/-;GGGG

rs1161032867 in FUS gene and Movement Disorders PMID 20385912 2010 Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis.

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

PMID 26362943 2015 De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.

PMID 23474818 2013 ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules.

PMID 22863194 2012 Exome sequencing identifies FUS mutations as a cause of essential tremor.

PMID 24280224 2014 Intranuclear aggregation of mutant FUS/TLS as a molecular pathomechanism of amyotrophic lateral sclerosis.

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