FUS gene homepage

General information
Gene symbol FUS
Gene name fused in sarcoma
Chromosome 16
Chromosomal band p11.2
Imprinted Unknown
Genomic reference NG_012889.2
Transcript reference NM_004960.3
Exon/intron information NM_004960.3 exon/intron table
Associated with diseases ALS-6, Tremor, hereditary essential, 4
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 126
Unique public DNA variants reported 73
Individuals with public variants 132
Hidden variants 2
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created April 29, 2010
Date last updated February 02, 2018
Version FUS:180202

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_004960.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/FUS
External URL Orphanet
HGNC 4010
Entrez Gene 2521
PubMed articles FUS
OMIM - Gene 137070
OMIM - Diseases ALS-6 (sclerosis, lateral, amyotrophic, type type 6 (ALS-6))
Tremor, hereditary essential, 4
HGMD FUS
GeneCards FUS
GeneTests FUS


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00008204 16 transcript variant 1 NM_004960.3 NP_004951.1 126


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