Gene: FUS (FUS RNA binding protein) Pan paniscus
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Symbol:
FUS
Name:
FUS RNA binding protein
Description:
ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); estrogen receptor binding (ortholog); INVOLVED IN cellular response to calcium ion (ortholog); mRNA splicing, via spliceosome (ortholog); mRNA stabilization (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis (ortholog); amyotrophic lateral sclerosis type 1 (ortholog); amyotrophic lateral sclerosis type 6 (ortholog); FOUND IN dendritic spine head (ortholog); nucleoplasm (ortholog); nucleus (ortholog)
Type:
protein-coding
RefSeq Status:
MODEL
Also known as:
fused in sarcoma; RNA-binding protein FUS
Orthologs:
Latest Assembly:
PanPan1.1 - Bonobo PanPan1.1 Assembly
Position:
Bonobo Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl PanPan1.1 16 31,551,035 - 31,562,494 (+) NCBI panpan1.1 PanPan1.1 Bonobo Cytomap 16 NCBI
JBrowse:
View Region in Genome Browser (JBrowse)
Model
Disease Annotations
Imported Annotations - ClinVar
amyotrophic lateral sclerosis type 1 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic Lateral Sclerosis, Dominant ClinVar PMID:22292843 more ... amyotrophic lateral sclerosis type 1 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic Lateral Sclerosis, Dominant ClinVar PMID:20124201 more ... amyotrophic lateral sclerosis type 1 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic Lateral Sclerosis, Dominant ClinVar PMID:21261515 more ... amyotrophic lateral sclerosis type 1 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic Lateral Sclerosis, Dominant ClinVar PMID:25741868 , PMID:28492532 amyotrophic lateral sclerosis type 1 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic Lateral Sclerosis, Dominant ClinVar amyotrophic lateral sclerosis type 1 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic Lateral Sclerosis, Dominant ClinVar PMID:25741868 , PMID:26467025 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:25741868 , PMID:26467025 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:20124201 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:12858291 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:21261515 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:19741215 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:22722621 , PMID:28492532 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:22863194 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis 6, autosomal recessive ClinVar PMID:19251627 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:28492532 , PMID:28642336 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:19251627 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:28273913 , PMID:28492532 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:26601740 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:28492532 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:20385912 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:12840784 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:20668259 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:19861302 , PMID:22863194 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:19861302 , PMID:20385912 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:19251627 , PMID:19251628 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:25741868 , PMID:28492532 amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:22292843 more ... amyotrophic lateral sclerosis type 6 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 6 ClinVar PMID:20660363 more ... branched-chain keto acid dehydrogenase kinase deficiency ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Branched-chain keto acid dehydrogenase kinase deficiency ClinVar PMID:25741868 dystonia ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Dystonia ClinVar PMID:25741868 essential tremor 4 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Tremor, hereditary essential, 4 ClinVar PMID:22863194 essential tremor 4 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Tremor, hereditary essential, 4 ClinVar PMID:22863194 more ... essential tremor 4 ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Tremor, hereditary essential, 4 ClinVar PMID:19861302 , PMID:22863194 genetic disease ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:19251627 more ... spinal muscular atrophy ISS RGD:1318882 9068941 ClinVar Annotator: match by term: Distal spinal muscular atrophy ClinVar
Gene Ontology Annotations
