Early onset dementia (encompassing fronto-temporal dementia and prion disease)
Gene: FUSEnsemblGeneIds (GRCh38): ENSG00000089280
EnsemblGeneIds (GRCh37): ENSG00000089280
OMIM: 137070, Gene2Phenotype
FUS is in 3 panels
2 reviews
simon mead (UCL)
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
ALS
Caroline Wright (Genomics England Curator)
Comment on list classification: Comment on list classification: Associated with ALS and on ALS panel; not definitely associated with FTLD in OMIM, ClinVar or literature - mostly ALS patients without dementiaCreated: 10 May 2016, 2:34 p.m.
Details
- Sources
-
- Expert Review Red
- UKGTN
- Phenotypes
-
- Dementia
- OMIM
- 137070
- Clinvar variants
- Variants in FUS
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Gene classified by Genomics England curator
Caroline Wright (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Gene classified by Genomics England curator
Caroline Wright (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)FUS was added to Early onset dementia (encompassing fronto-temporal dementia and prion disease)panel. Sources: UKGTN