Annotation Detail
Information
- Associated Genes
- TARDBP
- Associated Variants
-
TARDBP p.Gly348Cys (p.G348C)
(
ENST00000700088.1,
ENST00000621790.4,
ENST00000240185.8,
ENST00000649624.1,
ENST00000629725.2,
ENST00000639083.1,
ENST00000616545.4,
ENST00000315091.7 )
TARDBP p.Asn352Ser (p.N352S) ( ENST00000315091.7, ENST00000240185.8, ENST00000700088.1, ENST00000616545.4, ENST00000621790.4, ENST00000629725.2, ENST00000639083.1, ENST00000649624.1 )
TARDBP p.Gly348Cys (p.G348C) ( ENST00000700088.1, ENST00000240185.8, ENST00000315091.7, ENST00000616545.4, ENST00000621790.4, ENST00000629725.2, ENST00000639083.1, ENST00000649624.1 )
TARDBP p.Asn352Ser (p.N352S) ( ENST00000700088.1, ENST00000240185.8, ENST00000315091.7, ENST00000616545.4, ENST00000621790.4, ENST00000629725.2, ENST00000639083.1, ENST00000649624.1 ) - Associated Disease
- Impaired cognition
- Source Database
- DisGeNET
- Description
- We identified 2 missense mutations (G348C and the novel N352S) in TARDBP in 2 small kindreds with a hereditary form of ALS with early spinal onset resulting in fatal respiratory insufficiency without clinical relevant bulbar symptoms or signs of cognitive impairment.
- Pubmed
- 18779421
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00135720936040152
- Year of publication
- 2008
Drugs