Annotation Detail
Information
- Associated Genes
- NOTCH3
- Associated Variants
-
NOTCH3 p.Arg133Cys (p.R133C)
(
ENST00000263388.7 )
NOTCH3 p.Arg133Ser (p.R133S) ( ENST00000263388.7 )
NOTCH3 p.Arg133Cys (p.R133C) ( ENST00000263388.7 )
NOTCH3 p.Arg133Ser (p.R133S) ( ENST00000263388.7 ) - Associated Disease
- CADASIL Syndrome
- Source Database
- DisGeNET
- Description
- We have previously described a patient with cerebral autosomal-dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) caused by R133C mutation in NOTCH3 and with a concomitant myopathy caused by a G to A point mutation at base pair 5650 (5650G>A) in the gene encoding tRNA(Ala) in mitochondrial DNA (mtDNA).
- Pubmed
- 17276737
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.537478390901604
- Year of publication
- 2007
Drugs