Annotation Detail
Information
- Associated Genes
- PRNP
- Associated Variants
-
PRNP p.Glu200Lys (p.E200K)
(
ENST00000379440.9,
ENST00000424424.2,
ENST00000430350.2,
ENST00000457586.2 )
PRNP p.Val210Ile (p.V210I) ( ENST00000379440.9, ENST00000424424.2, ENST00000430350.2, ENST00000457586.2 )
PRNP p.Glu200Lys (p.E200K) ( ENST00000379440.9, ENST00000424424.2, ENST00000430350.2, ENST00000457586.2 )
PRNP p.Val210Ile (p.V210I) ( ENST00000379440.9, ENST00000424424.2, ENST00000430350.2, ENST00000457586.2 ) - Associated Disease
- fatal familial insomnia
- Source Database
- DisGeNET
- Description
- Interestingly, type of prion disease (sporadic vs. genetic) and the PRNP mutation (E200K vs. V210I and FFI), codon 129 genotype, and PrP(Sc) type affected RT-QuIC response.
- Pubmed
- 24809690
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.587816554605694
- Year of publication
- 2014
Drugs