Annotation Detail
Information
- Associated Genes
- PRNP
- Associated Variants
-
PRNP p.Asp178Asn (p.D178N)
(
ENST00000430350.2,
ENST00000457586.2,
ENST00000424424.2,
ENST00000379440.9 )
PRNP p.Asp178Asn (p.D178N) ( ENST00000424424.2, ENST00000379440.9, ENST00000457586.2, ENST00000430350.2 ) - Associated Disease
- fatal familial insomnia
- Source Database
- DisGeNET
- Description
- The authors present clinical, sleep, and neuroendocrine features of a patient with genetically confirmed fatal familial insomnia (D178N mutation with heterozygosity at codon 129 of the prion protein gene).
- Pubmed
- 15623717
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.587816554605694
- Year of publication
- 2004
Drugs