- Concept UI
- M000616231
- Registry Numbers
- 0
- Scope Note
- Membrane glycosylphosphatidylinositol-anchored glycoproteins that may aggregate into rod-like structures. The prion protein (PRNP) gene is characterized by five TANDEM REPEAT SEQUENCES that encode a highly unstable protein region of five octapeptide repeats. Mutations in the repeat region and elsewhere in this gene are associated with CREUTZFELDT-JAKOB DISEASE; FATAL FAMILIAL INSOMNIA; GERSTMANN-STRAUSSLER DISEASE; Huntington disease-like 1, and KURU.
- Terms
-
Prion Proteins
Preferred Term
Term UI
T033391
Date10/11/1991
LexicalTag
NON
ThesaurusID
NLM (1993)
-
PrP Proteins
Term UI
T033392
Date12/07/1993
LexicalTag
NON
ThesaurusID
NLM (1995)
-
Fatal Familial Insomnia Protein
Term UI
T000897859
Date03/29/2016
LexicalTag
NON
ThesaurusID
NLM (2017)
-
Prion Protein
Term UI
T000897856
Date03/29/2016
LexicalTag
NON
ThesaurusID
NLM (2017)
-
CD230 Antigen
Term UI
T000897857
Date03/29/2016
LexicalTag
ABX
ThesaurusID
NLM (2017)
-
Creutzfeldt-Jakob Disease Protein
Term UI
T000897858
Date03/29/2016
LexicalTag
NON
ThesaurusID
NLM (2017)
-
Major Prion Protein
Term UI
T000897855
Date03/29/2016
LexicalTag
NON
ThesaurusID
NLM (2017)