Search on: CREUTZFELDT JAKOB DISEASE PROTEIN 
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Descriptor English:   Prion Proteins 
Descriptor Spanish:   Proteínas Priónicas 
Descriptor Portuguese:   Proteínas Priônicas 
Synonyms English:   AltPrP
Alternative Prion Protein
CD230 Antigen
Creutzfeldt-Jakob Disease Protein
Fatal Familial Insomnia Protein
Major Prion Protein
Prion Protein
Antigen, CD230
Creutzfeldt Jakob Disease Protein
Prion Protein, Alternative
Prion Protein, Major
PrP Proteins  
Tree Number:   D12.776.395.550.448.600
D12.776.543.484.500.625
D12.776.543.550.418.600
D12.776.785.340
D23.050.301.264.035.534
D23.101.100.110.534
Definition English:   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. 
History Note English:   2017: for PRION PROTEINS use PRIONS 1991-2016 
Allowable Qualifiers English:  
AD administration & dosage AE adverse effects
AG agonists AN analysis
AI antagonists & inhibitors BI biosynthesis
BL blood CF cerebrospinal fluid
CS chemical synthesis CH chemistry
CL classification CT contraindications
DF deficiency DE drug effects
EC economics GE genetics
HI history IM immunology
IP isolation & purification ME metabolism
PK pharmacokinetics PD pharmacology
PH physiology PO poisoning
RE radiation effects SE secretion
ST standards SD supply & distribution
TU therapeutic use TO toxicity
UL ultrastructure UR urine
Record Number:   56625 
Unique Identifier:   D000072002 

Occurrence in VHL:
 

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