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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Prion Proteins [Chemical/Ingredient] | |
| Synonyms |
Creutzfeldt-Jakob Disease Protein Major Prion Protein Prion Protein CD230 Antigen Fatal Familial Insomnia Protein Prion Proteins PrP Proteins |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000193033 |
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| altLabel |
Creutzfeldt-Jakob Disease Protein Major Prion Protein Prion Protein CD230 Antigen Fatal Familial Insomnia Protein Prion Proteins PrP Proteins
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| cui |
C4082486
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| MESH DEFINITION |
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.
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| MESH DUI |
D000072002
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| MeSH name |
Prion Proteins
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|
| MESH UI |
M000616231
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| NDFRT kind |
INGREDIENT_KIND
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| notation |
N0000193033
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| NUI |
N0000193033
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|
| prefLabel |
Prion Proteins [Chemical/Ingredient]
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| tui |
T116
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| subClassOf |
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