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Medical Subject Headings
Preferred Name | Prion Proteins | |
Synonyms |
Creutzfeldt-Jakob Disease Protein Major Prion Protein Antigen, CD230 Alternative Prion Protein Prion Protein CD230 Antigen Prion Protein, Alternative Fatal Familial Insomnia Protein Creutzfeldt Jakob Disease Protein Prion Protein, Major PrP Proteins AltPrP |
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Definitions |
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. An overlapping open reading frame within the PRNP gene that encodes a protein which is smaller and structurally unrelated to major prion protein. |
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ID |
http://purl.bioontology.org/ontology/MESH/D000072002 |
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altLabel |
Creutzfeldt-Jakob Disease Protein Major Prion Protein Antigen, CD230 Alternative Prion Protein Prion Protein CD230 Antigen Prion Protein, Alternative Fatal Familial Insomnia Protein Creutzfeldt Jakob Disease Protein Prion Protein, Major PrP Proteins AltPrP
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AQL |
AD AE AG AI AN BI BL CF CH CL CS DE DF EC GE HI IM IP ME PD PH PK PO RE SD ST TO TU UL UR
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cui |
C4082486 C4255061
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DC |
1
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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. An overlapping open reading frame within the PRNP gene that encodes a protein which is smaller and structurally unrelated to major prion protein.
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DX |
20170101
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HN |
2017: for PRION PROTEINS use PRIONS 1991-2016
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Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000096 http://purl.bioontology.org/ontology/MESH/Q000172 http://purl.bioontology.org/ontology/MESH/Q000627 http://purl.bioontology.org/ontology/MESH/Q000648 http://purl.bioontology.org/ontology/MESH/Q000493 http://purl.bioontology.org/ontology/MESH/Q000494 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000138 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000008 http://purl.bioontology.org/ontology/MESH/Q000009 http://purl.bioontology.org/ontology/MESH/Q000032 http://purl.bioontology.org/ontology/MESH/Q000037 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000302 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000592 http://purl.bioontology.org/ontology/MESH/Q000737 http://purl.bioontology.org/ontology/MESH/Q000819 http://purl.bioontology.org/ontology/MESH/Q000502 http://purl.bioontology.org/ontology/MESH/Q000506 http://purl.bioontology.org/ontology/MESH/Q000187 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000633 http://purl.bioontology.org/ontology/MESH/Q000600 |
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Inverse of RB |
0
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Machine permutation |
2017; for PRION PROTEINS see PRIONS 1991-2016
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Mapped from |
http://purl.bioontology.org/ontology/MESH/C437319 |
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MDA |
20160708
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MMR |
20230316
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MN |
D12.776.395.550.448.600 D09.400.430.890.448.600 D12.776.543.550.418.600 D12.776.543.484.500.625 D12.776.785.340
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notation |
D000072002
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prefLabel |
Prion Proteins
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TERMUI |
T000897855 T000897859 T000897857 T033392 T000897856 T000897862 T033391 T000897863 T000897858
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TH |
NLM (1993) NLM (1995) NLM (2017)
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tui |
T116
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subClassOf |
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