2005, PrionDB.
This data was extracted from Medline abstracts and full texts (when available) in an automated manner.
The table below describes the selected point mutation and provides links to other documents. The sentence(s) where the point mutation Q212P was found are listed after the table.
The mutated residues are also indicated in the family sequence alignments and hyperlinked to the corresponding mutation pages.
| Point mutation: | Q212P | |
| Domain: | Not determined | |
| General numbering (PrionDB): | - | |
| Protein: | PRIO_HUMAN (PRNP) | Swiss-Prot Cross-reference table Family page |
| Other point mutations / same protein / same position | Point mutations at position 212 in PRIO_HUMAN | |
| Other point mutations / same protein | List of mutations in PRIO_HUMAN | |
| Family alignments |
Mammalian prion proteins Prion proteins (PRP, PRNP) | |
| Other point mutations / same position |
Position 212 in Mammalian prion proteins family Position 212 in Prion proteins (PRP, PRNP) family | |
| Reference: | A cluster of familial Creutzfeldt-Jakob disease mutations recapitulate conserved residues in Doppel: a case of molecular mimicry? Mastrangelo P, Serpell L, Dafforn T, Lesk A, Fraser P, Westaway D FEBS Lett 2002 Dec 4;532(1-2):21-6. | Medline |
| Other point mutations / same article | List | |
| Text source | HTML and PDF full texts | |
| Validation status | True positive |
Relevant sentences:
Q212P
cmbi.ru.nl), 22-Aug-2005