PrionDB: Point mutations extracted from the literature - PRND_HUMAN

2005, PrionDB.

This data was extracted from medline abstracts and full text papers (when available) in an automated manner.

Each point mutation is linked to the entry specific to the residue position. Citations are linked to the list of point mutations found in the corresponding articles. The last column allows you to go back to the original text via Medline.

Protein	PRND_HUMAN (PRND,DPL)	Swiss-Prot Cross-reference table Family page
Family alignments	Prion-like protein doppel precursor (PrPLP)

Mutation Location General numbering Reference
P56L Not determined Schroder B et al., Hum Genet 2001 Medline

P56P Not determined Schroder B et al., Hum Genet 2001 Medline

V136A Not determined Eghiaian F et al., Proc Natl Acad Sci U S A 2004 Medline

Mutation	Location	Reference
P56L	Not determined	Schroder B et al., Hum Genet 2001	Medline
P56P	Not determined	Schroder B et al., Hum Genet 2001	Medline
V136A	Not determined	Eghiaian F et al., Proc Natl Acad Sci U S A 2004	Medline

F.Horn (priondbcmbi.ru.nl), 22-Aug-2005