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Results for Proteins associated with the Gene: PRNP
PRNP
5621


Known Diseases associated with this Protein:
  CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED
  CREUTZFELDT-JAKOB DISEASE
  CREUTZFELDT-JAKOB DISEASE (CJD)
  CREUTZFELDT-JAKOB DISEASE, INCLUDED
  FATAL FAMILIAL INSOMNIA
  FATAL FAMILIAL INSOMNIA (FFI)
  FATAL FAMILIAL INSOMNIA, INCLUDED
  GERSTMANN-STRAUSSLER DISEASE
  GERSTMANN-STRAUSSLER DISEASE (GSD)
  KURU, PROTECTION AGAINST
  RECLASSIFIED - VARIANT OF UNKNOWN SIGNIFICANCE
  SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES
  SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES, INCLUDED
45
8
28
1
24
Tips:
 The Domains on the Default View are decided by HMMER's search E-Value of the Protein against the Domain model.
 Clicking a check box on the left will display or hide the corresponding domain(s).
 To view the Protein page, either click on the protein links in the box to the left or the blue bar above the Protein's graphic.


Default View:

Prion_bPrPp - pfam11587
PRP - smart00157



Default View:

Prion_bPrPp - pfam11587
PRP - smart00157
Prion - pfam00377


RefSeq Protein: NP_898902
   Default View:



Default View:

Prion_bPrPp - pfam11587
PRP - smart00157
Prion - pfam00377



Default View:

Prion_bPrPp - pfam11587
PRP - smart00157
Prion - pfam00377



Default View:

Prion_bPrPp - pfam11587
PRP - smart00157
Prion - pfam00377



Default View:

Prion_bPrPp - pfam11587
PRP - smart00157
Prion - pfam00377


RefSeq Protein: NP_000302
   Default View:




Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
NP_000302Prion_bPrPppfam115871282.3e-16
NP_000302PRPsmart00157232401.4e-158



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