Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 5621
  • Symbol: PRNP
  • Description: prion protein (Kanno blood group)

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Disease_Term Source Rank Other Values
Creutzfeldt-Jakob disease, 123400 (3) OMIM high
  • Genome region : 20p13
  • OMIM_ID : 123400 OMIM phenotype ID
  • OMIM_ID : 176640 OMIM gene ID
Gerstmann-Straussler disease, 137440 (3) OMIM high
  • Genome region : 20p13
  • OMIM_ID : 137440 OMIM phenotype ID
  • OMIM_ID : 176640 OMIM gene ID
Prion disease with protracted course, 606688 (3) OMIM high
  • Genome region : 20p13
  • OMIM_ID : 176640 OMIM gene ID
  • OMIM_ID : 606688 OMIM phenotype ID
Huntington disease-like 1, 603218 (3) OMIM high
  • Genome region : 20p13
  • OMIM_ID : 176640 OMIM gene ID
  • OMIM_ID : 603218 OMIM phenotype ID
{Kuru, susceptibility to}, 245300 (3) OMIM high
  • Genome region : 20p13
  • OMIM_ID : 176640 OMIM gene ID
  • OMIM_ID : 245300 OMIM phenotype ID
Insomnia, fatal familial, 600072 (3) OMIM high
  • Genome region : 20p13
  • OMIM_ID : 176640 OMIM gene ID
  • OMIM_ID : 600072 OMIM phenotype ID
Cerebral amyloid angiopathy, PRNP-related, 137440 (3) OMIM high
  • Genome region : 20p13
  • OMIM_ID : 137440 OMIM phenotype ID
  • OMIM_ID : 176640 OMIM gene ID
Platelet aggregation GWAS high
Creutzfeldt-Jakob disease GWAS high
Creutzfeldt-Jakob disease (sporadic) GWAS high
Prion diseases GWAS high
Creutzfeldt-Jakob disease (variant) GWAS high