Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking SNCA and Parkinson's disease in Homo sapiens.        

  • The association was inferred from mutant phenotype (IMP)
  •  
  • The annotation was made from Masliah E, etal., Science 2000 Feb 18;287(5456):1265-9.
  • 2 additional annotations were made from Masliah E, etal., Science 2000 Feb 18;287(5456):1265-9.
  • 416 RGD objects have been annotated to Parkinson's disease  (DOID:14330)
  • 42 papers in RGD have been used to annotate SNCA
  • Curation Notes: human gene in a mouse model


  • An association has been curated linking Snca and Parkinson's disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Masliah E, etal., Science 2000 Feb 18;287(5456):1265-9.
  • The annotation has been inferred from sequence orthology with SNCA (Homo sapiens) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Masliah E, etal., Science 2000 Feb 18;287(5456):1265-9.
  • 416 RGD objects have been annotated to Parkinson's disease  (DOID:14330)
  • 75 papers in RGD have been used to annotate Snca
  • Curation Notes: human gene in a mouse model


  • An association has been curated linking Snca and Parkinson's disease in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Masliah E, etal., Science 2000 Feb 18;287(5456):1265-9.
  • The annotation has been inferred from sequence orthology with SNCA (Homo sapiens) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Masliah E, etal., Science 2000 Feb 18;287(5456):1265-9.
  • 416 RGD objects have been annotated to Parkinson's disease  (DOID:14330)
  • 41 papers in RGD have been used to annotate Snca
  • Curation Notes: human gene in a mouse model


  • Go Back to source page   Continue to Ontology report