Send us a Message



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

GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking PPARGC1A and Huntington's disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • 5 additional annotations were made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • 212 RGD objects have been annotated to Huntington's disease  (DOID:12858)
  • 107 papers in RGD have been used to annotate PPARGC1A
  • Qualifier: no_association
  • Curation Notes: DNA:missense mutation:cds:pT612M (rs3736265) (human)


  • An association has been curated linking PPARGC1A and Huntington's disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • 5 additional annotations were made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • 212 RGD objects have been annotated to Huntington's disease  (DOID:12858)
  • 107 papers in RGD have been used to annotate PPARGC1A
  • Qualifier: onset
  • Curation Notes: DNA:snps, haplotypes:multiple (human)


  • An association has been curated linking Ppargc1a and Huntington's disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • The annotation has been inferred from sequence orthology with PPARGC1A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • 212 RGD objects have been annotated to Huntington's disease  (DOID:12858)
  • 175 papers in RGD have been used to annotate Ppargc1a
  • Qualifier: no_association
  • Curation Notes: DNA:missense mutation:cds:pT612M (rs3736265) (human)


  • An association has been curated linking Ppargc1a and Huntington's disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • The annotation has been inferred from sequence orthology with PPARGC1A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • 212 RGD objects have been annotated to Huntington's disease  (DOID:12858)
  • 175 papers in RGD have been used to annotate Ppargc1a
  • Qualifier: onset
  • Curation Notes: DNA:snps, haplotypes:multiple (human)


  • An association has been curated linking Ppargc1a and Huntington's disease in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • The annotation has been inferred from sequence orthology with PPARGC1A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • 212 RGD objects have been annotated to Huntington's disease  (DOID:12858)
  • 112 papers in RGD have been used to annotate Ppargc1a
  • Qualifier: no_association
  • Curation Notes: DNA:missense mutation:cds:pT612M (rs3736265) (human)


  • An association has been curated linking Ppargc1a and Huntington's disease in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • The annotation has been inferred from sequence orthology with PPARGC1A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Weydt P, etal., Mol Neurodegener. 2009 Jan 8;4:3. doi: 10.1186/1750-1326-4-3.
  • 212 RGD objects have been annotated to Huntington's disease  (DOID:12858)
  • 112 papers in RGD have been used to annotate Ppargc1a
  • Qualifier: onset
  • Curation Notes: DNA:snps, haplotypes:multiple (human)


  • Go Back to source page   Continue to Ontology report