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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Tnf and hemochromatosis in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Krayenbuehl PA, etal., Clin Chem. 2006 Aug;52(8):1552-8. Epub 2006 Jun 22.
  • The annotation has been inferred from sequence orthology with TNF (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 additional annotations were made from Krayenbuehl PA, etal., Clin Chem. 2006 Aug;52(8):1552-8. Epub 2006 Jun 22.
  • 24 RGD objects have been annotated to hemochromatosis  (DOID:2352)
  • 632 papers in RGD have been used to annotate Tnf
  • Curation Notes: DNA:SNP:promoter:-308G>A (human)


    • An association has been curated linking Tnf and hemochromatosis in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Fargion S, etal., Blood. 2001 Jun 15;97(12):3707-12.
  • The annotation has been inferred from sequence orthology with TNF (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Fargion S, etal., Blood. 2001 Jun 15;97(12):3707-12.
  • 24 RGD objects have been annotated to hemochromatosis  (DOID:2352)
  • 632 papers in RGD have been used to annotate Tnf
  • Curation Notes: DNA:SNP:promoter:-238G>A (rs361525) (human)


    • An association has been curated linking Tnf and hemochromatosis in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TNF (Homo sapiens) [(EXP) inferred from experiment]
  • 24 RGD objects have been annotated to hemochromatosis  (DOID:2352)
  • 632 papers in RGD have been used to annotate Tnf
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:16793930


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