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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Nod2 and Behcet's disease in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Uyar FA, etal., Clin Exp Rheumatol. 2004 Jul-Aug;22(4 Suppl 34):S50-2.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Uyar FA, etal., Clin Exp Rheumatol. 2004 Jul-Aug;22(4 Suppl 34):S50-2.
  • 73 RGD objects have been annotated to Behcet's disease  (DOID:13241)
  • 67 papers in RGD have been used to annotate Nod2
  • Qualifier: no_association
  • Curation Notes: DNA:mutations:cds:p.G908R,p.R702W,p.L1007fsinsC(human)

  • This annotation was curated on 2018-05-05 09:01:07.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Behcet's disease in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Kappen JH, etal., Rheumatology (Oxford). 2009 Nov;48(11):1375-7. doi: 10.1093/rheumatology/kep292. Epub 2009 Sep 11.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Kappen JH, etal., Rheumatology (Oxford). 2009 Nov;48(11):1375-7. doi: 10.1093/rheumatology/kep292. Epub 2009 Sep 11.
  • 73 RGD objects have been annotated to Behcet's disease  (DOID:13241)
  • 67 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snp, insertion:exons:p.R702W, p.L1007insC (human)

  • This annotation was curated on 2018-05-05 09:01:09.0 by RGD . For more information contact us

    An association has been curated linking Nod2 and Behcet's disease in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 73 RGD objects have been annotated to Behcet's disease  (DOID:13241)
  • 67 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Behcet's syndrome

  • This annotation was curated on 2019-10-08 13:09:58.0 by RGD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.