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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Nod2 and Behcet's disease in Chinchilla lanigera.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens)
  • 66 RGD objects have been annotated to Behcet's disease  (DOID:13241)
  • 2 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snp, insertion:exons:p.R702W, p.L1007insC (human)
  • Original References(s): PMID:19748964 REF_RGD_ID:8158059


    • An association has been curated linking Nod2 and Behcet's disease in Chinchilla lanigera.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens)
  • 66 RGD objects have been annotated to Behcet's disease  (DOID:13241)
  • 2 papers in RGD have been used to annotate Nod2
  • Qualifier: no_association
  • Curation Notes: DNA:mutations:cds:p.G908R,p.R702W,p.L1007fsinsC(human)
  • Original References(s): PMID:15515785 REF_RGD_ID:13204711


    • An association has been curated linking Nod2 and Behcet's disease in Chinchilla lanigera.        

  • 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]
  • 66 RGD objects have been annotated to Behcet's disease  (DOID:13241)
  • 2 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Behcet disease
  • Original References(s): PMID:28492532


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