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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking IL1B and antisynthetase syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:26896411 (Homo sapiens)
  • 1 RGD objects have been annotated to antisynthetase syndrome  (DOID:0080744)
  • 354 papers in RGD have been used to annotate IL1B
  • Curation Notes: ClinVar Annotator: match by term: Antisynthetase syndrome


  • An association has been curated linking IL1B and antisynthetase syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:26896409 (Homo sapiens)
  • 1 RGD objects have been annotated to antisynthetase syndrome  (DOID:0080744)
  • 354 papers in RGD have been used to annotate IL1B
  • Curation Notes: ClinVar Annotator: match by term: Antisynthetase syndrome


  • An association has been curated linking IL1B and antisynthetase syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:26896408 (Homo sapiens)
  • 1 RGD objects have been annotated to antisynthetase syndrome  (DOID:0080744)
  • 354 papers in RGD have been used to annotate IL1B
  • Curation Notes: ClinVar Annotator: match by term: Antisynthetase syndrome
  • Original References(s): PMID:18550579


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