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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking C3 and Nephropathy 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:15202220 (Homo sapiens)
  • 167 RGD objects have been annotated to Nephropathy  (HP:0000112)
  • 142 papers in RGD have been used to annotate C3
  • Curation Notes: ClinVar Annotator: match by term: Kidney disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C3 and Nephropathy 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:11626611 (Homo sapiens)
  • 167 RGD objects have been annotated to Nephropathy  (HP:0000112)
  • 142 papers in RGD have been used to annotate C3
  • Curation Notes: ClinVar Annotator: match by term: Kidney disease
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29888403


  • An association has been curated linking C3 and Nephropathy 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:155645411 (Homo sapiens)
  • 167 RGD objects have been annotated to Nephropathy  (HP:0000112)
  • 142 papers in RGD have been used to annotate C3
  • Curation Notes: ClinVar Annotator: match by term: Kidney disease
  • Original References(s): PMID:25741868


  • An association has been curated linking C3 and Nephropathy 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:11626265 (Homo sapiens)
  • 167 RGD objects have been annotated to Nephropathy  (HP:0000112)
  • 142 papers in RGD have been used to annotate C3
  • Curation Notes: ClinVar Annotator: match by term: Kidney disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C3 and Nephropathy 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:15172098 (Homo sapiens)
  • 167 RGD objects have been annotated to Nephropathy  (HP:0000112)
  • 142 papers in RGD have been used to annotate C3
  • Curation Notes: ClinVar Annotator: match by term: Kidney disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C3 and Nephropathy 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:10395514 (Homo sapiens)
  • 167 RGD objects have been annotated to Nephropathy  (HP:0000112)
  • 142 papers in RGD have been used to annotate C3
  • Curation Notes: ClinVar Annotator: match by term: Kidney disease
  • Original References(s): PMID:25741868


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