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1 Annotations Found.

An association has been curated linking Foxc2 and genetic disease in Rattus norvegicus.        

  • 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 FOXC2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 13282 RGD objects have been annotated to genetic disease  (DOID:630)
  • 14 papers in RGD have been used to annotate Foxc2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:12114478 PMID:16081467 PMID:19760751 PMID:25252123 PMID:25741868 PMID:27276711 PMID:28492532 PMID:28724617 PMID:31460188 PMID:32411386 PMID:33897756 PMID:35716761

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