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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking CASP8 and genetic disease 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:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens) & RGD:155930014|RGD:156053825|RGD:156126080|RGD:156185085|RGD:156271983|RGD:401880011|RGD:405735739|RGD:405735749|RGD:405736468|RGD:407476140 (Homo sapiens)
  • 27242 RGD objects have been annotated to genetic disease  (DOID:630)
  • 76 papers in RGD have been used to annotate CASP8
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking CASP8 and genetic disease 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:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens) & RGD:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens) & RGD:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens) & RGD:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens) & RGD:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens) & RGD:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens) & RGD:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens) & RGD:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens) & RGD:126744155|RGD:126771481|RGD:127248849|RGD:13820989|RGD:151781554|RGD:151817988|RGD:151882472|RGD:152032671|RGD:156068064 (Homo sapiens)
  • 27242 RGD objects have been annotated to genetic disease  (DOID:630)
  • 76 papers in RGD have been used to annotate CASP8
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


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