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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking KRAS 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:8563214 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 75 papers in RGD have been used to annotate KRAS
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:16474405 PMID:16987887 PMID:17056636 PMID:17704260 PMID:17875937 PMID:18958496 PMID:19020799 PMID:20949621 PMID:21686179 PMID:21784453 PMID:23885229 PMID:24033266 PMID:24803665 PMID:25359213 PMID:25741868 PMID:28492532 PMID:29493581


    • An association has been curated linking KRAS 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:8563212 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 75 papers in RGD have been used to annotate KRAS
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:16474404 PMID:16474405 PMID:16773572 PMID:17056636 PMID:17551339 PMID:17875937 PMID:18456719 PMID:20949621 PMID:21062266 PMID:21871821 PMID:24033266 PMID:24703799 PMID:25326637 PMID:25741868 PMID:28492532


    • An association has been curated linking KRAS 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:40887039 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 75 papers in RGD have been used to annotate KRAS
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:26854235


    • An association has been curated linking KRAS 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:8563217 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 75 papers in RGD have been used to annotate KRAS
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:17056636 PMID:18386799 PMID:20949621 PMID:26037647


    • An association has been curated linking KRAS 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:8563211 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 75 papers in RGD have been used to annotate KRAS
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:16474404 PMID:17056636 PMID:19396835 PMID:20949621 PMID:24033266 PMID:24803665 PMID:25741868 PMID:26242988 PMID:28492532 PMID:28650561 PMID:29493581


    • An association has been curated linking KRAS 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:8563206 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 75 papers in RGD have been used to annotate KRAS
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:12460918 PMID:15696205 PMID:16361624 PMID:16434492 PMID:16618717 PMID:17332249 PMID:17384584 PMID:18316791 PMID:18794081 PMID:19018267 PMID:19075190 PMID:19114683 PMID:19255327 PMID:19679400 PMID:19773371 PMID:20921462 PMID:20921465 PMID:20978259 PMID:21063026 PMID:21228335 PMID:21398618 PMID:21975775 PMID:22392911 PMID:22407852 PMID:22571758 PMID:22734028 PMID:2278970 PMID:23182985 PMID:23406027 PMID:24033266 PMID:24558511 PMID:24720724 PMID:25157968 PMID:2547513 PMID:25705018 PMID:25741868 PMID:25808193 PMID:26623049 PMID:28492532 PMID:3122217 PMID:3627975


    • An association has been curated linking KRAS 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:8609410 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 75 papers in RGD have been used to annotate KRAS
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266 PMID:24356096 PMID:24728327 PMID:25741868


    • An association has been curated linking KRAS 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:156068284|RGD:329369780|RGD:40887040|RGD:40887622 (Homo sapiens) & RGD:156068284|RGD:329369780|RGD:40887040|RGD:40887622 (Homo sapiens) & RGD:156068284|RGD:329369780|RGD:40887040|RGD:40887622 (Homo sapiens) & RGD:156068284|RGD:329369780|RGD:40887040|RGD:40887622 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 75 papers in RGD have been used to annotate KRAS
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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