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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Scn8a and epilepsy in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SCN8A (Homo sapiens) [(EXP) inferred from experiment]
  • 2802 RGD objects have been annotated to epilepsy  (DOID:1826)
  • 19 papers in RGD have been used to annotate Scn8a
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:23708187 PMID:29942082


    • An association has been curated linking Scn8a and epilepsy 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 SCN8A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2802 RGD objects have been annotated to epilepsy  (DOID:1826)
  • 19 papers in RGD have been used to annotate Scn8a
  • Curation Notes: ClinVar Annotator: match by term: Epilepsy | ClinVar Annotator: match by term: Seizures
  • Original References(s): PMID:25741868 PMID:26677014 PMID:26993267 PMID:27864847 PMID:28492532 PMID:28923014 PMID:29432985 PMID:30171078 PMID:30615093 PMID:31625145


    • An association has been curated linking Scn8a and epilepsy in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Scn8a (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2802 RGD objects have been annotated to epilepsy  (DOID:1826)
  • 19 papers in RGD have been used to annotate Scn8a


    • An association has been curated linking Scn8a and epilepsy 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 SCN8A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2802 RGD objects have been annotated to epilepsy  (DOID:1826)
  • 19 papers in RGD have been used to annotate Scn8a
  • Curation Notes: ClinVar Annotator: match by term: Epilepsy | ClinVar Annotator: match by term: Seizure
  • Original References(s): PMID:18414213 PMID:24888894 PMID:25741868 PMID:26677014 PMID:26993267 PMID:27210545 PMID:27864847 PMID:27875746 PMID:28492532 PMID:28923014 PMID:29432985 PMID:30171078 PMID:30185235 PMID:30615093 PMID:31625145 PMID:32581362


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