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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking Scn1b and developmental and epileptic encephalopathy 52 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 SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to developmental and epileptic encephalopathy 52  (DOID:0080455)
  • 21 papers in RGD have been used to annotate Scn1b
  • Curation Notes: ClinVar Annotator: match by term: Epileptic encephalopathy, early infantile, 52
  • Original References(s): PMID:28218389


  • An association has been curated linking Scn1b and developmental and epileptic encephalopathy 52 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 SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to developmental and epileptic encephalopathy 52  (DOID:0080455)
  • 21 papers in RGD have been used to annotate Scn1b
  • Curation Notes: ClinVar Annotator: match by term: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52
  • Original References(s): PMID:23148524


  • An association has been curated linking Scn1b and developmental and epileptic encephalopathy 52 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 SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to developmental and epileptic encephalopathy 52  (DOID:0080455)
  • 21 papers in RGD have been used to annotate Scn1b
  • Curation Notes: ClinVar Annotator: match by term: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52
  • Original References(s): PMID:19710327


  • An association has been curated linking Scn1b and developmental and epileptic encephalopathy 52 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to developmental and epileptic encephalopathy 52  (DOID:0080455)
  • 21 papers in RGD have been used to annotate Scn1b


  • An association has been curated linking Scn1b and developmental and epileptic encephalopathy 52 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 SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to developmental and epileptic encephalopathy 52  (DOID:0080455)
  • 21 papers in RGD have been used to annotate Scn1b
  • Curation Notes: ClinVar Annotator: match by term: Epileptic encephalopathy, early infantile, 52
  • Original References(s): PMID:21994374 PMID:22155597 PMID:22155598 PMID:22284586 PMID:22840528 PMID:23414114 PMID:23465283 PMID:23861362 PMID:24033266 PMID:25253298 PMID:25741868 PMID:26498160 PMID:27435932 PMID:27896052 PMID:28341588 PMID:28492532 PMID:28837624 PMID:29758173


  • An association has been curated linking Scn1b and developmental and epileptic encephalopathy 52 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 SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to developmental and epileptic encephalopathy 52  (DOID:0080455)
  • 21 papers in RGD have been used to annotate Scn1b
  • Curation Notes: ClinVar Annotator: match by term: Epileptic encephalopathy, early infantile, 52
  • Original References(s): PMID:25741868 PMID:28218389


  • An association has been curated linking Scn1b and developmental and epileptic encephalopathy 52 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 SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to developmental and epileptic encephalopathy 52  (DOID:0080455)
  • 21 papers in RGD have been used to annotate Scn1b
  • Curation Notes: ClinVar Annotator: match by term: Epileptic encephalopathy, early infantile, 52
  • Original References(s): PMID:25741868


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