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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Kcnt1 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 KCNT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2796 RGD objects have been annotated to epilepsy  (DOID:1826)
  • 7 papers in RGD have been used to annotate Kcnt1
  • Curation Notes: ClinVar Annotator: match by term: Epilepsy | ClinVar Annotator: match by term: Epilepsy syndrome | ClinVar Annotator: match by term: Seizure | ClinVar Annotator: match by term: Seizure disorder
  • Original References(s): PMID:17576681 PMID:18414213 PMID:23086396 PMID:23086397 PMID:24319675 PMID:24591078 PMID:25326635 PMID:25326637 PMID:25339316 PMID:25482562 PMID:25741868 PMID:26105150 PMID:26122718 PMID:26140313 PMID:26467025 PMID:26648591 PMID:26740507 PMID:26786403 PMID:27029629 PMID:27081515 PMID:27652284 PMID:28488083 PMID:28492532 PMID:28554332 PMID:28987752 PMID:29358611 PMID:29422393 PMID:30182418 PMID:9536098


  • An association has been curated linking Kcnt1 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 KCNT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2796 RGD objects have been annotated to epilepsy  (DOID:1826)
  • 7 papers in RGD have been used to annotate Kcnt1
  • Curation Notes: ClinVar Annotator: match by term: Epilepsy syndrome | ClinVar Annotator: match by term: Seizure
  • Original References(s): PMID:17576681 PMID:18414213 PMID:23086396 PMID:23086397 PMID:24319675 PMID:24591078 PMID:25326635 PMID:25326637 PMID:25339316 PMID:25482562 PMID:25741868 PMID:26105150 PMID:26122718 PMID:26140313 PMID:26467025 PMID:26648591 PMID:26740507 PMID:26786403 PMID:27029629 PMID:27081515 PMID:27652284 PMID:28488083 PMID:28492532 PMID:28554332 PMID:28987752 PMID:29100083 PMID:29358611 PMID:29422393 PMID:30182418 PMID:9536098


  • An association has been curated linking Kcnt1 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 KCNT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2796 RGD objects have been annotated to epilepsy  (DOID:1826)
  • 7 papers in RGD have been used to annotate Kcnt1
  • Curation Notes: ClinVar Annotator: match by term: Epilepsy | ClinVar Annotator: match by term: Epilepsy syndrome | ClinVar Annotator: match by term: Seizure
  • Original References(s): PMID:23086396 PMID:23086397 PMID:24319675 PMID:24591078 PMID:25326635 PMID:25326637 PMID:25482562 PMID:25741868 PMID:26122718 PMID:26140313 PMID:26648591 PMID:26740507 PMID:26993267 PMID:27029629 PMID:27081515 PMID:27652284 PMID:28492532 PMID:28987752 PMID:29100083 PMID:30182418


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