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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking KCNQ3 and benign familial neonatal epilepsy in Sus scrofa.        

  • 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 KCNQ3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 RGD objects have been annotated to benign familial neonatal epilepsy  (DOID:14777)
  • 0 papers in RGD have been used to annotate KCNQ3
  • Curation Notes: ClinVar Annotator: match by term: Benign familial neonatal epilepsy | ClinVar Annotator: match by term: Benign familial neonatal seizures
  • Original References(s): PMID:18249525 PMID:18625963 PMID:19344764 PMID:19464834 PMID:21703448 PMID:22612257 PMID:23020937 PMID:23146207 PMID:23596459 PMID:23934111 PMID:24375629 PMID:24851285 PMID:25052858 PMID:25740509 PMID:25741868 PMID:26350515 PMID:26467025 PMID:26582918 PMID:28135719 PMID:28492532 PMID:28628100 PMID:29358611 PMID:29655203 PMID:30348901 PMID:30578330 PMID:31177578 PMID:31238879 PMID:33004838 PMID:34356170


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