Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Kcnc3 and spinocerebellar ataxia type 13 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 KCNC3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 13  (DOID:0050963)
  • 13 papers in RGD have been used to annotate Kcnc3


  • An association has been curated linking Kcnc3 and spinocerebellar ataxia type 13 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 KCNC3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 13  (DOID:0050963)
  • 13 papers in RGD have been used to annotate Kcnc3
  • Curation Notes: ClinVar Annotator: match by term: KCNC3-related condition | ClinVar Annotator: match by term: Spinocerebellar ataxia type 13
  • Original References(s): PMID:10820125 PMID:16135769 PMID:16501573 PMID:18592334 PMID:19953606 PMID:20712895 PMID:21479265 PMID:21543613 PMID:22289912 PMID:22736459 PMID:22933745 PMID:23215817 PMID:23734863 PMID:23912307 PMID:24116147 PMID:25152487 PMID:25497598 PMID:25741868 PMID:25756792 PMID:25981959 PMID:26442672 PMID:26467025 PMID:28216058 PMID:28467418 PMID:28492532 PMID:30862666 PMID:32644043


  • An association has been curated linking Kcnc3 and spinocerebellar ataxia type 13 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 KCNC3 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 13  (DOID:0050963)
  • 13 papers in RGD have been used to annotate Kcnc3
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • Go Back to source page   Continue to Ontology report