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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking Csnk2b and autosomal dominant intellectual developmental disorder 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 CSNK2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 455 RGD objects have been annotated to autosomal dominant intellectual developmental disorder  (DOID:0060307)
  • 23 papers in RGD have been used to annotate Csnk2b
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant non-syndromic intellectual disability
  • Original References(s): PMID:25741868


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