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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Copb2 and primary autosomal recessive microcephaly 19 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 COPB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to primary autosomal recessive microcephaly 19  (DOID:0070281)
  • 10 papers in RGD have been used to annotate Copb2


  • An association has been curated linking Copb2 and primary autosomal recessive microcephaly 19 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 COPB2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to primary autosomal recessive microcephaly 19  (DOID:0070281)
  • 10 papers in RGD have been used to annotate Copb2
  • Curation Notes: ClinVar Annotator: match by term: COPB2-related condition | ClinVar Annotator: match by term: Microcephaly 19, primary, autosomal recessive
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29036432 PMID:34450031


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