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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Rnf168 and Riddle syndrome 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 RNF168 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Riddle syndrome  (DOID:0090113)
  • 7 papers in RGD have been used to annotate Rnf168


    • An association has been curated linking Rnf168 and Riddle syndrome 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 RNF168 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Riddle syndrome  (DOID:0090113)
  • 7 papers in RGD have been used to annotate Rnf168
  • Curation Notes: ClinVar Annotator: match by term: RIDDLE syndrome | ClinVar Annotator: match by term: RNF168-related condition
  • Original References(s): PMID:19203578 PMID:21394101 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking Rnf168 and Riddle syndrome in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Rnf168 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Riddle syndrome  (DOID:0090113)
  • 7 papers in RGD have been used to annotate Rnf168
  • Curation Notes: OMIM:611943


    • An association has been curated linking Rnf168 and Riddle syndrome 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 RNF168 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Riddle syndrome  (DOID:0090113)
  • 7 papers in RGD have been used to annotate Rnf168
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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