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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Rab3gap1 and Warburg micro 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 RAB3GAP1 (Homo sapiens) [(EXP) inferred from experiment]
  • 4 RGD objects have been annotated to Warburg micro syndrome  (DOID:0060237)
  • 7 papers in RGD have been used to annotate Rab3gap1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking Rab3gap1 and Warburg micro 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 RAB3GAP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Warburg micro syndrome  (DOID:0060237)
  • 7 papers in RGD have been used to annotate Rab3gap1
  • Curation Notes: ClinVar Annotator: match by OMIM:600118


  • An association has been curated linking Rab3gap1 and Warburg micro 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 RAB3GAP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Warburg micro syndrome  (DOID:0060237)
  • 7 papers in RGD have been used to annotate Rab3gap1
  • Curation Notes: ClinVar Annotator: match by term: Warburg micro syndrome
  • Original References(s): PMID:25741868 PMID:26467025


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