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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Nup188 and Sandestig-Stefanova 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 NUP188 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sandestig-Stefanova Syndrome  (DOID:9008661)
  • 3 papers in RGD have been used to annotate Nup188


  • An association has been curated linking Nup188 and Sandestig-Stefanova 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 NUP188 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sandestig-Stefanova Syndrome  (DOID:9008661)
  • 3 papers in RGD have been used to annotate Nup188
  • Curation Notes: ClinVar Annotator: match by term: SANDESTIG-STEFANOVA SYNDROME
  • Original References(s): PMID:32275884


  • An association has been curated linking Nup188 and Sandestig-Stefanova 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 NUP188 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sandestig-Stefanova Syndrome  (DOID:9008661)
  • 3 papers in RGD have been used to annotate Nup188
  • Curation Notes: ClinVar Annotator: match by term: SANDESTIG-STEFANOVA SYNDROME
  • Original References(s): PMID:32021605


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