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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking LOC100361018 and retinitis pigmentosa-deafness 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 C10orf105 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 1 papers in RGD have been used to annotate LOC100361018
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome


  • An association has been curated linking LOC100361018 and retinitis pigmentosa-deafness 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 C10orf105 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 1 papers in RGD have been used to annotate LOC100361018
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking LOC100361018 and retinitis pigmentosa-deafness 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 C10orf105 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 1 papers in RGD have been used to annotate LOC100361018
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:24033266 PMID:28492532


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