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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:24033266


  • An association has been curated linking Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome


  • An association has been curated linking Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:12075507 PMID:16963483 PMID:19683999 PMID:21174530 PMID:24033266 PMID:25741868 PMID:26969326 PMID:27018795 PMID:28492532


  • An association has been curated linking Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • 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 Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:18429043 PMID:21228398 PMID:21569298 PMID:22135276 PMID:22995991 PMID:24033266 PMID:25474345 PMID:25741868 PMID:28492532 PMID:30029624 PMID:30718709


  • An association has been curated linking Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Cdh23 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 CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to retinitis pigmentosa-deafness syndrome  (DOID:0110829)
  • 22 papers in RGD have been used to annotate Cdh23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome
  • Original References(s): PMID:24033266 PMID:28492532


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