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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Fth1 and autosomal dominant vitreoretinochoroidopathy 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 FTH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant vitreoretinochoroidopathy  (DOID:0111569)
  • 25 papers in RGD have been used to annotate Fth1
  • Curation Notes: ClinVar Annotator: match by term: Vitreoretinochoroidopathy


  • An association has been curated linking Fth1 and autosomal dominant vitreoretinochoroidopathy 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 FTH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant vitreoretinochoroidopathy  (DOID:0111569)
  • 25 papers in RGD have been used to annotate Fth1
  • Curation Notes: ClinVar Annotator: match by term: Vitreoretinochoroidopathy
  • Original References(s): PMID:14615048


  • An association has been curated linking Fth1 and autosomal dominant vitreoretinochoroidopathy 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 FTH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant vitreoretinochoroidopathy  (DOID:0111569)
  • 25 papers in RGD have been used to annotate Fth1
  • Curation Notes: ClinVar Annotator: match by term: Vitreoretinochoroidopathy
  • Original References(s): PMID:10453731 PMID:11713080 PMID:17898294 PMID:28492532


  • An association has been curated linking Fth1 and autosomal dominant vitreoretinochoroidopathy 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 FTH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant vitreoretinochoroidopathy  (DOID:0111569)
  • 25 papers in RGD have been used to annotate Fth1
  • Curation Notes: ClinVar Annotator: match by term: Vitreoretinochoroidopathy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Fth1 and autosomal dominant vitreoretinochoroidopathy 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 FTH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant vitreoretinochoroidopathy  (DOID:0111569)
  • 25 papers in RGD have been used to annotate Fth1
  • Curation Notes: ClinVar Annotator: match by term: Vitreoretinochoroidopathy
  • Original References(s): PMID:28492532


  • An association has been curated linking Fth1 and autosomal dominant vitreoretinochoroidopathy 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 FTH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant vitreoretinochoroidopathy  (DOID:0111569)
  • 25 papers in RGD have been used to annotate Fth1
  • Curation Notes: ClinVar Annotator: match by term: Vitreoretinochoroidopathy
  • Original References(s): PMID:28492532 PMID:28687848


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