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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:10545952


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:10749987


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:18924171


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:10545952 PMID:15210538 PMID:19879173 PMID:23643385 PMID:28492532


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:14994243


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:12020273


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:25741868


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:28492532


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:10545952 PMID:11673586 PMID:12020273 PMID:14970747 PMID:16326995 PMID:23643385 PMID:25741868


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:23643385 PMID:25959673 PMID:28492532


  • An association has been curated linking Ncaph2 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 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 NCAPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency  (DOID:0050713)
  • 4 papers in RGD have been used to annotate Ncaph2
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
  • Original References(s): PMID:23643385 PMID:25741868 PMID:28492532


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