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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease 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 COX10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: ClinVar Annotator: match by OMIM:220110


  • An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease 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 COX10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:25741868 PMID:32313153


  • An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease 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 COX10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:12928484 PMID:25741868 PMID:32313153


  • An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease 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 COX10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: ClinVar Annotator: match by term: Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency
  • Original References(s): PMID:28492532


  • An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease 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 COX10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:25741868


  • An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease 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 COX10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease 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 COX10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:23814038


  • An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Cox10 (Mus musculus) [(IEA) inferred from electronic annotation]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: OMIM:220110


  • An association has been curated linking Cox10 and cytochrome-c oxidase deficiency disease 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 COX10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate Cox10
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


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