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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking Cox15 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with COX15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  (DOID:0080358)
  • 13 papers in RGD have been used to annotate Cox15


  • An association has been curated linking Cox15 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2 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 COX15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  (DOID:0080358)
  • 13 papers in RGD have been used to annotate Cox15
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
  • Original References(s): PMID:12474143 PMID:15235026 PMID:21412973 PMID:2175025


  • An association has been curated linking Cox15 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2 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 COX15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  (DOID:0080358)
  • 13 papers in RGD have been used to annotate Cox15
  • Curation Notes: ClinVar Annotator: match by OMIM:615119
  • Original References(s): PMID:12474143


  • An association has been curated linking Cox15 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2 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 COX15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  (DOID:0080358)
  • 13 papers in RGD have been used to annotate Cox15
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2


  • An association has been curated linking Cox15 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2 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 COX15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  (DOID:0080358)
  • 13 papers in RGD have been used to annotate Cox15
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
  • Original References(s): PMID:28492532


  • An association has been curated linking Cox15 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2 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 COX15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  (DOID:0080358)
  • 13 papers in RGD have been used to annotate Cox15
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
  • Original References(s): PMID:25741868


  • An association has been curated linking Cox15 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2 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 COX15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  (DOID:0080358)
  • 13 papers in RGD have been used to annotate Cox15
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
  • Original References(s): PMID:15863660 PMID:21412973 PMID:22310368 PMID:26959537 PMID:32232962


  • An association has been curated linking Cox15 and fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2 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 COX15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  (DOID:0080358)
  • 13 papers in RGD have been used to annotate Cox15
  • Curation Notes: ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
  • Original References(s): PMID:15863660


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