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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

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


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


  • An association has been curated linking Tymp 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 TYMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 30 papers in RGD have been used to annotate Tymp
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:23643385 PMID:25959673 PMID:28492532


  • An association has been curated linking Tymp 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 TYMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 30 papers in RGD have been used to annotate Tymp
  • Curation Notes: ClinVar Annotator: match by term: Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency
  • Original References(s): PMID:12529715 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Tymp 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 TYMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 30 papers in RGD have been used to annotate Tymp
  • Curation Notes: ClinVar Annotator: match by term: Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Tymp 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 TYMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 30 papers in RGD have been used to annotate Tymp
  • Curation Notes: ClinVar Annotator: match by term: Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency
  • Original References(s): PMID:23643385 PMID:25741868 PMID:28492532


  • An association has been curated linking Tymp 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 TYMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 31 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 30 papers in RGD have been used to annotate Tymp
  • 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


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