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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking COX15 and mitochondrial complex IV deficiency nuclear type 6 in Sus scrofa.        

  • 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 mitochondrial complex IV deficiency nuclear type 6  (DOID:0080358)
  • 0 papers in RGD have been used to annotate COX15


    • An association has been curated linking COX15 and mitochondrial complex IV deficiency nuclear type 6 in Sus scrofa.        

  • 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 mitochondrial complex IV deficiency nuclear type 6  (DOID:0080358)
  • 0 papers in RGD have been used to annotate COX15
  • Curation Notes: ClinVar Annotator: match by term: COX15-related condition | ClinVar Annotator: match by term: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
  • Original References(s): PMID:12474143 PMID:15235026 PMID:15863660 PMID:16199547 PMID:17576681 PMID:21412973 PMID:2175025 PMID:22310368 PMID:25741868 PMID:26940873 PMID:26959537 PMID:28492532 PMID:31102535 PMID:31967322 PMID:32232962 PMID:33746038 PMID:9536098


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