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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Atpaf2 and mitochondrial complex V (ATP synthase) deficiency nuclear type 1 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 ATPAF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to mitochondrial complex V (ATP synthase) deficiency nuclear type 1  (DOID:0050768)
  • 5 papers in RGD have been used to annotate Atpaf2


  • An association has been curated linking Atpaf2 and mitochondrial complex V (ATP synthase) deficiency nuclear type 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with ATPAF2 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to mitochondrial complex V (ATP synthase) deficiency nuclear type 1  (DOID:0050768)
  • 5 papers in RGD have been used to annotate Atpaf2
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking Atpaf2 and mitochondrial complex V (ATP synthase) deficiency nuclear type 1 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 ATPAF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to mitochondrial complex V (ATP synthase) deficiency nuclear type 1  (DOID:0050768)
  • 5 papers in RGD have been used to annotate Atpaf2
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
  • Original References(s): PMID:14757859 PMID:16199547 PMID:25741868 PMID:28492532 PMID:34440436


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