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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Ndufa2 and nuclear type mitochondrial complex I deficiency 13 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 NDUFA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 13  (DOID:0112076)
  • 10 papers in RGD have been used to annotate Ndufa2
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13
  • Original References(s): PMID:32154054


    • An association has been curated linking Ndufa2 and nuclear type mitochondrial complex I deficiency 13 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 NDUFA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 13  (DOID:0112076)
  • 10 papers in RGD have been used to annotate Ndufa2
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13
  • Original References(s): PMID:27159321 PMID:28857146


    • An association has been curated linking Ndufa2 and nuclear type mitochondrial complex I deficiency 13 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 NDUFA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 13  (DOID:0112076)
  • 10 papers in RGD have been used to annotate Ndufa2
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13
  • Original References(s): PMID:25741868 PMID:28857146


    • An association has been curated linking Ndufa2 and nuclear type mitochondrial complex I deficiency 13 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 NDUFA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 13  (DOID:0112076)
  • 10 papers in RGD have been used to annotate Ndufa2
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13
  • Original References(s): PMID:18513682


    • An association has been curated linking Ndufa2 and nuclear type mitochondrial complex I deficiency 13 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 NDUFA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 13  (DOID:0112076)
  • 10 papers in RGD have been used to annotate Ndufa2


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