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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking NDUFS4 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:156164022 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 14 papers in RGD have been used to annotate NDUFS4
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking NDUFS4 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10409734 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 14 papers in RGD have been used to annotate NDUFS4
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking NDUFS4 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:156150558 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 14 papers in RGD have been used to annotate NDUFS4
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:11165261 PMID:20433953 PMID:28844695


    • An association has been curated linking NDUFS4 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8570773 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 14 papers in RGD have been used to annotate NDUFS4
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:19107570 PMID:19364667 PMID:20818383 PMID:24020637 PMID:25741868 PMID:28492532


    • An association has been curated linking NDUFS4 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens) & RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens) & RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens) & RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens) & RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens) & RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens) & RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens) & RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens) & RGD:14394268|RGD:156254028|RGD:329395035|RGD:401760603|RGD:401765970|RGD:401894310|RGD:405806512|RGD:407526010|RGD:407526013 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 14 papers in RGD have been used to annotate NDUFS4
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking NDUFS4 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10410781|RGD:156330451 (Homo sapiens) & RGD:10410781|RGD:156330451 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 14 papers in RGD have been used to annotate NDUFS4
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


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