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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking NDUFA9 and nuclear type mitochondrial complex I deficiency 26 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:8602203 (Homo sapiens)
  • 1 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 26  (DOID:0112086)
  • 7 papers in RGD have been used to annotate NDUFA9
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26
  • Original References(s): PMID:22114105


    • An association has been curated linking NDUFA9 and nuclear type mitochondrial complex I deficiency 26 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 26  (DOID:0112086)
  • 7 papers in RGD have been used to annotate NDUFA9


    • An association has been curated linking NDUFA9 and nuclear type mitochondrial complex I deficiency 26 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:13827736 (Homo sapiens)
  • 1 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 26  (DOID:0112086)
  • 7 papers in RGD have been used to annotate NDUFA9
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26
  • Original References(s): PMID:25741868 PMID:28671271


    • An association has been curated linking NDUFA9 and nuclear type mitochondrial complex I deficiency 26 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:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens) & RGD:10409935|RGD:10410148|RGD:10411373|RGD:10411658|RGD:12837252|RGD:13529823|RGD:150412547|RGD:15102799|RGD:8660125|RGD:8692185|RGD:8692186|RGD:8692188 (Homo sapiens)
  • 1 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 26  (DOID:0112086)
  • 7 papers in RGD have been used to annotate NDUFA9
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26 | ClinVar Annotator: match by term: NDUFA9-related condition
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking NDUFA9 and nuclear type mitochondrial complex I deficiency 26 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:21072323|RGD:34890845|RGD:42723724 (Homo sapiens) & RGD:21072323|RGD:34890845|RGD:42723724 (Homo sapiens) & RGD:21072323|RGD:34890845|RGD:42723724 (Homo sapiens)
  • 1 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 26  (DOID:0112086)
  • 7 papers in RGD have been used to annotate NDUFA9
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26


    • An association has been curated linking NDUFA9 and nuclear type mitochondrial complex I deficiency 26 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:126727714|RGD:12742402|RGD:155797403|RGD:404998810|RGD:404998815 (Homo sapiens) & RGD:126727714|RGD:12742402|RGD:155797403|RGD:404998810|RGD:404998815 (Homo sapiens) & RGD:126727714|RGD:12742402|RGD:155797403|RGD:404998810|RGD:404998815 (Homo sapiens) & RGD:126727714|RGD:12742402|RGD:155797403|RGD:404998810|RGD:404998815 (Homo sapiens) & RGD:126727714|RGD:12742402|RGD:155797403|RGD:404998810|RGD:404998815 (Homo sapiens)
  • 1 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 26  (DOID:0112086)
  • 7 papers in RGD have been used to annotate NDUFA9
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26
  • Original References(s): PMID:25741868


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