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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking NDUFV2-AS1 and nuclear type mitochondrial complex I deficiency 7 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:155267959 (Homo sapiens)
  • 3 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 7  (DOID:0112092)
  • 0 papers in RGD have been used to annotate NDUFV2-AS1
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7
  • Original References(s): PMID:25741868 PMID:30369941


    • An association has been curated linking NDUFV2-AS1 and nuclear type mitochondrial complex I deficiency 7 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:14351004 (Homo sapiens)
  • 3 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 7  (DOID:0112092)
  • 0 papers in RGD have been used to annotate NDUFV2-AS1
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7
  • Original References(s): PMID:25741868 PMID:26008862 PMID:28492532


    • An association has been curated linking NDUFV2-AS1 and nuclear type mitochondrial complex I deficiency 7 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:10411548|RGD:11637304|RGD:151351417|RGD:243054616|RGD:405291382 (Homo sapiens) & RGD:10411548|RGD:11637304|RGD:151351417|RGD:243054616|RGD:405291382 (Homo sapiens) & RGD:10411548|RGD:11637304|RGD:151351417|RGD:243054616|RGD:405291382 (Homo sapiens) & RGD:10411548|RGD:11637304|RGD:151351417|RGD:243054616|RGD:405291382 (Homo sapiens) & RGD:10411548|RGD:11637304|RGD:151351417|RGD:243054616|RGD:405291382 (Homo sapiens)
  • 3 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 7  (DOID:0112092)
  • 0 papers in RGD have been used to annotate NDUFV2-AS1
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7
  • Original References(s): PMID:25741868


    • An association has been curated linking NDUFV2-AS1 and nuclear type mitochondrial complex I deficiency 7 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:126742557|RGD:150332903 (Homo sapiens) & RGD:126742557|RGD:150332903 (Homo sapiens)
  • 3 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 7  (DOID:0112092)
  • 0 papers in RGD have been used to annotate NDUFV2-AS1
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7


    • An association has been curated linking NDUFV2-AS1 and nuclear type mitochondrial complex I deficiency 7 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:10411089 (Homo sapiens)
  • 3 RGD objects have been annotated to nuclear type mitochondrial complex I deficiency 7  (DOID:0112092)
  • 0 papers in RGD have been used to annotate NDUFV2-AS1
  • Curation Notes: ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7
  • Original References(s): PMID:28492532


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