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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11665601 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11665315 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11666134 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11666484 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11665225 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11665764 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:25741868


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11665336 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:25741868


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11665386 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:25741868


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11665969 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:25741868


  • An association has been curated linking DNM1L and myopathy, lactic acidosis, and sideroblastic anemia 2 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:11665712 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 15 papers in RGD have been used to annotate DNM1L
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:25741868 PMID:28492532


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