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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by OMIM:614388
  • Original References(s): PMID:17460227 PMID:20696759


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by OMIM:614388
  • Original References(s): PMID:17460227


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by OMIM:614388


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by OMIM:614388
  • Original References(s): PMID:26825290


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by OMIM:614388
  • Original References(s): PMID:26825290 PMID:27328748


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by OMIM:614388
  • Original References(s): PMID:27328748


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by term: Encephalopathy due to defective mitochondrial and peroxisomal fission 1
  • Original References(s): PMID:25741868 PMID:30850373


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by term: Encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission
  • Original References(s): PMID:25326635 PMID:25741868 PMID:26931468


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by term: Encephalopathy due to defective mitochondrial and peroxisomal fission 1
  • Original References(s): PMID:20696759 PMID:25741868 PMID:26604000 PMID:27145208 PMID:28492532 PMID:29877124


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by term: Encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission
  • Original References(s): PMID:18414213 PMID:20696759 PMID:26604000


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by term: Encephalopathy due to defective mitochondrial and peroxisomal fission 1
  • Original References(s): PMID:20696759 PMID:26931468 PMID:31587467


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by term: Encephalopathy due to defective mitochondrial and peroxisomal fission 1
  • Original References(s): PMID:25741868


  • An association has been curated linking Dnm1l and encephalopathy due to defective mitochondrial and peroxisomal fission 1 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 DNM1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to encephalopathy due to defective mitochondrial and peroxisomal fission 1  (DOID:0070347)
  • 27 papers in RGD have been used to annotate Dnm1l
  • Curation Notes: ClinVar Annotator: match by term: Encephalopathy due to defective mitochondrial and peroxisomal fission 1
  • Original References(s): PMID:25741868 PMID:26992161


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