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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Slc25a4 and mitochondrial DNA depletion syndrome 12b 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 SLC25A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to mitochondrial DNA depletion syndrome 12b  (DOID:0080335)
  • 40 papers in RGD have been used to annotate Slc25a4


  • An association has been curated linking Slc25a4 and mitochondrial DNA depletion syndrome 12b 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 SLC25A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to mitochondrial DNA depletion syndrome 12b  (DOID:0080335)
  • 40 papers in RGD have been used to annotate Slc25a4
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial DNA depletion syndrome 12b (cardiomyopathic type), autosomal recessive
  • Original References(s): PMID:25732997


  • An association has been curated linking Slc25a4 and mitochondrial DNA depletion syndrome 12b 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 SLC25A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to mitochondrial DNA depletion syndrome 12b  (DOID:0080335)
  • 40 papers in RGD have been used to annotate Slc25a4
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial DNA depletion syndrome 12b (cardiomyopathic type), autosomal recessive
  • Original References(s): PMID:25732997 PMID:7609449 PMID:8479824


  • An association has been curated linking Slc25a4 and mitochondrial DNA depletion syndrome 12b 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 SLC25A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to mitochondrial DNA depletion syndrome 12b  (DOID:0080335)
  • 40 papers in RGD have been used to annotate Slc25a4
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial DNA depletion syndrome 12b (cardiomyopathic type), autosomal recessive
  • Original References(s): PMID:22187496


  • An association has been curated linking Slc25a4 and mitochondrial DNA depletion syndrome 12b 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 SLC25A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to mitochondrial DNA depletion syndrome 12b  (DOID:0080335)
  • 40 papers in RGD have been used to annotate Slc25a4
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial DNA depletion syndrome 12b (cardiomyopathic type), autosomal recessive
  • Original References(s): PMID:25741868


  • An association has been curated linking Slc25a4 and mitochondrial DNA depletion syndrome 12b 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 SLC25A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to mitochondrial DNA depletion syndrome 12b  (DOID:0080335)
  • 40 papers in RGD have been used to annotate Slc25a4
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial DNA depletion syndrome 12b (cardiomyopathic type), autosomal recessive
  • Original References(s): PMID:16155110 PMID:25741868


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