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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking Nfu1 and multiple mitochondrial dysfunctions syndrome 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 NFU1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to multiple mitochondrial dysfunctions syndrome 1  (DOID:0080133)
  • 6 papers in RGD have been used to annotate Nfu1


  • An association has been curated linking Nfu1 and multiple mitochondrial dysfunctions syndrome 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 NFU1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to multiple mitochondrial dysfunctions syndrome 1  (DOID:0080133)
  • 6 papers in RGD have been used to annotate Nfu1
  • Curation Notes: ClinVar Annotator: match by term: Multiple mitochondrial dysfunctions syndrome 1
  • Original References(s): PMID:28492532


  • An association has been curated linking Nfu1 and multiple mitochondrial dysfunctions syndrome 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 NFU1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to multiple mitochondrial dysfunctions syndrome 1  (DOID:0080133)
  • 6 papers in RGD have been used to annotate Nfu1
  • Curation Notes: ClinVar Annotator: match by OMIM:605711
  • Original References(s): PMID:22077971


  • An association has been curated linking Nfu1 and multiple mitochondrial dysfunctions syndrome 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 NFU1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to multiple mitochondrial dysfunctions syndrome 1  (DOID:0080133)
  • 6 papers in RGD have been used to annotate Nfu1
  • Curation Notes: ClinVar Annotator: match by term: Multiple mitochondrial dysfunctions syndrome 1


  • An association has been curated linking Nfu1 and multiple mitochondrial dysfunctions syndrome 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 NFU1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to multiple mitochondrial dysfunctions syndrome 1  (DOID:0080133)
  • 6 papers in RGD have been used to annotate Nfu1
  • Curation Notes: ClinVar Annotator: match by OMIM:605711
  • Original References(s): PMID:11156534 PMID:21944046 PMID:22077971


  • An association has been curated linking Nfu1 and multiple mitochondrial dysfunctions syndrome 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 NFU1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to multiple mitochondrial dysfunctions syndrome 1  (DOID:0080133)
  • 6 papers in RGD have been used to annotate Nfu1
  • Curation Notes: ClinVar Annotator: match by term: Multiple mitochondrial dysfunctions syndrome 1
  • Original References(s): PMID:25477904


  • An association has been curated linking Nfu1 and multiple mitochondrial dysfunctions syndrome 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 NFU1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to multiple mitochondrial dysfunctions syndrome 1  (DOID:0080133)
  • 6 papers in RGD have been used to annotate Nfu1
  • Curation Notes: ClinVar Annotator: match by term: Multiple mitochondrial dysfunctions syndrome 1
  • Original References(s): PMID:25741868


  • An association has been curated linking Nfu1 and multiple mitochondrial dysfunctions syndrome 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 NFU1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to multiple mitochondrial dysfunctions syndrome 1  (DOID:0080133)
  • 6 papers in RGD have been used to annotate Nfu1
  • Curation Notes: ClinVar Annotator: match by term: Multiple mitochondrial dysfunctions syndrome 1
  • Original References(s): PMID:24033266


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