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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by OMIM:300855
  • Original References(s): PMID:25099252


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by OMIM:300855
  • Original References(s): PMID:25741868 PMID:27094817


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by OMIM:300855
  • Original References(s): PMID:23020937 PMID:25099252 PMID:25741868 PMID:27094817


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:25741868 PMID:28708303


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:25326635 PMID:25741868


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:25741868 PMID:28327206


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:25741868


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:29558889


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:25489052


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:18414213 PMID:25741868 PMID:27094817


  • An association has been curated linking Naa10 and Ogden syndrome 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 NAA10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Ogden syndrome  (DOID:0050781)
  • 5 papers in RGD have been used to annotate Naa10
  • Curation Notes: ClinVar Annotator: match by term: N-terminal acetyltransferase deficiency
  • Original References(s): PMID:25741868 PMID:27094817 PMID:28492532 PMID:31127942 PMID:31174490


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