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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking Maoa and Brunner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with MAOA (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:8211186


  • An association has been curated linking Maoa and Brunner 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 MAOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa


  • An association has been curated linking Maoa and Brunner 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 MAOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa
  • Curation Notes: ClinVar Annotator: match by OMIM:300615
  • Original References(s): PMID:25807999


  • An association has been curated linking Maoa and Brunner 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 MAOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa
  • Curation Notes: ClinVar Annotator: match by OMIM:300615
  • Original References(s): PMID:8211186


  • An association has been curated linking Maoa and Brunner 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 MAOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa
  • Curation Notes: ClinVar Annotator: match by OMIM:300615
  • Original References(s): PMID:24169519


  • An association has been curated linking Maoa and Brunner 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 MAOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa
  • Curation Notes: ClinVar Annotator: match by term: BRUNNER SYNDROME
  • Original References(s): PMID:25741868


  • An association has been curated linking Maoa and Brunner 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 MAOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa
  • Curation Notes: ClinVar Annotator: match by term: Monoamine oxidase A deficiency
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Maoa and Brunner 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 MAOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa
  • Curation Notes: ClinVar Annotator: match by term: BRUNNER SYNDROME
  • Original References(s): PMID:11700166, PMID:25807999


  • An association has been curated linking Maoa and Brunner 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 MAOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Brunner syndrome  (DOID:0060693)
  • 18 papers in RGD have been used to annotate Maoa
  • Curation Notes: ClinVar Annotator: match by term: Monoamine oxidase A deficiency
  • Original References(s): PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.