Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1
  • Original References(s): PMID:25741868


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1
  • Original References(s): PMID:18470948


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1
  • Original References(s): PMID:16906565 PMID:18470948


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1
  • Original References(s): PMID:15821734


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1
  • Original References(s): PMID:18671284


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1
  • Original References(s): PMID:18470948 PMID:20301770


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1
  • Original References(s): PMID:15821734 PMID:18470948 PMID:20301770 PMID:25741868


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1
  • Original References(s): PMID:15821734 PMID:18470948 PMID:20301770


  • An association has been curated linking Mycn and Feingold 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Feingold Syndrome 1  (DOID:9004844)
  • 6 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Feingold syndrome 1


  • Go Back to source page   Continue to Ontology report