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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by OMIM:615547
  • Original References(s): PMID:24076603


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by OMIM:615547


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by OMIM:615547
  • Original References(s): PMID:24076603 PMID:24088041 PMID:26633545


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-yang syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-Yang syndrome
  • Original References(s): PMID:25473036 PMID:25741868 PMID:27195816 PMID:27632685 PMID:28492532 PMID:29599419


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-yang syndrome
  • Original References(s): PMID:27195816


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-Yang syndrome
  • Original References(s): PMID:25741868 PMID:32860008


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-yang syndrome
  • Original References(s): PMID:26365340


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-Yang syndrome
  • Original References(s): PMID:24076603 PMID:25741868 PMID:26365340 PMID:27195816 PMID:28492532 PMID:31680349


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-yang syndrome
  • Original References(s): PMID:24076603 PMID:25326635 PMID:25741868


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-Yang syndrome
  • Original References(s): PMID:25741868 PMID:27195816 PMID:28281571


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-yang syndrome
  • Original References(s): PMID:25741868 PMID:27195816


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-Yang syndrome
  • Original References(s): PMID:27195816 PMID:29581464


  • An association has been curated linking Magel2 and Schaaf-Yang 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 MAGEL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Schaaf-Yang syndrome  (DOID:0111715)
  • 3 papers in RGD have been used to annotate Magel2
  • Curation Notes: ClinVar Annotator: match by term: Schaaf-Yang syndrome
  • Original References(s): PMID:31397880


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