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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking NSD1 and Weaver syndrome in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 7 RGD objects have been annotated to Weaver syndrome  (DOID:14731)
  • 16 papers in RGD have been used to annotate NSD1
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:12807965


    • An association has been curated linking NSD1 and Weaver syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9683220 (Homo sapiens)
  • 7 RGD objects have been annotated to Weaver syndrome  (DOID:14731)
  • 16 papers in RGD have been used to annotate NSD1
  • Curation Notes: ClinVar Annotator: match by term: Weaver syndrome
  • Original References(s): PMID:18414213 PMID:28492532


    • An association has been curated linking NSD1 and Weaver syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11593824 (Homo sapiens)
  • 7 RGD objects have been annotated to Weaver syndrome  (DOID:14731)
  • 16 papers in RGD have been used to annotate NSD1
  • Curation Notes: ClinVar Annotator: match by term: Weaver syndrome
  • Original References(s): PMID:28492532


    • An association has been curated linking NSD1 and Weaver syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11655652 (Homo sapiens)
  • 7 RGD objects have been annotated to Weaver syndrome  (DOID:14731)
  • 16 papers in RGD have been used to annotate NSD1
  • Curation Notes: ClinVar Annotator: match by term: Weaver syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking NSD1 and Weaver syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens) & RGD:11587710|RGD:11646014|RGD:11646680|RGD:11647503|RGD:11648067|RGD:11648410|RGD:11648457|RGD:11649073|RGD:11650568|RGD:11653651|RGD:11660407 (Homo sapiens)
  • 7 RGD objects have been annotated to Weaver syndrome  (DOID:14731)
  • 16 papers in RGD have been used to annotate NSD1
  • Curation Notes: ClinVar Annotator: match by term: Weaver syndrome


    • An association has been curated linking NSD1 and Weaver syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10052575|RGD:11583236|RGD:9683246 (Homo sapiens) & RGD:10052575|RGD:11583236|RGD:9683246 (Homo sapiens) & RGD:10052575|RGD:11583236|RGD:9683246 (Homo sapiens)
  • 7 RGD objects have been annotated to Weaver syndrome  (DOID:14731)
  • 16 papers in RGD have been used to annotate NSD1
  • Curation Notes: ClinVar Annotator: match by term: Weaver syndrome
  • Original References(s): PMID:25741868 PMID:28492532


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