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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking NSD2 and Wittwer 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:11666023 (Homo sapiens)
  • 5 RGD objects have been annotated to Wittwer Syndrome  (DOID:9001308)
  • 7 papers in RGD have been used to annotate NSD2
  • Curation Notes: ClinVar Annotator: match by term: Wittwer syndrome
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking NSD2 and Wittwer 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:11666272|RGD:151662256 (Homo sapiens) & RGD:11666272|RGD:151662256 (Homo sapiens)
  • 5 RGD objects have been annotated to Wittwer Syndrome  (DOID:9001308)
  • 7 papers in RGD have been used to annotate NSD2
  • Curation Notes: ClinVar Annotator: match by term: Wittwer syndrome
  • Original References(s): PMID:28492532


    • An association has been curated linking NSD2 and Wittwer 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:14349897|RGD:14349953|RGD:14349955 (Homo sapiens) & RGD:14349897|RGD:14349953|RGD:14349955 (Homo sapiens) & RGD:14349897|RGD:14349953|RGD:14349955 (Homo sapiens)
  • 5 RGD objects have been annotated to Wittwer Syndrome  (DOID:9001308)
  • 7 papers in RGD have been used to annotate NSD2
  • Curation Notes: ClinVar Annotator: match by term: Wittwer syndrome
  • Original References(s): PMID:11252005 PMID:25741868 PMID:29760529 PMID:29892088 PMID:30345613


    • An association has been curated linking NSD2 and Wittwer 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:126743732|RGD:127244320|RGD:150452574|RGD:150551821|RGD:155642565 (Homo sapiens) & RGD:126743732|RGD:127244320|RGD:150452574|RGD:150551821|RGD:155642565 (Homo sapiens) & RGD:126743732|RGD:127244320|RGD:150452574|RGD:150551821|RGD:155642565 (Homo sapiens) & RGD:126743732|RGD:127244320|RGD:150452574|RGD:150551821|RGD:155642565 (Homo sapiens) & RGD:126743732|RGD:127244320|RGD:150452574|RGD:150551821|RGD:155642565 (Homo sapiens)
  • 5 RGD objects have been annotated to Wittwer Syndrome  (DOID:9001308)
  • 7 papers in RGD have been used to annotate NSD2
  • Curation Notes: ClinVar Annotator: match by term: Wittwer syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking NSD2 and Wittwer 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:11666816|RGD:11666838|RGD:11666973|RGD:11667025 (Homo sapiens) & RGD:11666816|RGD:11666838|RGD:11666973|RGD:11667025 (Homo sapiens) & RGD:11666816|RGD:11666838|RGD:11666973|RGD:11667025 (Homo sapiens) & RGD:11666816|RGD:11666838|RGD:11666973|RGD:11667025 (Homo sapiens)
  • 5 RGD objects have been annotated to Wittwer Syndrome  (DOID:9001308)
  • 7 papers in RGD have been used to annotate NSD2
  • Curation Notes: ClinVar Annotator: match by term: Wittwer syndrome


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