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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by OMIM:601358
  • Original References(s): PMID:22366787


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by OMIM:601358
  • Original References(s): PMID:25326637


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by OMIM:601358
  • Original References(s): PMID:25741868


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by OMIM:601358
  • Original References(s): PMID:22426308


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by OMIM:601358
  • Original References(s): PMID:19606471 PMID:22366787


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by OMIM:601358
  • Original References(s): PMID:22822383


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(EXP) inferred from experiment]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:22366787


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by OMIM:601358


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by OMIM:601358
  • Original References(s): PMID:18414213


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by term: Nicolaides-Baraitser syndrome
  • Original References(s): PMID:22366787 PMID:25326635 PMID:25741868


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by term: Nicolaides-Baraitser syndrome
  • Original References(s): PMID:25326635 PMID:25741868


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by term: Nicolaides-Baraitser syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by term: Nicolaides-Baraitser syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by term: Nicolaides-Baraitser syndrome
  • Original References(s): PMID:22366787 PMID:23752187 PMID:25169058 PMID:27099726 PMID:27665729 PMID:28824374 PMID:30459321


  • An association has been curated linking Smarca2 and Nicolaides Baraitser 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 SMARCA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Nicolaides Baraitser Syndrome  (DOID:9003531)
  • 13 papers in RGD have been used to annotate Smarca2
  • Curation Notes: ClinVar Annotator: match by term: Nicolaides-Baraitser syndrome
  • Original References(s): PMID:22366787 PMID:25741868


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