Send us a Message



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

GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:28492532


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:22426308 PMID:25741868


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by OMIM:607174
  • Original References(s): PMID:23377182


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(EXP) inferred from experiment]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:23377182


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:25169753 PMID:25741868 PMID:28492532


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:16199547 PMID:23377182 PMID:28492532


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Qualifier: susceptibility


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:23377182 PMID:28492532


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:25741868


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking Smarce1 and familial meningioma 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 SMARCE1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to familial meningioma  (DOID:4586)
  • 10 papers in RGD have been used to annotate Smarce1
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:28166811 PMID:28492532


  • Go Back to source page   Continue to Ontology report