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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Nf2 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 NF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to familial meningioma  (DOID:4586)
  • 21 papers in CRRD have been used to annotate Nf2
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Nf2 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 NF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to familial meningioma  (DOID:4586)
  • 21 papers in CRRD have been used to annotate Nf2
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:25741868, PMID:28492532, PMID:30311386


  • An association has been curated linking Nf2 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 NF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to familial meningioma  (DOID:4586)
  • 21 papers in CRRD have been used to annotate Nf2
  • Qualifier: susceptibility


  • An association has been curated linking Nf2 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 NF2 (Homo sapiens) [(EXP) inferred from experiment]
  • 8 CRRD objects have been annotated to familial meningioma  (DOID:4586)
  • 21 papers in CRRD have been used to annotate Nf2
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking Nf2 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 NF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to familial meningioma  (DOID:4586)
  • 21 papers in CRRD have been used to annotate Nf2
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:25741868


  • An association has been curated linking Nf2 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 NF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to familial meningioma  (DOID:4586)
  • 21 papers in CRRD have been used to annotate Nf2
  • Curation Notes: ClinVar Annotator: match by term: Meningioma, familial
  • Original References(s): PMID:20553997, PMID:25741868, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.