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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Snrpb and cerebrocostomandibular 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 SNRPB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to cerebrocostomandibular syndrome  (DOID:0111248)
  • 14 papers in RGD have been used to annotate Snrpb
  • Curation Notes: ClinVar Annotator: match by term: RIB GAP DEFECTS WITH MICROGNATHIA
  • Original References(s): PMID:25047197, PMID:25504470


  • An association has been curated linking Snrpb and cerebrocostomandibular 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 SNRPB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to cerebrocostomandibular syndrome  (DOID:0111248)
  • 14 papers in RGD have been used to annotate Snrpb
  • Curation Notes: ClinVar Annotator: match by term: RIB GAP DEFECTS WITH MICROGNATHIA
  • Original References(s): PMID:25047197


  • An association has been curated linking Snrpb and cerebrocostomandibular 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 SNRPB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to cerebrocostomandibular syndrome  (DOID:0111248)
  • 14 papers in RGD have been used to annotate Snrpb
  • Curation Notes: ClinVar Annotator: match by term: RIB GAP DEFECTS WITH MICROGNATHIA
  • Original References(s): PMID:25047197, PMID:25504470, PMID:26240113, PMID:26971886


  • An association has been curated linking Snrpb and cerebrocostomandibular 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 SNRPB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to cerebrocostomandibular syndrome  (DOID:0111248)
  • 14 papers in RGD have been used to annotate Snrpb
  • Curation Notes: ClinVar Annotator: match by term: RIB GAP DEFECTS WITH MICROGNATHIA
  • Original References(s): PMID:25047197, PMID:25504470, PMID:26971886


  • An association has been curated linking Snrpb and cerebrocostomandibular 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 SNRPB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to cerebrocostomandibular syndrome  (DOID:0111248)
  • 14 papers in RGD have been used to annotate Snrpb


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