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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Lrp5 and Worth 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 LRP5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Worth syndrome  (DOID:0080037)
  • 32 papers in RGD have been used to annotate Lrp5


  • An association has been curated linking Lrp5 and Worth 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 LRP5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Worth syndrome  (DOID:0080037)
  • 32 papers in RGD have been used to annotate Lrp5
  • Curation Notes: ClinVar Annotator: match by term: Worth disease
  • Original References(s): PMID:1002767 PMID:12579474


  • An association has been curated linking Lrp5 and Worth 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 LRP5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Worth syndrome  (DOID:0080037)
  • 32 papers in RGD have been used to annotate Lrp5
  • Curation Notes: ClinVar Annotator: match by term: Worth disease
  • Original References(s): PMID:11883972 PMID:12579474


  • An association has been curated linking Lrp5 and Worth 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 LRP5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Worth syndrome  (DOID:0080037)
  • 32 papers in RGD have been used to annotate Lrp5
  • Curation Notes: ClinVar Annotator: match by term: Worth disease
  • Original References(s): PMID:1002767 PMID:10434540 PMID:11701785 PMID:12015390 PMID:12579474 PMID:25741868


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