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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Sost and autosomal dominant craniodiaphyseal dysplasia 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 SOST (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant craniodiaphyseal dysplasia  (DOID:0080807)
  • 13 papers in RGD have been used to annotate Sost


  • An association has been curated linking Sost and autosomal dominant craniodiaphyseal dysplasia 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 SOST (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to autosomal dominant craniodiaphyseal dysplasia  (DOID:0080807)
  • 13 papers in RGD have been used to annotate Sost
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking Sost and autosomal dominant craniodiaphyseal dysplasia 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 SOST (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant craniodiaphyseal dysplasia  (DOID:0080807)
  • 13 papers in RGD have been used to annotate Sost
  • Curation Notes: ClinVar Annotator: match by term: Craniodiaphyseal dysplasia, autosomal dominant
  • Original References(s): PMID:17853455 PMID:21221996 PMID:25741868


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