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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Tnfrsf11a and autosomal recessive osteopetrosis 7 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 TNFRSF11A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive osteopetrosis 7  (DOID:0110946)
  • 19 papers in RGD have been used to annotate Tnfrsf11a


  • An association has been curated linking Tnfrsf11a and autosomal recessive osteopetrosis 7 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 TNFRSF11A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive osteopetrosis 7  (DOID:0110946)
  • 19 papers in RGD have been used to annotate Tnfrsf11a
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia | ClinVar Annotator: match by term: Autosomal recessive osteopetrosis 7
  • Original References(s): PMID:15231021 PMID:17576681 PMID:18606301 PMID:19940926 PMID:24033266 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking Tnfrsf11a and autosomal recessive osteopetrosis 7 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 TNFRSF11A (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to autosomal recessive osteopetrosis 7  (DOID:0110946)
  • 19 papers in RGD have been used to annotate Tnfrsf11a
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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