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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Wnt1 and osteogenesis imperfecta type 15 in Heterocephalus glaber.        

  • 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 WNT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 0 papers in RGD have been used to annotate Wnt1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15 | ClinVar Annotator: match by term: WNT1-related condition
  • Original References(s): PMID:22653731 PMID:23434763 PMID:23499309 PMID:23499310 PMID:23656646 PMID:25010833 PMID:25741868 PMID:27450065 PMID:28116328 PMID:28492532 PMID:28528193 PMID:28725987 PMID:29481978 PMID:29499418 PMID:29620724 PMID:30715774 PMID:30896082 PMID:30913006 PMID:33093841 PMID:33195954 PMID:34335676 PMID:36056132 PMID:36595228


    • An association has been curated linking Wnt1 and osteogenesis imperfecta type 15 in Heterocephalus glaber.        

  • 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 WNT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 0 papers in RGD have been used to annotate Wnt1


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