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GENE - TERM ANNOTATION REPORT

13 Annotations Found.

An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13831411 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13786148 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15
  • Original References(s): PMID:25741868 PMID:29481978


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Qualifier: susceptibility


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:150459291 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: WNT1-related condition
  • Original References(s): PMID:25741868 PMID:27450065 PMID:28492532 PMID:28725987 PMID:30715774 PMID:30913006 PMID:33093841 PMID:33195954 PMID:34335676 PMID:36056132


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:152999568 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15
  • Original References(s): PMID:23499309 PMID:25741868


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:151351348 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15
  • Original References(s): PMID:23434763 PMID:23499309 PMID:23499310 PMID:25741868 PMID:28492532 PMID:29499418 PMID:30896082 PMID:30913006


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8611923 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15
  • Original References(s): PMID:22653731 PMID:23499309 PMID:23499310 PMID:23656646 PMID:28492532 PMID:28528193 PMID:29620724


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10449639|RGD:15151357|RGD:151846397|RGD:152027288 (Homo sapiens) & RGD:10449639|RGD:15151357|RGD:151846397|RGD:152027288 (Homo sapiens) & RGD:10449639|RGD:15151357|RGD:151846397|RGD:152027288 (Homo sapiens) & RGD:10449639|RGD:15151357|RGD:151846397|RGD:152027288 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 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:25741868 PMID:28492532


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9693673 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15
  • Original References(s): PMID:23434763 PMID:23499309 PMID:25010833 PMID:28116328 PMID:28492532


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8611920|RGD:8611921|RGD:8611922 (Homo sapiens) & RGD:8611920|RGD:8611921|RGD:8611922 (Homo sapiens) & RGD:8611920|RGD:8611921|RGD:8611922 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15
  • Original References(s): PMID:23499309


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:150520394|RGD:152979438|RGD:243059375|RGD:243062165|RGD:28877591 (Homo sapiens) & RGD:150520394|RGD:152979438|RGD:243059375|RGD:243062165|RGD:28877591 (Homo sapiens) & RGD:150520394|RGD:152979438|RGD:243059375|RGD:243062165|RGD:28877591 (Homo sapiens) & RGD:150520394|RGD:152979438|RGD:243059375|RGD:243062165|RGD:28877591 (Homo sapiens) & RGD:150520394|RGD:152979438|RGD:243059375|RGD:243062165|RGD:28877591 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15
  • Original References(s): PMID:25741868


    • An association has been curated linking WNT1 and osteogenesis imperfecta type 15 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8611924|RGD:8611925 (Homo sapiens) & RGD:8611924|RGD:8611925 (Homo sapiens)
  • 2 RGD objects have been annotated to osteogenesis imperfecta type 15  (DOID:0110347)
  • 14 papers in RGD have been used to annotate WNT1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 15
  • Original References(s): PMID:23434763


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