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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking SNX22 and osteogenesis imperfecta 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:153347124 (Homo sapiens)
  • 76 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 3 papers in RGD have been used to annotate SNX22
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta
  • Original References(s): PMID:25741868


    • An association has been curated linking SNX22 and osteogenesis imperfecta 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:10449742 (Homo sapiens)
  • 76 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 3 papers in RGD have been used to annotate SNX22
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SNX22 and osteogenesis imperfecta 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:8565920 (Homo sapiens)
  • 76 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 3 papers in RGD have been used to annotate SNX22
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta
  • Original References(s): PMID:19781681 PMID:28492532


    • An association has been curated linking SNX22 and osteogenesis imperfecta 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:151746776 (Homo sapiens)
  • 76 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 3 papers in RGD have been used to annotate SNX22
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta
  • Original References(s): PMID:28242392 PMID:28492532 PMID:32392875 PMID:34659339 PMID:35583673


    • An association has been curated linking SNX22 and osteogenesis imperfecta 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:11558879|RGD:11635093|RGD:11635149|RGD:11635414|RGD:11635780|RGD:153346244 (Homo sapiens) & RGD:11558879|RGD:11635093|RGD:11635149|RGD:11635414|RGD:11635780|RGD:153346244 (Homo sapiens) & RGD:11558879|RGD:11635093|RGD:11635149|RGD:11635414|RGD:11635780|RGD:153346244 (Homo sapiens) & RGD:11558879|RGD:11635093|RGD:11635149|RGD:11635414|RGD:11635780|RGD:153346244 (Homo sapiens) & RGD:11558879|RGD:11635093|RGD:11635149|RGD:11635414|RGD:11635780|RGD:153346244 (Homo sapiens) & RGD:11558879|RGD:11635093|RGD:11635149|RGD:11635414|RGD:11635780|RGD:153346244 (Homo sapiens)
  • 76 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 3 papers in RGD have been used to annotate SNX22
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis Imperfecta, Recessive | ClinVar Annotator: match by term: Osteogenesis imperfecta


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