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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:28492532


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by OMIM:610915
  • Original References(s): PMID:17277775


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: OSTEOGENESIS IMPERFECTA, TYPE VIII
  • Original References(s): PMID:19088120, PMID:25741868


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:17277775, PMID:19088120, PMID:22281939, PMID:25741868, PMID:27509835, PMID:28492532, PMID:29150909


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:19088120, PMID:28492532


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:17277775, PMID:18566967, PMID:19088120, PMID:22281939, PMID:28492532, PMID:29499418


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:25741868


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:17277775, PMID:19088120, PMID:28492532


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:26634552, PMID:28492532


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:26634552


  • An association has been curated linking P3h1 and osteogenesis imperfecta type 8 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 P3H1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to osteogenesis imperfecta type 8  (DOID:0110336)
  • 8 papers in RGD have been used to annotate P3h1
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta type 8
  • Original References(s): PMID:24498616, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.