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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Ovol2 and posterior polymorphous corneal dystrophy 1 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 OVOL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 4 papers in RGD have been used to annotate Ovol2
  • Curation Notes: ClinVar Annotator: match by term: POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY
  • Original References(s): PMID:26749309


    • An association has been curated linking Ovol2 and posterior polymorphous corneal dystrophy 1 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 OVOL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 4 papers in RGD have been used to annotate Ovol2
  • Curation Notes: ClinVar Annotator: match by term: POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY
  • Original References(s): PMID:26749309 PMID:4900143


    • An association has been curated linking Ovol2 and posterior polymorphous corneal dystrophy 1 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 OVOL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 4 papers in RGD have been used to annotate Ovol2
  • Curation Notes: ClinVar Annotator: match by term: POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY
  • Original References(s): PMID:16303937 PMID:23049806 PMID:26749309


    • An association has been curated linking Ovol2 and posterior polymorphous corneal dystrophy 1 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 OVOL2 (Homo sapiens) [(EXP) inferred from experiment]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 4 papers in RGD have been used to annotate Ovol2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:26749309


    • An association has been curated linking Ovol2 and posterior polymorphous corneal dystrophy 1 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 OVOL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 4 papers in RGD have been used to annotate Ovol2


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