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GENE - TERM ANNOTATION REPORT

13 Annotations Found.

An association has been curated linking Vsx1 and posterior polymorphous corneal dystrophy 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Valleix S, etal., Invest Ophthalmol Vis Sci. 2006 Jan;47(1):48-54.
  • The annotation has been inferred from sequence orthology with VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Valleix S, etal., Invest Ophthalmol Vis Sci. 2006 Jan;47(1):48-54.
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: DNA:missense mutation:cds:p.H244R (human)


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:15623752 PMID:21976959


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: Posterior polymorphous corneal dystrophy 1
  • Original References(s): PMID:11978762 PMID:15623752 PMID:16303937 PMID:19763142 PMID:21976959 PMID:24033266 PMID:7795607


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:11978762 PMID:22171159


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:28492532


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:25741868


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:23592923 PMID:24033266 PMID:28492532


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:16384943 PMID:28492532


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:11978762 PMID:16303937 PMID:21976959


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:11978762 PMID:18216574 PMID:21976959


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:26879370


    • An association has been curated linking Vsx1 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 VSX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in RGD have been used to annotate Vsx1
  • Curation Notes: ClinVar Annotator: match by term: MAUMENEE CORNEAL DYSTROPHY
  • Original References(s): PMID:18626569 PMID:28492532


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