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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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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 CRRD objects have been annotated to posterior polymorphous corneal dystrophy 1  (DOID:0110855)
  • 15 papers in CRRD 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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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.