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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by OMIM:163500
  • Original References(s): PMID:17044014, PMID:8075643


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:22334370, PMID:24033266, PMID:25472526, PMID:26667666, PMID:28492532, PMID:28981474


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:28041643, PMID:30311386, PMID:7724547


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:22334370, PMID:28492532


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:28492532


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:24938718, PMID:28912962, PMID:30718709


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:28492532, PMID:30029497


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:25999674, PMID:27588261, PMID:28492532, PMID:30029497


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:28041643


  • An association has been curated linking Pde6b and congenital stationary night blindness autosomal dominant 2 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 PDE6B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital stationary night blindness autosomal dominant 2  (DOID:0110863)
  • 14 papers in CRRD have been used to annotate Pde6b
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, autosomal dominant 2
  • Original References(s): PMID:25741868, 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.