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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx


  • An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx
  • Curation Notes: ClinVar Annotator: match by OMIM:310500
  • Original References(s): PMID:11062472


  • An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx
  • Curation Notes: ClinVar Annotator: match by OMIM:310500
  • Original References(s): PMID:11062471


  • An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx
  • Curation Notes: ClinVar Annotator: match by OMIM:310500
  • Original References(s): PMID:16670814


  • An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, type 1A
  • Original References(s): PMID:17392683 PMID:23406521 PMID:28492532


  • An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, type 1A
  • Original References(s): PMID:23406521 PMID:28492532


  • An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, type 1A


  • An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, type 1A
  • Original References(s): PMID:28492532


  • An association has been curated linking Nyx and congenital stationary night blindness 1A 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 NYX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital stationary night blindness 1A  (DOID:0110870)
  • 7 papers in RGD have been used to annotate Nyx
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, type 1A
  • Original References(s): PMID:11062472 PMID:25741868 PMID:28492532


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