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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking OPN1LW and red color blindness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to red color blindness  (DOID:13910)
  • 6 papers in RGD have been used to annotate OPN1LW


  • An association has been curated linking OPN1LW and red color blindness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8561737 (Homo sapiens)
  • 1 RGD objects have been annotated to red color blindness  (DOID:13910)
  • 6 papers in RGD have been used to annotate OPN1LW
  • Curation Notes: ClinVar Annotator: match by term: Protan defect
  • Original References(s): PMID:12051694


  • An association has been curated linking OPN1LW and red color blindness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8561736 (Homo sapiens)
  • 1 RGD objects have been annotated to red color blindness  (DOID:13910)
  • 6 papers in RGD have been used to annotate OPN1LW
  • Curation Notes: ClinVar Annotator: match by term: Protan defect
  • Original References(s): PMID:15094734 PMID:25741868 PMID:8666378


  • An association has been curated linking OPN1LW and red color blindness in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to red color blindness  (DOID:13910)
  • 6 papers in RGD have been used to annotate OPN1LW
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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