Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking OPN1SW and blue 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 blue color blindness  (DOID:11661)
  • 6 papers in RGD have been used to annotate OPN1SW


  • An association has been curated linking OPN1SW and blue 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:127315208 (Homo sapiens)
  • 1 RGD objects have been annotated to blue color blindness  (DOID:11661)
  • 6 papers in RGD have been used to annotate OPN1SW
  • Curation Notes: ClinVar Annotator: match by term: Tritanopia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking OPN1SW and blue 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:8594847 (Homo sapiens)
  • 1 RGD objects have been annotated to blue color blindness  (DOID:11661)
  • 6 papers in RGD have been used to annotate OPN1SW
  • Curation Notes: ClinVar Annotator: match by term: Blue color blindness
  • Original References(s): PMID:1531728 PMID:28492532


  • An association has been curated linking OPN1SW and blue 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:8594846 (Homo sapiens)
  • 1 RGD objects have been annotated to blue color blindness  (DOID:11661)
  • 6 papers in RGD have been used to annotate OPN1SW
  • Curation Notes: ClinVar Annotator: match by term: Blue color blindness
  • Original References(s): PMID:1531728 PMID:28492532


  • An association has been curated linking OPN1SW and blue 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 blue color blindness  (DOID:11661)
  • 6 papers in RGD have been used to annotate OPN1SW
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking OPN1SW and blue 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:151830054 (Homo sapiens)
  • 1 RGD objects have been annotated to blue color blindness  (DOID:11661)
  • 6 papers in RGD have been used to annotate OPN1SW
  • Curation Notes: ClinVar Annotator: match by term: Blue color blindness
  • Original References(s): PMID:28492532


  • An association has been curated linking OPN1SW and blue 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:8594848 (Homo sapiens)
  • 1 RGD objects have been annotated to blue color blindness  (DOID:11661)
  • 6 papers in RGD have been used to annotate OPN1SW
  • Curation Notes: ClinVar Annotator: match by term: Blue color blindness
  • Original References(s): PMID:1386496 PMID:28492532 PMID:2937147 PMID:31816670


  • Go Back to source page   Continue to Ontology report