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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking OPN1MW and red-green 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:8561741 (Homo sapiens)
  • 2 RGD objects have been annotated to red-green color blindness  (DOID:13909)
  • 6 papers in RGD have been used to annotate OPN1MW
  • Curation Notes: ClinVar Annotator: match by term: Deutan defect
  • Original References(s): PMID:12626747


    • An association has been curated linking OPN1MW and red-green 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:8561739 (Homo sapiens)
  • 2 RGD objects have been annotated to red-green color blindness  (DOID:13909)
  • 6 papers in RGD have been used to annotate OPN1MW
  • Curation Notes: ClinVar Annotator: match by term: Deutan defect
  • Original References(s): PMID:11772996 PMID:1302020 PMID:15094734 PMID:19421413 PMID:2788922 PMID:8666378


    • An association has been curated linking OPN1MW and red-green 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
  • 2 RGD objects have been annotated to red-green color blindness  (DOID:13909)
  • 6 papers in RGD have been used to annotate OPN1MW


    • An association has been curated linking OPN1MW and red-green 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:8561740|RGD:8561742 (Homo sapiens) & RGD:8561740|RGD:8561742 (Homo sapiens)
  • 2 RGD objects have been annotated to red-green color blindness  (DOID:13909)
  • 6 papers in RGD have been used to annotate OPN1MW
  • Curation Notes: ClinVar Annotator: match by term: Deutan defect
  • Original References(s): PMID:12051694


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