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GENE - TERM ANNOTATION REPORT

37 Annotations Found.

An association has been curated linking PDE6B and fundus dystrophy 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:8599291 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:25741868 PMID:28041643 PMID:28492532 PMID:28981474 PMID:29472945 PMID:34906470 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:14698469 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:30718709


    • An association has been curated linking PDE6B and fundus dystrophy 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:13516290 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:27353947 PMID:28492532 PMID:30646425


    • An association has been curated linking PDE6B and fundus dystrophy 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:14746795 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532 PMID:28559085 PMID:30924848


    • An association has been curated linking PDE6B and fundus dystrophy 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:12895265 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:27898983 PMID:28492532 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:13435059 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:17576681 PMID:22334370 PMID:25741868 PMID:28041643 PMID:28492532 PMID:30718709 PMID:9536098


    • An association has been curated linking PDE6B and fundus dystrophy 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:26906148 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:23105016 PMID:24828262 PMID:25525159 PMID:25741868 PMID:27588261 PMID:28492532 PMID:34906470 PMID:8394174 PMID:8595886 PMID:9238087


    • An association has been curated linking PDE6B and fundus dystrophy 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:10050145 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25741868 PMID:28492532 PMID:34906470


    • An association has been curated linking PDE6B and fundus dystrophy 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:26909934 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:25741868 PMID:28130426 PMID:28492532 PMID:34906470 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:9688749 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:16199547 PMID:22334370 PMID:24033266 PMID:25097241 PMID:25741868 PMID:28041643 PMID:28224992 PMID:28492532 PMID:30718709 PMID:34906470 PMID:7724547 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:14693745 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:24265693 PMID:25741868 PMID:26766544 PMID:28492532 PMID:30646425 PMID:34906470 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:26910494 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:28492532 PMID:30998820 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:26906683 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:16199547 PMID:22334370 PMID:28492532 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:26904302 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25097241 PMID:25741868 PMID:28492532 PMID:30924848 PMID:33691693


    • An association has been curated linking PDE6B and fundus dystrophy 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:8639692 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:24938718 PMID:28492532 PMID:28912962 PMID:30718709 PMID:30998820 PMID:33576794


    • An association has been curated linking PDE6B and fundus dystrophy 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:11093795 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:24033266 PMID:27208204 PMID:28492532 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:26910376 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25356976 PMID:28492532 PMID:29641573


    • An association has been curated linking PDE6B and fundus dystrophy 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:10448572 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:12525556 PMID:17267005 PMID:25823529 PMID:28041643 PMID:28492532 PMID:30998820


    • An association has been curated linking PDE6B and fundus dystrophy 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:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens) & RGD:11593029|RGD:13795171|RGD:26909304|RGD:26909308|RGD:26909439|RGD:26910377|RGD:26910445|RGD:26910543|RGD:26910561|RGD:26910703|RGD:28901291|RGD:405264305|RGD:405264306|RGD:405264308|RGD:405264310|RGD:405264314|RGD:405264316|RGD:405264317|RGD:405264318|RGD:405264320|RGD:405264321|RGD:405264323|RGD:405264325|RGD:405264326|RGD:405264328|RGD:405264330|RGD:405264331|RGD:405264336|RGD:405264338|RGD:405264339|RGD:405264340|RGD:405264342|RGD:405264344|RGD:405264402|RGD:405264424|RGD:405264425|RGD:405264426|RGD:9481040 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy


    • An association has been curated linking PDE6B and fundus dystrophy 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:14395808 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:25741868 PMID:27588261 PMID:28492532 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:151747767 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532 PMID:33177553


    • An association has been curated linking PDE6B and fundus dystrophy 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:38483270 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25356976 PMID:28492532


    • An association has been curated linking PDE6B and fundus dystrophy 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:9480273 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25324289 PMID:28492532 PMID:30718709


    • An association has been curated linking PDE6B and fundus dystrophy 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:8599293 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25356976 PMID:25741868 PMID:25827439 PMID:26155838 PMID:28492532 PMID:29785639 PMID:30718709 PMID:7724547 PMID:8394174


    • An association has been curated linking PDE6B and fundus dystrophy 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:9480274 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25741868 PMID:25827439 PMID:26155838 PMID:28492532 PMID:9543643


    • An association has been curated linking PDE6B and fundus dystrophy 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:8563488 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:8394174


    • An association has been curated linking PDE6B and fundus dystrophy 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:15100326|RGD:15192518|RGD:8692378 (Homo sapiens) & RGD:15100326|RGD:15192518|RGD:8692378 (Homo sapiens) & RGD:15100326|RGD:15192518|RGD:8692378 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking PDE6B and fundus dystrophy 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:26885253 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532 PMID:31054281


    • An association has been curated linking PDE6B and fundus dystrophy 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:12907467 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:18310263 PMID:25356976 PMID:25741868 PMID:28492532 PMID:31054281


    • An association has been curated linking PDE6B and fundus dystrophy 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:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens) & RGD:10050632|RGD:11582850|RGD:11587842|RGD:11588423|RGD:11589353|RGD:11593608|RGD:11593840|RGD:126761622|RGD:127272925|RGD:151728606|RGD:151742070|RGD:15179391|RGD:151842336|RGD:151864987|RGD:152121722|RGD:26906793|RGD:26909756|RGD:26910175|RGD:26922013|RGD:28894965|RGD:28901474|RGD:38465387|RGD:38497549|RGD:38499071|RGD:402502394|RGD:405180867|RGD:405235614 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532


    • An association has been curated linking PDE6B and fundus dystrophy 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:38490131 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532 PMID:33177553 PMID:33946315


    • An association has been curated linking PDE6B and fundus dystrophy 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:12899983 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532 PMID:28981474 PMID:36819107


    • An association has been curated linking PDE6B and fundus dystrophy 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:26910564 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532 PMID:36460718


    • An association has been curated linking PDE6B and fundus dystrophy 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:14698657 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30029497 PMID:30718709 PMID:31630094 PMID:33090715 PMID:34906470 PMID:35836572 PMID:36460718


    • An association has been curated linking PDE6B and fundus dystrophy 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:26911007 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:16199547 PMID:22334370 PMID:26355662 PMID:28492532 PMID:30054919 PMID:3203739 PMID:35272565 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:26909730|RGD:26910190 (Homo sapiens) & RGD:26909730|RGD:26910190 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:22334370 PMID:28492532 PMID:8394174 PMID:8595886


    • An association has been curated linking PDE6B and fundus dystrophy 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:26909452|RGD:26910529 (Homo sapiens) & RGD:26909452|RGD:26910529 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 12 papers in RGD have been used to annotate PDE6B
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532 PMID:30998820


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