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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking CTNNA1 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:26909703 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 19 papers in RGD have been used to annotate CTNNA1
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy


    • An association has been curated linking CTNNA1 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:13435022 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 19 papers in RGD have been used to annotate CTNNA1
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:25741868 PMID:28041643 PMID:28492532 PMID:33137351


    • An association has been curated linking CTNNA1 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:14712935 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 19 papers in RGD have been used to annotate CTNNA1
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532 PMID:30515673 PMID:32051609 PMID:34425242


    • An association has been curated linking CTNNA1 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:14702018|RGD:14712951|RGD:14743596|RGD:26901121|RGD:26910360 (Homo sapiens) & RGD:14702018|RGD:14712951|RGD:14743596|RGD:26901121|RGD:26910360 (Homo sapiens) & RGD:14702018|RGD:14712951|RGD:14743596|RGD:26901121|RGD:26910360 (Homo sapiens) & RGD:14702018|RGD:14712951|RGD:14743596|RGD:26901121|RGD:26910360 (Homo sapiens) & RGD:14702018|RGD:14712951|RGD:14743596|RGD:26901121|RGD:26910360 (Homo sapiens)
  • 1015 RGD objects have been annotated to fundus dystrophy  (DOID:8501)
  • 19 papers in RGD have been used to annotate CTNNA1
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:28492532


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