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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking CACNA1C and Brugada syndrome 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:10044905 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking CACNA1C and Brugada syndrome 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:8600661 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Brugada syndrome
  • Original References(s): PMID:17224476 PMID:20817017 PMID:22385640 PMID:22581653


    • An association has been curated linking CACNA1C and Brugada syndrome 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:8600660 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:17224476 PMID:20817017 PMID:22581653 PMID:23414114 PMID:24033266 PMID:24183960 PMID:25333069 PMID:25741868 PMID:28492532 PMID:34222376


    • An association has been curated linking CACNA1C and Brugada syndrome 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:8690390 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:20817017 PMID:25633834 PMID:25741868 PMID:28492532


    • An association has been curated linking CACNA1C and Brugada syndrome 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:8623370 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:20817017 PMID:22581653 PMID:23861362 PMID:25741868 PMID:28492532


    • An association has been curated linking CACNA1C and Brugada syndrome 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:8623368 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Brugada syndrome (shorter-than-normal QT interval)
  • Original References(s): PMID:20817017 PMID:22581653 PMID:23414114 PMID:24055113 PMID:25637381 PMID:28492532


    • An association has been curated linking CACNA1C and Brugada syndrome 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:8623369 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:20817017 PMID:22581653 PMID:24033266 PMID:25741868 PMID:28492532 PMID:31539150 PMID:31737537


    • An association has been curated linking CACNA1C and Brugada syndrome 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:12741276 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:25637381 PMID:25741868 PMID:28492532


    • An association has been curated linking CACNA1C and Brugada syndrome 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:8640333 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:20817017 PMID:22840528 PMID:23861362 PMID:25633834 PMID:25741868 PMID:27662471 PMID:28492532 PMID:28750076


    • An association has been curated linking CACNA1C and Brugada syndrome 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:10044908 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:23631430 PMID:25741868 PMID:27231019 PMID:28341588 PMID:28492532 PMID:31293105 PMID:31737537


    • An association has been curated linking CACNA1C and Brugada syndrome 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:10046254 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:23861362 PMID:25637381 PMID:25741868 PMID:28492532 PMID:32145446


    • An association has been curated linking CACNA1C and Brugada syndrome 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:26902883 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Brugada syndrome
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


    • An association has been curated linking CACNA1C and Brugada syndrome 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:10044526 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Brugada syndrome
  • Original References(s): PMID:25633834 PMID:25741868 PMID:28492532 PMID:30279520


    • An association has been curated linking CACNA1C and Brugada syndrome 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:8623367 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Brugada syndrome
  • Original References(s): PMID:20817017 PMID:22581653 PMID:25741868 PMID:28492532 PMID:30172029 PMID:30662450


    • An association has been curated linking CACNA1C and Brugada syndrome 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:10044883|RGD:11546030|RGD:11551711|RGD:11621183|RGD:8690367 (Homo sapiens) & RGD:10044883|RGD:11546030|RGD:11551711|RGD:11621183|RGD:8690367 (Homo sapiens) & RGD:10044883|RGD:11546030|RGD:11551711|RGD:11621183|RGD:8690367 (Homo sapiens) & RGD:10044883|RGD:11546030|RGD:11551711|RGD:11621183|RGD:8690367 (Homo sapiens) & RGD:10044883|RGD:11546030|RGD:11551711|RGD:11621183|RGD:8690367 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Brugada syndrome | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
  • Original References(s): PMID:28492532


    • An association has been curated linking CACNA1C and Brugada syndrome 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:11607688|RGD:11652084|RGD:11657559|RGD:11657659 (Homo sapiens) & RGD:11607688|RGD:11652084|RGD:11657559|RGD:11657659 (Homo sapiens) & RGD:11607688|RGD:11652084|RGD:11657559|RGD:11657659 (Homo sapiens) & RGD:11607688|RGD:11652084|RGD:11657559|RGD:11657659 (Homo sapiens)
  • 178 RGD objects have been annotated to Brugada syndrome  (DOID:0050451)
  • 15 papers in RGD have been used to annotate CACNA1C
  • Curation Notes: ClinVar Annotator: match by term: Brugada syndrome


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