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GENE - TERM ANNOTATION REPORT

25 Annotations Found.

An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by OMIM:163800
  • Original References(s): PMID:17646576


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by OMIM:163800
  • Original References(s): PMID:16407510


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by OMIM:163800
  • Original References(s): PMID:25145517 PMID:25145518 PMID:27173043


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:12750403


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by OMIM:163800
  • Original References(s): PMID:20693575 PMID:25145518 PMID:27173043


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:21615589 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by OMIM:163800
  • Original References(s): PMID:25145517


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:21615589 PMID:25741868 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28086167 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:21615589 PMID:23623143 PMID:23861362 PMID:24033266 PMID:24569893 PMID:25145517 PMID:25467552 PMID:25642760 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:25741868 PMID:26467025


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:28254188 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:15123648 PMID:19748888 PMID:20662977 PMID:23075627 PMID:24492017 PMID:24569893 PMID:25642760 PMID:27553229 PMID:28204831 PMID:28350118


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:23623143 PMID:23861362 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:23861362 PMID:25145518 PMID:25145519 PMID:25642760 PMID:25741868 PMID:26467025 PMID:27173043 PMID:27659478 PMID:28104484 PMID:28182231 PMID:28254189 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28341588 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:23861362 PMID:25741868


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:21615589 PMID:23623143 PMID:23631727 PMID:25741868 PMID:26467025 PMID:27439367 PMID:27553229


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:23623143 PMID:25741868 PMID:26467025 PMID:27182706 PMID:28492532


  • An association has been curated linking Hcn4 and Sick Sinus Syndrome 2, Autosomal Dominant in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with HCN4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Sick Sinus Syndrome 2, Autosomal Dominant  (DOID:9003749)
  • 20 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Sick sinus syndrome 2, autosomal dominant
  • Original References(s): PMID:25145517 PMID:25741868 PMID:27173043 PMID:28492532


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