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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking Clcn2 and Familial Hyperaldosteronism, Type II in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with CLCN2 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Familial Hyperaldosteronism, Type II  (DOID:9006303)
  • 14 papers in RGD have been used to annotate Clcn2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:29403011


  • An association has been curated linking Clcn2 and Familial Hyperaldosteronism, Type II 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 CLCN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Familial Hyperaldosteronism, Type II  (DOID:9006303)
  • 14 papers in RGD have been used to annotate Clcn2
  • Curation Notes: ClinVar Annotator: match by term: Hyperaldosteronism, familial, type II
  • Original References(s): PMID:19861545 PMID:23542698 PMID:25907736


  • An association has been curated linking Clcn2 and Familial Hyperaldosteronism, Type II 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 CLCN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Familial Hyperaldosteronism, Type II  (DOID:9006303)
  • 14 papers in RGD have been used to annotate Clcn2
  • Curation Notes: ClinVar Annotator: match by term: Hyperaldosteronism, familial, type II
  • Original References(s): PMID:29403012


  • An association has been curated linking Clcn2 and Familial Hyperaldosteronism, Type II 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 CLCN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Familial Hyperaldosteronism, Type II  (DOID:9006303)
  • 14 papers in RGD have been used to annotate Clcn2
  • Curation Notes: ClinVar Annotator: match by term: Hyperaldosteronism, familial, type II
  • Original References(s): PMID:29403011


  • An association has been curated linking Clcn2 and Familial Hyperaldosteronism, Type II 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 CLCN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Familial Hyperaldosteronism, Type II  (DOID:9006303)
  • 14 papers in RGD have been used to annotate Clcn2


  • An association has been curated linking Clcn2 and Familial Hyperaldosteronism, Type II 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 CLCN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Familial Hyperaldosteronism, Type II  (DOID:9006303)
  • 14 papers in RGD have been used to annotate Clcn2
  • Curation Notes: ClinVar Annotator: match by term: FH II
  • Original References(s): PMID:19191339 PMID:25741868


  • An association has been curated linking Clcn2 and Familial Hyperaldosteronism, Type II 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 CLCN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Familial Hyperaldosteronism, Type II  (DOID:9006303)
  • 14 papers in RGD have been used to annotate Clcn2
  • Curation Notes: ClinVar Annotator: match by term: Hyperaldosteronism, familial, type II
  • Original References(s): PMID:19861545 PMID:23542698 PMID:25907736 PMID:29403011


  • An association has been curated linking Clcn2 and Familial Hyperaldosteronism, Type II 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 CLCN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Familial Hyperaldosteronism, Type II  (DOID:9006303)
  • 14 papers in RGD have been used to annotate Clcn2
  • Curation Notes: ClinVar Annotator: match by term: Hyperaldosteronism, familial, type II
  • Original References(s): PMID:25741868


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