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GENE - TERM ANNOTATION REPORT

20 Annotations Found.

An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by OMIM:601678
  • Original References(s): PMID:8640224


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by OMIM:601678
  • Original References(s): PMID:9355073


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by OMIM:601678
  • Original References(s): PMID:19513753


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by OMIM:601678


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:28095294


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:26963954


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:25741868


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:28893421


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:25741868 PMID:26467025


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:28492532


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:12761241 PMID:15167446 PMID:19096086 PMID:20219833 PMID:25326637 PMID:26467025 PMID:28000888 PMID:28095294 PMID:30113482 PMID:9585600


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:18391953 PMID:21157372 PMID:21209010 PMID:24253496


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:24550759 PMID:26467025 PMID:28492532


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:19602640 PMID:26467025 PMID:28492532


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:20219833 PMID:25741868 PMID:28492532


  • An association has been curated linking Slc12a1 and Bartter disease type 1 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 SLC12A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Bartter disease type 1  (DOID:0110142)
  • 19 papers in RGD have been used to annotate Slc12a1
  • Curation Notes: ClinVar Annotator: match by term: Bartter syndrome, type 1, antenatal
  • Original References(s): PMID:23897314 PMID:28492532


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