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GENE - TERM ANNOTATION REPORT

32 Annotations Found.

An association has been curated linking CLCNKB and Bartter disease type 3 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:21070305 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24830959 PMID:26920127 PMID:28381550 PMID:28492532 PMID:29254190


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:8560011 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:10906158 PMID:11102542


    • An association has been curated linking CLCNKB and Bartter disease type 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:13809141 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:17185149 PMID:25741868 PMID:26467025


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:13529494 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24033266 PMID:25741868


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:243049775 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:31690835


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:21073939 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24058621 PMID:24830959 PMID:25741868 PMID:25810436 PMID:26467025 PMID:28288174 PMID:28492532 PMID:28555925 PMID:32576985


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:8597585 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:10831588 PMID:10906158 PMID:11734858 PMID:21631963 PMID:23703872 PMID:23991001 PMID:25741868 PMID:25810436 PMID:26467025 PMID:28381550 PMID:28492532 PMID:31115572 PMID:32857947 PMID:9326936


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:8560012 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:11102542 PMID:25741868


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:41406236 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:28492532


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:151756507 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24830959 PMID:25741868 PMID:28492532


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:21070309 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:21865213 PMID:28381550 PMID:28492532 PMID:31803959 PMID:31834604


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:38460525 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:10906158 PMID:24830959 PMID:25741868 PMID:26920127 PMID:28381550 PMID:28492532 PMID:29254190


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:13470863 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:17185149 PMID:24830959 PMID:25525159 PMID:25810436 PMID:26467025 PMID:26920127 PMID:28381550 PMID:28492532 PMID:29254190


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:150536485 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:21415153 PMID:24058621 PMID:24271511 PMID:24830959 PMID:25741868 PMID:28381550 PMID:28492532


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:8597584 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:15875219 PMID:24830959 PMID:25741868 PMID:28492532 PMID:31803959 PMID:33532864 PMID:9326936


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:8597588 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:15531551 PMID:16902263 PMID:17622951 PMID:24830959 PMID:24965226 PMID:25741868 PMID:26920127 PMID:28381550 PMID:28492532 PMID:29254190


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:11350682 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24830959 PMID:25741868 PMID:26920127 PMID:28381550 PMID:28492532 PMID:29254190 PMID:31672324


    • An association has been curated linking CLCNKB and Bartter disease type 3 in Homo sapiens.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Clcnkb (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: OMIM:607364


    • An association has been curated linking CLCNKB and Bartter disease type 3 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:405281692 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:25741916


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:38598741 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:20810575 PMID:24830959 PMID:25741868 PMID:26920127 PMID:28381550 PMID:28492532 PMID:29254190 PMID:30773290


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:10405791 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24830959 PMID:25326637 PMID:25741868 PMID:26920127 PMID:28381550 PMID:28492532 PMID:29254190 PMID:31672324


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:13531146 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:13611927|RGD:21070306 (Homo sapiens) & RGD:13611927|RGD:21070306 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24830959 PMID:25741868 PMID:26920127 PMID:28381550 PMID:28492532 PMID:29254190


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:12833145|RGD:13478059|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens) & RGD:12833145|RGD:13478059|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens) & RGD:12833145|RGD:13478059|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens) & RGD:12833145|RGD:13478059|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens) & RGD:12833145|RGD:13478059|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens) & RGD:12833145|RGD:13478059|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens) & RGD:12833145|RGD:13478059|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens) & RGD:12833145|RGD:13478059|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:8597583|RGD:8597586|RGD:8597587 (Homo sapiens) & RGD:8597583|RGD:8597586|RGD:8597587 (Homo sapiens) & RGD:8597583|RGD:8597586|RGD:8597587 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:9326936


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:12838494|RGD:13481618|RGD:13808933 (Homo sapiens) & RGD:12838494|RGD:13481618|RGD:13808933 (Homo sapiens) & RGD:12838494|RGD:13481618|RGD:13808933 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:41406732|RGD:41406774 (Homo sapiens) & RGD:41406732|RGD:41406774 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:25741868 PMID:33532864


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:11634331|RGD:21070310|RGD:21070312 (Homo sapiens) & RGD:11634331|RGD:21070310|RGD:21070312 (Homo sapiens) & RGD:11634331|RGD:21070310|RGD:21070312 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens) & RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370|RGD:8621371 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:25741868


    • An association has been curated linking CLCNKB and Bartter disease type 3 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:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens) & RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15128451|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151728709|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
  • 5 RGD objects have been annotated to Bartter disease type 3  (DOID:0110144)
  • 8 papers in RGD have been used to annotate CLCNKB
  • Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
  • Original References(s): PMID:25741868 PMID:28492532


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