Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

23 Annotations Found.

An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:11933197 PMID:12661046 PMID:18337730 PMID:28492532 PMID:8112288 PMID:8845168


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:12661046 PMID:14639587 PMID:19949657 PMID:23113340 PMID:24625573 PMID:28492532


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:18263754 PMID:20301529 PMID:28492532


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:25741868


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:18337100


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:10533075 PMID:18220014 PMID:25741868 PMID:26467025 PMID:28492532 PMID:7981750 PMID:8112288 PMID:8857727 PMID:8857733 PMID:9122265


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:10690989 PMID:11840191 PMID:12390967 PMID:1379744 PMID:17932099 PMID:17990293 PMID:18337730 PMID:18807109 PMID:21204798 PMID:23739125 PMID:26467025 PMID:28492532 PMID:8301644 PMID:8533761 PMID:9040760


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:21045501 PMID:25741868 PMID:26467025 PMID:27118449 PMID:27415035 PMID:28492532 PMID:28706458


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:10737121 PMID:12163078 PMID:25741868 PMID:25749817 PMID:26467025 PMID:28492532 PMID:29606556 PMID:8533761 PMID:8845168


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:10430417 PMID:10644771 PMID:10665666 PMID:11840191 PMID:11933197 PMID:12390967 PMID:15162127 PMID:15980168 PMID:17107341 PMID:17932099 PMID:17990293 PMID:18337100 PMID:18337730 PMID:18807109 PMID:20301529 PMID:22094069 PMID:22197187 PMID:22649220 PMID:22995991 PMID:23097607 PMID:23739125 PMID:24033266 PMID:24349310 PMID:25741868 PMID:26096614 PMID:26467025 PMID:27142102 PMID:27296017 PMID:27614575 PMID:28492532 PMID:29606556 PMID:7874130 PMID:8533761 PMID:8845168


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:10051520 PMID:10962018 PMID:12390967 PMID:23739125 PMID:24349310 PMID:25036107 PMID:25741868 PMID:26467025 PMID:28492532 PMID:7581380 PMID:8845168 PMID:8857727


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:10690989 PMID:17654559 PMID:17932099 PMID:18337730 PMID:21221019 PMID:21698652 PMID:22094069 PMID:22407275 PMID:22521272 PMID:22641783 PMID:23113340 PMID:23739125 PMID:23933576 PMID:24037712 PMID:24088041 PMID:24304580 PMID:24349310 PMID:24452722 PMID:25741868 PMID:26467025 PMID:26510092 PMID:26633545 PMID:27199537 PMID:27266866 PMID:27614575 PMID:28492532 PMID:7874130 PMID:8533761


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:12456816 PMID:25741868 PMID:26467025 PMID:28492532 PMID:7581380 PMID:8845168 PMID:9736777


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:25741868 PMID:26467025


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:17932099 PMID:18337100 PMID:22094069 PMID:23739125 PMID:24037712 PMID:24349310 PMID:24920213 PMID:25088311 PMID:25741868 PMID:26467025 PMID:28427807 PMID:28492532 PMID:29606556 PMID:31544778 PMID:8533761 PMID:9158157 PMID:9736777


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:32117034


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:17932099 PMID:18337100 PMID:18337730 PMID:22094069 PMID:22649220 PMID:23739125 PMID:23893571 PMID:24349310 PMID:25741868 PMID:26467025 PMID:28492532 PMID:7581380 PMID:7951215 PMID:8533761 PMID:8571958


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:21221019 PMID:23408874 PMID:25088311 PMID:25741868 PMID:28492532


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:23739125 PMID:24452722 PMID:25741868 PMID:28492532


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:12390967 PMID:15786415 PMID:17932099 PMID:18337730 PMID:18816629 PMID:21387378 PMID:22995991 PMID:24037712 PMID:25741868 PMID:26467025 PMID:28492532 PMID:28662944 PMID:29606556 PMID:9736777


  • An association has been curated linking Clcn1 and Myotonia Congenita, 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 CLCN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Myotonia Congenita, Autosomal Dominant  (DOID:9001336)
  • 11 papers in RGD have been used to annotate Clcn1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myotonia, autosomal dominant form
  • Original References(s): PMID:25741868 PMID:26260254 PMID:27415035 PMID:28166811 PMID:28492532 PMID:28706458 PMID:31567646


  • Go Back to source page   Continue to Ontology report