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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:28492532


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:8651643


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:17686188 PMID:28492532


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:10562302 PMID:28492532


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:20562457 PMID:27391121 PMID:28492532 PMID:8872460


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:20562457 PMID:27375219 PMID:27391121 PMID:28492532 PMID:8872460


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:25741868


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Chrnb1 and congenital myasthenic syndrome 2A 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 CHRNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 2A  (DOID:0110681)
  • 14 papers in RGD have been used to annotate Chrnb1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 2a, slow-channel
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


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