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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking Chrna1 and congenital myasthenic syndrome 1B 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 CHRNA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 13 papers in RGD have been used to annotate Chrna1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 1B, fast-channel
  • Original References(s): PMID:12588888


  • An association has been curated linking Chrna1 and congenital myasthenic syndrome 1B 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 CHRNA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 13 papers in RGD have been used to annotate Chrna1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 1B, fast-channel
  • Original References(s): PMID:10195214


  • An association has been curated linking Chrna1 and congenital myasthenic syndrome 1B 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 CHRNA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 13 papers in RGD have been used to annotate Chrna1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 1B, fast-channel
  • Original References(s): PMID:15079006 PMID:7254233


  • An association has been curated linking Chrna1 and congenital myasthenic syndrome 1B 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 CHRNA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 13 papers in RGD have been used to annotate Chrna1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 1B, fast-channel
  • Original References(s): PMID:18806275


  • An association has been curated linking Chrna1 and congenital myasthenic syndrome 1B 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 CHRNA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 13 papers in RGD have been used to annotate Chrna1


  • An association has been curated linking Chrna1 and congenital myasthenic syndrome 1B 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 CHRNA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 13 papers in RGD have been used to annotate Chrna1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 1B, fast-channel
  • Original References(s): PMID:18806275 PMID:28492532


  • An association has been curated linking Chrna1 and congenital myasthenic syndrome 1B 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 CHRNA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 13 papers in RGD have been used to annotate Chrna1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 1B, fast-channel
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Chrna1 and congenital myasthenic syndrome 1B 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 CHRNA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 13 papers in RGD have been used to annotate Chrna1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 1B, fast-channel
  • Original References(s): PMID:25741868


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