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1 Annotations Found.

An association has been curated linking LOC687707 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 C17orf107 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital myasthenic syndrome 1B  (DOID:0110662)
  • 1 papers in RGD have been used to annotate LOC687707
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 1B, fast-channel
  • Original References(s): PMID:17878953 PMID:26467025 PMID:28492532 PMID:8755487

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