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1 Annotations Found.

An association has been curated linking Slc5a7 and congenital myasthenic syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC5A7 (Homo sapiens) [(EXP) inferred from experiment]
  • 57 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 20 papers in RGD have been used to annotate Slc5a7
  • Curation Notes: CTD Direct Evidence: marker/mechanism

  • This annotation was curated on 2019-10-08 04:41:33.0 by RGD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.