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GENE - TERM ANNOTATION REPORT

18 Annotations Found.

An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11623300 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11615518 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11659241 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11663487 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11631086 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:28903845 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:17363247


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11632271 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11630230 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11618465 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:28908016 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11631556 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11655209 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11628863 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11629339 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11626222 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11627802 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11645007 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking MINK1 and congenital myasthenic syndrome in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11628307 (Homo sapiens)
  • 86 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate MINK1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


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