Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

191 Annotations Found.

An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11558102 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12892400 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26916903 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617306 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14712281 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:15137803 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26897504 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8602851 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13785013 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:19396839 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:15150407 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13812423 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:15100315 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13465709 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14740419 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8640432 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617303 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11637532 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11351849 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26888053 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14741582 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26913368 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8640436 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:17559086 PMID:17878207 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14712479 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11641327 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:21520333 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13817470 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11643079 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14720795 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8602853 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg syndrome
  • Original References(s): PMID:14627679 PMID:17878207 PMID:21102627 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26919792 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11643551 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11599342 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:17597323 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13496718 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617318 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13535774 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11644108 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11643606 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11636103 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26895011 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:9692930 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:26467025 PMID:27124789 PMID:28492532 PMID:28688748


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8596046 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:14627679 PMID:25814170 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617288 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13473509 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14728074 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:9692931 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26918885 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:24144914 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11639598 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11348150 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:11165248 PMID:14627679 PMID:20961758 PMID:25741868 PMID:26809617 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13215155 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14735404 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12740210 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:17878207 PMID:18177472 PMID:18752264 PMID:19266496 PMID:25741868 PMID:27065010 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26906637 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14723907 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617316 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617277 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11577477 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:26130484 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13809492 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11350280 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617272 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13212373 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617274 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26900192 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:9691350 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:26633542 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12883159 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8596050 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:18177472 PMID:18414213 PMID:21228398 PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14730774 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26920426 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13529283 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13491643 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617290 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13806341 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26907049 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14723047 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13515810 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13819220 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38499526 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11639800 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38478734 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13806973 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11635944 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:21520333 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13492453 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26886678 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11637205 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:21520333 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26915606 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11543733 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38460246 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617268 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13504410 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11640464 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13516399 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14717349 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12841360 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14724421 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11643920 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13789867 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617300 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13807775 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11638309 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:21520333 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11546237 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38493388 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:15113741 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8596054 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:17597323 PMID:17878207 PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11550896 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532 PMID:28785732


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38488194 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13837680 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14715539 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13484915 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13817972 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617304 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38492809 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13807751 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14714355 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14719956 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:17044012 PMID:17878207 PMID:18752264 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13523872 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13523835 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8596053 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:11165248 PMID:17034757 PMID:19179078 PMID:22275357 PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14738688 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11547989 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38482746 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26906562 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:17878207 PMID:18752264 PMID:19266496 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13786535 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:17878207 PMID:18177472 PMID:18752264 PMID:19266496 PMID:27065010 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13617265 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11644117 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13811734 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13810184 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:9691347 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38498792 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11640643 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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 FKTN (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: DNA:insertion:exon:c.1167insA (human)
  • Original References(s): PMID:19266496 REF_RGD_ID:11576320


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38472790 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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 FKTN (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14735580 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38475357 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38461945 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38499755 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13515666 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11636432 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12886332 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11654095 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13518028 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:20620061 PMID:25741868 PMID:28492532 PMID:28680109


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11547160 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38500069 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:18752264 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11637272 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13477983 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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 Fktn (Mus musculus)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Original References(s): PMID:24824861 REF_RGD_ID:11537406


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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 FKTN (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Original References(s): PMID:9690476 REF_RGD_ID:1598929


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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 FKTN (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: DNA:missense mutation, nonsense mutation, insertions: :multiple
  • Original References(s): PMID:10545611 REF_RGD_ID:11062579


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12847995 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11552056 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12886545 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:9691349 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:26467025 PMID:26636822 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14726233 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8640439 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:21520333 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:9691351 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12840286 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8602854 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14717610 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11642707 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14713374 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12838006 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12891669 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26904986 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:12891797 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8602855 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13816295 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26900856 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13822680 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13516116 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8640440 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26919184 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:21520333 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13471072 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:26905137 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:15170625 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8557275 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscle eye brain disease
  • Original References(s): PMID:10545611 PMID:17044012 PMID:17878207 PMID:18177472 PMID:18752264 PMID:19266496 PMID:23757202 PMID:24144914 PMID:25741868 PMID:27065010 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8596044 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:19179078 PMID:19842201 PMID:20961758 PMID:25814170 PMID:28492532 PMID:9690476


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:11642224 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:13819384 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14741878 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:21067307 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:15134787 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:14710692 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38480203 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:15833426 PMID:22275357 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8602852 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8596047 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:17044012 PMID:17878207 PMID:19179078 PMID:19299310 PMID:19396839 PMID:20961758 PMID:25821721 PMID:26923585 PMID:28492532 PMID:30060766


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8640437 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:18414213 PMID:22037554 PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38482447 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532 PMID:28785732


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38475854 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38490615 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38494628 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38480277 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:38487928 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Walker-Warburg syndrome in Sus scrofa.        

  • 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:8640442 (Homo sapiens)
  • 33 RGD objects have been annotated to Walker-Warburg syndrome  (DOID:0050560)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Walker-Warburg congenital muscular dystrophy
  • Original References(s): PMID:22958903 PMID:23757202 PMID:25741868 PMID:28492532 PMID:28759667


  • Go Back to source page   Continue to Ontology report