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GENE - TERM ANNOTATION REPORT

13 Annotations Found.

An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • 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 Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:17559086 PMID:17878207 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:26130484 PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:18177472 PMID:18414213 PMID:21228398 PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:14627679 PMID:17878207 PMID:21102627 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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:8640429 (Homo sapiens)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:19015585 PMID:23582336 PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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:8640441 (Homo sapiens)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:19015585 PMID:23582336 PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:18414213 PMID:22037554 PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and Congenital Muscular Dystrophy with Central Nervous System Involvement 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)
  • 1 RGD objects have been annotated to Congenital Muscular Dystrophy with Central Nervous System Involvement  (DOID:9006181)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, with central nervous system involvement
  • Original References(s): PMID:17044012 PMID:17878207 PMID:19179078 PMID:19299310 PMID:19396839 PMID:20961758 PMID:25821721 PMID:26923585 PMID:28492532 PMID:30060766


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