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GENE - TERM ANNOTATION REPORT

21 Annotations Found.

An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8602851 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11577477 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:26130484 PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:9692931 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11547160 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11543733 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11552056 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:12838006 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8557275 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • 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-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8596050 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:18177472 PMID:18414213 PMID:21228398 PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8602853 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • 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-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11550896 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532 PMID:28785732


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11546237 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:13529283 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8640440 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8640436 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • 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-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:9691349 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:26636822 PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8596045 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1
  • Original References(s): PMID:19342235 PMID:25741868


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8640437 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:18414213 PMID:22037554 PMID:25741868 PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8602852 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKTN and congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8596047 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • 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 congenital muscular dystrophy-dystroglycanopathy type A1 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:11547989 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A1  (DOID:0111237)
  • 0 papers in RGD have been used to annotate FKTN
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:28492532


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