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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:12882160 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
  • Original References(s): PMID:18036232 PMID:21296577 PMID:25135358 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:8643024 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:14647208 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:13617292 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:16368217 PMID:25741868 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:8596349 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
  • Original References(s): PMID:11741828 PMID:12666124 PMID:14647208 PMID:15060126 PMID:15574464 PMID:15580560 PMID:15833432 PMID:15886712 PMID:16634037 PMID:16786213 PMID:17554798 PMID:18060779 PMID:18593008 PMID:18639457 PMID:19820980 PMID:19835634 PMID:19900540 PMID:21220724 PMID:21228398 PMID:22264518 PMID:22981120 PMID:23576288 PMID:23591631 PMID:24033266 PMID:24447024 PMID:25048216 PMID:25560911 PMID:25741868 PMID:26363967 PMID:26467025 PMID:26574668 PMID:26833294 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:11641483 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:11348442 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
  • Original References(s): PMID:14647208 PMID:15060126 PMID:24447024 PMID:25741868 PMID:27848944 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:8596360 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:12666124 PMID:15060126 PMID:15121789 PMID:16476814 PMID:16634037 PMID:18639457 PMID:19155270 PMID:26923585 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:11580531 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
  • Original References(s): PMID:14647208 PMID:18639457 PMID:23800702 PMID:25741868 PMID:25987458 PMID:27439679 PMID:28492532 PMID:28931339 PMID:30003095


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:13488908 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:13500873 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:8659562 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:14647208 PMID:18414213 PMID:25741868 PMID:26467025 PMID:27439679 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:11644197 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:30564623


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:8596348 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
  • Original References(s): PMID:11592034 PMID:12471058 PMID:15574464 PMID:17554798 PMID:19900540 PMID:23591631 PMID:25741868


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:8596347 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:11592034 PMID:12666124 PMID:12707425 PMID:14742276 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:8596353 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:12654965 PMID:14652796 PMID:15574464 PMID:16368217 PMID:18671187 PMID:19955119 PMID:23420653 PMID:23894383 PMID:26467025 PMID:28454995 PMID:28492532


  • An association has been curated linking FKRP and congenital muscular dystrophy-dystroglycanopathy type A1 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:8596362 (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 FKRP
  • Curation Notes: ClinVar Annotator: match by term: HARD syndrome
  • Original References(s): PMID:17336067 PMID:25741868 PMID:28492532 PMID:29065428 PMID:31041397 PMID:31671740


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