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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:14701864 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:13808894 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:14706086 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:14703084 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:38483807 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:8571247 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:23453667


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:13495391 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:14710832 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:26915097 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


  • An association has been curated linking TBCE and congenital muscular dystrophy-dystroglycanopathy type A11 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:12838355 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate TBCE
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • Original References(s): PMID:28492532


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