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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking TSPAN1 and congenital muscular dystrophy-dystroglycanopathy type A3 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:8557832 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A3  (DOID:0111236)
  • 0 papers in RGD have been used to annotate TSPAN1
  • Curation Notes: ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3
  • Original References(s): PMID:11709191


  • An association has been curated linking TSPAN1 and congenital muscular dystrophy-dystroglycanopathy type A3 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:8617319 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A3  (DOID:0111236)
  • 0 papers in RGD have been used to annotate TSPAN1
  • Curation Notes: ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3
  • Original References(s): PMID:11709191 PMID:12788071 PMID:12849864


  • An association has been curated linking TSPAN1 and congenital muscular dystrophy-dystroglycanopathy type A3 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:10406084 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A3  (DOID:0111236)
  • 0 papers in RGD have been used to annotate TSPAN1
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3
  • Original References(s): PMID:25741868


  • An association has been curated linking TSPAN1 and congenital muscular dystrophy-dystroglycanopathy type A3 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:8557835 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A3  (DOID:0111236)
  • 0 papers in RGD have been used to annotate TSPAN1
  • Curation Notes: ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED
  • Original References(s): PMID:15236414 PMID:16427280 PMID:17906881 PMID:21361872 PMID:25390965 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking TSPAN1 and congenital muscular dystrophy-dystroglycanopathy type A3 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:8557831 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A3  (DOID:0111236)
  • 0 papers in RGD have been used to annotate TSPAN1
  • Curation Notes: ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3
  • Original References(s): PMID:11709191 PMID:12788071 PMID:12849864


  • An association has been curated linking TSPAN1 and congenital muscular dystrophy-dystroglycanopathy type A3 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:8557836 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A3  (DOID:0111236)
  • 0 papers in RGD have been used to annotate TSPAN1
  • Curation Notes: ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3
  • Original References(s): PMID:15236414 PMID:16427280 PMID:17030669 PMID:17559086 PMID:19299310 PMID:20215985 PMID:21361872 PMID:22323514 PMID:22522420 PMID:27493216


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