Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking FKRP and autosomal recessive limb-girdle muscular dystrophy type 2I in Homo sapiens.        

  • The association was inferred from mutant phenotype (IMP)
  •  
  • The annotation was made from Qiao C, etal., Mol Ther. 2014 Nov;22(11):1890-9. doi: 10.1038/mt.2014.141. Epub 2014 Jul 22.
  • 2 additional annotations were made from Qiao C, etal., Mol Ther. 2014 Nov;22(11):1890-9. doi: 10.1038/mt.2014.141. Epub 2014 Jul 22.
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2I  (DOID:0110299)
  • 20 papers in RGD have been used to annotate FKRP
  • Qualifier: treatment


  • An association has been curated linking Fkrp and autosomal recessive limb-girdle muscular dystrophy type 2I in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Qiao C, etal., Mol Ther. 2014 Nov;22(11):1890-9. doi: 10.1038/mt.2014.141. Epub 2014 Jul 22.
  • The annotation has been inferred from sequence orthology with FKRP (Homo sapiens) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Qiao C, etal., Mol Ther. 2014 Nov;22(11):1890-9. doi: 10.1038/mt.2014.141. Epub 2014 Jul 22.
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2I  (DOID:0110299)
  • 23 papers in RGD have been used to annotate Fkrp
  • Qualifier: treatment


  • An association has been curated linking Fkrp and autosomal recessive limb-girdle muscular dystrophy type 2I in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Qiao C, etal., Mol Ther. 2014 Nov;22(11):1890-9. doi: 10.1038/mt.2014.141. Epub 2014 Jul 22.
  • The annotation has been inferred from sequence orthology with FKRP (Homo sapiens) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Qiao C, etal., Mol Ther. 2014 Nov;22(11):1890-9. doi: 10.1038/mt.2014.141. Epub 2014 Jul 22.
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2I  (DOID:0110299)
  • 22 papers in RGD have been used to annotate Fkrp
  • Qualifier: treatment


  • Go Back to source page   Continue to Ontology report