Send us a Message

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


1 Annotations Found.

An association has been curated linking GPX1 and autosomal recessive limb-girdle muscular dystrophy type 2P 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:26895460 (Homo sapiens)
  • 13 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2P  (DOID:0110293)
  • 0 papers in RGD have been used to annotate GPX1
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C9
  • Original References(s): PMID:20234391 PMID:28492532

  • Go Back to source page   Continue to Ontology report