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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Dpm3 and Congenital Disorder of Glycosylation Type 1O in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with DPM3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Congenital Disorder of Glycosylation Type 1O  (DOID:9006227)
  • 5 papers in RGD have been used to annotate Dpm3


  • An association has been curated linking Dpm3 and Congenital Disorder of Glycosylation Type 1O in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with DPM3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Congenital Disorder of Glycosylation Type 1O  (DOID:9006227)
  • 5 papers in RGD have been used to annotate Dpm3
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1O | ClinVar Annotator: match by term: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, DPM3-RELATED
  • Original References(s): PMID:19576565 PMID:28492532 PMID:29246662 PMID:31469168


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