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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Tnpo3 and autosomal dominant limb-girdle muscular dystrophy type 2 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 TNPO3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 RGD objects have been annotated to autosomal dominant limb-girdle muscular dystrophy type 2  (DOID:0110304)
  • 5 papers in RGD have been used to annotate Tnpo3


    • An association has been curated linking Tnpo3 and autosomal dominant limb-girdle muscular dystrophy type 2 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 TNPO3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 RGD objects have been annotated to autosomal dominant limb-girdle muscular dystrophy type 2  (DOID:0110304)
  • 5 papers in RGD have been used to annotate Tnpo3
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant limb-girdle muscular dystrophy type 1F | ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 1F
  • Original References(s): PMID:11222786 PMID:16199547 PMID:17576681 PMID:23543484 PMID:23667635 PMID:25741868 PMID:28492532 PMID:30567601 PMID:31071488 PMID:31217819 PMID:31674007 PMID:31953240 PMID:9536098


    • An association has been curated linking Tnpo3 and autosomal dominant limb-girdle muscular dystrophy type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TNPO3 (Homo sapiens) [(EXP) inferred from experiment]
  • 8 RGD objects have been annotated to autosomal dominant limb-girdle muscular dystrophy type 2  (DOID:0110304)
  • 5 papers in RGD have been used to annotate Tnpo3
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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