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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Pdgfra and hypereosinophilic syndrome 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 PDGFRA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 28 RGD objects have been annotated to hypereosinophilic syndrome  (DOID:999)
  • 71 papers in RGD have been used to annotate Pdgfra


    • An association has been curated linking Pdgfra and hypereosinophilic syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Cools J, etal., N Engl J Med. 2003 Mar 27;348(13):1201-14.
  • The annotation has been inferred from sequence orthology with PDGFRA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Cools J, etal., N Engl J Med. 2003 Mar 27;348(13):1201-14.
  • 28 RGD objects have been annotated to hypereosinophilic syndrome  (DOID:999)
  • 71 papers in RGD have been used to annotate Pdgfra
  • Curation Notes: DNA:translocation: (human)


    • An association has been curated linking Pdgfra and hypereosinophilic syndrome 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 PDGFRA (Homo sapiens) [(EXP) inferred from experiment]
  • 28 RGD objects have been annotated to hypereosinophilic syndrome  (DOID:999)
  • 71 papers in RGD have been used to annotate Pdgfra
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:16778211 PMID:28347583 PMID:31036733


    • An association has been curated linking Pdgfra and hypereosinophilic syndrome 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 PDGFRA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 28 RGD objects have been annotated to hypereosinophilic syndrome  (DOID:999)
  • 71 papers in RGD have been used to annotate Pdgfra
  • Curation Notes: ClinVar Annotator: match by term: Hypereosinophilic syndrome, idiopathic, resistant to imatinib | ClinVar Annotator: match by term: Idiopathic hypereosinophilic syndrome
  • Original References(s): PMID:12660384 PMID:17576681 PMID:20071345 PMID:20169295 PMID:22473090 PMID:22703879 PMID:22718859 PMID:23752188 PMID:24033266 PMID:24728327 PMID:25336117 PMID:25741868 PMID:26928227 PMID:27153395 PMID:27854218 PMID:28492532 PMID:28873162 PMID:30093976 PMID:30359545 PMID:30389923 PMID:33332384 PMID:35101336 PMID:9536098


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