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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Hnrnpa1 and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3 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 HNRNPA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3  (DOID:0111386)
  • 33 papers in RGD have been used to annotate Hnrnpa1
  • Curation Notes: ClinVar Annotator: match by OMIM:615424
  • Original References(s): PMID:20116073 PMID:23455423 PMID:25616961


  • An association has been curated linking Hnrnpa1 and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3 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 HNRNPA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3  (DOID:0111386)
  • 33 papers in RGD have been used to annotate Hnrnpa1


  • An association has been curated linking Hnrnpa1 and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3 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 HNRNPA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3  (DOID:0111386)
  • 33 papers in RGD have been used to annotate Hnrnpa1
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3
  • Original References(s): PMID:25741868


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