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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Hnrnpa2b1 and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 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 HNRNPA2B1 (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 2  (DOID:0111384)
  • 28 papers in RGD have been used to annotate Hnrnpa2b1
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2
  • Original References(s): PMID:28492532


  • An association has been curated linking Hnrnpa2b1 and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 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 HNRNPA2B1 (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 2  (DOID:0111384)
  • 28 papers in RGD have been used to annotate Hnrnpa2b1
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Hnrnpa2b1 and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 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 HNRNPA2B1 (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 2  (DOID:0111384)
  • 28 papers in RGD have been used to annotate Hnrnpa2b1
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2
  • Original References(s): PMID:11891683, PMID:23455423


  • An association has been curated linking Hnrnpa2b1 and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 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 HNRNPA2B1 (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 2  (DOID:0111384)
  • 28 papers in RGD have been used to annotate Hnrnpa2b1


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.