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GENE - TERM ANNOTATION REPORT

3 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 Chinchilla lanigera.        

  • 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)
  • 1 papers in RGD have been used to annotate Hnrnpa2b1


    • 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 Chinchilla lanigera.        

  • 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)
  • 1 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 | ClinVar Annotator: match by term: MULTISYSTEM PROTEINOPATHY 2
  • Original References(s): PMID:11891683 PMID:16199547 PMID:17576681 PMID:23455423 PMID:25741868 PMID:28389692 PMID:28492532 PMID:29358076 PMID:9536098


    • 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 Chinchilla lanigera.        

  • 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)
  • 1 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:16199547 PMID:17576681 PMID:23455423 PMID:25741868 PMID:27990297 PMID:28389692 PMID:28492532 PMID:29358076 PMID:35484142 PMID:9536098


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