Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:3178
  • Symbol:HNRNPA1
  • Description:heterogeneous nuclear ribonucleoprotein A1

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Disease_Term Source Rank Other Values
?Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3, 615424 (3) OMIM high
  • Genome region :12q13.13
  • OMIM_ID :164017OMIM gene ID
  • OMIM_ID :615424OMIM phenotype ID
Amyotrophic lateral sclerosis 20, 615426 (3) OMIM high
  • Genome region :12q13.13
  • OMIM_ID :164017OMIM gene ID
  • OMIM_ID :615426OMIM phenotype ID