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 : 164017 OMIM gene ID
  • OMIM_ID : 615424 OMIM phenotype ID
Amyotrophic lateral sclerosis 20, 615426 (3) OMIM high
  • Genome region : 12q13.13
  • OMIM_ID : 164017 OMIM gene ID
  • OMIM_ID : 615426 OMIM phenotype ID