Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 1778
  • Symbol: DYNC1H1
  • Description: dynein cytoplasmic 1 heavy chain 1

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Disease_Term Source Rank Other Values
Charcot-Marie-Tooth disease, axonal, type 20, 614228 (3) OMIM high
  • Genome region : 14q32.31
  • OMIM_ID : 600112 OMIM gene ID
  • OMIM_ID : 614228 OMIM phenotype ID
Mental retardation, autosomal dominant 13, 614563 (3) OMIM high
  • Genome region : 14q32.31
  • OMIM_ID : 600112 OMIM gene ID
  • OMIM_ID : 614563 OMIM phenotype ID
Spinal muscular atrophy, lower extremity-predominant 1, AD, 158600 (3) OMIM high
  • Genome region : 14q32.31
  • OMIM_ID : 158600 OMIM phenotype ID
  • OMIM_ID : 600112 OMIM gene ID