Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:6329
  • Symbol:SCN4A
  • Description:sodium voltage-gated channel alpha subunit 4

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Disease_Term Source Rank Other Values
Hyperkalemic periodic paralysis, type 2, 170500 (3) OMIM high
  • Genome region :17q23.3
  • OMIM_ID :170500OMIM phenotype ID
  • OMIM_ID :603967OMIM gene ID
Paramyotonia congenita, 168300 (3) OMIM high
  • Genome region :17q23.3
  • OMIM_ID :168300OMIM phenotype ID
  • OMIM_ID :603967OMIM gene ID
Hypokalemic periodic paralysis, type 2, 613345 (3) OMIM high
  • Genome region :17q23.3
  • OMIM_ID :603967OMIM gene ID
  • OMIM_ID :613345OMIM phenotype ID
Myasthenic syndrome, congenital, 16, 614198 (3) OMIM high
  • Genome region :17q23.3
  • OMIM_ID :603967OMIM gene ID
  • OMIM_ID :614198OMIM phenotype ID
Myotonia congenita, atypical, acetazolamide-responsive, 608390 (3) OMIM high
  • Genome region :17q23.3
  • OMIM_ID :603967OMIM gene ID
  • OMIM_ID :608390OMIM phenotype ID