Gene table: search width pubmed_id = 26700687


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Severe foetal hypokinesia related to SCN4A - (AR)
16.33
26700687
SCN4A (17q23-q25.3)
Sodium channel, voltage-gated, type IV, alpha
* Hyperkalemic periodic paralysis - HYPP
* Myotonia potassium-aggravatd
* Sodium-channel myasthenia
* Myasthenic syndrome, acetazolamide-responsive
* Myasthenic syndrome, congenital, 16 - CMS16
* Severe foetal hypokinesia related to SCN4A
* Congenital Myopathy 22B, severe fetal - CMYP22B
* Congenital Myopathy 22A, classic - CMYP22A
* Hyperkalemic periodic paralysis, type 2 - HOKPP2
* Paramyotonia congenita of Von Eulenburg - PMC
* Potassium-aggravated myotonia