Gene table: search width pubmed_id = 7889574


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Long QT syndrome (Romano-Ward syndrome) - (AD)
7.7
7889574
SCN5A (3p21)
Voltage-gated sodium channel type V alpha
* Progressive familial heart block, type I - PFHBI
* Cardiomyopathy, dilated, 1E - CMD1E
* Sick Sinus Syndrome 1, autosomal recessive - SSS1
* Ventricular fibrillation, idiopathic - IVF
* Ventricular fibrillation, paroxysmal familial - VF
* Hereditary bundle branch system defect - HBBD
* Cardiac conduction defect, progressive - PCCD
* Brugada syndrome - SCN5A
* Long QT syndrome-3 - LQT3