| ID | Sequence | Length | GC content |
|---|---|---|---|
| GCUCUCUGCCCGCUAACUUUCCCGAGCCCCGACCGGCGGCGCAGAGCUC… | 4085 nt | 0.5518 | |
| AGUCCUUUCCAGGGGAGAAAUGGAGAAUGAUGGAGGGUGGCCCAGGCGG… | 4480 nt | 0.5444 | |
| GCUCUCUGCCCGCUAACUUUCCCGAGCCCCGACCGGCGGCGCAGAGCUC… | 4487 nt | 0.5505 |
The protein encoded by this gene is one of several sodium channel beta subunits. These subunits interact with voltage-gated alpha subunits to change sodium channel kinetics. The encoded transmembrane protein forms interchain disulfide bonds with SCN2A. Defects in this gene are a cause of long QT syndrome type 10 (LQT10). Three protein-coding and one non-coding transcript variant have been found for this gene.[provided by RefSeq, Mar 2009]
A study in humans demonstrated that the SCN4B was listed among differentially expressed cardiac-related genes in sudden unexplained death (SUD) cases, with mutations reported in ion channelopathies or cardiomyopathies [Neubauer et al. DOI:10.1007/S00414-025-03414-4]. In a mouse model of myocardial infarction, the SCN4B mRNA, a component of the Nav1.4 channel, was decreased in ischemic heart tissue three days after coronary artery ligation and was identified as a predicted target of miR-125a and miR-351 [Williams et al. DOI:10.1152/physiolgenomics.00041.2020].