CACNB1: Difference between revisions
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Latest revision as of 05:42, 17 March 2025
CACNB1 is a gene that encodes the beta subunit of a calcium channel. This gene is located on the chromosome 17 in humans. The protein encoded by this gene is a part of the voltage-gated calcium channel complex, which plays a crucial role in the calcium signaling pathway.
Function[edit]
The CACNB1 gene encodes the beta-1 subunit of a voltage-dependent calcium channel. This subunit plays a key role in the assembly, trafficking, and function of the calcium channel. The calcium channel, composed of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits, mediates the influx of calcium ions into the cell upon membrane polarization. The beta-1 subunit increases the peak calcium current and shifts the voltage dependencies of activation and inactivation of the calcium channel to more negative voltages.
Clinical Significance[edit]
Mutations in the CACNB1 gene have been associated with Brugada syndrome, a genetic disorder that can cause a dangerous irregular heartbeat or sudden unexpected death in seemingly healthy individuals.
Research[edit]
Research on the CACNB1 gene is ongoing, with studies investigating its role in various diseases and conditions, including cardiovascular diseases, neurological disorders, and certain types of cancer.
See Also[edit]
References[edit]
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