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The official name of this gene is “calcium channel, voltage-dependent, beta 4 subunit.”
CACNB4 is the gene's official symbol. The CACNB4 gene is also known by other names, listed below.
The CACNB4 gene belongs to a family of genes that provide instructions for making calcium channels. These channels, which transport positively charged calcium atoms (calcium ions) into cells, play a key role in a cell's ability to generate and transmit electrical signals. Calcium ions are involved in many different cellular functions, including cell-to-cell communication, the tensing of muscle fibers (muscle contraction), and the regulation of certain genes.
Calcium channels are each made up of a large alpha-1 (α1) subunit, which forms the hole (pore) through which calcium ions can flow. Each channel also includes several smaller subunits, which regulate the channel's activity and interact with various proteins inside and outside the cell. The CACNB4 gene provides instructions for making a regulatory subunit called beta-4 (β4). This subunit is most often associated with calcium channels in the brain, particularly the part of the brain that is involved in coordinating movements (the cerebellum).
In the brain, calcium channels play an essential role in communication between nerve cells (neurons). These channels help control the release of neurotransmitters, which are chemicals that relay signals from one neuron to another. Researchers believe that calcium channels are also involved in the survival of neurons and the ability of these cells to change and adapt over time (plasticity).
The CACNB4 gene belongs to a family of genes called CACN (calcium channels).
A gene family is a group of genes that share important characteristics. Classifying individual genes into families helps researchers describe how genes are related to each other. For more information, see What are gene families? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genefamilies) in the Handbook.
Researchers have identified at least one mutation in the CACNB4 gene that is likely to cause episodic ataxia. This mutation, which was found in a French-Canadian family with episodic ataxia type 5 (EA5), changes a single protein building block (amino acid) in the calcium channel β4 subunit. Specifically, it replaces the amino acid cysteine with the amino acid phenylalanine at position 104 (written as Cys104Phe or C104F). Scientists speculate that this genetic change may alter the ability of the β4 subunit to interact with other proteins and in some way disrupt the normal function of calcium channels in the brain. It is unclear how these effects may lead to episodes of uncoordinated movement and the other signs and symptoms of episodic ataxia.
Mutations in the CACNB4 gene have been associated with epilepsy in a small number of families. One of these mutations prematurely stops protein production at position 482 (written as Arg482Ter or R482X). This mutation results in an abnormally shortened β4 subunit that is missing a region critical for interaction with the larger α1 subunit. Calcium channels made with the altered β4 subunit close more quickly than usual, reducing the flow of calcium ions into the cell. Impaired calcium ion transport likely disrupts communication between nerve cells, causing seizures in people with this genetic change.
Another CACNB4 mutation, Cys104Phe, appears to cause epilepsy in at least one family. This genetic change (described above) has also been found in an unrelated family with episodic ataxia. Researchers are uncertain why this single mutation appears to underlie two different neurological conditions. They suspect that other genetic and environmental factors may be involved.
Cytogenetic Location: 2q23.3
Molecular Location on chromosome 2: base pairs 151,832,771 to 152,099,988
The CACNB4 gene is located on the long (q) arm of chromosome 2 at position 23.3.
More precisely, the CACNB4 gene is located from base pair 151,832,771 to base pair 152,099,988 on chromosome 2.
See How do geneticists indicate the location of a gene? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genelocation) in the Handbook.
You and your healthcare professional may find the following resources about CACNB4 helpful.
You may also be interested in these resources, which are designed for genetics professionals and researchers.
See How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.
amino acid ; ataxia ; calcium ; cell ; cerebellum ; channel ; contraction ; cysteine ; epilepsy ; gene ; ions ; ion transport ; juvenile ; mutation ; neurological ; neuron ; neurotransmitters ; phenylalanine ; plasticity ; protein ; subunit ; voltage
You may find definitions for these and many other terms in the Genetics Home Reference Glossary.
The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.