CACNB2

Voltage-dependent L-type calcium channel subunit beta-2 is a protein that in humans is encoded by the CACNB2 gene.

Clinical significance

Mutation in the CACNB2 gene are associated with Brugada syndrome, autism, attention deficit-hyperactivity disorder (ADHD), bipolar disorder, major depressive disorder, and schizophrenia.

See also

Voltage-dependent calcium channel

References

Further reading

External links

GeneReviews/NIH/NCBI/UW entry on Brugada syndrome

CACNB2 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)

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