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