CACNB2
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Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). Voltage-dependent L-type calcium channel subunit beta-2 is a protein that in humans is encoded by the CACNB2 gene.[1][2][3]
Clinical significance
[edit | edit source]Mutation in the CACNB2 gene are associated with Brugada syndrome, autism, attention deficit-hyperactivity disorder (ADHD), bipolar disorder, major depressive disorder, and schizophrenia.[4]
See also
[edit | edit source]References
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Further reading
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External links
[edit | edit source]- GeneReviews/NIH/NCBI/UW entry on Brugada syndrome
- CACNB2+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- Human CACNB2 genome location and CACNB2 gene details page in the UCSC Genome Browser.
