Entrez 783 | Ensembl ENSG00000165995 | |
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Aliases CACNB2, CACNLB2, CAVB2, MYSB, calcium voltage-gated channel auxiliary subunit beta 2 External IDs MGI: 894644 HomoloGene: 75191 GeneCards: 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.
References
CACNB2 Wikipedia(Text) CC BY-SA