This gene encodes one of three calmodulin proteins which are members of the EF-hand calcium-binding protein family. Calcium-induced activation of calmodulin regulates and modulates the function of cardiac ion channels. Two pseudogenes have been identified on chromosome 7 and X. Multiple transcript variants encoding different isoforms have been found for this gene.A missense mutation in the CALM1 gene has been associated with ventricular tachycardia.[provided by RefSeq, May 2020]
- G2/M transition of mitotic cell cycle
- MAPK cascade
- Microtubule cytoskeleton organization
- Response to amphetamine
- Regulation of heart rate
- Long qt syndrome 14
- Ventricular tachycardia, catecholaminergic polymorphic, 4
- Catecholaminergic polymorphic ventricular tachycardia
- Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy
- Long qt syndrome 1
CALM3 localizations – Subcellular Localization Database