The trimeric intracellular cation-selective channels or TRIC proteins are a group of homo-trimeric cation channel proteins of ~300 residues in the ER membrane. There are two known TRIC proteins, TRIC-A and TRIC-B.
TRICs are permeable to both Na<sup>+</sup> and K<sup>+</sup> but not divalent cations like Ca<sup>2+</sup>. They exhibit marked voltage-dependence, becoming more open when the cytosol is more positively charged than the ER lumen.
TRIC-A is predominantly expressed in excitable tissues including brain and skeletal muscle. TRIC-A activity is thought to support RyR1-mediated efflux of Ca<sup>2+</sup> ions from the sarcoplasmic reticulum into the cytosol.
K<sup>+</sup> flux into the ER through TRIC-B is thought to support IP<sub>3</sub>-induced efflux of Ca<sup>2+</sup> ions through IP<sub>3</sub>-gated Ca<sup>2+</sup> channels in the ER membrane.
TRIC-A has been implicated in the regulation of arterial blood pressure through regulating the excitability of vascular smooth muscle cells. Several single-nucleotide polymorphisms (SNPs) in close proximity to the TRIC-A locus and, in future, may serve as an important biomarker in the diagnosis of essential hypertension
Null mutations in TMEM38B encoding TRIC-B are an uncommon but relatively severe cause of autosomal recessive osteogenesis imperfecta or "brittle bone disease".