TMEM38B

TRIC-B is permeable to both Na⁺ and K⁺ but not divalent cations like Ca²⁺.^[4] The channel exhibits marked voltage-dependence, becoming more open when the cytosol is more positively charged than the ER lumen. There at least four major sub-conductance states (with 80%, 60%, 46% and 30% of the conductance of the fully-opened channel).^[4] TMEM38B-knockout mice exhibit reduced IP₃-receptor-mediated Ca²⁺ release.^[4] As such, K⁺ flux into the ER through TRIC-B is thought to support IP₃-induced efflux of Ca²⁺ ions through IP₃-gated Ca²⁺ channels in the ER membrane.

Null mutations in TMEM38B reduce the levels of functional TRIC-B in heterozygotes and abolish expression of functional TRIC-B in homozygotes. Such mutations are an uncommon but relatively severe cause of autosomal recessive osteogenesis imperfecta or "brittle bone disease".^[5]

• TMEM38A
• Trimeric intracellular cation-selective channel