Automated description from the Alliance of Genome Resources (Release 7.4.0)
Enables intracellularly cAMP-activated cation channel activity. Acts upstream of or within in utero embryonic development; monoatomic cation transport; and regulation of heart contraction. Located in axon. Is expressed in several structures, including eye; future brain; heart; septum transversum; and venous system. Human ortholog(s) of this gene implicated in Brugada syndrome 8; Gilles de la Tourette syndrome; idiopathic generalized epilepsy; and sick sinus syndrome. Orthologous to human HCN4 (hyperpolarization activated cyclic nucleotide gated potassium channel 4).
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