Automated description from the Alliance of Genome Resources (Release 7.4.0)
Enables leak channel activity and monoatomic cation channel activity. Involved in monoatomic cation transmembrane transport and regulation of resting membrane potential. Predicted to be part of monoatomic ion channel complex. Predicted to be active in plasma membrane. Is expressed in brain and spinal cord gray matter. Human ortholog(s) of this gene implicated in congenital limbs-face contractures-hypotonia-developmental delay syndrome. Orthologous to human NALCN (sodium leak channel, non-selective).
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