Automated description from the Alliance of Genome Resources
Exhibits steroid binding activity. Involved in several processes, including cellular sodium ion homeostasis; excretion; and regulation of synaptic vesicle exocytosis. Localizes to the GABA-ergic synapse and glutamatergic synapse. Used to study autosomal dominant pseudohypoaldosteronism type 1. Human ortholog(s) of this gene implicated in autosomal dominant pseudohypoaldosteronism type 1 and pseudohypoaldosteronism. Is expressed in several structures, including central nervous system and genitourinary system. Orthologous to human NR3C2 (nuclear receptor subfamily 3 group C member 2).