Predicted to enable identical protein binding activity. Involved in cellular potassium ion homeostasis; membrane hyperpolarization; and positive regulation of transporter activity. Located in plasma membrane. Human ortholog(s) of this gene implicated in progressive myoclonus epilepsy 3. Orthologous to human KCTD7 (potassium channel tetramerization domain containing 7). [provided by Alliance of Genome Resources, Apr 2022]