Automated description from the Alliance of Genome Resources (Release 3.1.1)
Predicted to have transcription factor binding activity. Involved in aorta development and coronary vasculature development. Localizes to nucleus. Is expressed in several structures, including brain; embryo mesenchyme; genitourinary system; limb; and sensory organ. Used to study autosomal recessive Robinow syndrome and velocardiofacial syndrome. Human ortholog(s) of this gene implicated in progressive myoclonus epilepsy 1B. Orthologous to human PRICKLE1 (prickle planar cell polarity protein 1).