Automated description from the Alliance of Genome Resources
Predicted to have transcription factor binding activity. Involved in aorta development and coronary vasculature development. Localizes to the nucleus. Used to study autosomal recessive Robinow syndrome and velocardiofacial syndrome. Human ortholog(s) of this gene implicated in progressive myoclonus epilepsy. Orthologous to human PRICKLE1 (prickle planar cell polarity protein 1).