Automated description from the Alliance of Genome Resources
Predicted to have lysophospholipase activity. Involved in angiogenesis and animal organ morphogenesis. Predicted to localize to the endoplasmic reticulum and membrane. Human ortholog(s) of this gene implicated in Boucher-Neuhauser syndrome; Laurence-Moon syndrome; Oliver-McFarlane syndrome; and hereditary spastic paraplegia 39. Is expressed in several structures, including brain; cranial nerve; epithelium; extraembryonic component; and genitourinary system. Orthologous to human PNPLA6 (patatin like phospholipase domain containing 6).