Automated description from the Alliance of Genome Resources
Predicted to have CD4 receptor binding activity. Predicted to localize to the cytosol; intracellular membrane-bounded organelle; and trans-Golgi network transport vesicle. Human ortholog(s) of this gene implicated in Mast syndrome and hereditary spastic paraplegia. Is expressed in extraembryonic component; head mesenchyme; tongue; and vertebral axis musculature. Orthologous to human SPG21 (SPG21 abhydrolase domain containing, maspardin).