Automated description from the Alliance of Genome Resources
Predicted to have phosphatidylinositol-3-phosphate binding activity. Predicted to be involved in double-strand break repair via homologous recombination and regulation of cytokinesis. Predicted to localize to the centrosome and midbody. Used to study hereditary spastic paraplegia 15. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 15. Is expressed in central nervous system; retina inner nuclear layer; and retina outer nuclear layer. Orthologous to human ZFYVE26 (zinc finger FYVE-type containing 26).