Automated description from the Alliance of Genome Resources (Release 7.0.0)
Acts upstream of or within visual perception. Predicted to be located in cell projection; endoplasmic reticulum; and membrane. Used to study congenital stationary night blindness 1F. Human ortholog(s) of this gene implicated in congenital stationary night blindness 1F. Orthologous to human LRIT3 (leucine rich repeat, Ig-like and transmembrane domains 3).