Enables voltage-gated calcium channel activity. Acts upstream of or within several processes, including neuron projection morphogenesis; retina development in camera-type eye; and visual perception. Predicted to be located in membrane and neuronal cell body. Predicted to be integral component of membrane. Predicted to be part of voltage-gated calcium channel complex. Used to study congenital stationary night blindness 2A. Human ortholog(s) of this gene implicated in Aland Island eye disease; X-linked cone-rod dystrophy 3; congenital stationary night blindness; and congenital stationary night blindness 2A. Orthologous to human CACNA1F (calcium voltage-gated channel subunit alpha1 F). [provided by Alliance of Genome Resources, Apr 2022]