Nckx30C - Nckx30C

Enables calcium, potassium:sodium antiporter activity. Involved in calcium ion transmembrane transport; compound eye development; and sodium ion transport. Located in membrane. Is expressed in several structures, including adult optic lobe; brain; head; imaginal disc; and synaptic neuropil domain. Human ortholog(s) of this gene implicated in congenital stationary night blindness 1D. Orthologous to several human genes including SLC24A2 (solute carrier family 24 member 2). [provided by Alliance of Genome Resources, Dec 2024]

NCBI Orthologs

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