Gene: SLC24A1

Alternate names for this Gene: CSNB1D|HsT17412|NCKX|NCKX1|RODX

Gene Summary: This gene encodes a member of the potassium-dependent sodium/calcium exchanger protein family. The encoded protein plays an important role in sodium/calcium exchange in retinal rod and cone photoreceptors by mediating the extrusion of one calcium ion and one potassium ion in exchange for four sodium ions. Mutations in this gene may play a role in congenital stationary night blindness. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Gene is located in Chromosome: 15

Location in Chromosome : 15q22.31

Description of this Gene: solute carrier family 24 member 1

Type of Gene: protein-coding

Gene: INTS14

Alternate names for this Gene: C15orf44|VWA9

Gene Summary:

Gene is located in Chromosome: 15

Location in Chromosome : 15q22.31

Description of this Gene: integrator complex subunit 14

Type of Gene: protein-coding