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The CNGA3 protein is an alpha subunit of cyclic nucleotide-gated (CNG) cation channels found in cone photoreceptors. These channels are crucial for color vision, allowing the influx of cations in the dark and closing upon light exposure during phototransduction. Mutations in CNGA3 cause several inherited retinal disorders, including achromatopsia and cone dystrophy.
Modulation of ion flow in response to cGMP levels
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