opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan - Protein

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Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency. [J Opt Soc Am A Opt Image Sci V...]
Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency.
Neitz M, Krekling ED, Hagen LA, Pedersen HR, Rowlan J, Barborek R, Neitz J, Crain A, Baraas RC. J Opt Soc Am A Opt Image Sci Vis. 2020 Apr 1; 37(4):A26-A34.
Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities. [Vision Res. 2012]
Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities.
Baraas RC, Hagen LA, Dees EW, Neitz M. Vision Res. 2012 Nov 15; 73:1-9. Epub 2012 Sep 26.
A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect. [Vis Neurosci. 2006]
A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect.
Gunther KL, Neitz J, Neitz M. Vis Neurosci. 2006 May-Aug; 23(3-4):403-9.

RefSeq genomic sequence
See the genomic reference sequence for the OPN1SW gene (NG_009094.1).
RefSeq protein
See the reference protein sequence for short-wave-sensitive opsin 1 (NP_001372054.1).

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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
reagent reviews [ExactAntigen/Labome]
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