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Disease Info Card
Color Vision Defect
Information about Color Vision Defect: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Color Vision Defect
Most recent studies have shown that Color Vision Defect shares some biological mechanisms with achromatopsia, age-related-macular-degeneration, atrophy, blind-vision, color-blindness, color-blindness-red, color-blindness-red-green, confusion, disorder-of-eye, disorder-of-the-optic-nerve, dystrophy, glaucoma, nystagmus, optic-atrophy, optic-neuritis, retinal-degeneration, retinal-diseases, retinitis-pigmentosa, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Color Vision Defect, and have been seen in publications frequently: Aging, Cell Death, Coagulation, Excretion, Flight, Gene Conversion, Hypersensitivity, Localization, Mating, Pathogenesis, Phototransduction, Pigmentation, Reflex, Regeneration, Secretion, Synaptic Transmission, Translation, Transport, Visual Behavior, Visual Perception
Quite a number of genes have been found to play important roles in Color Vision Defect, such as CNGA3, CNGB3, COX5A, ERG, F9, FMOD, G6PD, GNAT2, GUCY2D, KCNH2, NOL3, PMEL, RHO, RPGR, TNFSF14, UBL4A. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.