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Disease Info Card
Color Blindness
Information about Color Blindness: 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 Blindness
Most recent studies have shown that Color Blindness shares some biological mechanisms with abnormal-color-vision, achromatopsia, acquired-color-vision-deficiency, atrophy, bipolar-disorder, blind-vision, cardiovascular-diseases, color-blindness-red, color-blindness-red-green, color-vision-defect, congenital-color-blindness, disorder-of-eye, dystrophy, glucosephosphate-dehydrogenase-deficiency, nystagmus, optic-atrophy, retinal-diseases, retinitis-pigmentosa, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Color Blindness, and have been seen in publications frequently: Aging, Blood Coagulation, Coagulation, Developmental Process, Flight, Gene Conversion, Glycosylation, Localization, Optomotor Response, Pathogenesis, Phototaxis, Phototransduction, Protein Glycosylation, Reflex, Secretion, Translation, Transport, Transposition, Visual Behavior, Visual Perception
Quite a number of genes have been found to play important roles in Color Blindness, such as ABO, CCDC6, CNGA3, CNGB3, ERG, F8, F9, G6PD, GNAT2, KCNH2, PTCH1, RET, RHCE, RHD, RHO, TAS2R38, 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.