Disease Info Card

Retinal Dystrophies

Information about Retinal Dystrophies: 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 Retinal Dystrophies

Most recent studies have shown that Retinal Dystrophies shares some biological mechanisms with abnormal-degeneration, age-related-macular-degeneration, amaurosis, atrophy, bardet-biedl-syndrome, blind-vision, dystrophy, hereditary-retinal-dystrophy, leber-congenital-amaurosis, night-blindness, obesity, polydactyly, retinal-degeneration, retinal-diseases, retinitis-pigmentosa, stargardts-disease, visual-impairment.

Among the many pathways, these few ones have gauged particular interests from scientists studying Retinal Dystrophies, and have been seen in publications frequently: Aging, Cell Cycle, Cell Death, Cell Proliferation, Cellular Localization, Dna Repair, Intraflagellar Transport, Localization, Neuroprotection, Pathogenesis, Phagocytosis, Phototransduction, Pigmentation, Programmed Cell Death, Protein Transport, Reflex, Regeneration, Secretion, Translation, Transport

Quite a number of genes have been found to play important roles in Retinal Dystrophies, such as ABCA4, AIPL1, ARPP21, BEST1, CLTA, CRB1, CRX, ERG, GUCY2D, KCNH2, PRPH, PTPRC, RHO, RPE, RPE65, RPGR, RPGRIP1, TNFSF14. 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.

Retinal Dystrophies Related Genes

click to see detail information for each gene

ABCA4 AIPL1 ARPP21
BEST1 CLTA CRB1
CRX ERG GUCY2D
KCNH2 PRPH PTPRC
RHO RPE RPE65
RPGR RPGRIP1 TNFSF14