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Disease Info Card
Albinism, Ocular
Information about Albinism, Ocular: 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 Albinism, Ocular
Most recent studies have shown that Albinism, Ocular shares some biological mechanisms with albinism, albinism-oculocutaneous, blind-vision, congenital-nystagmus, disorder-of-eye, genetic-diseases-x-linked, hypopigmentation-disorder, hypoplasia, myopia, night-blindness, nystagmus, ocular-albinism-type-i, photophobia, refractive-errors, retinal-diseases, retinitis-pigmentosa, steroid-sulfatase-deficiency-disease, strabismus, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Albinism, Ocular, and have been seen in publications frequently: Cell Death, Cell Migration, Cellular Localization, Chromosome Segregation, Developmental Maturation, Eye Pigmentation, Glycosylation, Innervation, Intracellular Signal Transduction, Localization, Melanosome Transport, Neuroprotection, Pathogenesis, Pigment Accumulation, Pigmentation, Reflex, Response To Uv, Transport, Vasculogenesis, Visual Perception
Quite a number of genes have been found to play important roles in Albinism, Ocular, such as ERG, FZD4, GPR143, GPR151, KCNH2, LGR6, LPAR3, MRGPRX1, MRGPRX3, MRGPRX4, OCA2, OXER1, RPE, SLC45A2, STS, TNFSF14, TYR, TYRP1, VN1R17P. 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.