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Disease Info Card
Ocular Albinism, Type I
Information about Ocular Albinism, Type I: 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 Ocular Albinism, Type I
Most recent studies have shown that Ocular Albinism, Type I shares some biological mechanisms with albinism, albinism-ocular, albinism-oculocutaneous, congenital-nystagmus, disorder-of-eye, genetic-diseases-x-linked, hypopigmentation-disorder, hypoplasia, ichthyoses, ichthyosis-x-linked, kallmann-syndrome, melanoma, microphthalmos, nystagmus, photophobia, pigmentation-disorders, sex-chromosome-aberrations, steroid-sulfatase-deficiency-disease, strabismus.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ocular Albinism, Type I, and have been seen in publications frequently: Cellular Localization, Eye Development, Eye Pigmentation, Glycosylation, Intracellular Signal Transduction, Intracellular Transport, Localization, Melanosome Transport, Pathogenesis, Pigmentation, Secretory Pathway, Translation, Transport
Quite a number of genes have been found to play important roles in Ocular Albinism, Type I, such as FZD4, GPR143, GPR151, GPRC6A, LAMP1, LGR6, LPAR3, MLANA, MRGPRX1, MRGPRX3, MRGPRX4, OCA2, OXER1, RPE, STS, 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.