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Disease Info Card
Ectopia Lentis
Information about Ectopia Lentis: 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 Ectopia Lentis
Most recent studies have shown that Ectopia Lentis shares some biological mechanisms with arachnodactyly, blepharoptosis, cataract, congenital-ectopia, connective-tissue-diseases, dislocations, disorder-of-eye, glaucoma, homocystinuria, intraocular-lymphoma, lens-dislocation, lens-subluxation, marfan-syndrome, myopia, pathological-dilatation, retinal-detachment, subluxation-of-joint, weill-marchesani-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ectopia Lentis, and have been seen in publications frequently: Aging, Bone Resorption, Coagulation, Dehiscence, Excretion, Lipoprotein Transport, Localization, Pathogenesis, Pigment Accumulation, Pigmentation, Proteolysis, Reflex, Secretion, Sulfation, Tissue Homeostasis, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Ectopia Lentis, such as ADAMTS10, ADAMTSL4, CALCR, CBS, EGF, ELN, FBN1, FBN2, LTBP2, LTBP3, MTHFR, PAX6, PTCH1, RET, SUOX, TAS2R38, TGFBR1. 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.