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Disease Info Card
Eye Abnormalities
Information about Eye Abnormalities: 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 Eye Abnormalities
Most recent studies have shown that Eye Abnormalities shares some biological mechanisms with anophthalmos, blind-vision, cataract, cleft-palate, congenital-abnormality, congenital-heart-defects, congenital-ocular-coloboma-(disorder), corneal-diseases, cytogenetic-abnormality, disorder-of-eye, dysplasia, glaucoma, hypoplasia, microphthalmos, nervousness, retinal-detachment, retinal-diseases, strabismus, tooth-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Eye Abnormalities, and have been seen in publications frequently: Angiogenesis, Brain Development, Cell Adhesion, Cell Cycle, Cell Death, Cell Differentiation, Cell Migration, Cell Proliferation, Eye Development, Eye Morphogenesis, Gastrulation, Glycosylation, Localization, Mating, Pathogenesis, Pigmentation, Programmed Cell Death, Reflex, System Development, Translation
Quite a number of genes have been found to play important roles in Eye Abnormalities, such as BMP4, CAT, CRAT, FKTN, FOXC1, GJA1, GLYAT, IKBKG, PAX2, PAX6, PITX2, POMGNT1, POMT1, SHH, SS18L1, TP63. 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.