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Disease Info Card
Fundus Coloboma
Information about Fundus Coloboma: 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 Fundus Coloboma
Most recent studies have shown that Fundus Coloboma shares some biological mechanisms with blind-vision, cataract, congenital-abnormality, congenital-coloboma-of-iris, congenital-ocular-coloboma-(disorder), corneal-diseases, developmental-delay-(disorder), disorder-of-eye, dysplasia, eye-abnormalities, hypoplasia, microphthalmos, neoplasms, optic-nerve-hypoplasia, pathologic-neovascularization, retinal-detachment, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Fundus Coloboma, and have been seen in publications frequently: Bone Maturation, Cell Cycle, Cell Differentiation, Cell Fate Specification, Cell Proliferation, Dorsal Closure, Enucleation, Eye Development, Eye Morphogenesis, Fertilization, Glycosylation, Hyperphosphorylation, Localization, Neural Tube Closure, Neurogenesis, Pathogenesis, Protein Glycosylation, Regulation Of Signaling, Stem Cell Proliferation, Tube Closure
Quite a number of genes have been found to play important roles in Fundus Coloboma, such as BMP4, CAT, CRAT, FN1, GDF6, GLYAT, KDM2B, MAPK8, PAX2, PAX6, RAX, RPE, RYBP, SALL1, SHH, SIX3, SKI, SOX2, TFAP2A. 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.