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Disease Info Card
Cryptophthalmos
Information about Cryptophthalmos: 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 Cryptophthalmos
Most recent studies have shown that Cryptophthalmos shares some biological mechanisms with anophthalmos, atresia, bulla, cleft-lip, congenital-abnormality, congenital-absence, congenital-absence-of-kidney, congenital-ocular-coloboma-(disorder), corneal-diseases, craniofacial-abnormalities, cryptophthalmos-syndrome, dysplasia, eye-abnormalities, hypoplasia, microphthalmos, orbital-separation-excessive, stenosis, syndactyly, urogenital-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cryptophthalmos, and have been seen in publications frequently: Basement Membrane Assembly, Cell Adhesion, Cell Death, Fin Development, Fin Morphogenesis, Localization, Lung Development, Lung Growth, Membrane Assembly, Organ Morphogenesis, Ossification, Pathogenesis, Programmed Cell Death, Translation
Quite a number of genes have been found to play important roles in Cryptophthalmos, such as CALM1, CALM2, CALM3, ERG, FN1, FRAS1, FREM1, FREM2, FREM3, GRIP1, LGALS12, MRPL28, NCOA2, NPHS1, OTX2, SOX2. 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.