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Disease Info Card
Aniridia
Information about Aniridia: 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 Aniridia
Most recent studies have shown that Aniridia shares some biological mechanisms with aphakia, cataract, congenital-abnormality, corneal-diseases, cytogenetic-abnormality, disorder-of-eye, eye-abnormalities, eye-injuries, glaucoma, hypoplasia, intraocular-pressure-disorder, kidney-neoplasm, neoplasms, nephroblastoma, nystagmus, urogenital-abnormalities, wagr-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Aniridia, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Migration, Dehiscence, Enucleation, Epithelial Cell Migration, Eye Development, Eye Morphogenesis, Insulin Secretion, Localization, Metaphase, Mitotic Recombination, Oncogenesis, Pathogenesis, Pigmentation, Reflex, Secretion, System Development, Translation, Wound Healing
Quite a number of genes have been found to play important roles in Aniridia, such as BRCA1, CAT, CRAT, EXOSC1, FOXC1, FSHB, GLYAT, INS, PAX6, PITX2, SUB1, VEGFA, WT1. 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.