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Disease Info Card
Charge Syndrome
Information about Charge Syndrome: 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 Charge Syndrome
Most recent studies have shown that Charge Syndrome shares some biological mechanisms with atresia, choanal-atresia, complete-hearing-loss, congenital-abnormality, congenital-heart-defects, congenital-ocular-coloboma-(disorder), cytogenetic-abnormality, developmental-delay-(disorder), developmental-disabilities, digeorge-syndrome, dysplasia, growth-disorders, heart-diseases, hypogonadism, hypoplasia, nervousness, pathologic-fistula, sensorineural-hearing-loss-(disorder), tracheoesophageal-fistula.
Among the many pathways, these few ones have gauged particular interests from scientists studying Charge Syndrome, and have been seen in publications frequently: Atp-dependent Chromatin Remodeling, Cell Migration, Cell Motility, Cell Proliferation, Chromatin Remodeling, Ear Morphogenesis, Excretion, Eye Development, Innervation, Methylation, Neurogenesis, Olfactory Bulb Development, Ossification, Pathogenesis, Reflex, Secretion, Segmentation, Stem Cell Proliferation, Tissue Development, Transposition
Quite a number of genes have been found to play important roles in Charge Syndrome, such as ABCB6, BMP4, CDH20, CHD2, CHD7, FABP6, FBN1, FGF8, FGFR1, ITGA2B, ITGB3, PROK2, PROKR2, SOX2, SS18L1, STS, TBX1. 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.