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Disease Info Card
Townes Syndrome
Information about Townes 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 Townes Syndrome
Most recent studies have shown that Townes Syndrome shares some biological mechanisms with anus-imperforate, atresia, complete-hearing-loss, congenital-abnormality, congenital-absence, congenital-hand-deformities, congenital-heart-defects, developmental-disabilities, dysplasia, goldenhar-syndrome-with-ipsilateral-radial-defect, haploinsufficiency, hypoplasia, limb-deformities-congenital, middle-lobe-syndrome, pathologic-fistula, polydactyly, radial-polydactyly, sensorineural-hearing-loss-(disorder).
Among the many pathways, these few ones have gauged particular interests from scientists studying Townes Syndrome, and have been seen in publications frequently: Cell Development, Cell Differentiation, Cell Division, Cell Fate Determination, Cell Fate Specification, Cell Proliferation, Gastrulation, Glomerular Filtration, Gonad Development, Kidney Development, Limb Development, Liver Development, Localization, Metanephros Development, Neurogenesis, Pathogenesis, Regeneration, Stem Cell Differentiation, Stem Cell Proliferation, Ureteric Bud Invasion
Quite a number of genes have been found to play important roles in Townes Syndrome, such as CBX1, EYA1, FGF4, GLI3, HNF1B, KIR3DL2, PAX2, SALL1, SALL2, SALL3, SALL4, SHH, SIX1, SRCIN1, TBX5, TERF1, UBE2I. 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.