Disease Info Card

Branchio-oto-renal Syndrome

Information about Branchio-oto-renal 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 Branchio-oto-renal Syndrome

Most recent studies have shown that Branchio-oto-renal Syndrome shares some biological mechanisms with branchial-clefts-congenital-disorder, branchioma, branchiooculofacial-syndrome, cleft-lip, complete-hearing-loss, conductive-hearing-loss, congenital-abnormality, congenital-absence, congenital-absence-of-kidney, dysplasia, eye-abnormalities, head-and-neck-neoplasms, hearing-loss-mixed-conductive-sensorineural, hearing-problem, hypoplasia, kidney-diseases, kidney-failure, pathologic-fistula, sensorineural-hearing-loss-(disorder), stenosis.

Among the many pathways, these few ones have gauged particular interests from scientists studying Branchio-oto-renal Syndrome, and have been seen in publications frequently: Cell Migration, Ear Development, Ear Morphogenesis, Electron Transport, Electron Transport Chain, Eye Development, Eye Morphogenesis, Glomerular Filtration, Inner Ear Development, Innervation, Kidney Development, Localization, Middle Ear Morphogenesis, Neurogenesis, Nuclear Export, Organ Development, Pathogenesis, Reflex, Respiratory Electron Transport Chain, Transport

Quite a number of genes have been found to play important roles in Branchio-oto-renal Syndrome, such as BMP4, CDCA8, DACH1, EYA1, EYA2, EYA3, GJB2, HNF1B, MB, NEUROD1, POU3F4, SALL1, SHARPIN, SIX1, SIX5, SLC26A4, TBX1, 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.