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Disease Info Card
Pendred's Syndrome
Information about Pendred's 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 Pendred's Syndrome
Most recent studies have shown that Pendred's Syndrome shares some biological mechanisms with adenoma, carcinoma, complete-hearing-loss, congenital-hypothyroidism, deaf-mutism, deafness-congenital, diarrhea, dysplasia, follicular-thyroid-carcinoma, goiter, graves-disease, hypothyroidism, malignant-neoplasm-of-thyroid, malignant-neoplasms, neoplasms, nodular-goiter, sensorineural-hearing-loss-(disorder), thyroid-diseases, thyroid-neoplasm.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pendred's Syndrome, and have been seen in publications frequently: Anion Transport, Cell Proliferation, Chloride Transport, Ear Development, Excretion, Fertilization, Glycosylation, Immune Response, Inner Ear Development, Iodide Transport, Ion Transport, Localization, Pathogenesis, Pigmentation, Protein Phosphorylation, Reverse Transcription, Secretion, Sperm Motility, Sulfate Transport, Transport
Quite a number of genes have been found to play important roles in Pendred's Syndrome, such as CFTR, FOXI1, GJB2, HES1, HMGCL, KCNJ10, LIPC, MPZL2, NKX2-1, PTGDS, SLC26A2, SLC26A3, SLC26A4, SLC26A5, SLC5A8, TG, THPO, TPO. 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.