Pendred syndrome is an autosomal recessive disorder characterized by congenital deafness and thyroid goiter. This syndrome is caused by mutation of the gene encoding Pendrin (SLC26A4), a 780 amino acid transmembrane protein that functions as an iodide/chl
Pathway
Multifunctional anion exchangers, organism-specific biosystem; SLC-mediated transmembrane transport, organism-specific biosystem; Transmembrane transport of small molecules, organism-specific biosystem; Transport of inorganic cations/anions and amino acids/oligopeptides, organism-specific biosystem;
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