靶标：
SLC26A4
产品别名：
DFNB4； EVA； PDS； TDH2B； SLC26A4； solute carrier family 26 member 4； solute carrier family 26 member 4； pendrin； sodium-independent chloride/iodide transporter； solute carrier family 26 (anion exchanger), member 4； 溶质载体家族26成员4(SLC26A4)； 钠碘单独转运蛋白SLC26A4；
背景信息：
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008],
