Your search for "slc26a4" returned 368 TaqMan® SNP Genotyping Assays
solute carrier family 26 member 4
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]
DFNB4, EVA, PDS, PENDRIN, SLC26A4, TDH2B
Please enter the information below and press OK to send your cart to Core Services for purchase.