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SLC26A4

Official Full Name
solute carrier family 26 member 4
Organism
Homo sapiens
GeneID
5172
Background
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]
Synonyms
EVA; PDS; DFNB4; TDH2B;

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