1 antibody, AAC1 antibody, ANT antibody, ANT 1 antibody, ANT1 antibody, PEO2 antibody, PEO3 antibody, T1 antibody, AU019225 antibody, Ant1 antibody, ant antibody, ant1 antibody, peo2 antibody, peo3 antibody, MANT1 antibody, SLC25A5 antibody, fa22e07 antibody, wu:fa22e07 antibody, zgc:77591 antibody, slc25a4 antibody, solute carrier family 25 member 4 antibody, solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 antibody, adenine nucleotide translocator antibody, solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4 antibody, solute carrier family 25 member 4 L homeolog antibody, SLC25A4 antibody, Slc25a4 antibody, slc25a4 antibody, ANT1 antibody, slc25a4.L antibody
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. Synonyms: EVA, PDS, DFNB4, TDH2B