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FIGURE: 1 / 3
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
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.
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Protein Aliases: sodium-independent chloride/iodide transporter; solute carrier family 26 (anion exchanger), member 4; unnamed protein product
Gene Aliases: DFNB4; EVA; PDS; TDH2B
UniProt ID: (Human) O43511
Entrez Gene ID: (Human) 5172
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