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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC26A4-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : SLC26A4
Gene Name : Solute carrier family 26 member 4
Chromosome : CHR 7: 107,660,634-107,717,808
Locus : 7q22.3
Alt. Genes : CLEC3A
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