SLC26A4 Back

solute carrier family 26, member 4

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NCBI Description of SLC26A4

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.

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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


SLC26A4 is highly significantly mutated in
SLC26A4 is significantly mutated in
SLC26A4 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for SLC26A4