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.|
Community Annotation of SLC26A4 Add / Edit SLC26A4: Annotations
No community annotations yet for SLC26A4.
• "Mouse over" a mutation to see details.
Click on a tumor type to see its full list of significant genes.