| Protein Name | solute carrier family 26 member 4 |
|---|---|
| Organism | Homo sapiens |
| Gene ID | 5172 |
| Gene Symbol | SLC26A4 |
| UniProt | O43511 (S26A4_HUMAN) |
| Relationships |
Total Number of functionally related compound(s) :
110
Total Number of Articles : 198 |
Description |
solute carrier family 26 member 4 |
| Gene Summary |
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] |
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