SLC26A4
solute carrier family 26 (anion exchanger), member 4
Sinónimos:
DFNB4, EVA, PDS, TDH2B
Especie:
Human SLC26A4 (5172), Mouse Slc26a4 (23985), Rat Slc26a4 (29440), domestic guinea pig Slc26a4 (100718397), Domestic Rabbit SLC26A4 (100345415), naked mole-rat Slc26a4 (101702473), cow SLC26A4 (530241), sheep SLC26A4 (101104654), Zebrafish slc26a4 (563818), Horse SLC26A4 (100060222) ...Más
ID UniProtKB:
ID del gen:
- Human(5172) 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]
- Mouse(23985) solute carrier family 26, member 4
- Rat(29440) solute carrier family 26 (anion exchanger), member 4
- domestic guinea pig(100718397) solute carrier family 26, member 4
- Domestic Rabbit(100345415) solute carrier family 26, member 4
- naked mole-rat(101702473) solute carrier family 26, member 4
- cow(530241) solute carrier family 26, member 4
- sheep(101104654) solute carrier family 26, member 4
- Zebrafish(563818) solute carrier family 26, member 4
- Horse(100060222) solute carrier family 26, member 4
- domestic cat(101095090) solute carrier family 26, member 4
- dog(483263) solute carrier family 26, member 4
- chicken(427845) solute carrier family 26, member 4
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