QuickView for pendrin (gene)

Gene Symbol:

SLC26A4 Homo sapiens

Full name:

solute carrier family 26 member 4

Synonyms:

DFNB4, EVA, PDS, TDH2B, pendrin, sodium-independent chloride/iodide transporter, solute carrier family 26 (anion exchanger), member 4, truncated solute carrier family 26

Genomic Location:

Chr 7: 107088316-107145490

Description:

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.

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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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Gallus gallus ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus ,  Danio rerio

External Links:

Entrez Gene

miRNA binding sites
(Source: TargetScan):

Predicted Gene Targets for miR-26 ,  Predicted Gene Targets for miR-495 ,  Predicted Gene Targets for miR-496

Cytogenetic Map:

7q22.3

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