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SLC26A4


Official Full Name
solute carrier family 26 member 4
Organism
Homo sapiens
Gene ID
5172
Background
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]
Synonyms
EVA; PDS; DFNB4; TDH2B

Cat.No. Product Name Price
SHH409968 shRNA set against Human SLC26A4 (NM_000441.1) Inquiry
SHH409972 shRNA set against Mouse SLC26A4 (NM_011867.3) Inquiry
SHH409976 shRNA set against Rat SLC26A4 (NM_019214.1) Inquiry
SHL004284 shRNA set against Human SLC26A4(NM_000441.1) Inquiry
SHL004302 shRNA set against Rat Slc26a4(NM_019214.1) Inquiry
SHL004338 shRNA set against Mouse Slc26a4(NM_011867.3) Inquiry
SHW013465 shRNA set against Danio rerio SLC26A4 (NM_001165915) Inquiry
Cat.No. Product Name Price
CDFH017817 Human SLC26A4 cDNA Clone(NM_000441.1) Inquiry
CDFR011510 Rat Slc26a4 cDNA Clone(NM_019214.1) Inquiry
MiUTR1H-09496 SLC26A4 miRNA 3'UTR clone Inquiry
MiUTR1M-10826 SLC26A4 miRNA 3'UTR clone Inquiry
MiUTR1R-07435 SLC26A4 miRNA 3'UTR clone Inquiry
CDCB174940 Danio rerio SLC26A4 ORF Clone (NM_001165915) Inquiry
CDCB190526 Rabbit SLC26A4 ORF clone (XM_002712039.2) Inquiry
CDCH081684 human SLC26A4 ORF clone (NM_000441.1) Inquiry
CDCR251479 Mouse Slc26a4 ORF Clone(NM_011867.3) Inquiry
CDCR378373 Rat Slc26a4 ORF Clone(NM_019214.1) Inquiry
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