SLC26A4 Products

Antibodies
SLC26A4 Antibody
SLC26A4 Antibody
NBP1-60106
Species: Hu
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
SLC26A4 Antibody
SLC26A4 Antibody
NBP1-85237
Species: Hu, Rat
Applications: ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
SLC26A4 Antibody (3D2)
SLC26A4 Antibody (3D2)
H00005172-M03
Species: Hu
Applications: ELISA
Host: Mouse Monoclonal
Proteins
SLC26A4 Partial Recombinant P ...
SLC26A4 Partial Recombinant Protein
H00005172-Q01
Species: Hu
Applications: WB, ELISA, PA
SLC26A4 Recombinant Protein
SLC26A4 Recombinant Protein
H00005172-P01
Species: Hu
Applications: WB, ELISA, PA
SLC26A4 Recombinant Protein A ...
SLC26A4 Recombinant Protein Antigen
NBP1-85237PEP
Species: Hu
Applications: AC
RNAi
SLC26A4 RNAi
SLC26A4 RNAi
H00005172-R01
Species: Hu

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. [provided by RefSeq]

Bioinformatics

Entrez Human
Uniprot Human
Human
Human
Product By Gene ID 5172
Alternate Names
  • Solute carrier family 26 member 4
  • DFNB4
  • pendrin
  • Sodium-independent chloride/iodide transporter
  • PDSTDH2B
  • EVA
  • solute carrier family 26, member 4

Bioinformatics Tool for SLC26A4

Discover related pathways, diseases and genes to SLC26A4. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
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