SLC26A3 Products

Description

SLC26A3 is encoded by this gene is a transmembrane glycoprotein that functions as a sulfate transporter. It is localized to the mucosa of the lower intestinal tract, particularly to the apical membrane of columnar epithelium and some goblet cells. Mutations in this gene have been associated with congenital chloride diarrhea.

Bioinformatics

Entrez	1811 Human
Uniprot	AAH25671 Human NM_000111 Human NP_000102 Human
Product By Gene ID	1811
Alternate Names	chloride anion exchanger CLD congenital chloride diarrhea down-regulated in adenoma protein DRADown-regulated in adenoma Protein DRA Solute carrier family 26 member 3 solute carrier family 26, member 3

Related SLC26A3 Blog Posts

Check out the latest blog posts on SLC26A3.

Antibody Therapies and the New Generation of DNA Sequencing Our antibody database is primarily focused on protein-coding genes. Although they form only 1% of the total human genome, these important genes account for 85% of the mutations that lead to disease.DNA sequencing (defining the sequence of the 4 base...    Read more.

Next-Gen DNA Sequencing and SLC26A3 Research The SLC26A3, also known as DRA (downregulated-in-adenoma) gene is a member of the sulphate anion transporter family, serving an important role in the exchange and transport of chloride, bicarbonate and sulphate ions at plasma membrane sites. We at Nov...    Read more.

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