Slc26a2 Gene Summary [Rat]

Predicted to enable inorganic anion transmembrane transporter activity and organic anion transmembrane transporter activity. Involved in sulfate transmembrane transport. Located in apical plasma membrane and microvillus membrane. Human ortholog(s) of this gene implicated in bone disease (multiple). Orthologous to human SLC26A2 (solute carrier family 26 member 2). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
Slc26a2
Official Name
solute carrier family 26 member 2 [Source:RGD Symbol;Acc:620622]
Ensembl ID
ENSRNOG00000018082
Bio databases IDs NCBI: 117267 Ensembl: ENSRNOG00000018082
Aliases solute carrier family 26 member 2
Synonyms D5S1708, diastrophic dysplasia sulphate transporter, DTD, DTDST, EDM4, MST153, MSTP157, solute carrier family 26 member 2, solute carrier family 26 (sulfate transporter), member 2, solute carrier family 26 (sulphate transporter), member 2, ST-OB
Species
Rat, Rattus norvegicus
OrthologiesHumanMouse

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in rat Slc26a2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Sulfate permease family
  • PRK11660
  • sulfate transporter
  • high affinity sulphate transporter 1
  • inorganic anion exchanger
  • sulphate transporter and anti-sigma factor antagonist domain
  • transporter

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • atelosteogenesis type II
  • achondrogenesis type IB
  • multiple epiphyseal dysplasia 4
  • colon cancer
  • diastrophic dysplasia
  • osteochondrodysplasia
  • anaplastic thyroid carcinoma
  • anaplastic thyroid cancer
  • connective tissue disorder
  • 3MC syndrome type 2
regulated by
regulates
  • sulfate
  • hydroxide ion
  • sialyl lewis X
  • iodide
  • oxalic acid
  • sialyl 6-sulfo Lewis X
  • chloride
  • mitomycin C
  • nitrate
  • bromide
role in cell
  • differentiation
  • growth
  • proliferation
  • exchange in

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Plasma Membrane
  • cellular membrane
  • apical membrane
  • microvilli

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the rat Slc26a2 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • sulfate transport
  • ossification
  • chondrocyte differentiation
  • chondrocyte proliferation
  • oxalate transport
  • bicarbonate transport

Cellular Component

Where in the cell the gene product is active
  • microvillus membrane
  • extracellular vesicular exosome
  • membrane
  • plasma membrane
  • apical plasma membrane

Molecular Function

What the gene product does at the molecular level
  • secondary active sulfate transmembrane transporter activity
  • oxalate transmembrane transporter activity
  • inorganic anion exchanger activity
  • chloride transmembrane transporter activity
  • bicarbonate transmembrane transporter activity
  • sulfate transmembrane transporter activity

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.