2. Gene
  3. Slc26a2 - solute carrier family 26 (sulfate transporter), member 2 Gene

Slc26a2 - solute carrier family 26 (sulfate transporter), member 2 Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Mus musculus

Also known as Dtd; ST-OB

Gene ID: 13521 | Gene type: protein coding

About Slc26a2

Summary

Predicted to enable anion transmembrane transporter activity. Predicted to be involved in ossification and sulfate transmembrane transport. Predicted to be located in apical plasma membrane and microvillus membrane. Predicted to be integral component of plasma membrane. Is expressed in several structures, including alimentary system; brain; genitourinary system; sensory organ; and skeleton. Used to study diastrophic dysplasia. 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 2022]

Slc26a2 Products(1)

mRNA Protein Name
NM_007885.2 NP_031911.1 sulfate transporter
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables solute:inorganic anion antiporter activity IDA
IDA: Inferred from direct assay
20219950 MGI
enables sulfate transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
15703192 MGI
Biological Process GO Annotation Evidence Reference Source
involved in chondrocyte differentiation IMP
IMP: Inferred from mutant phenotype
24302720 MGI
involved in chondrocyte proliferation IMP
IMP: Inferred from mutant phenotype
24302720 MGI
involved in sulfate transmembrane transport IMP
IMP: Inferred from mutant phenotype
24302720 MGI
Cellular Component GO Annotation Evidence Reference Source
is active in plasma membrane IMP
IMP: Inferred from mutant phenotype
15703192 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

sulfate transporter

diastrophic dysplasia protein homolog

solute carrier family 26 member 2

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS13136 SLC26A2 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc26a2 NCBI NCBI:1836