2. Gene
  3. Slc26a2 - solute carrier family 26 member 2 Gene

Slc26a2 - solute carrier family 26 member 2 Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Rattus norvegicus

Also known as Dtdst

Gene ID: 117267 | Gene type: protein coding

About Slc26a2

Summary

Enables sulfate transmembrane transporter activity. Involved in ossification and sulfate 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 2022]

Slc26a2 Products(1)

mRNA Protein Name
NM_057127.1 NP_476468.1 sulfate transporter
Gene Ontology
  • Biological Process
  • Cellular Component
Biological Process GO Annotation Evidence Reference Source
involved in sulfate transmembrane transport IDA
IDA: Inferred from direct assay
9575183 RGD
Cellular Component GO Annotation Evidence Reference Source
located in apical plasma membrane IDA
IDA: Inferred from direct assay
20369363 RGD
located in microvillus membrane IDA
IDA: Inferred from direct assay
20369363 RGD
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 (anion exchanger), member 2

solute carrier family 26 (sulfate transporter), 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