Slc26a2 - solute carrier family 26 member 2 Gene

Also Known as Dtdst

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 117267

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 References Source
involved in sulfate transmembrane transport IDA
IDA: Inferred from direct assay
9575183 RGD
Cellular Component GO Annotation Evidence References 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

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