Early Detection Research Network

SLC26A2

Aliases:
This biomarker is also known as:
  • solute carrier family 26 member 2,
  • diastrophic dysplasia protein,
  • MST153,
  • sulfate transporter,
  • Diastrophic dysplasia protein,
  • EDM4,
  • diastrophic dysplasia sulfate transporter,
  • DTD,
  • DTDST,
  • solute carrier family 26 (sulfate transporter), member 2,
  • sulfate anion transporter 1,
  • Solute carrier family 26 member 2,
  • MSTP157,
  • D5S1708,
  • SLC26A2,

Description…

From NCBI Gene: The diastrophic dysplasia sulfate transporter is a transmembrane glycoprotein implicated in the pathogenesis of several human chondrodysplasias. It apparently is critical in cartilage for sulfation of proteoglycans and matrix organization. [provided by RefSeq, Jul 2008]

Datasets

There are no datasets associated with this biomarker.

Attributes
QA State: Under Review
Type: Gene
HGNC Name: SLC26A2

This biomarker is currently being annotated or is under review. You must be logged in or do not have permission to view any additional information. Contact the Informatics Center if you should have access to this biomarker.

This biomarker is currently being annotated or is under review. You must be logged in or do not have permission to view any additional information. Contact the Informatics Center if you should have access to this biomarker.

This biomarker is currently being annotated or is under review. You must be logged in or do not have permission to view any additional information. Contact the Informatics Center if you should have access to this biomarker.

This biomarker is currently being annotated or is under review. You must be logged in or do not have permission to view any additional information. Contact the Informatics Center if you should have access to this biomarker.

Version 5.0.2