SLC26A2

Aliases
  • D5S1708
  • DTD
  • DTDST
  • Diastrophic dysplasia protein
  • EDM4
  • MST153
  • MSTP157
  • SLC26A2
  • Solute carrier family 26 member 2
  • diastrophic dysplasia protein
  • diastrophic dysplasia sulfate transporter
  • solute carrier family 26 (sulfate transporter), member 2
  • solute carrier family 26 member 2
  • sulfate anion transporter 1
  • sulfate transporter
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]
Attributes
QA State
Under Review
Type
Gene
HGNC Name
SLC26A2
Certifications
  • None
QA State for Prostate
Under Review

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.