solute carrier family 26 (anion exchanger), member 2
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]
Gene aliases
D5S1708,
DTD,
DTDST,
EDM4,
MSTP157
Chromosome
5
Map location
5q31-q34
Gene type
protein-coding
Gene Ontology (GO) terms enrichment
Database references
Statistics for SLC26A2
| Domains | |
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| PTMs | |
| Protein entries | |
| Sequence variants | |
| Cell lines/tissues | |
| Pathways involved in | |
| Protein-Protein Interactions |
Sequence variants for SLC26A2
List of cell lines/tissues that have SLC26A2 sequence variants
List of pathways where SLC26A2 is involved
| Pathway name | Pathway source |
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Protein-Protein Interaction Network for SLC26A2
Network key
Number of sequence variations per gene
Protein identification for SLC26A2
Browse by protein identification methods
| Identification method | Quantitative data available |
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