SLC26A2 Sulfate transporter. May play a role in endochondral bone formation. Belongs to the SLC26A/SulP transporter (TC 2.A.53) family. Ubiquitously expressed. Note: This description may include information from UniProtKB.
Protein type: Membrane protein, integral; Membrane protein, multi-pass; Transporter; Transporter, SLC family
Chromosomal Location of Human Ortholog: 5q32
Cellular Component:  apical plasma membrane; integral component of plasma membrane; membrane; microvillus membrane; plasma membrane
Molecular Function:  secondary active sulfate transmembrane transporter activity; sulfate transmembrane transporter activity
Biological Process:  3'-phosphoadenosine 5'-phosphosulfate biosynthetic process; bicarbonate transport; chloride transmembrane transport; ion transport; ossification; oxalate transport; sulfate transmembrane transport
Disease: Achondrogenesis, Type Ib; Atelosteogenesis, Type Ii; Diastrophic Dysplasia; Epiphyseal Dysplasia, Multiple, 4
Reference #:  P50443 (UniProtKB)
Alt. Names/Synonyms: D5S1708; Diastrophic dysplasia protein; diastrophic dysplasia sulfate transporter; DTD; DTDST; EDM4; MST153; MSTP157; S26A2; SLC26A2; solute carrier family 26 (sulfate transporter), member 2; Solute carrier family 26 member 2; sulfate anion transporter 1; Sulfate transporter
Gene Symbols: SLC26A2
Molecular weight: 81,662 Da
Basal Isoelectric point: 8.67  Predict pI for various phosphorylation states
Select Structure to View Below

SLC26A2

Protein Structure Not Found.

Cross-references to other databases:  STRING  |  cBioPortal  |  Wikipedia  |  Reactome  |  neXtProt  |  Protein Atlas  |  BioGPS  |  Pfam  |  Phospho.ELM  |  NetworKIN  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene