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Gene: SLC26A2 (solute carrier family 26 member 2) Homo sapiens
Symbol: SLC26A2
Name: solute carrier family 26 member 2
Description: Exhibits sulfate transmembrane transporter activity. Involved in sulfate transmembrane transport. Localizes to integral component of plasma membrane. Implicated in bone disease (multiple).
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: D5S1708; diastrophic dysplasia protein; diastrophic dysplasia sulfate transporter; DTD; DTDST; EDM4; MST153; MSTP157; solute carrier family 26 (anion exchanger), member 2; solute carrier family 26 (sulfate transporter), member 2; sulfate anion transporter 1; sulfate transporter
Mus musculus (house mouse) : Slc26a2 (solute carrier family 26 (sulfate transporter), member 2)  MGI  Alliance
Rattus norvegicus (Norway rat) : Slc26a2 (solute carrier family 26 member 2)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Slc26a2 (solute carrier family 26 member 2)
Pan paniscus (bonobo/pygmy chimpanzee) : SLC26A2 (solute carrier family 26 member 2)
Canis lupus familiaris (dog) : SLC26A2 (solute carrier family 26 member 2)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Slc26a2 (solute carrier family 26 member 2)
Sus scrofa (pig) : SLC26A2 (solute carrier family 26 member 2)
Chlorocebus sabaeus (African green monkey) : SLC26A2 (solute carrier family 26 member 2)
Heterocephalus glaber (naked mole-rat) : Slc26a2 (solute carrier family 26 member 2)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Human AssemblyChrPosition (strand)SourceGenome Browsers
GRCh38 Ensembl5149,960,758 - 149,993,455 (+)EnsemblGRCh38hg38GRCh38
GRCh38 Ensembl5149,960,737 - 149,993,455 (+)EnsemblGRCh38hg38GRCh38
GRCh385149,960,758 - 149,987,400 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh375149,340,300 - 149,366,963 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365149,320,493 - 149,347,156 (+)NCBINCBI36hg18NCBI36
Build 345149,320,638 - 149,347,155NCBI
Celera5145,421,686 - 145,448,348 (+)NCBI
Cytogenetic Map5q32NCBI
HuRef5144,488,253 - 144,514,927 (+)NCBIHuRef
CHM1_15148,772,975 - 148,799,655 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)

Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Phenotype Annotations
References - curated
References - uncurated


Comparative Map Data
Position Markers
miRNA Target Status


RNA-SEQ Expression


Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
More on SLC26A2
Alliance Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 732217
Created: 2004-01-12
Species: Homo sapiens
Last Modified: 2020-04-28
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.