Slc26a2 - solute carrier family 26 (sulfate transporter), member 2 Gene
Also Known as Dtd; ST-OB
Species: Mus musculus
Summary
Predicted to enable anion transmembrane transporter activity. Predicted to be involved in ossification and sulfate transmembrane transport. Predicted to be located in apical plasma membrane and microvillus membrane. Predicted to be integral component of plasma membrane. Is expressed in several structures, including alimentary system; brain; genitourinary system; sensory organ; and skeleton. Used to study diastrophic dysplasia. Human ortholog(s) of this gene implicated in bone disease (multiple). Orthologous to human SLC26A2 (solute carrier family 26 member 2). [provided by Alliance of Genome Resources, Apr 2022]
Slc26a2 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_007885.2 | NP_031911.1 | sulfate transporter |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables solute:inorganic anion antiporter activity |
IDA
IDA: Inferred from direct assay
|
20219950 | MGI |
| enables sulfate transmembrane transporter activity |
IMP
IMP: Inferred from mutant phenotype
|
15703192 | MGI |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in chondrocyte differentiation |
IMP
IMP: Inferred from mutant phenotype
|
24302720 | MGI |
| involved in chondrocyte proliferation |
IMP
IMP: Inferred from mutant phenotype
|
24302720 | MGI |
| involved in sulfate transmembrane transport |
IMP
IMP: Inferred from mutant phenotype
|
24302720 | MGI |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| is active in plasma membrane |
IMP
IMP: Inferred from mutant phenotype
|
15703192 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
sulfate transporter |
|