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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
solute carrier family 26 member 2
Summary
- Gene Symbol
-
- SLC26A2
- Aliases
-
- DTDST
- diastrophic dysplasia sulfate transporter
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Cell membrane
- Disease variant
- Dwarfism
- Glycoprotein
- Phosphoprotein
- Reference proteome
- Transmembrane helix
- Transport
- Proteins
| UniProt | Protein Name |
|---|---|
| P50443 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| oxalate transport | ||
| ossification | ||
| chondrocyte proliferation | ||
| bicarbonate transport | ||
| chondrocyte differentiation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| microvillus membrane | ||
| plasma membrane | ||
| membrane |
|
|
| apical plasma membrane | ||
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| secondary active sulfate transmembrane transporter activity | ||
| chloride transmembrane transporter activity | ||
| oxalate transmembrane transporter activity | ||
| solute:inorganic anion antiporter activity | ||
| sulfate transmembrane transporter activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:4258 | Weissenbacher-Zweymuller syndrome | |
| DOID:445 | Bartter disease | |
| DOID:446 | primary hyperaldosteronism | |
| DOID:4480 | achondroplasia | |
| DOID:4766 | embryoma | |
| DOID:480 | movement disease | |
| DOID:5403 | microcystic adenoma | |
| DOID:5517 | stomach carcinoma | |
| DOID:5672 | large intestine cancer | |
| DOID:6000 | congestive heart failure |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001440 | Metatarsal synostosis |
| HP:0001511 | Intrauterine growth retardation |
| HP:0001518 | Small for gestational age |
| HP:0001522 | Death in infancy |
| HP:0001537 | Umbilical hernia |
| HP:0001538 | Protuberant abdomen |
| HP:0001561 | Polyhydramnios |
| HP:0001591 | Bell-shaped thorax |
| HP:0001602 | Laryngeal stenosis |
| HP:0001609 | Hoarse voice |
| Disease ID | Disease Name |
|---|---|
| OMIM:256050 |
|
| OMIM:600972 |
|
| OMIM:222600 |
|
| ORPHA:628 |
|
| OMIM:226900 |
|
| ORPHA:93298 |
|
| ORPHA:93307 |
|
| ORPHA:56304 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 105821510 | PROCO11588 | ||
| 856111 | SGD:S000006207 | ||
| 109057031 | CYPCA85162 | ||
| 103738097 | NANGA20180 | ||
| 116451276 | CORMO04234 | ||
| 103263372 | CARSF13054 | ||
| 115615562 | STRHB13122 |
