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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
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001234 | Hitchhiker thumb |
| HP:0001249 | Intellectual disability |
| HP:0001252 | Hypotonia |
| HP:0001357 | Plagiocephaly |
| HP:0001371 | Flexion contracture |
| HP:0001373 | Joint dislocation |
| HP:0001376 | Limitation of joint mobility |
| HP:0001382 | Joint hypermobility |
| HP:0001385 | Hip dysplasia |
| HP:0001387 | Joint stiffness |
| 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 |
|---|---|---|---|
| 100556372 | ANOCA03179 | ||
| 107082690 | CYPVA04653 | ||
| 114027840 | VOMUR08700 | ||
| 100952772 | OTOGA18379 | ||
| 102785415 | NEOBR17714 | ||
| 102019592 | CHILA04746 | ||
| 108243959 | KRYMA20022 | ||
| 105717014 | AOTNA00127 | ||
| 110192814 | PHACI31525 | ||
| 101039305 | SAIBB23094 |
