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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:11476 | osteoporosis | |
| DOID:11527 | laryngostenosis | |
| DOID:11569 | neurocirculatory asthenia | |
| DOID:11836 | clubfoot | |
| DOID:12028 | Conn's syndrome | |
| DOID:12175 | dyshormonogenic goiter | |
| DOID:12185 | otosclerosis | |
| DOID:12721 | multiple epiphyseal dysplasia | |
| DOID:12798 | mucopolysaccharidosis | |
| DOID:12799 | mucopolysaccharidosis II |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002654 | Multiple epiphyseal dysplasia |
| HP:0002656 | Epiphyseal dysplasia |
| HP:0002751 | Kyphoscoliosis |
| HP:0002786 | Tracheobronchomalacia |
| HP:0002808 | Kyphosis |
| HP:0002812 | Coxa vara |
| HP:0002829 | Arthralgia |
| HP:0002857 | Genu valgum |
| HP:0002938 | Lumbar hyperlordosis |
| HP:0002947 | Cervical kyphosis |
| 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 |
