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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: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: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 |
|---|---|---|---|
| 111232705 | SERDU08213 | ||
| 108417923 | PYGNA03831 | ||
| 101965720 | ICTTR07462 | ||
| 103140084 | POEFO07745 | ||
| 101615559 | JACJA16422 | ||
| 118319364 | SCOMX05014 | ||
| 100225222 | TAEGU04549 | ||
| 103244785 | CHLSB11104 | ||
| 108532051 | RHIBE02229 | ||
| 104670404 | RHIRO28069 |
