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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 |
|---|---|---|
| sulfate transport | ||
| sulfate transmembrane transport | ||
| chloride transmembrane transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| microvillus membrane | ||
| plasma membrane | ||
| membrane |
|
|
| apical plasma membrane | ||
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| bicarbonate 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:0014667 | disease of metabolism | |
| DOID:0050581 | brachydactyly | |
| DOID:0050648 | atelosteogenesis | |
| DOID:0060185 | Clostridium difficile colitis | |
| DOID:0060229 | Baraitser-Winter syndrome | |
| DOID:0060232 | branchiootic syndrome | |
| DOID:0060249 | scoliosis | |
| DOID:0060316 | orofaciodigital syndrome I | |
| DOID:0060320 | inguinal hernia | |
| DOID:0060321 | umbilical hernia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0006703 | Aplasia/Hypoplasia of the lungs |
| HP:0008110 | Equinovarus deformity |
| HP:0008434 | Hypoplastic cervical vertebrae |
| HP:0008608 | Hypertrophic auricular cartilage |
| HP:0008752 | Laryngeal cartilage malformation |
| HP:0008802 | Hypoplasia of the femoral head |
| HP:0008807 | Acetabular dysplasia |
| HP:0008826 | Dislocation of the femoral head |
| HP:0008829 | Delayed femoral head ossification |
| HP:0008848 | Moderately short stature |
| 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 |
|---|---|---|---|
| 179357 | WB:WBGene00013963 | ||
| 189085 | WB:WBGene00020914 | ||
| 189195 | WB:WBGene00012259 | ||
| 39996 | FB:FBgn0036770 | ||
| 103191307 | CALMI45344 | ||
| 102347458 | LATCH08051 | ||
| 557046 | ZFIN:ZDB-GENE-030717-3 | DANRE07491 | |
| 103047169 | ASTMX04717 | ||
| 108269293 | ICTPU34117 | ||
| 113573351 | ELEEL13196 |
