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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: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:0000316 | Hypertelorism |
| HP:0000331 | Short chin |
| HP:0000343 | Long philtrum |
| HP:0000347 | Micrognathia |
| HP:0000363 | Abnormal earlobe morphology |
| HP:0000365 | Hearing impairment |
| HP:0000368 | Low-set, posteriorly rotated ears |
| HP:0000369 | Low-set ears |
| HP:0000377 | Abnormal pinna morphology |
| HP:0000396 | Overfolded helix |
| 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 |
|---|---|---|---|
| 108710958 | Xenbase:XB-GENE-17330073 | ||
| 108713240 | Xenbase:XB-GENE-17330889 | ||
| 108713241 | Xenbase:XB-GENE-17330074 | ||
| 100494417 | Xenbase:XB-GENE-997399 | ||
| 101950986 | CHRPI02566 | ||
| 113433670 | PSETE03868 | ||
| 104913251 | MELGA04079 | ||
| 103817533 | SERCA12556 | ||
| 100075512 | ORNAN29403 | ||
| 100916422 | SARHA13108 |
