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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:0110716 | Warburg micro syndrome 1 | |
| DOID:0110717 | Warburg micro syndrome 2 | |
| DOID:0110718 | Warburg micro syndrome 3 | |
| DOID:0110719 | Warburg micro syndrome 4 | |
| DOID:0110946 | autosomal recessive osteopetrosis 7 | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:1002 | endometritis | |
| DOID:10534 | stomach cancer | |
| DOID:10690 | mastitis | |
| DOID:11383 | cryptorchidism |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000023 | Inguinal hernia |
| HP:0000028 | Cryptorchidism |
| HP:0000175 | Cleft palate |
| HP:0000218 | High palate |
| HP:0000219 | Thin upper lip vermilion |
| HP:0000256 | Macrocephaly |
| HP:0000272 | Malar flattening |
| HP:0000286 | Epicanthus |
| HP:0000293 | Full cheeks |
| 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 |
