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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:0060327 | omphalocele | |
| DOID:0060359 | Sakati-Nyhan syndrome | |
| DOID:0060380 | orofaciodigital syndrome X | |
| DOID:0060599 | Nance-Horan syndrome | |
| DOID:0060703 | Muenke Syndrome | |
| DOID:0060744 | Pendred Syndrome | |
| DOID:0070300 | multiple epiphyseal dysplasia 4 | |
| DOID:0080055 | achondrogenesis type IB | |
| DOID:0090001 | Fraser syndrome | |
| DOID:0110213 | isolated cleft palate |
- 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 |
|---|---|---|---|
| 100388764 | CALJA25925 | ||
| 105589871 | CERAT28141 | ||
| 102121787 | MACFA36689 | ||
| 709998 | MACMU37940 | ||
| 105466878 | MACNE08058 | ||
| 101010114 | PAPAN31527 | ||
| 105543438 | MANLE16402 | ||
| 101150948 | GORGO33190 | ||
| 100976756 | PANPA32912 | ||
| 742297 | PANTR36548 |
