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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
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 |
|---|---|---|
| ossification |
|
|
| chondrocyte differentiation | ||
| sulfate transport |
|
|
| bicarbonate transport | ||
| oxalate transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane | ||
| membrane | ||
| apical plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| solute:inorganic anion antiporter activity | ||
| secondary active sulfate transmembrane transporter activity | ||
| bicarbonate transmembrane transporter activity | ||
| chloride transmembrane transporter activity | ||
| sulfate transmembrane transporter activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- transporter
- Functional Category
-
- E: Amino acid transport and metabolism
- P: Inorganic ion transport and metabolism
- T: Signal transduction mechanisms
| InterPro |
|---|
| SLC26A/SulP transporter domain |
| SLC26A/SulP transporter |
| STAS domain superfamily |
| STAS domain |
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:0050581 | brachydactyly | |
| DOID:0050648 | atelosteogenesis | |
| DOID:0070300 | multiple epiphyseal dysplasia 4 | |
| DOID:0080055 | achondrogenesis type IB | |
| DOID:14687 | diastrophic dysplasia | |
| DOID:2256 | osteochondrodysplasia | |
| DOID:2300 | spondylolysis | |
| DOID:676 | juvenile rheumatoid arthritis |
- 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:600972 |
|
| OMIM:222600 |
|
| OMIM:226900 |
|
| ORPHA:56304 |
|
| OMIM:256050 |
|
| ORPHA:628 |
|
| ORPHA:93298 |
|
| ORPHA:93307 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 1811 | SGD:S000006207 | ||
| 1836 | Xenbase:XB-GENE-997399 | ||
| 10861 | SGD:S000006207 | ||
| 13487 | SGD:S000006207 | ||
| 13521 | Xenbase:XB-GENE-997399 | MOUSE23375 | |
| 65010 | SGD:S000006207 | ||
| 80979 | SGD:S000006207 | ||
| 83819 | SGD:S000006207 | ||
| 114629 | SGD:S000006207 | ||
| 115019 | SGD:S000006207 |
