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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Sulfate transporter
Summary
- UniProt ID
- P50443
- Gene Symbol
-
- SLC26A2
- DTD
- DTDST
- Organism
- Homo sapiens (human)
External Links
- The Human Metabolome Database
- HMDBP02805
- RaftProt
- P50443
Annotation
- Keyword
-
- 3D-structure
- Cell membrane
- Disease variant
- Dwarfism
- Glycoprotein
- Phosphoprotein
- Reference proteome
- Transmembrane helix
- Transport
- Gene Ontology (GO)
| GO Term |
|---|
| ossification |
| chondrocyte differentiation |
| sulfate transport |
| sulfate transmembrane transport |
| chondrocyte proliferation |
| GO Term |
|---|
| plasma membrane |
| membrane |
| extracellular exosome |
| apical plasma membrane |
| microvillus membrane |
Sequence
MSSESKEQHNVSPRDSAEGNDSYPSGIHLELQRESSTDFKQFETNDQCRPYHRILIERQEKSDTNFKEFVIKKLQKNCQCSPAKAKNMILGFLPVLQWLPKYDLKKNILGDVMSGLIVGILLVPQSIAYSLLAGQEPVYGLYTSFFASIIYFLLGTSRHISVGIFGVLCLMIGETVDRELQKAGYDNAHSAPSLGMVSNGSTLLNHTSDRICDKSCYAIMVGSTVTFIAGVYQVAMGFFQVGFVSVYLSDALLSGFVTGASFTILTSQAKYLLGLNLPRTNGVGSLITTWIHVFRNIHKTNLCDLITSLLCLLVLLPTKELNEHFKSKLKAPIPIELVVVVAATLASHFGKLHENYNSSIAGHIPTGFMPPKVPEWNLIPSVAVDAIAISIIGFAITVSLSEMFAKKHGYTVKANQEMYAIGFCNIIPSFFHCFTTSAALAKTLVKESTGCHTQLSGVVTALVLLLVLLVIAPLFYSLQKSVLGVITIVNLRGALRKFRDLPKMWSISRMDTVIWFVTMLSSALLSTEIGLLVGVCFSIFCVILRTQKPKSSLLGLVEESEVFESVSAYKNLQIKPGIKIFRFVAPLYYINKECFKSALYKQTVNPILIKVAWKKAAKRKIKEKVVTLGGIQDEMSVQLSHDPLELHTIVIDCSAIQFLDTAGIHTLKEVRRDYEAIGIQVLLAQCNPTVRDSLTNGEYCKKEEENLLFYSVYEAMAFAEVSKNQKGVCVPNGLSLSSD
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Defective SLC26A2 causes chondrodysplasias | Homo sapiens |
| Multifunctional anion exchangers | Homo sapiens |
| Transport and synthesis of PAPS | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| 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 | |
| DOID:0110716 | Warburg micro syndrome 1 |
