# Solute carrier family 26 member 2

> mammalian protein found in Homo sapiens

**Wikidata**: [Q7390819](https://www.wikidata.org/wiki/Q7390819)  
**Source**: https://4ort.xyz/entity/solute-carrier-family-26-member-2


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P50443)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P50443)
5. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P50443)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P50443&geneProductId=UniProtKB:P50443)
7. [The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping](http://www.ebi.ac.uk/QuickGO/annotations?protein=P50443&geneProductId=UniProtKB:P50443)
8. [The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P50443)
9. [Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P50443)
10. [In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine](http://www.ebi.ac.uk/QuickGO/annotations?protein=P50443&geneProductId=UniProtKB:P50443)
11. [Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene](http://www.ebi.ac.uk/QuickGO/annotations?protein=P50443&geneProductId=UniProtKB:P50443)
12. [In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P50443)
13. Ensembl Release 99
14. Transporter Classification database