# Solute carrier family 52 member 2

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21100632](https://www.wikidata.org/wiki/Q21100632)  
**Source**: https://4ort.xyz/entity/solute-carrier-family-52-member-2-q21100632


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9HAB3)
3. Q20641742
4. [A proteome-scale map of the human interactome network](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9HAB3)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9HAB3)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9HAB3&geneProductId=UniProtKB:Q9HAB3)
7. [Identification and comparative functional characterization of a new human riboflavin transporter hRFT3 expressed in the brain](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9HAB3&geneProductId=UniProtKB:Q9HAB3)
8. [Identification and comparative functional characterization of a new human riboflavin transporter hRFT3 expressed in the brain](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9HAB3)
9. [SLC52A2 [p.P141T] and SLC52A3 [p.N21S] causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transporters](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9HAB3)
10. Ensembl Release 99
11. Transporter Classification database