# Solute carrier family 52 member 3

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21124460](https://www.wikidata.org/wiki/Q21124460)  
**Source**: https://4ort.xyz/entity/solute-carrier-family-52-member-3-q21124460


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9NQ40)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9NQ40&geneProductId=UniProtKB:Q9NQ40)
5. [Identification and comparative functional characterization of a new human riboflavin transporter hRFT3 expressed in the brain](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9NQ40&geneProductId=UniProtKB:Q9NQ40)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9NQ40)
7. [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:Q9NQ40)
8. [Effect of clinical mutations on functionality of the human riboflavin transporter-2 (hRFT-2)](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9NQ40)
9. [Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9NQ40)
10. Ensembl Release 99
11. Transporter Classification database