# Solute carrier family 13 member 5

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21124419](https://www.wikidata.org/wiki/Q21124419)  
**Source**: https://4ort.xyz/entity/solute-carrier-family-13-member-5


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q86YT5)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86YT5)
5. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86YT5)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q86YT5&geneProductId=UniProtKB:Q86YT5)
7. [Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86YT5)
8. Ensembl Release 99
9. UMLS 2023
10. Transporter Classification database