# Solute carrier family 25 member 15

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21124255](https://www.wikidata.org/wiki/Q21124255)  
**Source**: https://4ort.xyz/entity/solute-carrier-family-25-member-15


## References

1. UniProt
2. Q20641742
3. [Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9Y619&geneProductId=UniProtKB:Q9Y619)
4. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9Y619&geneProductId=UniProtKB:Q9Y619)
5. [Cloning and characterization of human ORNT2: a second mitochondrial ornithine transporter that can rescue a defective ORNT1 in patients with the hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a urea cycle disorder](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9Y619&geneProductId=UniProtKB:Q9Y619)
6. [The mitochondrial ornithine transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9Y619&geneProductId=UniProtKB:Q9Y619)
7. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9Y619)
8. [Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9Y619)
9. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9Y619)
10. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9Y619&geneProductId=UniProtKB:Q9Y619)
11. Ensembl Release 99
12. Transporter Classification database