Solute carrier family 25 member 15

mammalian protein found in Homo sapiens
Protein protein Q21124255
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Solute carrier family 25 member 15

Summary

Solute carrier family 25 member 15 is a protein[1].

Key Facts

  • Solute carrier family 25 member 15's instance of is recorded as protein[2].
  • Solute carrier family 25 member 15's UniProt protein ID is recorded as Q9Y619[3].
  • Solute carrier family 25 member 15's part of is recorded as Ornithine translocase[4].
  • Solute carrier family 25 member 15's RefSeq protein ID is recorded as NP_055067[5].
  • Solute carrier family 25 member 15's molecular function is recorded as L-ornithine transmembrane transporter activity[6].
  • Solute carrier family 25 member 15's molecular function is recorded as transmembrane transporter activity[7].
  • Solute carrier family 25 member 15's molecular function is recorded as L-ornithine transmembrane transporter activity[8].
  • Solute carrier family 25 member 15's cell component is recorded as membrane[9].
  • Solute carrier family 25 member 15's cell component is recorded as mitochondrion[10].
  • Solute carrier family 25 member 15's cell component is recorded as mitochondrial inner membrane[11].
  • Solute carrier family 25 member 15's cell component is recorded as integral component of membrane[12].
  • Solute carrier family 25 member 15's cell component is recorded as mitochondrial inner membrane[13].
  • Solute carrier family 25 member 15's cell component is recorded as integral component of membrane[14].
  • Solute carrier family 25 member 15's biological process is recorded as urea cycle[15].
  • Solute carrier family 25 member 15's biological process is recorded as mitochondrial transport[16].
  • Solute carrier family 25 member 15's biological process is recorded as mitochondrial L-ornithine transmembrane transport[17].
  • Solute carrier family 25 member 15's biological process is recorded as mitochondrial L-ornithine transmembrane transport[18].
  • Solute carrier family 25 member 15's encoded by is recorded as SLC25A15[19].
  • Solute carrier family 25 member 15's found in taxon is recorded as Homo sapiens[20].
  • Solute carrier family 25 member 15's Ensembl protein ID is recorded as ENSP00000342267[21].
  • Solute carrier family 25 member 15's Ensembl protein ID is recorded as ENSP00000415826[22].
  • Solute carrier family 25 member 15's Ensembl protein ID is recorded as ENSP00000431429[23].
  • Solute carrier family 25 member 15's Transporter Classification Database ID is recorded as 2.A.29.19.2[24].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . Q905695. Retrieved . wikidata.org.
  2. [3] . Q905695. Retrieved . wikidata.org.
  3. [4] . Retrieved . wikidata.org.
  4. [5] . Q20641742. Retrieved . wikidata.org.
  5. [6] . Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  6. [7] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  7. [8] . Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  8. [9] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  9. [10] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] . Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] . Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] . Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] . Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] . Q905695. Retrieved . wikidata.org.
  19. [20] . Q905695. Retrieved . wikidata.org.
  20. [21] . Ensembl Release 99. wikidata.org.
  21. [22] . Ensembl Release 99. wikidata.org.
  22. [23] . Ensembl Release 99. wikidata.org.
  23. [24] . Transporter Classification database. Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). Solute carrier family 25 member 15. Retrieved May 3, 2026, from https://4ort.xyz/entity/solute-carrier-family-25-member-15
MLA “Solute carrier family 25 member 15.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/solute-carrier-family-25-member-15.
BibTeX @misc{4ortxyz_solute-carrier-family-25-member-15_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Solute carrier family 25 member 15}}, year = {2026}, url = {https://4ort.xyz/entity/solute-carrier-family-25-member-15}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Solute carrier family 25 member 15 — https://4ort.xyz/entity/solute-carrier-family-25-member-15 (retrieved 2026-05-03)

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