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Derlin 2

mammalian protein found in Homo sapiens
Protein protein Q5262654
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Derlin 2

Summary

Derlin 2 is a protein[1].

Key Facts

  • Derlin 2's instance of is recorded as protein[2].
  • Derlin 2's UniProt protein ID is recorded as Q9GZP9[3].
  • Derlin 2's part of is recorded as Derlin[4].
  • Derlin 2's part of is recorded as Endoplasmic Reticular Retrotranslocon[5].
  • Derlin 2's RefSeq protein ID is recorded as NP_001291706[6].
  • Derlin 2's RefSeq protein ID is recorded as NP_001291708[7].
  • Derlin 2's RefSeq protein ID is recorded as NP_057125[8].
  • Derlin 2's molecular function is recorded as protein binding[9].
  • Derlin 2's cell component is recorded as integral component of membrane[10].
  • Derlin 2's cell component is recorded as integral component of endoplasmic reticulum membrane[11].
  • Derlin 2's cell component is recorded as late endosome[12].
  • Derlin 2's cell component is recorded as early endosome[13].
  • Derlin 2's cell component is recorded as endoplasmic reticulum membrane[14].
  • Derlin 2's cell component is recorded as endoplasmic reticulum[15].
  • Derlin 2's cell component is recorded as membrane[16].
  • Derlin 2's cell component is recorded as endoplasmic reticulum quality control compartment[17].
  • Derlin 2's cell component is recorded as signal recognition particle receptor complex[18].
  • Derlin 2's cell component is recorded as signal recognition particle[19].
  • Derlin 2's cell component is recorded as membrane[20].
  • Derlin 2's biological process is recorded as endoplasmic reticulum unfolded protein response[21].
  • Derlin 2's biological process is recorded as positive regulation of cell growth[22].
  • Derlin 2's biological process is recorded as retrograde protein transport, ER to cytosol[23].
  • Derlin 2's biological process is recorded as response to unfolded protein[24].
  • Derlin 2's biological process is recorded as negative regulation of retrograde protein transport, ER to cytosol[25].
  • Derlin 2's biological process is recorded as positive regulation of cell population proliferation[26].

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] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Q20641742. Retrieved . wikidata.org.
  6. [7] ↑ . Q20641742. Retrieved . wikidata.org.
  7. [8] ↑ . Q20641742. Retrieved . wikidata.org.
  8. [9] ↑ . Derlin-2 and Derlin-3 are regulated by the mammalian unfolded protein response and are required for ER-associated degradation. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  9. [10] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] ↑ . Derlin-2 and Derlin-3 are regulated by the mammalian unfolded protein response and are required for ER-associated degradation. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] ↑ . GOA. 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] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] ↑ . Pre-emptive Quality Control Protects the ER from Protein Overload via the Proximity of ERAD Components and SRP. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] ↑ . Pre-emptive Quality Control Protects the ER from Protein Overload via the Proximity of ERAD Components and SRP. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] ↑ . Derlin-2 and Derlin-3 are regulated by the mammalian unfolded protein response and are required for ER-associated degradation. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] ↑ . Cloning and characterization of F-LANa, upregulated in human liver cancer. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . Derlin-2 and Derlin-3 are regulated by the mammalian unfolded protein response and are required for ER-associated degradation. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] ↑ . Identification of ERAD components essential for dislocation of the null Hong Kong variant of α-1-antitrypsin (NHK). Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] ↑ . Cloning and characterization of F-LANa, upregulated in human liver cancer. Retrieved . ebi.ac.uk. Provenance: wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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). Derlin 2. Retrieved May 3, 2026, from https://4ort.xyz/entity/derlin-2
MLA “Derlin 2.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/derlin-2.
BibTeX @misc{4ortxyz_derlin-2_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Derlin 2}}, year = {2026}, url = {https://4ort.xyz/entity/derlin-2}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Derlin 2 — https://4ort.xyz/entity/derlin-2 (retrieved 2026-05-03)

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