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Opioid receptor, mu 1

mammalian protein found in Rattus norvegicus
Protein protein Q28561662
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Opioid receptor, mu 1

Summary

Opioid receptor, mu 1 is a protein[1].

Key Facts

  • Opioid receptor, mu 1's instance of is recorded as protein[2].
  • Opioid receptor, mu 1's UniProt protein ID is recorded as P33535[3].
  • Opioid receptor, mu 1's part of is recorded as Mu opioid receptor[4].
  • Opioid receptor, mu 1's part of is recorded as GPCR, rhodopsin-like, 7TM, protein family[5].
  • Opioid receptor, mu 1's has part is recorded as GPCR, rhodopsin-like, 7TM[6].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001033686[7].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001033688[8].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001033689[9].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001033690[10].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001291662[11].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001291663[12].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001291664[13].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001291665[14].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001291666[15].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001291667[16].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_001291669[17].
  • Opioid receptor, mu 1's RefSeq protein ID is recorded as NP_037203[18].
  • Opioid receptor, mu 1's molecular function is recorded as G-protein alpha-subunit binding[19].
  • Opioid receptor, mu 1's molecular function is recorded as G protein-coupled receptor activity[20].
  • Opioid receptor, mu 1's molecular function is recorded as beta-endorphin receptor activity[21].
  • Opioid receptor, mu 1's molecular function is recorded as G protein-coupled opioid receptor activity[22].
  • Opioid receptor, mu 1's molecular function is recorded as voltage-gated calcium channel activity[23].
  • Opioid receptor, mu 1's molecular function is recorded as protein binding[24].
  • Opioid receptor, mu 1's molecular function is recorded as protein C-terminus binding[25].
  • Opioid receptor, mu 1's molecular function is recorded as protein domain specific binding[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] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  6. [7] ↑ . Q20641742. Retrieved . wikidata.org.
  7. [8] ↑ . Q20641742. Retrieved . wikidata.org.
  8. [9] ↑ . Q20641742. Retrieved . wikidata.org.
  9. [10] ↑ . Q20641742. Retrieved . wikidata.org.
  10. [11] ↑ . Q20641742. Retrieved . wikidata.org.
  11. [12] ↑ . Q20641742. Retrieved . wikidata.org.
  12. [13] ↑ . Q20641742. Retrieved . wikidata.org.
  13. [14] ↑ . Q20641742. Retrieved . wikidata.org.
  14. [15] ↑ . Q20641742. Retrieved . wikidata.org.
  15. [16] ↑ . Q20641742. Retrieved . wikidata.org.
  16. [17] ↑ . Q20641742. Retrieved . wikidata.org.
  17. [18] ↑ . Q20641742. Retrieved . wikidata.org.
  18. [19] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . The μ-Opioid Receptor Down-Regulates Differently from the δ-Opioid Receptor: Requirement of a High Affinity Receptor/G Protein Complex Formation. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . Activation of μ opioid receptors inhibits transient high- and low-threshold Ca 2+ currents, but spares a sustained current. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] ↑ . Formation of mu-/kappa-opioid receptor heterodimer is sex-dependent and mediates female-specific opioid analgesia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] ↑ . Heterodimerization of opioid receptor-like 1 and mu-opioid receptors impairs the potency of micro receptor agonist. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] ↑ . Interaction of the mu-opioid receptor with GPR177 (Wntless) inhibits Wnt secretion: potential implications for opioid dependence. 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). Opioid receptor, mu 1. Retrieved May 3, 2026, from https://4ort.xyz/entity/opioid-receptor-mu-1-q28561662
MLA “Opioid receptor, mu 1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/opioid-receptor-mu-1-q28561662.
BibTeX @misc{4ortxyz_opioid-receptor-mu-1-q28561662_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Opioid receptor, mu 1}}, year = {2026}, url = {https://4ort.xyz/entity/opioid-receptor-mu-1-q28561662}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Opioid receptor, mu 1 — https://4ort.xyz/entity/opioid-receptor-mu-1-q28561662 (retrieved 2026-05-03)

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