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Bardet-Biedl syndrome 4

mammalian protein found in Homo sapiens
Protein protein Q21112595
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Summary

Bardet-Biedl syndrome 4 is a protein[1].

Key Facts

  • Bardet-Biedl syndrome 4's instance of is recorded as protein[2].
  • Bardet-Biedl syndrome 4's UniProt protein ID is recorded as Q96RK4[3].
  • Bardet-Biedl syndrome 4's part of is recorded as Tetratricopeptide-like helical domain superfamily[4].
  • Bardet-Biedl syndrome 4's part of is recorded as Tetratricopeptide repeat-containing domain, protein family[5].
  • Bardet-Biedl syndrome 4's part of is recorded as Tetratricopeptide repeat family[6].
  • Bardet-Biedl syndrome 4's has part is recorded as Tetratricopeptide repeat-containing domain[7].
  • Bardet-Biedl syndrome 4's has part is recorded as tetratricopeptide repeat[8].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as NP_001239607[9].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as NP_001307594[10].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as NP_149017[11].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as XP_011520150[12].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as XP_011520151[13].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as XP_011520153[14].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as XP_016877939[15].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as XP_016877941[16].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as XP_016877942[17].
  • Bardet-Biedl syndrome 4's RefSeq protein ID is recorded as XP_016877943[18].
  • Bardet-Biedl syndrome 4's molecular function is recorded as microtubule motor activity[19].
  • Bardet-Biedl syndrome 4's molecular function is recorded as dynactin binding[20].
  • Bardet-Biedl syndrome 4's molecular function is recorded as alpha-tubulin binding[21].
  • Bardet-Biedl syndrome 4's molecular function is recorded as protein binding[22].
  • Bardet-Biedl syndrome 4's molecular function is recorded as beta-tubulin binding[23].
  • Bardet-Biedl syndrome 4's cell component is recorded as cytoplasm[24].
  • Bardet-Biedl syndrome 4's cell component is recorded as ciliary basal body[25].
  • Bardet-Biedl syndrome 4's cell component is recorded as centrosome[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . UniProt. Retrieved . wikidata.org.
  2. [3] ↑ . UniProt. Retrieved . wikidata.org.
  3. [4] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  7. [8] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: 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] ↑ . The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] ↑ . A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] ↑ . The centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSome. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] ↑ . Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] ↑ . GOA. 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). Bardet-Biedl syndrome 4. Retrieved May 3, 2026, from https://4ort.xyz/entity/bardet-biedl-syndrome-4
MLA “Bardet-Biedl syndrome 4.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/bardet-biedl-syndrome-4.
BibTeX @misc{4ortxyz_bardet-biedl-syndrome-4_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Bardet-Biedl syndrome 4}}, year = {2026}, url = {https://4ort.xyz/entity/bardet-biedl-syndrome-4}, note = {Accessed: 2026-05-03}}
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