Bardet-Biedl syndrome 1

mammalian protein found in Homo sapiens
Protein protein Q21112592
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Bardet-Biedl syndrome 1

Summary

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

Key Facts

  • Bardet-Biedl syndrome 1's instance of is recorded as protein[2].
  • Bardet-Biedl syndrome 1's UniProt protein ID is recorded as Q8NFJ9[3].
  • Bardet-Biedl syndrome 1's part of is recorded as Quinoprotein alcohol dehydrogenase-like superfamily[4].
  • Bardet-Biedl syndrome 1's part of is recorded as Bardet-Biedl syndrome 1 protein[5].
  • Bardet-Biedl syndrome 1's part of is recorded as Bardet-Biedl syndrome 1, N-terminal domain, protein family[6].
  • Bardet-Biedl syndrome 1's has part is recorded as Bardet-Biedl syndrome 1, N-terminal[7].
  • Bardet-Biedl syndrome 1's RefSeq protein ID is recorded as NP_078925[8].
  • Bardet-Biedl syndrome 1's molecular function is recorded as smoothened binding[9].
  • Bardet-Biedl syndrome 1's molecular function is recorded as patched binding[10].
  • Bardet-Biedl syndrome 1's molecular function is recorded as protein binding[11].
  • Bardet-Biedl syndrome 1's molecular function is recorded as patched binding[12].
  • Bardet-Biedl syndrome 1's molecular function is recorded as smoothened binding[13].
  • Bardet-Biedl syndrome 1's cell component is recorded as cytoplasm[14].
  • Bardet-Biedl syndrome 1's cell component is recorded as ciliary basal body[15].
  • Bardet-Biedl syndrome 1's cell component is recorded as cytosol[16].
  • Bardet-Biedl syndrome 1's cell component is recorded as centrosome[17].
  • Bardet-Biedl syndrome 1's cell component is recorded as cell projection[18].
  • Bardet-Biedl syndrome 1's cell component is recorded as BBSome[19].
  • Bardet-Biedl syndrome 1's cell component is recorded as membrane[20].
  • Bardet-Biedl syndrome 1's cell component is recorded as plasma membrane[21].
  • Bardet-Biedl syndrome 1's cell component is recorded as cilium[22].
  • Bardet-Biedl syndrome 1's cell component is recorded as microtubule organizing center[23].
  • Bardet-Biedl syndrome 1's cell component is recorded as ciliary membrane[24].
  • Bardet-Biedl syndrome 1's cell component is recorded as axoneme[25].
  • Bardet-Biedl syndrome 1's cell component is recorded as cytoskeleton[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] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  7. [8] . Q20641742. Retrieved . wikidata.org.
  8. [9] . BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  9. [10] . BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] . Bardet-Biedl syndrome proteins 1 and 3 regulate the ciliary trafficking of polycystic kidney disease 1 protein. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] . BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] . BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] . Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] . GOA. 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] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. 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 1. Retrieved May 3, 2026, from https://4ort.xyz/entity/bardet-biedl-syndrome-1
MLA “Bardet-Biedl syndrome 1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/bardet-biedl-syndrome-1.
BibTeX @misc{4ortxyz_bardet-biedl-syndrome-1_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Bardet-Biedl syndrome 1}}, year = {2026}, url = {https://4ort.xyz/entity/bardet-biedl-syndrome-1}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Bardet-Biedl syndrome 1 — https://4ort.xyz/entity/bardet-biedl-syndrome-1 (retrieved 2026-05-03)

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