McKusick-Kaufman syndrome

mammalian protein found in Mus musculus
Protein protein Q21496604
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McKusick-Kaufman syndrome

Summary

McKusick-Kaufman syndrome is a protein[1].

Key Facts

  • McKusick-Kaufman syndrome's instance of is recorded as protein[2].
  • McKusick-Kaufman syndrome's subclass of is recorded as protein[3].
  • McKusick-Kaufman syndrome's UniProt protein ID is recorded as Q9JI70[4].
  • McKusick-Kaufman syndrome's part of is recorded as McKusick-Kaufman/Bardet-Biedl syndromes putative chaperonin[5].
  • McKusick-Kaufman syndrome's part of is recorded as GroEL-like apical domain superfamily[6].
  • McKusick-Kaufman syndrome's part of is recorded as GroEL-like equatorial domain superfamily[7].
  • McKusick-Kaufman syndrome's part of is recorded as TCP-1-like chaperonin intermediate domain superfamily[8].
  • McKusick-Kaufman syndrome's RefSeq protein ID is recorded as NP_001135418[9].
  • McKusick-Kaufman syndrome's RefSeq protein ID is recorded as NP_001273910[10].
  • McKusick-Kaufman syndrome's RefSeq protein ID is recorded as NP_001273912[11].
  • McKusick-Kaufman syndrome's RefSeq protein ID is recorded as NP_067502[12].
  • McKusick-Kaufman syndrome's RefSeq protein ID is recorded as XP_036018330[13].
  • McKusick-Kaufman syndrome's RefSeq protein ID is recorded as XP_036018331[14].
  • McKusick-Kaufman syndrome's molecular function is recorded as nucleotide binding[15].
  • McKusick-Kaufman syndrome's molecular function is recorded as ATP binding[16].
  • McKusick-Kaufman syndrome's molecular function is recorded as protein folding chaperone activity[17].
  • McKusick-Kaufman syndrome's molecular function is recorded as unfolded protein binding[18].
  • McKusick-Kaufman syndrome's molecular function is recorded as unfolded protein binding[19].
  • McKusick-Kaufman syndrome's cell component is recorded as ciliary basal body[20].
  • McKusick-Kaufman syndrome's cell component is recorded as cytosol[21].
  • McKusick-Kaufman syndrome's cell component is recorded as centrosome[22].
  • McKusick-Kaufman syndrome's cell component is recorded as kinociliary basal body[23].
  • McKusick-Kaufman syndrome's cell component is recorded as intracellular anatomical structure[24].
  • McKusick-Kaufman syndrome's cell component is recorded as microtubule organizing center[25].
  • McKusick-Kaufman syndrome's cell component is recorded as motile cilium[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] . Q905695. Retrieved . wikidata.org.
  4. [5] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  5. [6] . InterPro Release 71.0. ebi.ac.uk. Provenance: 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] . 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] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] . Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis. 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] . Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] . Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia. 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). McKusick-Kaufman syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/mckusick-kaufman-syndrome-q21496604
MLA “McKusick-Kaufman syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/mckusick-kaufman-syndrome-q21496604.
BibTeX @misc{4ortxyz_mckusick-kaufman-syndrome-q21496604_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{McKusick-Kaufman syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/mckusick-kaufman-syndrome-q21496604}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): McKusick-Kaufman syndrome — https://4ort.xyz/entity/mckusick-kaufman-syndrome-q21496604 (retrieved 2026-05-03)

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