WD repeat domain 19

mammalian protein found in Mus musculus
Protein protein Q21990311
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WD repeat domain 19

Summary

WD repeat domain 19 is a protein[1].

Key Facts

  • WD repeat domain 19's instance of is recorded as protein[2].
  • WD repeat domain 19's subclass of is recorded as protein[3].
  • WD repeat domain 19's UniProt protein ID is recorded as Q3UGF1[4].
  • WD repeat domain 19's RefSeq protein ID is recorded as NP_700440[5].
  • WD repeat domain 19's RefSeq protein ID is recorded as NP_001346808[6].
  • WD repeat domain 19's RefSeq protein ID is recorded as NP_001346809[7].
  • WD repeat domain 19's molecular function is recorded as molecular function[8].
  • WD repeat domain 19's cell component is recorded as cytoplasm[9].
  • WD repeat domain 19's cell component is recorded as cell projection[10].
  • WD repeat domain 19's cell component is recorded as intraciliary transport particle A[11].
  • WD repeat domain 19's cell component is recorded as photoreceptor connecting cilium[12].
  • WD repeat domain 19's cell component is recorded as nucleoplasm[13].
  • WD repeat domain 19's cell component is recorded as motile cilium[14].
  • WD repeat domain 19's cell component is recorded as cytoskeleton[15].
  • WD repeat domain 19's cell component is recorded as photoreceptor outer segment[16].
  • WD repeat domain 19's cell component is recorded as non-motile cilium[17].
  • WD repeat domain 19's cell component is recorded as cilium[18].
  • WD repeat domain 19's cell component is recorded as nuclear body[19].
  • WD repeat domain 19's cell component is recorded as cilium[20].
  • WD repeat domain 19's cell component is recorded as intraciliary transport particle A[21].
  • WD repeat domain 19's biological process is recorded as digestive system development[22].
  • WD repeat domain 19's biological process is recorded as myotome development[23].
  • WD repeat domain 19's biological process is recorded as ciliary receptor clustering involved in smoothened signaling pathway[24].
  • WD repeat domain 19's biological process is recorded as nervous system process[25].
  • WD repeat domain 19's biological process is recorded as in utero embryonic development[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] . Q20641742. Retrieved . wikidata.org.
  5. [6] . Q20641742. Retrieved . wikidata.org.
  6. [7] . Q20641742. Retrieved . wikidata.org.
  7. [8] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  8. [9] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  9. [10] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] . Essential role of nephrocystin in photoreceptor intraflagellar transport in mouse. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] . Caenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory cilia. 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] . Caenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory cilia. 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] . Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] . Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] . The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] . Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] . Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies. Retrieved . ebi.ac.uk. Provenance: wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

📑 Cite this page

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). WD repeat domain 19. Retrieved May 3, 2026, from https://4ort.xyz/entity/wd-repeat-domain-19
MLA “WD repeat domain 19.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/wd-repeat-domain-19.
BibTeX @misc{4ortxyz_wd-repeat-domain-19_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{WD repeat domain 19}}, year = {2026}, url = {https://4ort.xyz/entity/wd-repeat-domain-19}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): WD repeat domain 19 — https://4ort.xyz/entity/wd-repeat-domain-19 (retrieved 2026-05-03)

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