Nephrocystin 3

mammalian protein found in Homo sapiens
Protein protein Q21117131
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Nephrocystin 3

Summary

Nephrocystin 3 is a protein[1].

Key Facts

  • Nephrocystin 3's instance of is recorded as protein[2].
  • Nephrocystin 3's UniProt protein ID is recorded as Q7Z494[3].
  • Nephrocystin 3's part of is recorded as Tetratricopeptide-like helical domain superfamily[4].
  • Nephrocystin 3's part of is recorded as P-loop containing nucleoside triphosphate hydrolase[5].
  • Nephrocystin 3's part of is recorded as Tetratricopeptide repeat-containing domain, protein family[6].
  • Nephrocystin 3's part of is recorded as Tetratricopeptide repeat family[7].
  • Nephrocystin 3's has part is recorded as Tetratricopeptide repeat-containing domain[8].
  • Nephrocystin 3's has part is recorded as tetratricopeptide repeat[9].
  • Nephrocystin 3's RefSeq protein ID is recorded as NP_694972[10].
  • Nephrocystin 3's molecular function is recorded as protein binding[11].
  • Nephrocystin 3's cell component is recorded as cell projection[12].
  • Nephrocystin 3's cell component is recorded as cytosol[13].
  • Nephrocystin 3's cell component is recorded as cilium[14].
  • Nephrocystin 3's cell component is recorded as extracellular region[15].
  • Nephrocystin 3's biological process is recorded as Wnt signaling pathway[16].
  • Nephrocystin 3's biological process is recorded as determination of liver left/right asymmetry[17].
  • Nephrocystin 3's biological process is recorded as determination of pancreatic left/right asymmetry[18].
  • Nephrocystin 3's biological process is recorded as lung development[19].
  • Nephrocystin 3's biological process is recorded as atrial septum development[20].
  • Nephrocystin 3's biological process is recorded as heart looping[21].
  • Nephrocystin 3's biological process is recorded as convergent extension involved in gastrulation[22].
  • Nephrocystin 3's biological process is recorded as ureter development[23].
  • Nephrocystin 3's biological process is recorded as regulation of Wnt signaling pathway, planar cell polarity pathway[24].
  • Nephrocystin 3's biological process is recorded as negative regulation of canonical Wnt signaling pathway[25].
  • Nephrocystin 3's biological process is recorded as epithelial cilium movement involved in determination of left/right asymmetry[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] . wikidata.org.
  7. [8] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  8. [9] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  9. [10] . Q20641742. Retrieved . wikidata.org.
  10. [11] . Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] . GOA. 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] . Identification of a gene for renal-hepatic-pancreatic dysplasia by microarray-based homozygosity mapping. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] . Identification of a gene for renal-hepatic-pancreatic dysplasia by microarray-based homozygosity mapping. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] . Identification of a gene for renal-hepatic-pancreatic dysplasia by microarray-based homozygosity mapping. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] . Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] . Identification of a gene for renal-hepatic-pancreatic dysplasia by microarray-based homozygosity mapping. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] . Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] . Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] . Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. 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). Nephrocystin 3. Retrieved May 3, 2026, from https://4ort.xyz/entity/nephrocystin-3
MLA “Nephrocystin 3.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/nephrocystin-3.
BibTeX @misc{4ortxyz_nephrocystin-3_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Nephrocystin 3}}, year = {2026}, url = {https://4ort.xyz/entity/nephrocystin-3}, note = {Accessed: 2026-05-03}}
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