Clarin 1

mammalian protein found in Homo sapiens
Protein protein Q21102417
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Clarin 1

Summary

Clarin 1 is a protein[1].

Key Facts

  • Clarin 1's instance of is recorded as protein[2].
  • Clarin 1's UniProt protein ID is recorded as P58418[3].
  • Clarin 1's part of is recorded as Clarin[4].
  • Clarin 1's part of is recorded as transporter of unknown biochemical mechanism[5].
  • Clarin 1's RefSeq protein ID is recorded as NP_001182723[6].
  • Clarin 1's RefSeq protein ID is recorded as NP_001243748[7].
  • Clarin 1's RefSeq protein ID is recorded as NP_443721[8].
  • Clarin 1's RefSeq protein ID is recorded as NP_777367[9].
  • Clarin 1's cell component is recorded as integral component of membrane[10].
  • Clarin 1's cell component is recorded as microvillus[11].
  • Clarin 1's cell component is recorded as plasma membrane[12].
  • Clarin 1's cell component is recorded as membrane[13].
  • Clarin 1's cell component is recorded as lamellipodium[14].
  • Clarin 1's cell component is recorded as microtubule[15].
  • Clarin 1's cell component is recorded as trans-Golgi network transport vesicle[16].
  • Clarin 1's cell component is recorded as stereocilium[17].
  • Clarin 1's cell component is recorded as basal part of cell[18].
  • Clarin 1's biological process is recorded as photoreceptor cell maintenance[19].
  • Clarin 1's biological process is recorded as sensory perception of light stimulus[20].
  • Clarin 1's biological process is recorded as positive regulation of lamellipodium assembly[21].
  • Clarin 1's biological process is recorded as hearing[22].
  • Clarin 1's biological process is recorded as equilibrioception[23].
  • Clarin 1's biological process is recorded as response to stimulus[24].
  • Clarin 1's biological process is recorded as visual perception[25].
  • Clarin 1's biological process is recorded as actin filament organization[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] . Retrieved . wikidata.org.
  5. [6] . Q20641742. Retrieved . wikidata.org.
  6. [7] . Q20641742. Retrieved . wikidata.org.
  7. [8] . Q20641742. Retrieved . wikidata.org.
  8. [9] . Q20641742. Retrieved . wikidata.org.
  9. [10] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] . Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton. 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] . Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton. 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] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] . Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] . Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] . Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] . Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] . Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability. 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] . Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton. 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). Clarin 1. Retrieved May 3, 2026, from https://4ort.xyz/entity/clarin-1
MLA “Clarin 1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/clarin-1.
BibTeX @misc{4ortxyz_clarin-1_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Clarin 1}}, year = {2026}, url = {https://4ort.xyz/entity/clarin-1}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Clarin 1 — https://4ort.xyz/entity/clarin-1 (retrieved 2026-05-03)

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