SCN11A

protein-coding gene in the species Homo sapiens
Gene gene Q14914141
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SCN11A

Summary

SCN11A is a gene[1]. SCN11A ranks in the top 2% of gene entities by monthly Wikipedia readership (8 views/month).[2]

Key Facts

  • SCN11A's instance of is recorded as gene[3].
  • SCN11A is a type of protein-coding gene[4].
  • SCN11A's HomoloGene ID is recorded as 8041[5].
  • SCN11A's genomic start is recorded as 38887260[6].
  • SCN11A's genomic start is recorded as 38845764[7].
  • SCN11A's genomic end is recorded as 38992052[8].
  • SCN11A's genomic end is recorded as 39052157[9].
  • SCN11A's ortholog is recorded as Scn11a[10].
  • SCN11A's ortholog is recorded as Scn11a[11].
  • SCN11A's ortholog is recorded as para[12].
  • SCN11A's encodes is recorded as Sodium voltage-gated channel alpha subunit 11[13].
  • SCN11A's found in taxon is recorded as Homo sapiens[14].
  • SCN11A's chromosome is recorded as human chromosome 3[15].
  • SCN11A's genetic association is recorded as hereditary sensory and autonomic neuropathy type 7[16].
  • SCN11A's genetic association is recorded as autosomal dominant hereditary sensory and autonomic neuropathy[17].
  • SCN11A's genetic association is recorded as familial episodic pain syndrome with predominantly lower limb involvement[18].
  • SCN11A's strand orientation is recorded as reverse strand[19].
  • SCN11A's exact match is recorded as http://identifiers.org/ncbigene/11280[20].
  • SCN11A's cytogenetic location is recorded as 3p22.2[21].
  • SCN11A's expressed in is recorded as buccal mucosa cell[22].
  • SCN11A's expressed in is recorded as spinal ganglia[23].
  • SCN11A's expressed in is recorded as testicle[24].
  • SCN11A's expressed in is recorded as trigeminal ganglion[25].
  • SCN11A's expressed in is recorded as gonad[26].
  • SCN11A's expressed in is recorded as left testis[27].

Why It Matters

SCN11A ranks in the top 2% of gene entities by monthly Wikipedia readership (8 views/month).[2]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . ensembl Release 106. wikidata.org.
  2. [4] . Ensembl Release 87. wikidata.org.
  3. [5] . Q20641742. Retrieved . wikidata.org.
  4. [6] . ensembl Release 106. wikidata.org.
  5. [7] . ensembl Release 106. wikidata.org.
  6. [8] . ensembl Release 106. wikidata.org.
  7. [9] . ensembl Release 106. wikidata.org.
  8. [10] . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  9. [11] . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  10. [12] . Orthologous MAtrix. omabrowser.org. Provenance: wikidata.org.
  11. [13] . Q905695. Retrieved . wikidata.org.
  12. [14] . ensembl Release 106. wikidata.org.
  13. [15] . ensembl Release 106. wikidata.org.
  14. [16] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  15. [17] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  16. [18] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  17. [19] . ensembl Release 106. wikidata.org.
  18. [20] . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  19. [21] . Q20641742. Retrieved . wikidata.org.
  20. [22] . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  21. [23] . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  22. [24] . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  23. [25] . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  24. [26] . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  25. [27] . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). SCN11A. Retrieved May 3, 2026, from https://4ort.xyz/entity/scn11a
MLA “SCN11A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/scn11a.
BibTeX @misc{4ortxyz_scn11a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{SCN11A}}, year = {2026}, url = {https://4ort.xyz/entity/scn11a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): SCN11A — https://4ort.xyz/entity/scn11a (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 14d ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    Hgnc gene symbol SCN11A
    Genetic association hereditary sensory and autonomic neuropathy type 7, autosomal dominant hereditary sensory and autonomic neuropathy, familial episodic pain syndrome with predominantly lower limb involvement
    Refseq rna id NM_001287223, NM_014139, XM_011533321 +6
    Microsoft academic id (discontinued) 2777776202
    + 22 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||gsw */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/32527|batch #32527]]: human gene name and description in Alemannic"
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