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 October 5, 2026, from https://4ort.xyz/entity/scn11a
MLA “SCN11A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 5 Oct. 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: 2026-10-05}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): SCN11A — https://4ort.xyz/entity/scn11a (retrieved 2026-10-05)

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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. 19w 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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