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BCAP31

protein-coding gene in the species Homo sapiens
Class type of: protein-coding gene Q18035057

Facts

13 properties
Instance of
gene
Subclass of
protein-coding gene
Chromosome
human X chromosome[13]
Cytogenetic location
Xq28[16]
Encodes
B cell receptor associated protein 31[11]
Expressed in
left adrenal gland, right adrenal gland, right adrenal cortex, left adrenal cortex, mucosa of transverse colon, stromal cell of endometrium, skin of leg, skin of abdomen, Brodmann area 10, islet of Langerhans[17][18][19][20][21][22][23][24][25][26]
Found in taxon
Homo sapiens[12]
Genetic association
severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome[14]
Genomic end
152990152, 153724565[6][7]
Genomic start
152965947, 153700492[4][5]
HomoloGene ID
38095[3]
Ortholog
Bcap31, Bcap31, bcap31, CG13887, Y54G2A.18[8][9][10]
Strand orientation
reverse strand[15]
🏷️ Also known as
en 6C6-AG en BAP31 en BCAP31 en B cell receptor associated protein 31 en B-cell receptor associated protein 31 en B-cell receptor-associated protein 31 en CDM en DDCH en DXS1357E

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Summary

BCAP31 is a gene[1]. BCAP31 is a type of protein-coding gene[2].

References

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

Direct Wikidata claims

  1. [2] ↑ . NCBI homo sapiens annotation release 107. Retrieved . wikidata.org.
  2. [3] ↑ . NCBI Gene. Retrieved . wikidata.org.
  3. [4] ↑ . ensembl Release 106. wikidata.org.
  4. [5] ↑ . ensembl Release 106. wikidata.org.
  5. [6] ↑ . ensembl Release 106. wikidata.org.
  6. [7] ↑ . ensembl Release 106. wikidata.org.
  7. [8] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  8. [9] ↑ . HomoloGene build68. wikidata.org.
  9. [10] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  10. [11] ↑ . UniProt. Retrieved . wikidata.org.
  11. [12] ↑ . ensembl Release 106. wikidata.org.
  12. [13] ↑ . ensembl Release 106. wikidata.org.
  13. [14] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  14. [15] ↑ . ensembl Release 106. wikidata.org.
  15. [16] ↑ . NCBI Gene. Retrieved . wikidata.org.
  16. [17] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  17. [18] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  18. [19] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  19. [20] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  20. [21] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  21. [22] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  22. [23] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  23. [24] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  24. [25] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  25. [26] ↑ . Bgee. Retrieved . bgee.org. 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). BCAP31. Retrieved November 3, 2026, from https://4ort.xyz/entity/bcap31
MLA “BCAP31.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 Nov. 2026, https://4ort.xyz/entity/bcap31.
BibTeX @misc{4ortxyz_bcap31_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{BCAP31}}, year = {2026}, url = {https://4ort.xyz/entity/bcap31}, note = {Accessed: 2026-11-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): BCAP31 — https://4ort.xyz/entity/bcap31 (retrieved 2026-11-03)

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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. 24w ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    HGNC gene symbol → BCAP31
    Genetic association → severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
    RefSeq RNA ID → NM_005745, NM_001139441, NM_001139457 +1
    Exact match → http://identifiers.org/ncbigene/10134
    + 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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.