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Wnt family member 10A

mammalian protein found in Homo sapiens
Protein protein Q21123978
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Wnt family member 10A

Summary

Wnt family member 10A is a protein[1].

Key Facts

  • Wnt family member 10A's instance of is recorded as protein[2].
  • Wnt family member 10A's UniProt protein ID is recorded as Q9GZT5[3].
  • Wnt family member 10A's part of is recorded as Wnt-10 protein[4].
  • Wnt family member 10A's part of is recorded as Wnt protein, conserved site, protein family[5].
  • Wnt family member 10A's has part is recorded as Wnt protein, conserved site[6].
  • Wnt family member 10A's RefSeq protein ID is recorded as NP_079492[7].
  • Wnt family member 10A's RefSeq protein ID is recorded as XP_011510231[8].
  • Wnt family member 10A's RefSeq protein ID is recorded as XP_011510232[9].
  • Wnt family member 10A's molecular function is recorded as frizzled binding[10].
  • Wnt family member 10A's molecular function is recorded as signaling receptor binding[11].
  • Wnt family member 10A's molecular function is recorded as receptor ligand activity[12].
  • Wnt family member 10A's cell component is recorded as extracellular region[13].
  • Wnt family member 10A's cell component is recorded as extracellular space[14].
  • Wnt family member 10A's biological process is recorded as skin development[15].
  • Wnt family member 10A's biological process is recorded as odontogenesis[16].
  • Wnt family member 10A's biological process is recorded as tongue development[17].
  • Wnt family member 10A's biological process is recorded as hair follicle development[18].
  • Wnt family member 10A's biological process is recorded as positive regulation of gene expression[19].
  • Wnt family member 10A's biological process is recorded as regulation of odontogenesis of dentin-containing tooth[20].
  • Wnt family member 10A's biological process is recorded as multicellular organism development[21].
  • Wnt family member 10A's biological process is recorded as neural crest cell differentiation[22].
  • Wnt family member 10A's biological process is recorded as neuron differentiation[23].
  • Wnt family member 10A's biological process is recorded as epidermis morphogenesis[24].
  • Wnt family member 10A's biological process is recorded as hair follicle morphogenesis[25].
  • Wnt family member 10A's biological process is recorded as cell fate commitment[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] ↑ . wikidata.org.
  5. [6] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  6. [7] ↑ . Q20641742. Retrieved . wikidata.org.
  7. [8] ↑ . Q20641742. Retrieved . wikidata.org.
  8. [9] ↑ . Q20641742. Retrieved . wikidata.org.
  9. [10] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] ↑ . Mapping of Wnt-Frizzled interactions by multiplex CRISPR targeting of receptor gene families.. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] ↑ . Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] ↑ . Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] ↑ . Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] ↑ . Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] ↑ . Phenotypic variability associated with WNT10A nonsense mutations. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] ↑ . Phenotypic variability associated with WNT10A nonsense mutations. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. 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). Wnt family member 10A. Retrieved May 3, 2026, from https://4ort.xyz/entity/wnt-family-member-10a
MLA “Wnt family member 10A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/wnt-family-member-10a.
BibTeX @misc{4ortxyz_wnt-family-member-10a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Wnt family member 10A}}, year = {2026}, url = {https://4ort.xyz/entity/wnt-family-member-10a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Wnt family member 10A — https://4ort.xyz/entity/wnt-family-member-10a (retrieved 2026-05-03)

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