Teratocarcinoma-derived growth factor

mouse protein (annotated by UniProtKB/Swiss-Prot P51865)
Protein protein Q21989640
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Summary

Teratocarcinoma-derived growth factor is a protein[1].

Key Facts

  • Teratocarcinoma-derived growth factor's instance of is recorded as protein[2].
  • Teratocarcinoma-derived growth factor's UniProt protein ID is recorded as P51865[3].
  • Teratocarcinoma-derived growth factor's part of is recorded as Teratocarcinoma-derived growth factor Cripto[4].
  • Teratocarcinoma-derived growth factor's part of is recorded as Cryptic/Cripto, CFC domain, protein family[5].
  • Teratocarcinoma-derived growth factor's part of is recorded as EGF-like domain, protein family[6].
  • Teratocarcinoma-derived growth factor's part of is recorded as EGF-like, conserved site, protein family[7].
  • Teratocarcinoma-derived growth factor's has part is recorded as EGF-like, conserved site[8].
  • Teratocarcinoma-derived growth factor's has part is recorded as EGF-like domain[9].
  • Teratocarcinoma-derived growth factor's has part is recorded as Cryptic/Cripto, CFC domain[10].
  • Teratocarcinoma-derived growth factor's PDB structure ID is recorded as 2J5H[11].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as coreceptor activity[12].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as type I activin receptor binding[13].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as Wnt-protein binding[14].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as protein binding[15].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as nodal binding[16].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as growth factor activity[17].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as signaling receptor binding[18].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as signaling receptor binding[19].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as nodal binding[20].
  • Teratocarcinoma-derived growth factor's molecular function is recorded as activin receptor binding[21].
  • Teratocarcinoma-derived growth factor's cell component is recorded as cytoplasm[22].
  • Teratocarcinoma-derived growth factor's cell component is recorded as Golgi apparatus[23].
  • Teratocarcinoma-derived growth factor's cell component is recorded as membrane[24].
  • Teratocarcinoma-derived growth factor's cell component is recorded as plasma membrane[25].
  • Teratocarcinoma-derived growth factor's cell component is recorded as cell surface[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . UniProt. Retrieved . wikidata.org.
  3. [4] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  8. [9] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  9. [10] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  10. [11] ↑ . UniProt. Retrieved . wikidata.org.
  11. [12] ↑ . Nodal signals to Smads through Cripto-dependent and Cripto-independent mechanisms. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] ↑ . Nodal signals to Smads through Cripto-dependent and Cripto-independent mechanisms. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] ↑ . Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] ↑ . GRP78 and Cripto form a complex at the cell surface and collaborate to inhibit transforming growth factor beta signaling and enhance cell growth. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] ↑ . Dual roles of Cripto as a ligand and coreceptor in the nodal signaling pathway. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] ↑ . Identification and biological characterization of an epidermal growth factor-related protein: cripto-1. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . Dual roles of Cripto as a ligand and coreceptor in the nodal signaling pathway. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] ↑ . Netrin-1 can affect morphogenesis and differentiation of the mouse mammary gland. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . Detection and location of amphiregulin and Cripto-1 expression in the developing postnatal mouse mammary gland. 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] ↑ . GOA. 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). Teratocarcinoma-derived growth factor. Retrieved May 3, 2026, from https://4ort.xyz/entity/teratocarcinoma-derived-growth-factor
MLA “Teratocarcinoma-derived growth factor.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/teratocarcinoma-derived-growth-factor.
BibTeX @misc{4ortxyz_teratocarcinoma-derived-growth-factor_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Teratocarcinoma-derived growth factor}}, year = {2026}, url = {https://4ort.xyz/entity/teratocarcinoma-derived-growth-factor}, note = {Accessed: 2026-05-03}}
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