DNA segment, Chr 7, ERATO Doi 443, expressed

mammalian protein found in Mus musculus
Protein protein Q21424994
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Summary

DNA segment, Chr 7, ERATO Doi 443, expressed is a protein[1].

Key Facts

  • DNA segment, Chr 7, ERATO Doi 443, expressed's instance of is recorded as protein[2].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's subclass of is recorded as protein[3].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's UniProt protein ID is recorded as D2J0Y4[4].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's part of is recorded as (E2-independent) E3 ubiquitin-conjugating enzyme FATS[5].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's part of is recorded as ALMS motif domain, protein family[6].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's has part is recorded as ALMS motif[7].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as NP_001074800[8].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as NP_001186870[9].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as XP_011240203[10].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as XP_011240204[11].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as XP_011240205[12].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as XP_011240206[13].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as XP_011240207[14].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as XP_011240208[15].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's RefSeq protein ID is recorded as XP_011240209[16].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's molecular function is recorded as histone deacetylase binding[17].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's molecular function is recorded as alpha-actinin binding[18].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's molecular function is recorded as protein binding[19].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's molecular function is recorded as histone deacetylase binding[20].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's molecular function is recorded as ubiquitin protein ligase activity[21].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's molecular function is recorded as transferase activity[22].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's cell component is recorded as cytoplasm[23].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's cell component is recorded as microtubule organizing center[24].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's cell component is recorded as centrosome[25].
  • DNA segment, Chr 7, ERATO Doi 443, expressed's cell component is recorded as cytoskeleton[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . UniProt. Retrieved . wikidata.org.
  2. [3] ↑ . UniProt. Retrieved . wikidata.org.
  3. [4] ↑ . UniProt. Retrieved . wikidata.org.
  4. [5] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  7. [8] ↑ . Q20641742. Retrieved . wikidata.org.
  8. [9] ↑ . Q20641742. Retrieved . wikidata.org.
  9. [10] ↑ . Q20641742. Retrieved . wikidata.org.
  10. [11] ↑ . Q20641742. Retrieved . wikidata.org.
  11. [12] ↑ . Q20641742. Retrieved . wikidata.org.
  12. [13] ↑ . Q20641742. Retrieved . wikidata.org.
  13. [14] ↑ . Q20641742. Retrieved . wikidata.org.
  14. [15] ↑ . Q20641742. Retrieved . wikidata.org.
  15. [16] ↑ . Q20641742. Retrieved . wikidata.org.
  16. [17] ↑ . An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] ↑ . FATS is an E2-independent ubiquitin ligase that stabilizes p53 and promotes its activation in response to DNA damage. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] ↑ . FATS is an E2-independent ubiquitin ligase that stabilizes p53 and promotes its activation in response to DNA damage. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . GOA. 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). DNA segment, Chr 7, ERATO Doi 443, expressed. Retrieved May 3, 2026, from https://4ort.xyz/entity/dna-segment-chr-7-erato-doi-443-expressed
MLA “DNA segment, Chr 7, ERATO Doi 443, expressed.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/dna-segment-chr-7-erato-doi-443-expressed.
BibTeX @misc{4ortxyz_dna-segment-chr-7-erato-doi-443-expressed_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{DNA segment, Chr 7, ERATO Doi 443, expressed}}, year = {2026}, url = {https://4ort.xyz/entity/dna-segment-chr-7-erato-doi-443-expressed}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): DNA segment, Chr 7, ERATO Doi 443, expressed — https://4ort.xyz/entity/dna-segment-chr-7-erato-doi-443-expressed (retrieved 2026-05-03)

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