Glycogen synthase 1, muscle

mammalian protein found in Mus musculus
Protein protein Q21496445
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Glycogen synthase 1, muscle

Summary

Glycogen synthase 1, muscle is a protein[1].

Key Facts

  • Glycogen synthase 1, muscle's instance of is recorded as protein[2].
  • Glycogen synthase 1, muscle's subclass of is recorded as protein[3].
  • Glycogen synthase 1, muscle's UniProt protein ID is recorded as Q9Z1E4[4].
  • Glycogen synthase 1, muscle's part of is recorded as Glycogen synthase, subgroup[5].
  • Glycogen synthase 1, muscle's RefSeq protein ID is recorded as NP_109603[6].
  • Glycogen synthase 1, muscle's molecular function is recorded as transferase activity[7].
  • Glycogen synthase 1, muscle's molecular function is recorded as glycosyltransferase activity[8].
  • Glycogen synthase 1, muscle's molecular function is recorded as glycogen (starch) synthase activity[9].
  • Glycogen synthase 1, muscle's molecular function is recorded as catalytic activity[10].
  • Glycogen synthase 1, muscle's molecular function is recorded as protein binding[11].
  • Glycogen synthase 1, muscle's molecular function is recorded as protein kinase binding[12].
  • Glycogen synthase 1, muscle's molecular function is recorded as glycogen synthase activity, transferring glucose-1-phosphate[13].
  • Glycogen synthase 1, muscle's molecular function is recorded as glucose binding[14].
  • Glycogen synthase 1, muscle's molecular function is recorded as glycogen (starch) synthase activity[15].
  • Glycogen synthase 1, muscle's molecular function is recorded as glucose binding[16].
  • Glycogen synthase 1, muscle's molecular function is recorded as protein kinase binding[17].
  • Glycogen synthase 1, muscle's molecular function is recorded as glycogen synthase activity, transferring glucose-1-phosphate[18].
  • Glycogen synthase 1, muscle's molecular function is recorded as protein binding[19].
  • Glycogen synthase 1, muscle's cell component is recorded as cytoplasm[20].
  • Glycogen synthase 1, muscle's cell component is recorded as inclusion body[21].
  • Glycogen synthase 1, muscle's cell component is recorded as cytoplasm[22].
  • Glycogen synthase 1, muscle's biological process is recorded as development of the heart[23].
  • Glycogen synthase 1, muscle's biological process is recorded as metabolism[24].
  • Glycogen synthase 1, muscle's biological process is recorded as glycogen biosynthetic process[25].
  • Glycogen synthase 1, muscle's biological process is recorded as glycogen metabolic process[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] . Q905695. Retrieved . wikidata.org.
  4. [5] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  5. [6] . Q20641742. Retrieved . wikidata.org.
  6. [7] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  7. [8] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  8. [9] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  9. [10] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] . Deficiency of a Glycogen Synthase-associated Protein, Epm2aip1, Causes Decreased Glycogen Synthesis and Hepatic Insulin Resistance. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] . Deficiency of a Glycogen Synthase-associated Protein, Epm2aip1, Causes Decreased Glycogen Synthesis and Hepatic Insulin Resistance. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] . A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori's disease. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] . A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori's disease. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] . A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori's disease. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] . Abnormal cardiac development in the absence of heart glycogen. 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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APA 4ort.xyz Knowledge Graph. (2026). Glycogen synthase 1, muscle. Retrieved May 3, 2026, from https://4ort.xyz/entity/glycogen-synthase-1-muscle
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BibTeX @misc{4ortxyz_glycogen-synthase-1-muscle_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Glycogen synthase 1, muscle}}, year = {2026}, url = {https://4ort.xyz/entity/glycogen-synthase-1-muscle}, note = {Accessed: 2026-05-03}}
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