Hexosaminidase A

mammalian protein found in Mus musculus
Protein protein Q21984075
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Hexosaminidase A

Summary

Hexosaminidase An is a protein[1].

Key Facts

  • Hexosaminidase A's instance of is recorded as protein[2].
  • Hexosaminidase A's UniProt protein ID is recorded as P29416[3].
  • Hexosaminidase A's part of is recorded as beta-hexosaminidase[4].
  • Hexosaminidase A's part of is recorded as Beta-hexosaminidase-like, domain 2[5].
  • Hexosaminidase A's part of is recorded as glycoside hydrolase superfamily[6].
  • Hexosaminidase A's part of is recorded as membrane protein[7].
  • Hexosaminidase A's part of is recorded as Glycoside hydrolase family 20, catalytic domain, protein family[8].
  • Hexosaminidase A's part of is recorded as Beta-hexosaminidase, eukaryotic type, N-terminal domain, protein family[9].
  • Hexosaminidase A's has part is recorded as Glycoside hydrolase family 20, catalytic domain[10].
  • Hexosaminidase A's has part is recorded as Beta-hexosaminidase, eukaryotic type, N-terminal[11].
  • Hexosaminidase A's RefSeq protein ID is recorded as NP_034551[12].
  • Hexosaminidase A's RefSeq protein ID is recorded as XP_017168625[13].
  • Hexosaminidase A's molecular function is recorded as hydrolase activity, hydrolyzing O-glycosyl compounds[14].
  • Hexosaminidase A's molecular function is recorded as acetylglucosaminyltransferase activity[15].
  • Hexosaminidase A's molecular function is recorded as hydrolase activity, acting on glycosyl bonds[16].
  • Hexosaminidase A's molecular function is recorded as beta-N-acetylhexosaminidase activity[17].
  • Hexosaminidase A's molecular function is recorded as protein heterodimerization activity[18].
  • Hexosaminidase A's molecular function is recorded as hydrolase activity[19].
  • Hexosaminidase A's molecular function is recorded as N-acetyl-beta-D-galactosaminidase activity[20].
  • Hexosaminidase A's cell component is recorded as azurophil granule[21].
  • Hexosaminidase A's cell component is recorded as lysosome[22].
  • Hexosaminidase A's cell component is recorded as membrane[23].
  • Hexosaminidase A's biological process is recorded as glycosaminoglycan metabolic process[24].
  • Hexosaminidase A's biological process is recorded as skeletal system development[25].
  • Hexosaminidase A's biological process is recorded as sexual reproduction[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] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  5. [6] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  10. [11] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  11. [12] . Q20641742. Retrieved . wikidata.org.
  12. [13] . Q20641742. Retrieved . 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] . Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease. 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] . 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] . Dynamics of major histocompatibility complex class II compartments during B cell receptor-mediated cell activation. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] . Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] . Mice deficient in all forms of lysosomal beta-hexosaminidase show mucopolysaccharidosis-like pathology. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] . Characterization of the testis and epididymis in mouse models of human Tay Sachs and Sandhoff diseases and partial determination of accumulated gangliosides. Retrieved . ebi.ac.uk. Provenance: wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). Hexosaminidase A. Retrieved May 3, 2026, from https://4ort.xyz/entity/hexosaminidase-a
MLA “Hexosaminidase A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hexosaminidase-a.
BibTeX @misc{4ortxyz_hexosaminidase-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Hexosaminidase A}}, year = {2026}, url = {https://4ort.xyz/entity/hexosaminidase-a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Hexosaminidase A — https://4ort.xyz/entity/hexosaminidase-a (retrieved 2026-05-03)

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