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TPP1

protein-coding gene in the species Homo sapiens
Class type of: protein-coding gene Q18021526
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Summary

TPP1 is a gene[1]. TPP1 is a type of protein-coding gene[2].

Key Facts

  • HomoloGene ID: 335[3]
  • Genomic start: 6634000[4], 6612768[5]
  • Genomic end: 6640692[6], 6619448[7]
  • Ortholog: Tpp1[8]
  • Encodes: tripeptidyl peptidase 1[9]
  • Found in taxon: Homo sapiens[10]
  • Chromosome: human chromosome 11[11]
  • Genetic association: neuronal ceroid lipofuscinosis 2[12], autosomal recessive spinocerebellar ataxia 7[13], neuronal ceroid lipofuscinosis[14]
  • Strand orientation: reverse strand[15]
  • Cytogenetic location: 11p15.4[16]
  • Expressed in: retinal pigment epithelium[17], dorsal motor nucleus of vagus nerve[18], inferior olivary nucleus[19], right adrenal cortex[20], germinal epithelium[21], visceral pleura[22], stromal cell of endometrium[23], left adrenal gland[24], spleen[25], parietal pleura[26]

References

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

Direct Wikidata claims

  1. [2] ↑ . Ensembl Release 87. wikidata.org.
  2. [3] ↑ . NCBI Gene. Retrieved . wikidata.org.
  3. [4] ↑ . ensembl Release 106. wikidata.org.
  4. [5] ↑ . ensembl Release 106. wikidata.org.
  5. [6] ↑ . ensembl Release 106. wikidata.org.
  6. [7] ↑ . ensembl Release 106. wikidata.org.
  7. [8] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  8. [9] ↑ . UniProt. Retrieved . wikidata.org.
  9. [10] ↑ . ensembl Release 106. wikidata.org.
  10. [11] ↑ . ensembl Release 106. wikidata.org.
  11. [12] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  12. [13] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  13. [14] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  14. [15] ↑ . ensembl Release 106. wikidata.org.
  15. [16] ↑ . NCBI Gene. Retrieved . wikidata.org.
  16. [17] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  17. [18] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  18. [19] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  19. [20] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  20. [21] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  21. [22] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  22. [23] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  23. [24] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  24. [25] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  25. [26] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

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). TPP1. Retrieved October 30, 2026, from https://4ort.xyz/entity/tpp1
MLA “TPP1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 30 Oct. 2026, https://4ort.xyz/entity/tpp1.
BibTeX @misc{4ortxyz_tpp1_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{TPP1}}, year = {2026}, url = {https://4ort.xyz/entity/tpp1}, note = {Accessed: 2026-10-30}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 23w ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    Genetic association → neuronal ceroid lipofuscinosis 2, autosomal recessive spinocerebellar ataxia 7, neuronal ceroid lipofuscinosis
    Subclass of → —
    Chromosome → human chromosome 11
    Strand orientation → reverse strand
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||gsw */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/32527|batch #32527]]: human gene name and description in Alemannic"
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