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PEX19

protein-coding gene in the species Homo sapiens
Class type of: protein-coding gene Q18030971

Facts

13 properties
Instance of
gene
Subclass of
protein-coding gene[2]
Chromosome
human chromosome 1[13]
Cytogenetic location
1q23.2[17]
Encodes
Peroxisomal biogenesis factor 19[11]
Expressed in
muscle of thigh, gastrocnemius muscle, Skeletal muscle tissue of biceps brachii, ventricular zone, epithelium of colon, abdominal fat, thoracic diaphragm, subcutaneous adipose tissue, islet of Langerhans, right lobe of liver[18][19][20][21][22][23][24][25][26][27]
Found in taxon
Homo sapiens[12]
Genetic association
Zellweger spectrum disorder, Zellweger syndrome[14][15]
Genomic end
160286348, 160256138[6][7]
Genomic start
160246602, 160276807[4][5]
HomoloGene ID
134253[3]
Ortholog
Pex19, LOC100911356, LOC102548286, Pex19, pex19, Pex19[8][9][10]
Strand orientation
reverse strand[16]
🏷️ Also known as
en D1S2223E en HK33 en PBD12A en peroxisomal biogenesis factor 19 en PEX19 en PMP1 en PMPI en PXF en PXMP1

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Summary

PEX19 is a gene[1].

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. wikidata.org.
  8. [9] ↑ . HomoloGene build68. wikidata.org.
  9. [10] ↑ . HomoloGene build68. wikidata.org.
  10. [11] ↑ . UniProt. Retrieved . wikidata.org.
  11. [12] ↑ . ensembl Release 106. wikidata.org.
  12. [13] ↑ . ensembl Release 106. wikidata.org.
  13. [14] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  14. [15] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  15. [16] ↑ . ensembl Release 106. wikidata.org.
  16. [17] ↑ . NCBI Gene. Retrieved . 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.
  26. [27] ↑ . 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). PEX19. Retrieved November 6, 2026, from https://4ort.xyz/entity/pex19
MLA “PEX19.” 4ort.xyz Knowledge Graph, 4ort.xyz, 6 Nov. 2026, https://4ort.xyz/entity/pex19.
BibTeX @misc{4ortxyz_pex19_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{PEX19}}, year = {2026}, url = {https://4ort.xyz/entity/pex19}, note = {Accessed: 2026-11-06}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): PEX19 — https://4ort.xyz/entity/pex19 (retrieved 2026-11-06)

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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. 24w ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    HGNC gene symbol → PEX19
    Genetic association → Zellweger spectrum disorder, Zellweger syndrome
    RefSeq RNA ID → NR_036493, NM_001131039, NM_001193644 +2
    Exact match → http://identifiers.org/ncbigene/5824
    + 23 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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