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PEX7

protein-coding gene in the species Homo sapiens
Class type of: protein-coding gene Q18030463

Facts

13 properties
Instance of
gene
Subclass of
protein-coding gene
Chromosome
human chromosome 6[11]
Cytogenetic location
6q23.3[16]
Encodes
peroxisomal biogenesis factor 7[9]
Expressed in
retinal pigment epithelium, sperm, right adrenal gland, right adrenal cortex, left adrenal gland, secondary oocyte, gonad, body of pancreas, left adrenal cortex, kidney tubule[17][18][19][20][21][22][23][24][25][26]
Found in taxon
Homo sapiens[10]
Genetic association
rhizomelic chondrodysplasia punctata type 1, Zellweger spectrum disorder, adult Refsum disease[12][13][14]
Genomic end
137235075, 136913934[6][7]
Genomic start
136822564, 137143717[4][5]
HomoloGene ID
242[3]
Ortholog
Pex7, Pex7, pex7, Pex7[8]
Strand orientation
forward strand[15]
🏷️ Also known as
en PBD9B en peroxisomal biogenesis factor 7 en PEX7 en PTS2R en RCDP1 en RD
🔖 Identifiers · 10
Ensembl gene ID
ENSG00000112357
Ensembl transcript ID
ENST00000541292, ENST00000318471, ENST00000367756, ENST00000679286, ENST00000678593, ENST00000678002, ENST00000678557
Entrez Gene ID
5191
Exact match
identifiers.org
Google Knowledge Graph ID
/g/11fy_qm8f3
HGNC ID
8860
HGNC gene symbol
PEX7
OMIM ID
601757
RefSeq RNA ID
NM_000288, XM_005267019, XM_006715502, XM_047418874
UMLS CUI
C1418479

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Summary

PEX7 is a gene[1]. PEX7 is a type of protein-coding gene[2].

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] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  13. [14] ↑ . Open Targets Platform. Retrieved . platform.opentargets.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). PEX7. Retrieved November 4, 2026, from https://4ort.xyz/entity/pex7-q18030463
MLA “PEX7.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Nov. 2026, https://4ort.xyz/entity/pex7-q18030463.
BibTeX @misc{4ortxyz_pex7-q18030463_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{PEX7}}, year = {2026}, url = {https://4ort.xyz/entity/pex7-q18030463}, note = {Accessed: 2026-11-04}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): PEX7 — https://4ort.xyz/entity/pex7-q18030463 (retrieved 2026-11-04)

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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 → PEX7
    Genetic association → rhizomelic chondrodysplasia punctata type 1, Zellweger spectrum disorder, adult Refsum disease
    RefSeq RNA ID → NM_000288, XM_005267019, XM_006715502 +1
    Exact match → http://identifiers.org/ncbigene/5191
    + 21 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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.