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Gene entry

XPNPEP2

X-prolyl aminopeptidase 2

Chromosome
X
Cytoband
Xq26.1
Variants (rsID)
20

XPNPEP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq26.1). Its official name is “X-prolyl aminopeptidase 2”. The reference table lists 20 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs3747343Benignsingle nucleotide variant
  • rs3788853Risk factorsingle nucleotide variantSusceptibility to angioedema induced by ACE inhibitors

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.