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Gene entry

XPNPEP3

X-prolyl aminopeptidase 3

Chromosome
22
Cytoband
22q13.2
Variants (rsID)
15

XPNPEP3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q13.2). Its official name is “X-prolyl aminopeptidase 3”. The reference table lists 15 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

  • rs143719656Conflicting interpretationssingle nucleotide variantNephronophthisis-like nephropathy 1
  • rs146023695Conflicting interpretationssingle nucleotide variantNephronophthisis-like nephropathy 1
  • rs267607179Pathogenicsingle nucleotide variantNephronophthisis-like nephropathy 1

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.