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Gene entry

PEX14

peroxisomal biogenesis factor 14

Chromosome
1
Cytoband
1p36.22
Variants (rsID)
38

PEX14 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.22). Its official name is “peroxisomal biogenesis factor 14”. The reference table lists 38 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs12061667Benignsingle nucleotide variantPeroxisome biogenesis disorder 13A (Zellweger)|Peroxisome biogenesis disorder, complementation group K
  • rs36083022Benignsingle nucleotide variantPeroxisome biogenesis disorder 13A (Zellweger)|Peroxisome biogenesis disorder, complementation group K
  • rs616488Benignsingle nucleotide variantPeroxisome biogenesis disorder, complementation group K
  • rs77261230Benignsingle nucleotide variantPeroxisome biogenesis disorder 13A (Zellweger)|Peroxisome biogenesis disorder, complementation group K
  • rs143412169Conflicting interpretationssingle nucleotide variantPeroxisome biogenesis disorder 13A (Zellweger)|Peroxisome biogenesis disorder, complementation group K
  • rs200154696Conflicting interpretationssingle nucleotide variantPeroxisome biogenesis disorder 13A (Zellweger)|Peroxisome biogenesis disorder, complementation group K
  • rs41274484Conflicting interpretationssingle nucleotide variantPeroxisome biogenesis disorder 13A (Zellweger)|Peroxisome biogenesis disorder, complementation group K

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.