Gene entry
PEX26
peroxisomal biogenesis factor 26
- Chromosome
- 22
- Cytoband
- 22q11.21
- Variants (rsID)
- 16
PEX26 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q11.21). Its official name is “peroxisomal biogenesis factor 26”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs12484657Benignsingle nucleotide variantPeroxisome biogenesis disorder 1A (Zellweger)|Peroxisome biogenesis disorder 7A (Zellweger)|Peroxisome biogenesis disorder 7B|Peroxisome biogenesis disorder 7A (Zellweger)
- rs45489191Benignsingle nucleotide variantPeroxisome biogenesis disorder 7A (Zellweger)
- rs149153003Conflicting interpretationssingle nucleotide variantPeroxisome biogenesis disorder 7A (Zellweger)|Peroxisome biogenesis disorder 7A (Zellweger)|Peroxisome biogenesis disorder 7B
- rs45567240Conflicting interpretationssingle nucleotide variantPeroxisome biogenesis disorder 7A (Zellweger)|Peroxisome biogenesis disorder 7B|Peroxisome biogenesis disorder 7A (Zellweger)
- rs62641228Pathogenicsingle nucleotide variantPeroxisome biogenesis disorder 7B|Peroxisome biogenesis disorder 7B|Peroxisome biogenesis disorder 7A (Zellweger)|Peroxisome biogenesis disorder
- rs61752132Uncertain significancesingle nucleotide variantPeroxisome biogenesis disorder 7B|Peroxisome biogenesis disorder 7A (Zellweger)|Peroxisome biogenesis disorder 7A (Zellweger)|Peroxisome biogenesis disorder 7B
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.