Gene entry
PEX10
peroxisomal biogenesis factor 10
- Chromosome
- 1
- Cytoband
- 1p36.32
- Variants (rsID)
- 11
PEX10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.32). Its official name is “peroxisomal biogenesis factor 10”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs139345520Benignsingle nucleotide variantPeroxisome biogenesis disorder 6A (Zellweger)|Peroxisome biogenesis disorder, complementation group 7|Zellweger spectrum disorders
- rs146452560Benignsingle nucleotide variantPeroxisome biogenesis disorder 6A (Zellweger)|Peroxisome biogenesis disorder, complementation group 7|Zellweger spectrum disorders
- rs35082957Benignsingle nucleotide variantPeroxisome biogenesis disorder 6A (Zellweger)|Peroxisome biogenesis disorder, complementation group 7|Zellweger spectrum disorders
- rs375032738Conflicting interpretationssingle nucleotide variantPeroxisome biogenesis disorder 6A (Zellweger)|Peroxisome biogenesis disorder, complementation group 7
- rs61750435PathogenicDuplicationPeroxisome biogenesis disorder 6A (Zellweger)|Peroxisome biogenesis disorder 6B|Peroxisome biogenesis disorder, complementation group 7|Peroxisome biogenesis disorder|Zellweger spectrum disorders
- rs61752093PathogenicDeletionPeroxisome biogenesis disorder 6B|Peroxisome biogenesis disorder 6A (Zellweger)|Peroxisome biogenesis disorder|Peroxisome biogenesis disorder, complementation group 7|Zellweger spectrum disorders
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.