Gene entry
PEX19
peroxisomal biogenesis factor 19
- Chromosome
- 1
- Cytoband
- 1q23.2
- Variants (rsID)
- 3
PEX19 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q23.2). Its official name is “peroxisomal biogenesis factor 19”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs141133579Benignsingle nucleotide variantPeroxisome biogenesis disorder 12A (Zellweger)
- rs11550119Conflicting interpretationssingle nucleotide variantPeroxisome biogenesis disorder 12A (Zellweger)
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.