Gene entry
HPGD
15-hydroxyprostaglandin dehydrogenase
- Chromosome
- 4
- Cytoband
- 4q34.1
- Variants (rsID)
- 16
HPGD is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q34.1). Its official name is “15-hydroxyprostaglandin dehydrogenase”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs1050145Benignsingle nucleotide variantHypertrophic osteoarthropathy, primary, autosomal recessive, 1|Isolated congenital digital clubbing
- rs8752Benignsingle nucleotide variantHypertrophic osteoarthropathy, primary, autosomal recessive, 1|Isolated congenital digital clubbing
- rs121434480Pathogenicsingle nucleotide variantCranioosteoarthropathy|Hypertrophic osteoarthropathy, primary, autosomal recessive, 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.