HPGD

hydroxyprostaglandin dehydrogenase 15-(NAD)

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

This gene encodes a member of the short-chain nonmetalloenzyme alcohol dehydrogenase protein family. The encoded enzyme is responsible for the metabolism of prostaglandins, which function in a variety of physiologic and cellular processes such as inflammation. Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

From UniProt:

Prostaglandin inactivation. Contributes to the regulation of events that are under the control of prostaglandin levels. Catalyzes the NAD-dependent dehydrogenation of lipoxin A4 to form 15-oxo-lipoxin A4. Inhibits in vivo proliferation of colon cancer cells.

From NCBI Gene:

  • Digital clubbing, isolated congenital
  • Pachydermoperiostosis syndrome

From UniProt:

Isolated congenital nail clubbing (ICNC): A rare genodermatosis characterized by enlargement of the nail plate and terminal segments of the fingers and toes, resulting from proliferation of the connective tissues between the nail matrix and the distal phalanx. It is usually symmetrical and bilateral (in some cases unilateral). In nail clubbing usually the distal end of the nail matrix is relatively high compared to the proximal end, while the nail plate is complete but its dimensions and diameter more or less vary in comparison to normal. There may be different fingers and toes involved to varying degrees. Some fingers or toes are spared, but the thumbs are almost always involved. [MIM:119900]

Cranioosteoarthropathy (COA): A form of osteoarthropathy characterized by swelling of the joints, digital clubbing, hyperhidrosis, delayed closure of the fontanels, periostosis, and variable patent ductus arteriosus. Pachydermia is not a prominent feature. [MIM:259100]

Hypertrophic osteoarthropathy, primary, autosomal recessive, 1 (PHOAR1): A disease characterized by digital clubbing, periostosis, acroosteolysis, painful joint enlargement, and variable features of pachydermia that include thickened facial skin and a thickened scalp. Other developmental anomalies include delayed closure of the cranial sutures and congenital heart disease. [MIM:259100]

Cytogenetic Location: 4q34-q35, which is the long (q) arm of chromosome 4 between positions 34 and 35

Molecular Location: base pairs 174,490,177 to 174,522,898 on chromosome 4 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 4q34-q35, which is the long (q) arm of chromosome 4 between positions 34 and 35
  • 15-PGDH
  • PGDH
  • PGDH1
  • PHOAR1
  • SDR36C1