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Gene : HPGD Homo sapiens
Name  ? 15-hydroxyprostaglandin dehydrogenase Cytological Location  4q34.1
Brief Description  15-hydroxyprostaglandin dehydrogenase
Description  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]
  • synonyms:
  • SDR36C1,
  • HPGD,
  • uc003itu.3,
  • SDR36C1,
  • HGNC:5154,
  • OTTHUMG00000160772,
  • hydroxyprostaglandin dehydrogenase 15-(NAD),
  • PGDH1,
  • 15-PGDH,
  • PHOAR1,
  • short chain dehydrogenase/reductase family 36C, member 1,
  • PGDH,
  • NM_000860,
  • 15-hydroxyprostaglandin dehydrogenase (NAD(+))
  • identifiers:
  • 3248,
  • ENSG00000164120,
  • HPGD

Genome feature

Region: gene ? Length: 32724  
Location: 4:174490175-174522898 reverse strand Cyto location: 4q34.1


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11 Pathways

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Gene -> HPO annotation (Human Phenotype Ontology)

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Disease

2 Diseases

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11 Pathways

937 SN Ps

5 Cross References

17 Data Sets

8 Homologues

0 Located Features

97 Rna Seq Results





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