AAB53034.1
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UniProt Secondary Accession #
UniProt Related Accession #
NCBI Official Full Name
15-hydroxyprostaglandin dehydrogenase
NCBI Official Synonym Full Names
hydroxyprostaglandin dehydrogenase 15-(NAD)
NCBI Official Synonym Symbols
PGDH; PGDH1; PHOAR1; 15-PGDH; SDR36C1 [Similar Products]
NCBI Protein Information
15-hydroxyprostaglandin dehydrogenase [NAD(+)]; 15-hydroxyprostaglandin dehydrogenase [NAD(+)]; prostaglandin dehydrogenase 1; NAD+-dependent 15-hydroxyprostaglandin dehydrogenase; short chain dehydrogenase/reductase family 36C, member 1
UniProt Protein Name
15-hydroxyprostaglandin dehydrogenase [NAD(+)]
UniProt Synonym Protein Names
Prostaglandin dehydrogenase 1
UniProt Synonym Gene Names
UniProt Entry Name
PGDH_HUMAN
NCBI Summary for HPGD
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]
UniProt Comments for HPGD
HPGD: 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. Defects in HPGD are the cause of hypertrophic osteoarthropathy, primary, autosomal recessive, type 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. Defects in HPGD are the cause of cranioosteoarthropathy (COA). A form of osterarthropathy 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. Defects in HPGD are a cause of isolated congenital nail clubbing (ICNC); also called clubbing of digits or hereditary acropachy. ICNC is 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. Belongs to the short-chain dehydrogenases/reductases (SDR) family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Oxidoreductase; EC 1.1.1.141; Tumor suppressor
Chromosomal Location of Human Ortholog: 4q34-q35
Cellular Component: basolateral plasma membrane; cytosol
Molecular Function: protein homodimerization activity; 15-hydroxyprostaglandin dehydrogenase (NAD+) activity; catalytic activity; NAD binding; prostaglandin E receptor activity
Biological Process: ovulation; lipoxygenase pathway; transforming growth factor beta receptor signaling pathway; cyclooxygenase pathway; arachidonic acid metabolic process; parturition; female pregnancy; prostaglandin metabolic process; negative regulation of cell cycle
Disease: Digital Clubbing, Isolated Congenital; Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1
Research Articles on HPGD
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Products associated with HPGD elisa kit
Pathways associated with HPGD elisa kit
Diseases associated with HPGD elisa kit
Disease Name |
Pubmed Publications |
Osteoarthropathy, Primary Hypertrophic Antibodies |
>15 publications with HPGD and Osteoarthropathy, Primary Hypertrophic |
HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1 Antibodies |
>15 publications with HPGD and HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1 |
Inflammation Antibodies |
>9 publications with HPGD and Inflammation |
Breast Neoplasms Antibodies |
>3 publications with HPGD and Breast Neoplasms |
Fetal Growth Retardation Antibodies |
>2 publications with HPGD and Fetal Growth Retardation |
Fibrosis Antibodies |
>2 publications with HPGD and Fibrosis |
Prostatic Neoplasms Antibodies |
>2 publications with HPGD and Prostatic Neoplasms |
Arthritis, Rheumatoid Antibodies |
>1 publications with HPGD and Arthritis, Rheumatoid |
Neoplasms, Experimental Antibodies |
>1 publications with HPGD and Neoplasms, Experimental |
Hypertrophy Antibodies |
>1 publications with HPGD and Hypertrophy |
Organs/Tissues associated with HPGD elisa kit
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