HPGD - 15-hydroxyprostaglandin dehydrogenase Gene

Also Known as PGDH; PGDH1; PHOAR1; 15-PGDH; SDR36C1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3248

About HPGD

Cytogenetic location: 4q34.1 Genomic coordinates (GRCh38): 4:174,490,175-174,522,893 (from NCBI)

This gene has 14 transcripts (splice variants), 205 orthologues and is associated with 6 phenotypes. Biased expression in urinary bladder (RPKM 176.8), stomach (RPKM 67.9) and 11 other tissues.

Summary

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]

HPGD Products (8)

mRNA Protein Name
NM_001256305.2 NP_001243234.1 15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 4
NM_001363574.2 NP_001350503.1 15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 6
NM_001256301.1 NP_001243230.1 15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 3
XR_938728.3
NM_000860.6 NP_000851.2 15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 1
NM_001256307.2 NP_001243236.1 15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 3
NM_001256306.2 NP_001243235.1 15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 5
NM_001145816.3 NP_001139288.1 15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 2
Molecular Function GO Annotation Evidence References Source
enables 15-hydroxyprostaglandin dehydrogenase (NAD+) activity IDA
IDA: Inferred from direct assay
2025296 GOA
enables 15-hydroxyprostaglandin dehydrogenase (NAD+) activity IMP
IMP: Inferred from mutant phenotype
8086429 GOA
enables NAD binding IDA
IDA: Inferred from direct assay
10198228 GOA
enables NAD+ binding IDA
IDA: Inferred from direct assay
16828555 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
21072165 GOA
enables oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor IDA
IDA: Inferred from direct assay
16757471 GOA
enables prostaglandin E receptor activity IDA
IDA: Inferred from direct assay
10198228 GOA
Biological Process GO Annotation Evidence References Source
involved in female pregnancy IDA
IDA: Inferred from direct assay
15531523 GOA
involved in negative regulation of cell cycle IDA
IDA: Inferred from direct assay
15574495 GOA
involved in parturition IDA
IDA: Inferred from direct assay
15531523 GOA
involved in prostaglandin metabolic process IDA
IDA: Inferred from direct assay
16828555 GOA
involved in regulation of prostaglandin catabolic process IMP
IMP: Inferred from mutant phenotype
8086429 GOA
involved in transforming growth factor beta receptor signaling pathway IDA
IDA: Inferred from direct assay
15574495 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

HPGD Protein Structure

adh_short

adh_short: short chain dehydrogenase (6 - 166)

  • 0
  • 100
  • 200
  • 266 a.a.
Protein Preferred Names Protein Names

15-hydroxyprostaglandin dehydrogenase [NAD(+)]

  • 15-hydroxyprostaglandin dehydrogenase (NAD(+))

  • NAD+-dependent 15-hydroxyprostaglandin dehydrogenase

  • eicosanoid/docosanoid dehydrogenase

  • hydroxyprostaglandin dehydrogenase 15-(NAD)

  • prostaglandin dehydrogenase 1

  • short chain dehydrogenase/reductase family 36C member 1

Recombinant HPGD Proteins

Cat. No. Product Name Accession Purity
HY-P70297 15-PGDH/HPGD Protein, Human (HEK293, His) P15428-1 (M1-Q266) ≥ 95%, as determined by reducing SDS-PAGE.

HPGD Antibodies

Cat. No. Product Name Application Reactivity
HY-P81351 15 PGDH Antibody (YA1096) IHC-P Human
HY-P81351A 15 PGDH Antibody (YA1096)(PBS only) IHC-P Human

Related Diseases

Diseases Alias
Colorectal Adenoma
  • Colorectal Adenomas

  • Adenoma Of Large Intestine

Colon Adenoma
  • Adenomatous Polyp Of Colon

Gastric Tubular Adenocarcinoma
  • Tubular Adenocarcinoma Of Stomach

Gastritis, Familial Giant Hypertrophic
  • Menetrier Disease

  • Gastric Mucosal Hypertrophy

  • Giant Hypertrophic Gastritis

  • Hypertrophic Gastropathy

  • Gastritis, Hypertrophic

  • Familial Giant Hypertrophic Gastritis

  • Giant Rugal Hypertrophy Of Stomach

  • Hypertrophic Gastritis

  • Gastroenteropathy, Protein Losing

  • Giant Hypertrophic Gastropathy

  • Giant Hypertrophy Of The Gastric Mucosa

  • Hypoproteinemic Hypertrophic Gastropathy

  • Menetrier'S Disease

  • Giant Hypertrophic Hypersecretory Gastritis

Lung Cancer Susceptibility 3
  • Lung Adenocarcinoma

  • Adenocarcinoma Of Lung

  • LNCR3

  • Adenocarcinoma Of Lung, Susceptibility To

  • Bronchogenic Lung Adenocarcinoma

  • Nonsmall Cell Adenocarcinoma

  • Adenocarcinoma Lung

  • Lung Adenocarcinomas

  • Non-Small Cell Adenocarcinoma

Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1
  • Cranioosteoarthropathy

  • PHOAR1

  • Pachydermoperiostosis, Autosomal Recessive

  • Touraine-Solente-Gole Syndrome

  • Pho, Autosomal Recessive

  • Pdp, Autosomal Recessive

  • Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1

  • Cranio Osteoarthropathy

  • Cranio-Osteoarthropathy

  • Currarino Disease

  • Currarino Idiopathic Osteoarthropathy

  • Reginato-Schiapachasse Syndrome

  • Touraine-Solente-Golé Syndrome

  • COA

  • Pachydermoperiostosis Autosomal Recessive

  • Pdp Autosomal Recessive

  • Pho Autosomal Recessive

  • Osteoarthropathy, Hypertrophic, Primary, Autosomal Recessive, Type 1

  • Osteoarthropathy, Primary Hypertrophic

  • Reginato Schiapachasse Syndrome

Patent Ductus Arteriosus 1
  • Patent Ductus Arteriosus

  • PDA1

  • Pda

  • Ductus Arteriosus, Patent

  • Patent Ductus Arteriosus, Susceptibility To

  • Patent Ductus Botalli

  • Patency Of The Ductus Arteriosus

  • Patent Ductus Arteriosus Familial

  • Ductus Arteriosus Patent

  • Patent Ductus Arteriosus - Persisting Type

Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Primary Hypertrophic Osteoarthropathy
  • Pachydermoperiostosis Syndrome

  • Osteoarthropathy, Primary Hypertrophic

  • Pachydermoperiostosis Of Nail

  • Idiopathic Hypertrophic Osteoarthropathy

  • Pho

Acroosteolysis
  • Acro-Osteolysis

Ureteral Obstruction
Colonic Benign Neoplasm
  • Colon Neoplasm

  • Colonic Mass

  • Colonic Tumor

  • Neoplasm Of Colon

  • Neoplasm Of The Colon

  • Colonic Neoplasms

  • Colon Cancer

  • Colon Carcinoma Nos

  • Colonic Cancer

  • Metastatic Colon Cancer Nos

Lymphangioma
  • Lymphatic Malformation

  • Lymphatic Malformations

  • Benign Lymphangioma

  • Congenital Lymphangioma

  • Lymphangiomas

Periostitis
Digital Clubbing, Isolated Congenital
  • Isolated Congenital Digital Clubbing

  • DIGC

  • Clubbing Of Digits

  • Acropachy, Hereditary

  • Isolated Congenital Acropachy

  • Isolated Congenital Nail Clubbing

  • Hereditary Acropachy

Secondary Hypertrophic Osteoarthropathy
  • Osteoarthropathy, Secondary Hypertrophic

  • Bamberger-Marie Disease

  • Hpoa - Hypertrophic Pulmonary Osteoarthropathy

  • Hypertrophic Pulmonary Osteoarthropathy

  • Marie Bamberger Disease

Heart Disease
  • Heart Failure

  • Congenital Heart Disease

  • Heart Diseases

  • Congenital Heart Defects

  • Congenital Heart Defect

  • Congenital Anomaly Of Heart

  • Heart Defect

  • Heart Malformation

  • Heart-Congenital Defect

  • Congenital Heart Disorder

  • Heart Defects Congenital

  • Heart Defects, Congenital

  • Heart Defects

  • Heart Disease, Congenital

  • Disease, Heart, Congenital

  • Congestive Heart Failure

Acromegaloid Changes, Cutis Verticis Gyrata, And Corneal Leukoma
  • Pachydermoperiostosis

  • Rosenthal-Kloepfer Syndrome

  • Pdp

  • Acromegaloid Changes, Cutis Verticis Gyrata And Corneal Leukoma

  • Idiopathic Hypertrophic Osteoarthropathy

  • Primary Hypertrophic Osteoarthropathy

  • Touraine Solente Gole Syndrome

  • Touraine-Solente-Gole Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus HPGD VGNC VGNC:56973
Macaca mulatta HPGD VGNC VGNC:73512
Felis catus HPGD VGNC VGNC:67638
Canis familiaris HPGD VGNC VGNC:49605
Mus musculus HPGD MGD MGI:108085
Rattus norvegicus HPGD RGD RGD:620087
Others HPGD NCBI