GediPNet logo

HPGD (15-hydroxyprostaglandin dehydrogenase)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3248
Gene nameGene Name - the full gene name approved by the HGNC.
15-hydroxyprostaglandin dehydrogenase
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
HPGD
SynonymsGene synonyms aliases
15-PGDH, PGDH, PGDH1, PHOAR1, SDR36C1
ChromosomeChromosome number
4
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q34.1
SummarySummary of gene provided in NCBI Entrez 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 inflamma
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs121434480 C>G Pathogenic Missense variant, coding sequence variant, non coding transcript variant, intron variant
rs121434481 A>G Pathogenic Missense variant, coding sequence variant, genic downstream transcript variant, intron variant
rs375335006 G>A,C Likely-pathogenic Coding sequence variant, missense variant, intron variant, genic downstream transcript variant
rs587776676 GGTCTACAAC>TG Pathogenic Intron variant, frameshift variant, non coding transcript variant, coding sequence variant, 5 prime UTR variant
rs587777719 AG>- Pathogenic Intron variant, frameshift variant, non coding transcript variant, coding sequence variant, 5 prime UTR variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT053173 hsa-miR-21-5p In situ hybridization, Luciferase reporter assay, qRT-PCR, Western blot 24699315
MIRT719015 hsa-miR-664a-3p HITS-CLIP 19536157
MIRT719014 hsa-miR-4289 HITS-CLIP 19536157
MIRT719013 hsa-miR-486-5p HITS-CLIP 19536157
MIRT719012 hsa-miR-4742-3p HITS-CLIP 19536157
Transcription factors
Transcription factor Regulation Reference
CREB1 Unknown 10650939
ERG Unknown 21178489
ETS1 Unknown 10650939
NFIL3 Unknown 1620116
SNAI2 Repression 17575121
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001822 Process Kidney development IEA
GO:0004957 Function Prostaglandin E receptor activity IDA 10198228
GO:0005654 Component Nucleoplasm IDA
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005829 Component Cytosol IDA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P15428
Protein name 15-hydroxyprostaglandin dehydrogenase [NAD(+)] (15-PGDH) (EC 1.1.1.141) (Eicosanoid/docosanoid dehydrogenase [NAD(+)]) (EC 1.1.1.-, EC 1.1.1.232) (Prostaglandin dehydrogenase 1) (Short chain dehydrogenase/reductase family 36C member 1)
Protein function Catalyzes the NAD-dependent dehydrogenation (oxidation) of a broad array of hydroxylated polyunsaturated fatty acids (mainly eicosanoids and docosanoids, including prostaglandins, lipoxins and resolvins), yielding their corresponding keto (oxo)
PDB 2GDZ , 8CVN , 8CWL , 8FD8
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00106 adh_short
6 199
short chain dehydrogenase
Domain
Sequence
Sequence length 266
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Arachidonic acid metabolism
Transcriptional misregulation in cancer
  Synthesis of Lipoxins (LX)
Biosynthesis of D-series resolvins
Biosynthesis of E-series 18(S)-resolvins
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Anemia Anemia rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966, rs137853122, rs137853123, rs786205060, rs267607121, rs121908584, rs80338697, rs80338699, rs120074166, rs120074167, rs1050828, rs74575103, rs137852314, rs5030868, rs137852316, rs137852317, rs137852318, rs137852319, rs137852320, rs137852321, rs137852322, rs137852323, rs137852324, rs72554665, rs387906468, rs5030872, rs137852326, rs137852333, rs137852327, rs137852328, rs137852329, rs137852330, rs137852331, rs137852332, rs137852334, rs137852335, rs137852336, rs137852339, rs76645461, rs137852340, rs137852341, rs78478128, rs137852343, rs137852344, rs137852345, rs587776730, rs137852346, rs137852347, rs137852349, rs2070404412, rs2070350038, rs2070350009, rs137852303, rs137852304, rs33946267, rs34378160, rs33933298, rs11549407, rs35724775, rs34598529, rs41469945, rs267607201, rs80338694, rs80338696, rs387907018, rs398123546, rs78365220, rs587777100, rs587777101, rs483352840, rs869312752, rs765487627, rs1557229599, rs1557230040, rs1555524842, rs782090947, rs1358275550, rs1557229736, rs1557230573, rs1556323334, rs1233124208, rs1293528130, rs146864395, rs1595503440, rs1603411214, rs137852325, rs1575247302, rs1603411177, rs1336651679, rs782322505
Arthritis Arthritis, Degenerative polyarthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470
Cerebral palsy Cerebral Palsy rs121918149, rs75184679, rs730880264, rs587777428, rs797045067, rs767399782, rs564185858, rs886039513
Currarino triad Currarino triad rs121912546, rs121912547, rs1563700090, rs1563700419, rs121912548, rs121912549, rs1554594329 18500342, 21438135
Unknown
Disease name Disease term dbSNP ID References
Acne Acne
Mallet finger Acquired deformity of finger
Acrosteolysis Acro-Osteolysis
Arthropathy Arthropathy

| © 2021, Biomedical Informatics Centre, NIRRH |
ICMR-National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400012
Tel: +91-22-24192104, Fax No: +91-22-24139412