Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3248
Gene name Gene Name - the full gene name approved by the HGNC.
15-hydroxyprostaglandin dehydrogenase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HPGD
Synonyms (NCBI Gene) Gene synonyms aliases
15-PGDH, PGDH, PGDH1, PHOAR1, SDR36C1
Disease Acronyms (UniProt) Disease acronyms from UniProt database
PHOAR1
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q34.1
Summary Summary 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
SNPs SNP 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
miRNA miRNA 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 IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601688 5154 ENSG00000164120
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
Tissue specificity TISSUE SPECIFICITY: Detected in colon epithelium (at protein level). {ECO:0000269|PubMed:15574495}.
Sequence
Sequence length 266
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  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 Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Anemia Anemia rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966
View all (89 more)
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 term Disease name Evidence References Source
Osteomyelitis Osteomyelitis ClinVar
Ptosis Blepharoptosis, Ptosis ClinVar
Cranioosteoarthropathy cranio-osteoarthropathy GenCC
Pachydermoperiostosis Syndrome pachydermoperiostosis GenCC
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 25735395, 26683690, 30531928
Adenoma Inhibit 23960441
Adenoma Associate 29769213
Arteriovenous Fistula Associate 40597829
Arthritis Rheumatoid Inhibit 26082314
Breast Neoplasms Associate 25003827, 28206964, 35617355, 36077333
Carcinogenesis Associate 20635443, 27561985, 30531928, 40095474
Carcinogenesis Inhibit 23960441
Carcinoma Intraductal Noninfiltrating Associate 19393583
Carcinoma Squamous Cell Inhibit 25735395