HPGD (15-hydroxyprostaglandin dehydrogenase)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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3248 |
Gene nameGene Name - the full gene name approved by the HGNC.
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15-hydroxyprostaglandin dehydrogenase |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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HPGD |
SynonymsGene synonyms aliases
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15-PGDH, PGDH, PGDH1, PHOAR1, SDR36C1 |
ChromosomeChromosome number
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4 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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4q34.1 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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.
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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 |
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miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00106 |
adh_short |
6 → 199 |
short chain dehydrogenase |
Domain |
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Sequence |
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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.
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Associated diseases
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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 |
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Arthritis |
Arthritis, Degenerative polyarthritis |
rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 |
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Cerebral palsy |
Cerebral Palsy |
rs121918149, rs75184679, rs730880264, rs587777428, rs797045067, rs767399782, rs564185858, rs886039513 |
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Currarino triad |
Currarino triad |
rs121912546, rs121912547, rs1563700090, rs1563700419, rs121912548, rs121912549, rs1554594329 |
18500342, 21438135 |
Hypertrophic osteoarthropathy |
Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant, HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1 |
rs121434480, rs587776676, rs548208942, rs1559943990, rs387906806, rs1559927542, rs751192029, rs370769816, rs387907295, rs387907296, rs387907297, rs577045722, rs587777719, rs776813259, rs1085307096, rs765249238, rs774795340, rs375335006, rs1576428882, rs1576467025 |
18500342, 25526675, 24816859, 18500342 |
Megalencephaly, polymicrogyria, polydactyly, hydrocephalus syndrome |
Medullary carcinoma |
rs587776934, rs587776935, rs397514605, rs397514606, rs587777624, rs886041100, rs886041591, rs1057519801, rs1064795602, rs1568636630 |
11352223 |
Osteomyelitis |
Osteomyelitis |
rs11125529, rs10936599, rs7675998, rs398652, rs755017 |
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Osteoporosis |
Osteoporosis |
rs72658152, rs72667023, rs587776916, rs72656370, rs768615287 |
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Palmoplantar keratoderma |
Keratoderma, Palmoplantar |
rs59616921, rs1568039793, rs746488412, rs200564757, rs1567027297, rs781596375, rs1567027610, rs398123054, rs398123055, rs398123056, rs398123057, rs398122949, rs398122950, rs397515639, rs398122951, rs397515640, rs397515641, rs142859678, rs797044479, rs577442939, rs672601344, rs568609861, rs1057518846, rs1182196436, rs1567037561 |
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Patent ductus arteriosus |
Patent ductus arteriosus |
rs80338911, rs879253870, rs879253871, rs879255278, rs879255279, rs879253872 |
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Prostate cancer |
Malignant neoplasm of prostate |
rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 |
17013881 |
Scoliosis |
Scoliosis, unspecified |
rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Acne |
Acne |
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Mallet finger |
Acquired deformity of finger |
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Acrosteolysis |
Acro-Osteolysis |
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Arthropathy |
Arthropathy |
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Congenital pectus excavatum |
Congenital pectus excavatum |
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Cranioosteoarthropathy |
CRANIOOSTEOARTHROPATHY, Reginato Schiapachasse syndrome, Cranio-osteoarthropathy |
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18500342, 21438135, 25526675, 18500342, 21438135 |
Cutis verticis gyrata |
Cutis verticis gyrata |
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Eczema |
Eczema |
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Gynecomastia |
Gynecomastia |
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Hereditary clubbing |
Hereditary clubbing |
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18805827, 18500342, 25526675 |
High palate |
Byzanthine arch palate |
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Lung neoplasms |
Lung Neoplasms |
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Malabsorption syndrome |
Malabsorption Syndrome |
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Osteopenia |
Osteopenia |
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Pachydermoperiostosis syndrome |
Osteoarthropathy, Primary Hypertrophic, Pachydermoperiostosis |
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18500342, 25526675 |
Palmoplantar keratosis |
Palmoplantar Keratosis |
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Peptic ulcer |
Peptic Ulcer |
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Prostatic neoplasms |
Prostatic Neoplasms |
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17013881 |
Ptosis |
Blepharoptosis, Ptosis |
rs139920573 |
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Seborrheic dermatitis |
Seborrheic dermatitis |
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Skin neoplasms |
Skin Neoplasms |
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Thyroid neoplasm |
Thyroid Neoplasm |
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11352223 |
Thyroid carcinoma |
Thyroid carcinoma |
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11352223 |
Thyroid gland follicular adenoma |
Thyroid Gland Follicular Adenoma |
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11352223 |
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