Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5731
Gene name Gene Name - the full gene name approved by the HGNC.
Prostaglandin E receptor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PTGER1
Synonyms (NCBI Gene) Gene synonyms aliases
EP1
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.12
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the G protein-coupled receptor family. This protein is one of four receptors identified for prostaglandin E2 (PGE2). Through a phosphatidylinositol-calcium second messenger system, G-Q proteins mediate this
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT2080144 hsa-miR-1587 CLIP-seq
MIRT2080145 hsa-miR-1915 CLIP-seq
MIRT2080146 hsa-miR-4417 CLIP-seq
MIRT2080147 hsa-miR-4492 CLIP-seq
MIRT2080148 hsa-miR-4498 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004955 Function Prostaglandin receptor activity IEA
GO:0004957 Function Prostaglandin E receptor activity IBA
GO:0004957 Function Prostaglandin E receptor activity IDA 8253813
GO:0004957 Function Prostaglandin E receptor activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
176802 9593 ENSG00000160951
Protein
UniProt ID P34995
Protein name Prostaglandin E2 receptor EP1 subtype (PGE receptor EP1 subtype) (PGE2 receptor EP1 subtype) (Prostanoid EP1 receptor)
Protein function Receptor for prostaglandin E2 (PGE2). The activity of this receptor is mediated by G(q) proteins which activate a phosphatidylinositol-calcium second messenger system. May play a role as an important modulator of renal function. Implicated the s
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 49 351 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Abundant in kidney. Lower level expression in lung, skeletal muscle and spleen, lowest expression in testis and not detected in liver brain and heart.
Sequence
Sequence length 402
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
Neuroactive ligand-receptor interaction
Human cytomegalovirus infection
Pathways in cancer
  Prostanoid ligand receptors
G alpha (q) signalling events
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Urolithiasis Urolithiasis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Asthma Aspirin Induced Inhibit 20587336
Breast Neoplasms Associate 16570043, 17906615
Bronchiolitis Obliterans Syndrome Associate 21940790
Carcinogenesis Associate 36436093
Carcinoma Hepatocellular Associate 15294900, 22555372
Cholangiocarcinoma Associate 24839005
Chondrosarcoma Associate 20178602
Colorectal Neoplasms Inhibit 17906615
Cystitis Interstitial Associate 25595860
Delayed Cranial Ossification due to CBFB Haploinsufficiency Associate 20648052