PTGER3
prostaglandin E receptor 3
Summary
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). This receptor may have many biological functions, which involve digestion, nervous system, kidney reabsorption, and uterine contraction activities. Studies of the mouse counterpart suggest that this receptor may also mediate adrenocorticotropic hormone response as well as fever generation in response to exogenous and endogenous stimuli. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17131479 | 1:71,357,687 | C/G | intron variant | — |
| rs521870 | 1:71,404,337 | T/C | — | — |
| rs758250767 | 1:71,418,635 | G/C | — | uncertain significance |
| rs762342468 | 1:71,418,696 | T/A | — | uncertain significance |
| rs1650929005 | 1:71,418,735 | C/T | — | uncertain significance |
| rs977214 | 1:71,426,260 | A/G | intron variant | — |
| rs573688 | 1:71,426,569 | T/C | intron variant | — |
| rs6665776 | 1:71,427,842 | C/A | intron variant | — |
| rs594454 | 1:71,430,468 | G/T | intron variant | — |
| rs909848 | 1:71,443,150 | T/A | — | — |
| rs2050066 | 1:71,455,135 | T/C | intron variant | — |
| rs6424414 | 1:71,455,470 | T/C | intron variant | — |
| rs2300167 | 1:71,458,162 | T/C | intron variant | — |
| rs1308330278 | 1:71,477,997 | C/A | — | uncertain significance |
| rs2525118441 | 1:71,478,076 | A/G | — | uncertain significance |
| rs1178993163 | 1:71,478,094 | T/C | — | uncertain significance |
| rs1196939574 | 1:71,478,130 | A/G | — | uncertain significance |
| rs66904764 | 1:71,493,639 | T/C | intron variant | — |
| rs2817866 | 1:71,503,447 | G/A | intron variant | — |
| rs777193036 | 1:71,512,441 | C/T | — | uncertain significance |
| rs2525441443 | 1:71,512,567 | A/G | — | uncertain significance |
| rs747455158 | 1:71,512,771 | A/G | — | uncertain significance |
| rs2525449488 | 1:71,513,047 | G/A | — | uncertain significance |
| rs1328620495 | 1:71,513,140 | G/C | — | uncertain significance |
| rs5669 | 1:71,513,150 | G/C | — | benign |
| rs1314974804 | 1:71,513,197 | T/G | — | likely benign |
| rs200764199 | 1:71,513,214 | C/T | — | uncertain significance |
| rs755042142 | 1:71,513,238 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.