PTGFRN
prostaglandin F2 receptor inhibitor
Summary
Predicted to be involved in myoblast fusion involved in skeletal muscle regeneration. Predicted to act upstream of or within lipid droplet organization. Located in cell surface. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2526539381 | 1:117,452,863 | T/C | — | uncertain significance |
| rs2806864 | 1:117,469,781 | C/G | intron variant | — |
| rs1469959312 | 1:117,484,391 | T/C | — | uncertain significance |
| rs916948746 | 1:117,484,430 | A/T | — | uncertain significance |
| rs1352465849 | 1:117,484,530 | G/T | — | uncertain significance |
| rs77895792 | 1:117,484,581 | C/T | — | benign |
| rs781449023 | 1:117,484,612 | G/T | — | uncertain significance |
| rs368215880 | 1:117,484,684 | G/C | — | uncertain significance |
| rs1242213837 | 1:117,484,699 | G/T | — | uncertain significance |
| rs777577579 | 1:117,487,343 | C/G | — | uncertain significance |
| rs80123219 | 1:117,487,344 | G/A | — | benign |
| rs1483261547 | 1:117,487,378 | G/A | — | uncertain significance |
| rs368166849 | 1:117,487,396 | G/A | — | uncertain significance |
| rs1231086395 | 1:117,487,456 | G/C | — | uncertain significance |
| rs2526607960 | 1:117,487,489 | G/A | — | uncertain significance |
| rs1322918645 | 1:117,487,528 | C/G | — | uncertain significance |
| rs886350311 | 1:117,487,532 | G/A | — | uncertain significance |
| rs2526608288 | 1:117,487,537 | G/T | — | uncertain significance |
| rs145790245 | 1:117,487,567 | G/A | — | conflicting classifications of pathogenicity |
| rs143781613 | 1:117,487,583 | T/C | — | uncertain significance |
| rs142424201 | 1:117,487,607 | A/G | — | likely benign |
| rs188883808 | 1:117,487,613 | C/T | — | uncertain significance |
| rs532025214 | 1:117,487,642 | G/A | — | uncertain significance |
| rs137888350 | 1:117,487,679 | C/T | — | uncertain significance |
| rs4546904 | 1:117,487,711 | T/A | missense variant | — |
| rs1650270302 | 1:117,491,822 | G/T | — | uncertain significance |
| rs756551810 | 1:117,491,840 | G/A | — | uncertain significance |
| rs2526618383 | 1:117,491,852 | G/A | — | uncertain significance |
| rs762637949 | 1:117,491,910 | G/A | — | uncertain significance |
| rs761385816 | 1:117,491,918 | G/T | — | uncertain significance |
| rs150849305 | 1:117,491,922 | C/T | — | uncertain significance |
| rs751655171 | 1:117,491,969 | G/A | — | uncertain significance |
| rs768367518 | 1:117,491,988 | G/A | — | uncertain significance |
| rs561296592 | 1:117,492,036 | A/G | — | uncertain significance |
| rs753167793 | 1:117,492,038 | G/A | — | uncertain significance |
| rs550219557 | 1:117,492,102 | A/T | — | uncertain significance |
| rs2526619418 | 1:117,492,105 | T/C | — | uncertain significance |
| rs2526619929 | 1:117,492,132 | G/T | — | uncertain significance |
| rs750587095 | 1:117,492,158 | G/A | — | likely benign |
| rs74408251 | 1:117,499,548 | A/T | intron variant | — |
| rs745346068 | 1:117,503,906 | G/A | — | uncertain significance |
| rs144591822 | 1:117,503,976 | G/A | — | uncertain significance |
| rs771208031 | 1:117,504,009 | G/A | — | uncertain significance |
| rs201152399 | 1:117,504,021 | A/G | — | uncertain significance |
| rs535434092 | 1:117,504,035 | G/A | — | uncertain significance |
| rs1334931799 | 1:117,504,044 | G/A | — | uncertain significance |
| rs140632746 | 1:117,504,056 | G/A | — | uncertain significance |
| rs1650662181 | 1:117,504,107 | G/A | — | uncertain significance |
| rs367593504 | 1:117,504,153 | G/A | — | uncertain significance |
| rs6658749 | 1:117,504,193 | C/T | — | benign |
| rs2526646690 | 1:117,504,200 | G/T | — | uncertain significance |
| rs142302653 | 1:117,504,221 | C/T | — | uncertain significance |
| rs142161951 | 1:117,509,538 | G/A | — | uncertain significance |
| rs2526661821 | 1:117,509,715 | C/A | — | uncertain significance |
| rs150391268 | 1:117,509,732 | G/T | — | likely benign |
| rs201653450 | 1:117,509,885 | G/C | — | uncertain significance |
| rs148576999 | 1:117,509,933 | G/A | — | likely benign |
| rs573022952 | 1:117,511,173 | T/G | — | — |
| rs759408038 | 1:117,516,862 | A/G | — | uncertain significance |
| rs1570676251 | 1:117,516,879 | G/C | — | uncertain significance |
| rs6657819 | 1:117,526,905 | G/C | intron variant | — |
| rs1301904948 | 1:117,527,311 | C/T | — | uncertain significance |
| rs78836817 | 1:117,527,340 | T/A | — | uncertain significance |
| rs193251352 | 1:117,527,380 | T/G | — | uncertain significance |
| rs1362979313 | 1:117,527,407 | C/T | — | uncertain significance |
| rs145914956 | 1:117,527,430 | C/T | — | uncertain significance |
| rs17036676 | 1:117,527,444 | C/T | — | benign |
| rs778853881 | 1:117,527,490 | C/G | — | uncertain significance |
| rs532216050 | 1:117,527,523 | C/T | — | uncertain significance |
| rs778535659 | 1:117,529,523 | T/G | — | uncertain significance |
| rs747572385 | 1:117,529,537 | T/C | — | uncertain significance |
| rs140355100 | 1:117,529,548 | C/T | — | uncertain significance |
| rs144307532 | 1:117,529,560 | C/T | — | uncertain significance |
| rs770761276 | 1:117,529,561 | G/A | — | uncertain significance |
| rs771573075 | 1:117,529,583 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.