PTGR3
prostaglandin reductase 3
Summary
Predicted to enable 15-oxoprostaglandin 13-oxidase [NAD(P)+] activity. Predicted to be involved in negative regulation of fat cell differentiation. Located in mitochondrion. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs634687 | 18:72,906,960 | T/G | downstream gene variant | — |
| rs757955275 | 18:72,913,384 | T/G | — | uncertain significance |
| rs372819128 | 18:72,913,435 | T/A | — | uncertain significance |
| rs147233998 | 18:72,913,453 | C/A | — | uncertain significance |
| rs763668764 | 18:72,913,466 | C/T | — | uncertain significance |
| rs140713450 | 18:72,913,506 | G/C | — | uncertain significance |
| rs2511866527 | 18:72,913,541 | T/A | — | uncertain significance |
| rs762391408 | 18:72,913,544 | C/T | — | likely benign |
| rs141337829 | 18:72,913,642 | G/A | — | uncertain significance |
| rs534224169 | 18:72,913,660 | G/A | — | uncertain significance |
| rs1220289397 | 18:72,913,669 | G/A | — | uncertain significance |
| rs146651397 | 18:72,913,771 | T/C | — | uncertain significance |
| rs1002604887 | 18:72,913,841 | T/C | — | uncertain significance |
| rs143468645 | 18:72,913,885 | T/G | — | uncertain significance |
| rs766437241 | 18:72,913,954 | C/T | — | uncertain significance |
| rs1034445520 | 18:72,914,032 | G/A | — | uncertain significance |
| rs1430270722 | 18:72,914,159 | T/C | — | uncertain significance |
| rs149346224 | 18:72,914,203 | A/G | — | uncertain significance |
| rs768718857 | 18:72,914,231 | G/C | — | uncertain significance |
| rs1215256225 | 18:72,914,279 | C/T | — | uncertain significance |
| rs2639990 | 18:72,915,551 | T/C | intron variant | — |
| rs899535485 | 18:72,920,812 | G/A | — | uncertain significance |
| rs2511874588 | 18:72,920,860 | T/G | — | likely benign |
| rs201759106 | 18:72,920,865 | G/T | — | uncertain significance |
| rs763670392 | 18:72,920,896 | G/A | — | uncertain significance |
| rs752787245 | 18:72,920,922 | T/A | — | uncertain significance |
| rs777008296 | 18:72,920,980 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.