PXDNL
peroxidasin like
Summary
Predicted to enable heme binding activity and peroxidase activity. Predicted to be involved in hydrogen peroxide catabolic process. Predicted to be located in endoplasmic reticulum; extracellular region; and plasma membrane. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants164 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1349473459 | 8:52,232,479 | A/C | — | uncertain significance |
| rs1052704 | 8:52,232,487 | G/T | — | benign |
| rs199528987 | 8:52,232,512 | C/T | — | uncertain significance |
| rs2536738710 | 8:52,232,542 | G/A | — | uncertain significance |
| rs962965318 | 8:52,232,549 | G/A | — | uncertain significance |
| rs2536738822 | 8:52,232,554 | A/C | — | uncertain significance |
| rs180687856 | 8:52,233,365 | G/A | — | benign |
| rs201816215 | 8:52,233,381 | C/T | — | likely benign |
| rs755986290 | 8:52,233,388 | C/T | — | uncertain significance |
| rs751791668 | 8:52,233,407 | T/G | — | uncertain significance |
| rs7827446 | 8:52,233,408 | C/T | — | benign |
| rs781589832 | 8:52,233,414 | T/C | — | uncertain significance |
| rs748474859 | 8:52,233,416 | T/C | — | likely benign |
| rs2536742935 | 8:52,233,455 | T/C | — | uncertain significance |
| rs138123996 | 8:52,252,193 | G/T | — | benign |
| rs141860007 | 8:52,252,305 | T/G | — | benign |
| rs2536807637 | 8:52,252,311 | T/A | — | uncertain significance |
| rs16916011 | 8:52,252,320 | A/G | — | benign |
| rs11774588 | 8:52,258,429 | A/T | — | benign |
| rs755848253 | 8:52,258,454 | G/A | — | uncertain significance |
| rs147301930 | 8:52,258,494 | T/A | — | likely benign |
| rs1209261623 | 8:52,284,475 | T/A | — | uncertain significance |
| rs2536919705 | 8:52,284,485 | G/C | — | uncertain significance |
| rs751508764 | 8:52,284,524 | A/C | — | uncertain significance |
| rs1199283378 | 8:52,284,553 | C/A | — | uncertain significance |
| rs117752382 | 8:52,284,560 | A/T | — | benign |
| rs1807133948 | 8:52,284,600 | A/C | — | uncertain significance |
| rs201097388 | 8:52,284,609 | G/A | — | uncertain significance |
| rs371854791 | 8:52,284,619 | C/G | — | uncertain significance |
| rs771965713 | 8:52,287,226 | C/T | — | uncertain significance |
| rs28407367 | 8:52,287,230 | G/A | — | benign |
| rs2536929928 | 8:52,287,242 | C/T | — | uncertain significance |
| rs200654236 | 8:52,287,255 | G/A | — | likely benign |
| rs1407067131 | 8:52,287,257 | G/T | — | uncertain significance |
| rs202104971 | 8:52,287,283 | C/T | — | uncertain significance |
| rs371171299 | 8:52,287,284 | C/T | — | uncertain significance |
| rs184546026 | 8:52,287,295 | G/A | — | likely benign |
| rs1028440511 | 8:52,320,651 | G/A | — | uncertain significance |
| rs149385606 | 8:52,320,710 | A/T | — | likely benign |
| rs1808489131 | 8:52,320,730 | G/A | — | uncertain significance |
| rs749277291 | 8:52,320,782 | G/C | — | likely benign |
| rs74731075 | 8:52,320,786 | G/A | — | benign |
| rs768885889 | 8:52,320,792 | T/C | — | uncertain significance |
| rs148571691 | 8:52,320,799 | C/T | — | likely benign |
| rs145542518 | 8:52,320,832 | G/C | — | likely benign |
| rs757140816 | 8:52,320,850 | G/A | — | uncertain significance |
| rs566662597 | 8:52,320,909 | A/T | — | uncertain significance |
| rs781169573 | 8:52,320,931 | G/A | — | likely benign |
| rs2537051225 | 8:52,320,963 | A/G | — | uncertain significance |
| rs79130173 | 8:52,321,034 | A/G | — | benign |
| rs73678557 | 8:52,321,068 | T/C | — | benign |
| rs1434666248 | 8:52,321,077 | T/C | — | uncertain significance |
| rs1284252950 | 8:52,321,111 | G/A | — | uncertain significance |
| rs2537052822 | 8:52,321,186 | C/T | — | uncertain significance |
| rs2130886922 | 8:52,321,236 | G/C | — | likely benign |
| rs141024159 | 8:52,321,238 | G/A | — | benign |
| rs2977020 | 8:52,321,243 | T/C | — | benign |
| rs2537053492 | 8:52,321,249 | T/G | — | uncertain significance |
| rs759582960 | 8:52,321,257 | C/T | — | uncertain significance |
| rs761960247 | 8:52,321,269 | G/A | — | uncertain significance |
| rs758688968 | 8:52,321,292 | A/G | — | likely benign |
| rs745676964 | 8:52,321,347 | C/T | — | uncertain significance |
| rs1163232086 | 8:52,321,352 | G/C | — | uncertain significance |
| rs201569799 | 8:52,321,357 | C/T | — | uncertain significance |
| rs373830011 | 8:52,321,573 | T/A | — | uncertain significance |
| rs367770672 | 8:52,321,585 | G/A | — | uncertain significance |
| rs1808536055 | 8:52,321,604 | C/T | — | uncertain significance |
| rs200513898 | 8:52,321,642 | G/A | — | uncertain significance |
| rs11985241 | 8:52,321,686 | C/T | — | benign |
| rs563086442 | 8:52,321,777 | G/C | — | uncertain significance |
| rs1808548433 | 8:52,321,788 | T/A | — | uncertain significance |
| rs376470459 | 8:52,321,798 | C/A | — | uncertain significance |
| rs369170887 | 8:52,321,802 | G/A | — | likely benign |
| rs376832376 | 8:52,321,835 | G/T | — | likely benign |
| rs11992240 | 8:52,321,843 | G/C | — | benign |
| rs771643052 | 8:52,321,867 | A/G | — | uncertain significance |
| rs2537059488 | 8:52,321,877 | A/G | — | likely benign |
| rs1304685868 | 8:52,321,891 | G/A | — | uncertain significance |
| rs1244267078 | 8:52,321,911 | C/G | — | uncertain significance |
| rs550046007 | 8:52,321,917 | G/C | — | uncertain significance |
| rs1242794741 | 8:52,321,933 | G/A | — | uncertain significance |
| rs765030106 | 8:52,321,957 | C/T | — | uncertain significance |
| rs201280324 | 8:52,321,966 | G/A | — | benign |
| rs565390923 | 8:52,321,998 | G/A | — | uncertain significance |
| rs369143018 | 8:52,322,011 | C/T | — | uncertain significance |
| rs986221061 | 8:52,322,050 | G/C | — | uncertain significance |
| rs199983847 | 8:52,322,110 | T/C | — | uncertain significance |
| rs79920259 | 8:52,323,868 | C/T | — | benign |
| rs753198619 | 8:52,323,887 | C/T | — | uncertain significance |
| rs202110442 | 8:52,323,921 | G/A | — | uncertain significance |
| rs113122662 | 8:52,325,731 | G/A | — | uncertain significance |
| rs114874273 | 8:52,325,766 | A/G | — | likely benign |
| rs16916207 | 8:52,325,767 | G/T | — | benign |
| rs10504119 | 8:52,325,796 | A/G | — | benign |
| rs79635112 | 8:52,329,649 | C/T | intron variant | — |
| rs1183487397 | 8:52,336,153 | T/G | — | uncertain significance |
| rs758565106 | 8:52,336,154 | G/T | — | uncertain significance |
| rs1465349795 | 8:52,336,158 | G/A | — | uncertain significance |
| rs16916235 | 8:52,336,182 | C/T | — | benign |
| rs180899557 | 8:52,336,225 | C/T | — | uncertain significance |
Showing 100 of 164 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.