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.