QPCTL

glutaminyl-peptide cyclotransferase like

Summary

Enables glutaminyl-peptide cyclotransferase activity and zinc ion binding activity. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants36 total

rsidPosition (GRCh37)AllelesClassClinVar
rs77229235519:46,195,989C/Tuncertain significance
rs214612125419:46,195,999T/Guncertain significance
rs251364259819:46,196,124T/Cuncertain significance
rs251364268319:46,196,143A/Guncertain significance
rs251364275419:46,196,167G/Tuncertain significance
rs130643102419:46,196,671G/Auncertain significance
rs77218699419:46,196,783C/Tuncertain significance
rs55287998119:46,198,729G/Auncertain significance
rs76538851919:46,198,752T/Auncertain significance
rs36899458719:46,198,780T/Guncertain significance
rs140924245919:46,198,794G/Auncertain significance
rs8033986419:46,198,825G/Abenign
rs94351967819:46,198,846A/Guncertain significance
rs75048144919:46,198,876C/Tuncertain significance
rs102211069619:46,198,950C/Guncertain significance
rs15018411919:46,200,670C/Tupstream gene variant
rs5792589419:46,201,582C/Tintron variant
rs96133981219:46,201,809C/Guncertain significance
rs54427081419:46,201,913G/Auncertain significance
rs37545028119:46,201,941C/Tuncertain significance
rs77159730819:46,202,062C/Tuncertain significance
rs20143517619:46,202,123G/Auncertain significance
rs14501687419:46,202,131C/Tuncertain significance
rs19962561319:46,202,143C/Tuncertain significance
rs228701919:46,202,172C/Tintron variant
rs725619719:46,202,822A/Gintron variant
rs75042219819:46,205,068A/Guncertain significance
rs37356130719:46,205,071G/Auncertain significance
rs129768155519:46,205,076A/Guncertain significance
rs74639261119:46,206,183T/Cuncertain significance
rs13804620819:46,206,190G/Alikely benign
rs119303609119:46,206,219C/Tuncertain significance
rs196783786519:46,206,225C/Auncertain significance
rs93568977719:46,206,239C/Tuncertain significance
rs11722057319:46,206,249C/Tlikely benign
rs77545143719:46,206,267G/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.