ZDHHC11

zDHHC palmitoyltransferase 11

Summary

Enables signaling adaptor activity. Involved in antiviral innate immune response and positive regulation of defense response to virus by host. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants60 total

rsidPosition (GRCh37)AllelesClassClinVar
rs17383517705:801,248T/Cuncertain significance
rs3768571685:801,263T/Cuncertain significance
rs7704370845:801,273T/Auncertain significance
rs14453325795:801,279C/Glikely benign
rs74450175:813,070T/Cupstream gene variant
rs7645030215:814,887T/Cuncertain significance
rs1443767685:814,888A/Glikely benign
rs2009552485:814,895G/Auncertain significance
rs1917575905:814,915G/Clikely benign
rs68756885:818,479C/Tdownstream gene variant
rs7776938085:819,650G/Auncertain significance
rs5720012575:819,653C/Tuncertain significance
rs1488057105:819,657C/Guncertain significance
rs1416229655:819,669C/Tuncertain significance
rs1999811835:819,682C/Glikely benign
rs1478149105:819,708G/Auncertain significance
rs3767014565:821,980G/Cuncertain significance
rs7681058215:821,994G/Auncertain significance
rs28784675:825,331T/Guncertain significance
rs117451325:831,486G/Tintron variant
rs7568517175:833,890C/Guncertain significance
rs7687182545:837,498C/Tuncertain significance
rs7627618805:837,505A/Guncertain significance
rs15612749605:837,535T/Cuncertain significance
rs5281164355:837,553C/Tuncertain significance
rs7750302915:837,590T/Cuncertain significance
rs38228105:840,357G/Alikely benign
rs12003086405:840,646G/Auncertain significance
rs13280782385:840,705G/Cuncertain significance
rs2005735995:840,720G/Auncertain significance
rs17446820845:840,753A/Cuncertain significance
rs3695793515:843,732G/Auncertain significance
rs7465309615:843,735C/Tuncertain significance
rs3710353355:843,754C/Tuncertain significance
rs1442124715:843,759T/Cuncertain significance
rs7490985775:843,775A/Guncertain significance
rs3759648575:843,787C/Tlikely benign
rs17454845135:843,825G/Clikely benign
rs7750534135:847,662C/Guncertain significance
rs5752282095:847,685G/Alikely benign
rs13174112225:847,698T/Cuncertain significance
rs9050706965:847,727G/Cuncertain significance
rs12206646105:848,709C/Tuncertain significance
rs7464276995:848,718C/Tuncertain significance
rs7477724275:848,739G/Auncertain significance
rs7583414445:848,765C/Guncertain significance
rs3741512135:850,498C/Guncertain significance
rs7809127685:850,500T/Cuncertain significance
rs25311213775:850,504C/Tuncertain significance
rs2016909525:850,514C/Guncertain significance
rs1442935405:850,526C/Tlikely benign
rs11884621075:850,600A/Cuncertain significance
rs17470231355:850,605A/Tuncertain significance
rs1470922945:850,639G/Auncertain significance
rs12211617215:850,641G/Auncertain significance
rs7623039655:850,644G/Auncertain significance
rs1426409015:850,662T/Cuncertain significance
rs1926299795:850,677T/Guncertain significance
rs1503546465:850,687C/Abenign
rs2021905345:850,702C/Tlikely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.