PLCD4

phospholipase C delta 4

Summary

This gene encodes a member of the delta class of phospholipase C enzymes. Phospholipase C enzymes play a critical role in many cellular processes by hydrolyzing phosphatidylinositol 4,5-bisphosphate into two intracellular second messengers, inositol 1,4,5-trisphosphate and diacylglycerol. Expression of this gene may be a marker for cancer. [provided by RefSeq, Jan 2011]

Known Variants55 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75629732:219,471,455T/Cupstream gene variant
rs8328052:219,473,737T/G
rs8328062:219,473,914A/Tintron variant
rs7616323512:219,480,467C/Tuncertain significance
rs3695502682:219,480,688G/Tuncertain significance
rs15750156082:219,480,689T/Cuncertain significance
rs2000316712:219,480,733C/Tlikely benign
rs3733623012:219,480,755C/Tuncertain significance
rs4857652:219,480,804G/Aregulatory region variant
rs24695271722:219,483,334G/Tuncertain significance
rs2018963702:219,483,412C/Tuncertain significance
rs24695275992:219,483,418T/Guncertain significance
rs24695278322:219,483,482T/Cuncertain significance
rs7738535952:219,483,497T/Cuncertain significance
rs2010002912:219,483,506T/Cuncertain significance
rs2009729232:219,483,521G/Auncertain significance
rs2008633932:219,483,526G/Cuncertain significance
rs1401943962:219,483,536G/Alikely benign
rs2002228522:219,486,203G/Auncertain significance
rs5641168742:219,486,263C/Tuncertain significance
rs7547145592:219,486,264G/Auncertain significance
rs7484685292:219,487,442C/Tuncertain significance
rs3702009302:219,487,460C/Auncertain significance
rs16959467332:219,487,547T/Clikely benign
rs5348636702:219,492,850G/Tuncertain significance
rs7658515622:219,492,862C/Auncertain significance
rs16961975642:219,492,896A/Guncertain significance
rs7707235602:219,494,252C/Tuncertain significance
rs7762491942:219,494,253G/Auncertain significance
rs2002586402:219,494,261C/Tuncertain significance
rs12529596652:219,494,267G/Auncertain significance
rs2010519962:219,495,382T/Cuncertain significance
rs24695636672:219,495,404A/Guncertain significance
rs2003312192:219,495,439G/Tuncertain significance
rs3754128582:219,495,443G/Alikely benign
rs2000999652:219,495,446A/Tuncertain significance
rs5273879252:219,495,484A/Guncertain significance
rs7711673452:219,495,503C/Tuncertain significance
rs617522102:219,496,909A/Glikely benign
rs7519003222:219,498,439T/Cuncertain significance
rs5299177512:219,498,866C/Tuncertain significance
rs5481139682:219,498,867G/Auncertain significance
rs2006889972:219,498,943G/Auncertain significance
rs3768384392:219,499,237C/Tuncertain significance
rs7557554402:219,499,249G/Auncertain significance
rs9395984822:219,500,547T/Cuncertain significance
rs7733360492:219,500,610G/Auncertain significance
rs7629523242:219,500,629G/Alikely benign
rs7816678982:219,500,651A/Guncertain significance
rs7679997142:219,500,996G/Auncertain significance
rs13136643902:219,501,052G/Alikely benign
rs7750963362:219,501,065G/Auncertain significance
rs7682409052:219,501,089C/Tuncertain significance
rs16967501922:219,501,107T/Cuncertain significance
rs7717372112:219,501,200G/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.