PKN1

protein kinase N1

Summary

The protein encoded by this gene belongs to the protein kinase C superfamily. This kinase is activated by Rho family of small G proteins and may mediate the Rho-dependent signaling pathway. This kinase can be activated by phospholipids and by limited proteolysis. The 3-phosphoinositide dependent protein kinase-1 (PDPK1/PDK1) is reported to phosphorylate this kinase, which may mediate insulin signals to the actin cytoskeleton. The proteolytic activation of this kinase by caspase-3 or related proteases during apoptosis suggests its role in signal transduction related to apoptosis. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]

Known Variants74 total

rsidPosition (GRCh37)AllelesClassClinVar
rs133570069019:14,544,337G/Auncertain significance
rs37756615319:14,552,000G/Auncertain significance
rs76060893419:14,552,016C/Tuncertain significance
rs77536822319:14,552,111C/Tuncertain significance
rs93346417119:14,552,180C/Tuncertain significance
rs88929236419:14,552,196A/Guncertain significance
rs124852528419:14,552,225G/Auncertain significance
rs6098498319:14,553,265T/Cintron variant
rs76099204019:14,554,321C/Tuncertain significance
rs251281562119:14,554,337C/Auncertain significance
rs37209914819:14,554,339G/Auncertain significance
rs5581438219:14,554,394G/Abenign
rs75071763219:14,557,241C/Tuncertain significance
rs135043412319:14,557,312A/Cuncertain significance
rs75924901019:14,557,323C/Tuncertain significance
rs55382232619:14,557,331G/Auncertain significance
rs97872223219:14,561,133G/Cuncertain significance
rs251282208119:14,561,150G/Cuncertain significance
rs76851205219:14,561,183T/Auncertain significance
rs20021928619:14,561,212T/Clikely benign
rs104538529819:14,561,262A/Guncertain significance
rs76320779719:14,561,728A/Cuncertain significance
rs76118952019:14,561,856C/Auncertain significance
rs75590257819:14,561,900T/Auncertain significance
rs77478586719:14,561,913C/Tuncertain significance
rs56095091919:14,562,662T/Cuncertain significance
rs54479072619:14,562,692C/Tuncertain significance
rs37372506719:14,562,699C/Guncertain significance
rs20011827119:14,562,712A/Glikely benign
rs19954021519:14,562,742C/Tuncertain significance
rs77129800219:14,562,745C/Guncertain significance
rs36837198919:14,562,746C/Auncertain significance
rs74640441619:14,562,757C/Tuncertain significance
rs75254664619:14,562,802C/Tuncertain significance
rs20011626319:14,568,890A/Tuncertain significance
rs118219657119:14,568,891C/Tuncertain significance
rs251282972519:14,568,899A/Guncertain significance
rs76296813419:14,568,915A/Glikely benign
rs20172581819:14,569,047C/Tuncertain significance
rs55620384119:14,569,075G/Auncertain significance
rs76098341119:14,569,083C/Tuncertain significance
rs20142382619:14,569,194C/Abenign
rs37734099119:14,574,655G/Auncertain significance
rs20081305619:14,574,718A/Guncertain significance
rs13962232819:14,574,764C/Tlikely benign
rs36926711519:14,574,772G/Auncertain significance
rs3430923819:14,574,897C/Abenign
rs75296829919:14,574,900G/Auncertain significance
rs207150369519:14,578,398A/Guncertain significance
rs76100610419:14,578,407G/Cuncertain significance
rs37229941319:14,578,566C/Auncertain significance
rs77330351219:14,578,589G/Auncertain significance
rs74715672019:14,578,700G/Auncertain significance
rs76028847919:14,578,727G/Auncertain significance
rs75810215419:14,578,755T/Cuncertain significance
rs18818810319:14,580,239C/Tuncertain significance
rs77413933519:14,580,269C/Tuncertain significance
rs126255156919:14,580,320C/Tuncertain significance
rs129809741919:14,580,565T/Cuncertain significance
rs37087592419:14,580,612C/Guncertain significance
rs75797928919:14,580,619G/Auncertain significance
rs156835290119:14,580,623A/Guncertain significance
rs20054540119:14,580,993G/Auncertain significance
rs75173318219:14,581,053C/Tuncertain significance
rs78023089319:14,581,064G/Auncertain significance
rs76713876919:14,582,393A/Guncertain significance
rs251284615119:14,582,430C/Tuncertain significance
rs145657362319:14,582,482C/Tlikely benign
rs207155965719:14,582,502C/Auncertain significance
rs74766549719:14,582,522C/Tuncertain significance
rs78146721719:14,582,553A/Guncertain significance
rs75082394819:14,582,555G/Auncertain significance
rs78055464719:14,582,558G/Auncertain significance
rs5611975419:14,582,584C/Tbenign

Gene information from NCBI Gene. Variant classifications from ClinVar.