KIR3DL3

killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3

Summary

Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several "framework" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the "framework" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]

Known Variants44 total

rsidPosition (GRCh37)AllelesClassClinVar
rs89211648119:55,236,006C/T—uncertain significance
rs251531438119:55,236,024T/C—uncertain significance
rs138541681919:55,237,617G/A—uncertain significance
rs146343395319:55,237,662T/C—uncertain significance
rs206815305619:55,237,667C/G—uncertain significance
rs37042321719:55,237,678G/A—uncertain significance
rs127017635619:55,237,746C/G—uncertain significance
rs77862011519:55,237,768C/T—uncertain significance
rs75696903319:55,237,774C/T—uncertain significance
rs77803627819:55,237,785G/C—likely benign
rs133124812819:55,239,128C/T—uncertain significance
rs206833769919:55,239,133G/C—uncertain significance
rs206834065319:55,239,148C/A—uncertain significance
rs147326334819:55,239,152G/A—uncertain significance
rs6213266519:55,239,168G/Tmissense variant—
rs144474676219:55,239,212C/A—uncertain significance
rs20159136119:55,239,218G/A—likely benign
rs54656287819:55,239,237C/T—likely benign
rs36788609719:55,239,242C/T—uncertain significance
rs75709206519:55,239,367G/A—uncertain significance
rs131649482719:55,240,992C/T—uncertain significance
rs129379009519:55,241,042C/T—uncertain significance
rs90395135419:55,241,078G/A—uncertain significance
rs117588535819:55,241,115G/T—uncertain significance
rs130382157819:55,241,145C/T—uncertain significance
rs120395280019:55,241,181G/A—uncertain significance
rs146240092019:55,241,184T/C—uncertain significance
rs86588722719:55,241,211C/T—likely benign
rs130520818519:55,241,232C/T—uncertain significance
rs60244419:55,246,731C/Tmissense variant—
rs66238619:55,246,741T/A—uncertain significance
rs120411606219:55,246,770C/A—uncertain significance
rs251547648319:55,246,794C/T—uncertain significance
rs117581804619:55,246,800C/T—uncertain significance
rs75278081719:55,246,803C/T—uncertain significance
rs18944534919:55,246,808G/C—uncertain significance
rs74566594419:55,247,293T/C—likely benign
rs206950103919:55,247,316G/A—uncertain significance
rs75569122419:55,247,457C/A—uncertain significance
rs74706989419:55,247,485T/G—uncertain significance
rs56409701519:55,247,492G/A—uncertain significance
rs75373530619:55,247,525C/G—conflicting classifications of pathogenicity
rs76501590419:55,247,540C/A—uncertain significance
rs36963734519:55,247,546A/G—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.