LILRB2
leukocyte immunoglobulin like receptor B2
Summary
This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1430091303 | 19:54,778,565 | C/T | — | uncertain significance |
| rs202182093 | 19:54,778,577 | G/A | — | uncertain significance |
| rs111579555 | 19:54,778,652 | G/A | — | uncertain significance |
| rs150493192 | 19:54,778,665 | G/A | — | uncertain significance |
| rs192506020 | 19:54,778,830 | G/A | intron variant | — |
| rs140268965 | 19:54,779,669 | G/A | intron variant | — |
| rs201537103 | 19:54,779,829 | T/C | — | likely benign |
| rs369899348 | 19:54,780,139 | C/A | — | uncertain significance |
| rs2080229671 | 19:54,780,267 | C/T | — | likely benign |
| rs2080232264 | 19:54,780,299 | C/A | — | uncertain significance |
| rs759287360 | 19:54,780,304 | C/G | — | uncertain significance |
| rs749515031 | 19:54,780,684 | C/T | — | uncertain significance |
| rs201896387 | 19:54,780,736 | C/T | — | likely benign |
| rs778175152 | 19:54,780,761 | A/C | — | likely benign |
| rs1379509942 | 19:54,780,780 | A/G | — | uncertain significance |
| rs400942 | 19:54,781,557 | T/C | upstream gene variant | — |
| rs148321423 | 19:54,781,773 | G/T | — | uncertain significance |
| rs777069556 | 19:54,782,123 | C/T | — | uncertain significance |
| rs188934193 | 19:54,782,135 | G/T | — | uncertain significance |
| rs4993136 | 19:54,782,136 | C/G | — | likely benign |
| rs4993135 | 19:54,782,150 | A/T | — | likely benign |
| rs2080344755 | 19:54,782,152 | A/G | — | uncertain significance |
| rs2080350756 | 19:54,782,212 | G/A | — | uncertain significance |
| rs774788417 | 19:54,782,244 | C/G | — | uncertain significance |
| rs530711389 | 19:54,782,268 | T/G | — | likely benign |
| rs751598076 | 19:54,782,272 | C/T | — | uncertain significance |
| rs139074135 | 19:54,782,277 | T/G | — | likely benign |
| rs767551261 | 19:54,782,279 | G/C | — | uncertain significance |
| rs199535116 | 19:54,782,364 | G/C | — | likely benign |
| rs758836194 | 19:54,782,371 | G/A | — | uncertain significance |
| rs771938857 | 19:54,782,411 | T/A | — | uncertain significance |
| rs773696400 | 19:54,782,703 | A/C | — | uncertain significance |
| rs1228920944 | 19:54,782,717 | A/G | — | uncertain significance |
| rs532414442 | 19:54,782,828 | C/T | — | uncertain significance |
| rs576231032 | 19:54,783,217 | A/G | — | uncertain significance |
| rs201233860 | 19:54,783,233 | A/G | — | uncertain significance |
| rs201592158 | 19:54,783,244 | T/C | — | uncertain significance |
| rs200902973 | 19:54,783,265 | C/G | — | uncertain significance |
| rs199599364 | 19:54,783,272 | A/T | — | uncertain significance |
| rs774001588 | 19:54,783,278 | G/A | — | likely benign |
| rs771929420 | 19:54,783,280 | G/C | — | uncertain significance |
| rs776949112 | 19:54,783,289 | C/T | — | likely benign |
| rs199771422 | 19:54,783,296 | G/A | — | uncertain significance |
| rs755735810 | 19:54,783,302 | C/T | — | uncertain significance |
| rs143879306 | 19:54,783,315 | G/A | — | likely benign |
| rs771068803 | 19:54,783,323 | C/G | — | uncertain significance |
| rs148633009 | 19:54,783,337 | C/T | — | likely benign |
| rs140619167 | 19:54,783,457 | A/C | — | uncertain significance |
| rs754938207 | 19:54,783,465 | G/T | — | uncertain significance |
| rs764710286 | 19:54,783,470 | G/A | — | uncertain significance |
| rs383925 | 19:54,783,521 | C/T | upstream gene variant | — |
| rs758695722 | 19:54,783,660 | A/C | — | uncertain significance |
| rs778315782 | 19:54,783,739 | T/C | — | uncertain significance |
| rs1420250290 | 19:54,783,768 | A/C | — | uncertain significance |
| rs781553478 | 19:54,783,786 | C/T | — | uncertain significance |
| rs777134019 | 19:54,783,810 | T/C | — | uncertain significance |
| rs111453734 | 19:54,783,836 | G/A | synonymous variant | Likely benign |
| rs1212091770 | 19:54,783,880 | G/T | — | uncertain significance |
| rs383369 | 19:54,784,130 | T/C | missense variant | — |
| rs437236 | 19:54,786,341 | C/G | upstream gene variant | — |
| rs116877265 | 19:54,786,375 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.