FCRL2
Fc receptor like 2
Summary
This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein has four extracellular C2-type immunoglobulin domains, a transmembrane domain and a cytoplasmic domain that contains one immunoreceptor-tyrosine activation motif and two immunoreceptor-tyrosine inhibitory motifs. This protein may be a prognostic marker for chronic lymphocytic leukemia. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Apr 2009]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139956304 | 1:157,716,564 | C/T | — | uncertain significance |
| rs758612307 | 1:157,718,396 | T/A | — | uncertain significance |
| rs759712456 | 1:157,718,715 | T/C | — | uncertain significance |
| rs745484920 | 1:157,718,746 | C/G | — | uncertain significance |
| rs1239488818 | 1:157,719,444 | G/C | — | uncertain significance |
| rs550773131 | 1:157,722,335 | C/A | — | — |
| rs569207310 | 1:157,725,859 | G/C | — | — |
| rs187642743 | 1:157,727,298 | C/T | intron variant | — |
| rs183702416 | 1:157,731,683 | G/A | intron variant | — |
| rs2525246205 | 1:157,736,692 | A/T | — | uncertain significance |
| rs149829829 | 1:157,737,066 | C/T | — | uncertain significance |
| rs1437165407 | 1:157,737,071 | T/C | — | uncertain significance |
| rs2525253089 | 1:157,737,164 | G/C | — | uncertain significance |
| rs1649583502 | 1:157,737,168 | C/T | — | likely benign |
| rs144781687 | 1:157,737,195 | T/C | — | uncertain significance |
| rs376615407 | 1:157,737,218 | T/C | — | uncertain significance |
| rs144215277 | 1:157,737,287 | C/T | — | uncertain significance |
| rs369279577 | 1:157,737,288 | G/A | — | uncertain significance |
| rs2525265929 | 1:157,738,209 | A/C | — | uncertain significance |
| rs774232460 | 1:157,738,237 | T/C | — | uncertain significance |
| rs1649700012 | 1:157,738,245 | T/C | — | uncertain significance |
| rs749857247 | 1:157,738,276 | C/T | — | uncertain significance |
| rs138710224 | 1:157,738,309 | G/T | missense variant | — |
| rs746087124 | 1:157,738,395 | C/T | — | uncertain significance |
| rs138011295 | 1:157,739,752 | C/A | — | uncertain significance |
| rs766083921 | 1:157,739,859 | C/T | — | likely benign |
| rs780265354 | 1:157,739,914 | C/T | — | uncertain significance |
| rs543447651 | 1:157,739,922 | A/G | — | uncertain significance |
| rs139872242 | 1:157,739,929 | G/A | — | uncertain significance |
| rs368390897 | 1:157,740,211 | T/C | — | uncertain significance |
| rs745793091 | 1:157,740,316 | A/G | — | uncertain significance |
| rs375921670 | 1:157,740,347 | A/T | — | uncertain significance |
| rs375240841 | 1:157,740,417 | C/T | — | uncertain significance |
| rs377455239 | 1:157,740,422 | G/T | — | uncertain significance |
| rs1312452990 | 1:157,740,432 | G/A | — | uncertain significance |
| rs753453396 | 1:157,740,436 | G/A | — | uncertain significance |
| rs144041840 | 1:157,740,438 | G/A | — | uncertain significance |
| rs2210909 | 1:157,744,848 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.