FCRL3
Fc receptor like 3
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 contains immunoreceptor-tyrosine activation motifs and immunoreceptor-tyrosine inhibitory motifs in its cytoplasmic domain and may play a role in regulation of the immune system. Mutations in this gene have been associated with rheumatoid arthritis, autoimmune thyroid disease, and systemic lupus erythematosus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs555967986 | 1:157,646,731 | C/T | — | — |
| rs11264793 | 1:157,647,526 | A/T | 3 prime UTR variant | — |
| rs529726252 | 1:157,647,784 | T/C | — | — |
| rs11264794 | 1:157,647,789 | C/G | — | — |
| rs79629970 | 1:157,648,463 | T/C | 3 prime UTR variant | — |
| rs2282284 | 1:157,648,543 | T/C | — | benign |
| rs200672131 | 1:157,648,601 | C/T | — | uncertain significance |
| rs142600487 | 1:157,648,630 | T/C | — | uncertain significance |
| rs2524874531 | 1:157,650,497 | T/C | — | uncertain significance |
| rs770643906 | 1:157,650,552 | C/T | — | uncertain significance |
| rs778720169 | 1:157,650,772 | A/T | — | uncertain significance |
| rs139426571 | 1:157,650,798 | T/C | — | likely benign |
| rs777673180 | 1:157,650,857 | G/A | — | likely benign |
| rs146903009 | 1:157,650,874 | C/T | — | benign |
| rs141955468 | 1:157,652,679 | A/G | intron variant | — |
| rs139081042 | 1:157,653,034 | C/T | — | uncertain significance |
| rs141518688 | 1:157,654,624 | G/A | intron variant | — |
| rs114856780 | 1:157,655,676 | A/T | intron variant | — |
| rs199966528 | 1:157,659,599 | C/T | — | likely benign |
| rs145354138 | 1:157,659,642 | C/T | — | uncertain significance |
| rs758631183 | 1:157,659,678 | C/A | — | uncertain significance |
| rs761616785 | 1:157,660,056 | A/G | — | uncertain significance |
| rs151320709 | 1:157,660,059 | G/A | — | uncertain significance |
| rs143115777 | 1:157,660,155 | C/T | — | uncertain significance |
| rs369176005 | 1:157,660,198 | C/T | — | uncertain significance |
| rs147268020 | 1:157,660,221 | G/A | — | uncertain significance |
| rs371736717 | 1:157,660,228 | A/C | — | uncertain significance |
| rs144058263 | 1:157,660,251 | A/G | — | uncertain significance |
| rs143597458 | 1:157,660,285 | C/T | — | uncertain significance |
| rs143813895 | 1:157,660,318 | C/T | — | uncertain significance |
| rs78256272 | 1:157,662,659 | G/A | intron variant | — |
| rs750260814 | 1:157,665,148 | T/C | — | likely benign |
| rs756403772 | 1:157,665,167 | T/C | — | uncertain significance |
| rs746248621 | 1:157,665,202 | G/A | — | uncertain significance |
| rs140279920 | 1:157,665,830 | T/C | — | likely benign |
| rs772016366 | 1:157,665,842 | C/T | — | uncertain significance |
| rs560196456 | 1:157,665,875 | C/T | — | likely benign |
| rs564259735 | 1:157,665,931 | T/A | — | uncertain significance |
| rs757865879 | 1:157,665,970 | A/G | — | uncertain significance |
| rs754875256 | 1:157,666,004 | A/G | — | uncertain significance |
| rs115903952 | 1:157,666,027 | G/T | — | likely benign |
| rs12041673 | 1:157,666,043 | G/A | — | benign |
| rs145953660 | 1:157,666,047 | C/G | — | uncertain significance |
| rs115596233 | 1:157,666,084 | C/A | — | benign |
| rs201499857 | 1:157,666,938 | C/T | — | likely benign |
| rs755220542 | 1:157,666,940 | T/C | — | uncertain significance |
| rs760066597 | 1:157,666,983 | G/C | — | uncertain significance |
| rs761802836 | 1:157,667,012 | G/T | — | uncertain significance |
| rs777897301 | 1:157,667,052 | C/T | — | uncertain significance |
| rs760856382 | 1:157,667,157 | G/A | — | uncertain significance |
| rs375297389 | 1:157,667,175 | G/A | — | uncertain significance |
| rs77395825 | 1:157,667,190 | C/T | — | uncertain significance |
| rs773307054 | 1:157,667,460 | A/G | — | uncertain significance |
| rs145082681 | 1:157,667,562 | A/T | — | uncertain significance |
| rs140499647 | 1:157,667,571 | A/G | — | likely benign |
| rs1318234267 | 1:157,667,614 | C/T | — | uncertain significance |
| rs140491666 | 1:157,667,693 | C/G | — | uncertain significance |
| rs758981784 | 1:157,668,263 | T/C | — | uncertain significance |
| rs149955856 | 1:157,668,314 | T/C | — | likely benign |
| rs761638478 | 1:157,668,354 | C/G | — | uncertain significance |
| rs752772268 | 1:157,668,378 | A/T | — | uncertain significance |
| rs7522061 | 1:157,668,390 | T/C | missense variant | — |
| rs137945167 | 1:157,668,419 | C/A | — | uncertain significance |
| rs2210912 | 1:157,668,701 | A/C | downstream gene variant | — |
| rs2210913 | 1:157,668,993 | C/T | downstream gene variant | — |
| rs3761959 | 1:157,669,278 | C/G | — | — |
| rs147133369 | 1:157,669,487 | T/C | — | uncertain significance |
| rs10489678 | 1:157,669,668 | G/C | — | — |
| rs375543095 | 1:157,670,276 | G/C | — | uncertain significance |
| rs945635 | 1:157,670,290 | C/T | — | — |
| rs11264799 | 1:157,670,757 | C/T | regulatory region variant | — |
| rs7528684 | 1:157,670,816 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.