FCRLA
Fc receptor like A
Summary
This gene encodes a protein similar to receptors for the Fc fragment of gamma immunoglobulin (IgG). These receptors, referred to as FCGRs, mediate the destruction of IgG-coated antigens and of cells induced by antibodies. This encoded protein is selectively expressed in B cells, and may be involved in their development. This protein may also be involved in the development of lymphomas. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Aug 2011]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138600205 | 1:161,677,073 | C/T | — | uncertain significance |
| rs377168024 | 1:161,677,107 | T/G | — | uncertain significance |
| rs1194320206 | 1:161,680,637 | G/A | — | uncertain significance |
| rs139913866 | 1:161,681,040 | G/A | — | uncertain significance |
| rs750920328 | 1:161,681,051 | G/A | — | uncertain significance |
| rs145767742 | 1:161,681,082 | C/T | — | uncertain significance |
| rs61741806 | 1:161,681,087 | A/G | — | benign |
| rs371004106 | 1:161,681,132 | G/A | — | uncertain significance |
| rs1683092238 | 1:161,681,151 | C/T | — | uncertain significance |
| rs376314134 | 1:161,681,165 | C/A | — | uncertain significance |
| rs765507997 | 1:161,681,741 | A/G | — | likely benign |
| rs34733000 | 1:161,681,753 | G/C | — | benign |
| rs1196148552 | 1:161,681,813 | C/T | — | uncertain significance |
| rs546820153 | 1:161,681,831 | G/A | — | likely benign |
| rs902086098 | 1:161,681,861 | G/A | — | uncertain significance |
| rs369619169 | 1:161,681,867 | A/G | — | uncertain significance |
| rs117378923 | 1:161,681,870 | G/A | — | benign |
| rs2524933558 | 1:161,681,871 | T/G | — | uncertain significance |
| rs139679038 | 1:161,682,480 | G/A | intron variant | — |
| rs144052294 | 1:161,682,865 | C/T | — | benign |
| rs2101663254 | 1:161,682,884 | G/T | — | uncertain significance |
| rs775704128 | 1:161,682,938 | G/A | — | likely benign |
| rs2524941862 | 1:161,683,026 | G/T | — | uncertain significance |
| rs1386093942 | 1:161,683,087 | G/C | — | uncertain significance |
| rs61741808 | 1:161,683,116 | G/A | — | benign |
| rs2524943478 | 1:161,683,151 | C/A | — | uncertain significance |
| rs148913495 | 1:161,683,567 | A/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.