FCER1A
Fc epsilon receptor Ia
Summary
The immunoglobulin epsilon receptor (IgE receptor) is the initiator of the allergic response. When two or more high-affinity IgE receptors are brought together by allergen-bound IgE molecules, mediators such as histamine that are responsible for allergy symptoms are released. This receptor is comprised of an alpha subunit, a beta subunit, and two gamma subunits. The protein encoded by this gene represents the alpha subunit. [provided by RefSeq, Aug 2011]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10908703 | 1:159,252,002 | G/A | regulatory region variant | — |
| rs2494262 | 1:159,253,672 | C/A | upstream gene variant | — |
| rs2427837 | 1:159,258,545 | G/A | upstream gene variant | — |
| rs118011213 | 1:159,262,944 | T/C | intron variant | — |
| rs2427824 | 1:159,265,062 | T/C | intron variant | — |
| rs6665683 | 1:159,265,128 | C/T | intron variant | — |
| rs12136904 | 1:159,265,892 | T/C | intron variant | — |
| rs7548864 | 1:159,267,255 | G/A | intron variant | — |
| rs2427827 | 1:159,271,811 | T/A | — | — |
| rs2251746 | 1:159,272,060 | T/C | intron variant | — |
| rs145202898 | 1:159,273,825 | A/G | — | uncertain significance |
| rs1342196294 | 1:159,273,841 | A/G | — | uncertain significance |
| rs750378478 | 1:159,273,847 | G/A | — | uncertain significance |
| rs2298804 | 1:159,273,892 | A/G | missense variant | benign |
| rs2298805 | 1:159,273,943 | G/A | missense variant | benign |
| rs138210256 | 1:159,273,965 | C/T | — | benign |
| rs2269718 | 1:159,275,706 | G/C | — | — |
| rs891224869 | 1:159,275,807 | G/A | — | uncertain significance |
| rs767306097 | 1:159,275,820 | G/T | — | uncertain significance |
| rs2524876615 | 1:159,275,831 | T/A | — | uncertain significance |
| rs2524876682 | 1:159,275,852 | A/G | — | uncertain significance |
| rs2524876736 | 1:159,275,861 | G/A | — | likely benign |
| rs747310680 | 1:159,275,864 | G/A | — | uncertain significance |
| rs767348260 | 1:159,275,920 | C/A | — | uncertain significance |
| rs756874081 | 1:159,275,949 | T/C | — | uncertain significance |
| rs145443280 | 1:159,275,976 | C/T | — | benign |
| rs2524877483 | 1:159,276,012 | C/T | — | uncertain significance |
| rs146511084 | 1:159,277,672 | G/T | — | uncertain significance |
| rs201635034 | 1:159,277,673 | G/C | — | uncertain significance |
| rs143576640 | 1:159,277,682 | T/G | — | uncertain significance |
| rs41264475 | 1:159,277,689 | A/C | — | benign |
| rs143419433 | 1:159,277,709 | C/T | — | benign |
| rs2494250 | 1:159,278,251 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.