IRAG2
inositol 1,4,5-triphosphate receptor associated 2
Summary
The protein encode dby this gene is expressed in a developmentally regulated manner in lymphoid cell lines and tissues. The protein is localized to the cytoplasmic face of the endoplasmic reticulum. [provided by RefSeq, Jul 2008]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11047759 | 12:25,170,545 | T/C | regulatory region variant | — |
| rs1683181 | 12:25,193,775 | A/T | — | — |
| rs7295158 | 12:25,194,305 | C/G | — | — |
| rs1117117 | 12:25,199,496 | A/G | intron variant | — |
| rs755476102 | 12:25,222,357 | A/C | — | uncertain significance |
| rs769411549 | 12:25,232,179 | A/G | — | uncertain significance |
| rs144164545 | 12:25,232,333 | G/A | — | uncertain significance |
| rs147316104 | 12:25,232,608 | T/A | — | uncertain significance |
| rs76425591 | 12:25,232,641 | C/T | — | uncertain significance |
| rs1206099817 | 12:25,232,685 | A/T | — | uncertain significance |
| rs1312719792 | 12:25,236,368 | G/C | — | uncertain significance |
| rs767717485 | 12:25,236,416 | A/G | — | uncertain significance |
| rs149941754 | 12:25,254,116 | G/A | — | uncertain significance |
| rs776741440 | 12:25,254,119 | G/A | — | uncertain significance |
| rs531075630 | 12:25,254,164 | T/C | — | uncertain significance |
| rs2548199997 | 12:25,254,167 | A/G | — | uncertain significance |
| rs2140239210 | 12:25,254,245 | C/T | — | uncertain significance |
| rs2548211096 | 12:25,256,777 | T/C | — | uncertain significance |
| rs2548212027 | 12:25,256,965 | A/G | — | uncertain significance |
| rs775148882 | 12:25,257,297 | G/A | — | uncertain significance |
| rs766820531 | 12:25,260,827 | A/G | — | likely benign |
| rs1036017113 | 12:25,260,888 | A/G | — | uncertain significance |
| rs755949382 | 12:25,260,902 | G/A | — | uncertain significance |
| rs2548239678 | 12:25,260,915 | A/G | — | uncertain significance |
| rs1949336394 | 12:25,260,984 | C/T | — | uncertain significance |
| rs766913522 | 12:25,260,987 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.