CRACR2A
calcium release activated channel regulator 2A
Summary
Enables GTPase activity and calcium ion binding activity. Involved in several processes, including activation of store-operated calcium channel activity; positive regulation of JNK cascade; and store-operated calcium entry. Located in several cellular components, including Golgi apparatus; Weibel-Palade body; and immunological synapse. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368941338 | 12:3,724,556 | C/T | — | uncertain significance |
| rs548678583 | 12:3,724,598 | T/G | — | uncertain significance |
| rs1358977728 | 12:3,728,445 | G/T | — | uncertain significance |
| rs368994549 | 12:3,728,454 | C/T | — | uncertain significance |
| rs374975538 | 12:3,728,463 | G/A | — | uncertain significance |
| rs2497459749 | 12:3,728,470 | T/G | — | uncertain significance |
| rs745311292 | 12:3,728,474 | C/T | — | uncertain significance |
| rs751604518 | 12:3,728,535 | C/A | — | uncertain significance |
| rs768992580 | 12:3,736,663 | A/G | — | uncertain significance |
| rs10848893 | 12:3,736,734 | T/C | — | benign |
| rs10848894 | 12:3,736,745 | T/C | — | benign |
| rs760727400 | 12:3,736,797 | T/C | — | uncertain significance |
| rs764222855 | 12:3,736,824 | G/A | — | uncertain significance |
| rs905715810 | 12:3,736,837 | T/C | — | likely benign |
| rs2497520409 | 12:3,736,840 | C/A | — | uncertain significance |
| rs765399992 | 12:3,736,860 | C/T | — | uncertain significance |
| rs17836183 | 12:3,736,940 | T/C | — | benign |
| rs375420342 | 12:3,742,796 | A/T | — | uncertain significance |
| rs1944412350 | 12:3,742,797 | A/G | — | uncertain significance |
| rs1016900077 | 12:3,742,841 | G/A | — | uncertain significance |
| rs145536162 | 12:3,747,284 | C/T | — | likely benign |
| rs532414144 | 12:3,747,324 | C/T | — | uncertain significance |
| rs1156518985 | 12:3,747,340 | T/C | — | uncertain significance |
| rs748957811 | 12:3,747,363 | G/A | — | uncertain significance |
| rs962413675 | 12:3,747,379 | C/A | — | uncertain significance |
| rs370926137 | 12:3,747,386 | G/C | — | uncertain significance |
| rs1484448376 | 12:3,747,390 | G/A | — | uncertain significance |
| rs1447850859 | 12:3,747,453 | G/A | — | uncertain significance |
| rs373216321 | 12:3,747,486 | C/T | — | uncertain significance |
| rs759439857 | 12:3,747,495 | C/T | — | uncertain significance |
| rs1333629609 | 12:3,747,499 | G/C | — | uncertain significance |
| rs760222760 | 12:3,747,502 | A/G | — | uncertain significance |
| rs917707075 | 12:3,747,504 | G/A | — | uncertain significance |
| rs368233027 | 12:3,747,610 | C/T | — | uncertain significance |
| rs4766152 | 12:3,750,128 | T/A | — | — |
| rs865893443 | 12:3,750,913 | C/G | — | uncertain significance |
| rs2497653433 | 12:3,750,934 | A/G | — | uncertain significance |
| rs2497654158 | 12:3,750,987 | C/A | — | uncertain significance |
| rs7297853 | 12:3,751,046 | T/C | — | benign |
| rs761233575 | 12:3,753,787 | G/A | — | uncertain significance |
| rs887304 | 12:3,757,548 | T/C | intron variant | benign |
| rs201378260 | 12:3,757,736 | C/T | — | uncertain significance |
| rs773874892 | 12:3,757,747 | C/T | — | uncertain significance |
| rs372821272 | 12:3,757,762 | G/A | — | uncertain significance |
| rs763119535 | 12:3,757,768 | C/T | — | uncertain significance |
| rs12229948 | 12:3,763,317 | A/G | — | benign |
| rs369767255 | 12:3,763,393 | T/G | — | uncertain significance |
| rs2497768762 | 12:3,763,405 | G/A | — | uncertain significance |
| rs1944859758 | 12:3,763,526 | C/A | — | no classification for the single variant |
| rs541326469 | 12:3,765,501 | C/A | — | uncertain significance |
| rs2497790774 | 12:3,765,539 | G/T | — | uncertain significance |
| rs10848906 | 12:3,768,705 | C/A | — | benign |
| rs767844257 | 12:3,768,764 | T/G | — | uncertain significance |
| rs36030417 | 12:3,782,647 | A/T | — | benign |
| rs747013591 | 12:3,782,652 | C/T | — | uncertain significance |
| rs17697920 | 12:3,782,701 | C/T | — | benign |
| rs2497954528 | 12:3,782,718 | C/T | — | uncertain significance |
| rs61907258 | 12:3,782,779 | A/G | — | benign |
| rs73049123 | 12:3,787,238 | T/C | intron variant | — |
| rs748749655 | 12:3,788,092 | C/A | — | uncertain significance |
| rs773895003 | 12:3,788,102 | C/A | — | uncertain significance |
| rs571600929 | 12:3,788,115 | T/G | — | uncertain significance |
| rs242018 | 12:3,788,145 | C/T | — | benign |
| rs1945393506 | 12:3,788,175 | T/C | — | no classification for the single variant |
| rs1367451908 | 12:3,788,183 | T/C | — | uncertain significance |
| rs3803135 | 12:3,788,188 | C/T | — | benign |
| rs375574366 | 12:3,788,202 | G/A | — | uncertain significance |
| rs242017 | 12:3,788,222 | G/A | — | benign |
| rs148809643 | 12:3,789,422 | C/T | — | uncertain significance |
| rs749668480 | 12:3,789,434 | G/T | — | uncertain significance |
| rs17836273 | 12:3,789,452 | C/T | — | benign |
| rs61537702 | 12:3,789,562 | G/C | — | benign |
| rs57335133 | 12:3,789,563 | G/A | — | benign |
| rs17780600 | 12:3,789,607 | T/G | — | benign |
| rs577454892 | 12:3,791,373 | C/T | — | — |
| rs140037248 | 12:3,796,633 | A/G | downstream gene variant | — |
| rs150886385 | 12:3,805,955 | C/T | — | uncertain significance |
| rs144314920 | 12:3,805,977 | A/C | — | uncertain significance |
| rs143641818 | 12:3,806,092 | C/G | — | uncertain significance |
| rs145705713 | 12:3,806,137 | G/C | — | uncertain significance |
| rs9788233 | 12:3,806,147 | T/C | — | benign |
| rs10848911 | 12:3,814,238 | G/A | regulatory region variant | — |
| rs4766165 | 12:3,840,045 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.