MAST2
microtubule associated serine/threonine kinase 2
Summary
Enables phosphatase binding activity. Predicted to be involved in several processes, including protein phosphorylation; regulation of interleukin-12 production; and spermatid differentiation. Predicted to be located in cytoplasm; cytoskeleton; and plasma membrane. Predicted to be active in microtubule cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants141 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1396679922 | 1:46,269,596 | C/T | — | uncertain significance |
| rs1051120550 | 1:46,269,605 | C/T | — | uncertain significance |
| rs1229800479 | 1:46,269,667 | C/T | — | uncertain significance |
| rs1020485123 | 1:46,269,709 | C/G | — | uncertain significance |
| rs1644064745 | 1:46,269,713 | C/G | — | uncertain significance |
| rs1644065016 | 1:46,269,721 | G/C | — | uncertain significance |
| rs11211194 | 1:46,282,084 | C/T | intron variant | — |
| rs6695809 | 1:46,285,461 | T/A | — | — |
| rs11211199 | 1:46,287,869 | T/C | intron variant | — |
| rs116664070 | 1:46,290,097 | C/G | — | benign |
| rs368611726 | 1:46,290,129 | C/A | — | uncertain significance |
| rs1236613579 | 1:46,290,159 | A/T | — | uncertain significance |
| rs1465040082 | 1:46,290,178 | A/G | — | uncertain significance |
| rs924817352 | 1:46,290,234 | C/G | — | uncertain significance |
| rs1157252832 | 1:46,290,250 | C/T | — | uncertain significance |
| rs752883369 | 1:46,295,125 | C/G | — | uncertain significance |
| rs771976410 | 1:46,295,135 | G/T | — | uncertain significance |
| rs7526532 | 1:46,295,672 | G/A | — | — |
| rs10789475 | 1:46,304,177 | C/G | intron variant | — |
| rs61783217 | 1:46,324,165 | T/A | — | — |
| rs12751443 | 1:46,324,191 | C/T | intron variant | — |
| rs12145287 | 1:46,325,002 | C/G | intron variant | — |
| rs10890359 | 1:46,336,635 | A/T | — | — |
| rs746410267 | 1:46,348,066 | T/C | — | uncertain significance |
| rs7515491 | 1:46,355,079 | A/C | — | — |
| rs34444543 | 1:46,358,862 | G/A | intron variant | — |
| rs61296343 | 1:46,359,271 | T/A | intron variant | — |
| rs140601200 | 1:46,366,025 | C/T | regulatory region variant | — |
| rs35945607 | 1:46,381,239 | G/A | — | — |
| rs34907901 | 1:46,405,214 | T/A | — | — |
| rs1196113701 | 1:46,420,431 | A/G | — | — |
| rs142661646 | 1:46,425,062 | C/T | — | benign |
| rs1204914972 | 1:46,425,120 | G/A | — | uncertain significance |
| rs7520050 | 1:46,432,105 | A/C | — | — |
| rs12760175 | 1:46,447,840 | G/C | intron variant | — |
| rs2523325324 | 1:46,463,403 | T/G | — | uncertain significance |
| rs774377481 | 1:46,463,411 | A/G | — | uncertain significance |
| rs1050107601 | 1:46,463,429 | C/T | — | uncertain significance |
| rs763839590 | 1:46,463,467 | C/T | — | uncertain significance |
| rs11589562 | 1:46,466,721 | T/C | intron variant | — |
| rs372615184 | 1:46,472,045 | C/T | — | uncertain significance |
| rs1407180498 | 1:46,472,057 | C/T | — | uncertain significance |
| rs202066492 | 1:46,476,447 | A/G | — | uncertain significance |
| rs779007034 | 1:46,476,449 | C/A | — | uncertain significance |
| rs200211912 | 1:46,476,523 | G/A | — | uncertain significance |
| rs527729571 | 1:46,476,566 | A/G | — | likely benign |
| rs201377643 | 1:46,481,799 | C/G | — | — |
| rs369921244 | 1:46,485,283 | G/A | — | uncertain significance |
| rs763749553 | 1:46,485,334 | A/G | — | likely benign |
| rs201649155 | 1:46,485,342 | C/T | — | likely benign |
| rs749944799 | 1:46,485,353 | G/A | — | uncertain significance |
| rs773913950 | 1:46,487,680 | A/G | — | uncertain significance |
| rs201576606 | 1:46,487,710 | G/A | — | uncertain significance |
| rs2523930607 | 1:46,487,737 | C/T | — | uncertain significance |
| rs1218606138 | 1:46,488,631 | T/G | — | uncertain significance |
| rs199547415 | 1:46,488,914 | G/C | — | likely benign |
| rs781306104 | 1:46,488,974 | A/C | — | uncertain significance |
| rs1646292303 | 1:46,489,542 | C/T | — | uncertain significance |
| rs765230688 | 1:46,489,620 | G/A | — | uncertain significance |
| rs761923801 | 1:46,491,418 | C/T | — | uncertain significance |
| rs785479 | 1:46,492,144 | C/T | regulatory region variant | — |
| rs1010065196 | 1:46,493,425 | C/T | — | uncertain significance |
| rs966314117 | 1:46,493,508 | G/C | — | uncertain significance |
| rs1424110975 | 1:46,494,522 | G/T | — | uncertain significance |
| rs191974594 | 1:46,494,589 | T/C | — | likely benign |
| rs376806114 | 1:46,495,146 | G/T | — | uncertain significance |
| rs142312565 | 1:46,495,155 | G/A | — | benign |
| rs2524174462 | 1:46,495,171 | T/G | — | uncertain significance |
| rs762356466 | 1:46,495,212 | C/G | — | uncertain significance |
| rs946354215 | 1:46,495,512 | A/G | — | uncertain significance |
| rs778825675 | 1:46,495,562 | C/G | — | uncertain significance |
| rs1015671091 | 1:46,495,622 | G/A | — | uncertain significance |
| rs772384498 | 1:46,495,804 | G/A | — | uncertain significance |
| rs760785043 | 1:46,495,809 | G/A | — | uncertain significance |
| rs201379913 | 1:46,495,813 | G/A | — | uncertain significance |
| rs540837696 | 1:46,496,279 | G/A | — | uncertain significance |
| rs199702861 | 1:46,496,298 | G/A | — | uncertain significance |
| rs376686790 | 1:46,496,319 | G/A | — | uncertain significance |
| rs923656781 | 1:46,496,321 | C/T | — | uncertain significance |
| rs367655419 | 1:46,496,322 | G/A | — | uncertain significance |
| rs755350919 | 1:46,496,330 | C/T | — | uncertain significance |
| rs778084119 | 1:46,496,341 | G/T | — | uncertain significance |
| rs187418587 | 1:46,496,343 | G/A | — | uncertain significance |
| rs1228229619 | 1:46,496,352 | G/A | — | uncertain significance |
| rs371392889 | 1:46,496,378 | G/A | — | uncertain significance |
| rs753126429 | 1:46,496,406 | G/A | — | uncertain significance |
| rs201897607 | 1:46,496,777 | C/T | — | likely benign |
| rs9429087 | 1:46,496,829 | A/G | — | benign |
| rs952272792 | 1:46,496,867 | G/T | — | uncertain significance |
| rs368847255 | 1:46,496,875 | G/A | — | uncertain significance |
| rs748579768 | 1:46,496,960 | C/G | — | uncertain significance |
| rs1407522125 | 1:46,497,066 | T/C | — | uncertain significance |
| rs778296919 | 1:46,497,140 | C/T | — | uncertain significance |
| rs775729504 | 1:46,497,155 | C/T | — | uncertain significance |
| rs751193932 | 1:46,497,221 | G/A | — | uncertain significance |
| rs9429088 | 1:46,497,500 | T/G | — | — |
| rs1024963583 | 1:46,497,861 | T/A | — | uncertain significance |
| rs1210119735 | 1:46,497,963 | A/G | — | likely benign |
| rs771819076 | 1:46,497,988 | G/A | — | uncertain significance |
| rs1442315473 | 1:46,498,015 | T/C | — | uncertain significance |
Showing 100 of 141 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.