AATK
apoptosis associated tyrosine kinase
Summary
The protein encoded by this gene contains a tyrosine kinase domain at the N-terminus and a proline-rich domain at the C-terminus. This gene is induced during apoptosis, and expression of this gene may be a necessary pre-requisite for the induction of growth arrest and/or apoptosis of myeloid precursor cells. This gene has been shown to produce neuronal differentiation in a neuroblastoma cell line. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]
Known Variants129 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1325036868 | 17:79,092,207 | C/A | — | uncertain significance |
| rs375075298 | 17:79,092,216 | T/A | — | likely benign |
| rs72854172 | 17:79,092,940 | C/T | regulatory region variant | — |
| rs377602747 | 17:79,093,198 | C/A | — | uncertain significance |
| rs375323038 | 17:79,093,233 | G/A | — | uncertain significance |
| rs2511480606 | 17:79,093,242 | G/C | — | uncertain significance |
| rs762229882 | 17:79,093,251 | G/A | — | uncertain significance |
| rs759721974 | 17:79,093,312 | C/T | — | uncertain significance |
| rs779468304 | 17:79,093,350 | G/A | — | uncertain significance |
| rs972537597 | 17:79,093,773 | C/A | — | uncertain significance |
| rs370847936 | 17:79,094,018 | C/T | — | uncertain significance |
| rs184348609 | 17:79,094,122 | C/T | — | uncertain significance |
| rs1338608572 | 17:79,094,125 | G/A | — | uncertain significance |
| rs2060684707 | 17:79,094,153 | G/C | — | uncertain significance |
| rs2511486204 | 17:79,094,171 | C/T | — | uncertain significance |
| rs375456982 | 17:79,094,177 | T/C | — | uncertain significance |
| rs202227008 | 17:79,094,220 | G/C | — | uncertain significance |
| rs758376255 | 17:79,094,291 | C/T | — | uncertain significance |
| rs1387901618 | 17:79,094,329 | G/T | — | uncertain significance |
| rs755839232 | 17:79,094,332 | C/T | — | uncertain significance |
| rs777262558 | 17:79,094,341 | C/T | — | uncertain significance |
| rs766304985 | 17:79,094,389 | T/A | — | uncertain significance |
| rs777088304 | 17:79,094,479 | G/A | — | uncertain significance |
| rs1409429646 | 17:79,094,552 | G/C | — | uncertain significance |
| rs530755124 | 17:79,094,579 | C/T | — | likely benign |
| rs774710532 | 17:79,094,609 | C/T | — | uncertain significance |
| rs763971455 | 17:79,094,644 | C/T | — | uncertain significance |
| rs201369084 | 17:79,094,672 | C/T | — | uncertain significance |
| rs2060690553 | 17:79,094,675 | G/A | — | uncertain significance |
| rs1343528129 | 17:79,094,680 | C/T | — | likely benign |
| rs1156771537 | 17:79,094,713 | G/A | — | uncertain significance |
| rs777133846 | 17:79,094,726 | C/T | — | uncertain significance |
| rs1471199490 | 17:79,094,772 | C/G | — | uncertain significance |
| rs2511487671 | 17:79,094,789 | G/A | — | uncertain significance |
| rs766988346 | 17:79,094,803 | C/T | — | likely benign |
| rs200848510 | 17:79,094,836 | G/A | — | uncertain significance |
| rs773881001 | 17:79,094,845 | G/A | — | uncertain significance |
| rs771502788 | 17:79,094,846 | C/T | — | uncertain significance |
| rs368451595 | 17:79,094,866 | C/G | — | uncertain significance |
| rs372798744 | 17:79,094,875 | G/A | — | uncertain significance |
| rs771746107 | 17:79,094,971 | G/A | — | uncertain significance |
| rs1453821155 | 17:79,095,010 | G/A | — | uncertain significance |
| rs775724959 | 17:79,095,031 | G/C | — | uncertain significance |
| rs760841585 | 17:79,095,035 | C/T | — | uncertain significance |
| rs535691964 | 17:79,095,079 | A/G | — | uncertain significance |
| rs751468990 | 17:79,095,104 | C/T | — | uncertain significance |
| rs2060697504 | 17:79,095,146 | C/G | — | uncertain significance |
| rs1479391367 | 17:79,095,174 | C/G | — | uncertain significance |
| rs753429015 | 17:79,095,253 | G/A | — | uncertain significance |
| rs375081520 | 17:79,095,284 | C/T | — | uncertain significance |
| rs555748656 | 17:79,095,304 | G/A | — | uncertain significance |
| rs1472929778 | 17:79,095,346 | G/A | — | uncertain significance |
| rs377469093 | 17:79,095,353 | G/A | — | likely benign |
| rs201365197 | 17:79,095,358 | C/T | — | uncertain significance |
| rs376216252 | 17:79,095,365 | C/T | — | uncertain significance |
| rs1299760821 | 17:79,095,409 | G/A | — | likely benign |
| rs865962912 | 17:79,095,464 | G/A | — | uncertain significance |
| rs762617969 | 17:79,095,503 | G/T | — | uncertain significance |
| rs370949748 | 17:79,095,506 | C/T | — | likely benign |
| rs1040218204 | 17:79,095,595 | G/T | — | uncertain significance |
| rs745474725 | 17:79,095,647 | C/T | — | uncertain significance |
| rs2511490446 | 17:79,095,709 | C/A | — | uncertain significance |
| rs767788616 | 17:79,095,712 | C/T | — | likely benign |
| rs369359391 | 17:79,095,721 | G/T | — | uncertain significance |
| rs1210818318 | 17:79,095,727 | C/A | — | uncertain significance |
| rs761945776 | 17:79,095,773 | G/A | — | uncertain significance |
| rs2511490660 | 17:79,095,787 | C/T | — | uncertain significance |
| rs368788026 | 17:79,095,845 | C/T | — | uncertain significance |
| rs773465655 | 17:79,095,871 | C/T | — | uncertain significance |
| rs377531479 | 17:79,095,895 | G/A | — | uncertain significance |
| rs749394790 | 17:79,095,916 | G/A | — | uncertain significance |
| rs1219322696 | 17:79,096,000 | C/A | — | uncertain significance |
| rs761477063 | 17:79,096,024 | G/A | — | uncertain significance |
| rs1435806265 | 17:79,096,043 | C/G | — | uncertain significance |
| rs768153497 | 17:79,096,052 | C/A | — | uncertain significance |
| rs1218906774 | 17:79,096,079 | T/C | — | uncertain significance |
| rs778994530 | 17:79,096,094 | C/T | — | uncertain significance |
| rs1335485689 | 17:79,096,151 | C/T | — | uncertain significance |
| rs1006363050 | 17:79,096,175 | C/A | — | uncertain significance |
| rs1464586498 | 17:79,096,186 | G/A | — | uncertain significance |
| rs776166038 | 17:79,096,208 | C/T | — | uncertain significance |
| rs1428422460 | 17:79,096,225 | T/G | — | uncertain significance |
| rs113124233 | 17:79,096,235 | G/A | — | uncertain significance |
| rs981754089 | 17:79,096,274 | C/G | — | uncertain significance |
| rs762067083 | 17:79,096,276 | G/A | — | uncertain significance |
| rs750541119 | 17:79,096,280 | C/T | — | uncertain significance |
| rs888195768 | 17:79,096,318 | C/T | — | uncertain significance |
| rs1249569273 | 17:79,096,352 | C/T | — | uncertain significance |
| rs1417011889 | 17:79,096,357 | G/C | — | uncertain significance |
| rs770682190 | 17:79,096,370 | C/T | — | uncertain significance |
| rs531974842 | 17:79,096,399 | G/A | — | uncertain significance |
| rs769348971 | 17:79,096,411 | G/A | — | uncertain significance |
| rs765480787 | 17:79,096,450 | C/T | — | uncertain significance |
| rs1475483135 | 17:79,096,478 | C/T | — | uncertain significance |
| rs1418841939 | 17:79,096,481 | G/A | — | uncertain significance |
| rs533169152 | 17:79,096,535 | T/G | — | uncertain significance |
| rs759642127 | 17:79,096,553 | G/T | — | uncertain significance |
| rs749746659 | 17:79,097,063 | G/A | — | uncertain significance |
| rs1229662442 | 17:79,097,090 | G/T | — | uncertain significance |
| rs1416630748 | 17:79,097,102 | G/A | — | uncertain significance |
Showing 100 of 129 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.