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

rsidPosition (GRCh37)AllelesClassClinVar
rs132503686817:79,092,207C/Auncertain significance
rs37507529817:79,092,216T/Alikely benign
rs7285417217:79,092,940C/Tregulatory region variant
rs37760274717:79,093,198C/Auncertain significance
rs37532303817:79,093,233G/Auncertain significance
rs251148060617:79,093,242G/Cuncertain significance
rs76222988217:79,093,251G/Auncertain significance
rs75972197417:79,093,312C/Tuncertain significance
rs77946830417:79,093,350G/Auncertain significance
rs97253759717:79,093,773C/Auncertain significance
rs37084793617:79,094,018C/Tuncertain significance
rs18434860917:79,094,122C/Tuncertain significance
rs133860857217:79,094,125G/Auncertain significance
rs206068470717:79,094,153G/Cuncertain significance
rs251148620417:79,094,171C/Tuncertain significance
rs37545698217:79,094,177T/Cuncertain significance
rs20222700817:79,094,220G/Cuncertain significance
rs75837625517:79,094,291C/Tuncertain significance
rs138790161817:79,094,329G/Tuncertain significance
rs75583923217:79,094,332C/Tuncertain significance
rs77726255817:79,094,341C/Tuncertain significance
rs76630498517:79,094,389T/Auncertain significance
rs77708830417:79,094,479G/Auncertain significance
rs140942964617:79,094,552G/Cuncertain significance
rs53075512417:79,094,579C/Tlikely benign
rs77471053217:79,094,609C/Tuncertain significance
rs76397145517:79,094,644C/Tuncertain significance
rs20136908417:79,094,672C/Tuncertain significance
rs206069055317:79,094,675G/Auncertain significance
rs134352812917:79,094,680C/Tlikely benign
rs115677153717:79,094,713G/Auncertain significance
rs77713384617:79,094,726C/Tuncertain significance
rs147119949017:79,094,772C/Guncertain significance
rs251148767117:79,094,789G/Auncertain significance
rs76698834617:79,094,803C/Tlikely benign
rs20084851017:79,094,836G/Auncertain significance
rs77388100117:79,094,845G/Auncertain significance
rs77150278817:79,094,846C/Tuncertain significance
rs36845159517:79,094,866C/Guncertain significance
rs37279874417:79,094,875G/Auncertain significance
rs77174610717:79,094,971G/Auncertain significance
rs145382115517:79,095,010G/Auncertain significance
rs77572495917:79,095,031G/Cuncertain significance
rs76084158517:79,095,035C/Tuncertain significance
rs53569196417:79,095,079A/Guncertain significance
rs75146899017:79,095,104C/Tuncertain significance
rs206069750417:79,095,146C/Guncertain significance
rs147939136717:79,095,174C/Guncertain significance
rs75342901517:79,095,253G/Auncertain significance
rs37508152017:79,095,284C/Tuncertain significance
rs55574865617:79,095,304G/Auncertain significance
rs147292977817:79,095,346G/Auncertain significance
rs37746909317:79,095,353G/Alikely benign
rs20136519717:79,095,358C/Tuncertain significance
rs37621625217:79,095,365C/Tuncertain significance
rs129976082117:79,095,409G/Alikely benign
rs86596291217:79,095,464G/Auncertain significance
rs76261796917:79,095,503G/Tuncertain significance
rs37094974817:79,095,506C/Tlikely benign
rs104021820417:79,095,595G/Tuncertain significance
rs74547472517:79,095,647C/Tuncertain significance
rs251149044617:79,095,709C/Auncertain significance
rs76778861617:79,095,712C/Tlikely benign
rs36935939117:79,095,721G/Tuncertain significance
rs121081831817:79,095,727C/Auncertain significance
rs76194577617:79,095,773G/Auncertain significance
rs251149066017:79,095,787C/Tuncertain significance
rs36878802617:79,095,845C/Tuncertain significance
rs77346565517:79,095,871C/Tuncertain significance
rs37753147917:79,095,895G/Auncertain significance
rs74939479017:79,095,916G/Auncertain significance
rs121932269617:79,096,000C/Auncertain significance
rs76147706317:79,096,024G/Auncertain significance
rs143580626517:79,096,043C/Guncertain significance
rs76815349717:79,096,052C/Auncertain significance
rs121890677417:79,096,079T/Cuncertain significance
rs77899453017:79,096,094C/Tuncertain significance
rs133548568917:79,096,151C/Tuncertain significance
rs100636305017:79,096,175C/Auncertain significance
rs146458649817:79,096,186G/Auncertain significance
rs77616603817:79,096,208C/Tuncertain significance
rs142842246017:79,096,225T/Guncertain significance
rs11312423317:79,096,235G/Auncertain significance
rs98175408917:79,096,274C/Guncertain significance
rs76206708317:79,096,276G/Auncertain significance
rs75054111917:79,096,280C/Tuncertain significance
rs88819576817:79,096,318C/Tuncertain significance
rs124956927317:79,096,352C/Tuncertain significance
rs141701188917:79,096,357G/Cuncertain significance
rs77068219017:79,096,370C/Tuncertain significance
rs53197484217:79,096,399G/Auncertain significance
rs76934897117:79,096,411G/Auncertain significance
rs76548078717:79,096,450C/Tuncertain significance
rs147548313517:79,096,478C/Tuncertain significance
rs141884193917:79,096,481G/Auncertain significance
rs53316915217:79,096,535T/Guncertain significance
rs75964212717:79,096,553G/Tuncertain significance
rs74974665917:79,097,063G/Auncertain significance
rs122966244217:79,097,090G/Tuncertain significance
rs141663074817:79,097,102G/Auncertain significance

Showing 100 of 129 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.