TAOK3
TAO kinase 3
Summary
The protein encoded by this gene is a serine/threonine protein kinase that activates the p38/MAPK14 stress-activated MAPK cascade but inhibits the basal activity of the MAPK8/JNK cascade. The encoded protein is a member of the GCK subfamily of STE20-like kinases. [provided by RefSeq, Oct 2016]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs80282091 | 12:118,588,863 | C/T | — | uncertain significance |
| rs774571205 | 12:118,588,930 | G/A | — | uncertain significance |
| rs795484 | 12:118,589,862 | T/A | — | — |
| rs143511282 | 12:118,590,137 | G/A | — | benign |
| rs2501291632 | 12:118,598,158 | C/T | — | uncertain significance |
| rs752845950 | 12:118,598,170 | A/G | — | likely benign |
| rs267603331 | 12:118,599,706 | G/A | — | uncertain significance |
| rs1188491568 | 12:118,599,732 | A/G | — | uncertain significance |
| rs371188778 | 12:118,610,288 | C/T | — | uncertain significance |
| rs555589014 | 12:118,610,329 | T/C | — | uncertain significance |
| rs575733900 | 12:118,610,357 | T/A | — | uncertain significance |
| rs538340533 | 12:118,610,364 | G/C | — | uncertain significance |
| rs112263526 | 12:118,610,422 | T/C | — | uncertain significance |
| rs113227670 | 12:118,614,502 | T/A | intron variant | — |
| rs2501641988 | 12:118,615,022 | T/G | — | uncertain significance |
| rs2501642536 | 12:118,615,079 | T/C | — | uncertain significance |
| rs1255797024 | 12:118,615,127 | A/G | — | uncertain significance |
| rs762530228 | 12:118,619,246 | G/A | — | uncertain significance |
| rs2499927341 | 12:118,619,340 | G/A | — | uncertain significance |
| rs77139493 | 12:118,619,415 | G/A | — | likely benign |
| rs2499990716 | 12:118,627,631 | G/A | — | uncertain significance |
| rs1232154281 | 12:118,636,903 | C/T | — | uncertain significance |
| rs61945174 | 12:118,636,987 | C/T | missense variant | — |
| rs1170278559 | 12:118,637,028 | A/G | — | uncertain significance |
| rs192488251 | 12:118,637,151 | C/T | intron variant | — |
| rs535119046 | 12:118,639,118 | A/G | — | uncertain significance |
| rs759178115 | 12:118,639,164 | C/A | — | uncertain significance |
| rs1219239968 | 12:118,639,196 | G/T | — | uncertain significance |
| rs2038758343 | 12:118,651,834 | T/G | — | uncertain significance |
| rs2500306938 | 12:118,651,835 | G/T | — | uncertain significance |
| rs776377386 | 12:118,651,840 | G/A | — | uncertain significance |
| rs752446691 | 12:118,673,379 | C/T | — | uncertain significance |
| rs148463198 | 12:118,673,387 | T/C | — | uncertain significance |
| rs864622030 | 12:118,673,402 | A/G | — | uncertain significance |
| rs772111018 | 12:118,674,296 | A/T | — | — |
| rs760730356 | 12:118,675,928 | A/T | — | uncertain significance |
| rs753748513 | 12:118,675,933 | T/C | — | uncertain significance |
| rs2500681515 | 12:118,677,070 | A/G | — | uncertain significance |
| rs75202604 | 12:118,681,284 | C/T | — | uncertain significance |
| rs111763375 | 12:118,681,298 | T/C | — | benign |
| rs2500741316 | 12:118,681,308 | A/C | — | uncertain significance |
| rs78318782 | 12:118,681,329 | A/G | — | likely benign |
| rs963518684 | 12:118,682,721 | T/G | — | uncertain significance |
| rs708865 | 12:118,683,533 | A/C | upstream gene variant | — |
| rs12296288 | 12:118,685,725 | G/A | downstream gene variant | — |
| rs138803724 | 12:118,692,586 | G/A | intron variant | — |
| rs78662524 | 12:118,693,338 | G/T | — | uncertain significance |
| rs61945215 | 12:118,693,341 | A/G | — | uncertain significance |
| rs61946067 | 12:118,740,957 | T/C | intron variant | — |
| rs751143897 | 12:118,748,559 | C/G | — | — |
| rs115981023 | 12:118,751,105 | G/A | intron variant | — |
| rs575579185 | 12:118,759,751 | A/G | — | — |
| rs6490177 | 12:118,796,085 | C/A | intron variant | — |
| rs566804813 | 12:118,802,090 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.