NUAK1
NUAK family kinase 1
Summary
Enables p53 binding activity and protein serine/threonine kinase activity. Involved in protein phosphorylation; regulation of cell adhesion; and regulation of cellular senescence. Located in cytoplasm; microtubule cytoskeleton; and nuclear lumen. Implicated in uterine fibroid. Biomarker of uterine fibroid. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs779695417 | 12:106,460,645 | T/C | — | likely benign |
| rs776270199 | 12:106,460,674 | C/T | — | uncertain significance |
| rs151011578 | 12:106,460,681 | G/A | — | uncertain significance |
| rs201772373 | 12:106,460,712 | G/T | — | uncertain significance |
| rs762178790 | 12:106,460,770 | C/T | — | uncertain significance |
| rs141618950 | 12:106,460,782 | C/A | — | likely benign |
| rs1324493779 | 12:106,460,785 | G/T | — | uncertain significance |
| rs777676118 | 12:106,460,792 | G/A | — | uncertain significance |
| rs2541495252 | 12:106,460,814 | G/C | — | uncertain significance |
| rs2541495256 | 12:106,460,815 | T/A | — | uncertain significance |
| rs186215853 | 12:106,460,846 | C/T | — | uncertain significance |
| rs938846208 | 12:106,460,959 | A/G | — | likely benign |
| rs760225538 | 12:106,460,963 | T/C | — | likely benign |
| rs2541495446 | 12:106,460,994 | G/C | — | uncertain significance |
| rs776076144 | 12:106,461,032 | C/A | — | uncertain significance |
| rs201594672 | 12:106,461,069 | G/T | — | uncertain significance |
| rs1220374576 | 12:106,461,073 | C/T | — | uncertain significance |
| rs376346267 | 12:106,461,077 | T/A | — | likely benign |
| rs2541495630 | 12:106,461,112 | C/T | — | uncertain significance |
| rs111758972 | 12:106,461,115 | C/T | — | benign |
| rs779212474 | 12:106,461,185 | T/A | — | uncertain significance |
| rs56353131 | 12:106,461,213 | C/T | — | benign |
| rs747705556 | 12:106,461,214 | G/T | — | uncertain significance |
| rs1384994807 | 12:106,461,217 | A/T | — | uncertain significance |
| rs749654957 | 12:106,461,238 | G/A | — | uncertain significance |
| rs2541495772 | 12:106,461,245 | G/A | — | uncertain significance |
| rs144124030 | 12:106,461,301 | C/A | — | uncertain significance |
| rs202168878 | 12:106,461,317 | T/G | — | uncertain significance |
| rs2541495898 | 12:106,461,329 | T/G | — | uncertain significance |
| rs2541495928 | 12:106,461,347 | T/A | — | uncertain significance |
| rs139881229 | 12:106,461,466 | G/A | — | uncertain significance |
| rs1458958342 | 12:106,461,626 | C/T | — | uncertain significance |
| rs2541496341 | 12:106,461,672 | C/G | — | uncertain significance |
| rs766746646 | 12:106,464,560 | T/G | — | uncertain significance |
| rs141538558 | 12:106,464,612 | G/T | — | uncertain significance |
| rs55667101 | 12:106,464,616 | G/A | — | benign |
| rs187524260 | 12:106,467,048 | C/T | — | — |
| rs1320753304 | 12:106,480,569 | C/G | — | uncertain significance |
| rs551240873 | 12:106,500,233 | A/G | — | uncertain significance |
| rs142220131 | 12:106,500,308 | A/G | — | benign |
| rs770530605 | 12:106,532,223 | T/C | — | uncertain significance |
| rs2541540356 | 12:106,532,250 | A/T | — | uncertain significance |
| rs760586653 | 12:106,532,370 | C/T | — | uncertain significance |
| rs1390261166 | 12:106,532,373 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.