NEK11
NIMA related kinase 11
Summary
This gene encodes a member of the never in mitosis gene A family of kinases. The encoded protein localizes to the nucleoli, and may function with NEK2A in the S-phase checkpoint. The encoded protein appears to play roles in DNA replication and response to genotoxic stress. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2009]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs766328860 | 3:130,748,565 | C/A | — | uncertain significance |
| rs2064498385 | 3:130,748,590 | G/T | — | uncertain significance |
| rs1297418958 | 3:130,748,619 | A/G | — | uncertain significance |
| rs138488290 | 3:130,748,648 | A/G | — | likely benign |
| rs776665091 | 3:130,748,715 | G/C | — | uncertain significance |
| rs1389271 | 3:130,785,106 | G/C | — | — |
| rs1560300733 | 3:130,799,286 | T/A | — | uncertain significance |
| rs145554448 | 3:130,799,356 | A/G | — | uncertain significance |
| rs750640296 | 3:130,799,418 | A/G | — | uncertain significance |
| rs200944744 | 3:130,828,651 | G/A | — | uncertain significance |
| rs749410135 | 3:130,828,669 | T/C | — | uncertain significance |
| rs745678976 | 3:130,828,701 | C/T | — | uncertain significance |
| rs2535660362 | 3:130,828,741 | T/C | — | uncertain significance |
| rs759742040 | 3:130,851,614 | T/C | — | uncertain significance |
| rs2084751472 | 3:130,851,621 | A/G | — | uncertain significance |
| rs114884358 | 3:130,852,702 | G/A | — | uncertain significance |
| rs2149600909 | 3:130,852,710 | G/T | — | uncertain significance |
| rs145728410 | 3:130,852,725 | C/T | — | uncertain significance |
| rs2536599705 | 3:130,852,730 | A/G | — | uncertain significance |
| rs1369612748 | 3:130,852,773 | A/G | — | uncertain significance |
| rs138742765 | 3:130,852,792 | G/A | — | likely benign |
| rs2537236823 | 3:130,871,329 | A/G | — | uncertain significance |
| rs777979775 | 3:130,871,356 | A/G | — | uncertain significance |
| rs374241502 | 3:130,871,362 | C/G | — | uncertain significance |
| rs1029814163 | 3:130,873,907 | A/T | — | uncertain significance |
| rs2537348338 | 3:130,873,931 | T/G | — | uncertain significance |
| rs2092117785 | 3:130,884,277 | G/C | — | uncertain significance |
| rs760450934 | 3:130,884,329 | G/A | — | uncertain significance |
| rs112860756 | 3:130,884,341 | A/G | — | uncertain significance |
| rs764947085 | 3:130,884,354 | T/G | — | uncertain significance |
| rs180926777 | 3:130,903,576 | A/G | — | benign |
| rs145914506 | 3:130,947,448 | G/T | — | uncertain significance |
| rs773616867 | 3:130,947,463 | A/G | — | uncertain significance |
| rs375664389 | 3:130,947,465 | C/T | — | likely benign |
| rs138864243 | 3:130,947,466 | G/A | — | likely benign |
| rs200588944 | 3:130,962,296 | C/T | — | uncertain significance |
| rs201804637 | 3:130,962,297 | G/A | — | likely benign |
| rs2540218060 | 3:130,962,298 | T/A | — | uncertain significance |
| rs755820840 | 3:130,962,326 | G/T | — | uncertain significance |
| rs116395665 | 3:130,992,403 | T/A | — | benign |
| rs756406910 | 3:131,068,415 | A/G | — | uncertain significance |
| rs375166102 | 3:131,068,483 | G/A | — | uncertain significance |
| rs201023084 | 3:131,068,495 | C/T | — | uncertain significance |
| rs144423438 | 3:131,068,496 | G/C | — | uncertain significance |
| rs144885382 | 3:131,068,519 | C/T | — | uncertain significance |
| rs145872163 | 3:131,068,567 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.