MINK1
misshapen like kinase 1
Summary
This gene encodes a serine/threonine kinase belonging to the germinal center kinase (GCK) family. The protein is structurally similar to the kinases that are related to NIK and may belong to a distinct subfamily of NIK-related kinases within the GCK family. Studies of the mouse homolog indicate an up-regulation of expression in the course of postnatal mouse cerebral development and activation of the cJun N-terminal kinase (JNK) and the p38 pathways. [provided by RefSeq, Mar 2016]
Known Variants77 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375578873 | 17:4,736,884 | C/T | — | likely benign |
| rs1204453989 | 17:4,736,898 | C/T | — | uncertain significance |
| rs184353610 | 17:4,743,995 | A/T | intron variant | — |
| rs72835026 | 17:4,764,132 | G/A | upstream gene variant | — |
| rs112477024 | 17:4,767,587 | G/C | intron variant | — |
| rs180682759 | 17:4,774,574 | C/T | upstream gene variant | — |
| rs181807530 | 17:4,774,814 | C/G | upstream gene variant | — |
| rs72835045 | 17:4,780,795 | G/A | downstream gene variant | — |
| rs149700045 | 17:4,782,644 | A/G | downstream gene variant | — |
| rs2508837781 | 17:4,784,524 | G/C | — | uncertain significance |
| rs866810377 | 17:4,786,745 | C/T | — | — |
| rs2508929135 | 17:4,788,782 | T/G | — | uncertain significance |
| rs2508946436 | 17:4,789,417 | C/A | — | uncertain significance |
| rs1361010127 | 17:4,789,840 | C/T | — | uncertain significance |
| rs1353857219 | 17:4,790,428 | G/A | — | uncertain significance |
| rs2508992817 | 17:4,790,970 | A/G | — | uncertain significance |
| rs992035569 | 17:4,790,985 | A/T | — | uncertain significance |
| rs1456033048 | 17:4,791,003 | C/G | — | uncertain significance |
| rs1198604179 | 17:4,791,071 | C/T | — | uncertain significance |
| rs2509070757 | 17:4,793,951 | T/C | — | uncertain significance |
| rs2509070930 | 17:4,793,960 | G/C | — | uncertain significance |
| rs202107334 | 17:4,794,254 | G/C | — | uncertain significance |
| rs200592676 | 17:4,794,407 | G/C | — | uncertain significance |
| rs377523648 | 17:4,794,883 | G/A | — | likely benign |
| rs997002786 | 17:4,794,904 | G/A | — | uncertain significance |
| rs201027643 | 17:4,794,960 | C/G | — | likely benign |
| rs772451241 | 17:4,794,970 | C/A | — | uncertain significance |
| rs199633382 | 17:4,794,973 | C/A | — | uncertain significance |
| rs575955726 | 17:4,794,985 | C/T | — | uncertain significance |
| rs1968836636 | 17:4,794,997 | G/A | — | uncertain significance |
| rs1360141819 | 17:4,795,448 | C/G | — | uncertain significance |
| rs775990736 | 17:4,795,467 | C/T | — | likely benign |
| rs765417119 | 17:4,795,484 | C/T | — | uncertain significance |
| rs186368496 | 17:4,795,523 | G/A | — | uncertain significance |
| rs746560008 | 17:4,795,702 | G/A | — | uncertain significance |
| rs145314084 | 17:4,795,722 | A/C | — | likely benign |
| rs1383692801 | 17:4,795,765 | C/T | — | uncertain significance |
| rs1194459303 | 17:4,795,971 | G/A | — | uncertain significance |
| rs755667301 | 17:4,795,977 | C/G | — | uncertain significance |
| rs549182164 | 17:4,796,000 | G/A | — | uncertain significance |
| rs202128229 | 17:4,796,017 | C/G | — | uncertain significance |
| rs762380486 | 17:4,796,049 | G/A | — | uncertain significance |
| rs374378662 | 17:4,796,055 | G/T | — | uncertain significance |
| rs752913346 | 17:4,796,321 | G/A | — | uncertain significance |
| rs368988996 | 17:4,796,343 | C/T | — | uncertain significance |
| rs1969029395 | 17:4,796,354 | C/T | — | uncertain significance |
| rs747456065 | 17:4,796,771 | C/T | — | uncertain significance |
| rs1320642869 | 17:4,796,790 | T/C | — | uncertain significance |
| rs750069696 | 17:4,796,836 | C/G | — | likely benign |
| rs878884288 | 17:4,797,351 | A/G | — | uncertain significance |
| rs544525710 | 17:4,797,353 | C/A | — | likely benign |
| rs201290530 | 17:4,797,368 | G/A | — | uncertain significance |
| rs201847306 | 17:4,797,531 | C/T | — | benign |
| rs767561840 | 17:4,797,540 | G/T | — | uncertain significance |
| rs200852679 | 17:4,797,587 | C/T | — | uncertain significance |
| rs1404782489 | 17:4,797,843 | G/C | — | uncertain significance |
| rs375516051 | 17:4,797,883 | G/A | — | uncertain significance |
| rs370042103 | 17:4,798,460 | G/A | — | uncertain significance |
| rs2509187457 | 17:4,798,519 | C/T | — | likely benign |
| rs1460714985 | 17:4,798,674 | G/A | — | uncertain significance |
| rs770558865 | 17:4,798,728 | C/T | — | uncertain significance |
| rs1371779157 | 17:4,798,765 | T/G | — | uncertain significance |
| rs376392487 | 17:4,798,782 | A/G | — | uncertain significance |
| rs2509204333 | 17:4,799,035 | G/T | — | uncertain significance |
| rs374714718 | 17:4,799,305 | C/T | — | likely benign |
| rs752334893 | 17:4,799,310 | G/A | — | uncertain significance |
| rs369976237 | 17:4,799,540 | A/C | — | uncertain significance |
| rs774988040 | 17:4,799,549 | G/A | — | uncertain significance |
| rs75741630 | 17:4,799,553 | C/T | — | benign |
| rs369985962 | 17:4,799,772 | G/C | — | uncertain significance |
| rs2509238885 | 17:4,799,857 | A/C | — | uncertain significance |
| rs752226964 | 17:4,799,978 | G/C | — | uncertain significance |
| rs779185115 | 17:4,800,035 | C/T | — | uncertain significance |
| rs772442734 | 17:4,800,045 | C/T | — | likely benign |
| rs767984504 | 17:4,800,517 | C/T | — | uncertain significance |
| rs200856469 | 17:4,800,559 | C/G | — | uncertain significance |
| rs779959099 | 17:4,800,560 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.