NRK
Nik related kinase
Summary
The mouse ortholog of this gene encodes a protein kinase required for JNK activation. The encoded protein may be involved in the induction of actin polymerization in late embryogenesis.[provided by RefSeq, Jun 2010]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs112593620 | X:105,065,381 | C/T | regulatory region variant | — |
| rs2544749154 | X:105,066,863 | G/A | — | uncertain significance |
| rs1297242 | X:105,092,279 | G/T | intron variant | — |
| rs11092545 | X:105,101,580 | A/T | upstream gene variant | — |
| rs2544794937 | X:105,124,225 | G/A | — | uncertain significance |
| rs1176988972 | X:105,125,726 | G/A | — | conflicting classifications of pathogenicity |
| rs2544801617 | X:105,132,346 | A/G | — | likely benign |
| rs2544801670 | X:105,132,370 | A/G | — | likely benign |
| rs1261166799 | X:105,139,463 | G/T | — | uncertain significance |
| rs2544815057 | X:105,149,284 | G/A | — | uncertain significance |
| rs879071844 | X:105,149,293 | G/A | — | uncertain significance |
| rs377064886 | X:105,149,332 | G/A | — | uncertain significance |
| rs1190032459 | X:105,150,539 | A/T | — | uncertain significance |
| rs377144577 | X:105,152,737 | C/T | — | benign |
| rs2544818383 | X:105,152,757 | C/T | — | uncertain significance |
| rs917736775 | X:105,152,819 | C/T | — | uncertain significance |
| rs200574475 | X:105,152,867 | G/A | — | uncertain significance |
| rs144119374 | X:105,152,946 | G/A | — | benign |
| rs748826488 | X:105,152,964 | G/C | — | uncertain significance |
| rs754558243 | X:105,152,970 | T/G | — | uncertain significance |
| rs747808806 | X:105,152,984 | G/T | — | uncertain significance |
| rs2544819626 | X:105,153,272 | G/C | — | uncertain significance |
| rs373316175 | X:105,153,306 | A/G | — | uncertain significance |
| rs2040266280 | X:105,153,461 | A/G | — | uncertain significance |
| rs367975216 | X:105,153,464 | C/T | — | uncertain significance |
| rs200904424 | X:105,153,557 | G/C | — | uncertain significance |
| rs371793705 | X:105,153,625 | C/A | — | likely benign |
| rs777965913 | X:105,153,726 | G/T | — | uncertain significance |
| rs752431910 | X:105,153,796 | A/G | — | likely benign |
| rs33936206 | X:105,153,813 | G/T | — | uncertain significance |
| rs779676790 | X:105,153,818 | C/G | — | uncertain significance |
| rs893329656 | X:105,153,851 | G/A | — | uncertain significance |
| rs199807026 | X:105,156,700 | C/G | — | benign |
| rs748073147 | X:105,156,742 | A/G | — | uncertain significance |
| rs62605033 | X:105,157,655 | G/A | intron variant | — |
| rs192589373 | X:105,159,737 | C/T | — | benign |
| rs750638676 | X:105,159,741 | C/T | — | uncertain significance |
| rs202170693 | X:105,159,767 | C/T | — | uncertain significance |
| rs1317412707 | X:105,161,598 | G/A | — | uncertain significance |
| rs748722097 | X:105,161,610 | A/G | — | uncertain significance |
| rs776883441 | X:105,166,012 | C/T | — | uncertain significance |
| rs1383738331 | X:105,166,027 | G/A | — | uncertain significance |
| rs2520357768 | X:105,166,035 | G/T | — | uncertain significance |
| rs1923082159 | X:105,167,159 | C/A | — | uncertain significance |
| rs376128030 | X:105,167,200 | C/T | — | uncertain significance |
| rs2040476659 | X:105,167,239 | C/T | — | uncertain significance |
| rs193030679 | X:105,167,279 | G/A | — | uncertain significance |
| rs371339898 | X:105,167,417 | A/G | — | uncertain significance |
| rs747242923 | X:105,168,755 | C/T | — | uncertain significance |
| rs762539895 | X:105,168,830 | T/C | — | likely benign |
| rs1167347025 | X:105,168,885 | G/C | — | uncertain significance |
| rs980074417 | X:105,168,947 | G/A | — | uncertain significance |
| rs2520388079 | X:105,168,957 | T/G | — | uncertain significance |
| rs41300163 | X:105,168,992 | C/A | — | uncertain significance |
| rs777002408 | X:105,178,262 | G/A | — | likely benign |
| rs2520460779 | X:105,178,278 | A/G | — | uncertain significance |
| rs368674115 | X:105,178,293 | G/C | — | uncertain significance |
| rs775920538 | X:105,178,302 | C/T | — | likely benign |
| rs188996722 | X:105,178,329 | A/G | — | benign |
| rs377439740 | X:105,179,167 | G/T | — | uncertain significance |
| rs372760080 | X:105,179,219 | A/G | — | uncertain significance |
| rs1294120667 | X:105,179,238 | C/G | — | likely benign |
| rs1201565981 | X:105,179,247 | A/G | — | likely benign |
| rs755263364 | X:105,181,515 | G/A | — | uncertain significance |
| rs544266682 | X:105,181,527 | G/A | — | uncertain significance |
| rs2040682216 | X:105,181,539 | T/C | — | uncertain significance |
| rs56136869 | X:105,183,904 | T/C | — | benign |
| rs778421031 | X:105,183,912 | C/A | — | uncertain significance |
| rs1421389660 | X:105,187,989 | T/C | — | uncertain significance |
| rs769469390 | X:105,189,871 | T/C | — | uncertain significance |
| rs1010577750 | X:105,189,898 | A/G | — | uncertain significance |
| rs200616257 | X:105,189,958 | T/C | — | likely benign |
| rs2520569238 | X:105,190,380 | T/C | — | uncertain significance |
| rs747362643 | X:105,193,576 | A/C | — | uncertain significance |
| rs777092523 | X:105,193,613 | G/T | — | uncertain significance |
| rs181878602 | X:105,193,708 | G/A | — | uncertain significance |
| rs372460980 | X:105,197,071 | T/C | — | uncertain significance |
| rs774608160 | X:105,197,118 | C/T | — | uncertain significance |
| rs201279660 | X:105,199,518 | C/T | — | likely benign |
| rs369253049 | X:105,199,550 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.