MOK
MOK protein kinase
Summary
This gene belongs to the MAP kinase superfamily. The gene was found to be regulated by caudal type transcription factor 2 (Cdx2) protein. The encoded protein, which is localized to epithelial cells in the intestinal crypt, may play a role in growth arrest and differentiation of cells of upper crypt and lower villus regions. Multiple alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Dec 2012]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs778326923 | 14:102,695,636 | C/T | — | uncertain significance |
| rs2509958843 | 14:102,695,637 | C/T | — | uncertain significance |
| rs2509958968 | 14:102,695,642 | C/T | — | uncertain significance |
| rs774958063 | 14:102,695,648 | A/G | — | uncertain significance |
| rs1290953916 | 14:102,695,649 | T/C | — | uncertain significance |
| rs2509959597 | 14:102,695,669 | T/C | — | uncertain significance |
| rs767356918 | 14:102,695,681 | T/C | — | uncertain significance |
| rs767585856 | 14:102,695,822 | G/T | — | uncertain significance |
| rs370862359 | 14:102,695,859 | C/T | — | uncertain significance |
| rs2509965221 | 14:102,695,891 | G/A | — | uncertain significance |
| rs950904649 | 14:102,695,903 | A/C | — | uncertain significance |
| rs750706626 | 14:102,695,912 | G/A | — | uncertain significance |
| rs909385616 | 14:102,695,921 | A/G | — | uncertain significance |
| rs374806877 | 14:102,695,925 | T/G | — | uncertain significance |
| rs781739262 | 14:102,695,967 | G/C | — | uncertain significance |
| rs142160037 | 14:102,698,091 | C/T | — | uncertain significance |
| rs376559474 | 14:102,698,093 | G/A | — | likely benign |
| rs2509996947 | 14:102,698,125 | T/A | — | uncertain significance |
| rs1403898066 | 14:102,698,881 | T/C | — | uncertain significance |
| rs779981179 | 14:102,698,896 | T/C | — | uncertain significance |
| rs754455482 | 14:102,698,915 | C/T | — | likely benign |
| rs753928824 | 14:102,698,959 | G/A | — | uncertain significance |
| rs149225385 | 14:102,698,972 | G/T | — | uncertain significance |
| rs554700010 | 14:102,699,016 | A/C | — | uncertain significance |
| rs763765191 | 14:102,700,037 | G/C | — | uncertain significance |
| rs374797176 | 14:102,700,053 | C/T | — | uncertain significance |
| rs764383623 | 14:102,700,100 | T/C | — | uncertain significance |
| rs2510034105 | 14:102,700,119 | G/A | — | uncertain significance |
| rs34440178 | 14:102,711,201 | G/C | intron variant | — |
| rs757188060 | 14:102,717,153 | C/A | — | uncertain significance |
| rs1597366601 | 14:102,717,253 | G/A | — | likely benign |
| rs546771266 | 14:102,717,290 | C/T | — | uncertain significance |
| rs1306942878 | 14:102,717,302 | A/G | — | uncertain significance |
| rs1388855605 | 14:102,717,306 | C/T | — | uncertain significance |
| rs2274815 | 14:102,718,052 | G/A | intron variant | — |
| rs149850506 | 14:102,718,093 | C/G | — | benign |
| rs2510189311 | 14:102,718,104 | T/C | — | uncertain significance |
| rs912972442 | 14:102,718,290 | A/G | — | uncertain significance |
| rs1214695054 | 14:102,718,291 | T/G | — | uncertain significance |
| rs145834415 | 14:102,718,302 | A/C | — | uncertain significance |
| rs116212806 | 14:102,719,242 | A/G | intron variant | — |
| rs77401355 | 14:102,729,523 | C/T | regulatory region variant | — |
| rs750938879 | 14:102,732,170 | C/T | — | uncertain significance |
| rs147983922 | 14:102,732,188 | T/C | — | uncertain significance |
| rs751319494 | 14:102,749,816 | T/C | — | uncertain significance |
| rs34114580 | 14:102,749,824 | C/G | — | uncertain significance |
| rs746409818 | 14:102,749,896 | G/A | — | uncertain significance |
| rs2210315 | 14:102,764,820 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.