UNKL
unk like zinc finger
Summary
This gene encodes a RING finger protein that may function in Rac signaling. It can bind to Brg/Brm-associated factor 60b and can promote its ubiquitination. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2013]
Known Variants78 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs193302860 | 16:1,413,031 | C/T | missense variant | uncertain significance |
| rs375931700 | 16:1,416,284 | G/A | — | uncertain significance |
| rs774410822 | 16:1,416,353 | T/A | — | uncertain significance |
| rs146279538 | 16:1,416,847 | C/T | downstream gene variant | — |
| rs201695778 | 16:1,417,263 | T/C | — | uncertain significance |
| rs1390054794 | 16:1,417,293 | C/G | — | uncertain significance |
| rs778670919 | 16:1,417,302 | G/A | — | uncertain significance |
| rs758262484 | 16:1,417,307 | C/A | — | uncertain significance |
| rs776186310 | 16:1,417,328 | T/A | — | uncertain significance |
| rs142115515 | 16:1,417,711 | G/C | — | uncertain significance |
| rs975651898 | 16:1,417,746 | C/T | — | uncertain significance |
| rs763860235 | 16:1,417,752 | G/A | — | uncertain significance |
| rs112578064 | 16:1,417,773 | G/A | — | uncertain significance |
| rs747346579 | 16:1,417,790 | A/G | — | uncertain significance |
| rs574018450 | 16:1,417,823 | A/G | — | uncertain significance |
| rs767195746 | 16:1,417,824 | C/T | — | uncertain significance |
| rs773342752 | 16:1,417,828 | G/C | — | uncertain significance |
| rs2035436164 | 16:1,417,842 | C/T | — | uncertain significance |
| rs899400977 | 16:1,420,155 | C/A | — | likely benign |
| rs1222762421 | 16:1,420,172 | G/A | — | uncertain significance |
| rs960596007 | 16:1,420,179 | A/C | — | uncertain significance |
| rs528273200 | 16:1,420,229 | G/A | — | uncertain significance |
| rs374643122 | 16:1,420,257 | C/T | — | likely benign |
| rs751894202 | 16:1,420,262 | G/A | — | uncertain significance |
| rs899962968 | 16:1,420,265 | G/A | — | uncertain significance |
| rs1011755667 | 16:1,420,268 | G/T | — | uncertain significance |
| rs568053065 | 16:1,420,274 | G/A | — | uncertain significance |
| rs756107808 | 16:1,420,286 | G/A | — | uncertain significance |
| rs539413184 | 16:1,420,326 | C/T | — | likely benign |
| rs775879748 | 16:1,420,349 | G/A | — | uncertain significance |
| rs763730083 | 16:1,421,573 | G/T | — | uncertain significance |
| rs201635710 | 16:1,421,606 | G/A | — | uncertain significance |
| rs2548301969 | 16:1,435,233 | T/C | — | likely benign |
| rs745494705 | 16:1,435,236 | C/T | — | likely benign |
| rs1202710553 | 16:1,435,253 | G/A | — | uncertain significance |
| rs957863158 | 16:1,435,256 | C/T | — | uncertain significance |
| rs901832537 | 16:1,435,257 | G/A | — | uncertain significance |
| rs2142091208 | 16:1,435,281 | T/G | — | uncertain significance |
| rs193075543 | 16:1,435,293 | T/C | — | likely benign |
| rs990454204 | 16:1,435,305 | C/T | — | likely benign |
| rs377623850 | 16:1,435,317 | G/C | — | uncertain significance |
| rs759754274 | 16:1,435,341 | C/T | — | uncertain significance |
| rs762823346 | 16:1,435,374 | C/T | — | uncertain significance |
| rs1207938715 | 16:1,440,671 | C/T | — | uncertain significance |
| rs769958409 | 16:1,440,676 | G/A | — | uncertain significance |
| rs761163570 | 16:1,440,689 | G/A | — | uncertain significance |
| rs1286185696 | 16:1,442,893 | T/C | — | uncertain significance |
| rs368812211 | 16:1,442,914 | G/A | — | uncertain significance |
| rs997552404 | 16:1,444,186 | G/A | — | uncertain significance |
| rs771326963 | 16:1,447,201 | G/A | — | uncertain significance |
| rs1230156408 | 16:1,447,232 | C/T | — | uncertain significance |
| rs2505478699 | 16:1,447,249 | G/A | — | uncertain significance |
| rs1029264919 | 16:1,447,251 | T/A | — | uncertain significance |
| rs1175360804 | 16:1,447,257 | C/A | — | uncertain significance |
| rs1468383327 | 16:1,447,259 | A/G | — | uncertain significance |
| rs1555458393 | 16:1,447,261 | T/C | — | uncertain significance |
| rs958360430 | 16:1,447,269 | G/T | — | uncertain significance |
| rs61738726 | 16:1,447,270 | T/A | — | uncertain significance |
| rs2142169790 | 16:1,447,276 | A/G | — | uncertain significance |
| rs61738727 | 16:1,447,278 | A/G | — | likely benign |
| rs2505479999 | 16:1,447,288 | G/A | — | uncertain significance |
| rs138649541 | 16:1,449,387 | C/T | — | uncertain significance |
| rs774326698 | 16:1,449,411 | C/T | — | uncertain significance |
| rs371849793 | 16:1,449,447 | C/T | — | uncertain significance |
| rs772548230 | 16:1,451,571 | T/C | — | uncertain significance |
| rs148808750 | 16:1,451,660 | G/A | — | likely benign |
| rs199858046 | 16:1,451,682 | G/C | — | uncertain significance |
| rs1441947990 | 16:1,453,206 | C/T | — | uncertain significance |
| rs375675925 | 16:1,453,223 | T/C | — | uncertain significance |
| rs1023388796 | 16:1,453,254 | C/T | — | uncertain significance |
| rs765903048 | 16:1,453,295 | A/G | — | uncertain significance |
| rs2505738678 | 16:1,463,959 | T/C | — | uncertain significance |
| rs775790549 | 16:1,464,626 | T/G | — | uncertain significance |
| rs750627084 | 16:1,464,631 | T/G | — | uncertain significance |
| rs2505748968 | 16:1,464,635 | C/T | — | uncertain significance |
| rs769005974 | 16:1,464,653 | C/A | — | uncertain significance |
| rs762323803 | 16:1,464,665 | C/A | — | uncertain significance |
| rs1053914711 | 16:1,464,667 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.