USP6NL
USP6 N-terminal like
Summary
Enables GTPase activator activity and small GTPase binding activity. Involved in several processes, including plasma membrane to endosome transport; positive regulation of GTPase activity; and retrograde transport, plasma membrane to Golgi. Located in cytoplasmic vesicle and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375255729 | 10:11,504,504 | G/A | — | uncertain significance |
| rs1157401983 | 10:11,504,538 | C/A | — | uncertain significance |
| rs764513668 | 10:11,504,547 | C/T | — | uncertain significance |
| rs745998452 | 10:11,504,594 | G/A | — | uncertain significance |
| rs2491162411 | 10:11,504,601 | C/T | — | uncertain significance |
| rs143605121 | 10:11,504,715 | C/T | — | uncertain significance |
| rs1195683004 | 10:11,504,811 | C/T | — | uncertain significance |
| rs2491166813 | 10:11,504,828 | A/G | — | uncertain significance |
| rs771778974 | 10:11,504,860 | G/C | — | uncertain significance |
| rs4418693 | 10:11,504,879 | T/C | — | uncertain significance |
| rs765638465 | 10:11,504,883 | C/G | — | uncertain significance |
| rs764415627 | 10:11,504,888 | G/A | — | uncertain significance |
| rs2491169808 | 10:11,504,933 | T/C | — | uncertain significance |
| rs77522325 | 10:11,505,024 | G/A | — | uncertain significance |
| rs1280325776 | 10:11,505,056 | C/T | — | uncertain significance |
| rs375123048 | 10:11,505,105 | G/C | — | uncertain significance |
| rs548713634 | 10:11,505,111 | T/C | — | uncertain significance |
| rs372585556 | 10:11,505,171 | G/A | — | uncertain significance |
| rs577600663 | 10:11,505,188 | G/A | — | uncertain significance |
| rs2491175694 | 10:11,505,203 | T/C | — | uncertain significance |
| rs2491176533 | 10:11,505,245 | C/T | — | likely benign |
| rs981085886 | 10:11,505,308 | T/A | — | uncertain significance |
| rs2491177764 | 10:11,505,314 | T/A | — | uncertain significance |
| rs753071947 | 10:11,505,329 | T/C | — | uncertain significance |
| rs568389319 | 10:11,505,386 | G/A | — | uncertain significance |
| rs2096226100 | 10:11,505,401 | C/A | — | uncertain significance |
| rs755125955 | 10:11,505,416 | A/G | — | uncertain significance |
| rs773663092 | 10:11,505,458 | G/A | — | uncertain significance |
| rs746900219 | 10:11,505,531 | G/A | — | uncertain significance |
| rs1310431665 | 10:11,505,575 | C/T | — | uncertain significance |
| rs377168113 | 10:11,505,656 | G/A | — | uncertain significance |
| rs747418074 | 10:11,505,680 | G/A | — | likely benign |
| rs540226752 | 10:11,505,711 | C/G | — | uncertain significance |
| rs2491185106 | 10:11,505,729 | T/G | — | uncertain significance |
| rs1480965360 | 10:11,505,734 | A/C | — | uncertain significance |
| rs113611342 | 10:11,505,743 | G/A | — | uncertain significance |
| rs772326982 | 10:11,505,754 | G/T | — | uncertain significance |
| rs370066019 | 10:11,505,770 | C/T | — | uncertain significance |
| rs757614959 | 10:11,505,783 | C/T | — | likely benign |
| rs750754502 | 10:11,505,801 | C/T | — | uncertain significance |
| rs755509746 | 10:11,505,813 | G/T | — | uncertain significance |
| rs754242907 | 10:11,523,793 | C/T | — | uncertain significance |
| rs575447541 | 10:11,523,795 | C/T | — | uncertain significance |
| rs747274593 | 10:11,523,844 | C/T | — | uncertain significance |
| rs2491313917 | 10:11,523,898 | C/G | — | uncertain significance |
| rs1371856372 | 10:11,527,057 | G/C | — | uncertain significance |
| rs768454923 | 10:11,527,173 | C/T | — | uncertain significance |
| rs1447044997 | 10:11,527,175 | A/C | — | uncertain significance |
| rs1833408455 | 10:11,527,221 | T/C | — | uncertain significance |
| rs372721793 | 10:11,531,133 | T/G | — | uncertain significance |
| rs1431168136 | 10:11,531,147 | G/T | — | uncertain significance |
| rs199595275 | 10:11,532,842 | T/C | — | uncertain significance |
| rs751888357 | 10:11,543,206 | A/G | — | uncertain significance |
| rs904873265 | 10:11,560,559 | G/C | — | uncertain significance |
| rs548466296 | 10:11,560,565 | T/A | — | uncertain significance |
| rs1364191025 | 10:11,569,513 | C/T | — | uncertain significance |
| rs186927997 | 10:11,635,568 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.