USP24
ubiquitin specific peptidase 24
Summary
Modification of cellular proteins by ubiquitin is an essential regulatory mechanism controlled by the coordinated action of multiple ubiquitin-conjugating and deubiquitinating enzymes. USP24 belongs to a large family of cysteine proteases that function as deubiquitinating enzymes (Quesada et al., 2004 [PubMed 14715245]).[supplied by OMIM, Mar 2008]
Known Variants102 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs13312 | 1:55,532,742 | G/A | — | — |
| rs375993189 | 1:55,538,492 | G/A | — | benign |
| rs775674913 | 1:55,539,572 | C/T | — | uncertain significance |
| rs1557523211 | 1:55,539,586 | G/A | — | likely pathogenic |
| rs487230 | 1:55,541,174 | A/G | missense variant | — |
| rs2523370539 | 1:55,542,966 | A/T | — | uncertain significance |
| rs2523370628 | 1:55,542,973 | T/C | — | uncertain significance |
| rs146157541 | 1:55,544,228 | T/C | — | uncertain significance |
| rs2523378536 | 1:55,544,233 | A/T | — | uncertain significance |
| rs199520748 | 1:55,545,230 | C/G | — | uncertain significance |
| rs2523385720 | 1:55,545,287 | G/A | — | uncertain significance |
| rs778463727 | 1:55,545,311 | C/T | — | uncertain significance |
| rs748058365 | 1:55,545,324 | T/C | — | likely benign |
| rs201970458 | 1:55,547,024 | T/C | — | uncertain significance |
| rs370609533 | 1:55,547,090 | C/T | — | uncertain significance |
| rs775448328 | 1:55,547,093 | C/T | — | uncertain significance |
| rs2100436322 | 1:55,548,979 | C/G | — | uncertain significance |
| rs779693037 | 1:55,549,027 | C/T | — | uncertain significance |
| rs761483218 | 1:55,549,470 | A/G | — | uncertain significance |
| rs772558243 | 1:55,551,635 | C/T | — | uncertain significance |
| rs1645242941 | 1:55,551,694 | C/T | — | uncertain significance |
| rs1209668582 | 1:55,555,384 | A/G | — | uncertain significance |
| rs2523462405 | 1:55,557,768 | A/G | — | uncertain significance |
| rs2523468067 | 1:55,558,552 | C/T | — | uncertain significance |
| rs767352650 | 1:55,560,953 | G/A | — | uncertain significance |
| rs375955336 | 1:55,560,959 | C/T | — | uncertain significance |
| rs773073230 | 1:55,562,225 | T/C | — | uncertain significance |
| rs972778533 | 1:55,562,724 | T/A | — | uncertain significance |
| rs2523496215 | 1:55,562,734 | A/G | — | uncertain significance |
| rs2523496512 | 1:55,562,763 | C/T | — | uncertain significance |
| rs61760215 | 1:55,562,787 | G/T | — | uncertain significance |
| rs189659168 | 1:55,563,340 | T/C | — | likely benign |
| rs2523502800 | 1:55,563,631 | T/G | — | uncertain significance |
| rs377650319 | 1:55,563,644 | G/A | — | uncertain significance |
| rs202160257 | 1:55,563,710 | G/C | — | uncertain significance |
| rs866465698 | 1:55,566,564 | C/T | — | uncertain significance |
| rs1384403309 | 1:55,571,847 | C/A | — | uncertain significance |
| rs774014262 | 1:55,572,983 | A/G | — | uncertain significance |
| rs61760214 | 1:55,572,991 | C/T | — | benign |
| rs1221205318 | 1:55,573,034 | T/C | — | uncertain significance |
| rs56349475 | 1:55,576,102 | T/C | intron variant | — |
| rs530804537 | 1:55,583,210 | G/A | — | — |
| rs191448950 | 1:55,584,844 | G/A | intron variant | — |
| rs555924829 | 1:55,586,323 | G/A | — | uncertain significance |
| rs370480612 | 1:55,586,425 | C/T | — | uncertain significance |
| rs17111648 | 1:55,588,895 | T/C | intron variant | — |
| rs200504319 | 1:55,589,231 | G/A | — | uncertain significance |
| rs2523696751 | 1:55,589,237 | C/A | — | uncertain significance |
| rs67171713 | 1:55,590,015 | T/C | intron variant | — |
| rs376599050 | 1:55,590,171 | G/A | — | uncertain significance |
| rs200212511 | 1:55,590,202 | G/A | — | uncertain significance |
| rs909762638 | 1:55,590,279 | G/C | — | uncertain significance |
| rs368211572 | 1:55,591,075 | G/A | — | uncertain significance |
| rs2523756896 | 1:55,595,157 | C/T | — | uncertain significance |
| rs185180972 | 1:55,598,026 | G/C | intron variant | — |
| rs201533659 | 1:55,600,058 | G/A | — | uncertain significance |
| rs776267770 | 1:55,603,244 | T/C | — | uncertain significance |
| rs2523827981 | 1:55,603,520 | A/G | — | uncertain significance |
| rs1223361998 | 1:55,604,282 | T/C | — | uncertain significance |
| rs778225378 | 1:55,604,312 | T/C | — | uncertain significance |
| rs768064814 | 1:55,604,335 | A/C | — | uncertain significance |
| rs2523835993 | 1:55,604,337 | G/A | — | uncertain significance |
| rs754017134 | 1:55,604,372 | C/T | — | uncertain significance |
| rs1557625169 | 1:55,607,292 | T/A | — | uncertain significance |
| rs1165226 | 1:55,608,005 | C/T | intron variant | — |
| rs1557627382 | 1:55,608,741 | T/C | — | uncertain significance |
| rs1646967223 | 1:55,609,825 | C/T | — | uncertain significance |
| rs192650149 | 1:55,612,676 | G/A | — | benign |
| rs1647071255 | 1:55,613,468 | T/C | — | uncertain significance |
| rs142943113 | 1:55,614,145 | C/T | — | benign |
| rs2523982287 | 1:55,619,571 | A/G | — | uncertain significance |
| rs370880246 | 1:55,619,851 | C/A | — | uncertain significance |
| rs772476534 | 1:55,619,904 | C/T | — | uncertain significance |
| rs1237349431 | 1:55,619,933 | T/A | — | uncertain significance |
| rs1223438138 | 1:55,620,138 | C/A | — | uncertain significance |
| rs1299696345 | 1:55,620,367 | G/A | — | uncertain significance |
| rs2100742511 | 1:55,620,394 | C/T | — | uncertain significance |
| rs1015272658 | 1:55,620,415 | T/C | — | uncertain significance |
| rs2524007962 | 1:55,622,649 | T/C | — | uncertain significance |
| rs551860796 | 1:55,622,992 | T/C | — | uncertain significance |
| rs763923289 | 1:55,623,033 | A/C | — | uncertain significance |
| rs377597161 | 1:55,624,648 | G/A | — | uncertain significance |
| rs1281264830 | 1:55,624,657 | C/T | — | uncertain significance |
| rs373685626 | 1:55,625,315 | C/T | — | uncertain significance |
| rs17111684 | 1:55,625,548 | C/T | intron variant | — |
| rs17111689 | 1:55,627,525 | C/G | intron variant | — |
| rs913408670 | 1:55,642,067 | C/A | — | uncertain significance |
| rs186427081 | 1:55,643,658 | T/C | — | benign |
| rs2524177406 | 1:55,643,673 | A/G | — | uncertain significance |
| rs762634378 | 1:55,643,733 | T/C | — | uncertain significance |
| rs376472846 | 1:55,643,756 | G/T | — | uncertain significance |
| rs1165225 | 1:55,644,266 | C/T | intron variant | — |
| rs287230 | 1:55,660,292 | G/A | — | — |
| rs12750160 | 1:55,674,000 | C/T | intron variant | — |
| rs287235 | 1:55,678,499 | G/A | — | — |
| rs2524442067 | 1:55,680,564 | C/T | — | uncertain significance |
| rs2524442320 | 1:55,680,579 | G/A | — | uncertain significance |
| rs755458665 | 1:55,680,659 | T/C | — | uncertain significance |
| rs1312808244 | 1:55,680,720 | T/C | — | uncertain significance |
| rs376590533 | 1:55,680,764 | T/C | — | uncertain significance |
Showing 100 of 102 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.