SENP2
SUMO specific peptidase 2
Summary
SUMO1 (UBL1; MIM 601912) is a small ubiquitin-like protein that can be covalently conjugated to other proteins. SENP2 is one of a group of enzymes that process newly synthesized SUMO1 into the conjugatable form and catalyze the deconjugation of SUMO1-containing species.[supplied by OMIM, Apr 2004]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6778977 | 3:185,302,532 | T/G | upstream gene variant | — |
| rs371947025 | 3:185,307,915 | A/G | — | uncertain significance |
| rs370601182 | 3:185,316,207 | T/G | — | uncertain significance |
| rs2474186170 | 3:185,316,301 | A/T | — | uncertain significance |
| rs2474187397 | 3:185,316,774 | T/C | — | uncertain significance |
| rs12374077 | 3:185,317,674 | G/A | — | — |
| rs768990972 | 3:185,318,622 | G/A | — | uncertain significance |
| rs13081203 | 3:185,322,643 | G/A | upstream gene variant | — |
| rs542148822 | 3:185,324,197 | A/G | — | uncertain significance |
| rs1286640039 | 3:185,327,114 | G/A | — | uncertain significance |
| rs79193891 | 3:185,327,128 | A/G | — | benign |
| rs143348143 | 3:185,329,450 | G/A | — | uncertain significance |
| rs147526977 | 3:185,329,527 | A/G | — | uncertain significance |
| rs960843455 | 3:185,329,532 | A/T | — | uncertain significance |
| rs35637544 | 3:185,329,958 | A/G | intron variant | — |
| rs183052599 | 3:185,330,391 | A/G | — | likely benign |
| rs6785918 | 3:185,330,631 | A/C | — | — |
| rs6762208 | 3:185,331,165 | C/A | — | benign |
| rs777238584 | 3:185,332,371 | A/C | — | uncertain significance |
| rs2474224500 | 3:185,335,287 | G/A | — | uncertain significance |
| rs770213102 | 3:185,335,290 | A/G | — | uncertain significance |
| rs1380597000 | 3:185,335,307 | C/T | — | uncertain significance |
| rs1277913990 | 3:185,335,308 | C/T | — | uncertain significance |
| rs2474227430 | 3:185,337,187 | C/T | — | uncertain significance |
| rs6784842 | 3:185,342,723 | C/A | — | — |
| rs144387716 | 3:185,347,580 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.