MINDY2
MINDY lysine 48 deubiquitinase 2
Summary
Enables peptidase activity and polyubiquitin modification-dependent protein binding activity. Predicted to be involved in chromatin remodeling and proteolysis. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs376730103 | 15:59,063,694 | A/T | — | uncertain significance |
| rs759937759 | 15:59,063,703 | G/C | — | uncertain significance |
| rs1595688260 | 15:59,063,721 | G/A | — | uncertain significance |
| rs1037468456 | 15:59,063,724 | T/A | — | uncertain significance |
| rs557342297 | 15:59,063,809 | C/G | — | uncertain significance |
| rs781111103 | 15:59,063,826 | C/T | — | uncertain significance |
| rs573394169 | 15:59,063,844 | G/T | — | uncertain significance |
| rs1595689028 | 15:59,063,902 | G/A | — | uncertain significance |
| rs182620597 | 15:59,063,905 | G/A | — | uncertain significance |
| rs1318160684 | 15:59,063,923 | C/T | — | uncertain significance |
| rs762642665 | 15:59,063,935 | C/T | — | uncertain significance |
| rs374853839 | 15:59,063,950 | T/C | — | likely benign |
| rs1900437526 | 15:59,064,069 | A/G | — | uncertain significance |
| rs944417978 | 15:59,064,145 | C/A | — | uncertain significance |
| rs754415482 | 15:59,064,157 | G/T | — | uncertain significance |
| rs768264473 | 15:59,064,192 | A/G | — | uncertain significance |
| rs547008527 | 15:59,064,249 | A/C | — | uncertain significance |
| rs754616116 | 15:59,064,254 | G/C | — | uncertain significance |
| rs369473023 | 15:59,064,261 | G/C | — | uncertain significance |
| rs199979863 | 15:59,064,270 | A/G | — | likely benign |
| rs79378213 | 15:59,064,292 | C/T | — | uncertain significance |
| rs139080301 | 15:59,074,347 | G/C | — | — |
| rs2548900946 | 15:59,080,129 | A/G | — | uncertain significance |
| rs145829831 | 15:59,092,364 | T/G | intron variant | — |
| rs752539072 | 15:59,094,559 | C/T | — | uncertain significance |
| rs7183811 | 15:59,108,658 | A/G | intron variant | — |
| rs529941729 | 15:59,112,356 | T/A | — | — |
| rs34849581 | 15:59,123,238 | G/A | intron variant | — |
| rs373513458 | 15:59,124,047 | A/G | — | uncertain significance |
| rs756047364 | 15:59,124,080 | C/T | — | uncertain significance |
| rs750303322 | 15:59,139,557 | A/G | — | uncertain significance |
| rs748363533 | 15:59,139,571 | G/A | — | uncertain significance |
| rs1396173727 | 15:59,139,668 | A/T | — | uncertain significance |
| rs376405828 | 15:59,143,980 | T/C | — | uncertain significance |
| rs199705219 | 15:59,144,018 | A/C | — | uncertain significance |
| rs117942397 | 15:59,144,022 | A/G | — | uncertain significance |
| rs369163190 | 15:59,144,133 | C/T | — | uncertain significance |
| rs946967412 | 15:59,146,775 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.