MIDN
midnolin
Summary
Enables molecular adaptor activity. Involved in proteasomal ubiquitin-independent protein catabolic process. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10425079 | 19:1,247,290 | T/C | regulatory region variant | — |
| rs971142541 | 19:1,250,308 | C/G | — | uncertain significance |
| rs2145484307 | 19:1,250,378 | C/T | — | uncertain significance |
| rs777300728 | 19:1,250,388 | G/C | — | uncertain significance |
| rs775440270 | 19:1,250,401 | C/T | — | uncertain significance |
| rs779945506 | 19:1,250,459 | G/A | — | uncertain significance |
| rs763117290 | 19:1,250,485 | C/A | — | uncertain significance |
| rs2513000871 | 19:1,250,492 | T/G | — | uncertain significance |
| rs781052615 | 19:1,250,526 | C/A | — | uncertain significance |
| rs2513001005 | 19:1,250,527 | A/G | — | uncertain significance |
| rs2513005025 | 19:1,251,863 | C/T | — | uncertain significance |
| rs73494666 | 19:1,253,642 | C/G | — | — |
| rs748137724 | 19:1,254,182 | C/T | — | uncertain significance |
| rs754784777 | 19:1,254,247 | C/T | — | uncertain significance |
| rs201144803 | 19:1,254,304 | G/A | — | likely benign |
| rs1338724071 | 19:1,254,316 | C/T | — | uncertain significance |
| rs748612554 | 19:1,254,343 | G/C | — | uncertain significance |
| rs751831100 | 19:1,254,357 | C/G | — | uncertain significance |
| rs201314448 | 19:1,254,359 | G/A | — | uncertain significance |
| rs1568789391 | 19:1,254,367 | T/A | — | uncertain significance |
| rs376802436 | 19:1,254,404 | C/T | — | uncertain significance |
| rs781569306 | 19:1,254,436 | G/A | — | uncertain significance |
| rs550865023 | 19:1,254,446 | G/A | — | uncertain significance |
| rs779545651 | 19:1,254,463 | A/G | — | uncertain significance |
| rs765726789 | 19:1,254,920 | C/T | — | uncertain significance |
| rs755812511 | 19:1,254,941 | C/G | — | uncertain significance |
| rs149674816 | 19:1,254,947 | C/T | — | likely benign |
| rs372488115 | 19:1,254,958 | T/C | — | uncertain significance |
| rs554393552 | 19:1,254,983 | C/T | — | uncertain significance |
| rs146446826 | 19:1,255,002 | C/T | — | likely benign |
| rs752070614 | 19:1,255,031 | C/G | — | uncertain significance |
| rs753475621 | 19:1,255,039 | G/A | — | uncertain significance |
| rs369704822 | 19:1,255,474 | G/A | — | uncertain significance |
| rs752565935 | 19:1,255,475 | G/A | — | uncertain significance |
| rs2511980798 | 19:1,255,552 | C/G | — | uncertain significance |
| rs758714390 | 19:1,255,564 | G/A | — | uncertain significance |
| rs150627531 | 19:1,255,573 | T/A | — | uncertain significance |
| rs1380821444 | 19:1,255,583 | C/T | — | uncertain significance |
| rs537901815 | 19:1,255,594 | G/A | — | uncertain significance |
| rs572411883 | 19:1,255,600 | G/A | — | likely benign |
| rs377416779 | 19:1,255,691 | C/T | — | uncertain significance |
| rs57586121 | 19:1,255,719 | A/G | regulatory region variant | — |
| rs532939242 | 19:1,256,158 | C/A | — | — |
| rs2081206523 | 19:1,256,996 | G/A | — | uncertain significance |
| rs149895689 | 19:1,257,027 | C/T | — | uncertain significance |
| rs747187886 | 19:1,257,091 | G/A | — | likely benign |
| rs763398874 | 19:1,257,099 | C/T | — | uncertain significance |
| rs143942530 | 19:1,257,128 | C/T | — | uncertain significance |
| rs142058269 | 19:1,257,136 | C/T | — | benign |
| rs147781717 | 19:1,257,137 | G/C | — | uncertain significance |
| rs539586624 | 19:1,257,146 | G/A | — | uncertain significance |
| rs2081209527 | 19:1,257,162 | G/C | — | uncertain significance |
| rs2511983867 | 19:1,257,215 | T/C | — | uncertain significance |
| rs1344096619 | 19:1,257,218 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.