MIDEAS
mitotic deacetylase associated SANT domain protein
Summary
Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants74 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2503059565 | 14:74,186,089 | A/G | — | uncertain significance |
| rs367952461 | 14:74,186,123 | C/T | — | uncertain significance |
| rs367637105 | 14:74,188,001 | G/A | — | uncertain significance |
| rs200140026 | 14:74,188,007 | T/C | — | uncertain significance |
| rs754024767 | 14:74,188,040 | G/A | — | uncertain significance |
| rs146014844 | 14:74,188,046 | C/T | — | uncertain significance |
| rs758867456 | 14:74,188,055 | C/T | — | uncertain significance |
| rs143153494 | 14:74,188,083 | T/C | — | uncertain significance |
| rs1390673377 | 14:74,188,106 | T/A | — | uncertain significance |
| rs60635070 | 14:74,188,164 | T/C | — | uncertain significance |
| rs148804472 | 14:74,189,447 | G/A | — | uncertain significance |
| rs779920233 | 14:74,192,022 | T/G | — | uncertain significance |
| rs2503076708 | 14:74,192,054 | T/C | — | uncertain significance |
| rs749019320 | 14:74,192,759 | G/A | — | uncertain significance |
| rs1224693032 | 14:74,192,774 | C/T | — | uncertain significance |
| rs139702995 | 14:74,192,801 | T/C | — | uncertain significance |
| rs2503081767 | 14:74,193,395 | G/A | — | uncertain significance |
| rs143218610 | 14:74,193,540 | C/G | — | uncertain significance |
| rs2503082569 | 14:74,193,575 | G/A | — | uncertain significance |
| rs2503082616 | 14:74,193,584 | C/T | — | uncertain significance |
| rs2503082726 | 14:74,193,603 | A/T | — | uncertain significance |
| rs200440320 | 14:74,194,177 | G/C | — | uncertain significance |
| rs1261090911 | 14:74,194,218 | T/G | — | uncertain significance |
| rs374258786 | 14:74,196,379 | T/C | — | uncertain significance |
| rs765961232 | 14:74,196,423 | T/C | — | uncertain significance |
| rs200009619 | 14:74,196,526 | C/T | — | uncertain significance |
| rs2503091842 | 14:74,196,534 | C/T | — | uncertain significance |
| rs201704789 | 14:74,196,645 | C/T | — | uncertain significance |
| rs568125826 | 14:74,196,722 | C/T | — | — |
| rs190973077 | 14:74,198,420 | C/T | intron variant | — |
| rs866633106 | 14:74,203,744 | C/A | — | uncertain significance |
| rs199689942 | 14:74,203,754 | T/C | — | uncertain significance |
| rs764264585 | 14:74,203,787 | C/T | — | uncertain significance |
| rs2503112157 | 14:74,203,828 | G/A | — | likely benign |
| rs149419468 | 14:74,203,844 | C/T | — | uncertain significance |
| rs2503112426 | 14:74,203,893 | G/C | — | uncertain significance |
| rs201977850 | 14:74,203,975 | C/T | — | uncertain significance |
| rs776767092 | 14:74,205,327 | T/G | — | uncertain significance |
| rs371659365 | 14:74,205,336 | C/T | — | uncertain significance |
| rs146209706 | 14:74,205,345 | C/T | — | uncertain significance |
| rs754884289 | 14:74,205,369 | C/T | — | uncertain significance |
| rs760323523 | 14:74,205,436 | G/A | — | uncertain significance |
| rs374583347 | 14:74,205,450 | C/T | — | uncertain significance |
| rs2053238530 | 14:74,205,460 | G/A | — | uncertain significance |
| rs370492474 | 14:74,205,498 | C/A | — | uncertain significance |
| rs368078040 | 14:74,205,508 | G/C | — | uncertain significance |
| rs201766970 | 14:74,205,594 | C/T | — | uncertain significance |
| rs1406164082 | 14:74,205,682 | G/A | — | uncertain significance |
| rs770422656 | 14:74,205,741 | G/T | — | uncertain significance |
| rs1394372436 | 14:74,205,750 | A/G | — | uncertain significance |
| rs765568789 | 14:74,205,774 | G/C | — | uncertain significance |
| rs370627322 | 14:74,205,790 | G/T | — | uncertain significance |
| rs377123380 | 14:74,205,805 | G/A | — | uncertain significance |
| rs754474089 | 14:74,205,816 | G/A | — | uncertain significance |
| rs2053245822 | 14:74,205,853 | C/T | — | uncertain significance |
| rs540631454 | 14:74,205,996 | G/A | — | uncertain significance |
| rs377433576 | 14:74,206,008 | G/A | — | uncertain significance |
| rs200341939 | 14:74,206,012 | G/C | — | uncertain significance |
| rs2503121319 | 14:74,206,165 | T/A | — | uncertain significance |
| rs772282790 | 14:74,206,173 | C/T | — | uncertain significance |
| rs1195872318 | 14:74,206,255 | C/T | — | likely benign |
| rs372198853 | 14:74,206,266 | G/A | — | uncertain significance |
| rs751590751 | 14:74,206,375 | C/T | — | uncertain significance |
| rs772877670 | 14:74,206,429 | C/T | — | uncertain significance |
| rs368267089 | 14:74,206,468 | G/A | — | uncertain significance |
| rs2503123483 | 14:74,206,548 | G/T | — | uncertain significance |
| rs746579424 | 14:74,206,549 | C/T | — | uncertain significance |
| rs1456266032 | 14:74,206,653 | C/T | — | likely benign |
| rs531361502 | 14:74,206,677 | T/C | — | uncertain significance |
| rs544453779 | 14:74,218,569 | C/T | — | — |
| rs114609788 | 14:74,223,967 | C/A | upstream gene variant | — |
| rs114165892 | 14:74,223,968 | C/T | — | — |
| rs11844552 | 14:74,224,577 | A/G | upstream gene variant | — |
| rs59862836 | 14:74,236,619 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.