MED24
mediator complex subunit 24
Summary
This gene encodes a component of the mediator complex (also known as TRAP, SMCC, DRIP, or ARC), a transcriptional coactivator complex thought to be required for the expression of almost all genes. The mediator complex is recruited by transcriptional activators or nuclear receptors to induce gene expression, possibly by interacting with RNA polymerase II and promoting the formation of a transcriptional pre-initiation complex. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs709591 | 17:38,175,561 | T/G | — | — |
| rs776426730 | 17:38,175,789 | G/A | — | uncertain significance |
| rs778521509 | 17:38,175,840 | G/A | — | uncertain significance |
| rs11555254 | 17:38,175,866 | G/A | — | benign |
| rs769754599 | 17:38,175,894 | G/A | — | uncertain significance |
| rs16965540 | 17:38,176,031 | T/C | — | benign |
| rs371639314 | 17:38,176,050 | C/T | — | uncertain significance |
| rs776987335 | 17:38,176,072 | C/T | — | uncertain significance |
| rs754812266 | 17:38,176,144 | G/A | — | uncertain significance |
| rs748099423 | 17:38,176,148 | G/A | — | uncertain significance |
| rs142219986 | 17:38,176,550 | G/A | — | uncertain significance |
| rs377258028 | 17:38,178,216 | G/A | — | uncertain significance |
| rs1428505324 | 17:38,178,232 | C/T | — | uncertain significance |
| rs2544063514 | 17:38,178,257 | C/T | — | uncertain significance |
| rs778699289 | 17:38,178,267 | G/A | — | uncertain significance |
| rs137866788 | 17:38,178,660 | C/T | — | uncertain significance |
| rs913807148 | 17:38,178,687 | G/A | — | uncertain significance |
| rs535594488 | 17:38,178,916 | G/A | — | uncertain significance |
| rs373136853 | 17:38,178,941 | T/C | — | uncertain significance |
| rs1982178235 | 17:38,178,946 | G/A | — | uncertain significance |
| rs2544067458 | 17:38,179,010 | G/T | — | uncertain significance |
| rs760297650 | 17:38,179,042 | C/T | — | likely pathogenic |
| rs201206358 | 17:38,179,043 | G/A | — | uncertain significance |
| rs748727353 | 17:38,179,061 | G/C | — | uncertain significance |
| rs4794824 | 17:38,179,290 | G/A | downstream gene variant | — |
| rs376616538 | 17:38,179,449 | T/A | — | uncertain significance |
| rs775356662 | 17:38,179,455 | G/A | — | uncertain significance |
| rs2302777 | 17:38,179,492 | A/G | synonymous variant | benign |
| rs780526993 | 17:38,179,526 | G/A | — | uncertain significance |
| rs865792448 | 17:38,179,590 | C/T | — | likely benign |
| rs764316767 | 17:38,179,605 | C/T | — | uncertain significance |
| rs2302778 | 17:38,179,667 | A/G | — | benign |
| rs373322107 | 17:38,182,488 | G/A | — | uncertain significance |
| rs532514222 | 17:38,182,512 | C/T | — | uncertain significance |
| rs926133816 | 17:38,183,176 | G/A | — | uncertain significance |
| rs765875029 | 17:38,185,091 | C/T | — | uncertain significance |
| rs1568162263 | 17:38,186,020 | G/C | — | likely pathogenic |
| rs2544100352 | 17:38,186,029 | G/A | — | uncertain significance |
| rs776776500 | 17:38,186,107 | G/A | — | uncertain significance |
| rs201474001 | 17:38,186,919 | A/T | — | — |
| rs150033509 | 17:38,187,428 | T/C | — | uncertain significance |
| rs149212946 | 17:38,187,845 | A/G | — | uncertain significance |
| rs373051060 | 17:38,189,352 | G/A | — | uncertain significance |
| rs141135892 | 17:38,189,353 | T/G | — | uncertain significance |
| rs762866058 | 17:38,189,358 | C/T | — | uncertain significance |
| rs143564076 | 17:38,189,407 | G/A | — | uncertain significance |
| rs201239361 | 17:38,189,635 | G/A | — | uncertain significance |
| rs370373019 | 17:38,189,642 | C/T | — | likely benign |
| rs558755458 | 17:38,189,643 | G/A | — | uncertain significance |
| rs1279260720 | 17:38,189,655 | T/C | — | uncertain significance |
| rs34585432 | 17:38,189,659 | C/T | — | benign |
| rs144621344 | 17:38,191,391 | T/C | — | uncertain significance |
| rs937319726 | 17:38,191,405 | C/T | — | uncertain significance |
| rs539466477 | 17:38,191,507 | C/G | — | uncertain significance |
| rs540415066 | 17:38,191,577 | T/C | — | uncertain significance |
| rs757233957 | 17:38,191,982 | G/A | — | uncertain significance |
| rs2544126793 | 17:38,192,010 | C/G | — | uncertain significance |
| rs142648771 | 17:38,195,234 | C/T | regulatory region variant | — |
| rs1461548225 | 17:38,209,600 | G/A | — | uncertain significance |
| rs764382545 | 17:38,209,758 | G/T | — | uncertain significance |
| rs751905493 | 17:38,209,766 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.