EDC4
enhancer of mRNA decapping 4
Summary
Predicted to be involved in deadenylation-independent decapping of nuclear-transcribed mRNA. Located in P-body and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs369362135 | 16:67,907,241 | C/G | — | uncertain significance |
| rs56374641 | 16:67,908,713 | G/A | — | — |
| rs147080619 | 16:67,909,863 | G/T | — | uncertain significance |
| rs770131587 | 16:67,909,868 | C/T | — | uncertain significance |
| rs373416466 | 16:67,909,878 | G/T | — | uncertain significance |
| rs979403180 | 16:67,909,995 | A/G | — | uncertain significance |
| rs1488444319 | 16:67,910,462 | G/A | — | uncertain significance |
| rs762255664 | 16:67,911,281 | C/T | — | uncertain significance |
| rs8060686 | 16:67,911,517 | T/C | synonymous variant | — |
| rs2544346066 | 16:67,911,669 | T/A | — | uncertain significance |
| rs111231628 | 16:67,911,677 | A/G | — | likely benign |
| rs752460333 | 16:67,911,695 | G/A | — | uncertain significance |
| rs757911873 | 16:67,911,701 | G/A | — | uncertain significance |
| rs757734244 | 16:67,911,725 | A/G | — | uncertain significance |
| rs200449852 | 16:67,912,101 | G/A | — | benign |
| rs750996360 | 16:67,912,126 | G/A | — | uncertain significance |
| rs1341348818 | 16:67,912,168 | G/A | — | uncertain significance |
| rs537335476 | 16:67,913,222 | T/G | — | benign |
| rs370365160 | 16:67,913,338 | G/A | — | uncertain significance |
| rs374190646 | 16:67,913,510 | G/A | — | uncertain significance |
| rs976591622 | 16:67,913,562 | T/C | — | uncertain significance |
| rs965430280 | 16:67,913,651 | A/G | — | uncertain significance |
| rs1290587567 | 16:67,913,755 | C/G | — | uncertain significance |
| rs2058058230 | 16:67,913,796 | G/A | — | uncertain significance |
| rs200787993 | 16:67,913,804 | A/G | — | uncertain significance |
| rs2544350976 | 16:67,913,973 | G/A | — | uncertain significance |
| rs1483388098 | 16:67,914,004 | T/C | — | uncertain significance |
| rs774350066 | 16:67,914,055 | G/A | — | uncertain significance |
| rs149227826 | 16:67,914,084 | C/G | — | uncertain significance |
| rs1406431717 | 16:67,914,469 | G/T | — | uncertain significance |
| rs995782313 | 16:67,914,623 | G/A | — | uncertain significance |
| rs1254283323 | 16:67,914,688 | C/G | — | uncertain significance |
| rs1190770002 | 16:67,914,745 | C/T | — | uncertain significance |
| rs188082306 | 16:67,914,848 | C/T | — | uncertain significance |
| rs376988427 | 16:67,915,186 | G/C | — | likely benign |
| rs145018702 | 16:67,915,239 | G/A | — | uncertain significance |
| rs138068113 | 16:67,915,264 | C/G | — | likely benign |
| rs149541951 | 16:67,915,284 | C/T | — | uncertain significance |
| rs1243411142 | 16:67,915,580 | C/A | — | uncertain significance |
| rs776151334 | 16:67,915,595 | C/T | — | uncertain significance |
| rs377386261 | 16:67,915,664 | C/T | — | uncertain significance |
| rs745548951 | 16:67,915,712 | G/A | — | uncertain significance |
| rs374187596 | 16:67,915,719 | G/T | — | uncertain significance |
| rs1020490579 | 16:67,915,895 | C/T | — | uncertain significance |
| rs1213062384 | 16:67,915,941 | C/T | — | uncertain significance |
| rs374486323 | 16:67,915,958 | G/A | — | uncertain significance |
| rs537517125 | 16:67,916,007 | C/T | — | uncertain significance |
| rs2544355773 | 16:67,916,409 | C/G | — | uncertain significance |
| rs139960780 | 16:67,916,606 | T/C | — | uncertain significance |
| rs2058074388 | 16:67,916,615 | G/A | — | uncertain significance |
| rs760900009 | 16:67,916,898 | G/A | — | uncertain significance |
| rs781090608 | 16:67,916,916 | G/A | — | uncertain significance |
| rs774525692 | 16:67,916,971 | G/A | — | uncertain significance |
| rs756025487 | 16:67,917,013 | G/C | — | uncertain significance |
| rs367900519 | 16:67,917,472 | C/T | — | uncertain significance |
| rs781543069 | 16:67,917,519 | G/A | — | uncertain significance |
| rs2544358503 | 16:67,917,573 | C/G | — | uncertain significance |
| rs370577533 | 16:67,917,859 | C/T | — | likely benign |
| rs1459242586 | 16:67,917,875 | G/A | — | uncertain significance |
| rs2544359485 | 16:67,917,959 | T/A | — | uncertain significance |
| rs1242356021 | 16:67,918,031 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.