DDX42
DEAD-box helicase 42
Summary
This gene encodes a member of the Asp-Glu-Ala-Asp (DEAD) box protein family. Members of this protein family are putative RNA helicases, and are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1464119250 | 17:61,864,474 | G/A | — | uncertain significance |
| rs2511380125 | 17:61,864,500 | C/T | — | uncertain significance |
| rs780858678 | 17:61,864,530 | G/T | — | uncertain significance |
| rs2511380289 | 17:61,864,609 | C/T | — | uncertain significance |
| rs150380771 | 17:61,869,806 | G/A | — | uncertain significance |
| rs2039640108 | 17:61,869,810 | A/C | — | uncertain significance |
| rs7220095 | 17:61,871,239 | T/A | — | — |
| rs117257623 | 17:61,874,043 | G/A | intron variant | — |
| rs758688060 | 17:61,882,465 | A/G | — | uncertain significance |
| rs200037987 | 17:61,882,476 | G/A | — | uncertain significance |
| rs2511398313 | 17:61,882,534 | G/A | — | uncertain significance |
| rs770365184 | 17:61,883,926 | G/T | — | uncertain significance |
| rs139264003 | 17:61,883,962 | T/C | — | uncertain significance |
| rs2511402059 | 17:61,886,187 | C/G | — | uncertain significance |
| rs137904708 | 17:61,886,223 | G/A | — | uncertain significance |
| rs970265933 | 17:61,886,953 | A/G | — | uncertain significance |
| rs753293991 | 17:61,887,906 | G/A | — | uncertain significance |
| rs2039916358 | 17:61,889,367 | C/A | — | uncertain significance |
| rs753747374 | 17:61,889,448 | A/G | — | uncertain significance |
| rs1247150060 | 17:61,889,566 | C/T | — | uncertain significance |
| rs142912378 | 17:61,890,617 | A/G | — | uncertain significance |
| rs2511408062 | 17:61,890,726 | A/G | — | uncertain significance |
| rs768006629 | 17:61,890,781 | C/T | — | likely benign |
| rs749778858 | 17:61,890,809 | A/G | — | uncertain significance |
| rs142666932 | 17:61,892,969 | A/T | — | uncertain significance |
| rs1343472038 | 17:61,894,304 | C/T | — | uncertain significance |
| rs2584628 | 17:61,894,578 | T/C | downstream gene variant | — |
| rs2511414227 | 17:61,895,067 | G/C | — | uncertain significance |
| rs775376583 | 17:61,895,117 | G/C | — | uncertain significance |
| rs748924801 | 17:61,895,190 | A/C | — | uncertain significance |
| rs372074381 | 17:61,895,219 | G/A | — | likely benign |
| rs753492498 | 17:61,895,255 | A/G | — | uncertain significance |
| rs974801161 | 17:61,895,304 | A/G | — | uncertain significance |
| rs1364480467 | 17:61,895,322 | A/G | — | likely benign |
| rs1229040755 | 17:61,895,340 | C/A | — | uncertain significance |
| rs2144596077 | 17:61,895,346 | G/T | — | uncertain significance |
| rs748213997 | 17:61,895,382 | G/A | — | uncertain significance |
| rs369378680 | 17:61,895,394 | G/C | — | uncertain significance |
| rs138535741 | 17:61,895,439 | G/A | — | uncertain significance |
| rs2040000470 | 17:61,895,450 | G/A | — | uncertain significance |
| rs200701706 | 17:61,895,604 | A/C | — | uncertain significance |
| rs2040005833 | 17:61,895,688 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.