ZFP36L2
ZFP36 like 2 zinc finger CCCH-type
Summary
This gene is a member of the TIS11 family of early response genes. Family members are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. [provided by RefSeq, Jul 2008]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1367173 | 2:43,449,385 | C/G | — | — |
| rs2466074758 | 2:43,451,562 | T/G | — | uncertain significance |
| rs1054059394 | 2:43,451,653 | G/C | — | uncertain significance |
| rs1249302931 | 2:43,451,673 | G/A | — | uncertain significance |
| rs1179958520 | 2:43,451,685 | C/G | — | uncertain significance |
| rs955034240 | 2:43,451,711 | G/A | — | uncertain significance |
| rs369421544 | 2:43,451,716 | C/T | — | likely benign |
| rs768383040 | 2:43,451,738 | C/A | — | uncertain significance |
| rs773123280 | 2:43,451,755 | C/G | — | uncertain significance |
| rs759629300 | 2:43,451,766 | G/A | — | uncertain significance |
| rs866804302 | 2:43,451,783 | G/A | — | uncertain significance |
| rs1344468585 | 2:43,451,814 | C/G | — | uncertain significance |
| rs1422734354 | 2:43,451,852 | G/A | — | uncertain significance |
| rs777385119 | 2:43,451,853 | C/T | — | uncertain significance |
| rs764688757 | 2:43,451,876 | G/A | — | uncertain significance |
| rs769881803 | 2:43,451,892 | C/A | — | uncertain significance |
| rs761958630 | 2:43,451,900 | G/T | — | uncertain significance |
| rs761125625 | 2:43,451,902 | C/T | — | likely benign |
| rs1296052564 | 2:43,451,954 | G/A | — | uncertain significance |
| rs149290349 | 2:43,451,957 | G/A | — | benign |
| rs772208081 | 2:43,451,958 | C/T | — | uncertain significance |
| rs763592426 | 2:43,451,976 | C/T | — | uncertain significance |
| rs1375456352 | 2:43,451,979 | A/G | — | uncertain significance |
| rs754906682 | 2:43,451,996 | G/C | — | uncertain significance |
| rs2466077305 | 2:43,452,010 | C/T | — | likely benign |
| rs373995498 | 2:43,452,021 | A/C | — | pathogenic |
| rs368436754 | 2:43,452,108 | G/A | — | likely benign |
| rs780478324 | 2:43,452,113 | G/A | — | uncertain significance |
| rs1048207781 | 2:43,452,128 | C/G | — | uncertain significance |
| rs890439531 | 2:43,452,129 | C/G | — | uncertain significance |
| rs7933 | 2:43,452,183 | A/G | — | benign |
| rs2466077921 | 2:43,452,191 | C/T | — | uncertain significance |
| rs745472270 | 2:43,452,204 | G/A | — | uncertain significance |
| rs761747459 | 2:43,452,222 | C/G | — | uncertain significance |
| rs201694029 | 2:43,452,286 | G/C | — | likely benign |
| rs8098 | 2:43,452,334 | G/A | — | benign |
| rs759784530 | 2:43,452,389 | C/G | — | uncertain significance |
| rs752046397 | 2:43,452,412 | C/A | — | likely benign |
| rs754529710 | 2:43,452,437 | T/C | — | uncertain significance |
| rs776760038 | 2:43,452,454 | C/T | — | likely benign |
| rs752332320 | 2:43,452,499 | C/G | — | uncertain significance |
| rs76867290 | 2:43,452,608 | A/T | — | benign |
| rs762367560 | 2:43,452,623 | C/T | — | uncertain significance |
| rs748333896 | 2:43,452,647 | C/T | — | uncertain significance |
| rs776988707 | 2:43,452,656 | G/A | — | uncertain significance |
| rs1392388641 | 2:43,452,657 | T/C | — | likely benign |
| rs369626026 | 2:43,452,664 | G/A | — | likely benign |
| rs1667073348 | 2:43,452,666 | C/T | — | uncertain significance |
| rs1027565558 | 2:43,452,669 | C/T | — | uncertain significance |
| rs933129143 | 2:43,452,689 | C/T | — | uncertain significance |
| rs200295188 | 2:43,452,693 | C/T | — | uncertain significance |
| rs781621391 | 2:43,452,707 | G/T | — | uncertain significance |
| rs1470276604 | 2:43,452,725 | C/T | — | uncertain significance |
| rs199815762 | 2:43,452,755 | G/A | — | uncertain significance |
| rs201963284 | 2:43,452,757 | A/C | — | benign |
| rs761844244 | 2:43,452,833 | C/A | — | uncertain significance |
| rs745522686 | 2:43,452,855 | T/C | — | uncertain significance |
| rs112694524 | 2:43,453,721 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.