ZSCAN2
zinc finger and SCAN domain containing 2
Summary
The protein encoded by this gene contains several copies of zinc finger motif, which is commonly found in transcriptional regulatory proteins. Studies in mice show that this gene is expressed during embryonic development, and specifically in the testis in adult mice, suggesting that it may play a role in regulating genes in germ cells. Alternative splicing of this gene results in several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7181273 | 15:85,143,490 | A/G | — | — |
| rs182736722 | 15:85,147,175 | T/G | — | uncertain significance |
| rs146866915 | 15:85,147,178 | C/T | — | uncertain significance |
| rs924725525 | 15:85,147,183 | G/A | — | uncertain significance |
| rs1240079877 | 15:85,147,206 | G/C | — | uncertain significance |
| rs1895293860 | 15:85,147,264 | G/A | — | uncertain significance |
| rs747355496 | 15:85,147,268 | A/G | — | uncertain significance |
| rs1567005824 | 15:85,147,295 | T/C | — | uncertain significance |
| rs577882298 | 15:85,147,315 | T/A | — | uncertain significance |
| rs756957470 | 15:85,147,348 | G/A | — | likely benign |
| rs772221668 | 15:85,147,376 | C/G | — | uncertain significance |
| rs150217069 | 15:85,147,385 | C/A | — | uncertain significance |
| rs761562959 | 15:85,147,394 | G/A | — | uncertain significance |
| rs1035970057 | 15:85,147,461 | G/T | — | uncertain significance |
| rs960297822 | 15:85,147,462 | C/G | — | uncertain significance |
| rs143139453 | 15:85,147,494 | G/T | — | uncertain significance |
| rs138899257 | 15:85,147,499 | G/A | — | uncertain significance |
| rs976618155 | 15:85,147,541 | T/C | — | uncertain significance |
| rs760384430 | 15:85,147,546 | C/G | — | uncertain significance |
| rs748455 | 15:85,149,575 | T/C | intron variant | — |
| rs2341185 | 15:85,152,937 | G/T | — | — |
| rs71395455 | 15:85,153,804 | A/C | — | — |
| rs7180952 | 15:85,162,551 | C/T | upstream gene variant | — |
| rs149816515 | 15:85,163,896 | G/A | — | likely benign |
| rs139722283 | 15:85,163,906 | C/A | — | uncertain significance |
| rs761717307 | 15:85,163,908 | C/G | — | uncertain significance |
| rs753315167 | 15:85,163,976 | A/G | — | likely benign |
| rs2505306220 | 15:85,164,012 | C/T | — | uncertain significance |
| rs142275625 | 15:85,164,013 | C/A | — | likely benign |
| rs376408615 | 15:85,164,039 | G/C | — | uncertain significance |
| rs151264960 | 15:85,164,049 | A/G | — | uncertain significance |
| rs373531511 | 15:85,164,154 | C/T | — | uncertain significance |
| rs748429984 | 15:85,164,246 | G/A | — | uncertain significance |
| rs1319190806 | 15:85,164,258 | T/G | — | uncertain significance |
| rs760990068 | 15:85,164,316 | A/G | — | uncertain significance |
| rs770722985 | 15:85,164,390 | A/T | — | uncertain significance |
| rs146224159 | 15:85,164,463 | G/A | — | uncertain significance |
| rs770506908 | 15:85,164,528 | G/A | — | uncertain significance |
| rs770122410 | 15:85,164,535 | G/A | — | uncertain significance |
| rs2505308875 | 15:85,164,539 | T/A | — | uncertain significance |
| rs761971075 | 15:85,164,564 | C/T | — | uncertain significance |
| rs146139234 | 15:85,164,597 | A/G | — | uncertain significance |
| rs202006776 | 15:85,164,643 | T/C | — | uncertain significance |
| rs2505309452 | 15:85,164,658 | C/G | — | uncertain significance |
| rs193921069 | 15:85,164,681 | C/A | — | uncertain significance |
| rs200358209 | 15:85,164,736 | G/A | — | uncertain significance |
| rs201050627 | 15:85,164,916 | C/A | — | uncertain significance |
| rs1241308042 | 15:85,164,919 | G/A | — | uncertain significance |
| rs200037418 | 15:85,164,942 | G/A | — | uncertain significance |
| rs773175399 | 15:85,164,966 | C/T | — | uncertain significance |
| rs146985684 | 15:85,164,967 | G/A | — | uncertain significance |
| rs376085668 | 15:85,164,990 | C/T | — | uncertain significance |
| rs150175069 | 15:85,164,991 | G/A | — | uncertain significance |
| rs761644924 | 15:85,165,000 | C/T | — | uncertain significance |
| rs1345773524 | 15:85,165,023 | C/T | — | uncertain significance |
| rs776805814 | 15:85,165,047 | C/T | — | uncertain significance |
| rs182456686 | 15:85,165,195 | A/C | — | uncertain significance |
| rs1212304590 | 15:85,165,204 | A/G | — | uncertain significance |
| rs1331867763 | 15:85,165,210 | T/C | — | uncertain significance |
| rs1161492290 | 15:85,165,212 | A/G | — | uncertain significance |
| rs570812618 | 15:85,166,526 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.