ZSCAN21
zinc finger and SCAN domain containing 21
Summary
Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs182685663 | 7:99,648,530 | G/A | intron variant | — |
| rs138713462 | 7:99,654,708 | A/G | — | uncertain significance |
| rs566511570 | 7:99,654,736 | A/G | — | uncertain significance |
| rs375145287 | 7:99,654,762 | C/T | — | uncertain significance |
| rs200464385 | 7:99,654,763 | G/T | — | uncertain significance |
| rs750102855 | 7:99,654,766 | A/G | — | uncertain significance |
| rs769583600 | 7:99,654,808 | G/A | — | uncertain significance |
| rs775625448 | 7:99,654,943 | T/C | — | uncertain significance |
| rs1303461267 | 7:99,654,990 | G/A | — | uncertain significance |
| rs201175038 | 7:99,655,003 | G/A | — | likely benign |
| rs2546835895 | 7:99,655,361 | A/C | — | uncertain significance |
| rs753003880 | 7:99,655,423 | A/G | — | uncertain significance |
| rs775082571 | 7:99,655,472 | G/T | — | uncertain significance |
| rs761647964 | 7:99,655,488 | C/A | — | uncertain significance |
| rs765252660 | 7:99,661,434 | G/A | — | uncertain significance |
| rs142262559 | 7:99,661,600 | A/C | — | uncertain significance |
| rs146827623 | 7:99,661,614 | G/A | — | likely benign |
| rs201249540 | 7:99,661,644 | C/T | — | uncertain significance |
| rs140607349 | 7:99,661,650 | A/G | — | uncertain significance |
| rs1584390519 | 7:99,661,663 | G/C | — | uncertain significance |
| rs753061917 | 7:99,661,681 | A/G | — | uncertain significance |
| rs1266099026 | 7:99,661,683 | A/G | — | uncertain significance |
| rs371809963 | 7:99,661,708 | G/C | — | uncertain significance |
| rs368423078 | 7:99,661,746 | T/C | — | uncertain significance |
| rs1463910762 | 7:99,661,831 | G/T | — | uncertain significance |
| rs774647848 | 7:99,661,873 | G/A | — | uncertain significance |
| rs201972786 | 7:99,662,065 | A/G | — | uncertain significance |
| rs747027091 | 7:99,662,095 | A/C | — | uncertain significance |
| rs2546846836 | 7:99,662,134 | C/T | — | uncertain significance |
| rs200907549 | 7:99,662,185 | A/G | — | uncertain significance |
| rs1267359398 | 7:99,662,236 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.