ZKSCAN5
zinc finger with KRAB and SCAN domains 5
Summary
This gene encodes a zinc finger protein of the Kruppel family. The protein contains a SCAN box and a KRAB A domain and may be involved in transcriptional regulation. A similar protein in mouse is differentially expressed in spermatogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs66509940 | 7:99,101,503 | C/A | — | — |
| rs759875739 | 7:99,103,723 | C/A | — | uncertain significance |
| rs769444251 | 7:99,103,804 | T/C | — | uncertain significance |
| rs2485238602 | 7:99,103,842 | C/T | — | uncertain significance |
| rs777649511 | 7:99,104,049 | A/G | — | uncertain significance |
| rs200939318 | 7:99,104,080 | A/G | — | uncertain significance |
| rs9656060 | 7:99,106,674 | C/T | intron variant | — |
| rs3901286 | 7:99,107,727 | C/A | intron variant | — |
| rs2485274636 | 7:99,110,095 | T/C | — | uncertain significance |
| rs61739592 | 7:99,110,105 | G/A | — | benign |
| rs2485275556 | 7:99,110,190 | A/G | — | uncertain significance |
| rs774509272 | 7:99,110,194 | C/T | — | uncertain significance |
| rs201540731 | 7:99,110,197 | G/A | — | likely benign |
| rs61735345 | 7:99,110,213 | T/C | — | benign |
| rs10230784 | 7:99,113,672 | G/A | intron variant | — |
| rs12533251 | 7:99,115,677 | G/A | intron variant | — |
| rs953017456 | 7:99,117,820 | A/C | — | uncertain significance |
| rs971871854 | 7:99,117,865 | A/T | — | uncertain significance |
| rs11761528 | 7:99,118,801 | C/G | — | — |
| rs7804551 | 7:99,119,110 | A/G | intron variant | — |
| rs10271582 | 7:99,121,950 | A/G | intron variant | — |
| rs756726901 | 7:99,123,439 | A/G | — | uncertain significance |
| rs756408825 | 7:99,123,501 | T/C | — | uncertain significance |
| rs756964645 | 7:99,123,511 | C/T | — | uncertain significance |
| rs746317129 | 7:99,123,540 | G/A | — | uncertain significance |
| rs1036014382 | 7:99,123,567 | C/A | — | uncertain significance |
| rs1467464458 | 7:99,123,594 | G/A | — | uncertain significance |
| rs114266714 | 7:99,123,668 | C/A | — | uncertain significance |
| rs115589475 | 7:99,123,669 | C/T | — | uncertain significance |
| rs1801772663 | 7:99,123,690 | G/A | — | uncertain significance |
| rs115361099 | 7:99,123,725 | C/A | — | uncertain significance |
| rs375672801 | 7:99,123,981 | G/A | — | uncertain significance |
| rs755254515 | 7:99,123,991 | C/T | — | uncertain significance |
| rs2485343680 | 7:99,124,012 | A/C | — | uncertain significance |
| rs779311944 | 7:99,128,838 | C/G | — | uncertain significance |
| rs768210094 | 7:99,128,856 | G/A | — | uncertain significance |
| rs139466060 | 7:99,129,238 | G/T | — | uncertain significance |
| rs761003233 | 7:99,129,310 | G/A | — | uncertain significance |
| rs377171311 | 7:99,129,326 | G/T | — | uncertain significance |
| rs1423907331 | 7:99,129,372 | G/A | — | uncertain significance |
| rs1802059195 | 7:99,129,435 | G/A | — | uncertain significance |
| rs147717830 | 7:99,129,438 | G/A | — | uncertain significance |
| rs751498627 | 7:99,129,486 | T/G | — | uncertain significance |
| rs1802073496 | 7:99,129,647 | A/T | — | uncertain significance |
| rs1250558500 | 7:99,129,849 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.