ZKSCAN1
zinc finger with KRAB and SCAN domains 1
Summary
This gene encodes a member of the Kruppel C2H2-type zinc-finger family of proteins. This encoded protein may function as a transcription factor that regulates the expression of GABA type-A receptors in the brain. Transcripts from this gene have been shown to form stable and abundant circular RNAs. Elevated expression of this gene has been observed in gastric cancer and the encoded protein may stimulate migration and invasion of human gastric cancer cells. [provided by RefSeq, Oct 2016]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs751541769 | 7:99,611,749 | G/A | — | — |
| rs118111035 | 7:99,613,106 | G/T | regulatory region variant | — |
| rs13243708 | 7:99,616,291 | T/A | — | — |
| rs6953441 | 7:99,617,067 | G/A | intron variant | — |
| rs6465761 | 7:99,620,277 | G/T | — | — |
| rs12531809 | 7:99,620,473 | G/T | regulatory region variant | — |
| rs374547741 | 7:99,621,158 | C/T | — | uncertain significance |
| rs2546795645 | 7:99,621,219 | G/C | — | uncertain significance |
| rs2546795790 | 7:99,621,288 | G/C | — | uncertain significance |
| rs1425079153 | 7:99,621,310 | C/T | — | uncertain significance |
| rs1167524040 | 7:99,621,311 | G/T | — | uncertain significance |
| rs1355735435 | 7:99,621,341 | G/A | — | uncertain significance |
| rs2546795964 | 7:99,621,377 | A/G | — | uncertain significance |
| rs1790694448 | 7:99,621,385 | C/T | — | uncertain significance |
| rs371646053 | 7:99,621,386 | G/A | — | uncertain significance |
| rs2546796089 | 7:99,621,460 | G/A | — | uncertain significance |
| rs1236986656 | 7:99,621,509 | C/T | — | uncertain significance |
| rs149163835 | 7:99,621,810 | G/A | — | uncertain significance |
| rs762671026 | 7:99,621,870 | G/A | — | uncertain significance |
| rs2546796874 | 7:99,621,895 | A/G | — | uncertain significance |
| rs759540374 | 7:99,621,898 | C/T | — | uncertain significance |
| rs202154703 | 7:99,621,913 | G/A | — | uncertain significance |
| rs148037051 | 7:99,621,928 | G/A | — | uncertain significance |
| rs12112642 | 7:99,625,199 | G/A | intron variant | — |
| rs1015538 | 7:99,626,035 | A/G | intron variant | — |
| rs142526628 | 7:99,627,484 | C/G | — | uncertain significance |
| rs199751793 | 7:99,627,510 | C/T | — | uncertain significance |
| rs1292329595 | 7:99,627,517 | A/C | — | uncertain significance |
| rs1791032869 | 7:99,627,534 | G/C | — | uncertain significance |
| rs889997036 | 7:99,627,566 | G/A | — | likely benign |
| rs750888190 | 7:99,627,893 | A/G | — | uncertain significance |
| rs12534494 | 7:99,629,480 | G/A | intron variant | — |
| rs2897075 | 7:99,630,342 | C/A | — | — |
| rs770020945 | 7:99,630,942 | A/G | — | uncertain significance |
| rs143925671 | 7:99,630,948 | A/G | — | uncertain significance |
| rs748381875 | 7:99,631,024 | A/G | — | uncertain significance |
| rs749806479 | 7:99,631,059 | A/G | — | uncertain significance |
| rs1042820454 | 7:99,631,405 | T/C | — | uncertain significance |
| rs2546809660 | 7:99,631,422 | C/A | — | uncertain significance |
| rs1224233696 | 7:99,631,538 | C/G | — | uncertain significance |
| rs193920886 | 7:99,631,582 | G/A | — | uncertain significance |
| rs774053631 | 7:99,631,797 | G/A | — | uncertain significance |
| rs777132056 | 7:99,637,953 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.