ZNF160
zinc finger protein 160
Summary
The protein encoded by this gene is a Kruppel-related zinc finger protein which is characterized by the presence of an N-terminal repressor domain, the Kruppel-associated box (KRAB). The KRAB domain is a potent repressor of transcription; thus this protein may function in transcription regulation. Multiple transcript variants have been found for this gene. [provided by RefSeq, Apr 2016]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1450318598 | 19:53,571,342 | T/G | — | uncertain significance |
| rs199941489 | 19:53,571,346 | T/C | — | uncertain significance |
| rs368030849 | 19:53,571,361 | C/T | — | uncertain significance |
| rs764811582 | 19:53,571,400 | T/C | — | uncertain significance |
| rs2514611662 | 19:53,571,413 | T/C | — | uncertain significance |
| rs187006418 | 19:53,571,424 | C/T | — | uncertain significance |
| rs749609507 | 19:53,571,445 | G/A | — | uncertain significance |
| rs867208455 | 19:53,571,496 | G/C | — | uncertain significance |
| rs147900399 | 19:53,571,532 | C/T | — | uncertain significance |
| rs1198512352 | 19:53,571,565 | A/C | — | uncertain significance |
| rs781059600 | 19:53,571,637 | C/T | — | uncertain significance |
| rs2514617092 | 19:53,571,653 | T/C | — | uncertain significance |
| rs75696757 | 19:53,571,664 | T/C | — | uncertain significance |
| rs762274825 | 19:53,571,677 | G/C | — | uncertain significance |
| rs147062809 | 19:53,571,679 | T/C | — | uncertain significance |
| rs1168925387 | 19:53,571,740 | C/G | — | uncertain significance |
| rs767974287 | 19:53,571,853 | C/A | — | uncertain significance |
| rs1454579644 | 19:53,571,865 | C/T | — | uncertain significance |
| rs756011876 | 19:53,571,868 | C/T | — | uncertain significance |
| rs182756863 | 19:53,571,973 | C/T | — | uncertain significance |
| rs1489244598 | 19:53,572,012 | G/C | — | uncertain significance |
| rs1393603141 | 19:53,572,147 | G/A | — | uncertain significance |
| rs772390990 | 19:53,572,180 | G/C | — | uncertain significance |
| rs201744012 | 19:53,572,183 | T/C | — | uncertain significance |
| rs374450747 | 19:53,572,219 | C/A | — | uncertain significance |
| rs766183370 | 19:53,572,225 | C/T | — | uncertain significance |
| rs528291148 | 19:53,572,237 | G/T | — | uncertain significance |
| rs769963439 | 19:53,572,324 | T/C | — | uncertain significance |
| rs763577358 | 19:53,572,456 | C/T | — | likely benign |
| rs753283790 | 19:53,572,457 | G/A | — | uncertain significance |
| rs145975178 | 19:53,572,482 | C/T | — | likely benign |
| rs745775825 | 19:53,572,651 | G/A | — | uncertain significance |
| rs776770115 | 19:53,572,658 | G/A | — | uncertain significance |
| rs375230703 | 19:53,572,886 | T/C | — | uncertain significance |
| rs772896795 | 19:53,572,942 | T/A | — | uncertain significance |
| rs61745786 | 19:53,573,142 | G/A | — | likely benign |
| rs144649266 | 19:53,573,209 | T/C | — | uncertain significance |
| rs2514655098 | 19:53,573,291 | G/C | — | uncertain significance |
| rs138893110 | 19:53,573,311 | T/C | — | uncertain significance |
| rs1568475555 | 19:53,573,339 | C/T | — | likely benign |
| rs1216556701 | 19:53,573,342 | T/C | — | uncertain significance |
| rs200786878 | 19:53,573,403 | G/C | — | uncertain significance |
| rs764180451 | 19:53,573,419 | C/T | — | uncertain significance |
| rs749779810 | 19:53,573,461 | G/A | — | uncertain significance |
| rs916630955 | 19:53,577,451 | G/C | — | uncertain significance |
| rs377678615 | 19:53,577,453 | T/G | — | uncertain significance |
| rs770557595 | 19:53,578,346 | C/T | — | uncertain significance |
| rs145465295 | 19:53,578,428 | C/G | — | uncertain significance |
| rs329709 | 19:53,578,432 | C/T | — | uncertain significance |
| rs535555897 | 19:53,591,768 | T/C | — | — |
| rs187171029 | 19:53,599,256 | A/T | intron variant | — |
| rs329721 | 19:53,600,422 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.