ZBTB4
zinc finger and BTB domain containing 4
Summary
Enables several functions, including DNA-binding transcription repressor activity, RNA polymerase II-specific; nucleotide binding activity; and protein homodimerization activity. Involved in DNA damage response and negative regulation of transcription by RNA polymerase II. Located in cytosol and nuclear body. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9217 | 17:7,363,088 | T/A | — | — |
| rs376572108 | 17:7,365,271 | G/A | — | likely benign |
| rs771824658 | 17:7,365,307 | T/G | — | uncertain significance |
| rs2070028218 | 17:7,365,363 | C/T | — | likely benign |
| rs1220080088 | 17:7,365,369 | G/A | — | uncertain significance |
| rs374895110 | 17:7,365,390 | C/T | — | uncertain significance |
| rs117313567 | 17:7,365,391 | G/A | — | benign |
| rs144404116 | 17:7,365,408 | G/A | — | uncertain significance |
| rs764402120 | 17:7,365,471 | G/C | — | uncertain significance |
| rs779638184 | 17:7,365,504 | C/T | — | uncertain significance |
| rs1381784557 | 17:7,365,519 | G/A | — | uncertain significance |
| rs776394800 | 17:7,365,528 | C/T | — | uncertain significance |
| rs2070032203 | 17:7,365,582 | T/C | — | uncertain significance |
| rs148845628 | 17:7,365,584 | C/T | — | benign |
| rs201823610 | 17:7,365,651 | G/A | — | uncertain significance |
| rs565524533 | 17:7,365,654 | C/T | — | uncertain significance |
| rs374891909 | 17:7,365,662 | A/G | — | uncertain significance |
| rs143452364 | 17:7,365,678 | A/G | — | uncertain significance |
| rs1215095322 | 17:7,365,701 | T/C | — | uncertain significance |
| rs544952940 | 17:7,365,711 | C/T | — | uncertain significance |
| rs752232401 | 17:7,365,774 | C/T | — | uncertain significance |
| rs921525176 | 17:7,365,801 | C/T | — | uncertain significance |
| rs145141617 | 17:7,365,863 | T/C | — | uncertain significance |
| rs375607129 | 17:7,366,029 | C/T | — | uncertain significance |
| rs2507899971 | 17:7,366,053 | C/G | — | uncertain significance |
| rs144235825 | 17:7,366,056 | C/T | — | likely benign |
| rs144607759 | 17:7,366,117 | A/G | — | benign |
| rs765167064 | 17:7,366,121 | C/T | — | uncertain significance |
| rs369864702 | 17:7,366,131 | G/A | — | uncertain significance |
| rs142183003 | 17:7,366,146 | G/A | — | uncertain significance |
| rs201838522 | 17:7,366,151 | G/T | — | uncertain significance |
| rs1177536226 | 17:7,366,161 | C/T | — | uncertain significance |
| rs151185987 | 17:7,366,166 | G/A | — | benign |
| rs140221380 | 17:7,366,190 | C/T | — | uncertain significance |
| rs751837963 | 17:7,366,211 | C/T | — | uncertain significance |
| rs374825213 | 17:7,366,233 | G/A | — | uncertain significance |
| rs767828341 | 17:7,366,250 | A/C | — | uncertain significance |
| rs762257816 | 17:7,366,614 | G/A | — | uncertain significance |
| rs776866837 | 17:7,366,668 | C/T | — | uncertain significance |
| rs35231078 | 17:7,366,685 | G/A | — | benign |
| rs777923085 | 17:7,366,814 | G/A | — | uncertain significance |
| rs759993233 | 17:7,366,826 | C/G | — | likely benign |
| rs1248808355 | 17:7,366,845 | C/T | — | uncertain significance |
| rs375136406 | 17:7,366,934 | G/A | — | uncertain significance |
| rs369663945 | 17:7,366,937 | G/A | — | uncertain significance |
| rs762883050 | 17:7,366,964 | G/A | — | uncertain significance |
| rs200263417 | 17:7,366,994 | T/G | — | uncertain significance |
| rs11871207 | 17:7,367,080 | G/A | — | benign |
| rs765367165 | 17:7,367,126 | G/C | — | uncertain significance |
| rs57185120 | 17:7,367,164 | G/A | — | benign |
| rs370247741 | 17:7,368,406 | T/C | — | — |
| rs759680223 | 17:7,369,120 | C/T | — | uncertain significance |
| rs749358442 | 17:7,369,186 | G/T | — | uncertain significance |
| rs112556486 | 17:7,369,188 | G/A | — | benign |
| rs375990313 | 17:7,369,226 | C/T | — | uncertain significance |
| rs142612732 | 17:7,369,274 | C/T | — | uncertain significance |
| rs2507923457 | 17:7,369,325 | T/C | — | likely benign |
| rs769025766 | 17:7,369,334 | G/A | — | uncertain significance |
| rs770330008 | 17:7,369,336 | G/A | — | uncertain significance |
| rs1195923896 | 17:7,369,342 | G/C | — | uncertain significance |
| rs1227034000 | 17:7,369,348 | C/T | — | uncertain significance |
| rs1292460009 | 17:7,369,349 | G/C | — | uncertain significance |
| rs752484461 | 17:7,369,381 | T/G | — | uncertain significance |
| rs1234013380 | 17:7,369,424 | G/A | — | uncertain significance |
| rs373720420 | 17:7,369,429 | C/T | — | uncertain significance |
| rs200575166 | 17:7,369,505 | C/T | — | likely benign |
| rs1252029121 | 17:7,369,571 | C/T | — | uncertain significance |
| rs764091066 | 17:7,369,748 | C/T | — | uncertain significance |
| rs754025057 | 17:7,369,751 | G/A | — | uncertain significance |
| rs1287702085 | 17:7,369,753 | G/A | — | uncertain significance |
| rs1377694585 | 17:7,369,825 | G/A | — | uncertain significance |
| rs780295998 | 17:7,369,846 | G/A | — | uncertain significance |
| rs140340146 | 17:7,369,962 | G/A | — | likely benign |
| rs567567878 | 17:7,369,988 | G/A | — | uncertain significance |
| rs12942267 | 17:7,372,637 | C/T | intron variant | — |
| rs8075009 | 17:7,374,508 | A/T | — | — |
| rs7209131 | 17:7,376,411 | C/G | — | — |
| rs55894190 | 17:7,383,238 | C/T | regulatory region variant | — |
| rs8076642 | 17:7,383,984 | A/T | — | — |
| rs8081271 | 17:7,384,628 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.