ZBTB38
zinc finger and BTB domain containing 38
Summary
The protein encoded by this gene is a zinc finger transcriptional activator that binds methylated DNA. The encoded protein can form homodimers or heterodimers through the zinc finger domains. In mouse, inhibition of this protein has been associated with apoptosis in some cell types. [provided by RefSeq, Jun 2010]
Known Variants89 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1983235 | 3:141,049,964 | C/T | regulatory region variant | — |
| rs28721484 | 3:141,053,279 | C/T | intron variant | — |
| rs568435345 | 3:141,053,290 | C/T | — | — |
| rs41379945 | 3:141,055,204 | T/C | intron variant | — |
| rs9857275 | 3:141,078,188 | C/A | intron variant | — |
| rs13100711 | 3:141,082,990 | C/A | — | — |
| rs6440003 | 3:141,094,209 | G/A | intron variant | — |
| rs4683605 | 3:141,094,769 | C/A | regulatory region variant | — |
| rs74734425 | 3:141,096,216 | C/T | intron variant | — |
| rs56243018 | 3:141,101,839 | A/C | upstream gene variant | — |
| rs9853018 | 3:141,101,961 | C/T | upstream gene variant | — |
| rs6763931 | 3:141,102,833 | G/A | regulatory region variant | — |
| rs6767786 | 3:141,104,180 | G/A | upstream gene variant | — |
| rs724016 | 3:141,105,570 | A/G | regulatory region variant | — |
| rs55715288 | 3:141,108,338 | C/T | regulatory region variant | — |
| rs6785012 | 3:141,109,348 | C/G | — | — |
| rs4683606 | 3:141,110,074 | A/G | intron variant | — |
| rs1582874 | 3:141,115,219 | T/A | — | — |
| rs13068733 | 3:141,118,028 | A/G | regulatory region variant | — |
| rs568652489 | 3:141,121,136 | C/T | — | — |
| rs2011092 | 3:141,124,607 | T/A | — | — |
| rs1344672 | 3:141,125,705 | C/G | regulatory region variant | — |
| rs57345461 | 3:141,126,825 | A/G | — | — |
| rs13099193 | 3:141,128,804 | G/T | — | — |
| rs144088519 | 3:141,130,814 | C/A | regulatory region variant | — |
| rs35225290 | 3:141,130,835 | C/A | — | — |
| rs1991431 | 3:141,133,450 | G/A | regulatory region variant | — |
| rs73872717 | 3:141,134,569 | C/T | intron variant | — |
| rs16851397 | 3:141,134,818 | A/G | regulatory region variant | — |
| rs9825379 | 3:141,137,035 | G/A | intron variant | — |
| rs77263552 | 3:141,140,361 | T/G | regulatory region variant | — |
| rs6763927 | 3:141,140,366 | A/T | regulatory region variant | — |
| rs9846396 | 3:141,140,968 | C/T | regulatory region variant | — |
| rs16851416 | 3:141,141,310 | C/T | intron variant | — |
| rs79474768 | 3:141,141,904 | T/C | intron variant | — |
| rs10513137 | 3:141,143,430 | G/A | intron variant | — |
| rs13069734 | 3:141,148,419 | G/A | intron variant | — |
| rs7625643 | 3:141,150,026 | A/G | intron variant | — |
| rs79767329 | 3:141,155,344 | G/T | intron variant | — |
| rs1409563531 | 3:141,161,309 | C/G | — | uncertain significance |
| rs758194400 | 3:141,161,316 | G/A | — | uncertain significance |
| rs777917847 | 3:141,161,603 | C/T | — | uncertain significance |
| rs1010416885 | 3:141,161,793 | G/A | — | uncertain significance |
| rs61732446 | 3:141,161,863 | G/C | — | benign |
| rs374266610 | 3:141,161,871 | C/A | — | uncertain significance |
| rs549239683 | 3:141,162,054 | C/T | — | uncertain significance |
| rs372150185 | 3:141,162,137 | G/A | — | uncertain significance |
| rs1336231737 | 3:141,162,246 | C/T | — | uncertain significance |
| rs770793547 | 3:141,162,294 | C/T | — | uncertain significance |
| rs767703438 | 3:141,162,330 | C/T | — | uncertain significance |
| rs760994636 | 3:141,162,338 | C/A | — | uncertain significance |
| rs555322688 | 3:141,162,393 | G/A | — | uncertain significance |
| rs2477749272 | 3:141,162,399 | A/T | — | uncertain significance |
| rs763454595 | 3:141,162,450 | G/A | — | uncertain significance |
| rs755597209 | 3:141,162,476 | G/A | — | uncertain significance |
| rs144419697 | 3:141,162,551 | G/A | — | uncertain significance |
| rs2477774817 | 3:141,162,602 | A/G | — | uncertain significance |
| rs200951296 | 3:141,162,627 | A/G | — | uncertain significance |
| rs560855672 | 3:141,162,816 | A/G | — | uncertain significance |
| rs544444513 | 3:141,162,935 | C/T | synonymous variant | — |
| rs372805442 | 3:141,162,948 | G/C | — | uncertain significance |
| rs772878081 | 3:141,162,975 | G/A | — | uncertain significance |
| rs767199699 | 3:141,162,999 | G/A | — | uncertain significance |
| rs752475828 | 3:141,163,025 | G/A | — | uncertain significance |
| rs200713441 | 3:141,163,029 | C/G | — | uncertain significance |
| rs17787670 | 3:141,163,074 | C/T | — | likely benign |
| rs199673050 | 3:141,163,079 | A/G | — | uncertain significance |
| rs781758965 | 3:141,163,094 | G/A | — | uncertain significance |
| rs750461389 | 3:141,163,167 | A/G | — | likely benign |
| rs1458030002 | 3:141,163,235 | T/C | — | uncertain significance |
| rs776609604 | 3:141,163,289 | C/T | — | uncertain significance |
| rs751823083 | 3:141,163,329 | G/A | — | uncertain significance |
| rs373442841 | 3:141,163,340 | G/A | — | likely benign |
| rs2477864100 | 3:141,163,461 | T/C | — | uncertain significance |
| rs775824805 | 3:141,163,524 | G/A | — | uncertain significance |
| rs752377477 | 3:141,163,596 | C/T | — | uncertain significance |
| rs3732867 | 3:141,163,655 | G/A | — | benign |
| rs200934918 | 3:141,163,665 | C/A | — | uncertain significance |
| rs1483159827 | 3:141,163,766 | G/A | — | uncertain significance |
| rs61732448 | 3:141,163,975 | G/A | — | benign |
| rs761566704 | 3:141,164,018 | C/G | — | uncertain significance |
| rs781132144 | 3:141,164,073 | C/T | — | uncertain significance |
| rs181837053 | 3:141,164,123 | G/C | — | uncertain significance |
| rs1465641877 | 3:141,164,133 | A/G | — | uncertain significance |
| rs2080976468 | 3:141,164,223 | A/G | — | uncertain significance |
| rs993564159 | 3:141,164,615 | C/G | — | uncertain significance |
| rs61732445 | 3:141,164,761 | A/G | — | benign |
| rs761943359 | 3:141,164,769 | A/G | — | likely benign |
| rs76129297 | 3:141,164,795 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.