ZBTB7A
zinc finger and BTB domain containing 7A
Summary
Enables several functions, including SMAD binding activity; nuclear androgen receptor binding activity; and transcription corepressor binding activity. Involved in several processes, including erythrocyte maturation; negative regulation of signal transduction; and regulation of nucleobase-containing compound metabolic process. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs75366827 | 19:4,042,808 | G/C | regulatory region variant | — |
| rs13437 | 19:4,045,518 | T/A | — | — |
| rs763235683 | 19:4,047,799 | C/A | — | uncertain significance |
| rs1481574996 | 19:4,047,842 | G/A | — | uncertain significance |
| rs2040442787 | 19:4,047,857 | G/A | — | uncertain significance |
| rs770355593 | 19:4,047,859 | C/A | — | uncertain significance |
| rs1162491256 | 19:4,047,860 | T/A | — | uncertain significance |
| rs774464131 | 19:4,047,894 | G/T | — | uncertain significance |
| rs2040443852 | 19:4,047,908 | C/T | — | uncertain significance |
| rs1199965484 | 19:4,047,950 | C/T | — | uncertain significance |
| rs770934571 | 19:4,047,960 | G/T | — | likely benign |
| rs572062539 | 19:4,047,969 | C/T | — | likely benign |
| rs2512265157 | 19:4,047,974 | T/G | — | uncertain significance |
| rs540793033 | 19:4,047,977 | G/C | — | uncertain significance |
| rs2512265185 | 19:4,047,979 | T/G | — | uncertain significance |
| rs776553754 | 19:4,047,980 | C/T | — | uncertain significance |
| rs2512265284 | 19:4,047,997 | A/C | — | uncertain significance |
| rs757820619 | 19:4,048,028 | C/A | — | uncertain significance |
| rs2144973693 | 19:4,048,151 | C/T | — | pathogenic |
| rs2512265735 | 19:4,048,180 | T/C | — | uncertain significance |
| rs72976986 | 19:4,050,424 | G/A | intron variant | — |
| rs72976987 | 19:4,052,920 | C/T | regulatory region variant | — |
| rs138413340 | 19:4,053,974 | G/A | — | likely benign |
| rs2144989424 | 19:4,053,982 | C/A | — | uncertain significance |
| rs2144989619 | 19:4,054,048 | C/G | — | uncertain significance |
| rs773655534 | 19:4,054,079 | G/C | — | pathogenic |
| rs2144989820 | 19:4,054,123 | G/A | — | pathogenic |
| rs2040540956 | 19:4,054,165 | A/G | — | likely benign |
| rs2040544134 | 19:4,054,291 | G/T | — | uncertain significance |
| rs2512275163 | 19:4,054,312 | C/A | — | uncertain significance |
| rs772567458 | 19:4,054,323 | C/G | — | uncertain significance |
| rs768701442 | 19:4,054,336 | C/T | — | uncertain significance |
| rs2512275410 | 19:4,054,381 | A/C | — | uncertain significance |
| rs2512275430 | 19:4,054,387 | A/C | — | uncertain significance |
| rs571325589 | 19:4,054,390 | C/T | — | likely benign |
| rs2512275570 | 19:4,054,423 | C/T | — | uncertain significance |
| rs1219158461 | 19:4,054,510 | G/A | — | uncertain significance |
| rs770017071 | 19:4,054,539 | G/A | — | uncertain significance |
| rs773326936 | 19:4,054,540 | T/G | — | uncertain significance |
| rs1410611113 | 19:4,054,649 | G/C | — | uncertain significance |
| rs1049614247 | 19:4,054,663 | C/A | — | uncertain significance |
| rs2144992969 | 19:4,054,732 | T/C | — | uncertain significance |
| rs757359614 | 19:4,054,733 | G/T | — | uncertain significance |
| rs1464136185 | 19:4,054,807 | G/A | — | uncertain significance |
| rs759224730 | 19:4,054,810 | C/T | — | likely benign |
| rs147200385 | 19:4,054,825 | C/G | — | likely benign |
| rs747990059 | 19:4,054,841 | C/G | — | uncertain significance |
| rs2040559235 | 19:4,054,858 | C/T | — | uncertain significance |
| rs2040560193 | 19:4,054,893 | A/T | — | uncertain significance |
| rs2512277307 | 19:4,054,932 | C/T | — | uncertain significance |
| rs2512277851 | 19:4,055,205 | A/C | — | uncertain significance |
| rs895330 | 19:4,060,707 | C/G | downstream gene variant | — |
| rs10415135 | 19:4,061,544 | C/T | regulatory region variant | — |
| rs66833742 | 19:4,063,486 | C/T | regulatory region variant | — |
| rs56356382 | 19:4,064,057 | T/C | regulatory region variant | — |
| rs188955288 | 19:4,067,314 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.