ZBTB8A
zinc finger and BTB domain containing 8A
Summary
Enables several functions, including DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II-specific DNA-binding transcription factor binding activity; and transcription coactivator binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants99 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2095761 | 1:33,004,010 | A/C | — | — |
| rs72652133 | 1:33,006,459 | G/A | regulatory region variant | — |
| rs12130958 | 1:33,006,973 | G/A | intron variant | — |
| rs12130985 | 1:33,007,000 | G/A | intron variant | — |
| rs12127598 | 1:33,007,086 | A/G | intron variant | — |
| rs12131078 | 1:33,007,344 | G/A | intron variant | — |
| rs12128448 | 1:33,007,352 | T/C | intron variant | — |
| rs72652139 | 1:33,007,872 | C/T | intron variant | — |
| rs7551056 | 1:33,008,123 | C/G | — | — |
| rs3938707 | 1:33,008,747 | T/C | intron variant | — |
| rs12129697 | 1:33,008,830 | A/C | — | — |
| rs12140665 | 1:33,008,905 | C/T | intron variant | — |
| rs4970538 | 1:33,009,019 | A/C | intron variant | — |
| rs112515903 | 1:33,009,308 | C/T | intron variant | — |
| rs12034923 | 1:33,009,310 | T/C | intron variant | — |
| rs143744476 | 1:33,009,515 | G/A | — | — |
| rs72652145 | 1:33,009,587 | T/C | intron variant | — |
| rs7523628 | 1:33,011,829 | G/T | — | — |
| rs7515775 | 1:33,011,952 | T/G | — | — |
| rs7513429 | 1:33,012,005 | A/G | intron variant | — |
| rs7513806 | 1:33,012,401 | A/T | regulatory region variant | — |
| rs114362018 | 1:33,013,582 | G/A | intron variant | — |
| rs139106495 | 1:33,013,603 | C/G | intron variant | — |
| rs12130349 | 1:33,014,484 | T/A | intron variant | — |
| rs72652154 | 1:33,014,769 | G/A | intron variant | — |
| rs12133914 | 1:33,015,281 | G/T | regulatory region variant | — |
| rs12133942 | 1:33,015,328 | G/C | — | — |
| rs7526259 | 1:33,016,071 | A/G | — | — |
| rs143461021 | 1:33,016,387 | G/A | intron variant | — |
| rs113582306 | 1:33,016,462 | G/A | intron variant | — |
| rs72652158 | 1:33,016,588 | C/A | — | — |
| rs72652159 | 1:33,016,645 | G/A | intron variant | — |
| rs72652160 | 1:33,016,681 | G/A | intron variant | — |
| rs57273223 | 1:33,016,753 | T/C | intron variant | — |
| rs72652163 | 1:33,016,884 | T/A | intron variant | — |
| rs7542646 | 1:33,017,736 | G/T | — | — |
| rs4970531 | 1:33,018,116 | T/A | intron variant | — |
| rs7547882 | 1:33,018,685 | A/G | intron variant | — |
| rs115844090 | 1:33,018,910 | G/C | intron variant | — |
| rs12134736 | 1:33,019,254 | A/G | intron variant | — |
| rs12134788 | 1:33,019,436 | A/G | intron variant | — |
| rs12136580 | 1:33,020,773 | A/G | intron variant | — |
| rs6692878 | 1:33,021,705 | C/G | — | — |
| rs7523019 | 1:33,021,965 | G/A | intron variant | — |
| rs6678350 | 1:33,024,774 | G/A | intron variant | — |
| rs7527766 | 1:33,025,897 | T/C | intron variant | — |
| rs12041245 | 1:33,026,367 | T/G | intron variant | — |
| rs72652171 | 1:33,026,830 | G/C | intron variant | — |
| rs113855138 | 1:33,027,858 | C/T | intron variant | — |
| rs72652175 | 1:33,029,472 | A/G | intron variant | — |
| rs143669010 | 1:33,031,587 | C/G | intron variant | — |
| rs28490395 | 1:33,032,855 | A/G | intron variant | — |
| rs72652181 | 1:33,035,556 | T/C | intron variant | — |
| rs55655845 | 1:33,035,949 | T/G | intron variant | — |
| rs10914578 | 1:33,036,603 | C/T | — | — |
| rs113839457 | 1:33,039,133 | G/A | intron variant | — |
| rs112063951 | 1:33,042,211 | A/G | intron variant | — |
| rs113163842 | 1:33,044,878 | C/T | intron variant | — |
| rs12118659 | 1:33,047,914 | A/G | intron variant | — |
| rs111464299 | 1:33,050,147 | T/C | intron variant | — |
| rs72652195 | 1:33,050,690 | G/T | — | — |
| rs111704697 | 1:33,050,703 | C/T | intron variant | — |
| rs12037251 | 1:33,051,327 | C/G | intron variant | — |
| rs12029991 | 1:33,051,423 | G/A | intron variant | — |
| rs12022230 | 1:33,051,685 | A/G | intron variant | — |
| rs55652000 | 1:33,052,348 | G/C | — | — |
| rs72652198 | 1:33,052,908 | G/A | intron variant | — |
| rs10753260 | 1:33,056,940 | G/T | intron variant | — |
| rs12134667 | 1:33,057,945 | C/G | intron variant | — |
| rs111453410 | 1:33,058,349 | C/G | — | — |
| rs150478201 | 1:33,058,596 | G/A | — | uncertain significance |
| rs370105933 | 1:33,058,739 | G/T | — | uncertain significance |
| rs201739762 | 1:33,058,749 | C/A | — | uncertain significance |
| rs758486075 | 1:33,058,779 | G/A | — | uncertain significance |
| rs766037712 | 1:33,058,906 | G/A | — | uncertain significance |
| rs1187707212 | 1:33,058,962 | G/C | — | uncertain significance |
| rs201922748 | 1:33,059,019 | C/T | — | uncertain significance |
| rs1044289980 | 1:33,059,020 | G/A | — | likely benign |
| rs1644505084 | 1:33,059,025 | C/T | — | uncertain significance |
| rs935456145 | 1:33,059,047 | C/G | — | uncertain significance |
| rs751707803 | 1:33,059,059 | G/A | — | uncertain significance |
| rs751583612 | 1:33,059,163 | A/C | — | uncertain significance |
| rs1424618043 | 1:33,059,167 | A/G | — | uncertain significance |
| rs200737625 | 1:33,059,197 | C/G | — | uncertain significance |
| rs201447099 | 1:33,059,218 | G/A | — | uncertain significance |
| rs761731405 | 1:33,059,242 | C/G | — | uncertain significance |
| rs148974909 | 1:33,059,310 | T/C | — | uncertain significance |
| rs61998256 | 1:33,059,343 | A/G | — | uncertain significance |
| rs768744678 | 1:33,060,667 | G/A | — | uncertain significance |
| rs6673492 | 1:33,062,346 | A/G | downstream gene variant | — |
| rs6684670 | 1:33,062,362 | G/A | downstream gene variant | — |
| rs72654007 | 1:33,063,164 | A/G | downstream gene variant | — |
| rs12030780 | 1:33,063,383 | T/C | downstream gene variant | — |
| rs7525687 | 1:33,065,067 | C/T | downstream gene variant | — |
| rs7539872 | 1:33,065,272 | T/C | downstream gene variant | — |
| rs1644565400 | 1:33,065,857 | T/C | — | uncertain significance |
| rs147884621 | 1:33,065,908 | A/G | — | uncertain significance |
| rs752526056 | 1:33,066,002 | T/G | — | uncertain significance |
| rs138766553 | 1:33,066,010 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.