ZZZ3
zinc finger ZZ-type containing 3
Summary
Enables histone reader activity; lysine-acetylated histone binding activity; and methylated histone binding activity. Involved in several processes, including chromatin organization; regulation of cell division; and regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. Part of ATAC complex. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1027354 | 1:78,031,433 | T/C | — | benign |
| rs144864059 | 1:78,031,434 | T/C | — | uncertain significance |
| rs144357575 | 1:78,031,441 | C/A | — | uncertain significance |
| rs2523745004 | 1:78,031,448 | G/C | — | uncertain significance |
| rs151252073 | 1:78,031,851 | T/C | — | uncertain significance |
| rs756412327 | 1:78,034,127 | A/G | — | uncertain significance |
| rs528143476 | 1:78,041,760 | T/G | — | uncertain significance |
| rs912975341 | 1:78,041,773 | T/C | — | uncertain significance |
| rs138802564 | 1:78,041,799 | C/T | — | uncertain significance |
| rs780035496 | 1:78,044,469 | T/C | — | uncertain significance |
| rs1379265761 | 1:78,044,475 | T/C | — | uncertain significance |
| rs971869832 | 1:78,044,482 | T/C | — | uncertain significance |
| rs201334965 | 1:78,045,291 | A/T | — | uncertain significance |
| rs200866808 | 1:78,045,321 | A/G | — | benign |
| rs759583280 | 1:78,046,696 | G/C | — | uncertain significance |
| rs2523926258 | 1:78,047,462 | T/C | — | uncertain significance |
| rs200975651 | 1:78,047,508 | T/C | — | likely benign |
| rs1485712725 | 1:78,047,543 | T/C | — | uncertain significance |
| rs1570422268 | 1:78,047,706 | G/A | — | uncertain significance |
| rs17381664 | 1:78,048,331 | T/C | intron variant | — |
| rs748154236 | 1:78,050,203 | T/G | — | uncertain significance |
| rs1570429085 | 1:78,050,279 | C/A | — | uncertain significance |
| rs12026939 | 1:78,075,002 | A/T | — | — |
| rs758766305 | 1:78,097,611 | T/C | — | uncertain significance |
| rs1017494857 | 1:78,097,694 | C/T | — | uncertain significance |
| rs776826290 | 1:78,097,718 | C/G | — | uncertain significance |
| rs1667861341 | 1:78,097,791 | C/T | — | uncertain significance |
| rs145476647 | 1:78,097,803 | T/C | — | uncertain significance |
| rs1384500710 | 1:78,097,806 | G/T | — | uncertain significance |
| rs749315714 | 1:78,097,850 | G/A | — | uncertain significance |
| rs760746735 | 1:78,097,898 | G/A | — | uncertain significance |
| rs1667882666 | 1:78,098,009 | T/G | — | uncertain significance |
| rs371735987 | 1:78,098,058 | T/C | — | uncertain significance |
| rs762712221 | 1:78,098,064 | C/T | — | uncertain significance |
| rs139323381 | 1:78,098,105 | C/T | — | uncertain significance |
| rs2524441731 | 1:78,098,186 | G/A | — | uncertain significance |
| rs1667899709 | 1:78,098,196 | T/C | — | uncertain significance |
| rs769452368 | 1:78,098,202 | G/A | — | uncertain significance |
| rs1458798810 | 1:78,098,220 | G/T | — | uncertain significance |
| rs2100849107 | 1:78,098,223 | C/A | — | uncertain significance |
| rs1478552962 | 1:78,098,250 | G/T | — | uncertain significance |
| rs368611525 | 1:78,098,251 | G/T | — | uncertain significance |
| rs150978320 | 1:78,098,289 | T/C | — | likely benign |
| rs150105207 | 1:78,098,304 | C/T | — | uncertain significance |
| rs766855556 | 1:78,098,306 | G/A | — | uncertain significance |
| rs2100850052 | 1:78,098,336 | T/C | — | uncertain significance |
| rs765733529 | 1:78,098,342 | A/C | — | uncertain significance |
| rs752942616 | 1:78,098,343 | C/T | — | uncertain significance |
| rs780027688 | 1:78,098,373 | T/C | — | uncertain significance |
| rs2524446415 | 1:78,098,477 | A/C | — | uncertain significance |
| rs1263548439 | 1:78,098,636 | G/A | — | uncertain significance |
| rs139215601 | 1:78,098,678 | C/T | — | uncertain significance |
| rs373232337 | 1:78,098,720 | C/T | — | uncertain significance |
| rs372264452 | 1:78,098,759 | T/C | — | uncertain significance |
| rs1557746509 | 1:78,098,762 | T/C | — | uncertain significance |
| rs375066082 | 1:78,098,790 | T/C | — | uncertain significance |
| rs140282569 | 1:78,098,992 | T/A | — | uncertain significance |
| rs759669457 | 1:78,099,017 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.