MZF1
myeloid zinc finger 1
Summary
Enables DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and protein homodimerization activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759082568 | 19:59,073,456 | C/G | — | uncertain significance |
| rs150107156 | 19:59,073,495 | G/C | — | uncertain significance |
| rs146120851 | 19:59,073,535 | G/T | — | uncertain significance |
| rs762382995 | 19:59,073,593 | G/T | — | uncertain significance |
| rs374723544 | 19:59,073,668 | C/T | — | uncertain significance |
| rs1568674438 | 19:59,073,712 | C/A | — | uncertain significance |
| rs772478991 | 19:59,073,737 | T/A | — | uncertain significance |
| rs551259916 | 19:59,073,857 | G/C | — | uncertain significance |
| rs770870517 | 19:59,073,914 | G/T | — | uncertain significance |
| rs1486469107 | 19:59,073,936 | C/A | — | uncertain significance |
| rs775124753 | 19:59,073,959 | A/G | — | uncertain significance |
| rs1283610346 | 19:59,073,966 | G/A | — | uncertain significance |
| rs748231804 | 19:59,074,029 | G/A | — | uncertain significance |
| rs772207279 | 19:59,074,030 | C/A | — | uncertain significance |
| rs61731801 | 19:59,074,060 | C/T | — | likely benign |
| rs150590904 | 19:59,074,104 | C/G | — | uncertain significance |
| rs777948499 | 19:59,074,121 | G/T | — | uncertain significance |
| rs201388932 | 19:59,074,133 | T/A | — | uncertain significance |
| rs1015134616 | 19:59,074,140 | C/T | — | uncertain significance |
| rs1389747611 | 19:59,074,160 | G/A | — | uncertain significance |
| rs911640755 | 19:59,074,189 | A/C | — | uncertain significance |
| rs2053958654 | 19:59,074,194 | G/A | — | uncertain significance |
| rs765638825 | 19:59,074,208 | G/A | — | uncertain significance |
| rs758676175 | 19:59,074,217 | G/A | — | uncertain significance |
| rs2514355032 | 19:59,074,300 | G/C | — | uncertain significance |
| rs1257443350 | 19:59,074,311 | A/T | — | uncertain significance |
| rs763508871 | 19:59,074,341 | T/C | — | uncertain significance |
| rs546958807 | 19:59,074,372 | G/C | — | uncertain significance |
| rs149020787 | 19:59,074,401 | C/T | — | uncertain significance |
| rs2228162 | 19:59,074,429 | C/T | synonymous variant | — |
| rs748787144 | 19:59,074,482 | C/G | — | uncertain significance |
| rs778314996 | 19:59,074,580 | C/T | — | uncertain significance |
| rs146251309 | 19:59,074,607 | G/A | — | uncertain significance |
| rs2514357529 | 19:59,074,613 | C/T | — | uncertain significance |
| rs2514357571 | 19:59,074,616 | C/A | — | uncertain significance |
| rs370089804 | 19:59,074,637 | C/T | — | uncertain significance |
| rs4756 | 19:59,074,653 | T/C | missense variant | — |
| rs372763261 | 19:59,074,702 | T/G | — | uncertain significance |
| rs775348375 | 19:59,074,724 | A/G | — | uncertain significance |
| rs2514358914 | 19:59,074,730 | A/G | — | uncertain significance |
| rs115308072 | 19:59,074,769 | A/C | — | benign |
| rs761152473 | 19:59,074,832 | C/A | — | uncertain significance |
| rs754161627 | 19:59,074,841 | G/T | — | uncertain significance |
| rs757896533 | 19:59,074,854 | C/G | — | uncertain significance |
| rs35126926 | 19:59,074,855 | T/C | — | benign |
| rs73068325 | 19:59,079,096 | C/T | intron variant | — |
| rs200148787 | 19:59,081,820 | T/G | — | uncertain significance |
| rs745598986 | 19:59,082,369 | G/A | — | uncertain significance |
| rs2514398866 | 19:59,082,419 | T/C | — | uncertain significance |
| rs745791475 | 19:59,082,434 | C/G | — | uncertain significance |
| rs2054152934 | 19:59,082,467 | G/A | — | uncertain significance |
| rs774773643 | 19:59,082,642 | C/T | — | uncertain significance |
| rs772140250 | 19:59,082,746 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.