ZNF441
zinc finger protein 441
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs372058 | 19:11,877,120 | C/T | upstream gene variant | — |
| rs779347922 | 19:11,888,487 | G/A | — | uncertain significance |
| rs1238163046 | 19:11,888,502 | G/A | — | uncertain significance |
| rs7248102 | 19:11,888,518 | G/C | — | benign |
| rs766467026 | 19:11,888,547 | G/A | — | uncertain significance |
| rs781277154 | 19:11,889,168 | A/G | — | uncertain significance |
| rs867196405 | 19:11,889,180 | C/A | — | uncertain significance |
| rs35459645 | 19:11,890,906 | A/G | — | benign |
| rs761260826 | 19:11,890,970 | G/A | — | uncertain significance |
| rs375428214 | 19:11,890,988 | T/C | — | uncertain significance |
| rs1975388324 | 19:11,891,009 | G/A | — | uncertain significance |
| rs144102390 | 19:11,891,145 | A/G | — | uncertain significance |
| rs1427005902 | 19:11,891,198 | A/G | — | uncertain significance |
| rs34816447 | 19:11,891,207 | C/T | — | uncertain significance |
| rs148272848 | 19:11,891,244 | G/T | — | uncertain significance |
| rs965723578 | 19:11,891,399 | T/C | — | uncertain significance |
| rs536115030 | 19:11,891,421 | T/G | — | uncertain significance |
| rs989314830 | 19:11,891,459 | C/A | — | uncertain significance |
| rs778146260 | 19:11,891,590 | T/G | — | uncertain significance |
| rs149982598 | 19:11,891,622 | G/T | — | uncertain significance |
| rs184549854 | 19:11,891,624 | A/G | — | uncertain significance |
| rs779635419 | 19:11,891,656 | G/T | — | uncertain significance |
| rs2512860795 | 19:11,891,784 | A/T | — | uncertain significance |
| rs759087202 | 19:11,891,996 | G/A | — | uncertain significance |
| rs1054013253 | 19:11,892,092 | T/C | — | uncertain significance |
| rs201148941 | 19:11,892,099 | T/C | — | uncertain significance |
| rs2512861032 | 19:11,892,122 | A/G | — | uncertain significance |
| rs140651700 | 19:11,892,175 | T/C | — | likely benign |
| rs781511935 | 19:11,892,231 | A/T | — | uncertain significance |
| rs372673223 | 19:11,892,398 | C/T | — | uncertain significance |
| rs80152996 | 19:11,892,553 | T/A | — | benign |
| rs286219 | 19:11,894,535 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.