ZNF358
zinc finger protein 358
Summary
Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in several processes, including embryonic forelimb morphogenesis; neural tube development; and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113394178 | 19:7,581,244 | C/A | regulatory region variant | — |
| rs1392603082 | 19:7,584,136 | G/A | — | uncertain significance |
| rs778486348 | 19:7,584,147 | G/C | — | uncertain significance |
| rs2022414017 | 19:7,584,175 | G/A | — | uncertain significance |
| rs1003025975 | 19:7,584,177 | C/A | — | uncertain significance |
| rs779709307 | 19:7,584,180 | G/A | — | uncertain significance |
| rs200448071 | 19:7,584,235 | T/C | — | uncertain significance |
| rs192434630 | 19:7,584,239 | C/T | — | benign |
| rs368029064 | 19:7,584,316 | A/T | — | uncertain significance |
| rs61742775 | 19:7,584,329 | C/G | — | benign |
| rs200118318 | 19:7,584,354 | G/A | — | uncertain significance |
| rs769064740 | 19:7,584,381 | C/T | — | uncertain significance |
| rs142712888 | 19:7,584,388 | C/T | — | uncertain significance |
| rs762322485 | 19:7,584,397 | C/T | — | likely benign |
| rs758341197 | 19:7,584,473 | C/T | — | likely benign |
| rs370159121 | 19:7,584,489 | G/T | — | uncertain significance |
| rs1237474867 | 19:7,584,505 | G/A | — | likely benign |
| rs142875126 | 19:7,584,532 | C/T | — | uncertain significance |
| rs2022427720 | 19:7,584,610 | G/T | — | uncertain significance |
| rs531337842 | 19:7,584,666 | C/A | — | uncertain significance |
| rs1018193838 | 19:7,584,698 | C/G | — | uncertain significance |
| rs748635343 | 19:7,584,841 | C/T | — | uncertain significance |
| rs761620782 | 19:7,584,939 | G/T | — | uncertain significance |
| rs2512461460 | 19:7,584,984 | A/G | — | uncertain significance |
| rs1162451114 | 19:7,585,095 | C/A | — | uncertain significance |
| rs2512462228 | 19:7,585,242 | G/A | — | uncertain significance |
| rs750676021 | 19:7,585,281 | G/A | — | uncertain significance |
| rs1303750340 | 19:7,585,305 | C/T | — | uncertain significance |
| rs2022448990 | 19:7,585,314 | G/C | — | uncertain significance |
| rs199871271 | 19:7,585,328 | A/G | — | likely benign |
| rs554724109 | 19:7,585,337 | T/A | — | likely benign |
| rs2512462733 | 19:7,585,350 | G/C | — | uncertain significance |
| rs2022455598 | 19:7,585,356 | G/A | — | uncertain significance |
| rs12977398 | 19:7,585,446 | C/T | — | likely benign |
| rs755614766 | 19:7,585,483 | T/A | — | uncertain significance |
| rs758246034 | 19:7,585,506 | C/T | — | uncertain significance |
| rs2022467346 | 19:7,585,584 | C/A | — | uncertain significance |
| rs147948386 | 19:7,585,606 | C/A | — | uncertain significance |
| rs372064298 | 19:7,585,665 | G/A | — | uncertain significance |
| rs1004656258 | 19:7,585,685 | C/A | — | uncertain significance |
| rs2512464168 | 19:7,585,771 | T/C | — | uncertain significance |
| rs1324490806 | 19:7,585,809 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.