ZFPM1
zinc finger protein, FOG family member 1
Summary
Enables RNA polymerase II-specific DNA-binding transcription factor binding activity and transcription corepressor activity. Involved in platelet formation; regulation of definitive erythrocyte differentiation; and regulation of gene expression. Part of transcription repressor complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants169 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs879627 | 16:88,522,541 | C/T | — | — |
| rs4782366 | 16:88,524,298 | T/C | — | — |
| rs67651018 | 16:88,527,222 | G/A | regulatory region variant | — |
| rs115287613 | 16:88,527,676 | C/T | — | — |
| rs4584807 | 16:88,528,125 | C/G | — | — |
| rs60037105 | 16:88,528,636 | T/A | regulatory region variant | — |
| rs904790 | 16:88,528,780 | T/A | — | — |
| rs4782369 | 16:88,531,861 | G/C | regulatory region variant | — |
| rs34139656 | 16:88,534,923 | A/G | regulatory region variant | — |
| rs34088055 | 16:88,535,670 | C/T | downstream gene variant | — |
| rs553759219 | 16:88,540,083 | C/G | — | — |
| rs55880988 | 16:88,546,253 | G/C | — | — |
| rs566571310 | 16:88,546,269 | C/G | — | — |
| rs55637647 | 16:88,549,264 | C/G | regulatory region variant | — |
| rs12927479 | 16:88,551,837 | A/C | — | — |
| rs3751673 | 16:88,552,370 | A/G | — | benign |
| rs559772457 | 16:88,552,392 | G/T | — | uncertain significance |
| rs1316063658 | 16:88,552,418 | A/C | — | uncertain significance |
| rs35867223 | 16:88,552,442 | C/A | — | uncertain significance |
| rs567366010 | 16:88,553,123 | G/C | — | — |
| rs146676651 | 16:88,555,463 | C/T | — | uncertain significance |
| rs148828760 | 16:88,555,464 | G/A | — | likely benign |
| rs34916016 | 16:88,555,502 | G/C | — | benign |
| rs558530910 | 16:88,555,540 | G/A | — | likely benign |
| rs62048971 | 16:88,556,004 | G/A | intron variant | — |
| rs11863449 | 16:88,558,172 | G/C | — | — |
| rs59865663 | 16:88,558,312 | G/A | regulatory region variant | — |
| rs113895617 | 16:88,559,511 | G/A | intron variant | — |
| rs74035504 | 16:88,559,699 | T/C | intron variant | — |
| rs118090537 | 16:88,559,762 | G/T | — | — |
| rs74035505 | 16:88,559,841 | C/G | — | — |
| rs74035506 | 16:88,559,851 | A/G | intron variant | — |
| rs62048974 | 16:88,560,082 | G/C | — | — |
| rs9939277 | 16:88,565,634 | G/A | regulatory region variant | — |
| rs12185173 | 16:88,566,368 | A/G | regulatory region variant | — |
| rs77639164 | 16:88,568,054 | A/C | intron variant | — |
| rs11645559 | 16:88,568,102 | C/G | intron variant | — |
| rs55824135 | 16:88,568,477 | T/C | intron variant | — |
| rs4782371 | 16:88,568,831 | T/C | — | — |
| rs75874899 | 16:88,570,013 | G/T | — | — |
| rs899732 | 16:88,570,480 | A/T | — | — |
| rs749679 | 16:88,570,816 | A/G | regulatory region variant | — |
| rs11076614 | 16:88,573,169 | G/T | — | — |
| rs147032017 | 16:88,580,796 | C/T | splice region variant | — |
| rs769825796 | 16:88,580,808 | G/A | — | likely benign |
| rs77013160 | 16:88,582,871 | G/T | intron variant | — |
| rs561981265 | 16:88,592,475 | C/T | — | — |
| rs551152203 | 16:88,593,271 | C/T | — | uncertain significance |
| rs114240624 | 16:88,593,296 | C/T | — | benign |
| rs7198952 | 16:88,594,123 | G/A | — | — |
| rs1326027137 | 16:88,594,445 | G/A | — | uncertain significance |
| rs914676088 | 16:88,594,478 | G/A | — | uncertain significance |
| rs775802670 | 16:88,594,496 | G/A | — | uncertain significance |
| rs201427325 | 16:88,594,511 | G/A | — | uncertain significance |
| rs753525901 | 16:88,594,544 | A/G | — | uncertain significance |
| rs1469510709 | 16:88,594,554 | C/A | — | uncertain significance |
| rs145401494 | 16:88,594,633 | C/T | — | likely benign |
| rs12923090 | 16:88,597,149 | C/T | intron variant | — |
| rs762672608 | 16:88,598,454 | G/A | — | uncertain significance |
| rs550839892 | 16:88,598,497 | G/A | — | uncertain significance |
| rs141766578 | 16:88,598,508 | G/A | — | uncertain significance |
| rs371828977 | 16:88,598,524 | C/T | — | uncertain significance |
| rs201051014 | 16:88,598,526 | G/A | — | uncertain significance |
| rs772973552 | 16:88,598,581 | C/A | — | uncertain significance |
| rs151065815 | 16:88,598,590 | G/A | — | uncertain significance |
| rs372953091 | 16:88,598,595 | A/G | — | uncertain significance |
| rs1388344586 | 16:88,598,628 | A/G | — | uncertain significance |
| rs150205611 | 16:88,599,080 | C/T | — | likely benign |
| rs200901030 | 16:88,599,114 | A/T | — | uncertain significance |
| rs1180036961 | 16:88,599,208 | A/G | — | uncertain significance |
| rs763202383 | 16:88,599,221 | T/G | — | uncertain significance |
| rs1391727101 | 16:88,599,248 | G/A | — | uncertain significance |
| rs138649888 | 16:88,599,255 | G/C | — | uncertain significance |
| rs764813520 | 16:88,599,316 | G/A | — | uncertain significance |
| rs770903760 | 16:88,599,559 | G/A | — | uncertain significance |
| rs2507851876 | 16:88,599,609 | T/C | — | uncertain significance |
| rs1267171760 | 16:88,599,627 | G/A | — | uncertain significance |
| rs758708134 | 16:88,599,628 | C/T | — | uncertain significance |
| rs757397198 | 16:88,599,639 | T/C | — | uncertain significance |
| rs1006654788 | 16:88,599,649 | T/A | — | uncertain significance |
| rs1912944251 | 16:88,599,651 | G/T | — | uncertain significance |
| rs1253251216 | 16:88,599,676 | C/T | — | uncertain significance |
| rs201915453 | 16:88,599,698 | G/C | — | benign |
| rs956525347 | 16:88,599,745 | G/A | — | uncertain significance |
| rs750433569 | 16:88,599,766 | T/C | — | likely benign |
| rs1038637817 | 16:88,599,781 | C/T | — | uncertain significance |
| rs771559762 | 16:88,599,804 | G/A | — | uncertain significance |
| rs1912970875 | 16:88,599,847 | G/A | — | uncertain significance |
| rs774538257 | 16:88,599,861 | A/G | — | uncertain significance |
| rs1314073394 | 16:88,599,870 | G/A | — | uncertain significance |
| rs766427111 | 16:88,599,904 | C/A | — | uncertain significance |
| rs747841274 | 16:88,599,931 | G/C | — | uncertain significance |
| rs776229994 | 16:88,599,950 | G/C | — | uncertain significance |
| rs574184583 | 16:88,599,962 | G/A | — | likely benign |
| rs374949892 | 16:88,599,996 | G/A | — | uncertain significance |
| rs774785297 | 16:88,600,017 | C/T | — | uncertain significance |
| rs1363034794 | 16:88,600,031 | G/C | — | uncertain significance |
| rs966153336 | 16:88,600,051 | C/G | — | uncertain significance |
| rs1474468637 | 16:88,600,056 | G/T | — | uncertain significance |
| rs747432198 | 16:88,600,083 | G/A | — | uncertain significance |
Showing 100 of 169 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.