ZFPM2
zinc finger protein, FOG family member 2
Summary
The zinc finger protein encoded by this gene is a widely expressed member of the FOG family of transcription factors. The family members modulate the activity of GATA family proteins, which are important regulators of hematopoiesis and cardiogenesis in mammals. It has been demonstrated that the protein can both activate and down-regulate expression of GATA-target genes, suggesting different modulation in different promoter contexts. A related mRNA suggests an alternatively spliced product but this information is not yet fully supported by the sequence. [provided by RefSeq, Jul 2008]
Known Variants309 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1811964183 | 8:106,331,179 | C/T | — | likely pathogenic |
| rs962852256 | 8:106,331,196 | C/G | — | likely benign |
| rs550883122 | 8:106,331,220 | G/C | — | likely benign |
| rs149902904 | 8:106,331,221 | C/G | — | likely benign |
| rs559322533 | 8:106,360,115 | A/T | — | — |
| rs17211035 | 8:106,377,941 | G/T | intron variant | — |
| rs34628728 | 8:106,379,363 | T/G | — | — |
| rs11774007 | 8:106,403,105 | G/T | intron variant | — |
| rs7830852 | 8:106,415,088 | A/G | intron variant | — |
| rs756938601 | 8:106,431,362 | C/G | — | benign |
| rs374926066 | 8:106,431,368 | C/A | — | likely benign |
| rs186003344 | 8:106,431,388 | C/T | — | likely benign |
| rs1811743355 | 8:106,431,403 | A/G | — | likely benign |
| rs1811743429 | 8:106,431,404 | G/A | — | uncertain significance |
| rs371244942 | 8:106,431,405 | A/G | — | uncertain significance |
| rs2536474697 | 8:106,431,409 | A/G | — | likely benign |
| rs121908601 | 8:106,431,420 | A/G | missense variant | pathogenic |
| rs769580025 | 8:106,431,421 | G/A | — | likely benign |
| rs199535268 | 8:106,431,452 | C/G | — | conflicting classifications of pathogenicity |
| rs1586358616 | 8:106,431,456 | T/G | — | uncertain significance |
| rs569356297 | 8:106,431,461 | G/A | — | conflicting classifications of pathogenicity |
| rs180852828 | 8:106,431,522 | G/A | — | benign |
| rs1404513559 | 8:106,431,523 | T/G | — | likely pathogenic |
| rs7003816 | 8:106,433,801 | A/G | downstream gene variant | — |
| rs11997028 | 8:106,456,033 | G/T | — | — |
| rs573002259 | 8:106,456,500 | T/G | — | benign |
| rs765866053 | 8:106,456,548 | G/T | — | likely benign |
| rs888264289 | 8:106,456,549 | G/A | — | uncertain significance |
| rs1353333391 | 8:106,456,559 | C/T | — | uncertain significance |
| rs200972094 | 8:106,456,566 | A/G | — | benign |
| rs755810063 | 8:106,456,569 | G/T | — | likely benign |
| rs563358406 | 8:106,456,588 | A/G | — | uncertain significance |
| rs371910925 | 8:106,456,593 | C/T | — | likely benign |
| rs772042320 | 8:106,456,594 | G/T | — | uncertain significance |
| rs202217256 | 8:106,456,600 | G/A | — | benign |
| rs367972104 | 8:106,456,618 | G/T | — | likely benign |
| rs11990012 | 8:106,456,683 | A/G | — | benign |
| rs7008556 | 8:106,464,271 | G/A | intron variant | — |
| rs2622633 | 8:106,509,975 | G/A | intron variant | — |
| rs4734869 | 8:106,512,828 | T/A | intron variant | — |
| rs57942103 | 8:106,513,461 | A/T | — | — |
| rs12678719 | 8:106,516,054 | C/G | intron variant | — |
| rs6997293 | 8:106,517,928 | T/A | — | — |
| rs7836542 | 8:106,534,443 | C/G | — | — |
| rs28416651 | 8:106,564,652 | G/A | intron variant | — |
| rs34826779 | 8:106,570,964 | G/T | intron variant | — |
| rs3735953 | 8:106,573,578 | C/T | — | benign |
| rs763335389 | 8:106,573,586 | T/C | — | likely benign |
| rs372818742 | 8:106,573,587 | G/A | — | likely benign |
| rs1815131947 | 8:106,573,611 | A/G | — | uncertain significance |
| rs764921045 | 8:106,573,622 | A/C | — | uncertain significance |
| rs121908602 | 8:106,573,623 | C/T | stop gained | pathogenic |
| rs2536827502 | 8:106,573,638 | C/T | — | pathogenic |
| rs1303627095 | 8:106,573,643 | G/T | — | uncertain significance |
| rs556443661 | 8:106,573,646 | A/G | — | likely benign |
| rs1815133154 | 8:106,573,647 | C/T | — | uncertain significance |
| rs772114579 | 8:106,573,653 | G/T | — | uncertain significance |
| rs1230477062 | 8:106,573,672 | C/T | — | uncertain significance |
| rs199814804 | 8:106,573,673 | G/A | — | likely benign |
| rs1484648379 | 8:106,573,705 | C/A | — | uncertain significance |
| rs374105222 | 8:106,573,724 | C/T | — | likely benign |
| rs377621810 | 8:106,573,725 | G/A | — | likely benign |
| rs12216772 | 8:106,573,919 | C/T | — | benign |
| rs6993770 | 8:106,581,528 | A/T | regulatory region variant | — |
| rs16873402 | 8:106,589,247 | C/T | intron variant | — |
| rs6987377 | 8:106,590,684 | A/G | intron variant | — |
| rs4602861 | 8:106,590,706 | A/G | intron variant | — |
| rs2343593 | 8:106,590,851 | T/C | — | — |
| rs17217757 | 8:106,613,321 | G/T | — | — |
| rs761799802 | 8:106,646,464 | C/A | — | likely benign |
| rs552410913 | 8:106,646,469 | T/C | — | benign |
| rs1167230345 | 8:106,646,476 | G/T | — | uncertain significance |
| rs200168135 | 8:106,646,489 | G/C | — | conflicting classifications of pathogenicity |
| rs370456245 | 8:106,646,495 | A/G | — | conflicting classifications of pathogenicity |
| rs373855468 | 8:106,646,497 | G/C | — | uncertain significance |
| rs200671886 | 8:106,646,516 | A/G | — | uncertain significance |
| rs2536997524 | 8:106,646,530 | T/A | — | uncertain significance |
| rs1333119540 | 8:106,646,548 | G/A | — | likely benign |
| rs2130839797 | 8:106,646,571 | T/C | — | uncertain significance |
| rs4734883 | 8:106,646,683 | A/T | — | benign |
| rs2218279 | 8:106,674,812 | T/C | — | benign |
| rs138466839 | 8:106,800,942 | A/T | — | benign |
| rs1359443682 | 8:106,800,975 | G/C | — | uncertain significance |
| rs754528675 | 8:106,800,977 | C/T | — | likely benign |
| rs758169109 | 8:106,800,995 | G/A | — | likely benign |
| rs2131136061 | 8:106,801,006 | T/C | — | uncertain significance |
| rs368572530 | 8:106,801,030 | T/C | — | uncertain significance |
| rs940374051 | 8:106,801,038 | G/A | — | uncertain significance |
| rs182216711 | 8:106,801,042 | G/C | — | likely benign |
| rs1439864085 | 8:106,801,073 | T/C | — | likely benign |
| rs774715438 | 8:106,801,075 | C/T | — | uncertain significance |
| rs373471482 | 8:106,801,077 | C/T | — | uncertain significance |
| rs1294020638 | 8:106,801,078 | G/A | — | uncertain significance |
| rs202204708 | 8:106,801,092 | A/G | — | conflicting classifications of pathogenicity |
| rs397514520 | 8:106,801,094 | T/G | missense variant | pathogenic |
| rs140283741 | 8:106,801,171 | G/A | — | benign |
| rs751110244 | 8:106,810,933 | C/T | — | likely benign |
| rs370717147 | 8:106,810,948 | G/T | — | likely benign |
| rs953556550 | 8:106,810,972 | T/G | — | uncertain significance |
| rs1477755260 | 8:106,810,973 | C/T | — | uncertain significance |
Showing 100 of 309 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.