TFDP2
transcription factor Dp-2
Summary
The gene is a member of the transcription factor DP family. The encoded protein forms heterodimers with the E2F transcription factors resulting in transcriptional activation of cell cycle regulated genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1441751325 | 3:141,671,404 | T/C | — | uncertain significance |
| rs377110493 | 3:141,671,419 | G/T | — | uncertain significance |
| rs868661792 | 3:141,671,517 | C/A | — | uncertain significance |
| rs745484514 | 3:141,671,537 | C/T | — | uncertain significance |
| rs1576434847 | 3:141,671,778 | T/C | — | uncertain significance |
| rs9815587 | 3:141,674,548 | C/A | intron variant | — |
| rs1346513680 | 3:141,678,617 | C/T | — | uncertain significance |
| rs374416424 | 3:141,678,618 | G/A | — | uncertain significance |
| rs1364114367 | 3:141,682,741 | G/T | — | uncertain significance |
| rs61756224 | 3:141,682,750 | T/C | missense variant | — |
| rs376975635 | 3:141,682,799 | C/T | — | uncertain significance |
| rs1026445351 | 3:141,688,970 | C/T | — | uncertain significance |
| rs534991564 | 3:141,697,385 | T/C | — | uncertain significance |
| rs753885153 | 3:141,697,505 | C/T | — | uncertain significance |
| rs1298190375 | 3:141,697,519 | C/T | — | uncertain significance |
| rs62283132 | 3:141,709,036 | C/T | intron variant | — |
| rs1511299 | 3:141,716,072 | T/C | intron variant | — |
| rs34464850 | 3:141,721,762 | G/C | intron variant | — |
| rs373959825 | 3:141,724,296 | A/G | — | uncertain significance |
| rs1038236702 | 3:141,724,333 | T/C | — | uncertain significance |
| rs2473433790 | 3:141,724,350 | G/A | — | uncertain significance |
| rs2473434145 | 3:141,724,383 | T/C | — | uncertain significance |
| rs6440057 | 3:141,728,308 | T/G | — | — |
| rs6781340 | 3:141,733,417 | G/C | — | — |
| rs13065446 | 3:141,737,842 | C/A | — | — |
| rs72990266 | 3:141,741,960 | G/A | intron variant | — |
| rs78768527 | 3:141,749,930 | T/C | intron variant | — |
| rs1397764 | 3:141,750,810 | A/G | intron variant | — |
| rs9863685 | 3:141,757,097 | A/C | — | — |
| rs6440060 | 3:141,762,853 | A/G | coding sequence variant | — |
| rs6791514 | 3:141,766,305 | C/A | — | — |
| rs2902144 | 3:141,771,248 | G/C | — | — |
| rs347692 | 3:141,785,395 | G/A | — | — |
| rs347685 | 3:141,807,137 | C/A | intron variant | — |
| rs7640665 | 3:141,813,172 | G/A | intron variant | — |
| rs147877018 | 3:141,813,349 | G/C | — | — |
| rs11705932 | 3:141,818,850 | C/T | intron variant | — |
| rs62284572 | 3:141,832,981 | C/G | — | — |
| rs7610920 | 3:141,843,888 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.