CDCA2
cell division cycle associated 2
Summary
This gene encodes a targeting subunit of the cell-cycle associated protein, protein phosphatase 1, with a role in targeting this protein to chromatin during anaphase. These two proteins comprise a phosphatase complex that is involved in nuclear envelope reformation and regulation of the DNA damage response. The encoded protein may also play a role in cancer progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201653606 | 8:25,317,780 | C/T | — | uncertain significance |
| rs768781688 | 8:25,317,804 | A/G | — | likely benign |
| rs1563255495 | 8:25,317,905 | G/A | — | likely benign |
| rs2487128284 | 8:25,317,962 | C/T | — | uncertain significance |
| rs145990893 | 8:25,317,966 | C/T | — | likely benign |
| rs115875864 | 8:25,317,987 | C/T | — | benign |
| rs2487128476 | 8:25,318,014 | C/T | — | uncertain significance |
| rs2487128562 | 8:25,318,041 | C/T | — | uncertain significance |
| rs775377218 | 8:25,319,596 | T/C | — | uncertain significance |
| rs35698191 | 8:25,321,845 | T/C | — | — |
| rs763098763 | 8:25,323,710 | G/A | — | uncertain significance |
| rs761133309 | 8:25,323,734 | G/A | — | uncertain significance |
| rs376754752 | 8:25,323,768 | A/G | — | uncertain significance |
| rs147918382 | 8:25,323,772 | G/A | — | uncertain significance |
| rs11779723 | 8:25,324,678 | T/C | intron variant | — |
| rs199899316 | 8:25,325,744 | G/T | — | uncertain significance |
| rs991221398 | 8:25,325,811 | A/C | — | likely benign |
| rs1486521925 | 8:25,325,844 | C/T | — | uncertain significance |
| rs765128435 | 8:25,325,859 | T/C | — | likely benign |
| rs2487153993 | 8:25,325,890 | C/G | — | uncertain significance |
| rs771817829 | 8:25,325,913 | C/A | — | uncertain significance |
| rs904669969 | 8:25,327,473 | C/T | — | uncertain significance |
| rs11775358 | 8:25,329,777 | T/C | — | — |
| rs11777745 | 8:25,333,516 | A/G | regulatory region variant | — |
| rs748807211 | 8:25,337,435 | A/G | — | uncertain significance |
| rs1252270949 | 8:25,337,437 | G/T | — | uncertain significance |
| rs202137737 | 8:25,337,443 | G/T | — | uncertain significance |
| rs369855468 | 8:25,337,459 | A/G | — | uncertain significance |
| rs112148375 | 8:25,337,481 | G/A | — | benign |
| rs150751889 | 8:25,337,562 | C/T | — | likely benign |
| rs1324777807 | 8:25,337,563 | C/T | — | uncertain significance |
| rs768273369 | 8:25,337,567 | C/T | — | uncertain significance |
| rs142322892 | 8:25,337,591 | G/A | — | uncertain significance |
| rs774640407 | 8:25,337,611 | T/C | — | uncertain significance |
| rs80267219 | 8:25,340,562 | T/G | intron variant | — |
| rs754847258 | 8:25,340,921 | T/C | — | uncertain significance |
| rs771078018 | 8:25,340,944 | T/A | — | uncertain significance |
| rs2487196884 | 8:25,340,963 | A/G | — | uncertain significance |
| rs769164843 | 8:25,341,505 | C/T | — | uncertain significance |
| rs143591039 | 8:25,341,592 | A/G | — | uncertain significance |
| rs755408049 | 8:25,341,604 | C/T | — | uncertain significance |
| rs761513414 | 8:25,341,635 | A/G | — | uncertain significance |
| rs1412604453 | 8:25,341,722 | A/G | — | uncertain significance |
| rs764574548 | 8:25,343,308 | G/A | — | uncertain significance |
| rs796564573 | 8:25,344,826 | A/G | — | uncertain significance |
| rs117565806 | 8:25,346,073 | G/C | — | uncertain significance |
| rs774826692 | 8:25,346,078 | G/A | — | uncertain significance |
| rs374095928 | 8:25,346,110 | A/C | — | uncertain significance |
| rs2487213990 | 8:25,346,114 | C/T | — | uncertain significance |
| rs115925873 | 8:25,346,133 | A/G | — | benign |
| rs2487214158 | 8:25,346,135 | A/C | — | uncertain significance |
| rs150912540 | 8:25,346,155 | A/G | — | uncertain significance |
| rs2321250 | 8:25,349,531 | C/T | intron variant | — |
| rs11996749 | 8:25,351,521 | T/C | intron variant | — |
| rs7826705 | 8:25,352,833 | T/G | — | — |
| rs11785275 | 8:25,356,017 | T/C | intron variant | — |
| rs1804549643 | 8:25,360,917 | G/C | — | likely benign |
| rs201987917 | 8:25,360,932 | G/A | — | uncertain significance |
| rs2487253798 | 8:25,360,958 | A/G | — | uncertain significance |
| rs144313074 | 8:25,361,000 | G/A | — | uncertain significance |
| rs4595133 | 8:25,362,561 | C/T | intron variant | — |
| rs112952792 | 8:25,362,757 | G/C | — | — |
| rs368357943 | 8:25,364,052 | G/A | — | uncertain significance |
| rs113799371 | 8:25,364,101 | G/A | — | uncertain significance |
| rs747423702 | 8:25,364,297 | A/T | — | uncertain significance |
| rs749123267 | 8:25,364,314 | C/G | — | uncertain significance |
| rs765467570 | 8:25,364,365 | A/C | — | uncertain significance |
| rs1804703145 | 8:25,364,413 | A/G | — | uncertain significance |
| rs73550865 | 8:25,364,443 | A/C | — | benign |
| rs750340537 | 8:25,364,584 | C/G | — | uncertain significance |
| rs1804712705 | 8:25,364,634 | A/G | — | uncertain significance |
| rs760384674 | 8:25,364,666 | A/T | — | uncertain significance |
| rs1804718018 | 8:25,364,749 | T/C | — | uncertain significance |
| rs3829009 | 8:25,364,834 | A/G | synonymous variant | — |
| rs201786275 | 8:25,364,854 | G/A | — | uncertain significance |
| rs139582947 | 8:25,364,889 | G/A | — | uncertain significance |
| rs1405083781 | 8:25,365,006 | G/C | — | uncertain significance |
| rs147641260 | 8:25,365,042 | G/A | — | uncertain significance |
| rs114180099 | 8:25,365,087 | G/T | — | uncertain significance |
| rs376561663 | 8:25,365,169 | G/A | — | uncertain significance |
| rs940693857 | 8:25,365,200 | G/C | — | uncertain significance |
| rs368980502 | 8:25,365,202 | G/A | — | uncertain significance |
| rs2487267820 | 8:25,365,220 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.