ZCWPW1
zinc finger CW-type and PWWP domain containing 1
Summary
Enables histone reader activity; methyl-CpG binding activity; and methylated histone binding activity. Predicted to be involved in meiosis I; positive regulation of DNA metabolic process; and spermatogenesis. Predicted to act upstream of or within homologous chromosome pairing at meiosis. Predicted to be located in XY body. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2484852217 | 7:99,998,675 | C/T | — | uncertain significance |
| rs377145270 | 7:99,998,792 | C/T | — | uncertain significance |
| rs2484856659 | 7:99,998,804 | G/A | — | uncertain significance |
| rs768959785 | 7:99,998,840 | G/A | — | uncertain significance |
| rs756575257 | 7:99,998,855 | A/C | — | uncertain significance |
| rs377758789 | 7:99,999,520 | T/C | — | uncertain significance |
| rs1218238019 | 7:99,999,572 | G/C | — | uncertain significance |
| rs1425267573 | 7:99,999,595 | G/T | — | uncertain significance |
| rs375737733 | 7:100,000,150 | G/T | — | uncertain significance |
| rs777789711 | 7:100,000,188 | C/A | — | uncertain significance |
| rs757466499 | 7:100,001,367 | C/G | — | uncertain significance |
| rs2484925736 | 7:100,001,387 | T/C | — | uncertain significance |
| rs368172772 | 7:100,001,830 | T/C | — | likely benign |
| rs76913697 | 7:100,002,772 | A/G | intron variant | — |
| rs2485000974 | 7:100,004,369 | G/A | — | uncertain significance |
| rs758061043 | 7:100,004,378 | G/A | — | uncertain significance |
| rs1476679 | 7:100,004,446 | C/T | regulatory region variant | — |
| rs200631169 | 7:100,004,852 | G/A | — | uncertain significance |
| rs2485021866 | 7:100,004,908 | T/G | — | uncertain significance |
| rs2485062114 | 7:100,006,166 | G/T | — | uncertain significance |
| rs373658826 | 7:100,006,267 | C/T | — | uncertain significance |
| rs68116612 | 7:100,006,493 | G/A | intron variant | — |
| rs535083608 | 7:100,007,089 | G/A | — | uncertain significance |
| rs2485087494 | 7:100,007,092 | G/A | — | uncertain significance |
| rs768346152 | 7:100,007,094 | G/A | — | likely benign |
| rs751884265 | 7:100,013,645 | T/A | — | uncertain significance |
| rs577472355 | 7:100,013,666 | C/T | — | likely benign |
| rs1411810673 | 7:100,014,713 | G/T | — | uncertain significance |
| rs537142241 | 7:100,014,779 | T/C | — | uncertain significance |
| rs1795429058 | 7:100,014,787 | A/T | — | uncertain significance |
| rs73161762 | 7:100,014,846 | C/T | intron variant | — |
| rs13222543 | 7:100,015,457 | C/T | intron variant | — |
| rs141450215 | 7:100,016,781 | T/C | — | benign |
| rs767714348 | 7:100,017,269 | G/A | — | uncertain significance |
| rs771059720 | 7:100,017,309 | C/T | — | uncertain significance |
| rs776630030 | 7:100,017,330 | T/C | — | uncertain significance |
| rs1247310468 | 7:100,017,476 | G/A | — | uncertain significance |
| rs147650625 | 7:100,021,996 | T/C | upstream gene variant | — |
| rs200701118 | 7:100,026,421 | G/T | — | — |
| rs148383191 | 7:100,027,003 | G/T | — | — |
| rs150881124 | 7:100,027,184 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.