MORC1
MORC family CW-type zinc finger 1
Summary
This gene encodes the human homolog of mouse morc and like the mouse protein it is testis-specific. Mouse studies support a testis-specific function since only male knockout mice are infertile; infertility is the only apparent defect. These studies further support a role for this protein early in spermatogenesis, possibly by affecting entry into apoptosis because testis from knockout mice show greatly increased numbers of apoptotic cells. [provided by RefSeq, Jan 2009]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201034263 | 3:108,677,826 | T/C | — | uncertain significance |
| rs1947009201 | 3:108,677,850 | G/A | — | uncertain significance |
| rs1156730181 | 3:108,677,904 | T/C | — | uncertain significance |
| rs369497112 | 3:108,677,967 | C/G | — | uncertain significance |
| rs1947138932 | 3:108,682,412 | C/T | — | uncertain significance |
| rs753247879 | 3:108,688,518 | G/T | — | uncertain significance |
| rs762537920 | 3:108,698,428 | G/C | — | uncertain significance |
| rs139035446 | 3:108,698,491 | T/C | — | uncertain significance |
| rs141491434 | 3:108,698,497 | A/G | — | uncertain significance |
| rs1947658836 | 3:108,698,506 | T/C | — | likely benign |
| rs73200691 | 3:108,699,510 | C/T | intron variant | — |
| rs2593957 | 3:108,703,025 | T/C | intron variant | — |
| rs1441729530 | 3:108,703,564 | T/C | — | uncertain significance |
| rs114067906 | 3:108,705,737 | A/T | — | benign |
| rs2895349 | 3:108,708,374 | G/A | intron variant | — |
| rs3804702 | 3:108,712,803 | T/A | — | — |
| rs1948379691 | 3:108,719,504 | G/A | — | uncertain significance |
| rs145567621 | 3:108,723,936 | T/C | — | uncertain significance |
| rs375060364 | 3:108,723,942 | T/A | — | uncertain significance |
| rs1178273988 | 3:108,751,658 | A/G | — | uncertain significance |
| rs146265277 | 3:108,754,295 | A/C | — | uncertain significance |
| rs1294606089 | 3:108,773,728 | G/A | — | uncertain significance |
| rs762259758 | 3:108,776,229 | A/G | — | uncertain significance |
| rs747855351 | 3:108,776,287 | C/T | — | likely benign |
| rs770722056 | 3:108,776,298 | T/C | — | uncertain significance |
| rs17225637 | 3:108,780,836 | T/A | — | benign |
| rs189624981 | 3:108,786,728 | A/C | intron variant | — |
| rs772708323 | 3:108,788,524 | T/C | — | uncertain significance |
| rs148630097 | 3:108,788,596 | G/T | — | likely benign |
| rs558965386 | 3:108,813,767 | T/C | — | uncertain significance |
| rs2530017467 | 3:108,813,820 | T/G | — | uncertain significance |
| rs948587781 | 3:108,813,846 | C/T | — | uncertain significance |
| rs764440236 | 3:108,813,867 | T/C | — | uncertain significance |
| rs2530018260 | 3:108,813,900 | G/T | — | uncertain significance |
| rs148062449 | 3:108,813,903 | T/C | — | uncertain significance |
| rs751430053 | 3:108,818,209 | C/T | — | uncertain significance |
| rs141763031 | 3:108,818,285 | T/C | — | uncertain significance |
| rs750328045 | 3:108,818,306 | T/C | — | uncertain significance |
| rs2530042878 | 3:108,819,277 | T/C | — | uncertain significance |
| rs557495347 | 3:108,825,089 | C/T | — | — |
| rs116328407 | 3:108,833,242 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.