ASZ1
ankyrin repeat, SAM and basic leucine zipper domain containing 1
Summary
Predicted to be involved in male meiotic nuclear division; spermatogenesis; and transposable element silencing. Predicted to be located in cytoplasm. Predicted to be active in pi-body. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143434974 | 7:117,003,790 | G/A | — | uncertain significance |
| rs891809327 | 7:117,003,802 | A/G | — | likely benign |
| rs142005201 | 7:117,008,679 | A/C | — | uncertain significance |
| rs746841209 | 7:117,008,736 | T/C | — | uncertain significance |
| rs537698945 | 7:117,008,771 | A/G | — | likely benign |
| rs10225824 | 7:117,012,023 | G/A | intron variant | — |
| rs12534129 | 7:117,018,135 | T/A | — | — |
| rs200268860 | 7:117,019,999 | C/T | — | uncertain significance |
| rs2485474542 | 7:117,021,088 | T/C | — | uncertain significance |
| rs964766582 | 7:117,022,142 | T/C | — | uncertain significance |
| rs1584724028 | 7:117,023,098 | C/T | — | uncertain significance |
| rs901683870 | 7:117,023,125 | C/G | — | uncertain significance |
| rs4730779 | 7:117,023,535 | G/T | — | — |
| rs780891217 | 7:117,024,805 | A/G | — | uncertain significance |
| rs186384831 | 7:117,025,844 | T/C | — | conflicting classifications of pathogenicity |
| rs1212886634 | 7:117,025,847 | T/C | — | uncertain significance |
| rs199851030 | 7:117,025,850 | G/C | — | uncertain significance |
| rs2188555 | 7:117,057,233 | G/A | intron variant | — |
| rs557326021 | 7:117,060,247 | G/A | — | uncertain significance |
| rs1278610422 | 7:117,062,318 | T/C | — | uncertain significance |
| rs144389578 | 7:117,062,333 | G/A | — | uncertain significance |
| rs558179484 | 7:117,062,347 | T/C | — | uncertain significance |
| rs2485542476 | 7:117,062,353 | A/G | — | uncertain significance |
| rs1797227603 | 7:117,066,906 | C/G | — | uncertain significance |
| rs776497887 | 7:117,066,935 | T/C | — | uncertain significance |
| rs117446983 | 7:117,066,978 | C/T | — | benign |
| rs1258777314 | 7:117,067,451 | C/A | — | uncertain significance |
| rs773542306 | 7:117,067,460 | C/G | — | uncertain significance |
| rs770188222 | 7:117,067,499 | G/C | — | uncertain significance |
| rs776130320 | 7:117,067,501 | G/C | — | uncertain significance |
| rs749959101 | 7:117,067,507 | G/C | — | uncertain significance |
| rs7808424 | 7:117,067,822 | T/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.