SPATA2
spermatogenesis associated 2
Summary
Enables signaling receptor complex adaptor activity and ubiquitin-specific protease binding activity. Involved in several processes, including protein deubiquitination; regulation of necroptotic process; and regulation of tumor necrosis factor-mediated signaling pathway. Located in cytoplasm; fibrillar center; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs147213348 | 20:48,522,167 | C/T | — | uncertain significance |
| rs2515605299 | 20:48,522,248 | G/C | — | uncertain significance |
| rs377592515 | 20:48,522,325 | C/T | — | uncertain significance |
| rs495337 | 20:48,522,330 | G/A | synonymous variant | — |
| rs2515605631 | 20:48,522,377 | A/T | — | uncertain significance |
| rs370232950 | 20:48,522,395 | G/A | — | uncertain significance |
| rs757810263 | 20:48,522,398 | C/T | — | uncertain significance |
| rs758496582 | 20:48,522,409 | G/T | — | uncertain significance |
| rs771563644 | 20:48,522,443 | C/T | — | uncertain significance |
| rs201467660 | 20:48,522,530 | G/A | — | uncertain significance |
| rs745616123 | 20:48,522,608 | G/A | — | uncertain significance |
| rs199677367 | 20:48,522,625 | T/C | — | uncertain significance |
| rs1272597831 | 20:48,522,628 | G/C | — | uncertain significance |
| rs777508744 | 20:48,522,722 | C/G | — | uncertain significance |
| rs775035283 | 20:48,522,736 | T/C | — | uncertain significance |
| rs775466543 | 20:48,522,743 | C/T | — | likely benign |
| rs764318852 | 20:48,522,745 | C/T | — | uncertain significance |
| rs183875038 | 20:48,522,793 | G/C | — | uncertain significance |
| rs757002791 | 20:48,522,811 | C/T | — | uncertain significance |
| rs2515606860 | 20:48,522,816 | C/A | — | uncertain significance |
| rs151336494 | 20:48,522,859 | A/G | — | uncertain significance |
| rs561055492 | 20:48,522,866 | C/T | — | uncertain significance |
| rs140549434 | 20:48,522,877 | G/A | — | uncertain significance |
| rs2515607042 | 20:48,522,881 | C/A | — | uncertain significance |
| rs2515607100 | 20:48,522,904 | A/C | — | uncertain significance |
| rs150044824 | 20:48,522,928 | C/T | — | uncertain significance |
| rs1241924805 | 20:48,522,961 | G/A | — | uncertain significance |
| rs753167164 | 20:48,523,030 | A/G | — | uncertain significance |
| rs193290030 | 20:48,523,085 | G/A | — | uncertain significance |
| rs753009677 | 20:48,523,091 | C/T | — | uncertain significance |
| rs2515607635 | 20:48,523,125 | C/A | — | uncertain significance |
| rs868504150 | 20:48,523,151 | C/T | — | uncertain significance |
| rs750485207 | 20:48,523,174 | T/C | — | uncertain significance |
| rs2515607827 | 20:48,523,208 | C/T | — | uncertain significance |
| rs765803229 | 20:48,523,291 | T/A | — | uncertain significance |
| rs201830184 | 20:48,523,309 | C/A | — | uncertain significance |
| rs753627563 | 20:48,523,334 | C/T | — | uncertain significance |
| rs778762862 | 20:48,523,355 | C/T | — | uncertain significance |
| rs199990371 | 20:48,524,745 | C/T | — | uncertain significance |
| rs150565930 | 20:48,524,766 | C/T | — | uncertain significance |
| rs750170146 | 20:48,524,780 | C/T | — | uncertain significance |
| rs373260117 | 20:48,524,803 | G/A | — | likely benign |
| rs559326954 | 20:48,524,844 | G/A | — | uncertain significance |
| rs2146831867 | 20:48,524,898 | C/T | — | uncertain significance |
| rs757636727 | 20:48,524,900 | C/T | — | uncertain significance |
| rs912432094 | 20:48,524,915 | C/T | — | uncertain significance |
| rs77667957 | 20:48,524,979 | G/A | — | uncertain significance |
| rs3787331 | 20:48,533,576 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.