SPATA33
spermatogenesis associated 33
Summary
Predicted to be involved in mitophagy. Predicted to act upstream of or within fertilization; flagellated sperm motility; and protein localization. Predicted to be located in male germ cell nucleus and sperm mitochondrial sheath. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants23 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs142356394 | 16:89,724,213 | G/T | — | uncertain significance |
| rs751840485 | 16:89,724,217 | C/T | — | uncertain significance |
| rs753224788 | 16:89,724,235 | G/C | — | uncertain significance |
| rs983465542 | 16:89,724,241 | T/C | — | uncertain significance |
| rs370564618 | 16:89,724,668 | A/G | — | uncertain significance |
| rs759041299 | 16:89,724,672 | G/C | — | uncertain significance |
| rs776726821 | 16:89,724,713 | T/G | — | uncertain significance |
| rs770080204 | 16:89,724,721 | C/T | — | uncertain significance |
| rs780150367 | 16:89,724,775 | C/T | — | uncertain significance |
| rs371560786 | 16:89,724,808 | C/T | — | likely benign |
| rs139902569 | 16:89,729,248 | C/G | upstream gene variant | — |
| rs542341099 | 16:89,734,530 | G/A | — | — |
| rs376966711 | 16:89,735,722 | C/A | — | uncertain significance |
| rs199540350 | 16:89,735,749 | C/G | — | uncertain significance |
| rs1010716610 | 16:89,735,766 | C/T | — | uncertain significance |
| rs200969086 | 16:89,735,773 | G/C | — | uncertain significance |
| rs147495310 | 16:89,735,775 | C/T | — | uncertain significance |
| rs1597809593 | 16:89,735,784 | G/C | — | uncertain significance |
| rs745572164 | 16:89,735,802 | G/A | — | uncertain significance |
| rs574253442 | 16:89,735,850 | G/A | — | uncertain significance |
| rs114292682 | 16:89,735,852 | C/T | — | uncertain significance |
| rs541395243 | 16:89,735,865 | C/T | — | uncertain significance |
| rs35063026 | 16:89,736,157 | C/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.