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.