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SPATA32

spermatogenesis associated 32

HCNC Approved Symbol
SPATA32 (HGNC:26349)
Genomic Coordinates
: - (17q21.31)
Synonyms
FLJ25414, AEP2, VAD1.2, C17orf46, TEX34
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SPATA32 - Gene browser | 3billion