Spata32 | spermatogenesis associated 32
Physiological systems
10 / 24 physiological systems tested
10 No significant impact
14 Not tested
Data collections
Gene metrics:0Significant phenotypes
0Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues
Human diseases caused by Spata32 mutations
The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.
Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.
External links
No external links available for Spata32.
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