Spem2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Spem2
SPEM family member 2
MGI:1918293

24 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Spem2^em1Smoc/Spem2^em1Smoc C57BL/6JSmoc-Spem2^em1Smoc/Smoc	abnormal acrosome assembly	J:354200
	abnormal acrosome morphology	J:354200
	abnormal sperm head morphology	J:354200
	abnormal sperm individualization	J:354200
	abnormal sperm midpiece morphology	J:354200
	abnormal sperm mitochondrial morphology	J:354200
	abnormal sperm nucleus morphology	J:354200
	abnormal sperm-egg fusion	J:354200
	abnormal spermatid morphology	J:354200
	abnormal spermiation	J:354200
	abnormal spermiogenesis	J:354200
	asthenozoospermia	J:354200
	decreased fertilization frequency	J:354200
	disorganized sperm mitochondrial sheath	J:354200
	normal homeostasis/metabolism phenotype	J:354200
	impaired acrosome reaction	J:354200
	impaired fertilization	J:354200
	impaired sperm migration in female genital tract	J:354200
	male infertility	J:354200
	multi-headed sperm	J:354200
	multiflagellated sperm	J:354200
	oligozoospermia	J:354200
	normal reproductive system phenotype	J:354200
	teratozoospermia	J:354200

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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