Dcun1d1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Dcun1d1
defective in cullin neddylation 1 domain containing 1
MGI:2150386

16 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Dcun1d1^{Gt(RRR261)Byg}/Dcun1d1^{Gt(RRR261)Byg} involves: 129P2/OlaHsd	abnormal sperm flagellum morphology	J:270036
	abnormal sperm head morphology	J:270036
	abnormal spermatogenesis	J:270036
	abnormal spermiogenesis	J:270036
	asthenozoospermia	J:270036
	decreased body size	J:262901, J:270036
	decreased fibroblast proliferation	J:262901
	decreased survivor rate	J:270036
	globozoospermia	J:270036
	lymphoid hypoplasia	J:262901
	male infertility	J:270036
	oligozoospermia	J:270036
	seminiferous tubule degeneration	J:270036
	spleen hypoplasia	J:262901
	teratozoospermia	J:270036
	testicular atrophy	J:270036

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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