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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Dcun1d1Gt(RRR261)Byg/Dcun1d1Gt(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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last database update
05/28/2024
MGI 6.13
The Jackson Laboratory