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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ccdc25
coiled-coil domain containing 25
MGI:1914429
12 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Ccdc25em1(IMPC)Mbp/Ccdc25+
C57BL/6N-Ccdc25em1(IMPC)Mbp/MbpMmucd
abnormal liver morphology J:211773
abnormal retina morphology J:211773
abnormal vitreous body morphology J:211773
absent optic nerve J:211773
cataract J:211773
enlarged heart J:211773
impaired glucose tolerance J:211773
no spontaneous movement J:211773
small spleen J:211773
Ccdc25em1(IMPC)Mbp/Ccdc25em1(IMPC)Mbp
C57BL/6N-Ccdc25em1(IMPC)Mbp/MbpMmucd
abnormal placenta morphology J:211773
abnormal placenta vasculature J:211773
no spontaneous movement J:211773
preweaning lethality, incomplete penetrance J:211773

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
11/19/2024
MGI 6.24
The Jackson Laboratory