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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cetn2
centrin 2
MGI:1347085
17 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cetn2tm1.1Wbae/Y
involves: 129 * FVB/N
abnormal brain ependyma motile cilium location or orientation J:211061
abnormal cerebrospinal fluid flow J:211061
abnormal olfactory epithelium cilium morphology J:211061
abnormal olfactory sensory neuron morphology J:211061
normal cellular phenotype J:211061
decreased body weight J:211061
dilated brain ventricle J:211061
dilated lateral ventricle J:211061
domed cranium J:211061
dysosmia J:211061
hydrocephaly J:211061
impaired olfaction J:211061
premature death J:211061
prenatal lethality, incomplete penetrance J:275959
normal vision/eye phenotype J:211061
weight loss J:211061
Cetn2tm1.1Wbae/Y
Tg(CAG-EGFP/CETN2)3-4Jgg/0
involves: 129 * BALB/c * C57BL/6 * FVB/N
no abnormal phenotype detected J:211061

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
04/09/2024
MGI 6.23
The Jackson Laboratory