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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Cetn2
centrin 2
MGI:1347085
16 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Cetn2tm1.1Wbae/Cetn2+
Cetn3tm1a(EUCOMM)Wtsi/Cetn3tm1a(EUCOMM)Wtsi
involves: 129 * C57BL/6J * C57BL/6N * FVB/N 		abnormal rod electrophysiology J:275959
decreased b-wave amplitude J:275959
Cetn2tm1.1Wbae/Y
Cetn3tm1a(EUCOMM)Wtsi/Cetn3tm1a(EUCOMM)Wtsi
involves: 129 * C57BL/6J * C57BL/6N * FVB/N 		abnormal cone electrophysiology J:275959
abnormal photoreceptor connecting cilium morphology J:275959
abnormal photoreceptor outer segment diameter J:275959
abnormal photoreceptor outer segment disc membrane morphology J:275959
abnormal retina cone cell outer segment morphology J:275959
abnormal rod electrophysiology J:275959
decreased a-wave amplitude J:275959
decreased b-wave amplitude J:275959
decreased litter size J:275959
disorganized photoreceptor outer segment J:275959
dysosmia J:275959
hydrocephaly J:275959
prenatal lethality, incomplete penetrance J:275959
retina photoreceptor degeneration J:275959
short photoreceptor outer segment J:275959
thin retina outer nuclear layer J:275959
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory