Cetn2 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cetn2
centrin 2
MGI:1347085

16 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Cetn2^tm1.1Wbae/Cetn2⁺ Cetn3^{tm1a(EUCOMM)Wtsi}/Cetn3^{tm1a(EUCOMM)Wtsi} involves: 129 * C57BL/6J * C57BL/6N * FVB/N	abnormal rod electrophysiology	J:275959
	decreased b-wave amplitude	J:275959
Cetn2^tm1.1Wbae/Y Cetn3^{tm1a(EUCOMM)Wtsi}/Cetn3^{tm1a(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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