Cct2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cct2
chaperonin containing TCP1 subunit 2
MGI:107186

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cct2^em1Itwa/Cct2⁺ involves: C57BL/6J	normal vision/eye phenotype	J:358007
Cct2^em1Itwa/Cct2^em1Itwa Not Specified	prenatal lethality, complete penetrance	J:358007
Cct2^em1Itwa/Cct2^em2Itwa involves: C57BL/6J	abnormal retina cone cell morphology	J:358007
	abnormal retina outer nuclear layer morphology	J:358007
	postnatal lethality, complete penetrance	J:358007
Cct2^em2Itwa/Cct2^em2Itwa involves: C57BL/6J	abnormal a-wave shape	J:358007
	abnormal electroretinogram waveform feature	J:358007
	abnormal photoreceptor connecting cilium morphology	J:358007
	retina outer nuclear layer degeneration	J:358007
	retina photoreceptor degeneration	J:358007

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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