Cgn Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cgn
cingulin
MGI:1927237

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cgn^tm1.1Citi/Cgn^tm1.1Citi B6.129-Cgn^tm1.1Citi	normal digestive/alimentary phenotype	J:200284
	increased susceptibility to injury	J:200284
	intestinal ulcer	J:200284
Cgn^{tm1b(KOMP)Wtsi}/Cgn^{tm1b(KOMP)Wtsi} B6N(Cg)-Cgn^{tm1b(KOMP)Wtsi}/J	abnormal embryo size	J:211773
	abnormal forebrain morphology	J:211773
	abnormal neural tube closure	J:211773
	abnormal tail morphology	J:211773
	cyanosis	J:211773
	hemorrhage	J:211773
	preweaning lethality, complete 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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