Cldn19 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cldn19
claudin 19
MGI:3033992

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cldn19^{tm1.1(KOMP)Vlcg}/Cldn19^{tm1.1(KOMP)Vlcg} B6N(Cg)-Cldn19^{tm1.1(KOMP)Vlcg}/J	abnormal sleep behavior	J:211773
	decreased circulating free fatty acids level	J:211773
	increased circulating sodium level	J:211773
	increased heart weight	J:211773
	shortened PQ interval	J:211773
	shortened PR interval	J:211773
	shortened ST segment	J:211773
Cldn19^tm1Sts/Cldn19^tm1Sts involves: 129S4/SvJae * C57BL/6	abnormal gait	J:99659
	abnormal Schwann cell morphology	J:99659
	impaired coordination	J:99659

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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