Cldn13 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cldn13
claudin 13
MGI:1913102

12 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cldn13^em1(IMPC)J/Cldn13^em1(IMPC)J C57BL/6NJ-Cldn13^em1(IMPC)J/J	abnormal coat/hair pigmentation	J:211773
	abnormal startle reflex	J:211773
	decreased fasting circulating glucose level	J:211773
	decreased grip strength	J:211773
	increased circulating alanine transaminase level	J:211773
	persistence of hyaloid vascular system	J:211773
Cldn13^{tm1.1(KOMP)Vlcg}/Cldn13^{tm1.1(KOMP)Vlcg} B6N(Cg)-Cldn13^{tm1.1(KOMP)Vlcg}/J	decreased blood urea nitrogen level	J:211773
	decreased fasting circulating glucose level	J:211773
	decreased mean corpuscular volume	J:211773
	increased circulating potassium level	J:211773
	increased circulating sodium level	J:211773
	increased erythrocyte cell number	J:211773
	increased hemoglobin content	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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