Cldn1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cldn1
claudin 1
MGI:1276109

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cldn1^{tm1b(NCOM)Mfgc}/Cldn1⁺ C57BL/6N-Cldn1^{tm1b(NCOM)Mfgc}/Tcp	abnormal retina morphology	J:211773
Cldn1^{tm1b(NCOM)Mfgc}/Cldn1^{tm1b(NCOM)Mfgc} C57BL/6N-Cldn1^{tm1b(NCOM)Mfgc}/Tcp	preweaning lethality, complete penetrance	J:211773
Cldn1^tm1Sts/Cldn1^tm1Sts involves: 129S4/SvJae * C57BL/6	abnormal hair growth	J:75447
	dehydration	J:75447
	hyperkeratosis	J:75447
	impaired skin barrier function	J:75447
	neonatal lethality, complete penetrance	J:75447
	thick epidermis	J:75447
	weight loss	J:75447
	wrinkled skin	J:75447

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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