Cldn9 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cldn9
claudin 9
MGI:1913100

11 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cldn9^em1(IMPC)H/Cldn9^em1(IMPC)H C57BL/6NTac-Cldn9^em1(IMPC)H/H	abnormal startle reflex	J:211773
	increased basophil cell number	J:211773
Cldn9^nmf329/Cldn9^nmf329 C57BL/6J-Cldn9^nmf329/J	abnormal organ of Corti morphology	J:152154
	abnormal perilymph physiology	J:152154
	absent startle reflex	J:87349, J:152154
	normal behavior/neurological phenotype	J:152154
	cochlear outer hair cell degeneration	J:152154
	deafness	J:87349, J:152154
	decreased cochlear outer hair cell number	J:152154
	decreased outer hair cell stereocilia number	J:152154
	increased or absent threshold for auditory brainstem response	J:87349, J:152154

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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