Slc7a14 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc7a14
solute carrier family 7 (cationic amino acid transporter, y+ system), member 14
MGI:3040688

12 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc7a14^em1Jin/Slc7a14^em1Jin C57BL/6J-Slc7a14^em1Jin	absent cochlear inner hair cells	J:323825
	absent inner hair cell stereocilia	J:323825
	decreased inner hair cell stereocilia number	J:323825
	decreased total retina thickness	J:323825
	fused inner hair cell stereocilia	J:323825
	normal hearing/vestibular/ear phenotype	J:323825
	increased or absent threshold for auditory brainstem response	J:323825
	sensorineural hearing loss	J:323825
	short photoreceptor outer segment	J:323825
Slc7a14^em1Jqu/Slc7a14^em1Jqu C57BL/6-Slc7a14^em1Jqu	abnormal eye electrophysiology	J:225228
	abnormal rod electrophysiology	J:225228
	absent inner hair cell stereocilia	J:323825
	decreased inner hair cell stereocilia number	J:323825
	decreased total retina thickness	J:225228
	fused inner hair cell stereocilia	J:323825
	normal hearing/vestibular/ear phenotype	J:323825
	increased or absent threshold for auditory brainstem response	J:323825
	sensorineural hearing loss	J:323825
	thin retina outer nuclear layer	J:225228

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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