Slitrk6 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slitrk6
SLIT and NTRK-like family, member 6
MGI:2443198

21 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slitrk6^tm1.1Jaru/Slitrk6^tm1.1Jaru B6.129P2-Slitrk6^tm1.1Jaru	abnormal cochlear hair cell morphology	J:155405
	abnormal cochlear IHC afferent innervation pattern	J:155405
	abnormal cochlear IHC efferent innervation pattern	J:155405
	abnormal cochlear OHC efferent innervation pattern	J:155405
	abnormal crista ampullaris morphology	J:155405
	abnormal crista ampullaris neuroepithelium morphology	J:155405
	abnormal lens morphology	J:201352
	abnormal neuron physiology	J:155405
	abnormal retina morphology	J:201352
	deafness	J:201352
	myopia	J:201352
	small cochlear ganglion	J:155405
	small vestibular ganglion	J:155405
Slitrk6^tm1.1Jaru/Slitrk6^tm1.1Jaru involves: 129P2/OlaHsd	abnormal behavior	J:169557
	abnormal vertical vestibuloocular reflex	J:169557
	normal behavior/neurological phenotype	J:169557
	decreased body weight	J:169557
	decreased locomotor activity	J:169557
	decreased startle reflex	J:169557
	hyperactivity	J:169557
	increased or absent threshold for auditory brainstem response	J:169557

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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