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Symbol
Name
ID
Slitrk6
SLIT and NTRK-like family, member 6
MGI:2443198
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Sensorineural hearing impairment
Disease(s) Associated with SLITRK6
high myopia-sensorineural deafness syndrome

Mouse Phenotypes
abnormal vertical vestibuloocular reflex
abnormal cochlear hair cell morphology
abnormal cochlear IHC afferent innervation pattern
abnormal cochlear IHC efferent innervation pattern
abnormal cochlear OHC efferent innervation pattern
abnormal crista ampullaris morphology
abnormal crista ampullaris neuroepithelium morphology
increased or absent threshold for auditory brainstem response
deafness
Availability Mouse Genotype
Slitrk6tm1.1Jaru/Slitrk6tm1.1Jaru

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory