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Symbol
Name
ID

Tomt
transmembrane O-methyltransferase
MGI:3769724

Phenotype annotations related to hearing/vestibular/ear

Darker colors indicate more annotations

Human Phenotypes	Abnormal vestibular function	Congenital sensorineural hearing impairment
Disease(s) Associated with LRTOMT	Abnormal vestibular function	Congenital sensorineural hearing impairment
autosomal recessive nonsyndromic deafness 63

Mouse Phenotypes		abnormal orientation of cochlear hair cell stereociliary bundles	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	organ of Corti degeneration	increased or absent threshold for auditory brainstem response	absent distortion product otoacoustic emissions	deafness
Availability	Mouse Genotype
	Tomt^m1Btlr/Tomt^m1Btlr

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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