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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
Congenital sensorineural hearing impairment
Disease(s) Associated with LRTOMT
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
Tomtm1Btlr/Tomtm1Btlr

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/13/2019
MGI 6.13
The Jackson Laboratory