Tomt Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Tomt
transmembrane O-methyltransferase
MGI:3769724

16 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tomt^m1Btlr/Tomt^m1Btlr C57BL/6J-Tomt^m1Btlr	abnormal orientation of cochlear hair cell stereociliary bundles	J:137493
	absent distortion product otoacoustic emissions	J:137493
	absent startle reflex	J:137493
	bidirectional circling	J:137493
	cochlear ganglion degeneration	J:137493
	cochlear inner hair cell degeneration	J:137493
	cochlear outer hair cell degeneration	J:137493
	deafness	J:137493
	decreased body weight	J:137493
	head tossing	J:137493
	hyperactivity	J:137493
	impaired balance	J:137493
	increased aggression towards male mice	J:137493
	increased or absent threshold for auditory brainstem response	J:137493
	normal nervous system phenotype	J:137493
	organ of Corti degeneration	J:137493
Tomt^m1Btlr/Tomt^m1Btlr involves: C3H/HeN * C57BL/6J	bidirectional circling	J:137493
	decreased body weight	J:137493
	head tossing	J:137493
	hyperactivity	J:137493
	increased aggression towards male mice	J:137493

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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