About Help FAQ

Symbol
Name
ID

Tomt
transmembrane O-methyltransferase
MGI:3769724

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Abnormal fundus morphology
Disease(s) Associated with LRTOMT	Abnormal fundus morphology
autosomal recessive nonsyndromic deafness 63

Mouse Phenotypes		abnormal retina blood vessel morphology	abnormal retina morphology	anophthalmia
Availability	Mouse Genotype	abnormal retina blood vessel morphology	abnormal retina morphology	anophthalmia
	Lrrc51^{tm1b(EUCOMM)Hmgu}/Lrrc51^{tm1b(EUCOMM)Hmgu}
	Tomt^em1(IMPC)Tcp/Tomt^em1(IMPC)Tcp

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 07/14/2026 MGI 6.24