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Symbol
Name
ID

Mettl5
methyltransferase 5, N6-adenosine
MGI:1922672

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Strabismus
Disease(s) Associated with METTL5	Strabismus
autosomal recessive intellectual developmental disorder 72

Mouse Phenotypes		abnormal retina vasculature morphology	abnormal optic disk morphology	abnormal iris morphology	iris synechia	abnormal cornea morphology	abnormal lens morphology	cataract	persistence of hyaloid vascular system	abnormal retina morphology	abnormal vitreous body morphology
Availability	Mouse Genotype	abnormal retina vasculature morphology	abnormal optic disk morphology	abnormal iris morphology	iris synechia	abnormal cornea morphology	abnormal lens morphology	cataract	persistence of hyaloid vascular system	abnormal retina morphology	abnormal vitreous body morphology
	Mettl5^{em1(IMPC)Hmgu}/Mettl5^{em1(IMPC)Hmgu}
	Mettl5^em1Schne/Mettl5^em1Schne

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 04/16/2024 MGI 6.23