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Symbol
Name
ID

Adamts10
ADAM metallopeptidase with thrombospondin type 1 motif 10
MGI:2449112

Phenotype annotations related to vision/eye

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Microspherophakia	Cataract	Ectopia lentis	High myopia	Visual loss	Glaucoma
Disease(s) Associated with ADAMTS10
Weill-Marchesani syndrome

Mouse Phenotypes		vision/eye phenotype	abnormal ciliary body morphology	abnormal ciliary process morphology	abnormal cilary zonule morphology	increased cornea thickness	decreased eye anterior chamber depth	abnormal vitreous body morphology
Availability	Mouse Genotype	vision/eye phenotype	abnormal ciliary body morphology	abnormal ciliary process morphology	abnormal cilary zonule morphology	increased cornea thickness	decreased eye anterior chamber depth	abnormal vitreous body morphology
	Adamts10^em1Cbal/Adamts10^em1Cbal
	Adamts10^em1Jku/Adamts10^em1Jku	*
	Adamts10^tm1Dgen/Adamts10^tm1Dgen

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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