About Help FAQ

Symbol
Name
ID

Vsx1
visual system homeobox 1
MGI:1890816

Phenotype annotations related to vision/eye

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

Human Phenotypes

Anterior synechiae of the anterior chamber

Abnormal corneal endothelium morphology

Abnormal Descemet membrane morphology

Thinning of Descemet membrane

Polymorphous posterior corneal dystrophy

Band keratopathy

Keratoconus

Astigmatism

Corneal opacity

Ectopia pupillae

Iris atrophy

Uveal ectropion

Photophobia

Glaucoma

Epiphora

Disease(s) Associated with VSX1

keratoconus

posterior polymorphous corneal dystrophy 1

Mouse Phenotypes		vision/eye phenotype	abnormal retina cone bipolar cell morphology	abnormal eye electrophysiology	abnormal cone electrophysiology
Availability	Mouse Genotype	vision/eye phenotype	abnormal retina cone bipolar cell morphology	abnormal eye electrophysiology	abnormal cone electrophysiology
	Vsx1^tm1Bhr/Vsx1^tm1Bhr	*
	Vsx1^tm1Mci/Vsx1^tm1Mci	*
	Vsx1^tm2Mci/Vsx1^tm2Mci	*
	Vsx1^tm1Bhr/Vsx1^tm2Bhr	*

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 07/08/2026 MGI 6.24