Symbol Name ID |
Vsx1
visual system homeobox 1 MGI:1890816 |
* | 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 |
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Availability | Mouse Genotype | ||||
Vsx1tm1Bhr/Vsx1tm1Bhr | * | ||||
Vsx1tm1Mci/Vsx1tm1Mci | * | ||||
Vsx1tm2Mci/Vsx1tm2Mci | * | ||||
Vsx1tm1Bhr/Vsx1tm2Bhr | * |
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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last database update 04/16/2024 MGI 6.23 |
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