Symbol Name ID |
Vsx2
visual system homeobox 2 MGI:88401 |
Darker colors indicate more annotations |
Human Phenotypes | Opacification of the corneal stroma |
Microphthalmia |
Disease(s) Associated with VSX2 | ||
isolated microphthalmia 2 |
Mouse Phenotypes | abnormal hyaloid artery morphology |
lacrimal gland hypertrophy |
abnormal retina ganglion cell morphology |
abnormal optic nerve morphology |
absent optic chiasm |
absent optic nerve |
abnormal retina pigment epithelium morphology |
abnormal retina pigmentation |
decreased eye pigmentation |
abnormal eye morphology |
abnormal lens morphology |
abnormal lens development |
small lens |
abnormal eye development |
abnormal optic cup morphology |
abnormal optic fissure morphology |
abnormal optic stalk morphology |
abnormal retina development |
abnormal retina progenitor cell morphology |
microphthalmia |
eyelids fail to open |
abnormal retina morphology |
disorganized retina layers |
decreased total retina thickness |
abnormal vitreous body morphology |
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Availability | Mouse Genotype | |||||||||||||||||||||||||
Vsx2or-2J/Vsx2or-2J | ||||||||||||||||||||||||||
Vsx2or-J/Vsx2or-J | ||||||||||||||||||||||||||
Vsx2or/Vsx2or | ||||||||||||||||||||||||||
Vsx2tm1.1Eml/Vsx2tm1.1Eml | ||||||||||||||||||||||||||
Vsx2tm1.1Itl/Vsx2tm1.1Itl | ||||||||||||||||||||||||||
Vsx2or-J/Vsx2tm1.1Eml |
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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