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Symbol
Name
ID

Ovol2
ovo like zinc finger 2
MGI:1338039

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Photophobia
Disease(s) Associated with OVOL2	Photophobia
posterior polymorphous corneal dystrophy 1

Mouse Phenotypes		abnormal embryonic neuroepithelium morphology	increased embryonic neuroepithelium thickness	incomplete rostral neuropore closure	open neural tube	spina bifida	abnormal forebrain development	decreased embryonic neuroepithelial cell proliferation
Availability	Mouse Genotype	abnormal embryonic neuroepithelium morphology	increased embryonic neuroepithelium thickness	incomplete rostral neuropore closure	open neural tube	spina bifida	abnormal forebrain development	decreased embryonic neuroepithelial cell proliferation
	Ovol2^tm1Sito/Ovol2^tm1Sito
	Ovol2^tm1Xdai/Ovol2^tm1Xdai

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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