Symbol Name ID |
Vax1
ventral anterior homeobox 1 MGI:1277163 |
Darker colors indicate more annotations |
Human Phenotypes | Agenesis of pineal gland |
Agenesis of corpus callosum |
Hippocampal malrotation |
Global developmental delay |
Disease(s) Associated with VAX1 | ||||
syndromic microphthalmia 11 |
Mouse Phenotypes | abnormal neuron differentiation |
abnormal axon guidance |
abnormal pituitary gland morphology |
abnormal forebrain development |
abnormal telencephalon development |
abnormal olfactory bulb development |
abnormal rostral migratory stream morphology |
holoprosencephaly |
lobar holoprosencephaly |
decreased forebrain size |
abnormal lateral ventricle morphology |
abnormal corpus callosum morphology |
absent corpus callosum |
abnormal anterior commissure morphology |
abnormal hypothalamus morphology |
abnormal olfactory bulb morphology |
abnormal postnatal subventricular zone morphology |
abnormal ependyma morphology |
abnormal optic nerve innervation |
abnormal lateral ganglionic eminence morphology |
abnormal optic nerve morphology |
absent optic chiasm |
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Availability | Mouse Genotype | ||||||||||||||||||||||
Vax1tm1Grl/Vax1tm1Grl | |||||||||||||||||||||||
Vax1tm1Pgr/Vax1tm1Pgr |
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 04/30/2024 MGI 6.23 |
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