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Symbol
Name
ID
Vax1
ventral anterior homeobox 1
MGI:1277163
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Vax1tm1Grl/Vax1tm1Grl
Vax1tm1Pgr/Vax1tm1Pgr

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory