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Symbol
Name
ID
Alx3
aristaless-like homeobox 3
MGI:1277097
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Anterior basal encephalocele
Cranium bifidum occultum
Pericallosal lipoma
Agenesis of corpus callosum
Intellectual disability
Disease(s) Associated with ALX3
frontonasal dysplasia 1

Mouse Phenotypes
abnormal embryonic neuroepithelium morphology
open neural tube
exencephaly
Availability Mouse Genotype
Alx3tm1Hubr/Alx3tm1Hubr

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
04/23/2024
MGI 6.23
The Jackson Laboratory