About   Help   FAQ
Symbol
Name
ID
Dlx5
distal-less homeobox 5
MGI:101926
Phenotype annotations related to nervous system
!Indicates phenotype varies with strain background.
Darker colors indicate more annotations
Human Phenotypes
Intellectual disability
Disease(s) Associated with DLX5
split hand-foot malformation 1

Mouse Phenotypes
abnormal axon extension
absent vomeronasal organ
small vomeronasal organ
open neural tube
abnormal brain development
abnormal rostral migratory stream morphology
abnormal olfactory bulb morphology
abnormal olfactory bulb granule cell morphology
abnormal olfactory bulb periglomerular cell morphology
abnormal mitral cell morphology
small olfactory bulb
abnormal sensory neuron innervation pattern
anencephaly
exencephaly
abnormal GABAergic neuron morphology
small trigeminal ganglion
abnormal olfactory nerve morphology
Availability Mouse Genotype
Dlx5/Dlx6tm1Levi/Dlx5/Dlx6tm1Levi
Dlx5tm1Jlr/Dlx5tm1Jlr
Dlx5tm1Levi/Dlx5tm1Levi
Dlx5tm1Jlr/Dlx5+ !

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory