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Symbol
Name
ID
Dcx
doublecortin
MGI:1277171
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Spasticity
Lateral ventricle dilatation
Hydrocephalus
Ventriculomegaly
Lissencephaly
Agyria
Pachygyria
Subcortical band heterotopia
Polymicrogyria
Agenesis of corpus callosum
Hypoplastic hippocampus
Gray matter heterotopia
Ataxia
Dysarthria
Atypical behavior
Intellectual disability
Intellectual disability, severe
Sleep abnormality
Global developmental delay
Profound global developmental delay
Motor delay
Seizure
Disease(s) Associated with DCX
subcortical band heterotopia
X-linked lissencephaly 1

Mouse Phenotypes
abnormal rostral migratory stream morphology
abnormal brain interneuron morphology
abnormal hippocampus morphology
abnormal hippocampus CA3 region morphology
abnormal hippocampal mossy fiber morphology
abnormal hippocampus pyramidal cell layer
abnormal inhibitory postsynaptic currents
Availability Mouse Genotype
Dcxtm1Caw/Dcx+
Dcxtm1.2Ffr/Y
Dcxtm1Caw/Y

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