Symbol Name ID |
Dcx
doublecortin MGI:1277171 |
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 |
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Availability | Mouse Genotype | |||||||
Dcxtm1Caw/Dcx+ | ||||||||
Dcxtm1.2Ffr/Y | ||||||||
Dcxtm1Caw/Y |
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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