Symbol Name ID |
Cux2
cut-like homeobox 2 MGI:107321 |
Darker colors indicate more annotations |
Human Phenotypes | Cerebellar atrophy |
Athetosis |
EEG abnormality |
Hypsarrhythmia |
Reduced eye contact |
Recurrent hand flapping |
Intellectual disability |
Dyskinesia |
Dystonia |
Gait disturbance |
Epileptic encephalopathy |
Developmental regression |
Global developmental delay |
Bilateral tonic-clonic seizure |
Generalized non-motor (absence) seizure |
Focal hemiclonic seizure |
Generalized myoclonic seizure |
Atonic seizure |
Tonic seizure |
Disease(s) Associated with CUX2 | |||||||||||||||||||
developmental and epileptic encephalopathy 67 |
Mouse Phenotypes | abnormal neuronal precursor proliferation |
abnormal neural tube morphology |
abnormal neural tube marginal layer morphology |
abnormal neural tube ventricular layer morphology |
increased brain size |
abnormal cerebral cortex morphology |
abnormal neocortex morphology |
thickened cerebral cortex |
abnormal embryonic/fetal subventricular zone morphology |
increased neuron number |
abnormal spinal cord interneuron morphology |
abnormal ventral spinal root morphology |
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Availability | Mouse Genotype | ||||||||||||
Cux2Gt(OST440231)Lex/Cux2Gt(OST440231)Lex | |||||||||||||
Cux2tm1.1Nieto/Cux2tm1.1Nieto |
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 08/02/2024 MGI 6.24 |
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